# terms

id: GO:0043898
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,3-dihydroxybiphenyl + O2 = 2-hydroxy-6-phenylhexa-2,4-dienoic acid.","definition_xrefs":["PMID:15715866","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen","termid":"GO:0016702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2,3-dihydroxybiphenyl 1,2-dioxygenase activity","synonyms":[{"name":"2,3-dihydroxybiphenyl-1,2-dioxygenase activity","type":"exact"},{"name":"BphC","type":"related"}],"termid":"GO:0043898"}


id: PBO:0049983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypoxia inducible lipid droplet associated","termid":"PBO:0049983"}


id: PBO:0060753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B3 pseudogene 3","termid":"PBO:0060753"}


id: GO:0047627
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5'-adenylyl sulfate + H2O = AMP + 2 H+ + sulfate.","definition_xrefs":["RHEA:17041","EC:3.6.2.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid anhydrides, in sulfonyl-containing anhydrides","termid":"GO:0016819"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"adenylylsulfatase activity","secondary_identifiers":["MetaCyc:ADENYLYLSULFATASE-RXN","KEGG_REACTION:R00531"],"synonyms":[{"name":"adenosine 5-phosphosulfate sulfohydrolase activity","type":"related"},{"name":"adenylylsulfate sulfohydrolase activity","type":"related"},{"name":"adenylylsulphatase activity","type":"exact"}],"termid":"GO:0047627"}


id: MONDO:0010075
data:
  {"annotated_genes":["SJAG_00183"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88532],"is_not":false,"summary":null,"term":"MONDO:0010075"}]},"cv_name":"mondo","definition":"Any spondyloepimetaphyseal dysplasia with joint laxity in which the cause of the disease is a mutation in the B3GALT6 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloepimetaphyseal dysplasia with joint laxity","termid":"MONDO:0019675"},{"relation_name":"is_a","term_name":"B3GALT6-congenital disorder of glycosylation","termid":"MONDO:0100586"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00183":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322","MONDO:0005497"],"is_obsolete":false,"name":"spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:271640","DOID:0112198","MEDGEN:865814","Orphanet:642099","UMLS:C4017377"],"synonyms":[{"name":"B3GALT6 spondyloepimetaphyseal dysplasia with joint laxity","type":"exact"},{"name":"SEMDJL","type":"broad"},{"name":"SEMDJL1","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia with JOINT laxity, type 1, with or without fractures","type":"related"},{"name":"spondyloepimetaphyseal dysplasia with joint laxity caused by mutation in B3GALT6","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia with joint laxity, Beighton type","type":"exact"},{"name":"spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures","type":"exact"}],"termid":"MONDO:0010075","terms_by_termid":{"MONDO:0010075":null},"xrefs":{"Monarch":{"xref_id":"0010075"}}}


id: FYPO:0000282
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A viability phenotype observed in the vegetative growth phase of the life cycle in which a cell is able to survive at a high temperature.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete viable cell at high temperature (obsolete FYPO:0000282)","synonyms":[{"name":"cell viable at high temperature","type":"exact"},{"name":"viable cell at high temperature during mitotic cell cycle","type":"related"},{"name":"viable cell at high temperature during vegetative growth","type":"exact"}],"termid":"FYPO:0000282"}


id: PBO:0040677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCAR1 pseudogene 2","termid":"PBO:0040677"}


id: GO:0051524
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell switches from bipolar cell growth to monopolar cell growth.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of monopolar cell polarity","termid":"GO:0061162"},{"relation_name":"is_a","term_name":"regulation of direction of cell growth","termid":"GO:0061389"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0008150","GO:0007163"],"is_obsolete":false,"name":"cell growth mode switching, bipolar to monopolar","termid":"GO:0051524"}


id: MONDO:0957456
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"dermatomyositis","termid":"MONDO:0016367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005336"],"is_obsolete":false,"name":"classical dermatomyositis","secondary_identifiers":["UMLS:C5816707","MEDGEN:1843411","Orphanet:645613"],"termid":"MONDO:0957456","xrefs":{"Monarch":{"xref_id":"0957456"}}}


id: GO:0016880
data:
  {"annotated_genes":["SJAG_04544","SJAG_01845","SJAG_00359"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78770],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017178"},{"annotations":[73214,61869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004356"}]},"cv_name":"molecular_function","definition":"Catalysis of the ligation of an acid to ammonia (NH3) or an amide via a carbon-nitrogen bond, with the concomitant hydrolysis of the diphosphate bond in ATP or a similar triphosphate.","definition_xrefs":["GOC:mah","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00359":null,"SJAG_01845":null,"SJAG_04544":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"acid-ammonia (or amide) ligase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"secondary_identifiers":["EC:6.3.1.-"],"synonyms":[{"name":"amide synthase activity","type":"exact"}],"termid":"GO:0016880","terms_by_termid":{"GO:0004356":null,"GO:0017178":null}}


id: PBO:0077261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane p24 trafficking protein 10 pseudogene 1","termid":"PBO:0077261"}


id: GO:0046376
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving GDP-alpha-D-mannosylchitobiosyldiphosphodolichol, a substance composed of mannosylchitobiosyldiphosphodolichol in glycosidic linkage with guanosine diphosphate.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid metabolic process","termid":"GO:0006644"},{"relation_name":"is_a","term_name":"glycolipid metabolic process","termid":"GO:0006664"},{"relation_name":"is_a","term_name":"terpenoid metabolic process","termid":"GO:0006721"},{"relation_name":"is_a","term_name":"nucleoside phosphate metabolic process","termid":"GO:0006753"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0006629","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"GDP-alpha-D-mannosylchitobiosyldiphosphodolichol metabolic process","synonyms":[{"name":"GDP-alpha-D-mannosylchitobiosyldiphosphodolichol metabolism","type":"exact"}],"termid":"GO:0046376"}


id: PBO:0051915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrin subunit beta 1 binding protein 2","termid":"PBO:0051915"}


id: GO:0034439
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of a lipoprotein by oxidation of the lipid group.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid oxidation","termid":"GO:0034440"},{"relation_name":"is_a","term_name":"lipoprotein oxidation","termid":"GO:0042161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"lipoprotein lipid oxidation","termid":"GO:0034439"}


id: GO:0043258
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A laminin complex composed of alpha4, beta2 and gamma1 polypeptide chains.","definition_xrefs":["PMID:10842354","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laminin complex","termid":"GO:0043256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"laminin-9 complex","synonyms":[{"name":"laminin-421 complex","type":"exact"}],"termid":"GO:0043258"}


id: GO:0015303
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: galactose or glucose(out) = galactose or glucose(in).","definition_xrefs":["TC:2.A.1.1.6"],"gene_count":0,"genotype_count":0,"name":"obsolete galactose, glucose uniporter activity (obsolete GO:0015303)","synonyms":[{"name":"galactose, glucose uniporter activity","type":"exact"}],"termid":"GO:0015303"}


id: MONDO:0020427
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Laubry-Pezzi syndrome is a rare, non-syndromic, congenital heart malformation characterized by the prolapse of an aortic valve cusp into a subjacent ventricular septal defect due to Venturi effect, resulting in aortic regurgitation. Patients typically present with symptoms of progressive aortic valve insufficiency, such as shortness of breath, heart palpitations, chest pain and exercise intolerance.","definition_xrefs":["Orphanet:99094"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital heart malformation","termid":"MONDO:0019512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Laubry-Pezzi syndrome","secondary_identifiers":["SCTID:764955006","UMLS:C4707235","MEDGEN:1643612","GARD:19646"],"synonyms":[{"name":"VSD with aortic insufficiency","type":"exact"},{"name":"ventricular septal defect with aortic insufficiency","type":"exact"}],"termid":"MONDO:0020427","xrefs":{"Monarch":{"xref_id":"0020427"}}}


id: MONDO:0044789
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma arising from the sweat glands. Most cases present as nodular lesions on the digits, usually in the hands. It is characterized by the presence of epithelial cells in the dermis forming nodules. Cystic structures containing papillary projections are also present. It may recur and metastasize, most commonly to the lungs.","definition_xrefs":["NCIT:C27534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary eccrine carcinoma","termid":"MONDO:0003531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"digital papillary eccrine carcinoma","secondary_identifiers":["ONCOTREE:ADPA","DOID:5590","UMLS:C1367789","MEDGEN:277955"],"synonyms":[{"name":"aggressive digital papillary adenocarcinoma","type":"exact"},{"name":"digit papillary eccrine carcinoma","type":"exact"},{"name":"digital papillary carcinoma","type":"exact"},{"name":"digital papillary carcinoma of skin","type":"exact"},{"name":"digital papillary eccrine carcinoma","type":"exact"},{"name":"papillary digital eccrine carcinoma","type":"exact"},{"name":"papillary eccrine carcinoma of digit","type":"exact"}],"termid":"MONDO:0044789","xrefs":{"Monarch":{"xref_id":"0044789"}}}


id: MONDO:0008340
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital ptosis is characterized by superior eyelid drop present at birth.","definition_xrefs":["Orphanet:91411"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ptosis","termid":"MONDO:0000728"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"ptosis, hereditary congenital, 1","secondary_identifiers":["UMLS:C1867438","MedDRA:10015996","NCIT:C27049","SCTID:268163008","HP:0007970","MESH:C566737","OMIM:178300","DOID:0060261","MEDGEN:357987","GARD:16798","ICD9:743.61"],"synonyms":[{"name":"PTOS1","type":"related"},{"name":"congenital eyelid ptosis","type":"exact"},{"name":"congenital ptosis","type":"exact"},{"name":"congenital ptosis (disease)","type":"exact"},{"name":"ptosis, congenital","type":"exact"},{"name":"ptosis, hereditary congenital 1","type":"related"},{"name":"ptosis, hereditary congenital, 1","type":"exact"}],"termid":"MONDO:0008340","xrefs":{"Monarch":{"xref_id":"0008340"}}}


id: GO:0033067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving macrolides, any of a large group of polyketide compounds that contain a large lactone ring with few or no double bonds and no nitrogen atoms, linked glycosidically to one or more sugar groups. The macrolides include the carbomycins, the erythromycins, oleandomycin, oligomycins, and the spiramycins, and act as antibiotics, mainly against Gram-positive bacteria.","definition_xrefs":["PMID:17298179","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antibiotic metabolic process","termid":"GO:0016999"},{"relation_name":"is_a","term_name":"polyketide metabolic process","termid":"GO:0030638"},{"relation_name":"is_a","term_name":"lactone metabolic process","termid":"GO:1901334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"macrolide metabolic process","synonyms":[{"name":"macrolide metabolism","type":"exact"}],"termid":"GO:0033067"}


id: PR:Q9HDV4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A lysine-specific demethylase 5A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lid2 complex component lid2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP19A11.06","secondary_identifiers":["UniProtKB:Q9HDV4"],"synonyms":[{"name":"Lid2C component lid2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPBP19A11.06","type":"related"},{"name":"Spom972h-KDM5A","type":"exact"}],"termid":"PR:Q9HDV4"}


id: PR:Q10284
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sks2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10284"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein sks2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1709.05","synonyms":[{"name":"Spom972h-sks2","type":"exact"},{"name":"heat shock cognate protein hsc1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10284"}


id: PBO:0031306
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_cell","termid":"PBO:0031306"}


id: PBO:0062290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily M member 1","termid":"PBO:0062290"}


id: MONDO:0054601
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated pituitary adenoma","termid":"MONDO:0017824"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pituitary adenoma 5, multiple types","secondary_identifiers":["UMLS:C4539685","DOID:0112008","OMIM:617540","MEDGEN:1615593"],"synonyms":[{"name":"PITA5","type":"related"},{"name":"pituitary adenoma 5, multiple types","type":"exact"}],"termid":"MONDO:0054601","xrefs":{"Monarch":{"xref_id":"0054601"}}}


id: PR:Q1MTN3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pic1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q1MTN3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inner centromere protein-related protein pic1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC336.15","synonyms":[{"name":"INCENP-related protein pic1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-pic1","type":"exact"}],"termid":"PR:Q1MTN3"}


id: GO:0141140
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont interferes with, inhibits or disrupts the normal execution of the immunoglobulin-mediated immune response of the host organism. One common mechanism by which this happens is the direct inhibition of immunoglobulin activity, by direct binding or modification. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:22256861","PMID:24753590","PMID:18426869"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host immune response","termid":"GO:0052562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host immunoglobulin-mediated immune response","synonyms":[{"name":"symbiont-mediated suppression of host immunoglobulin activity","type":"related"}],"termid":"GO:0141140"}


id: PBO:0047611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formin homology 2 domain containing 3","termid":"PBO:0047611"}


id: GO:0050246
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + NADPH + O2 + questin = demethylsulochrin + NADP+.","definition_xrefs":["RHEA:10836"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"questin monooxygenase (NADPH) activity","secondary_identifiers":["KEGG_REACTION:R02417","EC:1.14.13.43","MetaCyc:QUESTIN-MONOOXYGENASE-RXN"],"synonyms":[{"name":"questin oxygenase activity","type":"related"},{"name":"questin,NADPH:oxygen oxidoreductase (hydroxylating, anthraquinone-ring-opening)","type":"related"}],"termid":"GO:0050246"}


id: PBO:0059021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrix metallopeptidase 10","termid":"PBO:0059021"}


id: PR:Q9C109
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAP27G11.16 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C109"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein P27G11.16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP27G11.16","synonyms":[{"name":"Spom972h-SPAP27G11.16","type":"exact"}],"termid":"PR:Q9C109"}


id: PBO:0002475
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alternative splicing","termid":"PBO:0002475"}


id: MONDO:0021040
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015278"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm involving the pancreas.","definition_xrefs":["NCIT:C3305"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreas disorder","termid":"MONDO:0002356"},{"relation_name":"is_a","term_name":"digestive system neoplasm","termid":"MONDO:0021223"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"pancreatic neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["EFO:0003860","MEDGEN:18279","SCTID:126859007","UMLS:C0030297","ONCOTREE:PANCREAS","MESH:D010190"],"synonyms":[{"name":"neoplasm of pancreas","type":"exact"},{"name":"neoplasm of the pancreas","type":"exact"},{"name":"pancreas","type":"related"},{"name":"pancreas neoplasm","type":"exact"},{"name":"pancreas neoplasm (disease)","type":"exact"},{"name":"pancreas tumor","type":"exact"},{"name":"pancreas tumour","type":"exact"},{"name":"pancreatic neoplasm","type":"exact"},{"name":"pancreatic tumor","type":"exact"},{"name":"pancreatic tumour","type":"exact"},{"name":"tumor of pancreas","type":"exact"},{"name":"tumor of the pancreas","type":"exact"},{"name":"tumour of pancreas","type":"exact"},{"name":"tumour of the pancreas","type":"exact"}],"termid":"MONDO:0021040","terms_by_termid":{"MONDO:0015278":null},"xrefs":{"Monarch":{"xref_id":"0021040"}}}


id: GO:1901933
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of bicyclogermacrene.","definition_xrefs":["GOC:TermGenie","PMID:22867794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpene catabolic process","termid":"GO:0051763"},{"relation_name":"is_a","term_name":"bicyclogermacrene metabolic process","termid":"GO:1901932"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"bicyclogermacrene catabolic process","synonyms":[{"name":"bicyclogermacrene breakdown","type":"exact"},{"name":"bicyclogermacrene catabolism","type":"exact"},{"name":"bicyclogermacrene degradation","type":"exact"}],"termid":"GO:1901933"}


id: PBO:0062499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 8 subfamily D member 4","termid":"PBO:0062499"}


id: FYPO:0000146
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transcription regulation phenotype observed in the vegetative growth phase of the life cycle in which chromatin silencing is abnormal in centromeric regions. Chromatin silencing is the observed effect of processes that repress transcription in a region of the genome that is normally assembled into heterochromatin or CENP-A-containing chromatin (the latter is found at the centromere central core).","definition_xrefs":["PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin silencing","termid":"FYPO:0000144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0006551","FYPO:0001985","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abnormal chromatin silencing at centromere","synonyms":[{"name":"abnormal chromatin silencing at centromere during mitotic cell cycle","type":"related"},{"name":"abnormal chromatin silencing at centromere during vegetative growth","type":"exact"},{"name":"abnormal heterochromatin silencing at centromere","type":"related"}],"termid":"FYPO:0000146"}


id: PBO:0017857
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrolysis rate of maltose to glucose is 14.5 (uM min-1 ml-2)","termid":"PBO:0017857"}


id: PBO:0066943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 245","termid":"PBO:0066943"}


id: PBO:0091143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pig-Y, phosphatidylinositol N-acetylglucosaminyltransferase subunit Eri1","termid":"PBO:0091143"}


id: PBO:0053198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lymphatic endothelial transcriptional regulator lncRNA 1","termid":"PBO:0053198"}


id: GO:0052767
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of the alpha-(1->6) bonds of alpha-D-mannose residues in mannosyl-oligosaccharide.","definition_xrefs":["GOC:mengo_curators","PMID:1849817","PMID:2338081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannosyl-oligosaccharide mannosidase activity","termid":"GO:0015924"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016798","GO:0003824"],"is_obsolete":false,"name":"mannosyl-oligosaccharide 1,6-alpha-mannosidase activity","synonyms":[{"name":"1,6-alpha-mannosidase activity","type":"broad"},{"name":"1,6-alpha-mannosyl-oligosaccharide alpha-D-mannohydrolase activity","type":"exact"},{"name":"alpha-1,6-mannosidase activity","type":"broad"},{"name":"alpha-1,6-mannosyl-oligosaccharide alpha-D-mannohydrolase activity","type":"exact"}],"termid":"GO:0052767"}


id: PBO:0091582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase assembly protein Cox1102/ mitochondrial ribosomal protein Rsm2202, fusion protein","termid":"PBO:0091582"}


id: PBO:0054675
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2082","termid":"PBO:0054675"}


id: GO:0060897
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pattern specification process that results in the subdivision of an axis or axes of the neural plate in space to define an area or volume in which specific patterns of cell differentiation will take place or in which cells interpret a specific environment.","definition_xrefs":["GOC:sdb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regionalization","termid":"GO:0003002"},{"relation_name":"is_a","term_name":"neural plate pattern specification","termid":"GO:0060896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural plate regionalization","termid":"GO:0060897"}


id: PBO:0069750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1032, pseudogene","termid":"PBO:0069750"}


id: PBO:0060775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B8 pseudogene 1","termid":"PBO:0060775"}


id: PBO:0073118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short chain dehydrogenase/reductase family 42E, member 2","termid":"PBO:0073118"}


id: PBO:0048202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma-aminobutyric acid type A receptor subunit alpha6","termid":"PBO:0048202"}


id: GO:1903945
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hepatocyte apoptotic process.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:8649852"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hepatocyte apoptotic process","termid":"GO:1903943"},{"relation_name":"is_a","term_name":"positive regulation of epithelial cell apoptotic process","termid":"GO:1904037"},{"relation_name":"positively_regulates","term_name":"hepatocyte apoptotic process","termid":"GO:0097284"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of hepatocyte apoptotic process","synonyms":[{"name":"activation of hepatocyte apoptosis","type":"narrow"},{"name":"activation of hepatocyte apoptotic process","type":"narrow"},{"name":"positive regulation of hepatocyte apoptosis","type":"narrow"},{"name":"up regulation of hepatocyte apoptosis","type":"narrow"},{"name":"up regulation of hepatocyte apoptotic process","type":"exact"},{"name":"up-regulation of hepatocyte apoptosis","type":"narrow"},{"name":"up-regulation of hepatocyte apoptotic process","type":"exact"},{"name":"upregulation of hepatocyte apoptosis","type":"narrow"},{"name":"upregulation of hepatocyte apoptotic process","type":"exact"}],"termid":"GO:1903945"}


id: GO:1900378
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of secondary metabolite biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of biosynthetic process","termid":"GO:0009891"},{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"positively_regulates","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"positive regulation of secondary metabolite biosynthetic process","synonyms":[{"name":"activation of secondary metabolite biosynthesis","type":"exact"},{"name":"activation of secondary metabolite biosynthetic process","type":"narrow"},{"name":"positive regulation of secondary metabolite biosynthesis","type":"exact"},{"name":"up regulation of secondary metabolite biosynthesis","type":"exact"},{"name":"up regulation of secondary metabolite biosynthetic process","type":"exact"},{"name":"up-regulation of secondary metabolite biosynthesis","type":"exact"},{"name":"up-regulation of secondary metabolite biosynthetic process","type":"exact"},{"name":"upregulation of secondary metabolite biosynthesis","type":"exact"},{"name":"upregulation of secondary metabolite biosynthetic process","type":"exact"}],"termid":"GO:1900378"}


id: GO:0071575
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the plasma membrane consisting of the gene products that penetrate only the external side of the membrane.","definition_xrefs":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of external side of plasma membrane (obsolete GO:0071575)","synonyms":[{"name":"integral to external leaflet of plasma membrane","type":"exact"},{"name":"integral to external side of plasma membrane","type":"narrow"}],"termid":"GO:0071575"}


id: GO:0032382
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the directed movement of sterols within cells.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of sterol transport","termid":"GO:0032373"},{"relation_name":"is_a","term_name":"positive regulation of intracellular lipid transport","termid":"GO:0032379"},{"relation_name":"is_a","term_name":"regulation of intracellular sterol transport","termid":"GO:0032380"},{"relation_name":"positively_regulates","term_name":"intracellular sterol transport","termid":"GO:0032366"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of intracellular sterol transport","synonyms":[{"name":"activation of intracellular sterol transport","type":"narrow"},{"name":"stimulation of intracellular sterol transport","type":"narrow"},{"name":"up regulation of intracellular sterol transport","type":"exact"},{"name":"up-regulation of intracellular sterol transport","type":"exact"},{"name":"upregulation of intracellular sterol transport","type":"exact"}],"termid":"GO:0032382"}


id: GO:1904806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein oxidation.","definition_xrefs":["GOC:TermGenie","PMID:22719267","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein modification process","termid":"GO:0031399"},{"relation_name":"regulates","term_name":"protein oxidation","termid":"GO:0018158"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of protein oxidation","synonyms":[{"name":"regulation of protein amino acid oxidation","type":"exact"}],"termid":"GO:1904806"}


id: MONDO:0020725
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Anemia due to a disorder that is persistent or long-standing in nature.","definition_xrefs":["NCIT:C35659"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anemia","termid":"MONDO:0002280"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"anemia due to chronic disorder","secondary_identifiers":["UMLS:C0002873","ICD9:285.29","MEDGEN:507442","SCTID:234347009"],"synonyms":[{"name":"Secondary anaemia","type":"related"},{"name":"Secondary anemia","type":"related"},{"name":"anaemia due to Chronic Disorder","type":"related"},{"name":"anaemia of chronic disease","type":"exact"},{"name":"anaemia of chronic disorder","type":"related"},{"name":"anaemia of chronic illness","type":"exact"},{"name":"anaemia of chronic inflammation","type":"exact"},{"name":"anaemia of systemic disease","type":"related"},{"name":"anemia due to Chronic Disorder","type":"related"},{"name":"anemia due to chronic disorder","type":"exact"},{"name":"anemia of chronic disease","type":"exact"},{"name":"anemia of chronic disorder","type":"related"},{"name":"anemia of chronic illness","type":"exact"},{"name":"anemia of chronic inflammation","type":"exact"},{"name":"anemia of systemic disease","type":"related"}],"termid":"MONDO:0020725","xrefs":{"Monarch":{"xref_id":"0020725"}}}


id: PBO:0084828
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial protein required for outer membrane protein import; cooperates with Tom70p to import the subset of proteins with multiple alpha-helical transmembrane segments, including Ugo1p, Tom20p, and others; forms a complex with Mim2p in the outer membrane that functions as cation-selective channel for translocation of positively charged precursor segments; also has a role in assembly of Tom20p into the TOM complex","termid":"PBO:0084828"}


id: PBO:0088156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vesicle membrane receptor protein (v-SNARE); involved in the fusion between Golgi-derived secretory vesicles with the plasma membrane; proposed to be involved in endocytosis; member of the synaptobrevin/VAMP family of R-type v-SNARE proteins; SNC1 has a paralog, SNC2, that arose from the whole genome duplication","termid":"PBO:0088156"}


id: MONDO:0008013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Monosomy 9p is a rare chromosomal anomaly characterized by psychomotor developmental delay, facial dysmorphism (trigonocephaly, midface hypoplasia, upslanting palpebral fissures, dysplastic small ears, flat nasal bridge with anteverted nostrils and long philtrum, micrognathia, choanal atresia, short neck), single umbilical artery, omphalocele, inguinal or umbilical hernia, genital abnormalities (hypospadia, cryptorchidism), muscular hypotonia and scoliosis.","definition_xrefs":["Orphanet:261112"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of chromosome 9","termid":"MONDO:0016874"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 9p deletion syndrome","secondary_identifiers":["ICD9:758.39","DOID:0060732","OMIM:158170","MEDGEN:167073","UMLS:C0795830","SCTID:62599000","GARD:3773","MESH:C538024"],"synonyms":[{"name":"9p deletion","type":"exact"},{"name":"9p deletion syndrome","type":"exact"},{"name":"9p monosomy","type":"exact"},{"name":"9p syndrome","type":"exact"},{"name":"9p- syndrome","type":"exact"},{"name":"Alfi syndrome","type":"exact"},{"name":"chromosome 9p deletion","type":"exact"},{"name":"deletion 9p","type":"exact"},{"name":"monosomy 9p","type":"exact"},{"name":"monosomy 9p syndrome","type":"exact"},{"name":"monosomy type 9p","type":"exact"},{"name":"partial deletion of chromosome 9p","type":"exact"},{"name":"partial deletion of the short arm of chromosome 9","type":"exact"},{"name":"partial deletion of the short arm of chromosome type 9","type":"exact"},{"name":"partial monosomy 9p","type":"exact"},{"name":"partial monosomy of chromosome 9p","type":"exact"},{"name":"partial monosomy of the short arm of chromosome 9","type":"exact"}],"termid":"MONDO:0008013","xrefs":{"Monarch":{"xref_id":"0008013"}}}


id: PBO:0091870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alditol NADP+ 1-oxidoreductase activity","termid":"PBO:0091870"}


id: GO:0004583
data:
  {"annotated_genes":["SJAG_01950","SJAG_03656","SJAG_03764"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[81761],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042283"},{"annotations":[70726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106073"},{"annotations":[78964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042281"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of an alpha-D-glucosyl residue from dolichyl-phosphate D-glucose into a membrane lipid-linked oligosaccharide.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucosyltransferase activity","termid":"GO:0046527"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01950":null,"SJAG_03656":null,"SJAG_03764":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0016757","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"dolichyl-phosphate-glucose-glycolipid alpha-glucosyltransferase activity","references_by_uniquename":{"GO_REF:0000003":null,"GO_REF:0000033":null},"secondary_identifiers":["Reactome:R-HSA-446189","Reactome:R-HSA-446194","Reactome:R-HSA-4724330","Reactome:R-HSA-4724291","Reactome:R-HSA-446202"],"termid":"GO:0004583","terms_by_termid":{"GO:0042281":null,"GO:0042283":null,"GO:0106073":null}}


id: PBO:0091873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pho84 repressing sense RNA Prt2","termid":"PBO:0091873"}


id: FYPO:0005489
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a protein that is not normally found in the vacuolar membrane is observed there.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein mislocalized to vacuole","termid":"FYPO:0005514"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"protein mislocalized to vacuolar membrane","synonyms":[{"name":"ectopic protein localization to vacuolar membrane","type":"exact"},{"name":"protein mislocalised to vacuolar membrane","type":"exact"},{"name":"protein mislocalised to vacuolar membrane during vegetative growth","type":"exact"},{"name":"protein mislocalized to vacuolar membrane during mitotic cell cycle","type":"related"},{"name":"protein mislocalized to vacuolar membrane during vegetative growth","type":"exact"},{"name":"protein mislocalized to vacuole membrane","type":"exact"}],"termid":"FYPO:0005489"}


id: PBO:0002897
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"promoter contains UAS","termid":"PBO:0002897"}


id: PBO:0064082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylserine decarboxylase","termid":"PBO:0064082"}


id: _global:seeAlso
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"seeAlso","secondary_identifiers":["http://www.w3.org/2000/01/rdf-schema#seeAlso"],"termid":"_global:seeAlso","xrefs":{"Monarch":{"xref_id":"seeAlso"}}}


id: FYPO:0003296
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of ribosome binding by a gene product (usually a protein) in a mutant is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein complex binding","termid":"FYPO:0005232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000702"}],"interesting_parent_ids":["FYPO:0000702","FYPO:0000652","FYPO:0000257"],"is_obsolete":false,"name":"normal ribosome binding","termid":"FYPO:0003296"}


id: MONDO:1011948
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"navicular disease, non-human animal","secondary_identifiers":["OMIA:000704"],"termid":"MONDO:1011948","xrefs":{"Monarch":{"xref_id":"1011948"}}}


id: PBO:0076374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TGF-beta activated kinase 1 (MAP3K7) binding protein 2","termid":"PBO:0076374"}


id: MONDO:1010040
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pyloric stenosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyloric stenosis, non-human animal","secondary_identifiers":["OMIA:000843"],"termid":"MONDO:1010040","xrefs":{"Monarch":{"xref_id":"1010040"}}}


id: SO:0001688
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The boundary at which a restriction enzyme breaks the nucleotide sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide_cleavage_site","termid":"SO:0002204"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restriction_enzyme_cleavage_junction","synonyms":[{"name":"restriction enzyme cleavage junction","type":"exact"}],"termid":"SO:0001688"}


id: MONDO:0016454
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare axonal hereditary motor and sensory neuropathy characterized by infantile onset of slowly progressive distal motor weakness and atrophy (more severe in legs and moderate in arms) with mildly delayed motor development, hypotonia, and distal sensory impairment of all sensory modalities.","definition_xrefs":["Orphanet:228374"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Charcot-Marie-Tooth disease type 2","termid":"MONDO:0018993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease type 2B5","secondary_identifiers":["UMLS:C4749824","icd11.foundation:1603286685","GARD:17153","MEDGEN:1668955"],"synonyms":[{"name":"AR-CMT2B5","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 2B5","type":"exact"},{"name":"SEOAN due to NEFL deficiency","type":"exact"},{"name":"autosomal recessive Charcot-Marie-Tooth disease type 2B5","type":"exact"},{"name":"severe early-onset axonal neuropathy due to NEFL deficiency","type":"exact"},{"name":"severe early-onset axonal neuropathy due to light neurofilament subunit deficiency","type":"exact"}],"termid":"MONDO:0016454","xrefs":{"Monarch":{"xref_id":"0016454"}}}


id: GO:0061233
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the mesonephric glomerular basement membrane over time, from its formation to the mature structure. The mesonephric glomerular basement membrane is the basal laminal portion of the mesonephric glomerulus which performs the actual filtration.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular basement membrane development","termid":"GO:0032836"},{"relation_name":"part_of","term_name":"mesonephric glomerulus development","termid":"GO:0061224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric glomerular basement membrane development","termid":"GO:0061233"}


id: MONDO:1012522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"turning calves syndrome, cattle","secondary_identifiers":["OMIA:002150-9913"],"synonyms":[{"name":"syndrome des veaux tourneurs","type":"exact"}],"termid":"MONDO:1012522","xrefs":{"Monarch":{"xref_id":"1012522"}}}


id: GO:0042361
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of menaquinones, any of the quinone-derived compounds synthesized by intestinal bacteria. Structurally, menaquinones consist of a methylated naphthoquinone ring structure and side chains composed of a variable number of unsaturated isoprenoid residues. Menaquinones have vitamin K activity and are known as vitamin K2.","definition_xrefs":["PMID:37938463","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"menaquinone metabolic process","termid":"GO:0009233"},{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"menaquinone catabolic process","synonyms":[{"name":"menaquinone breakdown","type":"exact"},{"name":"menaquinone catabolism","type":"exact"},{"name":"menaquinone degradation","type":"exact"},{"name":"menatetrenone catabolic process","type":"exact"},{"name":"menatetrenone catabolism","type":"exact"},{"name":"multiprenylmenaquinone catabolic process","type":"exact"},{"name":"multiprenylmenaquinone catabolism","type":"exact"},{"name":"vitamin K2 catabolic process","type":"exact"},{"name":"vitamin K2 catabolism","type":"exact"}],"termid":"GO:0042361"}


id: PBO:0064680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 16","termid":"PBO:0064680"}


id: MONDO:0008492
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare syndrome characterized by hard, thick skin, usually on the entire body. The thickening of the skin can limit joint mobility and causes joints to be stuck in a bent position (flexion contractures). The onset of signs and symptoms can range from presenting at birth through childhood. Other signs and symptoms may include excessive hair growth (hypertrichosis), loss of body fat (lipodystrophy), scoliosis, muscle weakness, slow growth, and short stature. Weakness or paralysis of the eye muscles have also been reported. Stiff skin syndrome is caused by mutations (changes) in the FBN1 gene and is inherited in an autosomal dominant manner. Diagnosis is based on a clinical evaluation that is consistent with stiff skin syndrome, and the diagnosis can be confirmed with genetic testing. Treatment is based on the symptoms of each individual and may include physical therapy.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"stiff skin syndrome","secondary_identifiers":["DOID:0111561","icd11.foundation:642409035","GARD:5025","NCIT:C118636","MESH:C566112","MEDGEN:348877","Orphanet:2833","SCTID:765187004","UMLS:C1861456","OMIM:184900"],"synonyms":[{"name":"SSKS","type":"related"},{"name":"STIFF skin syndrome","type":"related"},{"name":"stiff skin syndrome","type":"exact"}],"termid":"MONDO:0008492","xrefs":{"Monarch":{"xref_id":"0008492"}}}


id: FYPO:0000219
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of oxidation of one or more specific proteins, or of specific protein sites, is increased, resulting in the accumulation of proteins with oxidative modifications including carbonylated proteins.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein modification during vegetative growth","termid":"FYPO:0000547"},{"relation_name":"is_a","term_name":"increased protein oxidation","termid":"FYPO:0003863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0002494","FYPO:0002274"],"is_obsolete":false,"name":"increased protein oxidation during vegetative growth","synonyms":[{"name":"accumulation of carbonylated proteins during vegetative growth","type":"related"},{"name":"increased level of disulfides during vegetative growth","type":"related"},{"name":"increased level of oxidised thiols in proteins during vegetative growth","type":"related"},{"name":"increased level of oxidized protein thiols during vegetative growth","type":"related"},{"name":"increased protein oxidation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000219"}


id: MONDO:0010179
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Isolated right ventricular hypoplasia (IRVH) is a rare congenital heart malformation characterized by underdevelopment of the right ventricle associated with patent foramen ovale or interauricular communication and normally developed tricuspid and pulmonary valves. IRVH manifests with severe cyanosis, congestive heart failure, and in severe cases, death in early infancy.","definition_xrefs":["Orphanet:439"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"hypoplastic right heart syndrome","termid":"MONDO:0020291"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isolated right ventricular hypoplasia","secondary_identifiers":["GARD:4721","MEDGEN:336377","UMLS:C1848587","SCTID:718135001","MESH:C535682","OMIM:277200"],"synonyms":[{"name":"Irvh","type":"related"},{"name":"hypoplasia of the right ventricle","type":"related"},{"name":"isolated hypoplasia of the right ventricle","type":"related"},{"name":"right ventricle hypoplasia","type":"related"},{"name":"right ventricular hypoplasia","type":"related"},{"name":"right ventricular hypoplasia, isolated","type":"related"}],"termid":"MONDO:0010179","xrefs":{"Monarch":{"xref_id":"0010179"}}}


id: GO:0046037
data:
  {"annotated_genes":["SJAG_04849","SJAG_01298","SJAG_04634","SJAG_06634","SJAG_00964"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[65367],"is_not":false,"summary":null,"term":"GO:0046037"},{"annotations":[59857,63912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006177"},{"annotations":[77381,103012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032263"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving GMP, guanosine monophosphate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide metabolic process","termid":"GO:0009150"},{"relation_name":"is_a","term_name":"purine ribonucleoside monophosphate metabolic process","termid":"GO:0009167"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00964":null,"SJAG_01298":null,"SJAG_04634":null,"SJAG_04849":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"GMP metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"GMP metabolism","type":"exact"}],"termid":"GO:0046037","terms_by_termid":{"GO:0006177":null,"GO:0032263":null,"GO:0046037":null}}


id: GO:0051750
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a (3E,5Z)-dienoyl-CoA = a (2E,4E)-(5,6-saturated)-dienoyl-CoA.","definition_xrefs":["PMID:16040662","RHEA:45240","PMID:11278886"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, transposing C=C bonds","termid":"GO:0016863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674"],"is_obsolete":false,"name":"delta(3,5)-delta(2,4)-dienoyl-CoA isomerase activity","secondary_identifiers":["EC:5.3.3.21","GO:0008416"],"synonyms":[{"name":"delta(3,5),delta(2,4)-dienoyl-coenzyme A isomerase activity","type":"exact"},{"name":"delta3,5-delta2,4-dienoyl-CoA isomerase activity","type":"exact"},{"name":"delta5-delta2,4-dienoyl-CoA isomerase activity","type":"related"}],"termid":"GO:0051750"}


id: PBO:0067946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 248","termid":"PBO:0067946"}


id: GO:0004808
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-aminomethyl-2-thiouridine34 in tRNA + S-adenosyl-L-methionine = 5-methylaminomethyl-2-thiouridine34 in tRNA + H+ + S-adenosyl-L-homocysteine. This enzyme specifically adds the terminal methyl group of 5-[(methylamino)methyl]-2-thiouridylate.","definition_xrefs":["RHEA:19569"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"},{"relation_name":"is_a","term_name":"tRNA (uridine) methyltransferase activity","termid":"GO:0016300"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016741","GO:0003824","GO:0003674","GO:0140098","GO:0140101","GO:0016740"],"is_obsolete":false,"name":"tRNA (5-methylaminomethyl-2-thiouridylate)(34)-methyltransferase activity","secondary_identifiers":["KEGG_REACTION:R00601","GO:0016425","EC:2.1.1.61","MetaCyc:RXN0-5144"],"synonyms":[{"name":"tRNA (5-methylaminomethyl-2-thiouridylate)-methyltransferase activity","type":"exact"},{"name":"tRNA 5-methylaminomethyl-2-thiouridylate 5'-methyltransferase activity","type":"related"}],"termid":"GO:0004808"}


id: GO:0060102
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen and cuticulin-based noncellular, multilayered structure that is synthesized by an underlying ectodermal (hypodermal) cell layer. The cuticle serves essential functions in body morphology, locomotion, and environmental protection. An example of this component is found in Caenorhabditis elegans.","definition_xrefs":["ISSN:15518507","GOC:dph","PMID:12619137","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specialized extracellular matrix","termid":"GO:0140047"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"cuticular extracellular matrix","synonyms":[{"name":"collagen and cuticulin-based cuticle extracellular matrix","type":"exact"},{"name":"collagen and cuticulin-based exoskeleton extracellular matrix","type":"related"},{"name":"cuticular ECM","type":"exact"}],"termid":"GO:0060102"}


id: GO:0102872
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-palmitoyl-2-linoleoyl-phosphatidylcholine + O2 + a reduced electron acceptor = 1-16:0-2-18:3-phosphatidylcholine + 2 H2O + an oxidized electron acceptor.","definition_xrefs":["PMID:15538555","PMID:8102138","GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-16:0-2-18:2-phosphatidylcholine desaturase activity (obsolete GO:0102872)","termid":"GO:0102872"}


id: PBO:0042035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCDC88C divergent transcript","termid":"PBO:0042035"}


id: GO:0050665
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of hydrogen peroxide (H2O2), a potentially harmful byproduct of aerobic cellular respiration which can cause damage to DNA.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrogen peroxide metabolic process","termid":"GO:0042743"},{"relation_name":"is_a","term_name":"reactive oxygen species biosynthetic process","termid":"GO:1903409"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"hydrogen peroxide biosynthetic process","synonyms":[{"name":"H2O2 biosynthetic process","type":"exact"},{"name":"hydrogen peroxide anabolism","type":"exact"},{"name":"hydrogen peroxide biosynthesis","type":"exact"},{"name":"hydrogen peroxide formation","type":"exact"},{"name":"hydrogen peroxide generation","type":"exact"},{"name":"hydrogen peroxide synthesis","type":"exact"}],"termid":"GO:0050665"}


id: GO:0002248
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events leading to growth of connective tissue when loss of tissues that are incapable of regeneration occurs, or when fibrinous exudate cannot be adequately cleared, as part of an inflammatory response.","definition_xrefs":["PMID:9639571","GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"connective tissue replacement","termid":"GO:0097709"},{"relation_name":"part_of","term_name":"wound healing involved in inflammatory response","termid":"GO:0002246"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"connective tissue replacement involved in inflammatory response wound healing","synonyms":[{"name":"connective tissue replacement during inflammatory response","type":"related"},{"name":"fibrosis during inflammatory response","type":"narrow"},{"name":"tissue fibrosis development","type":"narrow"}],"termid":"GO:0002248"}


id: FYPO:0007074
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing mycophenolic acid.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002057","FYPO:0002058","FYPO:0000257","FYPO:0000003","FYPO:0002060"],"is_obsolete":false,"name":"normal growth on mycophenolic acid","synonyms":[{"name":"normal cell population growth in presence of mycophenolic acid","type":"exact"},{"name":"normal cell population growth on MPA","type":"exact"},{"name":"normal cell population growth on mycophenolic acid","type":"exact"},{"name":"normal vegetative cell population growth on mycophenolic acid","type":"exact"}],"termid":"FYPO:0007074"}


id: PBO:0002684
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenylyl-sulfate kinase (predicted)","termid":"PBO:0002684"}


id: MONDO:0020118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dense granule disease (obsolete MONDO:0020118)","secondary_identifiers":["icd11.foundation:1930060978","Orphanet:98456"],"synonyms":[{"name":"Delta granule disease","type":"exact"}],"termid":"MONDO:0020118","xrefs":{"Monarch":{"xref_id":"0020118"}}}


id: GO:0071728
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the beak over time from its initial formation until its mature state. The avian beak is an external anatomical structure, in the head region, that is adapted for feeding self and young, catching prey, probing, etc. It encompasses, but is not restricted to, the maxilla, mandible, maxillary rhamphotheca, mandibular rhamphotheca, nostril, nasal fossa, nasal bones, egg tooth and rictus.","definition_xrefs":["ISBN:0702008729","GOC:lp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"beak development","termid":"GO:0071728"}


id: PBO:0027408
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_onset_of_protein_localization_to_cell_division_site","termid":"PBO:0027408"}


id: FYPO:0001219
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein measured in a cell during a cellular response to nitrogen starvation is higher than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level","termid":"FYPO:0000836"},{"relation_name":"is_a","term_name":"altered level of substance in cell during nitrogen starvation","termid":"FYPO:0004139"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0006551","FYPO:0000002"],"is_obsolete":false,"name":"increased protein level during cellular response to nitrogen starvation","synonyms":[{"name":"increased protein accumulation during cellular response to nitrogen starvation","type":"related"},{"name":"increased protein level during cellular response to nitrogen depletion","type":"exact"},{"name":"increased protein level during cellular response to nitrogen deprivation","type":"exact"},{"name":"increased protein level during nitrogen starvation","type":"exact"}],"termid":"FYPO:0001219"}


id: RO:HOM0000049
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Paralogy that involves genes from the same species.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_paralogy_relationship_with","termid":"RO:HOM0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_within-species_paralogy_relationship_with","synonyms":[{"name":"within-species paralogous to","type":"exact"}],"termid":"RO:HOM0000049"}


id: PBO:0028330
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_rDNA_separation","termid":"PBO:0028330"}


id: GO:1990279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of the activity of the transcription factor MBF.","definition_xrefs":["PMID:24006488"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of MBF transcription factor activity (obsolete GO:1990279)","synonyms":[{"name":"negative regulation of MBF transcription factor activity","type":"exact"}],"termid":"GO:1990279"}


id: FYPO:0008231
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of lactate dehydrogenase activity is increased.","definition_xrefs":["PMID:37787465"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000661","FYPO:0001985","FYPO:0000707","FYPO:0000654"],"is_obsolete":false,"name":"increased lactate dehydrogenase activity","termid":"FYPO:0008231"}


id: PBO:0085394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane Na+/Pi cotransporter; active in early growth phase; similar to phosphate transporters of Neurospora crassa; transcription regulated by inorganic phosphate concentrations and Pho4p; mutations in related human transporter genes hPit1 and hPit2 are associated with hyperphosphatemia-induced calcification of vascular tissue and familial idiopathic basal ganglia calcification","termid":"PBO:0085394"}


id: PBO:0004034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER protein translocation subcomplex subunit Sec63 (predicted)","termid":"PBO:0004034"}


id: GO:0052181
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism activates, maintains or increases the frequency, rate or extent of the resistance gene-dependent defense response of the symbiont. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by host of symbiont defense response (obsolete GO:0052181)","termid":"GO:0052181"}


id: GO:0043117
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the extent to which blood vessels can be pervaded by fluid.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vascular permeability","termid":"GO:0043114"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of vascular permeability","synonyms":[{"name":"activation of vascular permeability","type":"narrow"},{"name":"stimulation of vascular permeability","type":"narrow"},{"name":"up regulation of vascular permeability","type":"exact"},{"name":"up-regulation of vascular permeability","type":"exact"},{"name":"upregulation of vascular permeability","type":"exact"}],"termid":"GO:0043117"}


id: MONDO:0859574
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"annular epidermolytic ichthyosis","termid":"MONDO:0011870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0000426"],"is_obsolete":false,"name":"ichthyosis, annular epidermolytic, 2","secondary_identifiers":["UMLS:C5774264","MEDGEN:1824037","OMIM:620148"],"termid":"MONDO:0859574","xrefs":{"Monarch":{"xref_id":"0859574"}}}


id: SO:0001805
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A conserved polypeptide motif that can be recognized by both Fizzy/Cdc20- and FZR/Cdh1-activated anaphase-promoting complex/cyclosome (APC/C) and targets a protein for ubiquitination and subsequent degradation by the APC/C. The consensus sequence is RXXLXXXXN.","definition_xrefs":["PMID:12208841","PMID:1842691"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_conserved_motif","termid":"SO:0100017"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"destruction_box","synonyms":[{"name":"D-box","type":"exact"},{"name":"destruction box","type":"exact"}],"termid":"SO:0001805"}


id: PBO:0027418
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_localization_to_Golgi_apparatus","termid":"PBO:0027418"}


id: MONDO:0017060
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"iniencephaly","termid":"MONDO:0018968"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"open iniencephaly","secondary_identifiers":["MEDGEN:608900","GARD:20949","icd11.foundation:1778329323","Orphanet:268363","SCTID:203928008","UMLS:C0431285"],"termid":"MONDO:0017060","xrefs":{"Monarch":{"xref_id":"0017060"}}}


id: PBO:0070687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 58","termid":"PBO:0070687"}


id: PBO:0060861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIMA-related kinase 4 pseudogene 3","termid":"PBO:0060861"}


id: PBO:0029432
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_tyrosine_phosphorylation_during_cellular_response_to_hydrogen_peroxide","termid":"PBO:0029432"}


id: GO:0160111
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A structural network of microtubule inner proteins (MIPs) located inside the lumen of the A tubule of the axonemal microtubule doublet that helps stabilize the A tubule.","definition_xrefs":["PMID:29430673","PMID:37295417","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"A axonemal microtubule","termid":"GO:0097649"},{"relation_name":"part_of","term_name":"axonemal microtubule doublet inner sheath","termid":"GO:0160110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0015630"],"is_obsolete":false,"name":"axonemal A tubule inner sheath","termid":"GO:0160111"}


id: PBO:0049241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRM8 antisense RNA 1","termid":"PBO:0049241"}


id: PBO:0076843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TERF2 interacting protein pseudogene 1","termid":"PBO:0076843"}


id: GO:0021834
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The creation and reception of signals that guide olfactory bulb interneuron precursors down concentration gradients towards the olfactory bulb.","definition_xrefs":["GOC:dgh","GOC:cls","GOC:dph","GOC:jid","PMID:12626695","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative chemotaxis","termid":"GO:0050919"},{"relation_name":"part_of","term_name":"embryonic olfactory bulb interneuron precursor migration","termid":"GO:0021831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"chemorepulsion involved in embryonic olfactory bulb interneuron precursor migration","synonyms":[{"name":"negative chemotaxis involved in embryonic olfactory bulb interneuron precursor migration","type":"exact"}],"termid":"GO:0021834"}


id: GO:0047661
data:
  {"annotated_genes":["SJAG_04298","SJAG_00036"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[62977,66974],"is_not":false,"summary":null,"term":"GO:0047661"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: an L-amino acid = a D-amino acid.","definition_xrefs":["EC:5.1.1.10","MetaCyc:AMINO-ACID-RACEMASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"racemase and epimerase activity, acting on amino acids and derivatives","termid":"GO:0016855"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00036":null,"SJAG_04298":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"amino-acid racemase activity","references_by_uniquename":{"GO_REF:0000002":null},"secondary_identifiers":["RHEA:18317"],"synonyms":[{"name":"L-amino acid racemase activity","type":"related"}],"termid":"GO:0047661","terms_by_termid":{"GO:0047661":null}}


id: PBO:0012304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome assembly chaperone 4 (predicted)","termid":"PBO:0012304"}


id: MOD:00105
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-serine residue to L-serine amide.","definition_xrefs":["PubMed:743209","RESID:AA0096"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C1-amidated residue","termid":"MOD:00883"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-serine amide","synonyms":[{"name":"(2S)-2-amino-3-hydroxypropanamide","type":"exact"},{"name":"L-serine amide","type":"exact"},{"name":"MOD_RES Serine amide","type":"exact"},{"name":"SerN","type":"exact"},{"name":"amidated L-serine","type":"exact"},{"name":"serinamide","type":"exact"}],"termid":"MOD:00105"}


id: GO:0032449
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex comprising Bcl10, MALT1 and a CARD domain-containing protein (CARD9, CARD10 or CARD11); plays a role in signal transduction during NF-kappaB activation.","definition_xrefs":["PMID:30467369","PMID:12909454"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"CBM complex","synonyms":[{"name":"CARMA1-BCL10-Malt1 complex","type":"exact"}],"termid":"GO:0032449"}


id: PBO:0072936
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small Cajal body-specific RNA 16","termid":"PBO:0072936"}


id: MONDO:0019796
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acrocephalosyndactyly (ACS) syndromes represent a group of inherited congenital malformation disorders characterized by craniosynostosis and fusion or webbing of the fingers or toes, often with other associated manifestations.","definition_xrefs":["Orphanet:946"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"acrocephalosyndactyly","secondary_identifiers":["MEDGEN:267602","MedDRA:10000590","DOID:12960","ICD9:755.55","NCIT:C34348","SCTID:268262006","UMLS:C1510455"],"synonyms":[{"name":"ACS","type":"exact"},{"name":"acrocephalosyndactylia","type":"exact"},{"name":"acrocephalosyndactyly","type":"exact"}],"termid":"MONDO:0019796","xrefs":{"Monarch":{"xref_id":"0019796"}}}


id: MONDO:0011516
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"early response to neural induction gene","secondary_identifiers":["OMIM:605105","UMLS:C1854633","MEDGEN:344332"],"synonyms":[{"name":"Erni","type":"related"},{"name":"early response to neural induction gene","type":"exact"}],"termid":"MONDO:0011516","xrefs":{"Monarch":{"xref_id":"0011516"}}}


id: GO:0061448
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of a connective tissue over time, from its formation to the mature structure.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue development","termid":"GO:0009888"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"connective tissue development","termid":"GO:0061448"}


id: PBO:0072217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S19 binding protein 1","termid":"PBO:0072217"}


id: GO:0008228
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a microorganism (or other particulate material) is rendered more susceptible to phagocytosis by coating with an opsonin, a blood serum protein such as a complement component or antibody.","definition_xrefs":["ISBN:068340007X","ISBN:0781735149","GOC:add","GOC:mah","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune effector process","termid":"GO:0002252"},{"relation_name":"positively_regulates","term_name":"phagocytosis, recognition","termid":"GO:0006910"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"opsonization","secondary_identifiers":["Wikipedia:Opsonin"],"termid":"GO:0008228"}


id: MONDO:0007269
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial dilated cardiomyopathy with conduction defect due to LMNA mutation is a rare familial dilated cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy and elevated serum creatine kinase.","definition_xrefs":["Orphanet:300751"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"dilated cardiomyopathy 1A","secondary_identifiers":["GARD:18615","UMLS:C1449563","OMIM:115200","SCTID:766883006","MEDGEN:258500","DOID:0110425"],"synonyms":[{"name":"CDCD1","type":"exact"},{"name":"LMNA familial isolated dilated cardiomyopathy","type":"exact"},{"name":"cardiomyopathy dilated with conduction defect type 1","type":"exact"},{"name":"cardiomyopathy, congestive","type":"related"},{"name":"cardiomyopathy, dilated, 1A","type":"related"},{"name":"cardiomyopathy, dilated, type 1A","type":"exact"},{"name":"cardiomyopathy, dilated, with conduction defect 1","type":"related"},{"name":"cardiomyopathy, familial idiopathic","type":"related"},{"name":"cardiomyopathy, idiopathic dilated","type":"related"},{"name":"dilated cardiomyopathy 1A","type":"exact"},{"name":"dilated cardiomyopathy type 1A","type":"exact"},{"name":"dilated cardiomyopathy with conduction defect 1","type":"exact"},{"name":"familial dilated cardiomyopathy with conduction defect due to LMNA mutation","type":"exact"},{"name":"familial isolated dilated cardiomyopathy caused by mutation in LMNA","type":"exact"}],"termid":"MONDO:0007269","xrefs":{"Monarch":{"xref_id":"0007269"}}}


id: MONDO:0010219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"xylosidase deficiency","secondary_identifiers":["MEDGEN:336338","MESH:C564730","OMIM:278900","UMLS:C1848407"],"synonyms":[{"name":"xylosidase deficiency","type":"exact"}],"termid":"MONDO:0010219","xrefs":{"Monarch":{"xref_id":"0010219"}}}


id: PBO:0056313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase kinase 7","termid":"PBO:0056313"}


id: MONDO:0016723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pineocytoma is the least aggressive form of pineal parenchymal tumors, manifesting with symptoms such as Parinaud's syndrome (a group of eye movement abnormalities and pupil dysfunction, including deficiency in upward-gaze and convergence-retraction nystagmus), headaches, balance impairment, urinary incontinence, and changes in mood and that are not known to disseminate in a diffuse manner. They are usually associated with a good prognosis.","definition_xrefs":["Orphanet:251912"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign endocrine neoplasm","termid":"MONDO:0000627"},{"relation_name":"is_a","term_name":"benign neoplasm of brain","termid":"MONDO:0021451"},{"relation_name":"is_a","term_name":"pineal parenchymal cell neoplasm","termid":"MONDO:0024890"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pineocytoma","secondary_identifiers":["EFO:1000476","icd11.foundation:2055142333","GARD:8207","ICDO:9361/1","HP:0030407","NANDO:2200092","SCTID:255045009","UMLS:C0917890","MedDRA:10035059","NCIT:C6966","MEDGEN:183004","ONCOTREE:PINC","DOID:0081248"],"synonyms":[{"name":"Pineocytoma (WHO grade I)","type":"exact"},{"name":"benign pinealoma","type":"exact"},{"name":"pinealocytoma","type":"exact"},{"name":"pineocytoma","type":"exact"},{"name":"pineocytoma (disease)","type":"exact"},{"name":"pineocytoma, benign","type":"exact"}],"termid":"MONDO:0016723","xrefs":{"Monarch":{"xref_id":"0016723"}}}


id: GO:0032258
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cytoplasm to vacuole targeting pathway that uses machinery common with autophagy. The Cvt vesicle is formed when the receptor protein, Atg19, binds to the complexes of the target protein (aminopeptidase or alpha-mannosidase homododecamers), forming the Cvt complex. Atg11 binds to Atg9 and transports the Cvt complex to the pre-autophagosome (PAS). The phagophore membrane expands around the Cvt complex (excluding bulk cytoplasm) forming the Cvt vesicle. This pathway is mostly observed in yeast.","definition_xrefs":["PMID:12865942","PMID:15659643"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein targeting to vacuole","termid":"GO:0006623"},{"relation_name":"is_a","term_name":"process utilizing autophagic mechanism","termid":"GO:0061919"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006605"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006605","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"cytoplasm to vacuole targeting by the Cvt pathway","termid":"GO:0032258"}


id: GO:0047664
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction:4-aminoimidazole + H20 = imidazol-4-one + NH3.","definition_xrefs":["RHEA:22348"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines","termid":"GO:0016814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0016810"],"is_obsolete":false,"name":"aminoimidazolase activity","secondary_identifiers":["MetaCyc:R13-RXN","EC:3.5.4.8"],"synonyms":[{"name":"4-aminoimidazole aminohydrolase activity","type":"related"},{"name":"4-aminoimidazole hydrolase activity","type":"related"}],"termid":"GO:0047664"}


id: PBO:0038826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 33","termid":"PBO:0038826"}


id: PBO:0046399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPB41L4A antisense RNA 1","termid":"PBO:0046399"}


id: GO:0140628
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and stops, prevents, or reduces the activity of an outwardly rectifying potassium channel.","definition_xrefs":["PMID:28108814"],"direct_ancestors":[{"relation_name":"is_a","term_name":"potassium channel inhibitor activity","termid":"GO:0019870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0140678","GO:0098772","GO:0003674"],"is_obsolete":false,"name":"outward rectifier potassium channel inhibitor activity","termid":"GO:0140628"}


id: MONDO:0000869
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital fibrosis of the extraocular muscles (obsolete MONDO:0000869)","termid":"MONDO:0000869","xrefs":{"Monarch":{"xref_id":"0000869"}}}


id: PBO:0035823
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_stress_responsive_gene_mRNA_during_vegetative_growth","termid":"PBO:0035823"}


id: GO:0051349
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of lyase activity, the catalysis of the cleavage of C-C, C-O, C-N and other bonds by other means than by hydrolysis or oxidation, or conversely adding a group to a double bond.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catalytic activity","termid":"GO:0043085"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of lyase activity","synonyms":[{"name":"activation of lyase activity","type":"narrow"},{"name":"lyase activator","type":"exact"},{"name":"stimulation of lyase activity","type":"narrow"},{"name":"up regulation of lyase activity","type":"exact"},{"name":"up-regulation of lyase activity","type":"exact"},{"name":"upregulation of lyase activity","type":"exact"}],"termid":"GO:0051349"}


id: GO:0090323
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of a prostaglandin that contributes to the immune response. Prostaglandins are a group of biologically active metabolites which contain a cyclopentane ring.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostaglandin secretion","termid":"GO:0032310"},{"relation_name":"part_of","term_name":"immune response","termid":"GO:0006955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0023052","GO:0051179"],"is_obsolete":false,"name":"prostaglandin secretion involved in immune response","termid":"GO:0090323"}


id: PBO:0070550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 16","termid":"PBO:0070550"}


id: PBO:0114138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenine deaminase Dea3","termid":"PBO:0114138"}


id: PBO:0045561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 10","termid":"PBO:0045561"}


id: GO:0015575
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of mannitol from one side of a membrane to the other. Mannitol is the alditol derived from D-mannose by reduction of the aldehyde group.","definition_xrefs":["ISBN:0815340729","GOC:ai","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate transmembrane transporter activity","termid":"GO:0015144"},{"relation_name":"is_a","term_name":"polyol transmembrane transporter activity","termid":"GO:0015166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"mannitol transmembrane transporter activity","secondary_identifiers":["GO:0015586"],"synonyms":[{"name":"mannitol permease activity","type":"exact"}],"termid":"GO:0015575"}


id: GO:0050106
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + monomethyl sulfate = H+ + methanol + sulfate.","definition_xrefs":["EC:3.1.6.16","RHEA:14221"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfuric ester hydrolase activity","termid":"GO:0008484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"monomethyl-sulfatase activity","secondary_identifiers":["KEGG_REACTION:R01145","MetaCyc:MONOMETHYL-SULFATASE-RXN"],"synonyms":[{"name":"monomethyl-sulfate sulfohydrolase activity","type":"related"},{"name":"monomethyl-sulphatase activity","type":"exact"}],"termid":"GO:0050106"}


id: PBO:0018237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome assembly protein Sqt1 (predicted)","termid":"PBO:0018237"}


id: PBO:0031870
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved in Fungi","termid":"PBO:0031870"}


id: SO:0000790
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute describing a feature that is invalidated.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"status","termid":"SO:0000905"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"invalidated","termid":"SO:0000790"}


id: MONDO:0020669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the paranasal sinuses.","definition_xrefs":["NCIT:C7487"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system cancer","termid":"MONDO:0000376"},{"relation_name":"is_a","term_name":"sensory system cancer","termid":"MONDO:0000649"},{"relation_name":"is_a","term_name":"skull cancer","termid":"MONDO:0002132"},{"relation_name":"is_a","term_name":"paranasal sinus neoplasm","termid":"MONDO:0005289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"paranasal sinus cancer","secondary_identifiers":["MEDGEN:56305","UMLS:C0153474"],"synonyms":[{"name":"malignant accessory sinus neoplasm","type":"exact"},{"name":"malignant accessory sinus tumor","type":"exact"},{"name":"malignant accessory sinus tumour","type":"exact"},{"name":"malignant neoplasm of accessory sinus","type":"exact"},{"name":"malignant neoplasm of paranasal sinus","type":"exact"},{"name":"malignant neoplasm of the accessory sinus","type":"exact"},{"name":"malignant neoplasm of the paranasal sinus","type":"exact"},{"name":"malignant paranasal sinus neoplasm","type":"exact"},{"name":"malignant paranasal sinus tumor","type":"exact"},{"name":"malignant paranasal sinus tumour","type":"exact"},{"name":"malignant tumor of accessory sinus","type":"exact"},{"name":"malignant tumor of paranasal sinus","type":"exact"},{"name":"malignant tumor of the accessory sinus","type":"exact"},{"name":"malignant tumor of the paranasal sinus","type":"exact"},{"name":"malignant tumour of accessory sinus","type":"exact"},{"name":"malignant tumour of paranasal sinus","type":"exact"},{"name":"malignant tumour of the accessory sinus","type":"exact"},{"name":"malignant tumour of the paranasal sinus","type":"exact"}],"termid":"MONDO:0020669","xrefs":{"Monarch":{"xref_id":"0020669"}}}


id: MONDO:0001229
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diverticulitis that involves the small intestine.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diverticulitis","termid":"MONDO:0004235"},{"relation_name":"is_a","term_name":"small intestine disorder","termid":"MONDO:0024635"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"small intestine diverticulitis","secondary_identifiers":["SCTID:56165008","MEDGEN:540732","ICD9:562.02","ICD9:562.01","DOID:11223","UMLS:C0267502"],"synonyms":[{"name":"diverticulitis of small intestine","type":"exact"},{"name":"diverticulosis of small intestine with haemorrhage","type":"exact"},{"name":"diverticulosis of small intestine with hemorrhage","type":"exact"},{"name":"small intestine diverticulitis","type":"exact"}],"termid":"MONDO:0001229","xrefs":{"Monarch":{"xref_id":"0001229"}}}


id: PBO:0034414
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_process_that_acts_on_population_of","termid":"PBO:0034414"}


id: PBO:0054582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1985","termid":"PBO:0054582"}


id: PBO:0045876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation elongation factor 1 delta","termid":"PBO:0045876"}


id: MONDO:0022401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cortical malformations characterized by no gyri, broad gyri and/or an excessive number of abnormally small gyri that result in an irregular cortical surface with lumpy aspect.","definition_xrefs":["PMID:22333901"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"agyria pachygyria polymicrogyria","termid":"MONDO:0022401","xrefs":{"Monarch":{"xref_id":"0022401"}}}


id: PR:Q10327
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC32A11.02c gene.","definition_xrefs":["UniProtKB:Q10327","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C32A11.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC32A11.02c","synonyms":[{"name":"Spom972h-SPAC32A11.02c","type":"exact"}],"termid":"PR:Q10327"}


id: PBO:0072664
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reticulon 4 interacting protein 1","termid":"PBO:0072664"}


id: PBO:0030861
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_localization_to_medial_cortex","termid":"PBO:0030861"}


id: MONDO:0037870
data:
  {"annotated_genes":["SJAG_00944"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87500],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009603"}]},"cv_name":"mondo","definition":"A disease that has its basis in the disruption of valine metabolic process.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid metabolism disease","termid":"MONDO:0037871"},{"relation_name":"is_a","term_name":"disorder of organic acid metabolism","termid":"MONDO:0045022"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00944":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"valine metabolism disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:444756000","UMLS:C2919304","MEDGEN:753614"],"synonyms":[{"name":"disorder of valine metabolic process","type":"exact"},{"name":"disorder of valine metabolism","type":"exact"},{"name":"valine metabolic process disease","type":"exact"}],"termid":"MONDO:0037870","terms_by_termid":{"MONDO:0009603":null},"xrefs":{"Monarch":{"xref_id":"0037870"}}}


id: PBO:0117050
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MFSD14A antisense RNA 1","termid":"PBO:0117050"}


id: PBO:0052375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family member 19B, pseudogene","termid":"PBO:0052375"}


id: MONDO:0011543
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete BRCA3 (obsolete MONDO:0011543)","secondary_identifiers":["MESH:C565336","OMIM:605365"],"synonyms":[{"name":"BRCA3","type":"exact"},{"name":"Brcax","type":"related"},{"name":"breast cancer 3","type":"related"},{"name":"moved to 114480","type":"related"}],"termid":"MONDO:0011543","xrefs":{"Monarch":{"xref_id":"0011543"}}}


id: PBO:0078553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 43","termid":"PBO:0078553"}


id: GO:0046513
data:
  {"annotated_genes":["SJAG_02842","SJAG_01057","SJAG_02085","SJAG_02305","SJAG_01219","SJAG_04178"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75900,78598,79846,80662,80825,110661],"is_not":false,"summary":null,"term":"GO:0046513"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ceramides, any N-acylated sphingoid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ceramide metabolic process","termid":"GO:0006672"},{"relation_name":"is_a","term_name":"sphingolipid biosynthetic process","termid":"GO:0030148"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01057":null,"SJAG_01219":null,"SJAG_02085":null,"SJAG_02305":null,"SJAG_02842":null,"SJAG_04178":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"ceramide biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"ceramide anabolism","type":"exact"},{"name":"ceramide biosynthesis","type":"exact"},{"name":"ceramide formation","type":"exact"},{"name":"ceramide synthesis","type":"exact"}],"termid":"GO:0046513","terms_by_termid":{"GO:0046513":null}}


id: MONDO:1011701
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hematologic disorder, non-human animal","termid":"MONDO:1011319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"combined deficiency of factors IX and XII, non-human animal","secondary_identifiers":["OMIA:001526"],"termid":"MONDO:1011701","xrefs":{"Monarch":{"xref_id":"1011701"}}}


id: GO:0010113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of systemic acquired resistance.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of response to biotic stimulus","termid":"GO:0002832"},{"relation_name":"is_a","term_name":"regulation of systemic acquired resistance","termid":"GO:0010112"},{"relation_name":"is_a","term_name":"negative regulation of defense response","termid":"GO:0031348"},{"relation_name":"is_a","term_name":"negative regulation of response to external stimulus","termid":"GO:0032102"},{"relation_name":"negatively_regulates","term_name":"systemic acquired resistance","termid":"GO:0009627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of systemic acquired resistance","synonyms":[{"name":"down regulation of systemic acquired resistance","type":"exact"},{"name":"down-regulation of systemic acquired resistance","type":"exact"},{"name":"downregulation of systemic acquired resistance","type":"exact"},{"name":"inhibition of systemic acquired resistance","type":"narrow"}],"termid":"GO:0010113"}


id: PBO:0117186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPP6 antisense RNA 1","termid":"PBO:0117186"}


id: PBO:0035919
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_transport_along_microtubule_during_vegetative_growth","termid":"PBO:0035919"}


id: MONDO:0022850
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital sucrose isomaltose malabsorption (obsolete MONDO:0022850)","termid":"MONDO:0022850","xrefs":{"Monarch":{"xref_id":"0022850"}}}


id: GO:0001989
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the force with which the cardiac muscles of the heart pump blood through the circulatory system as part of the baroreceptor response to decreased blood pressure.","definition_xrefs":["ISBN:0721643949"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of the force of heart contraction involved in baroreceptor response to decreased systemic arterial blood pressure (obsolete GO:0001989)","synonyms":[{"name":"increased force of heart contraction during baroreceptor response to decreased systemic arterial blood pressure","type":"related"},{"name":"increased strength of cardiac contraction during baroreceptor response to decreased blood pressure","type":"related"},{"name":"positive regulation of the force of heart contraction during baroreceptor response to decreased systemic arterial blood pressure","type":"related"}],"termid":"GO:0001989"}


id: GO:0004450
data:
  {"annotated_genes":["SJAG_04362"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75594],"is_not":false,"summary":null,"term":"GO:0004450"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: isocitrate + NADP+ = 2-oxoglutarate + CO2 + NADPH.","definition_xrefs":["RHEA:19629"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isocitrate dehydrogenase [NAD(P)+] activity","termid":"GO:0004448"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04362":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"isocitrate dehydrogenase (NADP+) activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:ISOCITDEH-RXN","Reactome:R-HSA-389540","Reactome:R-HSA-450984","Reactome:R-HSA-389550","EC:1.1.1.42"],"synonyms":[{"name":"NADP isocitric dehydrogenase activity","type":"exact"},{"name":"NADP(+)-ICDH activity","type":"related"},{"name":"NADP(+)-IDH activity","type":"related"},{"name":"NADP(+)-linked isocitrate dehydrogenase activity","type":"exact"},{"name":"NADP-dependent isocitrate dehydrogenase activity","type":"exact"},{"name":"NADP-dependent isocitric dehydrogenase activity","type":"exact"},{"name":"NADP-linked isocitrate dehydrogenase activity","type":"exact"},{"name":"NADP-specific isocitrate dehydrogenase activity","type":"exact"},{"name":"dual-cofactor-specific isocitrate dehydrogenase activity","type":"related"},{"name":"isocitrate (NADP) dehydrogenase activity","type":"exact"},{"name":"isocitrate (nicotinamide adenine dinucleotide phosphate) dehydrogenase activity","type":"exact"},{"name":"isocitrate dehydrogenase (NADP) activity","type":"exact"},{"name":"isocitrate dehydrogenase (NADP-dependent) activity","type":"exact"},{"name":"isocitrate:NADP+ oxidoreductase (decarboxylating)","type":"exact"},{"name":"triphosphopyridine nucleotide-linked isocitrate dehydrogenase activity","type":"exact"}],"termid":"GO:0004450","terms_by_termid":{"GO:0004450":null}}


id: PR:Q9HE16
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- toe1 gene.","definition_xrefs":["UniProtKB:Q9HE16","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized transcriptional regulatory protein C1399.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1399.05c","synonyms":[{"name":"Spom972h-toe1","type":"exact"}],"termid":"PR:Q9HE16"}


id: GO:1900349
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of methane biosynthetic process from methylamine.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of amine metabolic process","termid":"GO:0033239"},{"relation_name":"is_a","term_name":"regulation of methane biosynthetic process from methylamine","termid":"GO:1900348"},{"relation_name":"is_a","term_name":"negative regulation of alkane biosynthetic process","termid":"GO:1901578"},{"relation_name":"is_a","term_name":"negative regulation of cellular respiration","termid":"GO:1901856"},{"relation_name":"negatively_regulates","term_name":"methane biosynthetic process from methylamine","termid":"GO:2001128"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006091"},{"rel_name":"regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"negative regulation of methane biosynthetic process from methylamine","synonyms":[{"name":"down regulation of methane biosynthetic process from methylamine","type":"exact"},{"name":"down-regulation of methane biosynthetic process from methylamine","type":"exact"},{"name":"downregulation of methane biosynthetic process from methylamine","type":"exact"},{"name":"inhibition of methane biosynthetic process from methylamine","type":"narrow"}],"termid":"GO:1900349"}


id: PBO:0069155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 407, pseudogene","termid":"PBO:0069155"}


id: MONDO:0021925
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the tracheobronchial tree.","definition_xrefs":["NCIT:C122784"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lower respiratory tract disorder","termid":"MONDO:0000270"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tracheobronchitis","secondary_identifiers":["MEDGEN:508208","UMLS:C0040586","icd11.foundation:1889351414","SCTID:13617004"],"synonyms":[{"name":"Tracheobronchitis","type":"related"},{"name":"tracheobronchitis","type":"exact"}],"termid":"MONDO:0021925","xrefs":{"Monarch":{"xref_id":"0021925"}}}


id: GO:0019683
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glyceraldehyde-3-phosphate, an important intermediate in glycolysis.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glyceraldehyde-3-phosphate metabolic process","termid":"GO:0019682"},{"relation_name":"is_a","term_name":"aldehyde catabolic process","termid":"GO:0046185"},{"relation_name":"is_a","term_name":"organophosphate catabolic process","termid":"GO:0046434"},{"relation_name":"is_a","term_name":"carbohydrate derivative catabolic process","termid":"GO:1901136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"glyceraldehyde-3-phosphate catabolic process","synonyms":[{"name":"glyceraldehyde 3-phosphate catabolic process","type":"exact"},{"name":"glyceraldehyde 3-phosphate catabolism","type":"exact"},{"name":"glyceraldehyde-3-phosphate breakdown","type":"exact"},{"name":"glyceraldehyde-3-phosphate catabolism","type":"exact"},{"name":"glyceraldehyde-3-phosphate degradation","type":"exact"}],"termid":"GO:0019683"}


id: GO:0032625
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-21 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"interleukin-21 production","secondary_identifiers":["GO:0072619","GO:0042238"],"synonyms":[{"name":"IL-21 production","type":"exact"},{"name":"interleukin-21 biosynthetic process","type":"narrow"},{"name":"interleukin-21 secretion","type":"narrow"}],"termid":"GO:0032625"}


id: PBO:0060092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 39","termid":"PBO:0060092"}


id: PBO:0039646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP1B1 pseudogene 2","termid":"PBO:0039646"}


id: PBO:0016064
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pombe Response Regulator","termid":"PBO:0016064"}


id: MONDO:0012291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any selective IgA deficiency disease in which the cause of the disease is a mutation in the TNFRSF13B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"selective IgA deficiency disease","termid":"MONDO:0001341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"immunoglobulin A deficiency 2","secondary_identifiers":["OMIM:609529","MESH:C536291","MEDGEN:372182","UMLS:C1836032","GARD:10198"],"synonyms":[{"name":"IGAD2","type":"related"},{"name":"IMMUNOGLOBULIN A deficiency 2","type":"related"},{"name":"IgA, selective deficiency of, TACI related","type":"related"},{"name":"IgA, selective deficiency of, TACI-related","type":"related"},{"name":"Immunoglobulin A, selective deficiency of, TACI related","type":"related"},{"name":"Immunoglobulin A, selective deficiency of, TACI-related","type":"related"},{"name":"Immunoglobulin a deficiency type 2","type":"exact"},{"name":"TNFRSF13B selective IgA deficiency disease","type":"exact"},{"name":"immunoglobulin a deficiency 2","type":"exact"},{"name":"selective IgA deficiency disease caused by mutation in TNFRSF13B","type":"exact"}],"termid":"MONDO:0012291","xrefs":{"Monarch":{"xref_id":"0012291"}}}


id: GO:0006015
data:
  {"annotated_genes":["SJAG_04882","SJAG_04970","SJAG_03811"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[64435,74163,75610],"is_not":false,"summary":null,"term":"GO:0006015"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 5-phosphoribose 1-diphosphate, also known as 5-phosphoribosyl-1-pyrophosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribose phosphate biosynthetic process","termid":"GO:0046390"},{"relation_name":"is_a","term_name":"5-phosphoribose 1-diphosphate metabolic process","termid":"GO:0046391"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03811":null,"SJAG_04882":null,"SJAG_04970":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"5-phosphoribose 1-diphosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-73843"],"synonyms":[{"name":"5-phosphoribose 1-diphosphate anabolism","type":"exact"},{"name":"5-phosphoribose 1-diphosphate biosynthesis","type":"exact"},{"name":"5-phosphoribose 1-diphosphate formation","type":"exact"},{"name":"5-phosphoribose 1-diphosphate synthesis","type":"exact"},{"name":"5-phosphoribosyl-1-pyrophosphate biosynthesis","type":"exact"},{"name":"5-phosphoribosyl-1-pyrophosphate biosynthetic process","type":"exact"},{"name":"PRPP biosynthetic process","type":"exact"}],"termid":"GO:0006015","terms_by_termid":{"GO:0006015":null}}


id: PBO:0005737
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"condensin subunit CuT3 Interacting protein","termid":"PBO:0005737"}


id: PBO:0061326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear pore complex interacting protein family member B4","termid":"PBO:0061326"}


id: PBO:0065275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 36","termid":"PBO:0065275"}


id: PBO:0063042
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatase domain containing paladin 1","termid":"PBO:0063042"}


id: PBO:0053216
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galectin 13","termid":"PBO:0053216"}


id: GO:0060112
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process which controls the timing of the type of sexual cycle seen in female mammals.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovulation cycle process","termid":"GO:0022602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"generation of ovulation cycle rhythm","synonyms":[{"name":"generation of estrus cycle rhythm","type":"exact"},{"name":"generation of menstrual cycle rhythm","type":"related"},{"name":"generation of oestrus cycle rhythm","type":"exact"}],"termid":"GO:0060112"}


id: PBO:0071246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 87","termid":"PBO:0071246"}


id: MONDO:1011254
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any progressive rod-cone degeneration that occurs in dogs due to a mutation in the PDE6A gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cone-rod dystrophy, non-human animal","termid":"MONDO:1012582"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rod-cone dysplasia, PDE6A-related, dog","secondary_identifiers":["OMIA:001314-9615"],"synonyms":[{"name":"retinal atrophy - rod-cone dysplasia 3, PDE6A-related, dog","type":"related"}],"termid":"MONDO:1011254","xrefs":{"Monarch":{"xref_id":"1011254"}}}


id: PBO:0052989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laminin subunit alpha 1","termid":"PBO:0052989"}


id: PBO:0027172
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_nucleus_during_mitotic_interphase","termid":"PBO:0027172"}


id: MONDO:1011280
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microphthalmia, isolated, with coloboma that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microphthalmia, isolated, with coloboma, non-human animal","termid":"MONDO:1010352"},{"relation_name":"is_a","term_name":"coloboma, dog","termid":"MONDO:1011214"},{"relation_name":"is_a","term_name":"microphthalmia, dog","termid":"MONDO:1011238"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microphthalmia, isolated, with coloboma, dog","secondary_identifiers":["OMIA:002151-9615"],"termid":"MONDO:1011280","xrefs":{"Monarch":{"xref_id":"1011280"}}}


id: GO:0033646
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any constituent part of the living contents of a host cell; the matter contained within (but not including) the plasma membrane, usually taken to exclude large vacuoles and masses of secretory or ingested material. In eukaryotes it includes the nucleus and cytoplasm. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host cell part","termid":"GO:0033643"},{"relation_name":"part_of","term_name":"host intracellular region","termid":"GO:0043656"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"host intracellular part","synonyms":[{"name":"host cell intracellular part","type":"exact"}],"termid":"GO:0033646"}


id: GO:1900414
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A regulation of transcription from RNA polymerase II promoter that results in regulation of cytokinesis.","definition_xrefs":["PMID:15509866","GOC:mah","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cytokinesis by regulation of transcription from RNA polymerase II promoter (obsolete GO:1900414)","termid":"GO:1900414"}


id: MONDO:0003022
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An angiosarcoma occurring in childhood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood malignant neoplasm","termid":"MONDO:0006517"},{"relation_name":"is_a","term_name":"angiosarcoma","termid":"MONDO:0016982"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"pediatric angiosarcoma","secondary_identifiers":["UMLS:C0279988","NCIT:C9174","MEDGEN:124687","DOID:4505"],"synonyms":[{"name":"angiosarcoma","type":"broad"},{"name":"angiosarcoma (disease) of childhood","type":"exact"},{"name":"childhood angiosarcoma","type":"exact"},{"name":"childhood angiosarcoma (disease)","type":"exact"},{"name":"childhood hemangiosarcoma","type":"exact"},{"name":"paediatric angiosarcoma (disease)","type":"exact"},{"name":"paediatric hemangiosarcoma","type":"exact"},{"name":"pediatric angiosarcoma","type":"exact"},{"name":"pediatric angiosarcoma (disease)","type":"exact"},{"name":"pediatric hemangiosarcoma","type":"exact"}],"termid":"MONDO:0003022","xrefs":{"Monarch":{"xref_id":"0003022"}}}


id: PBO:0074313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMAD3 divergent transcript","termid":"PBO:0074313"}


id: PBO:0109373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 7","termid":"PBO:0109373"}


id: PBO:0061535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear speckle splicing regulatory protein 1","termid":"PBO:0061535"}


id: GO:0141062
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The disruption of a tissue of another organism, leading to damage or temporary subversion of that tissue.","definition_xrefs":["PMID:26355030","PMID:27416066","PMID:34346770","PMID:11895956","PMID:28194160"],"gene_count":0,"genotype_count":0,"name":"obsolete disruption of tissue in another organism (obsolete GO:0141062)","synonyms":[{"name":"tissue necrosis in another organism","type":"exact"}],"termid":"GO:0141062"}


id: PBO:0090579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Utp13","termid":"PBO:0090579"}


id: GO:0075035
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which specialized features of the symbiont appressorium are acquired post initiation, to aid in infection of the host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formation of structure involved in a symbiotic process","termid":"GO:0044111"},{"relation_name":"part_of","term_name":"appressorium formation","termid":"GO:0075016"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"appressorium maturation","synonyms":[{"name":"appressorium maturation on or near host","type":"exact"},{"name":"maturation of appressorium on or near host","type":"related"},{"name":"maturation of symbiont appressorium on or near host","type":"exact"}],"termid":"GO:0075035"}


id: PBO:0110397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NUDT5 pseudogene 1","termid":"PBO:0110397"}


id: PBO:0013132
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPHerical shape","termid":"PBO:0013132"}


id: MONDO:0021243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the parotid gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parotid disorder","termid":"MONDO:0005899"},{"relation_name":"is_a","term_name":"neoplasm of major salivary gland","termid":"MONDO:0021368"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"parotid gland neoplasm","secondary_identifiers":["SCTID:126788000","EFO:0003873","UMLS:C0030581","NCIT:C3314","MEDGEN:18313"],"synonyms":[{"name":"neoplasm of parotid","type":"exact"},{"name":"neoplasm of parotid gland","type":"exact"},{"name":"neoplasm of the parotid","type":"exact"},{"name":"neoplasm of the parotid gland","type":"exact"},{"name":"parotid gland neoplasm (disease)","type":"exact"},{"name":"parotid gland tumor","type":"exact"},{"name":"parotid gland tumour","type":"exact"},{"name":"parotid neoplasm","type":"exact"},{"name":"parotid tumor","type":"exact"},{"name":"parotid tumour","type":"exact"},{"name":"tumor of parotid","type":"exact"},{"name":"tumor of parotid gland","type":"exact"},{"name":"tumor of the parotid","type":"exact"},{"name":"tumor of the parotid gland","type":"exact"},{"name":"tumour of parotid","type":"exact"},{"name":"tumour of parotid gland","type":"exact"},{"name":"tumour of the parotid","type":"exact"},{"name":"tumour of the parotid gland","type":"exact"}],"termid":"MONDO:0021243","xrefs":{"Monarch":{"xref_id":"0021243"}}}


id: PBO:0044796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin alpha 9, pseudogene","termid":"PBO:0044796"}


id: GO:0045670
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of osteoclast differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of myeloid leukocyte differentiation","termid":"GO:0002761"},{"relation_name":"regulates","term_name":"osteoclast differentiation","termid":"GO:0030316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of osteoclast differentiation","termid":"GO:0045670"}


id: GO:0100033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that regulates fungal-type cell wall biogenesis.","definition_xrefs":["GOC:obol","GOC:cjm"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of fungal-type cell wall biogenesis by transcription from RNA polymerase II promoter (obsolete GO:0100033)","termid":"GO:0100033"}


id: PBO:0081367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 205","termid":"PBO:0081367"}


id: FYPO:0005027
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an inviable cell that does not divide, has a larger diameter and volume than normal, contains two nuclei and more than one septum, and has an abnormal shape featuring a constriction at the center of the cell, corresponding to the cell division site. In some such cells, the diameter at the ends is much greater than in wild-type cells.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multinucleate multiseptate vegetative cell","termid":"FYPO:0001252"},{"relation_name":"is_a","term_name":"inviable septated vegetative cell with abnormal cell morphology","termid":"FYPO:0002452"},{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, swollen binucleate cell with central constriction","termid":"FYPO:0002987"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000032","FYPO:0000631","FYPO:0000004","FYPO:0001985"],"is_obsolete":false,"name":"inviable after spore germination, without cell division, swollen binucleate multiseptate cell with central constriction","synonyms":[{"name":"inviable after spore germination, binucleate without cell division, swollen with multiple septa","type":"exact"},{"name":"inviable after spore germination, undivided swollen binucleate multiseptate cell with central constriction","type":"exact"},{"name":"inviable after spore germination, without cell division, swollen binucleate multiseptate cell with central constriction, with nuclear division without cytokinesis","type":"exact"},{"name":"inviable after spore germination, without cell division, swollen binucleate multiseptate cell with constricted region at cell division site","type":"exact"},{"name":"inviable after spore germination, without cell division, swollen dumbbell-shaped binucleate multiseptate cell","type":"related"},{"name":"inviable following spore germination, without cell division, swollen binucleate multiseptate cell with central constriction","type":"exact"},{"name":"inviable germinated spore, without cell division, swollen binucleate multiseptate cell with central constriction","type":"exact"},{"name":"lethal after spore germination, without cell division, swollen binucleate multiseptate cell with central constriction","type":"exact"}],"termid":"FYPO:0005027"}


id: PBO:0074383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMG6 nonsense mediated mRNA decay factor","termid":"PBO:0074383"}


id: PBO:0081731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 662","termid":"PBO:0081731"}


id: MONDO:0002539
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete oligodendroglioma (obsolete MONDO:0002539)","termid":"MONDO:0002539","xrefs":{"Monarch":{"xref_id":"0002539"}}}


id: PBO:0066951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 253","termid":"PBO:0066951"}


id: GO:0120295
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-glutaminyl-[histone] + serotonin = 5-serotonyl-L-glutamyl-[histone] + NH4(+).","definition_xrefs":["GOC:sp","PMID:30867594"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide serotonyltransferase activity","termid":"GO:0120294"},{"relation_name":"is_a","term_name":"histone modifying activity","termid":"GO:0140993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016746","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"histone serotonyltransferase activity","termid":"GO:0120295"}


id: PBO:0053975
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1287","termid":"PBO:0053975"}


id: GO:1902225
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of acrosome reaction.","definition_xrefs":["PMID:23430248","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of acrosome reaction","termid":"GO:0060046"},{"relation_name":"is_a","term_name":"negative regulation of reproductive process","termid":"GO:2000242"},{"relation_name":"negatively_regulates","term_name":"acrosome reaction","termid":"GO:0007340"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of acrosome reaction","synonyms":[{"name":"down regulation of acrosome reaction","type":"exact"},{"name":"down-regulation of acrosome reaction","type":"exact"},{"name":"downregulation of acrosome reaction","type":"exact"},{"name":"inhibition of acrosome reaction","type":"narrow"}],"termid":"GO:1902225"}


id: PBO:0055610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 3049","termid":"PBO:0055610"}


id: FYPO:0008190
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to chromatin at the centromere central core is increased during the meiotic prophase I.","direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during meiosis","termid":"FYPO:0003549"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"increased protein localization to chromatin at centromere central core during meiotic prophase I","termid":"FYPO:0008190"}


id: GO:0015442
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ATP + H2O + (Na+ or H+)(in) = ADP + phosphate + (Na+ or H+)(out).","definition_xrefs":["TC:3.A.2.-.-"],"gene_count":0,"genotype_count":0,"name":"obsolete hydrogen-/sodium-translocating ATPase activity (obsolete GO:0015442)","synonyms":[{"name":"hydrogen-/sodium-translocating ATPase activity","type":"exact"},{"name":"proton-/sodium-translocating ATPase activity","type":"exact"}],"termid":"GO:0015442"}


id: PBO:0039549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD44 divergent transcript","termid":"PBO:0039549"}


id: PBO:0028918
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_transcription_during_glucose_starvation","termid":"PBO:0028918"}


id: PBO:0084200
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Histone variant H2AZ; exchanged for histone H2A in nucleosomes by the SWR1 complex; involved in transcriptional regulation through prevention of the spread of silent heterochromatin; Htz1p-containing nucleosomes facilitate RNA Pol II passage by affecting correct assembly and modification status of RNA Pol II elongation complexes and by favoring efficient nucleosome remodeling","termid":"PBO:0084200"}


id: PBO:0069294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 550, pseudogene","termid":"PBO:0069294"}


id: PBO:0034543
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_nucleus_during_cellular_response_to_hydroxyurea","termid":"PBO:0034543"}


id: PBO:0068937
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 180, pseudogene","termid":"PBO:0068937"}


id: MONDO:0006669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Endocarditis that is caused by an infection with a bacterial agent.","definition_xrefs":["NCIT:C128359"],"direct_ancestors":[{"relation_name":"is_a","term_name":"infective endocarditis","termid":"MONDO:0000565"},{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"bacterial endocarditis","secondary_identifiers":["MedDRA:10004019","MEDGEN:41779","HP:0006689","EFO:1000830","UMLS:C0014121","icd11.foundation:1924438986","SCTID:301183007","MESH:D004697"],"synonyms":[{"name":"Bacteria caused endocarditis (disease)","type":"exact"},{"name":"Bacteria endocarditis (disease)","type":"exact"},{"name":"bacterial endocarditis","type":"exact"},{"name":"bacterial endocarditis (disease)","type":"exact"}],"termid":"MONDO:0006669","xrefs":{"Monarch":{"xref_id":"0006669"}}}


id: PBO:0035758
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_histone_H3-K4_trimethylation_during_vegetative_growth","termid":"PBO:0035758"}


id: MONDO:0020129
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An instance of motor neuron disease that is acquired during the lifetime of the individual.","definition_xrefs":["MONDO:patterns/acquired"],"direct_ancestors":[{"relation_name":"is_a","term_name":"motor neuron disorder","termid":"MONDO:0020128"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"acquired motor neuron disease","secondary_identifiers":["MEDGEN:1842733","UMLS:C5680367","Orphanet:98506","GARD:19479"],"synonyms":[{"name":"acquired anterior horn cell disease","type":"exact"},{"name":"acquired motor neuron disease","type":"exact"}],"termid":"MONDO:0020129","xrefs":{"Monarch":{"xref_id":"0020129"}}}


id: PBO:0063850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein inhibitor of activated STAT 3","termid":"PBO:0063850"}


id: PBO:0113223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Multicopper oxidase; integral membrane protein with similarity to Fet3p; targeted to vacuole via AP-3 pathway; may have role in iron transport","termid":"PBO:0113223"}


id: PBO:0005854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-coA-sterol acyltransferase Are2 (predicted)","termid":"PBO:0005854"}


id: GO:0035470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of blood vessel formation when new vessels emerge from the proliferation of pre-existing blood vessels and contribute to the series of events that restore integrity to damaged vasculature.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of angiogenesis","termid":"GO:0045766"},{"relation_name":"is_a","term_name":"regulation of vascular wound healing","termid":"GO:0061043"},{"relation_name":"is_a","term_name":"positive regulation of wound healing","termid":"GO:0090303"},{"relation_name":"positively_regulates","term_name":"vascular wound healing","termid":"GO:0061042"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of vascular wound healing","termid":"GO:0035470"}


id: PBO:0027609
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_bis(5'-nucleosyl)-tetraphosphatase_(asymmetrical)_activity","termid":"PBO:0027609"}


id: PBO:0084097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Guanine nucleotide exchange factor (GEF) for Ria1p; essential protein involved in ribosome maturation; with Ria1p, promotes release of Tif6p from 60S ribosomal subunits in the cytoplasm so that they can assemble with 40S subunits to generate mature ribosomes; ortholog of the human protein (SBDS) responsible for autosomal recessive Shwachman-Bodian-Diamond Syndrome; highly conserved across archaea and eukaryotes","termid":"PBO:0084097"}


id: PATO:0000238
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000238 relative odor_acuity (obsolete PATO:0000238)","termid":"PATO:0000238"}


id: PBO:0066026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAN binding protein 9","termid":"PBO:0066026"}


id: PBO:0059960
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 5","termid":"PBO:0059960"}


id: PBO:0004844
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar membrane alkaline phosphatase (predicted)","termid":"PBO:0004844"}


id: PBO:0116803
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 109C (gene/pseudogene)","termid":"PBO:0116803"}


id: GO:0140691
data:
  {"annotated_genes":["SJAG_00195","SJAG_01819","SJAG_02469","SJAG_00886","SJAG_03070","SJAG_03460","SJAG_04266"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[100296,109102,110380,114746,115684,116801,117733],"is_not":false,"summary":null,"term":"GO:0140691"}]},"cv_name":"molecular_function","definition":"Binding to an RNA or an RNA-containing complex to assist the folding process.","definition_xrefs":["PMID:31165735"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular_function","termid":"GO:0003674"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00195":null,"SJAG_00886":null,"SJAG_01819":null,"SJAG_02469":null,"SJAG_03070":null,"SJAG_03460":null,"SJAG_04266":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674"],"is_obsolete":false,"name":"RNA folding chaperone","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140691","terms_by_termid":{"GO:0140691":null}}


id: PBO:0040332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit c locus 1 pseudogene 7","termid":"PBO:0040332"}


id: GO:0046335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ethanolamine (2-aminoethanol), an important water-soluble base of phospholipid (phosphatidylethanolamine).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ethanolamine metabolic process","termid":"GO:0006580"},{"relation_name":"is_a","term_name":"primary alcohol biosynthetic process","termid":"GO:0034309"},{"relation_name":"is_a","term_name":"biogenic amine biosynthetic process","termid":"GO:0042401"},{"relation_name":"is_a","term_name":"primary amino compound biosynthetic process","termid":"GO:1901162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"ethanolamine biosynthetic process","synonyms":[{"name":"ethanolamine anabolism","type":"exact"},{"name":"ethanolamine biosynthesis","type":"exact"},{"name":"ethanolamine formation","type":"exact"},{"name":"ethanolamine synthesis","type":"exact"}],"termid":"GO:0046335"}


id: GO:0080032
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + methyl (-)-jasmonate = H+ + jasmonate + methanol.","definition_xrefs":["PMID:18467465","PMID:15233793","RHEA:55372"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"methyl jasmonate esterase activity","secondary_identifiers":["MetaCyc:RXN-10767"],"synonyms":[{"name":"MEJA esterase activity","type":"exact"},{"name":"jasmonic acid methyl ester esterase activity","type":"exact"},{"name":"methyl JA esterase activity","type":"exact"}],"termid":"GO:0080032"}


id: PBO:0038767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin related protein 5","termid":"PBO:0038767"}


id: GO:0070856
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a light chain of a myosin VI complex.","definition_xrefs":["GOC:sart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myosin light chain binding","termid":"GO:0032027"},{"relation_name":"is_a","term_name":"myosin VI binding","termid":"GO:0070853"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0008092"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515","GO:0008092"],"is_obsolete":false,"name":"myosin VI light chain binding","termid":"GO:0070856"}


id: SO:0000602
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A short 3'-uridylated RNA that can form a duplex (except for its post-transcriptionally added oligo_U tail (SO:0000609)) with a stretch of mature edited mRNA.","direct_ancestors":[{"relation_name":"is_a","term_name":"ncRNA","termid":"SO:0000655"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guide_RNA","secondary_identifiers":["http://en.wikipedia.org/wiki/Guide_RNA"],"synonyms":[{"name":"INSDC_feature:ncRNA","type":"broad"},{"name":"INSDC_qualifier:guide_RNA","type":"exact"},{"name":"gRNA","type":"exact"},{"name":"guide RNA","type":"exact"}],"termid":"SO:0000602"}


id: GO:0046702
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of an L-fucosyl group from GDP-beta-L-fucose to a galactoside acceptor molecule, usually an N-glycan, to form an alpha(1,6)-fucosylated galactoside.","definition_xrefs":["PMID:12413479"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-(1->6)-fucosyltransferase activity","termid":"GO:0046921"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016757","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"galactoside 6-L-fucosyltransferase activity","termid":"GO:0046702"}


id: PBO:0109188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi alpha-1,2-mannosyltransferase Omh6","termid":"PBO:0109188"}


id: GO:0061973
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which bone which forms deep in the organism are generated and organized.","definition_xrefs":["PMID:14579374"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone morphogenesis","termid":"GO:0060349"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"membrane bone morphogenesis","termid":"GO:0061973"}


id: PBO:0000767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO conjugating enzyme Hus5","termid":"PBO:0000767"}


id: PR:O42658
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pterin-4-alpha-carbinolamine dehydratase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO01871"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pterin-4-alpha-carbinolamine dehydratase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC27D7.04","secondary_identifiers":["UniProtKB:O42658"],"synonyms":[{"name":"4-alpha-hydroxy-tetrahydropterin dehydratase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PCD (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PHS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PCBD1","type":"exact"},{"name":"overlapping meiotic transcript 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"pterin carbinolamine dehydratase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42658"}


id: GO:0072386
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of an organelle towards the plus end of a microtubule, mediated by motor proteins. This process begins with the attachment of an organelle to a microtubule, and ends when the organelle reaches its final destination.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle transport along microtubule","termid":"GO:0072384"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"plus-end-directed organelle transport along microtubule","synonyms":[{"name":"microtubule plus-end-directed organelle distribution","type":"narrow"},{"name":"microtubule plus-end-directed organelle localization","type":"exact"}],"termid":"GO:0072386"}


id: GO:0098632
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The binding by a cell-adhesion protein on the cell surface to an extracellular matrix component, to mediate adhesion of the cell to another cell.","definition_xrefs":["Wikipedia:Cell_adhesion"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell adhesion mediator activity","termid":"GO:0098631"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0098631"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488","GO:0098631"],"is_obsolete":false,"name":"cell-cell adhesion mediator activity","synonyms":[{"name":"cell-cell adhesion molecule","type":"exact"},{"name":"protein binding involved in cell-cell adhesion","type":"exact"}],"termid":"GO:0098632"}


id: GO:0044588
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to laminaribiose, a disaccharide.","definition_xrefs":["GOC:tt","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide binding","termid":"GO:0070492"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"laminaribiose binding","termid":"GO:0044588"}


id: GO:0016511
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete endothelin-converting enzyme activity (obsolete GO:0016511)","synonyms":[{"name":"endothelin-converting enzyme activity","type":"exact"}],"termid":"GO:0016511"}


id: MOD:00144
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct between a cysteine residue and the porphyrin compound heme b, (7,12-diethenyl-3,8,13,17-tetramethylporphyrin-2,18-dipropanoato)iron.","definition_xrefs":["PubMed:170910","PubMed:192772","DeltaMass:0","ChEBI:17627","PubMed:2536325","PubMed:9535866","RESID:AA0135","Unimod:390#C"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porphyrin modified residue","termid":"MOD:00699"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-cysteine residue","termid":"MOD:02067"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"heme-L-cysteine","synonyms":[{"name":"(12-ethenyl-7-[(1S)-1-([(2R)-2-amino-2-carboxyethyl]sulfanyl)ethyl]-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-bis[2-carboxyethyl]-N21,N22,N23,N24)-ferrate","type":"exact"},{"name":"4-[1-(S-cysteinyl)ethyl]protoporphyrin IX","type":"exact"},{"name":"BINDING Heme (covalent; via 1 link)","type":"exact"},{"name":"Heme","type":"related"},{"name":"HemeCys1","type":"exact"},{"name":"S-Heme (on Cysteine)","type":"exact"},{"name":"cysteinyl heme","type":"exact"},{"name":"heme","type":"related"},{"name":"heme-L-cysteine","type":"exact"}],"termid":"MOD:00144"}


id: PBO:0071576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L35 pseudogene 5","termid":"PBO:0071576"}


id: GO:1904740
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A transcription from RNA polymerase II promoter that results in positive regulation of filamentous growth of a population of unicellular organisms in response to starvation.","definition_xrefs":["GOC:rn","GOC:TermGenie","GO_REF:0000063","PMID:26448198"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by transcription from RNA polymerase II promoter (obsolete GO:1904740)","synonyms":[{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by RNA polymerase II transcription factor activity","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by gene-specific transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by general transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by specific transcription from RNA polymerase II promoter","type":"related"},{"name":"positive regulation of filamentous growth of a population of unicellular organisms in response to starvation by transcription from Pol II promoter","type":"exact"}],"termid":"GO:1904740"}


id: PBO:0039848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGAP15 antisense RNA 1","termid":"PBO:0039848"}


id: GO:0140331
data:
  {"annotated_genes":["SJAG_00669","SJAG_03050","SJAG_02516"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[60480,63674,70233],"is_not":false,"summary":null,"term":"GO:0140331"}]},"cv_name":"biological_process","definition":"The movement of an aminophospholipid molecule from one leaflet of a membrane bilayer to the opposite leaflet.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminophospholipid transport","termid":"GO:0015917"},{"relation_name":"is_a","term_name":"phospholipid translocation","termid":"GO:0045332"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00669":null,"SJAG_02516":null,"SJAG_03050":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0061024"],"is_obsolete":false,"name":"aminophospholipid translocation","references_by_uniquename":{"GO_REF:0000108":null},"termid":"GO:0140331","terms_by_termid":{"GO:0140331":null}}


id: PBO:0082627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of conserved R2TP complex (Rvb1-Rvb2-Tah1-Pih1); R2TP complex interacts with Hsp90 (Hsp82p and Hsc82p) to mediate assembly of large protein complexes such as box C/D snoRNPs and RNA polymerase II; contains a single TPR domain with at least two TPR motifs; plays a role in determining prion variants","termid":"PBO:0082627"}


id: PBO:0002149
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"focus formation at heterochromatic regions, Swi6_dependent","termid":"PBO:0002149"}


id: PBO:0113483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Telomere-linked gene, silencing of which is strictly Sir2-dependent","termid":"PBO:0113483"}


id: MONDO:0018482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete squamous cell carcinoma of stomach (obsolete MONDO:0018482)","termid":"MONDO:0018482","xrefs":{"Monarch":{"xref_id":"0018482"}}}


id: PBO:0114411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific microprotein","termid":"PBO:0114411"}


id: GO:0045985
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving pyrimidine nucleobases.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of pyrimidine nucleobase metabolic process","termid":"GO:0006142"},{"relation_name":"is_a","term_name":"positive regulation of nucleobase-containing compound metabolic process","termid":"GO:0045935"},{"relation_name":"is_a","term_name":"positive regulation of small molecule metabolic process","termid":"GO:0062013"},{"relation_name":"positively_regulates","term_name":"pyrimidine nucleobase metabolic process","termid":"GO:0006206"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"positively_regulates","termid":"GO:0055086"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"positive regulation of pyrimidine nucleobase metabolic process","synonyms":[{"name":"activation of pyrimidine base metabolic process","type":"narrow"},{"name":"positive regulation of pyrimidine base metabolic process","type":"exact"},{"name":"positive regulation of pyrimidine base metabolism","type":"exact"},{"name":"stimulation of pyrimidine base metabolic process","type":"narrow"},{"name":"up regulation of pyrimidine base metabolic process","type":"exact"},{"name":"up-regulation of pyrimidine base metabolic process","type":"exact"},{"name":"upregulation of pyrimidine base metabolic process","type":"exact"}],"termid":"GO:0045985"}


id: FYECO:0000390
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which torin1 was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ torin1","synonyms":[{"name":"Torin1","type":"exact"}],"termid":"FYECO:0000390"}


id: PBO:0062415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 46 pseudogene","termid":"PBO:0062415"}


id: PR:Q09831
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ppk14 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09831"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine-protein kinase ppk14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4G8.05","synonyms":[{"name":"Spom972h-ppk14","type":"exact"}],"termid":"PR:Q09831"}


id: PBO:0041145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basic transcription factor 3 like 4 pseudogene 4","termid":"PBO:0041145"}


id: MOD:01743
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"The protein modification reporter fragment produced by an Proteome Sciences TMT6plex-128 reagent acylated residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"TMT6plex-128 reporter+balance reagent acylated residue","termid":"MOD:01736"},{"relation_name":"derives_from","term_name":"cysTMT6plex-128 reporter+balance reagent cysteine disulfide","termid":"MOD:01825"},{"relation_name":"is_a","term_name":"TMT6plex reporter fragment","termid":"MOD:01716"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMT6plex-128 reporter fragment","synonyms":[{"name":"2,6-dimethyl-1-methylidenepiperidinium","type":"exact"},{"name":"Sixplex Tandem Mass Tag(TM)","type":"related"},{"name":"TMT6plex","type":"related"},{"name":"cysTMT6plex-128 reporter fragment","type":"exact"}],"termid":"MOD:01743"}


id: PBO:0074814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 15A","termid":"PBO:0074814"}


id: PBO:0041614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdk5 and Abl enzyme substrate 2","termid":"PBO:0041614"}


id: FYPO:0000725
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of methyl methanesulfonate than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0001985","FYPO:0005447","FYPO:0002682","FYPO:0000003"],"is_obsolete":false,"name":"resistance to methyl methanesulfonate","synonyms":[{"name":"resistance to MMS","type":"exact"},{"name":"resistance to methyl methanesulfonate during mitotic cell cycle","type":"related"},{"name":"resistance to methyl methanesulfonate during vegetative growth","type":"exact"},{"name":"resistance to methyl methanesulphonate","type":"exact"},{"name":"resistant to methyl methanesulfonate","type":"exact"}],"termid":"FYPO:0000725"}


id: PBO:0091409
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"during meiotic recombination Rad51 foci partially colocalize with linear elements","termid":"PBO:0091409"}


id: PBO:0086400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative divalent metal ion transporter involved in iron homeostasis; transcriptionally regulated by metal ions; member of the Nramp family of metal transport proteins; protein abundance increases in response to DNA replication stress","termid":"PBO:0086400"}


id: PBO:0001111
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, human WDR70 family","termid":"PBO:0001111"}


id: PBO:0077947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (anticodon AGC) 7-1","termid":"PBO:0077947"}


id: PBO:0052069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine acetyltransferase 8","termid":"PBO:0052069"}


id: PBO:0085634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in histone H2B ubiquitination; acts as cofactor for Bre1p; null mutant forms abnormally large cells, and homozygous diploid null mutant displays delayed premeiotic DNA synthesis and reduced efficiency of meiotic nuclear division","termid":"PBO:0085634"}


id: PBO:0087349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Spindle pole body-related intermediate filament protein; forms cell cycle-specific filaments between spindle pole bodies in dividing cells; localizes to poles and microtubules of spindle during anaphase and contributes to spindle stability; involved in Glc7p localization and regulation; relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0087349"}


id: PBO:0042871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CFAP100 divergent transcript","termid":"PBO:0042871"}


id: GO:0046671
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of programmed cell death that occurs in the retina.","definition_xrefs":["GOC:ai","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of programmed cell death","termid":"GO:0043069"},{"relation_name":"is_a","term_name":"regulation of retinal cell programmed cell death","termid":"GO:0046668"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"negatively_regulates","term_name":"retinal cell programmed cell death","termid":"GO:0046666"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of retinal cell programmed cell death","synonyms":[{"name":"down regulation of retinal programmed cell death","type":"exact"},{"name":"down-regulation of retinal programmed cell death","type":"exact"},{"name":"downregulation of retinal programmed cell death","type":"exact"},{"name":"inhibition of retinal programmed cell death","type":"narrow"},{"name":"negative regulation of retinal programmed cell death","type":"exact"}],"termid":"GO:0046671"}


id: GO:0061651
data:
  {"annotated_genes":["SJAG_01251"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94726],"is_not":false,"summary":null,"term":"GO:0061651"}]},"cv_name":"molecular_function","definition":"Isoenergetic transfer of Atg12 from one protein to another via the reaction X-Atg12 + Y = Y-Atg12 + X, where both the X-Atg12 and Y-Atg12 linkages are thioester bonds between the C-terminal amino acid of Atg12 and a sulfhydryl side group of a cysteine residue.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Atg12 transferase activity","termid":"GO:0019777"},{"relation_name":"is_a","term_name":"ubiquitin-like protein conjugating enzyme activity","termid":"GO:0061650"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01251":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0019787"}],"interesting_parent_ids":["GO:0019787","GO:0003824","GO:0140096","GO:0016740","GO:0016746","GO:0003674"],"is_obsolete":false,"name":"Atg12 conjugating enzyme activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"E2","type":"broad"}],"termid":"GO:0061651","terms_by_termid":{"GO:0061651":null}}


id: MONDO:0002514
data:
  {"annotated_genes":["SJAG_02049"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88434],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007256"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the liver parenchyma, bile ducts, and gallbladder. Representative examples of benign neoplasms include hepatocellular adenoma, bile duct adenoma, and gallbladder lipoma. Representative examples of malignant neoplasms include hepatocellular carcinoma, intrahepatic and extrahepatic cholangiocarcinoma, and gallbladder carcinoma.","definition_xrefs":["NCIT:C8614"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hepatobiliary disorder","termid":"MONDO:0002515"},{"relation_name":"is_a","term_name":"digestive system neoplasm","termid":"MONDO:0021223"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02049":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"hepatobiliary neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080355","MEDGEN:208891","UMLS:C0854196","EFO:0008550"],"synonyms":[{"name":"hepatic and biliary neoplasms","type":"exact"},{"name":"hepatic and biliary tumors","type":"exact"},{"name":"hepatic and biliary tumours","type":"exact"},{"name":"hepatic, biliary, and gallbladder neoplasms","type":"exact"},{"name":"hepato-biliary neoplasm","type":"exact"},{"name":"hepato-biliary tumor","type":"exact"},{"name":"hepato-biliary tumour","type":"exact"},{"name":"hepatobiliary benign neoplasm","type":"narrow"},{"name":"hepatobiliary neoplasm","type":"exact"},{"name":"hepatobiliary system neoplasm","type":"exact"},{"name":"hepatobiliary system neoplasm (disease)","type":"exact"},{"name":"hepatobiliary system tumor","type":"exact"},{"name":"hepatobiliary system tumour","type":"exact"},{"name":"hepatobiliary tumor","type":"exact"},{"name":"hepatobiliary tumors","type":"exact"},{"name":"hepatobiliary tumour","type":"exact"},{"name":"hepatobiliary tumours","type":"exact"},{"name":"liver and biliary neoplasm","type":"exact"},{"name":"liver and biliary system neoplasm","type":"exact"},{"name":"neoplasm of hepatobiliary system","type":"exact"},{"name":"tumor of hepatobiliary system","type":"exact"},{"name":"tumour of hepatobiliary system","type":"exact"}],"termid":"MONDO:0002514","terms_by_termid":{"MONDO:0007256":null},"xrefs":{"Monarch":{"xref_id":"0002514"}}}


id: PBO:0003659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SURF-family protein Shy1 (predicted)","termid":"PBO:0003659"}


id: GO:1905013
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of 'de novo' NAD biosynthetic process from L-tryptophan.","definition_xrefs":["GOC:bf","PMID:12140278","PMID:19843166","GO_REF:0000058","GOC:PARL","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of amine metabolic process","termid":"GO:0033239"},{"relation_name":"is_a","term_name":"negative regulation of amino acid metabolic process","termid":"GO:0045763"},{"relation_name":"is_a","term_name":"negative regulation of purine nucleotide biosynthetic process","termid":"GO:1900372"},{"relation_name":"is_a","term_name":"negative regulation of NAD metabolic process","termid":"GO:1902689"},{"relation_name":"is_a","term_name":"regulation of 'de novo' NAD biosynthetic process from L-tryptophan","termid":"GO:1905012"},{"relation_name":"negatively_regulates","term_name":"'de novo' NAD+ biosynthetic process from L-tryptophan","termid":"GO:0034354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0055086"},{"rel_name":"negatively_regulates","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0006520","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"negative regulation of 'de novo' NAD biosynthetic process from L-tryptophan","synonyms":[{"name":"down regulation of 'de novo' NAD biosynthetic process from tryptophan","type":"exact"},{"name":"down regulation of de novo NAD biosynthetic process from tryptophan","type":"related"},{"name":"down-regulation of 'de novo' NAD biosynthetic process from tryptophan","type":"exact"},{"name":"down-regulation of de novo NAD biosynthetic process from tryptophan","type":"related"},{"name":"downregulation of 'de novo' NAD biosynthetic process from tryptophan","type":"exact"},{"name":"downregulation of de novo NAD biosynthetic process from tryptophan","type":"related"},{"name":"inhibition of 'de novo' NAD biosynthetic process from tryptophan","type":"narrow"},{"name":"inhibition of de novo NAD biosynthetic process from tryptophan","type":"related"},{"name":"negative regulation of 'de novo' NAD biosynthetic process from tryptophan","type":"broad"},{"name":"negative regulation of de novo NAD biosynthetic process from tryptophan","type":"related"}],"termid":"GO:1905013"}


id: MONDO:0100013
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paratenonitis associated with intratendinous degeneration.","definition_xrefs":["PMID:14560540"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paratenonitis","termid":"MONDO:0100012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"paratenonitis with tendinosis","termid":"MONDO:0100013","xrefs":{"Monarch":{"xref_id":"0100013"}}}


id: GO:0070613
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein processing, a protein maturation process achieved by the cleavage of a peptide bond or bonds within a protein.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of proteolysis","termid":"GO:0030162"},{"relation_name":"is_a","term_name":"regulation of protein maturation","termid":"GO:1903317"},{"relation_name":"regulates","term_name":"protein processing","termid":"GO:0016485"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0051604"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0051604"],"is_obsolete":false,"name":"regulation of protein processing","secondary_identifiers":["GO:0010953"],"synonyms":[{"name":"regulation of protein maturation by peptide bond cleavage","type":"exact"}],"termid":"GO:0070613"}


id: PBO:0029434
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_curved_septated_vegetative_cell","termid":"PBO:0029434"}


id: PR:O94360
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mob1 gene.","definition_xrefs":["UniProtKB:O94360","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maintenance of ploidy protein mob1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC428.13c","synonyms":[{"name":"Spom972h-mob1","type":"exact"}],"termid":"PR:O94360"}


id: PBO:0024815
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-capable_of_part_of","termid":"PBO:0024815"}


id: PBO:0088918
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone lysine acetyltransferase Rtt109","termid":"PBO:0088918"}


id: PBO:0082369
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Basic helix-loop-helix (bHLH) transcription factor of the myc-family; activates transcription cooperatively with Pho2p in response to phosphate limitation; binding to 'CACGTG' motif is regulated by chromatin restriction, competitive binding of Cbf1p to the same DNA binding motif and cooperation with Pho2p; function is regulated by phosphorylation at multiple sites and by phosphate availability","termid":"PBO:0082369"}


id: PBO:0066949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 251","termid":"PBO:0066949"}


id: PBO:0075895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST7 antisense RNA 1","termid":"PBO:0075895"}


id: MONDO:1011963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proportionate dwarfism with inflammatory lesions, non-human animal","secondary_identifiers":["OMIA:001686"],"termid":"MONDO:1011963","xrefs":{"Monarch":{"xref_id":"1011963"}}}


id: PBO:0060049
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 37","termid":"PBO:0060049"}


id: GO:0080116
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of glucuronate to the xylan backbone of glucuronoxylan molecule.","definition_xrefs":["PMID:18980649"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucuronosyltransferase activity","termid":"GO:0015020"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016757","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"glucuronoxylan glucuronosyltransferase activity","termid":"GO:0080116"}


id: RO:0008501
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"An interaction relationship wherein a plant or algae is living on the outside surface of another plant.","direct_ancestors":[{"relation_name":"is_a","term_name":"symbiotically_interacts_with","termid":"RO:0002440"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epiphyte_of","termid":"RO:0008501"}


id: SO:0000305
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A modified nucleotide, i.e. a nucleotide other than A, T, C. G.","direct_ancestors":[{"relation_name":"is_a","term_name":"base","termid":"SO:0001236"},{"relation_name":"is_a","term_name":"epigenetically_modified_region","termid":"SO:0001720"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modified_DNA_base","synonyms":[{"name":"INSDC_feature:modified_base","type":"exact"},{"name":"modified base site","type":"exact"}],"termid":"SO:0000305"}


id: PBO:0057545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 661","termid":"PBO:0057545"}


id: PBO:0078362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon TTC) 7-1","termid":"PBO:0078362"}


id: GO:0007039
data:
  {"annotated_genes":["SJAG_03586","SJAG_04990","SJAG_00534","SJAG_04785","SJAG_01072","SJAG_01868","SJAG_03385"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77826,82127,89283,93638,96281,118687],"is_not":false,"summary":null,"term":"GO:0007039"},{"annotations":[101206],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1904352"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a protein in the vacuole, usually by the action of vacuolar proteases.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein catabolic process","termid":"GO:0030163"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00534":null,"SJAG_01072":null,"SJAG_01868":null,"SJAG_03385":null,"SJAG_03586":null,"SJAG_04785":null,"SJAG_04990":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030163"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0030163","GO:0008150"],"is_obsolete":false,"name":"protein catabolic process in the vacuole","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"vacuolar protein breakdown","type":"related"},{"name":"vacuolar protein catabolic process","type":"related"},{"name":"vacuolar protein catabolism","type":"related"},{"name":"vacuolar protein degradation","type":"related"}],"termid":"GO:0007039","terms_by_termid":{"GO:0007039":null,"GO:1904352":null}}


id: GO:0034612
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a tumor necrosis factor stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cytokine","termid":"GO:0034097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to tumor necrosis factor","synonyms":[{"name":"response to TNF","type":"exact"}],"termid":"GO:0034612"}


id: PBO:0054068
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1415","termid":"PBO:0054068"}


id: PBO:0108909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1191 pseudogene 3","termid":"PBO:0108909"}


id: GO:0036221
data:
  {"annotated_genes":["SJAG_01651"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98917],"is_not":false,"summary":null,"term":"GO:0036221"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: UTP + H2O = UMP + H+ + diphosphate.","definition_xrefs":["RHEA:29395","GOC:dgf","PMID:17899088"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside triphosphate diphosphatase activity","termid":"GO:0047429"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01651":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0047429"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0047429","GO:0003824"],"is_obsolete":false,"name":"UTP diphosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R00662"],"synonyms":[{"name":"uridine triphosphate pyrophosphohydrolase activity","type":"exact"}],"termid":"GO:0036221","terms_by_termid":{"GO:0036221":null}}


id: MONDO:1011426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Junctionalis epidermolysis bullosa that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolysis bullosa, non-human animal","termid":"MONDO:1010129"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"junctionalis epidermolysis bullosa , non-human animal","secondary_identifiers":["OMIA:000342"],"termid":"MONDO:1011426","xrefs":{"Monarch":{"xref_id":"1011426"}}}


id: MONDO:0019114
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Psychogenic movement disorders (PMD) are movement disorders that cannot be attributed to any known structural or neurochemical diseases, but represent the manifestation of an underlying psychiatric illness or malingering. Most cases of PMD fall in the psychiatric diagnostic category of conversion disorders of the motor subtype.","definition_xrefs":["Orphanet:71519"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psychogenic movement disorders","secondary_identifiers":["MedDRA:10072376","UMLS:C0752208","GARD:18914","icd11.foundation:1905355308","MEDGEN:155722"],"synonyms":[{"name":"psychogenic dystonia","type":"exact"}],"termid":"MONDO:0019114","xrefs":{"Monarch":{"xref_id":"0019114"}}}


id: MOD:00421
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue hydrogen atom on a carbon with a carbohydrate-like group through a glycosidic bond.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosylated residue","termid":"MOD:00693"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"C-glycosylated residue","synonyms":[{"name":"CGlycoRes","type":"exact"}],"termid":"MOD:00421"}


id: PBO:0083962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"General transcription elongation factor TFIIS; enables RNA polymerase II to read through blocks to elongation by stimulating cleavage of nascent transcripts stalled at transcription arrest sites; maintains RNAPII elongation activity on ribosomal protein genes during conditions of transcriptional stress","termid":"PBO:0083962"}


id: PBO:0087685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the NuA3 histone acetyltransferase complex; this complex acetylates histone H3; contains PHD finger domain that interacts with methylated histone H3","termid":"PBO:0087685"}


id: MONDO:0005021
data:
  {"annotated_genes":["SJAG_MIT13","SJAG_01754","SJAG_02919","SJAG_01322","SJAG_01139","SJAG_01240","SJAG_01209","SJAG_03145","SJAG_04567","SJAG_MIT03","SJAG_02611","SJAG_01671","SJAG_03815","SJAG_02431","SJAG_03703","SJAG_04231","SJAG_04621","SJAG_MIT15"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032592"},{"annotations":[88345,88344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030300"},{"annotations":[87337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859358"},{"annotations":[88159],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957545"},{"annotations":[87666,87665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008409"},{"annotations":[87979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012808"},{"annotations":[88249,88250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013198"},{"annotations":[88850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013339"},{"annotations":[86929,86930,86928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014073"},{"annotations":[87959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013261"},{"annotations":[87961,87960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013262"},{"annotations":[87469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012556"},{"annotations":[87331,87329,87330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010788"},{"annotations":[89009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013968"}]},"cv_name":"mondo","definition":"Cardiomyopathy which is characterized by dilation and contractile dysfunction of the left and right ventricles. It may be idiopathic, or it may result from a myocardial infarction, myocardial infection, or alcohol abuse. It is a cause of congestive heart failure.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intrinsic cardiomyopathy","termid":"MONDO:0000591"}],"gene_count":18,"genes_by_uniquename":{"SJAG_01139":null,"SJAG_01209":null,"SJAG_01240":null,"SJAG_01322":null,"SJAG_01671":null,"SJAG_01754":null,"SJAG_02431":null,"SJAG_02611":null,"SJAG_02919":null,"SJAG_03145":null,"SJAG_03703":null,"SJAG_03815":null,"SJAG_04231":null,"SJAG_04567":null,"SJAG_04621":null,"SJAG_MIT03":null,"SJAG_MIT13":null,"SJAG_MIT15":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"dilated cardiomyopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["HP:0001644","icd11.foundation:1916294688","NANDO:2200232","MEDGEN:2880","ICD10CM:I42.0","NANDO:2100057","DOID:12930","MedDRA:10056370","SCTID:195021004","NCIT:C84673","GARD:221","Orphanet:217604","EFO:0000407","UMLS:C0007193","ICD9:425.4","MESH:D002311"],"synonyms":[{"name":"congestive cardiomyopathy","type":"related"},{"name":"dilated cardiomyopathy","type":"exact"},{"name":"familial dilated cardiomyopathy","type":"related"},{"name":"idiopathic dilation cardiomyopathy","type":"related"},{"name":"primary dilated cardiomyopathy","type":"related"}],"termid":"MONDO:0005021","terms_by_termid":{"MONDO:0008409":null,"MONDO:0010788":null,"MONDO:0012556":null,"MONDO:0012808":null,"MONDO:0013198":null,"MONDO:0013261":null,"MONDO:0013262":null,"MONDO:0013339":null,"MONDO:0013968":null,"MONDO:0014073":null,"MONDO:0030300":null,"MONDO:0032592":null,"MONDO:0859358":null,"MONDO:0957545":null},"xrefs":{"Monarch":{"xref_id":"0005021"}}}


id: GO:0090431
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ester derivatives of alkyl caffeate.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catechol-containing compound biosynthetic process","termid":"GO:0009713"},{"relation_name":"is_a","term_name":"cinnamic acid ester biosynthetic process","termid":"GO:0009802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0019748"},{"rel_name":"part_of","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"alkyl caffeate ester biosynthetic process","synonyms":[{"name":"alkyl caffeate ester anabolism","type":"exact"},{"name":"alkyl caffeate ester biosynthesis","type":"exact"},{"name":"alkyl caffeate ester formation","type":"exact"},{"name":"alkyl caffeate ester synthesis","type":"exact"}],"termid":"GO:0090431"}


id: PBO:0056613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"male-enhanced antigen 1","termid":"PBO:0056613"}


id: GO:1905892
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of cellular response to thapsigargin.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:21803450","GOC:bc","GOC:aruk"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of cellular response to thapsigargin (obsolete GO:1905892)","synonyms":[{"name":"down regulation of cellular response to thapsigargin","type":"exact"},{"name":"down-regulation of cellular response to thapsigargin","type":"exact"},{"name":"downregulation of cellular response to thapsigargin","type":"exact"},{"name":"inhibition of cellular response to thapsigargin","type":"narrow"}],"termid":"GO:1905892"}


id: SO:0001657
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A binding site that, in the molecule, interacts selectively and non-covalently with a small molecule such as a drug, or hormone.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding_site","termid":"SO:0000409"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ligand_binding_site","synonyms":[{"name":"ligand binding site","type":"exact"}],"termid":"SO:0001657"}


id: MONDO:0015592
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Limbic encephalitis with LGI1 antibodies is a rare neuroimmunological disorder characterized by the onset of cognitive decline, psychiatric disturbances and seizures (distinctively faciobrachial dystonic seizures) in association with detection of LGI1 antibodies in serum or cerebrospinal fluid. Patients may present with confusion, hallucinations, vocalization, paranoia, tangentiality, aggressive outbursts and/or spatial disorientation, as well as obstinate hyponatremia. It is most often non-paraneoplastic, however comorbid tumors, such as small cell lung cancer and thymoma, have been reported.","definition_xrefs":["Orphanet:163908"],"direct_ancestors":[{"relation_name":"is_a","term_name":"postinfectious encephalitis","termid":"MONDO:0020068"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"limbic encephalitis with LGI1 antibodies","secondary_identifiers":["SCTID:763794005","MEDGEN:1645969","UMLS:C4706583","GARD:13406"],"synonyms":[{"name":"limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies","type":"exact"}],"termid":"MONDO:0015592","xrefs":{"Monarch":{"xref_id":"0015592"}}}


id: PBO:0089870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome regulatory subunit, ubiquitin-specific protease subunit Rpn11","termid":"PBO:0089870"}


id: PBO:0041246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 1 open reading frame 131","termid":"PBO:0041246"}


id: PBO:0077861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tropomyosin 3 pseudogene 2","termid":"PBO:0077861"}


id: SO:0002243
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene which codes for 23S_rRNA, which functions as a component of the large subunit of the ribosome in prokaryotes.","direct_ancestors":[{"relation_name":"is_a","term_name":"cytosolic_LSU_rRNA_gene","termid":"SO:0002361"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytosolic_rRNA_23S_gene","synonyms":[{"name":"23S rRNA gene","type":"exact"},{"name":"23S_rRNA_gene","type":"exact"}],"termid":"SO:0002243"}


id: PBO:0073465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sideroflexin 1","termid":"PBO:0073465"}


id: FYPO:0007261
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which telomere tethering at the nuclear periphery is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal telomere tethering at nuclear periphery during vegetative growth","termid":"FYPO:0001515"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased telomere tethering at nuclear periphery during vegetative growth","synonyms":[{"name":"decreased mitotic telomere tethering at nuclear periphery during vegetative growth","type":"exact"},{"name":"decreased telomere anchoring at nuclear periphery during vegetative growth","type":"exact"},{"name":"decreased telomere tethering at nuclear periphery during mitotic cell cycle","type":"related"},{"name":"decreased telomere tethering to NE during vegetative growth","type":"exact"},{"name":"reduced telomere tethering at nuclear periphery during vegetative growth","type":"exact"}],"termid":"FYPO:0007261"}


id: MONDO:1010983
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hydrocephalus that occurs in yellow-crowned parrot.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"hydrocephalus, non-human animal","termid":"MONDO:1010233"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrocephalus, yellow-crowned parrot","secondary_identifiers":["OMIA:000487-151761"],"termid":"MONDO:1010983","xrefs":{"Monarch":{"xref_id":"1010983"}}}


id: PBO:0038563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin binding transcription modulator","termid":"PBO:0038563"}


id: FYPO:0007527
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the cell tip is increased when the cell is subject to nitrogen starvation.","definition_xrefs":["PMID:27746023","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to cell tip","termid":"FYPO:0005987"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"increased protein localization to cell tip during nitrogen starvation","synonyms":[{"name":"increased protein localization to cell tip during nitrogen depletion","type":"exact"},{"name":"increased protein localization to cell tip during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0007527"}


id: PBO:0038444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angio associated migratory cell protein","termid":"PBO:0038444"}


id: PBO:0073727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLAM family member 8","termid":"PBO:0073727"}


id: GO:0102128
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4-dihydrocoumaroyl-CoA + 3 malonyl-CoA + 3 H+ = phloretin + 4 coenzyme A + 3 carbon dioxide.","definition_xrefs":["GOC:pz","PMID:20356611"],"gene_count":0,"genotype_count":0,"name":"obsolete chalcone synthase activity (obsolete GO:0102128)","termid":"GO:0102128"}


id: MONDO:0016686
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low-grade (WHO grade II) astrocytic neoplasm. It is characterized by diffuse infiltration of neighboring central nervous system structures. These lesions typically affect young adults and have a tendency for progression to anaplastic astrocytoma and glioblastoma. Based on the IDH genes mutation status, diffuse astrocytomas are classified as IDH-mutant, IDH-wildtype, and not otherwise specified.","definition_xrefs":["NCIT:C7173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"low-grade astrocytoma","termid":"MONDO:0016685"},{"relation_name":"is_a","term_name":"grade II glioma","termid":"MONDO:0021639"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diffuse astrocytoma","secondary_identifiers":["NANDO:2200085","ONCOTREE:DASTR","UMLS:C0280785","Orphanet:251595","DOID:4857","GARD:5907","MEDGEN:83708"],"synonyms":[{"name":"WHO grade II astrocytoma","type":"exact"},{"name":"astrocytoma, diffuse","type":"exact"},{"name":"astrocytoma, diffuse, malignant","type":"exact"},{"name":"diffuse astrocytoma","type":"exact"},{"name":"fibrillary astrocytoma (histologic variant)","type":"related"},{"name":"gemistocytic astrocytoma (histologic variant)","type":"related"},{"name":"grade II astrocytic neoplasm","type":"exact"},{"name":"grade II astrocytic tumor","type":"exact"},{"name":"grade II astrocytic tumour","type":"exact"},{"name":"grade II astrocytoma","type":"exact"},{"name":"low-grade diffuse astrocytoma","type":"related"},{"name":"protoplasmic astrocytoma (histologic variant)","type":"related"}],"termid":"MONDO:0016686","xrefs":{"Monarch":{"xref_id":"0016686"}}}


id: PBO:0054826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 2239","termid":"PBO:0054826"}


id: GO:0045428
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of nitric oxide.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biosynthetic process","termid":"GO:0009889"},{"relation_name":"is_a","term_name":"regulation of nitric oxide metabolic process","termid":"GO:0080164"},{"relation_name":"regulates","term_name":"nitric oxide biosynthetic process","termid":"GO:0006809"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of nitric oxide biosynthetic process","synonyms":[{"name":"regulation of nitric oxide anabolism","type":"exact"},{"name":"regulation of nitric oxide biosynthesis","type":"exact"},{"name":"regulation of nitric oxide formation","type":"exact"},{"name":"regulation of nitric oxide synthesis","type":"exact"}],"termid":"GO:0045428"}


id: MONDO:0004333
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant, ectopic ACTH secreting pancreatic neuroendocrine tumor, associated with Cushing's syndrome. The prognosis is usually poor.","definition_xrefs":["NCIT:C27466"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functional pancreatic neuroendocrine tumor","termid":"MONDO:0023206"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"pancreatic ACTH-producing neuroendocrine tumor","secondary_identifiers":["MEDGEN:233302","ICDO:8158/1","DOID:7697","UMLS:C1335300"],"synonyms":[{"name":"pancreatic ACTH hormone producing tumor","type":"related"},{"name":"pancreatic ACTH hormone producing tumour","type":"related"},{"name":"pancreatic ACTH producing NET","type":"exact"},{"name":"pancreatic ACTH producing neuroendocrine tumor","type":"exact"},{"name":"pancreatic ACTH producing neuroendocrine tumour","type":"exact"},{"name":"pancreatic ACTH producing tumor","type":"exact"},{"name":"pancreatic ACTH producing tumour","type":"exact"},{"name":"pancreatic ACTH-producing neuroendocrine tumor","type":"exact"},{"name":"pancreatic adrenocorticotropic hormone producing tumor","type":"exact"},{"name":"pancreatic adrenocorticotropic hormone producing tumour","type":"exact"}],"termid":"MONDO:0004333","xrefs":{"Monarch":{"xref_id":"0004333"}}}


id: MONDO:0033261
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0000426"],"is_obsolete":false,"name":"hearing loss, autosomal dominant 34, with or without inflammation","secondary_identifiers":["MEDGEN:1626346","UMLS:C4521680","DOID:0080270","OMIM:617772"],"synonyms":[{"name":"DFNA34","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 34","type":"narrow"},{"name":"deafness, autosomal dominant 34, with or without inflammation","type":"narrow"}],"termid":"MONDO:0033261","xrefs":{"Monarch":{"xref_id":"0033261"}}}


id: GO:0097292
data:
  {"annotated_genes":["SJAG_06634","SJAG_01298"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77383,110112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving XMP, xanthosine monophosphate.","definition_xrefs":["GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleotide metabolic process","termid":"GO:0009150"},{"relation_name":"is_a","term_name":"purine ribonucleoside monophosphate metabolic process","termid":"GO:0009167"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01298":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"XMP metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"XMP metabolism","type":"exact"}],"termid":"GO:0097292","terms_by_termid":{"GO:0032265":null}}


id: GO:0047831
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-ornithine = (2R,4S)-2,4-diaminopentanoate.","definition_xrefs":["RHEA:14893"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular aminotransferase activity","termid":"GO:0016869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"D-ornithine 4,5-aminomutase activity","secondary_identifiers":["KEGG_REACTION:R02461","MetaCyc:ORNMUTST-RXN","EC:5.4.3.5"],"synonyms":[{"name":"D-alpha-ornithine 5,4-aminomutase activity","type":"related"},{"name":"D-ornithine aminomutase activity","type":"related"}],"termid":"GO:0047831"}


id: GO:0004687
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + myosin-light-chain = ADP + myosin-light-chain phosphate.","definition_xrefs":["EC:2.7.11.18"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine kinase activity","termid":"GO:0004674"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016301","GO:0140096","GO:0004672","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"myosin light chain kinase activity","secondary_identifiers":["Reactome:R-HSA-5668978","Reactome:R-HSA-445813","RHEA:22004","MetaCyc:2.7.11.18-RXN"],"synonyms":[{"name":"ATP:myosin-light-chain O-phosphotransferase","type":"broad"},{"name":"ATP:myosin-light-chain O-phosphotransferase activity","type":"related"},{"name":"MLCK","type":"related"},{"name":"MLCkase activity","type":"related"},{"name":"STK18","type":"related"},{"name":"calcium/calmodulin-dependent myosin light chain kinase activity","type":"related"},{"name":"myosin kinase activity","type":"related"},{"name":"myosin light chain protein kinase activity","type":"related"},{"name":"myosin light-chain kinase","type":"broad"},{"name":"myosin light-chain kinase (phosphorylating)","type":"related"},{"name":"myosin light-chain kinase (phosphorylating) activity","type":"related"},{"name":"myosin light-chain kinase activity","type":"related"},{"name":"myosin-light-chain kinase activity","type":"exact"},{"name":"smooth-muscle-myosin-light-chain kinase activity","type":"narrow"}],"termid":"GO:0004687"}


id: PBO:0073593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SHOC2 leucine rich repeat scaffold protein","termid":"PBO:0073593"}


id: GO:0045850
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of nurse cell apoptotic process.","definition_xrefs":["GOC:mtg_apoptosis","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nurse cell apoptotic process","termid":"GO:0045477"},{"relation_name":"is_a","term_name":"positive regulation of apoptotic process involved in development","termid":"GO:1904747"},{"relation_name":"is_a","term_name":"positive regulation of reproductive process","termid":"GO:2000243"},{"relation_name":"positively_regulates","term_name":"nurse cell apoptotic process","termid":"GO:0045476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of nurse cell apoptotic process","synonyms":[{"name":"activation of nurse cell apoptosis","type":"narrow"},{"name":"positive regulation of nurse cell apoptosis","type":"narrow"},{"name":"stimulation of nurse cell apoptosis","type":"narrow"},{"name":"up regulation of nurse cell apoptosis","type":"exact"},{"name":"up-regulation of nurse cell apoptosis","type":"exact"},{"name":"upregulation of nurse cell apoptosis","type":"exact"}],"termid":"GO:0045850"}


id: GO:0061387
data:
  {"annotated_genes":["SJAG_03602"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[100244],"is_not":false,"summary":null,"term":"GO:0061387"}]},"cv_name":"biological_process","definition":"Any process that modulates the extent of cell growth.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell growth","termid":"GO:0001558"},{"relation_name":"part_of","term_name":"regulation of cell size","termid":"GO:0008361"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03602":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of extent of cell growth","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061387","terms_by_termid":{"GO:0061387":null}}


id: MONDO:0700101
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cancer, non-human animal","termid":"MONDO:1011828"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carcinoma, non-human animal","termid":"MONDO:0700101","xrefs":{"Monarch":{"xref_id":"0700101"}}}


id: PBO:0090413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate dehydrogenase (ubiquinone) cytochrome b subunit","termid":"PBO:0090413"}


id: MONDO:1012617
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any lysosomal storage disorder that occurs in dogs due to a mutation in the IDUA gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucopolysaccharidosis or mucopolysaccharidosis-like disorder, non-human animal","termid":"MONDO:1012581"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucopolysaccharidosis I, dog","secondary_identifiers":["OMIA:000664-9615"],"synonyms":[{"name":"Hurler syndrome, dog","type":"related"},{"name":"MPS I","type":"exact"}],"termid":"MONDO:1012617","xrefs":{"Monarch":{"xref_id":"1012617"}}}


id: PBO:0083944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Gamma-glutamyl phosphate reductase; catalyzes the second step in proline biosynthesis","termid":"PBO:0083944"}


id: PBO:0004325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA hairpin binding protein (predicted)","termid":"PBO:0004325"}


id: PBO:0042922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclic GMP-AMP synthase","termid":"PBO:0042922"}


id: PBO:0073149
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC24 homolog B, COPII coat complex component","termid":"PBO:0073149"}


id: PBO:0058621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6753","termid":"PBO:0058621"}


id: PBO:0042897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement factor H related 1","termid":"PBO:0042897"}


id: PBO:0079553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 6","termid":"PBO:0079553"}


id: PBO:0043289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain containing 7A","termid":"PBO:0043289"}


id: PBO:0110328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD36 pseudogene 2","termid":"PBO:0110328"}


id: PBO:0050400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein C pseudogene 1","termid":"PBO:0050400"}


id: PBO:0003274
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ssDNA binding within synthetase domain","termid":"PBO:0003274"}


id: PBO:0069627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 904, pseudogene","termid":"PBO:0069627"}


id: GO:0160126
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A gated channel activity that enables the transmembrane transfer of a calcium ion by a channel that opens in response to a change in pH.","definition_xrefs":["PMID:30930064","PMID:34767445"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligand-gated calcium channel activity","termid":"GO:0099604"},{"relation_name":"is_a","term_name":"pH-gated monoatomic ion channel activity","termid":"GO:0160128"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"pH-gated calcium channel activity","synonyms":[{"name":"pH-dependent calcium channel activity","type":"related"},{"name":"pH-sensitive calcium channel activity","type":"related"}],"termid":"GO:0160126"}


id: MONDO:0015480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Coloboma of superior eyelid is a rare developmental defect during embryogenesis characterized by a typically unilateral, partial or full-thickness, variably sized defect of the superior eyelid, ranging from a small notch to complete absence of the entire lid, which is commonly triangular in shape (with base at eyelid margin) and located on the medial third of the lid. It can occur isolated, associated with other anomalies (e.g. ocular/orbital and facial), or as part of a syndrome.","definition_xrefs":["Orphanet:155884"],"direct_ancestors":[{"relation_name":"is_a","term_name":"facial cleft","termid":"MONDO:0015411"},{"relation_name":"is_a","term_name":"coloboma of eyelid","termid":"MONDO:0020357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"coloboma of superior eyelid","secondary_identifiers":["UMLS:C1863872","MEDGEN:350283","SCTID:763132003","GARD:19977"],"synonyms":[{"name":"superior palpebral coloboma","type":"exact"}],"termid":"MONDO:0015480","xrefs":{"Monarch":{"xref_id":"0015480"}}}


id: FYPO:0000879
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which trimethylation of lysine at position 9 of histone H3 occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K9 trimethylation during vegetative growth","termid":"FYPO:0000787"},{"relation_name":"is_a","term_name":"increased histone H3-K9 methylation during vegetative growth","termid":"FYPO:0000871"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002494","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0002274"],"is_obsolete":false,"name":"increased histone H3-K9 trimethylation during vegetative growth","synonyms":[{"name":"increased histone H3 K9 trimethylation during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 trimethylation during mitotic cell cycle","type":"related"},{"name":"increased histone H3K9 trimethylation during vegetative growth","type":"exact"},{"name":"increased histone H3K9me3 during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K9 trimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0000879"}


id: GO:0047200
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-2,3,4,5-tetrahydrodipicolinate + acetyl-CoA + H2O = L-2-acetamido-6-oxopimelate + CoA.","definition_xrefs":["EC:2.3.1.89","RHEA:13085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-acetyltransferase activity","termid":"GO:0008080"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016746","GO:0003824"],"is_obsolete":false,"name":"tetrahydrodipicolinate N-acetyltransferase activity","secondary_identifiers":["KEGG_REACTION:R04364","MetaCyc:2.3.1.89-RXN"],"synonyms":[{"name":"acetyl-CoA:(S)-2,3,4,5-tetrahydrodipicolinate-2,6-dicarboxylate N2-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:(S)-2,3,4,5-tetrahydropyridine-2,6-dicarboxylate 2-N-acetyltransferase activity","type":"related"},{"name":"acetyl-CoA:L-2,3,4,5-tetrahydrodipicolinate N2-acetyltransferase activity","type":"related"},{"name":"tetrahydrodipicolinate acetylase activity","type":"related"},{"name":"tetrahydrodipicolinate:acetyl-CoA acetyltransferase activity","type":"related"}],"termid":"GO:0047200"}


id: FYPO:0005585
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of one or more triglycerides measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased cellular triglyceride level during vegetative growth","synonyms":[{"name":"decreased cellular TAG level during vegetative growth","type":"exact"},{"name":"decreased cellular triacylglycerol level during vegetative growth","type":"exact"},{"name":"decreased cellular triglyceride level during mitotic cell cycle","type":"related"},{"name":"decreased triglyceride accumulation during vegetative growth","type":"related"},{"name":"reduced cellular triglyceride level during vegetative growth","type":"exact"}],"termid":"FYPO:0005585"}


id: SO:0000830
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of a chromosome.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"},{"relation_name":"part_of","term_name":"chromosome","termid":"SO:0000340"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome_part","synonyms":[{"name":"chromosomal region","type":"exact"},{"name":"chromosomal_region","type":"exact"},{"name":"chromosome part","type":"exact"}],"termid":"SO:0000830"}


id: MOD:01591
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Modifications that have monoisotopic mass differences from their respective origins of 304.205359 Da.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modifications with monoisotopic mass differences that are nominally equal at a resolution below 0.000001 Da","termid":"MOD:01515"},{"relation_name":"is_a","term_name":"modifications with monoisotopic mass differences that are nominally equal at 304.199-304.206 Da","termid":"MOD:01592"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"modifications with monoisotopic mass differences that are nominally equal at 304.205359 Da","termid":"MOD:01591"}


id: FYPO:0008166
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the kinetochore of a chromosome does not occur during prometaphase of mitosis.","direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to kinetochore during mitotic prometaphase","termid":"FYPO:0008165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"abolished protein localization to kinetochore during mitotic prometaphase","termid":"FYPO:0008166"}


id: GO:0005736
data:
  {"annotated_genes":["SJAG_00731","SJAG_01313","SJAG_04261","SJAG_01562","SJAG_03144","SJAG_04106","SJAG_01698","SJAG_02101","SJAG_02070","SJAG_01765","SJAG_03956","SJAG_03468","SJAG_01444","SJAG_02653","SJAG_02871","SJAG_01128","SJAG_03578"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[58456,69191,71841,72806,75898,76277,76925,77278,77485,77592,78284,78706,79238,104355,106713,116074,117384],"is_not":false,"summary":null,"term":"GO:0005736"}]},"cv_name":"cellular_component","definition":"RNA polymerase I, one of three nuclear DNA-directed RNA polymerases found in all eukaryotes, is a multisubunit complex; typically it produces rRNAs. Two large subunits comprise the most conserved portion including the catalytic site and share similarity with other eukaryotic and bacterial multisubunit RNA polymerases. The remainder of the complex is composed of smaller subunits (generally ten or more), some of which are also found in RNA polymerase III and others of which are also found in RNA polymerases II and III. Although the core is competent to mediate ribonucleic acid synthesis, it requires additional factors to select the appropriate template.","definition_xrefs":["GOC:krc","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear DNA-directed RNA polymerase complex","termid":"GO:0055029"},{"relation_name":"part_of","term_name":"nucleolus","termid":"GO:0005730"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00731":null,"SJAG_01128":null,"SJAG_01313":null,"SJAG_01444":null,"SJAG_01562":null,"SJAG_01698":null,"SJAG_01765":null,"SJAG_02070":null,"SJAG_02101":null,"SJAG_02653":null,"SJAG_02871":null,"SJAG_03144":null,"SJAG_03468":null,"SJAG_03578":null,"SJAG_03956":null,"SJAG_04106":null,"SJAG_04261":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005730"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005730","GO:0005634"],"is_obsolete":false,"name":"RNA polymerase I complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"DNA-directed RNA polymerase I activity","type":"related"},{"name":"DNA-directed RNA polymerase I complex","type":"exact"}],"termid":"GO:0005736","terms_by_termid":{"GO:0005736":null}}


id: MONDO:0005496
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from epithelial cells of the bile duct","direct_ancestors":[{"relation_name":"is_a","term_name":"bile duct cancer","termid":"MONDO:0003059"},{"relation_name":"is_a","term_name":"carcinoma of liver and intrahepatic biliary tract","termid":"MONDO:0018531"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"bile duct carcinoma","secondary_identifiers":["EFO:0005540","NCIT:C27814","DOID:4897","MEDGEN:152840","UMLS:C0740277"],"synonyms":[{"name":"bile duct cancer","type":"broad"},{"name":"bile duct cancer (including cholangiocarcinoma)","type":"exact"},{"name":"bile duct carcinoma","type":"exact"},{"name":"carcinoma of bile duct","type":"exact"}],"termid":"MONDO:0005496","xrefs":{"Monarch":{"xref_id":"0005496"}}}


id: PBO:0058461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5190","termid":"PBO:0058461"}


id: GO:0090550
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a starvation stimulus, deprivation of molybdenum.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to starvation","termid":"GO:0042594"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to molybdenum starvation","termid":"GO:0090550"}


id: PATO:0000099
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000099 plant growth hormone sensitivity (obsolete PATO:0000099)","termid":"PATO:0000099"}


id: PBO:0004376
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.39","termid":"PBO:0004376"}


id: PR:O94545
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An importin-11 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04626","PANTHER:PTHR10997:SF7","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"importin beta-like protein kap113 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1322.06","secondary_identifiers":["UniProtKB:O94545"],"synonyms":[{"name":"Spom972h-IPO11","type":"exact"},{"name":"karyopherin-113 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94545"}


id: PBO:0080820
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XXYLT1 antisense RNA 1","termid":"PBO:0080820"}


id: PBO:0054186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1561","termid":"PBO:0054186"}


id: GO:0048162
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The stage in oogenesis when many layers of follicle cells surround the oocyte. There is a yolk nucleus (Balbiani's Body) near the germinal vesicle.","definition_xrefs":["GOC:mtg_sensu","ISBN:0198542771","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mammalian oogenesis stage","termid":"GO:0022605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"multi-layer follicle stage","synonyms":[{"name":"mammalian oogenesis stage 5","type":"exact"}],"termid":"GO:0048162"}


id: PBO:0028073
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_single_or_double_cell_division,_arrest_with_anucleate_cell_(obsolete_FYPO:0003761)","termid":"PBO:0028073"}


id: SO:0001637
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that encodes for ribosomal RNA.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ncRNA_gene","termid":"SO:0001263"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rRNA_gene","synonyms":[{"name":"rDNA","type":"exact"},{"name":"rRNA gene","type":"exact"}],"termid":"SO:0001637"}


id: PR:O94375
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rex4 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94375"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA exonuclease 4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1604.09c","synonyms":[{"name":"Spom972h-rex4","type":"exact"}],"termid":"PR:O94375"}


id: PBO:0040006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARL14EP pseudogene 1","termid":"PBO:0040006"}


id: GO:0051816
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The production of structures and/or molecules in an organism that are required for the acquisition and/or utilization of nutrients obtained from a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:cc"],"gene_count":0,"genotype_count":0,"name":"obsolete acquisition of nutrients from other organism during symbiotic interaction (obsolete GO:0051816)","termid":"GO:0051816"}


id: MONDO:0019609
data:
  {"annotated_genes":["SJAG_02788","SJAG_02693","SJAG_02997","SJAG_00891","SJAG_03440","SJAG_00702","SJAG_01165","SJAG_03324","SJAG_04763","SJAG_04146","SJAG_03781","SJAG_02619","SJAG_00326","SJAG_05950"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013948"},{"annotations":[88682],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054549"},{"annotations":[89053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013949"},{"annotations":[89051],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013950"},{"annotations":[89054],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013951"},{"annotations":[89055],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013952"},{"annotations":[89013,89012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013967"},{"annotations":[88642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008953"},{"annotations":[89003],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011101"},{"annotations":[88630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008954"},{"annotations":[88914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008736"},{"annotations":[89035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013927"},{"annotations":[89037],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013930"},{"annotations":[89038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013931"},{"annotations":[89040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013936"},{"annotations":[89042],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013937"},{"annotations":[89043],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013938"},{"annotations":[89041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013939"},{"annotations":[89046],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013942"},{"annotations":[89044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013943"},{"annotations":[89049],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013945"},{"annotations":[88091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009959"}]},"cv_name":"mondo","definition":"The most severe variant seen in the peroxisome biogenesis disorders that is characterized by neuronal migration defects in the brain, dysmorphic craniofacial features, profound hypotonia, neonatal seizures, and liver dysfunction.","definition_xrefs":["Orphanet:912"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"excluded_subClassOf","term_name":"obsolete nephropathy secondary to a storage or other metabolic disease (obsolete MONDO:0019743)","termid":"MONDO:0019743"},{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"peroxisome biogenesis disorder","termid":"MONDO:0019234"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00326":null,"SJAG_00702":null,"SJAG_00891":null,"SJAG_01165":null,"SJAG_02619":null,"SJAG_02693":null,"SJAG_02788":null,"SJAG_02997":null,"SJAG_03324":null,"SJAG_03440":null,"SJAG_03781":null,"SJAG_04146":null,"SJAG_04763":null,"SJAG_05950":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019053"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019053","MONDO:0005066","MONDO:0005244","MONDO:0005559"],"is_obsolete":false,"name":"Zellweger spectrum disorders","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:905","NCIT:C85239","NORD:1876","UMLS:C0043459","MEDGEN:21958","GARD:7917","ICD10CM:E71.510","SCTID:88469006","NANDO:1200760","MESH:D015211"],"synonyms":[{"name":"ZS","type":"exact"},{"name":"ZWS","type":"exact"},{"name":"Zellweger leukodystrophy","type":"related"},{"name":"Zellweger spectrum disorders","type":"exact"},{"name":"Zellweger syndrome","type":"exact"},{"name":"cerebrohepatorenal syndrome","type":"exact"},{"name":"congenital iron overload","type":"exact"}],"termid":"MONDO:0019609","terms_by_termid":{"MONDO:0008736":null,"MONDO:0008953":null,"MONDO:0008954":null,"MONDO:0009959":null,"MONDO:0011101":null,"MONDO:0013927":null,"MONDO:0013930":null,"MONDO:0013931":null,"MONDO:0013936":null,"MONDO:0013937":null,"MONDO:0013938":null,"MONDO:0013939":null,"MONDO:0013942":null,"MONDO:0013943":null,"MONDO:0013945":null,"MONDO:0013948":null,"MONDO:0013949":null,"MONDO:0013950":null,"MONDO:0013951":null,"MONDO:0013952":null,"MONDO:0013967":null,"MONDO:0054549":null},"xrefs":{"Monarch":{"xref_id":"0019609"}}}


id: FYPO:0008174
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the acetylation of lysine at position 16 of histone H4 in silent mating-type cassettes occurs to a higher extent than normal.","direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H4-K16 acetylation during vegetative growth","termid":"FYPO:0007632"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0002274","FYPO:0002494","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased histone H4-K16 acetylation at silent mating-type cassette during vegetative growth","termid":"FYPO:0008174"}


id: GO:0035144
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the anal fin are generated and organized. An anal fin is an unpaired medial fin on the ventral aspect near the caudal end of a fish, which provides lateral stability while swimming.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"medial fin morphogenesis","termid":"GO:0035141"},{"relation_name":"part_of","term_name":"anal fin development","termid":"GO:0033335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"anal fin morphogenesis","termid":"GO:0035144"}


id: PBO:0051943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inosine triphosphatase","termid":"PBO:0051943"}


id: MONDO:0003343
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioblastoma that arises from the retina. It is typically a sign of von Hippel-Lindau disease. It may also be seen as an isolated entity without systemic involvement.","definition_xrefs":["NCIT:C39783"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal vascular disorder","termid":"MONDO:0002311"},{"relation_name":"is_a","term_name":"hemangioblastoma","termid":"MONDO:0016748"},{"relation_name":"is_a","term_name":"hemangioma of retina","termid":"MONDO:0021541"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"retinal hemangioblastoma","secondary_identifiers":["DOID:5240","UMLS:C0730303","MEDGEN:152677"],"synonyms":[{"name":"hemangioblastoma of vasculature of retina","type":"exact"},{"name":"retinal capillary hemangioblastoma","type":"exact"},{"name":"retinal hemangioblastoma","type":"exact"},{"name":"vasculature of retina hemangioblastoma","type":"exact"}],"termid":"MONDO:0003343","xrefs":{"Monarch":{"xref_id":"0003343"}}}


id: PBO:0082281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AP-1 accessory protein; colocalizes with clathrin to the late-Golgi apparatus; involved in TGN-endosome transport; physically interacts with AP-1; similar to the mammalian p200; may interact with ribosomes; YJL207C is a non-essential gene","termid":"PBO:0082281"}


id: GO:0090383
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces the pH of the phagosome, measured by the concentration of the hydrogen ion.","definition_xrefs":["GOC:tb","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular pH reduction","termid":"GO:0051452"},{"relation_name":"part_of","term_name":"phagosome maturation","termid":"GO:0090382"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"phagosome acidification","synonyms":[{"name":"phagosomal acidification","type":"exact"}],"termid":"GO:0090383"}


id: PBO:0059640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 6","termid":"PBO:0059640"}


id: GO:0047832
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5D-5-O-methyl-chiro-inositol + NADP+ = 2D-5-O-methyl-2,3,5/4,6-pentahydroxycyclohexanone + H+ + NADPH.","definition_xrefs":["RHEA:20437","EC:1.1.1.142"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"D-pinitol dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R03498","MetaCyc:D-PINITOL-DEHYDROGENASE-RXN"],"synonyms":[{"name":"1D-3-O-methyl-chiro-inositol:NADP+ oxidoreductase activity","type":"related"},{"name":"5D-5-O-methyl-chiro-inositol:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0047832"}


id: GO:1901543
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of ent-pimara-8(14),15-diene biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of isoprenoid metabolic process","termid":"GO:0045827"},{"relation_name":"is_a","term_name":"negative regulation of lipid biosynthetic process","termid":"GO:0051055"},{"relation_name":"is_a","term_name":"regulation of ent-pimara-8(14),15-diene biosynthetic process","termid":"GO:1901542"},{"relation_name":"negatively_regulates","term_name":"ent-pimara-8(14),15-diene biosynthetic process","termid":"GO:1901541"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"negative regulation of ent-pimara-8(14),15-diene biosynthetic process","synonyms":[{"name":"down regulation of ent-pimara-8(14),15-diene anabolism","type":"exact"},{"name":"down regulation of ent-pimara-8(14),15-diene biosynthesis","type":"exact"},{"name":"down regulation of ent-pimara-8(14),15-diene biosynthetic process","type":"exact"},{"name":"down regulation of ent-pimara-8(14),15-diene formation","type":"exact"},{"name":"down regulation of ent-pimara-8(14),15-diene synthesis","type":"exact"},{"name":"down-regulation of ent-pimara-8(14),15-diene anabolism","type":"exact"},{"name":"down-regulation of ent-pimara-8(14),15-diene biosynthesis","type":"exact"},{"name":"down-regulation of ent-pimara-8(14),15-diene biosynthetic process","type":"exact"},{"name":"down-regulation of ent-pimara-8(14),15-diene formation","type":"exact"},{"name":"down-regulation of ent-pimara-8(14),15-diene synthesis","type":"exact"},{"name":"downregulation of ent-pimara-8(14),15-diene anabolism","type":"exact"},{"name":"downregulation of ent-pimara-8(14),15-diene biosynthesis","type":"exact"},{"name":"downregulation of ent-pimara-8(14),15-diene biosynthetic process","type":"exact"},{"name":"downregulation of ent-pimara-8(14),15-diene formation","type":"exact"},{"name":"downregulation of ent-pimara-8(14),15-diene synthesis","type":"exact"},{"name":"inhibition of ent-pimara-8(14),15-diene anabolism","type":"narrow"},{"name":"inhibition of ent-pimara-8(14),15-diene biosynthesis","type":"narrow"},{"name":"inhibition of ent-pimara-8(14),15-diene biosynthetic process","type":"narrow"},{"name":"inhibition of ent-pimara-8(14),15-diene formation","type":"narrow"},{"name":"inhibition of ent-pimara-8(14),15-diene synthesis","type":"narrow"},{"name":"negative regulation of ent-pimara-8(14),15-diene anabolism","type":"exact"},{"name":"negative regulation of ent-pimara-8(14),15-diene biosynthesis","type":"exact"},{"name":"negative regulation of ent-pimara-8(14),15-diene formation","type":"exact"},{"name":"negative regulation of ent-pimara-8(14),15-diene synthesis","type":"exact"}],"termid":"GO:1901543"}


id: GO:0022859
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transmembrane transfer of a solute by a channel that opens in response to dephosphorylation of one of its constituent parts.","definition_xrefs":["GOC:mtg_transport","ISBN:0815340729"],"gene_count":0,"genotype_count":0,"name":"obsolete dephosphorylation-gated channel activity (obsolete GO:0022859)","termid":"GO:0022859"}


id: FYPO:0003127
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of nitric oxide measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased cellular reactive oxygen species level during vegetative growth","termid":"FYPO:0002780"},{"relation_name":"is_a","term_name":"altered cellular nitric oxide level","termid":"FYPO:0006408"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased cellular nitric oxide level during vegetative growth","synonyms":[{"name":"decreased cellular NO level during vegetative growth","type":"exact"},{"name":"decreased cellular nitric oxide level during mitotic cell cycle","type":"related"},{"name":"decreased nitric oxide accumulation during vegetative growth","type":"related"},{"name":"reduced cellular nitric oxide level during vegetative growth","type":"exact"}],"termid":"FYPO:0003127"}


id: PBO:0063330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 pseudogene 6","termid":"PBO:0063330"}


id: PBO:0027472
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cyclosporin_A_binding","termid":"PBO:0027472"}


id: GO:0033233
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the addition of SUMO groups to a protein.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein modification by small protein conjugation or removal","termid":"GO:1903320"},{"relation_name":"regulates","term_name":"protein sumoylation","termid":"GO:0016925"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0070647"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0070647"],"is_obsolete":false,"name":"regulation of protein sumoylation","synonyms":[{"name":"regulation of sumoylation","type":"exact"}],"termid":"GO:0033233"}


id: GO:0090465
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A homeostatic process involved in the maintenance of a steady state level of arginine within a cell.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular amino acid homeostasis","termid":"GO:0080144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"intracellular arginine homeostasis","synonyms":[{"name":"arginine homeostasis","type":"exact"},{"name":"cellular arginine homeostasis","type":"exact"}],"termid":"GO:0090465"}


id: GO:0003376
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway initiated by sphingosine-1-phosphate binding to its receptor on the surface of a cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:14592418","GOC:ascb_2009","GOC:signaling","PMID:22001186"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"},{"relation_name":"is_a","term_name":"sphingolipid mediated signaling pathway","termid":"GO:0090520"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"sphingosine-1-phosphate receptor signaling pathway","secondary_identifiers":["GO:0001789"],"synonyms":[{"name":"S1P receptor signaling pathway","type":"exact"},{"name":"S1P signaling pathway","type":"related"},{"name":"S1P-activated G-protein coupled receptor signaling pathway","type":"exact"},{"name":"S1P-activated GPCR signaling pathway","type":"exact"},{"name":"S1P-stimulated signal transduction pathway","type":"exact"},{"name":"sphingolipid signaling pathway","type":"broad"},{"name":"sphingolipid signalling pathway","type":"broad"}],"termid":"GO:0003376"}


id: PBO:0001711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridoxine-pyridoxal-pyridoxamine kinase (predicted)","termid":"PBO:0001711"}


id: GO:0031767
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a gastric inhibitory polypeptide receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor binding","termid":"GO:0001664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"gastric inhibitory polypeptide receptor binding","synonyms":[{"name":"gastric inhibitory polypeptide receptor ligand","type":"narrow"}],"termid":"GO:0031767"}


id: PBO:0058088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4305","termid":"PBO:0058088"}


id: _global:starts_during
data:
  {"annotation_feature_type":"gene","cv_name":"external","direct_ancestors":[{"relation_name":"is_a","term_name":"temporally_related_to","termid":"_global:temporally_related_to"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"starts_during","secondary_identifiers":["RO:0002091"],"termid":"_global:starts_during"}


id: _global:during
data:
  {"annotation_feature_type":"gene","cv_name":"go/extensions/gorel","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"during","secondary_identifiers":["GOREL:0000002"],"termid":"_global:during"}


id: FYPO:0001945
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which protein secretion is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein transport during vegetative growth","termid":"FYPO:0004848"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0001312","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein secretion","synonyms":[{"name":"normal protein secretion during mitotic cell cycle","type":"related"},{"name":"normal protein secretion during vegetative growth","type":"exact"}],"termid":"FYPO:0001945"}


id: GO:0031943
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving glucocorticoids.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of steroid metabolic process","termid":"GO:0019218"},{"relation_name":"is_a","term_name":"regulation of hormone metabolic process","termid":"GO:0032350"},{"relation_name":"regulates","term_name":"glucocorticoid metabolic process","termid":"GO:0008211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of glucocorticoid metabolic process","synonyms":[{"name":"regulation of glucocorticoid metabolism","type":"exact"}],"termid":"GO:0031943"}


id: PBO:0066958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 260","termid":"PBO:0066958"}


id: MONDO:0020014
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare disease with odontological manifestation (obsolete MONDO:0020014)","secondary_identifiers":["Orphanet:98027"],"termid":"MONDO:0020014","xrefs":{"Monarch":{"xref_id":"0020014"}}}


id: PBO:0062652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 13 subfamily C member 2","termid":"PBO:0062652"}


id: MOD:00206
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamic acid residue to L-isoglutamyl-polyglycine.","definition_xrefs":["ChEBI:21343","PubMed:10074368","RESID:AA0201","PubMed:16368691","PubMed:7992051"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-glutamic acid residue","termid":"MOD:00906"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-isoglutamyl-polyglycine","synonyms":[{"name":"L-isoglutamyl-polyglycine","type":"exact"},{"name":"MOD_RES 5-glutamyl polyglycine","type":"exact"},{"name":"gamma-glutamylpolyglycine","type":"exact"}],"termid":"MOD:00206"}


id: GO:1903254
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving hercynylselenocysteine.","definition_xrefs":["PMID:24828577","GO_REF:0000068","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete hercynylselenocysteine metabolic process (obsolete GO:1903254)","synonyms":[{"name":"hercynylselenocysteine metabolism","type":"exact"}],"termid":"GO:1903254"}


id: GO:1900325
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of maltotriulose transport.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transport","termid":"GO:0051051"},{"relation_name":"is_a","term_name":"regulation of maltotriulose transport","termid":"GO:1900324"},{"relation_name":"negatively_regulates","term_name":"maltotriulose transport","termid":"GO:2001090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of maltotriulose transport","synonyms":[{"name":"down regulation of maltotriulose transport","type":"exact"},{"name":"down-regulation of maltotriulose transport","type":"exact"},{"name":"downregulation of maltotriulose transport","type":"exact"},{"name":"inhibition of maltotriulose transport","type":"narrow"}],"termid":"GO:1900325"}


id: PBO:0044625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"doublecortin domain containing 2C","termid":"PBO:0044625"}


id: FYPO:0005561
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which stable microtubule bundles are longer than normal. Stable microtubule bundles, also called Q-MT bundles, are found in quiescent cells.","definition_xrefs":["PomBase:mah","PMID:26124291"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton morphology during vegetative growth","termid":"FYPO:0001418"},{"relation_name":"is_a","term_name":"abnormal microtubule bundle","termid":"FYPO:0005558"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002399","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0000054"],"is_obsolete":false,"name":"long stable microtubule bundle","synonyms":[{"name":"elongated stable microtubule bundle","type":"exact"},{"name":"increased stable microtubule bundle length","type":"exact"},{"name":"long Q-MT bundles","type":"exact"},{"name":"long quiescent cell MT bundle","type":"exact"},{"name":"long quiescent cell microtubule bundle","type":"exact"},{"name":"long stable microtubule array","type":"related"},{"name":"long static microtubule bundle","type":"exact"}],"termid":"FYPO:0005561"}


id: PBO:0088789
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rheb GAP, hamartin Tsc1","termid":"PBO:0088789"}


id: PBO:0076443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 13 pseudogene 2","termid":"PBO:0076443"}


id: PBO:0054306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1698","termid":"PBO:0054306"}


id: PBO:0090823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIID complex subunit Taf13","termid":"PBO:0090823"}


id: PBO:0004151
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Xeroderma pigmentosum","termid":"PBO:0004151"}


id: PR:Q874R1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rho4 gene.","definition_xrefs":["UniProtKB:Q874R1","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP-binding protein rho4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16A10.04","synonyms":[{"name":"Spom972h-rho4","type":"exact"}],"termid":"PR:Q874R1"}


id: GO:0036355
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-tyrosine + S-adenosyl-L-methionine + reduced acceptor = 2-iminoacetate + 4-methylphenol + 5'-deoxyadenosine + L-methionine + acceptor + 2 H+.","definition_xrefs":["EC:4.1.99.19","MetaCyc:RXN-11319","GOC:crds","PMID:17403671"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-carbon lyase activity","termid":"GO:0016830"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"2-iminoacetate synthase activity","secondary_identifiers":["RHEA:26361"],"termid":"GO:0036355"}


id: GO:0180009
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: basic L-amino acid(in) + neutral L-amino acid(out) = basic L-amino acid(in) + neutral L-amino acid(out).","definition_xrefs":["PMID:23506863","PMID:8663357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"basic amino acid transmembrane transporter activity","termid":"GO:0015174"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"},{"relation_name":"is_a","term_name":"antiporter activity","termid":"GO:0015297"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"broad specificity neutral L-amino acid:basic L-amino acid antiporter activity","synonyms":[{"name":"neutral L-amino acid:cationic L-amino acid antiporter activity","type":"exact"},{"name":"neutral L-amino acid:dibasic L-amino acid antiporter activity","type":"exact"},{"name":"neutral L-amino acid:positively-charged polar L-amino acid antiporter activity","type":"exact"},{"name":"system b(0,+)-type activity","type":"related"}],"termid":"GO:0180009"}


id: PBO:0036145
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_transport_on_microtubule_tip_to_cell_tip_cortex_during_vegetative_growth","termid":"PBO:0036145"}


id: PBO:0085041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-essential conserved protein with a role in mRNA decapping; specifically affects the function of the decapping enzyme Dcp1p; mediates decay of the RPS28B mRNA via binding to both Rps28Bp (or Rps28Ap) and the RPS28B mRNA; mediates decay of the YRA1 mRNA by a different, translation-independent mechanism; localizes to cytoplasmic mRNA processing bodies; forms cytoplasmic foci upon DNA replication stress","termid":"PBO:0085041"}


id: PBO:0084634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Methyltransferase required for m3U2843 methylation of the 25S rRNA; S-adenosylmethionine-dependent; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm; YLR063W is not an essential gene","termid":"PBO:0084634"}


id: PBO:0086242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that localizes to the mitochondrial intermembrane space; localizes via the Mia40p-Erv1p system; contains twin cysteine-x(9)-cysteine motifs","termid":"PBO:0086242"}


id: GO:0034986
data:
  {"annotated_genes":["SJAG_01418","SJAG_03862"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[102395,115738],"is_not":false,"summary":null,"term":"GO:0034986"}]},"cv_name":"molecular_function","definition":"Directly binding to and delivering iron ions to a target protein.","definition_xrefs":["GOC:BHF","GOC:vk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metallochaperone activity","termid":"GO:0016530"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01418":null,"SJAG_03862":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140104"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0140104"],"is_obsolete":false,"name":"iron chaperone activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9854984","Reactome:R-HSA-9866272","Reactome:R-HSA-9854405"],"synonyms":[{"name":"iron carrier activity","type":"exact"}],"termid":"GO:0034986","terms_by_termid":{"GO:0034986":null}}


id: GO:0031119
data:
  {"annotated_genes":["SJAG_04065","SJAG_03572","SJAG_00088","SJAG_01172","SJAG_02978","SJAG_00319"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[64777,74693,77388,80229,104312,108058],"is_not":false,"summary":null,"term":"GO:0031119"}]},"cv_name":"biological_process","definition":"The intramolecular conversion of uridine to pseudouridine in a tRNA molecule.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudouridine synthesis","termid":"GO:0001522"},{"relation_name":"is_a","term_name":"tRNA modification","termid":"GO:0006400"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00088":null,"SJAG_00319":null,"SJAG_01172":null,"SJAG_02978":null,"SJAG_03572":null,"SJAG_04065":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006399"],"is_obsolete":false,"name":"tRNA pseudouridine synthesis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0031119","terms_by_termid":{"GO:0031119":null}}


id: PBO:0045780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectodysplasin A","termid":"PBO:0045780"}


id: PBO:0053798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1053","termid":"PBO:0053798"}


id: PBO:0074298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secreted LY6/PLAUR domain containing 1","termid":"PBO:0074298"}


id: PBO:0046436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"esophagus epithelial intergenic associated transcript","termid":"PBO:0046436"}


id: PBO:0057370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548al","termid":"PBO:0057370"}


id: PBO:0040029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"armadillo repeat containing X-linked 4","termid":"PBO:0040029"}


id: GO:0030732
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + L-methionine = S-adenosyl-L-homocysteine + S-methyl-L-methionine.","definition_xrefs":["EC:2.1.1.12"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016741"],"is_obsolete":false,"name":"methionine S-methyltransferase activity","secondary_identifiers":["RHEA:13761","MetaCyc:METHIONINE-S-METHYLTRANSFERASE-RXN"],"synonyms":[{"name":"S-adenosyl methionine:methionine methyl transferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:L-methionine S-methyltransferase activity","type":"related"},{"name":"S-adenosylmethionine transmethylase activity","type":"related"},{"name":"S-adenosylmethionine-methionine methyltransferase activity","type":"related"},{"name":"methionine methyltransferase activity","type":"related"}],"termid":"GO:0030732"}


id: GO:0046754
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The exit of a fully formed virion particles from the host cell by exocytosis via a host vesicle.","definition_xrefs":["PMID:33157038","ISBN:0072370319"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-lytic viral release","termid":"GO:0046753"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"viral exocytosis","synonyms":[{"name":"viral egress by exocytosis","type":"exact"}],"termid":"GO:0046754"}


id: PBO:0072169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15 pseudogene 6","termid":"PBO:0072169"}


id: MONDO:0009869
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pierre-Robin syndrome (or Pierre-Robin sequence) is characterized by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft.","definition_xrefs":["Orphanet:718"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome or malformation associated with head and neck malformations (obsolete MONDO:0015501)","termid":"MONDO:0015501"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"isolated Pierre-Robin syndrome","secondary_identifiers":["GARD:4347","icd11.foundation:136361299","SCTID:4602007","MESH:D010855","NORD:1579","MEDGEN:19310","OMIM:261800","UMLS:C0031900","NCIT:C85010"],"synonyms":[{"name":"PRBNS","type":"related"},{"name":"Pierre Robin Sequence","type":"exact"},{"name":"Pierre Robin sequence","type":"related"},{"name":"Pierre Robin syndrome","type":"related"},{"name":"Pierre Robin syndrome skeletal dysplasia polydactyly","type":"related"},{"name":"Pierre Robin's sequence","type":"related"},{"name":"Pierre Robins sequence","type":"related"},{"name":"Pierre-Robin syndrome","type":"related"},{"name":"Robin sequence","type":"related"},{"name":"Robin syndrome, Pierre","type":"related"},{"name":"glossoptosis, micrognathia, and cleft palate","type":"related"},{"name":"isolated Pierre Robin sequence","type":"exact"},{"name":"isolated Pierre Robin syndrome","type":"related"},{"name":"isolated Pierre-Robin syndrome","type":"exact"},{"name":"sequence, Pierre Robin","type":"related"},{"name":"sequence, Pierre Robin's","type":"related"},{"name":"sequence, Robin","type":"related"},{"name":"syndrome, Pierre Robin","type":"related"},{"name":"syndrome, Pierre-Robin","type":"related"}],"termid":"MONDO:0009869","xrefs":{"Monarch":{"xref_id":"0009869"}}}


id: PBO:0053918
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"long intergenic non-protein coding RNA 1215","termid":"PBO:0053918"}


id: PBO:0062705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily F member 4 pseudogene","termid":"PBO:0062705"}


id: MONDO:0034953
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndromic inherited retinal disorder (obsolete MONDO:0034953)","secondary_identifiers":["Orphanet:519325"],"termid":"MONDO:0034953","xrefs":{"Monarch":{"xref_id":"0034953"}}}


id: PBO:0077250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMED2 divergent transcript","termid":"PBO:0077250"}


id: PBO:0111872
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal-ubiquitin fusion protein","termid":"PBO:0111872"}


id: PBO:0000701
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiosis-specific splicing","termid":"PBO:0000701"}


id: PBO:0080347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 111 pseudogene","termid":"PBO:0080347"}


id: PBO:0000394
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.4","termid":"PBO:0000394"}


id: GO:0044145
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the progression of an organism from an initial condition to a later condition, occurring in, on or near the exterior of its host organism.","definition_xrefs":["GOC:pamgo_curators","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological process","termid":"GO:0050789"},{"relation_name":"regulates","term_name":"formation of structure involved in a symbiotic process","termid":"GO:0044111"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"modulation of formation of structure involved in a symbiotic process","synonyms":[{"name":"modulation of development of symbiont during interaction with host","type":"related"},{"name":"modulation of development of symbiont involved in interaction with host","type":"related"}],"termid":"GO:0044145"}


id: PBO:0051533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 3 receptor subunit alpha","termid":"PBO:0051533"}


id: PBO:0026756
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_hexavalent_chromium","termid":"PBO:0026756"}


id: PBO:0064868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory subunit 26 pseudogene 1","termid":"PBO:0064868"}


id: FYPO:0002167
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to ethyl methanesulfonate. Cells stop growing (and may die) at a concentration of ethyl methanesulfonate that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to DNA damaging agents","termid":"FYPO:0000266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0000139","FYPO:0005447","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to ethyl methanesulfonate","synonyms":[{"name":"hypersensitive to ethyl methanesulfonate","type":"exact"},{"name":"sensitive to EMS","type":"exact"},{"name":"sensitive to ethyl methanesulfonate during mitotic cell cycle","type":"related"},{"name":"sensitive to ethyl methanesulfonate during vegetative growth","type":"exact"},{"name":"sensitive to ethyl methanesulphonate","type":"exact"}],"termid":"FYPO:0002167"}


id: PBO:0081587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 514","termid":"PBO:0081587"}


id: MONDO:0004920
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"male reproductive system disorder","termid":"MONDO:0003150"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrocele","secondary_identifiers":["ICD9:603.9","MEDGEN:318568","UMLS:C1720771","ICD9:603.8","DOID:9912","SCTID:55434001"],"termid":"MONDO:0004920","xrefs":{"Monarch":{"xref_id":"0004920"}}}


id: GO:0002888
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of myeloid leukocyte mediated immunity.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte mediated immunity","termid":"GO:0002705"},{"relation_name":"is_a","term_name":"regulation of myeloid leukocyte mediated immunity","termid":"GO:0002886"},{"relation_name":"positively_regulates","term_name":"myeloid leukocyte mediated immunity","termid":"GO:0002444"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of myeloid leukocyte mediated immunity","synonyms":[{"name":"activation of myeloid leukocyte mediated immunity","type":"narrow"},{"name":"stimulation of myeloid leukocyte mediated immunity","type":"narrow"},{"name":"up regulation of myeloid leukocyte mediated immunity","type":"exact"},{"name":"up-regulation of myeloid leukocyte mediated immunity","type":"exact"},{"name":"upregulation of myeloid leukocyte mediated immunity","type":"exact"}],"termid":"GO:0002888"}


id: GO:0060622
data:
  {"annotated_genes":["SJAG_04666","SJAG_04771"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89326,94233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140748"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of ascospore wall beta-glucan biosynthetic process, the chemical reactions and pathways resulting in the formation of beta-glucans, compounds composed of glucose residues linked by beta-D-glucosidic bonds, found in the walls of ascospores.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"is_a","term_name":"regulation of fungal-type cell wall beta-glucan biosynthetic process","termid":"GO:0090093"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"ascospore wall beta-glucan biosynthetic process","termid":"GO:0034412"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04666":null,"SJAG_04771":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0071554"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0044085","GO:0007049","GO:0071554"],"is_obsolete":false,"name":"regulation of ascospore wall beta-glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0060622","terms_by_termid":{"GO:0140748":null}}


id: GO:0003258
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter that contributes to the differentiation of an endocardial precursor cell.","definition_xrefs":["GOC:mtg_heart"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter involved in endocardial precursor cell differentiation (obsolete GO:0003258)","termid":"GO:0003258"}


id: MONDO:0008092
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A leukocyte disease characterized by autosomal dominant inheritance of lifelong, persistent elevated neutrophil counts primarily consisting of segmented neutrophils that has material basis in heterozygous mutation in the CSF3R gene on chromosome 1p34.","definition_xrefs":["DOID:0090120"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"leukocyte disorder","termid":"MONDO:0004805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"hereditary neutrophilia","secondary_identifiers":["MESH:C563010","OMIM:162830","Orphanet:279943","SCTID:129639005","UMLS:C0543669","GARD:17287","MEDGEN:154252"],"synonyms":[{"name":"neutrophilia, hereditary","type":"related"}],"termid":"MONDO:0008092","xrefs":{"Monarch":{"xref_id":"0008092"}}}


id: MONDO:0013637
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"primary biliary cholangitis","termid":"MONDO:0005388"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0019303"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515","MONDO:0019303"],"is_obsolete":false,"name":"primary biliary cholangitis 5","secondary_identifiers":["MEDGEN:481832","OMIM:614221","GARD:15777","DOID:0070362","UMLS:C3280202"],"synonyms":[{"name":"PBC5","type":"related"},{"name":"biliary cirrhosis, primary, 5","type":"related"}],"termid":"MONDO:0013637","xrefs":{"Monarch":{"xref_id":"0013637"}}}


id: SO:0001196
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute describing a GNA sequence in the (S)-GNA enantiomer.","definition_xrefs":["CHEBI:48017"],"direct_ancestors":[{"relation_name":"is_a","term_name":"GNA","termid":"SO:0001192"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S_GNA","synonyms":[{"name":"S GNA","type":"exact"}],"termid":"SO:0001196"}


id: GO:0019781
data:
  {"annotated_genes":["SJAG_00878","SJAG_03950"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73102,81429],"is_not":false,"summary":null,"term":"GO:0019781"}]},"cv_name":"molecular_function","definition":"Catalysis of the initiation of the NEDD8 (RUB1) conjugation cascade.","definition_xrefs":["PMID:12646924"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-like modifier activating enzyme activity","termid":"GO:0008641"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00878":null,"SJAG_03950":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"NEDD8 activating enzyme activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:6.2.1.64","GO:0019944"],"synonyms":[{"name":"RUB1 activating enzyme activity","type":"exact"}],"termid":"GO:0019781","terms_by_termid":{"GO:0019781":null}}


id: GO:0016474
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A sodium ion-transporting two-sector ATPase complex that couples ATP hydrolysis to the transport of sodium ions across a concentration gradient. The complex comprises a membrane sector (V0) that carries out proton transport and a cytoplasmic compartment sector (V1) that catalyzes ATP hydrolysis.","definition_xrefs":["GOC:mah","PMID:15802565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sodium ion-transporting two-sector ATPase complex","termid":"GO:0016472"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"sodium ion-transporting V-type ATPase complex","synonyms":[{"name":"sodium-translocating V-type ATPase complex","type":"exact"}],"termid":"GO:0016474"}


id: PBO:0050695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family A (Hsp70) member 9 pseudogene 1","termid":"PBO:0050695"}


id: PBO:0084882
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial RNA polymerase specificity factor; has structural similarity to S-adenosylmethionine-dependent methyltransferases and functional similarity to bacterial sigma-factors; Mtf1p interacts with and stabilizes the Rpo41p-promoter complex, enhancing DNA bending and melting to facilitate pre-initiation open complex formation","termid":"PBO:0084882"}


id: MONDO:0008551
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A short-rib dysplasia characterized by thoracic dystrophy, laryngeal stenosis and a small pelvis.","definition_xrefs":["Orphanet:3317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thoracic malformation","termid":"MONDO:0015929"},{"relation_name":"is_a","term_name":"short rib dysplasia","termid":"MONDO:0019691"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thoracolaryngopelvic dysplasia","secondary_identifiers":["icd11.foundation:337990406","SCTID:723556008","GARD:5184","OMIM:187760","MEDGEN:349978","OMIM:187770","MESH:C536517","UMLS:C1861197"],"synonyms":[{"name":"Barnes syndrome","type":"exact"},{"name":"TLPD","type":"related"},{"name":"autosomal dominant thoracolaryngopelvic dysplasia","type":"related"},{"name":"thoracolaryngopelvic dysplasia","type":"exact"},{"name":"thoracopelvic dysostosis","type":"exact"}],"termid":"MONDO:0008551","xrefs":{"Monarch":{"xref_id":"0008551"}}}


id: GO:0032493
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a bacterial lipoprotein stimulus.","definition_xrefs":["PMID:12077222","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to molecule of bacterial origin","termid":"GO:0002237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to bacterial lipoprotein","termid":"GO:0032493"}


id: PBO:0079943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USH2A antisense RNA 2","termid":"PBO:0079943"}


id: PBO:0120255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADD2 antisense RNA 1","termid":"PBO:0120255"}


id: PBO:0030350
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_kinetochore_during_vegetative_growth","termid":"PBO:0030350"}


id: PBO:0017885
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae FPR1","termid":"PBO:0017885"}


id: GO:0070994
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a stimulus indicating oxidative stress is received and converted into a molecular signal.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to oxidative stress","termid":"GO:0006979"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of oxidative stress","termid":"GO:0070994"}


id: PR:P87053
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pof1 gene.","definition_xrefs":["UniProtKB:P87053","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box/WD repeat-containing protein pof1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC57A10.05c","synonyms":[{"name":"Spom972h-pof1","type":"exact"},{"name":"skp1-binding protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87053"}


id: GO:0032308
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the regulated release of a prostaglandin from a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of icosanoid secretion","termid":"GO:0032305"},{"relation_name":"is_a","term_name":"regulation of prostaglandin secretion","termid":"GO:0032306"},{"relation_name":"is_a","term_name":"positive regulation of secretion by cell","termid":"GO:1903532"},{"relation_name":"positively_regulates","term_name":"prostaglandin secretion","termid":"GO:0032310"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of prostaglandin secretion","synonyms":[{"name":"activation of prostaglandin secretion","type":"narrow"},{"name":"positive regulation of prostacyclin secretion","type":"narrow"},{"name":"stimulation of prostaglandin secretion","type":"narrow"},{"name":"up regulation of prostaglandin secretion","type":"exact"},{"name":"up-regulation of prostaglandin secretion","type":"exact"},{"name":"upregulation of prostaglandin secretion","type":"exact"}],"termid":"GO:0032308"}


id: PBO:0058724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6852","termid":"PBO:0058724"}


id: MONDO:0016529
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Duplication of the urethra is a rare congenital genitourinary anomaly, encompassing a wide spectrum of anatomic variants in which the urethra is partially or totally duplicated, which may be asymptomatic or cause symptoms such as incontinence, recurrent urinary infections and difficulty urinating.","definition_xrefs":["Orphanet:237"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"duplication of urethra","secondary_identifiers":["MEDGEN:75609","icd11.foundation:2069509755","SCTID:69015003","GARD:1975","UMLS:C0266348","ICD9:753.8"],"synonyms":[{"name":"urethral duplication","type":"related"}],"termid":"MONDO:0016529","xrefs":{"Monarch":{"xref_id":"0016529"}}}


id: SO:0000794
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A rescue region that is engineered.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"engineered","termid":"SO:0000783"},{"relation_name":"is_a","term_name":"rescue_region","termid":"SO:0000411"},{"relation_name":"is_a","term_name":"engineered_region","termid":"SO:0000804"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"engineered_rescue_region","synonyms":[{"name":"engineered rescue fragment","type":"exact"},{"name":"engineered rescue region","type":"exact"},{"name":"engineered rescue segment","type":"exact"}],"termid":"SO:0000794"}


id: PR:Q9P3U0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ubp2 gene.","definition_xrefs":["UniProtKB:Q9P3U0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin carboxyl-terminal hydrolase Ubp2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC328.06","synonyms":[{"name":"SPAC328.06","type":"related"},{"name":"Spom972h-ubp2","type":"exact"},{"name":"deubiquitinating enzyme 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin thioesterase 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-specific-processing protease 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P3U0"}


id: GO:0033825
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of the non-reducing terminal alpha-D-glucose residue from a 1,4-alpha-D-glucan to the 4-position of an alpha-D-glucan, thus bringing about the hydrolysis of oligosaccharides.","definition_xrefs":["EC:2.4.1.161"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucosyltransferase activity","termid":"GO:0046527"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016757","GO:0016740"],"is_obsolete":false,"name":"oligosaccharide 4-alpha-D-glucosyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.161-RXN"],"synonyms":[{"name":"1,4-alpha-D-glucan:1,4-alpha-D-glucan 4-alpha-D-glucosyltransferase activity","type":"related"},{"name":"1,4-alpha-glucan:1,4-alpha-glucan 4-alpha-glucosyltransferase activity","type":"related"},{"name":"amylase III activity","type":"related"}],"termid":"GO:0033825"}


id: GO:0009470
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete class IIa cytochrome c (obsolete GO:0009470)","synonyms":[{"name":"class IIa cytochrome c","type":"exact"}],"termid":"GO:0009470"}


id: PBO:0117064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NTSR1 antisense RNA 1","termid":"PBO:0117064"}


id: PBO:0050108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 18","termid":"PBO:0050108"}


id: GO:0060976
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the blood vessels of the heart over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel development","termid":"GO:0001568"},{"relation_name":"part_of","term_name":"heart development","termid":"GO:0007507"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"coronary vasculature development","synonyms":[{"name":"cardiac blood vessel development","type":"exact"},{"name":"cardiac vasculature development","type":"exact"},{"name":"coronary blood vessel development","type":"exact"},{"name":"heart blood vessel development","type":"exact"},{"name":"heart vasculature development","type":"exact"}],"termid":"GO:0060976"}


id: PBO:0034325
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-starts_before","termid":"PBO:0034325"}


id: GO:0018016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The methylation of the N-terminal proline of proteins to form the derivative N,N-dimethyl-L-proline.","definition_xrefs":["RESID:AA0066"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-terminal peptidyl-proline methylation","termid":"GO:0035568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"N-terminal peptidyl-proline dimethylation","termid":"GO:0018016"}


id: PBO:0068336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 44","termid":"PBO:0068336"}


id: PR:Q1MTR5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC15C4.06c gene.","definition_xrefs":["UniProtKB:Q1MTR5","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized RING finger membrane protein C15C4.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC15C4.06c","synonyms":[{"name":"Spom972h-SPBC15C4.06c","type":"exact"}],"termid":"PR:Q1MTR5"}


id: PBO:0083176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps TEL07R","termid":"PBO:0083176"}


id: GO:0035996
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Thin cylindrical membrane-covered projection on the surface of a rhabdomere.","definition_xrefs":["GOC:sart","PMID:14744998","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microvillus","termid":"GO:0005902"},{"relation_name":"part_of","term_name":"rhabdomere","termid":"GO:0016028"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"rhabdomere microvillus","termid":"GO:0035996"}


id: GO:0001922
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of regulating the proliferation and elimination of B cells of the B-1 subset such that the total number of B-1 B cells within a whole or part of an organism is stable over time in the absence of an outside stimulus. B-1 B cells are a distinct subset of B cells characterized as being CD5 positive, found predominantly in the peritoneum, pleural cavities, and spleen, and enriched for self-reactivity.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell homeostasis","termid":"GO:0001782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"B-1 B cell homeostasis","synonyms":[{"name":"B-1 B lymphocyte homeostasis","type":"exact"},{"name":"B-1 B-cell homeostasis","type":"exact"},{"name":"B-1 B-lymphocyte homeostasis","type":"exact"}],"termid":"GO:0001922"}


id: GO:0016186
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Separation of a synaptic vesicle from the presynaptic membrane.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete synaptic vesicle fission (obsolete GO:0016186)","synonyms":[{"name":"synaptic vesicle fission","type":"exact"}],"termid":"GO:0016186"}


id: PBO:0078353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon TTC) 1-1","termid":"PBO:0078353"}


id: PBO:0077999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF receptor associated factor 3","termid":"PBO:0077999"}


id: GO:1902893
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of microRNA (miRNA) gene transcription.","definition_xrefs":["GOC:dph","GOC:TermGenie","GOC:kmv","PMID:24699545","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA-templated transcription","termid":"GO:0006355"},{"relation_name":"is_a","term_name":"regulation of miRNA metabolic process","termid":"GO:2000628"},{"relation_name":"regulates","term_name":"miRNA transcription","termid":"GO:0061614"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006351","GO:0006355"],"is_obsolete":false,"name":"regulation of miRNA transcription","synonyms":[{"name":"regulation of miRNA gene transcription","type":"exact"},{"name":"regulation of microRNA gene transcription","type":"exact"},{"name":"regulation of pri-miRNA transcription by RNA polymerase II","type":"exact"},{"name":"regulation of pri-miRNA transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of primary miRNA gene transcription","type":"exact"}],"termid":"GO:1902893"}


id: PBO:0070828
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L13a pseudogene 7","termid":"PBO:0070828"}


id: PR:Q10210
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- swc3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10210"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SWR1 complex subunit swc3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4H3.02c","synonyms":[{"name":"Spom972h-swc3","type":"exact"}],"termid":"PR:Q10210"}


id: MONDO:0001656
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An abnormal dilation of the esophagus not due to obstruction.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"esophageal disorder","termid":"MONDO:0003749"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"megaesophagus","secondary_identifiers":["MEDGEN:6286","SCTID:70667005","DOID:13186","UMLS:C0025164","NCIT:C34811"],"termid":"MONDO:0001656","xrefs":{"Monarch":{"xref_id":"0001656"}}}


id: PBO:0060328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin IF","termid":"PBO:0060328"}


id: MONDO:0004177
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Abnormal growth of the cells of the urethra (lower urinary tract) without malignant characteristics.","definition_xrefs":["NCIT:C3619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign urinary system neoplasm","termid":"MONDO:0004180"},{"relation_name":"is_a","term_name":"urethra neoplasm","termid":"MONDO:0021239"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign urethral neoplasm","secondary_identifiers":["ICD9:223.81","SCTID:92466006","DOID:730","MEDGEN:57812","ICD10CM:D30.4","UMLS:C0154019"],"synonyms":[{"name":"benign neoplasm of the urethra","type":"exact"},{"name":"benign neoplasm of urethra","type":"exact"},{"name":"benign tumor of the urethra","type":"exact"},{"name":"benign tumor of urethra","type":"exact"},{"name":"benign tumour of the urethra","type":"exact"},{"name":"benign tumour of urethra","type":"exact"},{"name":"benign urethra neoplasm","type":"exact"},{"name":"benign urethra tumor","type":"exact"},{"name":"benign urethra tumour","type":"exact"},{"name":"benign urethral neoplasm","type":"exact"},{"name":"benign urethral tumor","type":"exact"},{"name":"benign urethral tumour","type":"exact"},{"name":"neoplasm. urethra","type":"exact"},{"name":"urethra benign neoplasm","type":"exact"},{"name":"urethral benign neoplasm","type":"related"}],"termid":"MONDO:0004177","xrefs":{"Monarch":{"xref_id":"0004177"}}}


id: GO:1903950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of AV node cell action potential.","definition_xrefs":["PMID:25281747","GOC:mtg_cardiac_conduct_nov11","GOC:nc","GO_REF:0000058","GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of action potential","termid":"GO:0045759"},{"relation_name":"is_a","term_name":"regulation of AV node cell action potential","termid":"GO:0098904"},{"relation_name":"negatively_regulates","term_name":"AV node cell action potential","termid":"GO:0086016"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of AV node cell action potential","synonyms":[{"name":"down regulation of AV node cardiac muscle cell action potential","type":"exact"},{"name":"down regulation of AV node cell action potential","type":"exact"},{"name":"down regulation of atrioventricular node cardiac muscle cell action potential","type":"exact"},{"name":"down-regulation of AV node cardiac muscle cell action potential","type":"exact"},{"name":"down-regulation of AV node cell action potential","type":"exact"},{"name":"down-regulation of atrioventricular node cardiac muscle cell action potential","type":"exact"},{"name":"downregulation of AV node cardiac muscle cell action potential","type":"exact"},{"name":"downregulation of AV node cell action potential","type":"exact"},{"name":"downregulation of atrioventricular node cardiac muscle cell action potential","type":"exact"},{"name":"inhibition of AV node cardiac muscle cell action potential","type":"narrow"},{"name":"inhibition of AV node cell action potential","type":"narrow"},{"name":"inhibition of atrioventricular node cardiac muscle cell action potential","type":"narrow"},{"name":"negative regulation of AV node cardiac muscle cell action potential","type":"exact"},{"name":"negative regulation of atrioventricular node cardiac muscle cell action potential","type":"exact"}],"termid":"GO:1903950"}


id: GO:0098955
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the presynaptic endosome membrane consisting of the gene products and protein complexes having either part of their peptide sequence embedded in the hydrophobic region of the membrane or some other covalently attached group such as a GPI anchor that is similarly embedded in the membrane.","definition_xrefs":["GOC:mah","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of presynaptic endosome membrane (obsolete GO:0098955)","synonyms":[{"name":"intrinsic to presynaptic endosome membrane","type":"exact"}],"termid":"GO:0098955"}


id: PBO:0076094
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syntaxin 1A","termid":"PBO:0076094"}


id: GO:0050496
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-glutamine residues by deamidation and esterification with omega-hydroxyceramide.","definition_xrefs":["RESID:AA0347","PMID:10411887"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-L-glutamyl 5-omega-hydroxyceramide ester biosynthetic process from peptidyl-glutamine (obsolete GO:0050496)","synonyms":[{"name":"peptidyl-L-glutamyl 5-omega-hydroxyceramide ester anabolism from peptidyl-glutamine","type":"exact"},{"name":"peptidyl-L-glutamyl 5-omega-hydroxyceramide ester formation from peptidyl-glutamine","type":"exact"},{"name":"peptidyl-L-glutamyl 5-omega-hydroxyceramide ester synthesis from peptidyl-glutamine","type":"exact"}],"termid":"GO:0050496"}


id: PBO:0069002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 246, pseudogene","termid":"PBO:0069002"}


id: PBO:0070069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear 26, pseudogene","termid":"PBO:0070069"}


id: MOD:01990
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a glycine residue to a glycinium (protonated glycine).","definition_xrefs":["ChEBI:64723","PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified glycine residue","termid":"MOD:00908"},{"relation_name":"is_a","term_name":"alpha-amino protonated residue","termid":"MOD:01700"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protonated glycine (glycinium) residue","termid":"MOD:01990"}


id: PBO:0060333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYO3B antisense RNA 1","termid":"PBO:0060333"}


id: PBO:0034630
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_nuclear_envelope_during_G0_to_G1_transition","termid":"PBO:0034630"}


id: PBO:0046652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"esterase activator","termid":"PBO:0046652"}


id: GO:0061544
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled release of a peptide from a cell in which the peptide acts as a neurotransmitter.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide secretion","termid":"GO:0002790"},{"relation_name":"is_a","term_name":"neurotransmitter secretion","termid":"GO:0007269"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"peptide secretion, neurotransmission","termid":"GO:0061544"}


id: FYPO:0009111
data:
  {"alleles_by_uniquename":{"SJAG_02527:allele-1":{"allele_type":"disruption","description":"RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage","gene_uniquename":"SJAG_02527","name":"lig4::KanMX6","uniquename":"SJAG_02527:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121140],"is_not":false,"summary":null,"term":"FYPO:0009111"}]},"cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population phenotype that reflects increased occurrence of flocculation. Flocculation is the non-sexual aggregation of single cells.","definition_xrefs":["PMID:35924983"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased flocculation","termid":"FYPO:0000155"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02527":null},"genotype_count":1,"genotypes_by_uniquename":{"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown":{"display_name":"lig4::KanMX6(RNA sequencing revealed that only the 5' end of the disrupted allele showed low RNA expression and coverage)[Knockdown]","display_uniquename":"lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02527:allele-1","expression":"Knockdown"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased flocculation during vegetative growth","references_by_uniquename":{"PMID:37233261":null},"single_locus_annotated_genes":["SJAG_02527"],"single_locus_genotype_uniquenames":["lig4::KanMX6-RNA_sequencing_revealed_that_only_the_5'_end_of_the_disrupted_allele_showed_low_RNA_expression_and_coverage-disruption-expression-knockdown"],"termid":"FYPO:0009111","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000081":null,"FYPO:0009111":null}}


id: PBO:0068430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, ribosomal 45S cluster 5","termid":"PBO:0068430"}


id: SO:0002174
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A deletion that is the result of base-calling or assembly error.","direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_alteration_artifact","termid":"SO:0002172"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deletion_artifact","synonyms":[{"name":"deletion artifact","type":"exact"}],"termid":"SO:0002174"}


id: PBO:0059719
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO2 pseudogene 27","termid":"PBO:0059719"}


id: GO:0047642
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-D-aldosyl1 beta-D-fructoside + D-aldose2 = D-aldose1 + alpha-D-aldosyl2 beta-D-fructoside.","definition_xrefs":["MetaCyc:ALDOSE-BETA-FRUCTOSYLTRANSFERASE-RXN","EC:2.4.1.162"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fructosyltransferase activity","termid":"GO:0050738"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016757","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"aldose beta-D-fructosyltransferase activity","synonyms":[{"name":"aldose b-D-fructosyltransferase activity","type":"exact"},{"name":"alpha-D-aldosyl-beta-D-fructoside:aldose 1-beta-D-fructosyltransferase activity","type":"related"}],"termid":"GO:0047642"}


id: GO:0052353
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism resulting in the breakdown of carbohydrate molecules within the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete catabolism by host of symbiont carbohydrate (obsolete GO:0052353)","termid":"GO:0052353"}


id: PBO:0029267
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_serine_phosphorylation_during_cellular_response_to_DNA_damage","termid":"PBO:0029267"}


id: PBO:0031096
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cell_population_growth_following_spore_germination","termid":"PBO:0031096"}


id: PBO:0051760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"importin 5 pseudogene 1","termid":"PBO:0051760"}


id: MONDO:0850054
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"hemophilia B leyden","secondary_identifiers":["MEDGEN:1845499","Orphanet:617930","UMLS:C5848256","GARD:22455"],"termid":"MONDO:0850054","xrefs":{"Monarch":{"xref_id":"0850054"}}}


id: PR:O14417
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mitotic spindle assembly checkpoint protein MAD2A that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:KER"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic spindle assembly checkpoint protein MAD2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC20F10.06","secondary_identifiers":["UniProtKB:O14417","PR:000035572"],"synonyms":[{"name":"Spom972h-MAD2L1","type":"exact"}],"termid":"PR:O14417"}


id: PBO:0063420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphodiesterase 3B","termid":"PBO:0063420"}


id: SO:0001070
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Region of polypeptide with a given structural property.","definition_xrefs":["SO:cb","EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_region","termid":"SO:0000839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"polypeptide_structural_region","secondary_identifiers":["BS:00337"],"synonyms":[{"name":"polypeptide structural region","type":"exact"},{"name":"structural_region","type":"related"}],"termid":"SO:0001070"}


id: GO:0004345
data:
  {"annotated_genes":["SJAG_02696","SJAG_02297","SJAG_02148"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[60324,63535,69677],"is_not":false,"summary":null,"term":"GO:0004345"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucose 6-phosphate + NADP+ = D-glucono-1,5-lactone 6-phosphate + NADPH + H+.","definition_xrefs":["EC:1.1.1.49"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02148":null,"SJAG_02297":null,"SJAG_02696":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"glucose-6-phosphate dehydrogenase activity","references_by_uniquename":{"GO_REF:0000002":null},"secondary_identifiers":["Reactome:R-HSA-70377","MetaCyc:GLU6PDEHYDROG-RXN","RHEA:15841"],"synonyms":[{"name":"6-phosphoglucose dehydrogenas","type":"related"},{"name":"6-phosphoglucose dehydrogenase activity","type":"exact"},{"name":"D-glucose 6-phosphate dehydrogenase activity","type":"exact"},{"name":"D-glucose-6-phosphate:NADP+ 1-oxidoreductase activity","type":"related"},{"name":"Entner-doudoroff enzyme","type":"related"},{"name":"G6PD activity","type":"related"},{"name":"G6PDH","type":"exact"},{"name":"GDH","type":"related"},{"name":"NADP-dependent glucose 6-phosphate dehydrogenase activity","type":"exact"},{"name":"NADP-glucose-6-phosphate dehydrogenase activity","type":"exact"},{"name":"Zwischenferment","type":"related"},{"name":"glucose 6-phosphate dehydrogenase (NADP) activity","type":"exact"},{"name":"glucose-6-phosphate 1-dehydrogenase activity","type":"exact"}],"termid":"GO:0004345","terms_by_termid":{"GO:0004345":null}}


id: GO:2001109
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lens epithelial cell proliferation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell proliferation","termid":"GO:0050678"},{"relation_name":"regulates","term_name":"lens epithelial cell proliferation","termid":"GO:0097166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of lens epithelial cell proliferation","termid":"GO:2001109"}


id: GO:0110149
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of biomineralization, the formation and deposition of mineral crystals by living organisms.","definition_xrefs":["PMID:22992051"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of biomineralization (obsolete GO:0110149)","synonyms":[{"name":"regulation of biomineral formation","type":"narrow"},{"name":"regulation of biomineralisation","type":"exact"},{"name":"regulation of mineralisation","type":"exact"},{"name":"regulation of mineralization","type":"exact"}],"termid":"GO:0110149"}


id: GO:0045939
data:
  {"annotated_genes":["SJAG_02104"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95694],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010895"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways involving steroids.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of steroid metabolic process","termid":"GO:0019218"},{"relation_name":"is_a","term_name":"negative regulation of lipid metabolic process","termid":"GO:0045833"},{"relation_name":"negatively_regulates","term_name":"steroid metabolic process","termid":"GO:0008202"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02104":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"negative regulation of steroid metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of steroid metabolic process","type":"exact"},{"name":"down-regulation of steroid metabolic process","type":"exact"},{"name":"downregulation of steroid metabolic process","type":"exact"},{"name":"inhibition of steroid metabolic process","type":"narrow"},{"name":"negative regulation of steroid metabolism","type":"exact"}],"termid":"GO:0045939","terms_by_termid":{"GO:0010895":null}}


id: PBO:0068482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 63, pseudogene","termid":"PBO:0068482"}


id: FYPO:0007701
data:
  {"alleles_by_uniquename":{"SJAG_04332:allele-1":{"allele_type":"amino_acid_mutation","description":"I30T,T572P","gene_uniquename":"SJAG_04332","name":"cdc25-D9","uniquename":"SJAG_04332:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121346],"is_not":false,"summary":null,"term":"FYPO:0007701"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, is longer than normal, has one nucleus, and the mitotic cell cycle is arrested with nuclei at the mitotic G2/M phase transition.","definition_xrefs":["PMID:33683349","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated mononucleate vegetative cell","termid":"FYPO:0004255"},{"relation_name":"is_a","term_name":"inviable elongated cell with cell cycle arrest at mitotic G2/M phase transition","termid":"FYPO:0007702"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04332":null},"genotype_count":1,"genotypes_by_uniquename":{"cdc25-D9-I30T,T572P-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"cdc25-D9(I30T,T572P aa)","display_uniquename":"cdc25-D9-I30T,T572P-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04332:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000005","FYPO:0000004","FYPO:0001320","FYPO:0000631","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"inviable elongated mononucleate cell with cell cycle arrest at mitotic G2/M phase transition","references_by_uniquename":{"PMID:25866389":null},"single_locus_annotated_genes":["SJAG_04332"],"single_locus_genotype_uniquenames":["cdc25-D9-I30T,T572P-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"inviable elongated mononucleate cell with cell cycle arrest at mitotic G2/M phase transition during mitotic cell cycle","type":"related"},{"name":"inviable elongated mononucleate cell with cell cycle arrest at mitotic G2/M phase transition during vegetative growth","type":"exact"},{"name":"inviable elongated mononucleate cell with cell cycle arrest in mitotic G2 phase","type":"related"},{"name":"inviable elongated mononucleate vegetative cell with cell cycle arrest at mitotic G2/M phase transition","type":"exact"},{"name":"lethal; elongated mononucleate cell with cell cycle arrest at mitotic G2/M phase transition","type":"exact"}],"termid":"FYPO:0007701","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000137":null,"FYPO:0007701":null,"FYPO_EXT:0000001":null}}


id: GO:0008829
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: dCTP + H2O = dUTP + NH3.","definition_xrefs":["EC:3.5.4.13"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines","termid":"GO:0016814"},{"relation_name":"is_a","term_name":"deaminase activity","termid":"GO:0019239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016810","GO:0016787"],"is_obsolete":false,"name":"dCTP deaminase activity","secondary_identifiers":["Reactome:R-HSA-180632","RHEA:22680","MetaCyc:DCTP-DEAM-RXN"],"synonyms":[{"name":"5-methyl-dCTP deaminase activity","type":"related"},{"name":"dCTP aminohydrolase activity","type":"related"},{"name":"deoxycytidine triphosphate deaminase activity","type":"related"}],"termid":"GO:0008829"}


id: PBO:0050516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox D cluster","termid":"PBO:0050516"}


id: GO:0102310
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: dTDP-4-dehydro-2,6-dideoxy-alpha-D-allose + NAD(P) = dTDP-(2R,6S)-6-hydroxy-2-methyl-3-oxo-3,6-dihydro-2H-pyran-4-olate + 2 H+ + NAD(P)H.","definition_xrefs":["GOC:pz","EC:1.17.1.-","MetaCyc:RXN-12940"],"gene_count":0,"genotype_count":0,"name":"obsolete dTDP-(2R,6S)-6-hydroxy-2-methyl-3-oxo-3,6-dihydro-2H-pyran-4-olate 3-ketoreductase (dTDP-4-dehydro-2,6-dideoxy-alpha-D-allose-forming) activity (obsolete GO:0102310)","termid":"GO:0102310"}


id: PBO:0064354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PM20D1 antisense RNA 1","termid":"PBO:0064354"}


id: GO:1901900
data:
  {"annotated_genes":["SJAG_03602","SJAG_04597","SJAG_02645"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96221],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140325"},{"annotations":[100242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120047"},{"annotations":[109793],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905391"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization to cell division site.","definition_xrefs":["GOC:dph","GOC:TermGenie","PMID:22573892"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization","termid":"GO:0032880"},{"relation_name":"regulates","term_name":"protein localization to cell division site","termid":"GO:0072741"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02645":null,"SJAG_03602":null,"SJAG_04597":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of protein localization to cell division site","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of protein localisation to cell division site","type":"exact"}],"termid":"GO:1901900","terms_by_termid":{"GO:0120047":null,"GO:0140325":null,"GO:1905391":null}}


id: GO:0050610
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 glutathione + H+ + methylarsonate = glutathione disulfide + H2O + methylarsonous acid.","definition_xrefs":["RHEA:15969","EC:1.20.4.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on phosphorus or arsenic in donors, disulfide as acceptor","termid":"GO:0030614"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"methylarsonate reductase activity","secondary_identifiers":["KEGG_REACTION:R05748","UM-BBD_reactionID:r0837","MetaCyc:1.20.4.2-RXN","Reactome:R-HSA-5696230"],"synonyms":[{"name":"MMA(V) reductase activity","type":"related"},{"name":"glutathione:methylarsonate oxidoreductase activity","type":"related"}],"termid":"GO:0050610"}


id: PBO:0002890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Smc5-6 complex SMC subunit Smc5","termid":"PBO:0002890"}


id: GO:0002087
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process carried out by the nervous system that is required for the proper control of respiratory gaseous exchange. This process occurs in the respiratory center of the brain in vertebrates.","definition_xrefs":["PMID:12458206","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of respiratory system process","termid":"GO:0044065"},{"relation_name":"is_a","term_name":"nervous system process","termid":"GO:0050877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of respiratory gaseous exchange by nervous system process","synonyms":[{"name":"neurological control of breathing","type":"exact"},{"name":"regulation of respiratory gaseous exchange by neurological system process","type":"exact"}],"termid":"GO:0002087"}


id: GO:0071613
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of granzyme B due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:rv","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"production of molecular mediator of immune response","termid":"GO:0002440"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"granzyme B production","termid":"GO:0071613"}


id: PATO:0001069
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001069 relative density (obsolete PATO:0001069)","termid":"PATO:0001069"}


id: MONDO:0014237
data:
  {"annotated_genes":["SJAG_01538","SJAG_04558"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87592,87593],"is_not":false,"summary":null,"term":"MONDO:0014237"}]},"cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the SYNE4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01538":null,"SJAG_04558":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 76","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:615540","DOID:0110524","UMLS:C3147083","GARD:22650","MEDGEN:811137"],"synonyms":[{"name":"DFNB76","type":"narrow"},{"name":"SYNE4 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 76","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 76","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in SYNE4","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 76","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 76","type":"exact"},{"name":"deafness, autosomal recessive 76","type":"narrow"},{"name":"deafness, autosomal recessive type 76","type":"narrow"}],"termid":"MONDO:0014237","terms_by_termid":{"MONDO:0014237":null},"xrefs":{"Monarch":{"xref_id":"0014237"}}}


id: GO:0019470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of trans-4-hydroxy-L-proline, C5H9NO3, a derivative of the amino acid proline.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"4-hydroxyproline metabolic process","termid":"GO:0019471"},{"relation_name":"is_a","term_name":"modified amino acid catabolic process","termid":"GO:0042219"},{"relation_name":"is_a","term_name":"L-amino acid catabolic process","termid":"GO:0170035"},{"relation_name":"is_a","term_name":"non-proteinogenic amino acid catabolic process","termid":"GO:0170044"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"trans-4-hydroxy-L-proline catabolic process","secondary_identifiers":["MetaCyc:HYDROXYPRODEG-PWY"],"synonyms":[{"name":"4-hydroxyproline breakdown","type":"exact"},{"name":"4-hydroxyproline catabolism","type":"exact"},{"name":"4-hydroxyproline degradation","type":"exact"}],"termid":"GO:0019470"}


id: MONDO:0023209
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"galactorrhea","termid":"MONDO:0009256"},{"relation_name":"is_a","term_name":"acquired hyperprolactinemia","termid":"MONDO:0024305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"galactorrhoea-hyperprolactinaemia","secondary_identifiers":["MESH:C535402","UMLS:C2930894","GARD:8400","MEDGEN:419279"],"synonyms":[{"name":"galactorrhea-hyperprolactinemia","type":"related"},{"name":"galactorrhoea-hyperprolactinaemia","type":"exact"},{"name":"hyperprolactinaemia","type":"related"}],"termid":"MONDO:0023209","xrefs":{"Monarch":{"xref_id":"0023209"}}}


id: PBO:0001833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP kinase Spk1","termid":"PBO:0001833"}


id: MONDO:0004607
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer involving a epiglottic vallecula.","definition_xrefs":["MONDO:patterns/cancer"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oropharynx cancer","termid":"MONDO:0004608"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"vallecula cancer","secondary_identifiers":["SCTID:363395000","UMLS:C0153386","MEDGEN:509271","DOID:8556","ICD10CM:C10.0","ICD9:146.3"],"synonyms":[{"name":"cancer of epiglottic vallecula","type":"exact"},{"name":"epiglottic vallecula cancer","type":"exact"},{"name":"malignant epiglottic vallecula neoplasm","type":"exact"},{"name":"malignant neoplasm of epiglottic vallecula","type":"exact"},{"name":"malignant tumor of vallecula","type":"exact"},{"name":"malignant tumour of vallecula","type":"exact"}],"termid":"MONDO:0004607","xrefs":{"Monarch":{"xref_id":"0004607"}}}


id: PBO:0087588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the ARP2/3 complex; ARP2/3 is required for the motility and integrity of cortical actin patches","termid":"PBO:0087588"}


id: PBO:0078354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Glu (anticodon TTC) 1-2","termid":"PBO:0078354"}


id: PR:O13810
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A glutamate 5-kinase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00832"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate 5-kinase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17H9.13c","secondary_identifiers":["UniProtKB:O13810"],"synonyms":[{"name":"GK (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-proB","type":"exact"},{"name":"gamma-glutamyl kinase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13810"}


id: GO:0060288
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of a lineage restriction boundary within a developing tissue which does not correspond to some morphological barrier.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"formation of anatomical boundary","termid":"GO:0048859"},{"relation_name":"part_of","term_name":"compartment pattern specification","termid":"GO:0007386"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"formation of a compartment boundary","synonyms":[{"name":"compartment boundary formation","type":"exact"}],"termid":"GO:0060288"}


id: PBO:0090096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPK cascade adaptor protein Ste4","termid":"PBO:0090096"}


id: PBO:0041705
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calmodulin 2","termid":"PBO:0041705"}


id: PBO:0016516
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae MID1","termid":"PBO:0016516"}


id: MONDO:0005243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Cushing syndrome (obsolete MONDO:0005243)","termid":"MONDO:0005243","xrefs":{"Monarch":{"xref_id":"0005243"}}}


id: FYPO:0003413
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is inviable, forms one or more branches near a septum, is elongated, and has more than one septum.","definition_xrefs":["PMID:18256290","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branched, elongated, multiseptate cell","termid":"FYPO:0000134"},{"relation_name":"is_a","term_name":"inviable elongated multiseptate vegetative cell","termid":"FYPO:0001494"},{"relation_name":"is_a","term_name":"inviable branched, elongated vegetative cell","termid":"FYPO:0002462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000631","FYPO:0000005","FYPO:0000002","FYPO:0000004"],"is_obsolete":false,"name":"inviable branched, elongated, multiseptate vegetative cell","synonyms":[{"name":"inviable branched, elongated, multiseptate cell during vegetative growth","type":"exact"},{"name":"inviable branched, elongated, multiseptate vegetative cell during mitotic cell cycle","type":"related"},{"name":"inviable branched, long, multiseptate cell","type":"exact"},{"name":"lethal; branched, elongated, multiseptate vegetative cell","type":"exact"}],"termid":"FYPO:0003413"}


id: MONDO:0022470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by arterial dissections, multiple lentigines, and cystic medial necrosis.","definition_xrefs":["PMID:7838191"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aortic dissection lentiginosis","termid":"MONDO:0022470","xrefs":{"Monarch":{"xref_id":"0022470"}}}


id: MONDO:0700141
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Melanoma occurring in a dog. It is the most common malignant tumor found in the mouths of dogs and also occurs frequently on the digits. All canine melanomas are locally invasive and malignant canine melanomas show a high rate of metastasis. Melanoma in dogs has been established as a relevant model for human melanoma.","definition_xrefs":["NCIT:C120298"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanoma, non-human animal","termid":"MONDO:0700132"},{"relation_name":"is_a","term_name":"canine neoplasm","termid":"MONDO:0700139"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canine melanoma","termid":"MONDO:0700141","xrefs":{"Monarch":{"xref_id":"0700141"}}}


id: PBO:0046782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EYA2 antisense RNA 1","termid":"PBO:0046782"}


id: PBO:0070417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II associated protein 2 pseudogene 1","termid":"PBO:0070417"}


id: PBO:0084041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPI-glycan remodelase; conserved phosphoesterase domain-containing protein; acts together with Emp24p/Erv25p in cargo exit from the ER; functional ortholog of mammalian GPI-glycan remodelase PGAP5; deletion confers sensitivity to 4-(N-(S-glutathionylacetyl)amino) phenylarsenoxide (GSAO)","termid":"PBO:0084041"}


id: GO:1990017
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Portion of a tanycyte that lies within the ependyma and contains the nucleus. A tanycyte is a specialized elongated ventricular ependymal cell that has processes that extend to the outer, or pial, surface of the CNS.","definition_xrefs":["NIF_Subcellular:sao401910342","ISBN:0195065719"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell body","termid":"GO:0044297"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"somatic portion of tanycyte","synonyms":[{"name":"somatic portion","type":"broad"}],"termid":"GO:1990017"}


id: MOD:01210
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamic acid residue to the copper(1+) glutamate salt.","definition_xrefs":["Unimod:531#E"],"direct_ancestors":[{"relation_name":"is_a","term_name":"copper containing modified residue","termid":"MOD:00742"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-glutamic acid residue","termid":"MOD:02068"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper(1+) L-glutamate","synonyms":[{"name":"Cation:Cu[I]","type":"related"},{"name":"Replacement of proton by copper","type":"related"},{"name":"cuprous salt","type":"exact"}],"termid":"MOD:01210"}


id: MONDO:0017554
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital radioulnar synostosis","termid":"MONDO:0017985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"radio-ulnar synostosis, unilateral","secondary_identifiers":["icd11.foundation:2026644976","GARD:21221","Orphanet:295217"],"synonyms":[{"name":"radio-ulnar fusion, unilateral","type":"exact"}],"termid":"MONDO:0017554","xrefs":{"Monarch":{"xref_id":"0017554"}}}


id: GO:0000438
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The core TFIIH complex when it is part of the general transcription factor TFIIH.","definition_xrefs":["GOC:ew","GOC:krc","PMID:22308316","PMID:22572993","PMID:7813015","PMID:14500720"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription factor TFIIH core complex","termid":"GO:0000439"},{"relation_name":"part_of","term_name":"transcription factor TFIIH holo complex","termid":"GO:0005675"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0005654","GO:0032991"],"is_obsolete":false,"name":"core TFIIH complex portion of holo TFIIH complex","secondary_identifiers":["GO:0000443"],"synonyms":[{"name":"SSL2-core TFIIH complex portion of holo TFIIH complex","type":"exact"}],"termid":"GO:0000438"}


id: FYPO:0000582
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the rate, or speed, of spore germination is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spore germination","termid":"FYPO:0000305"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased rate of spore germination","synonyms":[{"name":"reduced rate of spore germination","type":"exact"},{"name":"spore germination: decreased rate","type":"related"}],"termid":"FYPO:0000582"}


id: GO:0140934
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A deubiquitinase that cleaves ubiquitin from a histone protein to which it is conjugated.","definition_xrefs":["PMID:18206972","PMID:18226187"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deubiquitinase activity","termid":"GO:0101005"},{"relation_name":"is_a","term_name":"histone modifying activity","termid":"GO:0140993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787","GO:0140096","GO:0008233"],"is_obsolete":false,"name":"histone deubiquitinase activity","synonyms":[{"name":"histone deubiquitination","type":"related"}],"termid":"GO:0140934"}


id: PBO:0078418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gly (anticodon GCC) 1-4","termid":"PBO:0078418"}


id: GO:1902683
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of receptor localization to synapse.","definition_xrefs":["PMID:22252129","GOC:kmv","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of localization","termid":"GO:0032879"},{"relation_name":"regulates","term_name":"receptor localization to synapse","termid":"GO:0097120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of receptor localization to synapse","synonyms":[{"name":"regulation of receptor localisation to synapse","type":"exact"}],"termid":"GO:1902683"}


id: PBO:0001340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fun thirty related protein Fft3","termid":"PBO:0001340"}


id: MONDO:0019332
data:
  {"annotated_genes":["SJAG_05011"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86797],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007858"}]},"cv_name":"mondo","definition":"Punctate palmoplantar keratoderma type I (PPKP1), also known as Buschke-Fischer-Brauer syndrome, is a very rare hereditary skin disease characterized by irregularly distributed epidermal hyperkeratosis of the palms and soles with wide variation among patients..","definition_xrefs":["Orphanet:79501"],"direct_ancestors":[{"relation_name":"is_a","term_name":"punctate palmoplantar keratoderma","termid":"MONDO:0017675"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05011":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"punctate palmoplantar keratoderma type 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:372099","GARD:3103","SCTID:717184007","UMLS:C1835662"],"synonyms":[{"name":"Brauer-Buschke-Fischer syndrome","type":"related"},{"name":"Buschke-Fischer-Brauer syndrome","type":"exact"},{"name":"PPKP1","type":"exact"},{"name":"keratoderma, palmoplantar punctate type 1","type":"related"},{"name":"keratodermia palmoplantaris papulosa, Buschke-Fischer-Brauer type","type":"exact"},{"name":"punctate palmoplantar keratoderma type I","type":"related"},{"name":"type I punctate palmoplantar keratoderma","type":"related"}],"termid":"MONDO:0019332","terms_by_termid":{"MONDO:0007858":null},"xrefs":{"Monarch":{"xref_id":"0019332"}}}


id: GO:0010404
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a cell wall hydroxyproline-rich glycoprotein that consist of a core-protein backbone O-glycosylated by one or more complex carbohydrates.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell wall proteoglycan metabolic process","termid":"GO:0010384"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0071554","GO:0008150"],"is_obsolete":false,"name":"cell wall hydroxyproline-rich glycoprotein metabolic process","synonyms":[{"name":"cell wall hydroxyproline-rich glycoprotein metabolism","type":"exact"}],"termid":"GO:0010404"}


id: GO:0048161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The stage in oogenesis when a double layer of distinct follicle cells surrounds the oocyte. An example of this process is found in Mus musculus.","definition_xrefs":["GOC:jid","ISBN:0198542771","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mammalian oogenesis stage","termid":"GO:0022605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"double layer follicle stage","synonyms":[{"name":"mammalian oogenesis stage 4","type":"exact"}],"termid":"GO:0048161"}


id: PATO:0002475
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A position quality inhering in a bearer by virtue of the bearer's existing near the end of another entity.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"position","termid":"PATO:0000140"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subterminal","termid":"PATO:0002475"}


id: PBO:0085982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; relocalizes from vacuole to cytoplasm upon DNA replication stress","termid":"PBO:0085982"}


id: PBO:0077946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (anticodon AGC) 6-1","termid":"PBO:0077946"}


id: FYPO:0004443
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the prospore membrane is decreased during the second meiotic nuclear division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during meiosis","termid":"FYPO:0003549"},{"relation_name":"is_a","term_name":"decreased protein localization to prospore membrane","termid":"FYPO:0004442"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to prospore membrane during meiosis II","synonyms":[{"name":"decreased protein localisation to prospore membrane during meiosis II","type":"exact"},{"name":"decreased protein localization to forespore membrane during meiosis II","type":"exact"},{"name":"decreased protein localization to prospore membrane during second meiotic nuclear division","type":"exact"},{"name":"reduced protein localization to prospore membrane during meiosis II","type":"exact"}],"termid":"FYPO:0004443"}


id: PBO:0051266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IgA inducing protein","termid":"PBO:0051266"}


id: GO:1905327
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the tracheoesophageal septum. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:TermGenie","PMID:9731532","GO_REF:0000081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"tracheoesophageal septum formation","synonyms":[{"name":"esophagotracheal septum formation","type":"exact"},{"name":"tracheoesophageal ridges formation","type":"related"}],"termid":"GO:1905327"}


id: PBO:0004374
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates ace2","termid":"PBO:0004374"}


id: MONDO:0012172
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mitochondrial trifunctional protein (TFP) deficiency (TFPD) is a disorder of fatty acid oxidation characterized by a wide clinical spectrum ranging from severe neonatal manifestations including cardiomyopathy, hypoglycemia, metabolic acidosis, skeletal myopathy and neuropathy, liver disease and death to a mild phenotype with peripheral polyneuropathy, episodic rhabdomyolysis and pigmentary retinopathy..","definition_xrefs":["Orphanet:746"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"long chain 3-hydroxyacyl-CoA dehydrogenase deficiency","termid":"MONDO:0012173"},{"relation_name":"is_a","term_name":"inherited lipid metabolism disorder","termid":"MONDO:0002525"},{"relation_name":"is_a","term_name":"inborn mitochondrial myopathy","termid":"MONDO:0009637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005336","MONDO:0002525","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial trifunctional protein deficiency","secondary_identifiers":["NANDO:2201147","UMLS:C1969443","MEDGEN:370665","NCIT:C98991","GARD:3684","DOID:0111277","MESH:C566945","NANDO:2200515","NANDO:1200974","ICD9:277.85","OMIMPS:609015","icd11.foundation:1018083832","SCTID:237999008"],"synonyms":[{"name":"MTPD","type":"related"},{"name":"TFP deficiency","type":"exact"},{"name":"TFPD","type":"exact"},{"name":"mitochondrial trifunctional PROTEIN deficiency","type":"related"},{"name":"mitochondrial trifunctional protein deficiency","type":"exact"},{"name":"trifunctional Protein deficiency","type":"related"},{"name":"trifunctional Protein deficiency with myopathy and neuropathy","type":"related"}],"termid":"MONDO:0012172","xrefs":{"Monarch":{"xref_id":"0012172"}}}


id: FYPO:0000996
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which the cell tapers at one end to a diameter smaller than the other when the cell is subject to nitrogen starvation. The cell diameter at the narrow end is smaller than that of a wild-type cell.","definition_xrefs":["PMID:19366728","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tapered cell","termid":"FYPO:0000014"},{"relation_name":"is_a","term_name":"abnormal cell morphology during nitrogen starvation","termid":"FYPO:0000995"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"tapered cell during nitrogen starvation","synonyms":[{"name":"bottle-shaped cell during nitrogen starvation","type":"exact"},{"name":"cell morphology, bottle/skittle during nitrogen starvation","type":"exact"},{"name":"skittle-shaped cell during nitrogen starvation","type":"exact"},{"name":"tapered cell during nitrogen depletion","type":"exact"},{"name":"tapered cell during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0000996"}


id: PBO:0011460
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trancriptional repressor protein BolA domain (predicted)","termid":"PBO:0011460"}


id: GO:0097090
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process which results in the assembly, arrangement of constituent parts, or disassembly of a presynaptic membrane, including any proteins associated with the membrane, but excluding other cellular components. A presynaptic membrane is a specialized area of membrane of the axon terminal that faces the plasma membrane of the neuron or muscle fiber with which the axon terminal establishes a synaptic junction.","definition_xrefs":["GOC:sjp","GOC:pr","PMID:19730411","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane organization","termid":"GO:0061024"},{"relation_name":"part_of","term_name":"synapse organization","termid":"GO:0050808"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0008150"],"is_obsolete":false,"name":"presynaptic membrane organization","synonyms":[{"name":"pre-synaptic membrane organization","type":"exact"},{"name":"presynaptic membrane organisation","type":"exact"}],"termid":"GO:0097090"}


id: PBO:0052072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"katanin catalytic subunit A1 like 1","termid":"PBO:0052072"}


id: FYPO:0002319
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of lanosterol measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular sterol level","termid":"FYPO:0002327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular lanosterol level","synonyms":[{"name":"increased cellular lanosterol level during mitotic cell cycle","type":"related"},{"name":"increased cellular lanosterol level during vegetative growth","type":"exact"},{"name":"increased lanosterol accumulation","type":"related"}],"termid":"FYPO:0002319"}


id: MOD:00649
data:
  {"annotated_genes":["SJAG_00733","SJAG_00464","SJAG_02522","SJAG_03641"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[82426,82376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00050"},{"annotations":[82466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00126"},{"annotations":[82499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00127"}]},"cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with an acyl group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00464":null,"SJAG_00733":null,"SJAG_02522":null,"SJAG_03641":null},"genotype_count":0,"is_obsolete":false,"name":"acylated residue","references_by_uniquename":{"PMID:36408920":null},"synonyms":[{"name":"AcylRes","type":"exact"}],"termid":"MOD:00649","terms_by_termid":{"MOD:00050":null,"MOD:00126":null,"MOD:00127":null}}


id: PBO:0000442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase X family","termid":"PBO:0000442"}


id: PBO:0046599
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K9, member 1","termid":"PBO:0046599"}


id: SO:0000521
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene in rearranged configuration including at least one V-gene and one VDJ-gene.","direct_ancestors":[{"relation_name":"has_part","term_name":"V_gene_segment","termid":"SO:0000466"},{"relation_name":"has_part","term_name":"VDJ_gene_segment","termid":"SO:0000574"},{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_rearranged_gene_cluster","termid":"SO:0000938"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V_VDJ_cluster","synonyms":[{"name":"V VDJ cluster","type":"exact"},{"name":"V-(VDJ)-CLUSTER","type":"exact"}],"termid":"SO:0000521"}


id: PR:O59828
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- alr1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59828"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alanine racemase, catabolic (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC965.08c","synonyms":[{"name":"Spom972h-alr1","type":"exact"}],"termid":"PR:O59828"}


id: FYPO:0005917
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of RNA derived from subtelomeric heterochromatin regions is higher than normal. Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PMID:25798942"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during vegetative growth","termid":"FYPO:0000825"},{"relation_name":"is_a","term_name":"increased transcription","termid":"FYPO:0002875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000294","FYPO:0001320","FYPO:0006551","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased subtelomeric heterochromatin RNA level","synonyms":[{"name":"accumulation of subtelomere-derived RNA transcripts","type":"related"},{"name":"increased transcription at subtelomere","type":"narrow"},{"name":"increased transcription at subtelomeric heterochromatin during vegetative growth","type":"narrow"}],"termid":"FYPO:0005917"}


id: PBO:0111967
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dsl1/NZR complex secretory pathway protein RINT1 family","termid":"PBO:0111967"}


id: PBO:0091207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gln","termid":"PBO:0091207"}


id: PBO:0062564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 10 subfamily AD member 1","termid":"PBO:0062564"}


id: PBO:0044586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"D-box binding PAR bZIP transcription factor","termid":"PBO:0044586"}


id: PBO:0034770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDP-diacylglycerol-glycerol-3-phosphate3-phosphatidyltransferase Pgs1","termid":"PBO:0034770"}


id: PBO:0091968
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"III:g.1774235_1774236insGATC","termid":"PBO:0091968"}


id: GO:1903215
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein targeting to mitochondrion.","definition_xrefs":["GOC:bf","PMID:21370995","GOC:PARL","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein targeting to mitochondrion","termid":"GO:1903214"},{"relation_name":"is_a","term_name":"negative regulation of establishment of protein localization to mitochondrion","termid":"GO:1903748"},{"relation_name":"negatively_regulates","term_name":"protein targeting to mitochondrion","termid":"GO:0006626"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006605"},{"rel_name":"negatively_regulates","termid":"GO:0006605"}],"interesting_parent_ids":["GO:0006605","GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein targeting to mitochondrion","synonyms":[{"name":"down regulation of mitochondrial protein import","type":"related"},{"name":"down regulation of mitochondrial translocation","type":"related"},{"name":"down regulation of protein import into mitochondrion","type":"exact"},{"name":"down regulation of protein targeting to mitochondria","type":"exact"},{"name":"down regulation of protein targeting to mitochondrion","type":"exact"},{"name":"down regulation of protein-mitochondrial targeting","type":"exact"},{"name":"down-regulation of mitochondrial protein import","type":"related"},{"name":"down-regulation of mitochondrial translocation","type":"related"},{"name":"down-regulation of protein import into mitochondrion","type":"exact"},{"name":"down-regulation of protein targeting to mitochondria","type":"exact"},{"name":"down-regulation of protein targeting to mitochondrion","type":"exact"},{"name":"down-regulation of protein-mitochondrial targeting","type":"exact"},{"name":"downregulation of mitochondrial protein import","type":"related"},{"name":"downregulation of mitochondrial translocation","type":"related"},{"name":"downregulation of protein import into mitochondrion","type":"exact"},{"name":"downregulation of protein targeting to mitochondria","type":"exact"},{"name":"downregulation of protein targeting to mitochondrion","type":"exact"},{"name":"downregulation of protein-mitochondrial targeting","type":"exact"},{"name":"inhibition of mitochondrial protein import","type":"related"},{"name":"inhibition of mitochondrial translocation","type":"related"},{"name":"inhibition of protein import into mitochondrion","type":"narrow"},{"name":"inhibition of protein targeting to mitochondria","type":"narrow"},{"name":"inhibition of protein targeting to mitochondrion","type":"narrow"},{"name":"inhibition of protein-mitochondrial targeting","type":"narrow"},{"name":"negative regulation of mitochondrial protein import","type":"related"},{"name":"negative regulation of mitochondrial translocation","type":"related"},{"name":"negative regulation of protein import into mitochondrion","type":"exact"},{"name":"negative regulation of protein targeting to mitochondria","type":"exact"},{"name":"negative regulation of protein-mitochondrial targeting","type":"exact"}],"termid":"GO:1903215"}


id: GO:0000934
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A septum or cross wall which does not entirely span the space between two portions of cell wall and may contain a specialized central pore structure. A porous septum allows the movement of organelles and/or cytoplasm between compartments.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell septum","termid":"GO:0030428"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"porous cell septum","synonyms":[{"name":"porous septum","type":"broad"}],"termid":"GO:0000934"}


id: GO:1901363
data:
  {"annotated_genes":["SJAG_03115","SJAG_01877","SJAG_03602","SJAG_00330","SJAG_03927","SJAG_01458","SJAG_03897","SJAG_03486","SJAG_01534","SJAG_00853","SJAG_04265","SJAG_00412","SJAG_03660","SJAG_01432","SJAG_04552","SJAG_03495","SJAG_01179","SJAG_00597","SJAG_01499","SJAG_03732","SJAG_02640","SJAG_00392","SJAG_03240","SJAG_01245","SJAG_01081","SJAG_02595","SJAG_03923","SJAG_02994","SJAG_02242","SJAG_01254","SJAG_03374","SJAG_02236","SJAG_03533","SJAG_00332","SJAG_04762","SJAG_00718","SJAG_04856","SJAG_01137","SJAG_02429","SJAG_04495","SJAG_00993","SJAG_00256","SJAG_00031","SJAG_02656","SJAG_01052","SJAG_04081","SJAG_03915","SJAG_03567","SJAG_01679","SJAG_00986","SJAG_00488","SJAG_02370","SJAG_00427","SJAG_02686","SJAG_01878","SJAG_01379","SJAG_04465","SJAG_00815","SJAG_16456","SJAG_02428","SJAG_00466","SJAG_05024","SJAG_00906","SJAG_03345","SJAG_00996","SJAG_02827","SJAG_03562","SJAG_04178","SJAG_03961","SJAG_02838","SJAG_02200","SJAG_03592","SJAG_04507","SJAG_04980","SJAG_01080","SJAG_02748","SJAG_01019","SJAG_03526","SJAG_02496","SJAG_03987","SJAG_04121","SJAG_03850","SJAG_00106","SJAG_00931","SJAG_01010","SJAG_04745","SJAG_03557","SJAG_01376","SJAG_04599","SJAG_01215","SJAG_01546","SJAG_00773","SJAG_03828","SJAG_00830","SJAG_01148","SJAG_01731","SJAG_02378","SJAG_03320","SJAG_00364","SJAG_04577","SJAG_01530","SJAG_04874","SJAG_00790","SJAG_02723","SJAG_04842","SJAG_04030","SJAG_00881","SJAG_03585","SJAG_01070","SJAG_00610","SJAG_02604","SJAG_01881","SJAG_02897","SJAG_03290","SJAG_00878","SJAG_02206","SJAG_00356","SJAG_01435","SJAG_00475","SJAG_03071","SJAG_01315","SJAG_02288","SJAG_00430","SJAG_03436","SJAG_04052","SJAG_00359","SJAG_04183","SJAG_04167","SJAG_00980","SJAG_02643","SJAG_04469","SJAG_02420","SJAG_04258","SJAG_00084","SJAG_01855","SJAG_03457","SJAG_02610","SJAG_02713","SJAG_01938","SJAG_02887","SJAG_01259","SJAG_03813","SJAG_04757","SJAG_02431","SJAG_01587","SJAG_01618","SJAG_00857","SJAG_00633","SJAG_02906","SJAG_02721","SJAG_01040","SJAG_00638","SJAG_04760","SJAG_04589","SJAG_02599","SJAG_02015","SJAG_03236","SJAG_04665","SJAG_01831","SJAG_03479","SJAG_04351","SJAG_02509","SJAG_03811","SJAG_02889","SJAG_00871","SJAG_00757","SJAG_03967","SJAG_00875","SJAG_02348","SJAG_04118","SJAG_05015","SJAG_04865","SJAG_00353","SJAG_03160","SJAG_04187","SJAG_00169","SJAG_03959","SJAG_03312","SJAG_04277","SJAG_01695","SJAG_00937","SJAG_02295","SJAG_02601","SJAG_01339","SJAG_01791","SJAG_04355","SJAG_04210","SJAG_00464","SJAG_02822","SJAG_03336","SJAG_04186","SJAG_01669","SJAG_03237","SJAG_04461","SJAG_02104","SJAG_03501","SJAG_01018","SJAG_04480","SJAG_02558","SJAG_01063","SJAG_02180","SJAG_04114","SJAG_00964","SJAG_02619","SJAG_04743","SJAG_03096","SJAG_02825","SJAG_03157","SJAG_01447","SJAG_03471","SJAG_03659","SJAG_01837","SJAG_04612","SJAG_02704","SJAG_04032","SJAG_02226","SJAG_02615","SJAG_02233","SJAG_03376","SJAG_01807","SJAG_03371","SJAG_00706","SJAG_03799","SJAG_00281","SJAG_04627","SJAG_00995","SJAG_01383","SJAG_04551","SJAG_05372","SJAG_00235","SJAG_01131","SJAG_04366","SJAG_01684","SJAG_01620","SJAG_00381","SJAG_02545","SJAG_01311","SJAG_03485","SJAG_03140","SJAG_04270","SJAG_02460","SJAG_03193","SJAG_00208","SJAG_02520","SJAG_04233","SJAG_01696","SJAG_00409","SJAG_04678","SJAG_02697","SJAG_01084","SJAG_01510","SJAG_03743","SJAG_02835","SJAG_02267","SJAG_04544","SJAG_04650","SJAG_02084","SJAG_01613","SJAG_01859","SJAG_02464","SJAG_04692","SJAG_04154","SJAG_04054","SJAG_03257","SJAG_02187","SJAG_03676","SJAG_01611","SJAG_02148","SJAG_05018","SJAG_04394","SJAG_03362","SJAG_04549","SJAG_04268","SJAG_00420","SJAG_02360","SJAG_01825","SJAG_03909","SJAG_00863","SJAG_04004","SJAG_00779","SJAG_02457","SJAG_01352","SJAG_04657","SJAG_00690","SJAG_00707","SJAG_03728","SJAG_05230","SJAG_00801","SJAG_00234","SJAG_03932","SJAG_04230","SJAG_04288","SJAG_03730","SJAG_03684","SJAG_02563","SJAG_03626","SJAG_02684","SJAG_01797","SJAG_00968","SJAG_02926","SJAG_03363","SJAG_03209","SJAG_00963","SJAG_00344","SJAG_05213","SJAG_04157","SJAG_03903","SJAG_01762","SJAG_05313","SJAG_02313","SJAG_05340","SJAG_03703","SJAG_02712","SJAG_02366","SJAG_01164","SJAG_03306","SJAG_03449","SJAG_00390","SJAG_01942","SJAG_00678","SJAG_02077","SJAG_01774","SJAG_03355","SJAG_00252","SJAG_03036","SJAG_06622","SJAG_02785","SJAG_02564","SJAG_00930","SJAG_01024","SJAG_01000","SJAG_04457","SJAG_04509","SJAG_02736","SJAG_02680","SJAG_01671","SJAG_01438","SJAG_02336","SJAG_02875","SJAG_02426","SJAG_01405","SJAG_03451","SJAG_02878","SJAG_00293","SJAG_03950","SJAG_03067","SJAG_02592","SJAG_00342","SJAG_02848","SJAG_02517","SJAG_04276","SJAG_02950","SJAG_02571","SJAG_03785","SJAG_04362","SJAG_03384","SJAG_05295","SJAG_03077","SJAG_02249","SJAG_04845","SJAG_03689","SJAG_00956","SJAG_00402","SJAG_01235","SJAG_02061","SJAG_04343","SJAG_01268","SJAG_02997","SJAG_02498","SJAG_00436","SJAG_02205","SJAG_05249","SJAG_00653","SJAG_00661","SJAG_03982","SJAG_02876","SJAG_00114","SJAG_02142","SJAG_05105","SJAG_01500","SJAG_00712","SJAG_02294","SJAG_04285","SJAG_04477","SJAG_01945","SJAG_01787","SJAG_02796","SJAG_01558","SJAG_03570","SJAG_01358","SJAG_04470","SJAG_00358","SJAG_00300","SJAG_01456","SJAG_03048","SJAG_02791","SJAG_03137","SJAG_04777","SJAG_04988","SJAG_01577","SJAG_00378","SJAG_03578","SJAG_03313","SJAG_02287","SJAG_03475","SJAG_04206","SJAG_02292","SJAG_03529","SJAG_00432","SJAG_00265","SJAG_03985","SJAG_04655","SJAG_02808","SJAG_03688","SJAG_02872","SJAG_02489","SJAG_00729","SJAG_03188","SJAG_00983","SJAG_02074","SJAG_02331","SJAG_02734","SJAG_00605","SJAG_03804","SJAG_01680","SJAG_03434","SJAG_02618","SJAG_03349","SJAG_00766","SJAG_01075","SJAG_01789","SJAG_04042","SJAG_04700","SJAG_05276","SJAG_02760","SJAG_01571","SJAG_01351","SJAG_04738","SJAG_02698","SJAG_02286","SJAG_04367","SJAG_04410","SJAG_00663","SJAG_00039","SJAG_00186","SJAG_05030","SJAG_04468","SJAG_03496","SJAG_04974","SJAG_06597","SJAG_02302","SJAG_01805","SJAG_05231","SJAG_01198","SJAG_04000","SJAG_01176","SJAG_01002","SJAG_02945","SJAG_03866","SJAG_02708","SJAG_00669","SJAG_02364","SJAG_01863","SJAG_03497","SJAG_03206","SJAG_01471","SJAG_00583","SJAG_00855","SJAG_02824","SJAG_02305","SJAG_00424","SJAG_02382","SJAG_04511","SJAG_00533","SJAG_02342","SJAG_01159","SJAG_02135","SJAG_01182","SJAG_02182","SJAG_00786","SJAG_00599","SJAG_00673","SJAG_01718","SJAG_00845","SJAG_04147","SJAG_02400","SJAG_01419","SJAG_03712","SJAG_04652","SJAG_02527","SJAG_05304","SJAG_05022","SJAG_02038","SJAG_03534","SJAG_03854","SJAG_03658","SJAG_01937","SJAG_04537","SJAG_03453","SJAG_00118","SJAG_04280","SJAG_01449","SJAG_00103","SJAG_01221","SJAG_01240","SJAG_00360","SJAG_01373","SJAG_00609","SJAG_02991","SJAG_04001","SJAG_00329","SJAG_00136","SJAG_03852","SJAG_01575","SJAG_00203","SJAG_02605","SJAG_03145","SJAG_03671","SJAG_03887","SJAG_00337","SJAG_02725","SJAG_02183","SJAG_03669","SJAG_00198","SJAG_04634","SJAG_01197","SJAG_02399","SJAG_03438","SJAG_01918","SJAG_02444","SJAG_00637","SJAG_03896","SJAG_04755","SJAG_01953","SJAG_03946","SJAG_00027","SJAG_03011","SJAG_04573","SJAG_01944","SJAG_06621","SJAG_01344","SJAG_02923","SJAG_03017","SJAG_00168","SJAG_01668","SJAG_01186","SJAG_01929","SJAG_00495","SJAG_03832","SJAG_05019","SJAG_05025","SJAG_04597","SJAG_03708","SJAG_01402","SJAG_04862","SJAG_00097","SJAG_04486","SJAG_04334","SJAG_00042","SJAG_02977","SJAG_03886","SJAG_01874","SJAG_01653","SJAG_01677","SJAG_06642","SJAG_04849","SJAG_04189","SJAG_01410","SJAG_01400","SJAG_00649","SJAG_02858","SJAG_04772","SJAG_04126","SJAG_04622","SJAG_04003","SJAG_01644","SJAG_03386","SJAG_01851","SJAG_03275","SJAG_04669","SJAG_00616","SJAG_03613","SJAG_00048","SJAG_03141","SJAG_00933","SJAG_02879","SJAG_05173","SJAG_00947","SJAG_03545","SJAG_00840","SJAG_02738","SJAG_01816","SJAG_04435","SJAG_00331","SJAG_03277","SJAG_01489","SJAG_01595","SJAG_01012","SJAG_04039","SJAG_04810","SJAG_00403","SJAG_05194","SJAG_02058","SJAG_04094","SJAG_03061","SJAG_04666","SJAG_04761","SJAG_02741","SJAG_02022","SJAG_01297","SJAG_01766","SJAG_05332","SJAG_03753","SJAG_02598","SJAG_01082","SJAG_02696","SJAG_03846","SJAG_02856","SJAG_01769","SJAG_03898","SJAG_03720","SJAG_02895","SJAG_01522","SJAG_00636","SJAG_02199","SJAG_04055","SJAG_04232","SJAG_01391","SJAG_00004","SJAG_01664","SJAG_01152","SJAG_04375","SJAG_04473","SJAG_03709","SJAG_04734","SJAG_00244","SJAG_03409","SJAG_01903","SJAG_00111","SJAG_02374","SJAG_03914","SJAG_01724","SJAG_05027","SJAG_04125","SJAG_03069","SJAG_00650","SJAG_03798","SJAG_01047","SJAG_04156","SJAG_05353","SJAG_04372","SJAG_01162","SJAG_02384","SJAG_00226","SJAG_00851","SJAG_03152","SJAG_00660","SJAG_02602","SJAG_00582","SJAG_04946","SJAG_02596","SJAG_03055","SJAG_05209","SJAG_00486","SJAG_02488","SJAG_03342","SJAG_02661","SJAG_02392","SJAG_00174","SJAG_03421","SJAG_00999","SJAG_04203","SJAG_02972","SJAG_00370","SJAG_02575","SJAG_01885","SJAG_00443","SJAG_04312","SJAG_02297","SJAG_04150","SJAG_03129","SJAG_02521","SJAG_01964","SJAG_00604","SJAG_00984","SJAG_00457","SJAG_03461","SJAG_04482","SJAG_00500","SJAG_03679","SJAG_04409","SJAG_04287","SJAG_04459","SJAG_02176","SJAG_04320","SJAG_04064","SJAG_03861","SJAG_03102","SJAG_00564","SJAG_02082","SJAG_01129","SJAG_04387","SJAG_00887","SJAG_00414","SJAG_01277","SJAG_04145","SJAG_03224","SJAG_00243","SJAG_01704","SJAG_00150","SJAG_00798","SJAG_01466","SJAG_04566","SJAG_03780","SJAG_04608","SJAG_02394","SJAG_00541","SJAG_03948","SJAG_02421","SJAG_04747","SJAG_01616","SJAG_02720","SJAG_04282","SJAG_04693","SJAG_01041","SJAG_03476","SJAG_01544","SJAG_05290","SJAG_00988","SJAG_00898","SJAG_04840","SJAG_01181","SJAG_03892","SJAG_01615","SJAG_00884","SJAG_04038","SJAG_04970","SJAG_03174","SJAG_00044","SJAG_00231","SJAG_01354","SJAG_04882","SJAG_03789","SJAG_01474","SJAG_16455","SJAG_00447","SJAG_00516","SJAG_00529","SJAG_03213","SJAG_02468","SJAG_01693","SJAG_00659","SJAG_04857","SJAG_02171","SJAG_01909","SJAG_01799","SJAG_02690","SJAG_03072","SJAG_00502","SJAG_00704","SJAG_00938","SJAG_02353","SJAG_04149","SJAG_05010","SJAG_00714","SJAG_04940","SJAG_00972"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75681],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002055"},{"annotations":[71699,94668,74476,91032],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043531"},{"annotations":[71753,75678,90699,70349],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016208"},{"annotations":[57559,67907,57470,60596,90619,59205,70187,58576,69462,60130,70042,59333,63449,65256,57525,59088,69727,59695,70353,60281,64038,104081,58166,65589,59731,67943,66112,59429,64283,58943,61191,68104,57951,66413,67015,70086,59697,57626,115971,62603,58520,64189,59129,59742,91316,69437,58273,59721,68549,59942,64616,66556,70356,107323,114811,62257,93370,58910,68332,66858,69599,70702,57761,67401,63198,62273,63053,60825,59292,64904,70738,57595,68401,64895,58801,66326,58630,59485,63097,67878,67506,95511,117881,61816,62556,78206,66531,112934,60492,58020,69007,60616,69222,65266,61380,65418,63681,60551,58979,69791,65836,58244,67689,115917,92976,57363,67192,64205,69542,64473,66174,64088,67673,63596,60371,60853,58030,64887,58008,62822,67985,63690,68793,70080,70655,70849,71140,61151,61222,104492,107065,110005,61851,57744,62480,62766,66796,60791,68008,63129,64419,115448,67387,66831,61011,58827,64446,59021,61704,61670,57613,63381,65754,59552,63511,66493,110344,60769,64170,60705,59418,63636,65904,66199,67739,68821,58048,58580,66415,73840,60523,81961,110385,114812,63814,69779,59655,63876,67330,70706,62092,60364,66663,57662,58599,58704,70662,69043,60988,76069,107421,61757,71472,58728,68293,69072,58751,63249,66024,67043,69933,106467,59939,99310,69355,62890,64732,67552,69526,60380,66456,62069,64257,61345,70634,71499,60661,71403,59141,62087,63123,71150,91034,58424,71304,67857,58999,69606,57454,62116,67448,57096,57679,60110,59949,61062,61901,65673,62100,58848,70496,68050,60507,67466,69397,100613,57281,66434,61436,69583,63357,66501,65572,70398,65129,69119,71700,117624,64897,66043,66265,66606,119787,67524,57123,71116,58744,62908,63063,59362,66301,66917,68989,69375,59275,64099,68856,59054,64757,70984,57708,61654,74410,90891,105644,119848,61373,57421,66958,59826,65389,58172,61366,65250,74694,60094,66696,69452,65923,63564,71263,57446,64663,69634,70444,71247,116376,59268,57820,63465,67346,70156,57922,68248,67734,66629,60890,59030,62721,67751,61916,66703,69814,69850,75836,106143,67545,69350,69564,65106,112383,67239,62032,60470,61635,58227,70068,67525,68350,64986,66131,70826,61167,61339,57585,70571,68886,58626,90196,91663,70851,58793,62492,101916,57213,58394,59674,71257,101506,57996,69777,117560,66861,71178,74190,61092,70934,57505,66083,68505,70225,65430,62106,65017,59397,59104,105145,59520,62440,69131,60699,70599,59237,66020,69494,67537,61441,68968,64918,58397,68829,57372,65079,65166,60428,66313,70859,65365,62391,59496,59040,60227,58343,63071,64357,65647,62416,64164,70325,70306,70966,68187,71486,100955,64837,59231,69861,71250,58917,102922,69012,58358,60810,68273,58871,62244,66461,60072,60207,60168,63988,62113,65796,61790,62826,62541,59738,63713,71048,101156,68071,70466,67170,61290,63572,69154,69569,61767,64606,62641,67931,70422,98301,109782,113240,63134,70527,63507,60725,65276,68029,62690,57860,71124,67838,60388,57549,71385,58313,69091,70323,66467,68606,63620,70163,64368,67166,69440,62333,69587,59117,62552,68116,57750,67025,68981,67419,64250,68716,62670,59077,61729,58433,66181,68417,68469,64583,59348,65818,69027,69834,57564,61751,115035,61544,64398,58675,115279,64780,60203,71107,64431,65621,63587,79176,57500,57766,93961,57846,59932,60245,65724,70004,63721,64271,71298,74477,114946,67258,79525,114810,59593,61124,66851,59846,67831,59406,71503,59421,57166,57257,65736,57289,62973,59640,58718,68374,60344,67284,73465,65616,67156,70297,70343,69720,57808,68263],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005524"},{"annotations":[72718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030552"},{"annotations":[92664,89553],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002135"},{"annotations":[71998,114868,78009,59918,72656,73595,65690,71453,94156,61254,70681,71418,111528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071949"},{"annotations":[77804,80071,80810,80842,66119,120659,76297,78976,63359,60185,73495,95923,77966,61202,67211,77751,67112,77981,114654],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050660"},{"annotations":[66903,91193,78975,80806,80068,76293,65214,74462,71005,77979,65999,61245,60038,60180,68862,57606,63857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010181"},{"annotations":[76939,73989,93517,94241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019003"},{"annotations":[90700,117551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019002"},{"annotations":[119354,64642,79189,98321,57433,63828,67457,74267,79683,57387,106893,62671,79693,69503,75150,67890,65341,60571,66895,68966,60857,72792,64120,70539,59162,95212,115392,68191,79240,74497,59376,74110,70667,82121,77605,58249,73438,92895,76154,120356,120838,63675,75066,65353,69996,58410,63545,65698,61590,58294,70641,64815,81687,95265,59325,59972,58300,71509,93744,96041,103057,65816,76164,78179,110308,60446,69589,73986,71620,97575,61925,66425,62167,62614,79565,67255,98095,75035,76936,67647,72049,71074,65946,68732,80276,62922,63914,81898,61107,81870,105484,58381,75779],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005525"},{"annotations":[117552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905108"},{"annotations":[77663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036042"},{"annotations":[60654,59263,65986,58342,63581,62456,64452,63869,63759,71350,71462,65507,111251,120660,64266,111250,111253,111249,61630,70818],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051287"},{"annotations":[67275,58607,113826,60541,80487],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070403"},{"annotations":[67132,63580,111257,106283,65716,60326,63537,66001,111258,69679,60653,72814,82112,57779,69688,71461,95924,111256,65505,58890,116664,111260,65776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050661"},{"annotations":[59256],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070401"},{"annotations":[104865,116647,76129],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070402"},{"annotations":[60668,67750,76163,66584,73816,72268,75917,64454,66769,66353,66823,70412,71626,75076,112288,58152,65686,74199,58503,68921,81331,69412,67484,69458,67710,62397,57313,81044,70208,80148],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030170"},{"annotations":[112228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902444"},{"annotations":[65222,63327,61871],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032549"},{"annotations":[68509],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030975"},{"annotations":[65560,59360,57682,62498,74979,58924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030976"},{"annotations":[92670,93495],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002134"}]},"cv_name":"molecular_function","definition":"Binding to heterocyclic compound.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small molecule binding","termid":"GO:0036094"}],"gene_count":767,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00027":null,"SJAG_00031":null,"SJAG_00039":null,"SJAG_00042":null,"SJAG_00044":null,"SJAG_00048":null,"SJAG_00084":null,"SJAG_00097":null,"SJAG_00103":null,"SJAG_00106":null,"SJAG_00111":null,"SJAG_00114":null,"SJAG_00118":null,"SJAG_00136":null,"SJAG_00150":null,"SJAG_00168":null,"SJAG_00169":null,"SJAG_00174":null,"SJAG_00186":null,"SJAG_00198":null,"SJAG_00203":null,"SJAG_00208":null,"SJAG_00226":null,"SJAG_00231":null,"SJAG_00234":null,"SJAG_00235":null,"SJAG_00243":null,"SJAG_00244":null,"SJAG_00252":null,"SJAG_00256":null,"SJAG_00265":null,"SJAG_00281":null,"SJAG_00293":null,"SJAG_00300":null,"SJAG_00329":null,"SJAG_00330":null,"SJAG_00331":null,"SJAG_00332":null,"SJAG_00337":null,"SJAG_00342":null,"SJAG_00344":null,"SJAG_00353":null,"SJAG_00356":null,"SJAG_00358":null,"SJAG_00359":null,"SJAG_00360":null,"SJAG_00364":null,"SJAG_00370":null,"SJAG_00378":null,"SJAG_00381":null,"SJAG_00390":null,"SJAG_00392":null,"SJAG_00402":null,"SJAG_00403":null,"SJAG_00409":null,"SJAG_00412":null,"SJAG_00414":null,"SJAG_00420":null,"SJAG_00424":null,"SJAG_00427":null,"SJAG_00430":null,"SJAG_00432":null,"SJAG_00436":null,"SJAG_00443":null,"SJAG_00447":null,"SJAG_00457":null,"SJAG_00464":null,"SJAG_00466":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00488":null,"SJAG_00495":null,"SJAG_00500":null,"SJAG_00502":null,"SJAG_00516":null,"SJAG_00529":null,"SJAG_00533":null,"SJAG_00541":null,"SJAG_00564":null,"SJAG_00582":null,"SJAG_00583":null,"SJAG_00597":null,"SJAG_00599":null,"SJAG_00604":null,"SJAG_00605":null,"SJAG_00609":null,"SJAG_00610":null,"SJAG_00616":null,"SJAG_00633":null,"SJAG_00636":null,"SJAG_00637":null,"SJAG_00638":null,"SJAG_00649":null,"SJAG_00650":null,"SJAG_00653":null,"SJAG_00659":null,"SJAG_00660":null,"SJAG_00661":null,"SJAG_00663":null,"SJAG_00669":null,"SJAG_00673":null,"SJAG_00678":null,"SJAG_00690":null,"SJAG_00704":null,"SJAG_00706":null,"SJAG_00707":null,"SJAG_00712":null,"SJAG_00714":null,"SJAG_00718":null,"SJAG_00729":null,"SJAG_00757":null,"SJAG_00766":null,"SJAG_00773":null,"SJAG_00779":null,"SJAG_00786":null,"SJAG_00790":null,"SJAG_00798":null,"SJAG_00801":null,"SJAG_00815":null,"SJAG_00830":null,"SJAG_00840":null,"SJAG_00845":null,"SJAG_00851":null,"SJAG_00853":null,"SJAG_00855":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00871":null,"SJAG_00875":null,"SJAG_00878":null,"SJAG_00881":null,"SJAG_00884":null,"SJAG_00887":null,"SJAG_00898":null,"SJAG_00906":null,"SJAG_00930":null,"SJAG_00931":null,"SJAG_00933":null,"SJAG_00937":null,"SJAG_00938":null,"SJAG_00947":null,"SJAG_00956":null,"SJAG_00963":null,"SJAG_00964":null,"SJAG_00968":null,"SJAG_00972":null,"SJAG_00980":null,"SJAG_00983":null,"SJAG_00984":null,"SJAG_00986":null,"SJAG_00988":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_00996":null,"SJAG_00999":null,"SJAG_01000":null,"SJAG_01002":null,"SJAG_01010":null,"SJAG_01012":null,"SJAG_01018":null,"SJAG_01019":null,"SJAG_01024":null,"SJAG_01040":null,"SJAG_01041":null,"SJAG_01047":null,"SJAG_01052":null,"SJAG_01063":null,"SJAG_01070":null,"SJAG_01075":null,"SJAG_01080":null,"SJAG_01081":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01129":null,"SJAG_01131":null,"SJAG_01137":null,"SJAG_01148":null,"SJAG_01152":null,"SJAG_01159":null,"SJAG_01162":null,"SJAG_01164":null,"SJAG_01176":null,"SJAG_01179":null,"SJAG_01181":null,"SJAG_01182":null,"SJAG_01186":null,"SJAG_01197":null,"SJAG_01198":null,"SJAG_01215":null,"SJAG_01221":null,"SJAG_01235":null,"SJAG_01240":null,"SJAG_01245":null,"SJAG_01254":null,"SJAG_01259":null,"SJAG_01268":null,"SJAG_01277":null,"SJAG_01297":null,"SJAG_01311":null,"SJAG_01315":null,"SJAG_01339":null,"SJAG_01344":null,"SJAG_01351":null,"SJAG_01352":null,"SJAG_01354":null,"SJAG_01358":null,"SJAG_01373":null,"SJAG_01376":null,"SJAG_01379":null,"SJAG_01383":null,"SJAG_01391":null,"SJAG_01400":null,"SJAG_01402":null,"SJAG_01405":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01432":null,"SJAG_01435":null,"SJAG_01438":null,"SJAG_01447":null,"SJAG_01449":null,"SJAG_01456":null,"SJAG_01458":null,"SJAG_01466":null,"SJAG_01471":null,"SJAG_01474":null,"SJAG_01489":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01510":null,"SJAG_01522":null,"SJAG_01530":null,"SJAG_01534":null,"SJAG_01544":null,"SJAG_01546":null,"SJAG_01558":null,"SJAG_01571":null,"SJAG_01575":null,"SJAG_01577":null,"SJAG_01587":null,"SJAG_01595":null,"SJAG_01611":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01616":null,"SJAG_01618":null,"SJAG_01620":null,"SJAG_01644":null,"SJAG_01653":null,"SJAG_01664":null,"SJAG_01668":null,"SJAG_01669":null,"SJAG_01671":null,"SJAG_01677":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01684":null,"SJAG_01693":null,"SJAG_01695":null,"SJAG_01696":null,"SJAG_01704":null,"SJAG_01718":null,"SJAG_01724":null,"SJAG_01731":null,"SJAG_01762":null,"SJAG_01766":null,"SJAG_01769":null,"SJAG_01774":null,"SJAG_01787":null,"SJAG_01789":null,"SJAG_01791":null,"SJAG_01797":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_01807":null,"SJAG_01816":null,"SJAG_01825":null,"SJAG_01831":null,"SJAG_01837":null,"SJAG_01851":null,"SJAG_01855":null,"SJAG_01859":null,"SJAG_01863":null,"SJAG_01874":null,"SJAG_01877":null,"SJAG_01878":null,"SJAG_01881":null,"SJAG_01885":null,"SJAG_01903":null,"SJAG_01909":null,"SJAG_01918":null,"SJAG_01929":null,"SJAG_01937":null,"SJAG_01938":null,"SJAG_01942":null,"SJAG_01944":null,"SJAG_01945":null,"SJAG_01953":null,"SJAG_01964":null,"SJAG_02015":null,"SJAG_02022":null,"SJAG_02038":null,"SJAG_02058":null,"SJAG_02061":null,"SJAG_02074":null,"SJAG_02077":null,"SJAG_02082":null,"SJAG_02084":null,"SJAG_02104":null,"SJAG_02135":null,"SJAG_02142":null,"SJAG_02148":null,"SJAG_02171":null,"SJAG_02176":null,"SJAG_02180":null,"SJAG_02182":null,"SJAG_02183":null,"SJAG_02187":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02205":null,"SJAG_02206":null,"SJAG_02226":null,"SJAG_02233":null,"SJAG_02236":null,"SJAG_02242":null,"SJAG_02249":null,"SJAG_02267":null,"SJAG_02286":null,"SJAG_02287":null,"SJAG_02288":null,"SJAG_02292":null,"SJAG_02294":null,"SJAG_02295":null,"SJAG_02297":null,"SJAG_02302":null,"SJAG_02305":null,"SJAG_02313":null,"SJAG_02331":null,"SJAG_02336":null,"SJAG_02342":null,"SJAG_02348":null,"SJAG_02353":null,"SJAG_02360":null,"SJAG_02364":null,"SJAG_02366":null,"SJAG_02370":null,"SJAG_02374":null,"SJAG_02378":null,"SJAG_02382":null,"SJAG_02384":null,"SJAG_02392":null,"SJAG_02394":null,"SJAG_02399":null,"SJAG_02400":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_02426":null,"SJAG_02428":null,"SJAG_02429":null,"SJAG_02431":null,"SJAG_02444":null,"SJAG_02457":null,"SJAG_02460":null,"SJAG_02464":null,"SJAG_02468":null,"SJAG_02488":null,"SJAG_02489":null,"SJAG_02496":null,"SJAG_02498":null,"SJAG_02509":null,"SJAG_02517":null,"SJAG_02520":null,"SJAG_02521":null,"SJAG_02527":null,"SJAG_02545":null,"SJAG_02558":null,"SJAG_02563":null,"SJAG_02564":null,"SJAG_02571":null,"SJAG_02575":null,"SJAG_02592":null,"SJAG_02595":null,"SJAG_02596":null,"SJAG_02598":null,"SJAG_02599":null,"SJAG_02601":null,"SJAG_02602":null,"SJAG_02604":null,"SJAG_02605":null,"SJAG_02610":null,"SJAG_02615":null,"SJAG_02618":null,"SJAG_02619":null,"SJAG_02640":null,"SJAG_02643":null,"SJAG_02656":null,"SJAG_02661":null,"SJAG_02680":null,"SJAG_02684":null,"SJAG_02686":null,"SJAG_02690":null,"SJAG_02696":null,"SJAG_02697":null,"SJAG_02698":null,"SJAG_02704":null,"SJAG_02708":null,"SJAG_02712":null,"SJAG_02713":null,"SJAG_02720":null,"SJAG_02721":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02734":null,"SJAG_02736":null,"SJAG_02738":null,"SJAG_02741":null,"SJAG_02748":null,"SJAG_02760":null,"SJAG_02785":null,"SJAG_02791":null,"SJAG_02796":null,"SJAG_02808":null,"SJAG_02822":null,"SJAG_02824":null,"SJAG_02825":null,"SJAG_02827":null,"SJAG_02835":null,"SJAG_02838":null,"SJAG_02848":null,"SJAG_02856":null,"SJAG_02858":null,"SJAG_02872":null,"SJAG_02875":null,"SJAG_02876":null,"SJAG_02878":null,"SJAG_02879":null,"SJAG_02887":null,"SJAG_02889":null,"SJAG_02895":null,"SJAG_02897":null,"SJAG_02906":null,"SJAG_02923":null,"SJAG_02926":null,"SJAG_02945":null,"SJAG_02950":null,"SJAG_02972":null,"SJAG_02977":null,"SJAG_02991":null,"SJAG_02994":null,"SJAG_02997":null,"SJAG_03011":null,"SJAG_03017":null,"SJAG_03036":null,"SJAG_03048":null,"SJAG_03055":null,"SJAG_03061":null,"SJAG_03067":null,"SJAG_03069":null,"SJAG_03071":null,"SJAG_03072":null,"SJAG_03077":null,"SJAG_03096":null,"SJAG_03102":null,"SJAG_03115":null,"SJAG_03129":null,"SJAG_03137":null,"SJAG_03140":null,"SJAG_03141":null,"SJAG_03145":null,"SJAG_03152":null,"SJAG_03157":null,"SJAG_03160":null,"SJAG_03174":null,"SJAG_03188":null,"SJAG_03193":null,"SJAG_03206":null,"SJAG_03209":null,"SJAG_03213":null,"SJAG_03224":null,"SJAG_03236":null,"SJAG_03237":null,"SJAG_03240":null,"SJAG_03257":null,"SJAG_03275":null,"SJAG_03277":null,"SJAG_03290":null,"SJAG_03306":null,"SJAG_03312":null,"SJAG_03313":null,"SJAG_03320":null,"SJAG_03336":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03349":null,"SJAG_03355":null,"SJAG_03362":null,"SJAG_03363":null,"SJAG_03371":null,"SJAG_03374":null,"SJAG_03376":null,"SJAG_03384":null,"SJAG_03386":null,"SJAG_03409":null,"SJAG_03421":null,"SJAG_03434":null,"SJAG_03436":null,"SJAG_03438":null,"SJAG_03449":null,"SJAG_03451":null,"SJAG_03453":null,"SJAG_03457":null,"SJAG_03461":null,"SJAG_03471":null,"SJAG_03475":null,"SJAG_03476":null,"SJAG_03479":null,"SJAG_03485":null,"SJAG_03486":null,"SJAG_03495":null,"SJAG_03496":null,"SJAG_03497":null,"SJAG_03501":null,"SJAG_03526":null,"SJAG_03529":null,"SJAG_03533":null,"SJAG_03534":null,"SJAG_03545":null,"SJAG_03557":null,"SJAG_03562":null,"SJAG_03567":null,"SJAG_03570":null,"SJAG_03578":null,"SJAG_03585":null,"SJAG_03592":null,"SJAG_03602":null,"SJAG_03613":null,"SJAG_03626":null,"SJAG_03658":null,"SJAG_03659":null,"SJAG_03660":null,"SJAG_03669":null,"SJAG_03671":null,"SJAG_03676":null,"SJAG_03679":null,"SJAG_03684":null,"SJAG_03688":null,"SJAG_03689":null,"SJAG_03703":null,"SJAG_03708":null,"SJAG_03709":null,"SJAG_03712":null,"SJAG_03720":null,"SJAG_03728":null,"SJAG_03730":null,"SJAG_03732":null,"SJAG_03743":null,"SJAG_03753":null,"SJAG_03780":null,"SJAG_03785":null,"SJAG_03789":null,"SJAG_03798":null,"SJAG_03799":null,"SJAG_03804":null,"SJAG_03811":null,"SJAG_03813":null,"SJAG_03828":null,"SJAG_03832":null,"SJAG_03846":null,"SJAG_03850":null,"SJAG_03852":null,"SJAG_03854":null,"SJAG_03861":null,"SJAG_03866":null,"SJAG_03886":null,"SJAG_03887":null,"SJAG_03892":null,"SJAG_03896":null,"SJAG_03897":null,"SJAG_03898":null,"SJAG_03903":null,"SJAG_03909":null,"SJAG_03914":null,"SJAG_03915":null,"SJAG_03923":null,"SJAG_03927":null,"SJAG_03932":null,"SJAG_03946":null,"SJAG_03948":null,"SJAG_03950":null,"SJAG_03959":null,"SJAG_03961":null,"SJAG_03967":null,"SJAG_03982":null,"SJAG_03985":null,"SJAG_03987":null,"SJAG_04000":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04004":null,"SJAG_04030":null,"SJAG_04032":null,"SJAG_04038":null,"SJAG_04039":null,"SJAG_04042":null,"SJAG_04052":null,"SJAG_04054":null,"SJAG_04055":null,"SJAG_04064":null,"SJAG_04081":null,"SJAG_04094":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04125":null,"SJAG_04126":null,"SJAG_04145":null,"SJAG_04147":null,"SJAG_04149":null,"SJAG_04150":null,"SJAG_04154":null,"SJAG_04156":null,"SJAG_04157":null,"SJAG_04167":null,"SJAG_04178":null,"SJAG_04183":null,"SJAG_04186":null,"SJAG_04187":null,"SJAG_04189":null,"SJAG_04203":null,"SJAG_04206":null,"SJAG_04210":null,"SJAG_04230":null,"SJAG_04232":null,"SJAG_04233":null,"SJAG_04258":null,"SJAG_04265":null,"SJAG_04268":null,"SJAG_04270":null,"SJAG_04276":null,"SJAG_04277":null,"SJAG_04280":null,"SJAG_04282":null,"SJAG_04285":null,"SJAG_04287":null,"SJAG_04288":null,"SJAG_04312":null,"SJAG_04320":null,"SJAG_04334":null,"SJAG_04343":null,"SJAG_04351":null,"SJAG_04355":null,"SJAG_04362":null,"SJAG_04366":null,"SJAG_04367":null,"SJAG_04372":null,"SJAG_04375":null,"SJAG_04387":null,"SJAG_04394":null,"SJAG_04409":null,"SJAG_04410":null,"SJAG_04435":null,"SJAG_04457":null,"SJAG_04459":null,"SJAG_04461":null,"SJAG_04465":null,"SJAG_04468":null,"SJAG_04469":null,"SJAG_04470":null,"SJAG_04473":null,"SJAG_04477":null,"SJAG_04480":null,"SJAG_04482":null,"SJAG_04486":null,"SJAG_04495":null,"SJAG_04507":null,"SJAG_04509":null,"SJAG_04511":null,"SJAG_04537":null,"SJAG_04544":null,"SJAG_04549":null,"SJAG_04551":null,"SJAG_04552":null,"SJAG_04566":null,"SJAG_04573":null,"SJAG_04577":null,"SJAG_04589":null,"SJAG_04597":null,"SJAG_04599":null,"SJAG_04608":null,"SJAG_04612":null,"SJAG_04622":null,"SJAG_04627":null,"SJAG_04634":null,"SJAG_04650":null,"SJAG_04652":null,"SJAG_04655":null,"SJAG_04657":null,"SJAG_04665":null,"SJAG_04666":null,"SJAG_04669":null,"SJAG_04678":null,"SJAG_04692":null,"SJAG_04693":null,"SJAG_04700":null,"SJAG_04734":null,"SJAG_04738":null,"SJAG_04743":null,"SJAG_04745":null,"SJAG_04747":null,"SJAG_04755":null,"SJAG_04757":null,"SJAG_04760":null,"SJAG_04761":null,"SJAG_04762":null,"SJAG_04772":null,"SJAG_04777":null,"SJAG_04810":null,"SJAG_04840":null,"SJAG_04842":null,"SJAG_04845":null,"SJAG_04849":null,"SJAG_04856":null,"SJAG_04857":null,"SJAG_04862":null,"SJAG_04865":null,"SJAG_04874":null,"SJAG_04882":null,"SJAG_04940":null,"SJAG_04946":null,"SJAG_04970":null,"SJAG_04974":null,"SJAG_04980":null,"SJAG_04988":null,"SJAG_05010":null,"SJAG_05015":null,"SJAG_05018":null,"SJAG_05019":null,"SJAG_05022":null,"SJAG_05024":null,"SJAG_05025":null,"SJAG_05027":null,"SJAG_05030":null,"SJAG_05105":null,"SJAG_05173":null,"SJAG_05194":null,"SJAG_05209":null,"SJAG_05213":null,"SJAG_05230":null,"SJAG_05231":null,"SJAG_05249":null,"SJAG_05276":null,"SJAG_05290":null,"SJAG_05295":null,"SJAG_05304":null,"SJAG_05313":null,"SJAG_05332":null,"SJAG_05340":null,"SJAG_05353":null,"SJAG_05372":null,"SJAG_06597":null,"SJAG_06621":null,"SJAG_06622":null,"SJAG_06642":null,"SJAG_16455":null,"SJAG_16456":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"heterocyclic compound binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:1901363","terms_by_termid":{"GO:0002055":null,"GO:0002134":null,"GO:0002135":null,"GO:0005524":null,"GO:0005525":null,"GO:0010181":null,"GO:0016208":null,"GO:0019002":null,"GO:0019003":null,"GO:0030170":null,"GO:0030552":null,"GO:0030975":null,"GO:0030976":null,"GO:0032549":null,"GO:0036042":null,"GO:0043531":null,"GO:0050660":null,"GO:0050661":null,"GO:0051287":null,"GO:0070401":null,"GO:0070402":null,"GO:0070403":null,"GO:0071949":null,"GO:1902444":null,"GO:1905108":null}}


