# terms

id: MONDO:0026045
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Prurigonodularis (PN) is a skin disease in which hard crusty lumps are formed on the skin that itches intensely. Repetitive rubbing, scratching, and touching results in more lesions in the skin. The itching is so intense that people scratch themselves to the point of bleeding or pain. The lumps formed in the skin are hard, and have about a half inch across, with a dry and rough top that is often scratched open. They tend to be located in the areas most easily reached and are worse on the outer sides: arms, shoulders and legs. The trunk, face and even palms can also be affected. The exact cause is unknown but some factors triggering PN include liver and kidneys problems, nervous and mental conditions and other skin diseases. Prurigo nodulares, in some cases, can be seen in other diseases such as lymphoma, chronic autoimmune cholestatic hepatitis, HIV infection, severe anemia,or a chronic kidney disease-related itching known as uremic pruritus. Treatment is very difficult, and may include corticoids, antihistaminic and other medication such as thalidomide and similar (Lenalidomide). In some cases, cryotherapy, photochemotherapy and habit reversal therapy for the itch-scratch cycle has improved the symptoms. PN can last for many years, and the itching is so intense that may affect all the everyday activities.","definition_xrefs":["GARD:0007480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"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":"prurigo nodularis","secondary_identifiers":["MEDGEN:120471","ICD10CM:L28.1","UMLS:C0263353"],"termid":"MONDO:0026045","xrefs":{"Monarch":{"xref_id":"0026045"}}}


id: PBO:0087792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO E3 ligase; required for synaptonemal complex formation; localizes to synapsis initiation sites on meiotic chromosomes; associates with centromeres early in meiosis, then with chromosome axes and finally with double-strand break sites that are engaged in repair by crossovers; potential Cdc28p substrate","termid":"PBO:0087792"}


id: PBO:0054896
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 2310","termid":"PBO:0054896"}


id: PBO:0039471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 18A","termid":"PBO:0039471"}


id: GO:0030033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of a microvillus, a thin cylindrical membrane-covered projection on the surface of a cell.","definition_xrefs":["GOC:mah","ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microvillus organization","termid":"GO:0032528"},{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection assembly","termid":"GO:0120031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"microvillus assembly","synonyms":[{"name":"microvillus biogenesis","type":"related"}],"termid":"GO:0030033"}


id: PBO:0057559
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 708","termid":"PBO:0057559"}


id: MONDO:0019142
data:
  {"annotated_genes":["SJAG_02876","SJAG_01841","SJAG_02896","SJAG_04109","SJAG_05283","SJAG_04944","SJAG_01372","SJAG_03961"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87099],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008294"},{"annotations":[87243],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009902"},{"annotations":[87499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008296"},{"annotations":[87198],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030048"},{"annotations":[87652],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007369"},{"annotations":[87244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013000"},{"annotations":[86935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008319"},{"annotations":[87518],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008297"},{"annotations":[88170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957577"},{"annotations":[88514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010420"}]},"cv_name":"mondo","definition":"Porphyrias constitute a group of eight hereditary metabolic diseases characterized by intermittent neuro-visceral manifestations, cutaneous lesions or by the combination of both.","definition_xrefs":["Orphanet:738"],"direct_ancestors":[{"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":"hereditary photodermatosis","termid":"MONDO:0015951"},{"relation_name":"is_a","term_name":"inborn disorder of porphyrin metabolism","termid":"MONDO:0017754"},{"relation_name":"is_a","term_name":"porphyria","termid":"MONDO:0037939"}],"gene_count":8,"genes_by_uniquename":{"SJAG_01372":null,"SJAG_01841":null,"SJAG_02876":null,"SJAG_02896":null,"SJAG_03961":null,"SJAG_04109":null,"SJAG_04944":null,"SJAG_05283":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005093"],"is_obsolete":false,"name":"inherited porphyria","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MedDRA:10036181","DOID:13268","MedDRA:10061356","NCIT:C97096","UMLS:C1275125","SCTID:371628009","MEDGEN:698423","MESH:D011164","GARD:10353","NANDO:2200610","ICD9:277.1","SCTID:418470004"],"synonyms":[{"name":"Hematoporphyria","type":"related"},{"name":"Porphyrinopathy","type":"related"},{"name":"disorder of porphyrin and hem metabolism","type":"exact"},{"name":"disorder of porphyrin and heme metabolism","type":"broad"},{"name":"disorder of porphyrin metabolism","type":"broad"},{"name":"hereditary porphyria","type":"exact"},{"name":"porphyria","type":"broad"}],"termid":"MONDO:0019142","terms_by_termid":{"MONDO:0007369":null,"MONDO:0008294":null,"MONDO:0008296":null,"MONDO:0008297":null,"MONDO:0008319":null,"MONDO:0009902":null,"MONDO:0010420":null,"MONDO:0013000":null,"MONDO:0030048":null,"MONDO:0957577":null},"xrefs":{"Monarch":{"xref_id":"0019142"}}}


id: PBO:0002133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNARE Slt1 (predicted)","termid":"PBO:0002133"}


id: PBO:0001587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial hydrogen/potassium transport system protein (predicted)","termid":"PBO:0001587"}


id: PBO:0086162
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for respiratory growth; localized to both the nucleus and mitochondrion; may interact with transcription factors to mediate the transition to respiratory growth and activate transcription of nuclear and mitochondrial genes","termid":"PBO:0086162"}


id: PBO:0049095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 152","termid":"PBO:0049095"}


id: GO:0004177
data:
  {"annotated_genes":["SJAG_00181","SJAG_02033","SJAG_06636","SJAG_03022","SJAG_03744","SJAG_00969","SJAG_01088","SJAG_01896"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[63320,64809],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004239"},{"annotations":[57978,60678,99657,65601,64808,74382,76213,116314],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070006"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of a single N-terminal amino acid residue from a polypeptide chain.","definition_xrefs":["EC:3.4.11.-","PMID:24157837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exopeptidase activity","termid":"GO:0008238"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00181":null,"SJAG_00969":null,"SJAG_01088":null,"SJAG_01896":null,"SJAG_02033":null,"SJAG_03022":null,"SJAG_03744":null,"SJAG_06636":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0003674","GO:0003824","GO:0008233","GO:0016787"],"is_obsolete":false,"name":"aminopeptidase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-983162","https://www.ebi.ac.uk/merops/about/glossary.shtml#AMINOPEPTIDASE","Reactome:R-HSA-2534096","Reactome:R-HSA-1236954","MetaCyc:RXN0-5052"],"termid":"GO:0004177","terms_by_termid":{"GO:0004239":null,"GO:0070006":null}}


id: PBO:0061669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin 50 pseudogene 2","termid":"PBO:0061669"}


id: PR:O59737
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gyp1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59737"],"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":"GTPase-activating protein gyp1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC530.01","synonyms":[{"name":"GAP for ypt1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gyp1","type":"exact"}],"termid":"PR:O59737"}


id: PBO:0029044
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_arsenate","termid":"PBO:0029044"}


id: PBO:0028427
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_sodium_fluoride","termid":"PBO:0028427"}


id: PBO:0074475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMU1 pseudogene 1","termid":"PBO:0074475"}


id: PBO:0038441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha and gamma adaptin binding protein","termid":"PBO:0038441"}


id: MONDO:0002365
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangiopericytoma arising from the kidney.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangiopericytoma","termid":"MONDO:0005094"},{"relation_name":"is_a","term_name":"kidney neoplasm","termid":"MONDO:0021163"}],"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":"kidney hemangiopericytoma","secondary_identifiers":["NCIT:C4527","UMLS:C5848097","DOID:262","SCTID:254923001","MEDGEN:1847044"],"synonyms":[{"name":"hemangiopericytoma of kidney","type":"exact"},{"name":"hemangiopericytoma of the kidney","type":"exact"},{"name":"kidney hemangiopericytoma","type":"exact"},{"name":"kidney spindle cell tumor","type":"exact"},{"name":"kidney spindle cell tumour","type":"exact"},{"name":"renal hemangiopericytoma","type":"exact"}],"termid":"MONDO:0002365","xrefs":{"Monarch":{"xref_id":"0002365"}}}


id: MONDO:0006835
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A glomerular disorder characterized by the electron microscopic finding of loss of podocyte foot processes. Light microscopic examination does not show glomerular changes. Patients present with proteinuria and nephrotic syndrome.","definition_xrefs":["NCIT:C34844"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"nephrotic syndrome","termid":"MONDO:0005377"},{"relation_name":"is_a","term_name":"glomerulonephritis","termid":"MONDO:0002462"}],"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":"lipoid nephrosis","secondary_identifiers":["NANDO:2200112","MESH:D009402","MedDRA:10058325","DOID:10966","EFO:1001020","UMLS:C0027721","MEDGEN:10307","NANDO:1200720","SCTID:44785005"],"synonyms":[{"name":"MCNS","type":"related"},{"name":"idiopathic minimal change nephrotic syndrome","type":"related"},{"name":"lipoid nephrosis","type":"exact"},{"name":"minimal change disease","type":"exact"},{"name":"minimal change glomerulonephritis","type":"exact"},{"name":"minimal change glomerulopathy","type":"related"},{"name":"minimal change nephropathy","type":"exact"},{"name":"minimal change nephrotic syndrome","type":"related"},{"name":"nephrotic syndrome with lesion of minimal change glomerulonephritis","type":"related"},{"name":"nephrotic syndrome with lesion of minimal change nephrotic syndrome","type":"related"},{"name":"nil disease","type":"exact"}],"termid":"MONDO:0006835","xrefs":{"Monarch":{"xref_id":"0006835"}}}


id: FYPO:0000429
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the G0 to G1 transition begins later than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal G0 to G1 transition","termid":"FYPO:0002955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"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:0000002","FYPO:0001985","FYPO:0000631","FYPO:0005447"],"is_obsolete":false,"name":"delayed G0 to G1 transition","synonyms":[{"name":"delayed G0/G1 transition","type":"exact"},{"name":"delayed exit from G0","type":"exact"},{"name":"delayed exit from cell quiescence","type":"exact"},{"name":"slow cell population growth following nitrogen starvation","type":"related"}],"termid":"FYPO:0000429"}


id: MONDO:1010243
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cerebellar degeneration that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegenerative disease, non-human animal","termid":"MONDO:1012953"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebellar degeneration, non-human animal","secondary_identifiers":["OMIA:001221"],"termid":"MONDO:1010243","xrefs":{"Monarch":{"xref_id":"1010243"}}}


id: MONDO:1012931
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary chondrodysplasia that occurs in cattle due to a mutation in the EVC2 gene.","definition_xrefs":["PMID:24733244"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrodysplasia, non-human animal","termid":"MONDO:1010306"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondrodysplasia, EVC2-related, cattle","secondary_identifiers":["OMIA:002540-9913"],"synonyms":[{"name":"Ellis-van Creveld Syndrome, cattle","type":"related"},{"name":"bovine chondrodysplastic dwarfism","type":"related"}],"termid":"MONDO:1012931","xrefs":{"Monarch":{"xref_id":"1012931"}}}


id: PBO:0081949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc and ring finger 2 pseudogene 3","termid":"PBO:0081949"}


id: PBO:0054505
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 1905","termid":"PBO:0054505"}


id: PBO:0082252
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha subunit of the translation initiation factor eIF2; eIF2 is involved in identification of the start codon; phosphorylation of Ser51 is required for regulation of translation by inhibiting the exchange of GDP for GTP; protein abundance increases in response to DNA replication stress","termid":"PBO:0082252"}


id: PBO:0047681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FLNC antisense RNA 1","termid":"PBO:0047681"}


id: GO:0072002
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the Malpighian tubule over time, from its formation to the mature structure. A Malpighian tubule is a fine, thin-walled excretory tubule in insects which leads into the posterior part of the gut.","definition_xrefs":["PMID:19783135","FBbt:00005786","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ development","termid":"GO:0048513"},{"relation_name":"is_a","term_name":"renal tubule development","termid":"GO:0061326"}],"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":"Malpighian tubule development","termid":"GO:0072002"}


id: GO:0070968
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to pyrroloquinoline quinone, PQQ, the coenzyme or the prosthetic group of certain alcohol dehydrogenases and glucose dehydrogenases.","definition_xrefs":["GOC:dh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic acid binding","termid":"GO:0031406"},{"relation_name":"is_a","term_name":"heterocyclic compound binding","termid":"GO:1901363"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"pyrroloquinoline quinone binding","synonyms":[{"name":"PQQ binding","type":"exact"}],"termid":"GO:0070968"}


id: PBO:0028952
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-curved_cell_during_recovery_from_stationary_phase","termid":"PBO:0028952"}


id: GO:0141076
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process in which a symbiont interferes with, inhibits or disrupts a TRAF-mediated signal transduction in its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:31311877","PMID:22407319","PMID:20335533"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression of host TRAF-mediated signal transduction (obsolete GO:0141076)","synonyms":[{"name":"disruption of host TRAF-mediated signal transduction","type":"exact"},{"name":"inhibition of host TRAF-mediated signal transduction","type":"exact"},{"name":"inhibition of host TRAFs","type":"narrow"},{"name":"negative regulation of host TRAF-mediated signal transduction","type":"exact"},{"name":"suppression of host TRAF activity","type":"narrow"},{"name":"suppression of host TRAF-mediated signal transduction","type":"exact"},{"name":"suppression of host tumor necrosis factor receptor-associated factor signaling","type":"exact"},{"name":"symbiont-mediated suppression of host TRAF-mediated signal transduction","type":"related"}],"termid":"GO:0141076"}


id: GO:1903551
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of extracellular vesicular exosome assembly.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:24105262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of organelle assembly","termid":"GO:1902115"},{"relation_name":"regulates","term_name":"extracellular exosome assembly","termid":"GO:0071971"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of extracellular exosome assembly","synonyms":[{"name":"regulation of extracellular vesicular exosome assembly","type":"exact"}],"termid":"GO:1903551"}


id: MONDO:0004569
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A brachial plexus neuropathy caused by an injury in the brachial plexus network of nerves.","definition_xrefs":["PMID:39811497"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brachial plexus neuropathy","termid":"MONDO:0006683"}],"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":"brachial plexus neuropathy from injury","secondary_identifiers":["ICD9:353.0","MEDGEN:507501","DOID:8443","UMLS:C0006091"],"synonyms":[{"name":"brachial plexus lesion","type":"exact"},{"name":"brachial plexus lesions","type":"exact"}],"termid":"MONDO:0004569","xrefs":{"Monarch":{"xref_id":"0004569"}}}


id: PBO:0052346
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin family member 2C","termid":"PBO:0052346"}


id: MONDO:0022785
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleft palate cardiac defect ectrodactyly","termid":"MONDO:0022785","xrefs":{"Monarch":{"xref_id":"0022785"}}}


id: PBO:0084236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Imidazoleglycerol-phosphate dehydratase; catalyzes the sixth step in histidine biosynthesis; mutations cause histidine auxotrophy and sensitivity to Cu, Co, and Ni salts; transcription is regulated by general amino acid control via Gcn4p","termid":"PBO:0084236"}


id: PATO:0001674
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A concentration quality inhering in a bearer by virtue of the bearer's catalytic activity divided by the volume of the system.","definition_xrefs":["IUPAC:IUPAC"],"direct_ancestors":[{"relation_name":"is_a","term_name":"concentration of","termid":"PATO:0000033"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"catalytic (activity) concentration","termid":"PATO:0001674"}


id: FYPO:0007696
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the activity of a DNA strand exchange inhibitor is increased.","definition_xrefs":["PomBase:mah","PMID:33493431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity regulator phenotype","termid":"FYPO:0007690"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652"],"is_obsolete":false,"name":"increased DNA strand exchange inhibitor activity","synonyms":[{"name":"increased RecA-family recombinase inhibitor activity","type":"exact"},{"name":"increased negative regulation of RecA-family recombinase activity","type":"related"}],"termid":"FYPO:0007696"}


id: SO:0001972
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A histone 4 modification where the modification is the acetylation of the residue.","definition_xrefs":["ISBN:0815341059","SO:ke","EBI:nj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_acetylation_site","termid":"SO:0001702"}],"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":"histone_4_acetylation_site","synonyms":[{"name":"H4ac","type":"exact"},{"name":"histone 4 acetylation site","type":"exact"}],"termid":"SO:0001972"}


id: PBO:0091026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoskeleton adaptor for Rga7 GTPase activator Rng10","termid":"PBO:0091026"}


id: PBO:0073938
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 18 member A1","termid":"PBO:0073938"}


id: GO:0043237
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to laminin-1, a glycoprotein trimer with the subunit composition alpha1, beta1, gamma1.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laminin binding","termid":"GO:0043236"}],"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"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"laminin-1 binding","synonyms":[{"name":"laminin-111 binding","type":"exact"}],"termid":"GO:0043237"}


id: FYPO:0005062
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 methylation of lysine at position 4 of histone H3 in telomeric regions occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone methylation during vegetative growth","termid":"FYPO:0000869"},{"relation_name":"is_a","term_name":"abnormal histone H3-K4 methylation during vegetative growth","termid":"FYPO:0002330"},{"relation_name":"is_a","term_name":"abnormal histone methylation at telomere during vegetative growth","termid":"FYPO:0007375"}],"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:0002494"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0005447","FYPO:0002274","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased histone H3-K4 methylation at telomere during vegetative growth","synonyms":[{"name":"increased histone H3 K4 methylation at telomere","type":"exact"},{"name":"increased histone H3-K4 methylation at telomere during mitotic cell cycle during vegetative growth","type":"related"},{"name":"increased histone H3-K4 methylation at telomeric region","type":"exact"},{"name":"increased histone H3K4 methylation at telomere","type":"exact"},{"name":"increased histone H3K4me at telomere","type":"exact"},{"name":"increased histone lysine H3 K4 methylation at telomere","type":"exact"}],"termid":"FYPO:0005062"}


id: GO:0019148
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-cysteine + H2O = sulfide + NH3 + pyruvate.","definition_xrefs":["EC:4.4.1.15"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"D-cysteine desulfhydrase activity","secondary_identifiers":["MetaCyc:DCYSDESULF-RXN","RHEA:11268"],"synonyms":[{"name":"D-cysteine lyase activity","type":"related"},{"name":"D-cysteine sulfide-lyase (deaminating)","type":"related"},{"name":"D-cysteine sulfide-lyase (deaminating; pyruvate-forming)","type":"related"}],"termid":"GO:0019148"}


id: PBO:0004371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-directed RNA polymerase I complex large subunit Nuc1","termid":"PBO:0004371"}


id: GO:0008306
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Learning by associating a stimulus (the cause) with a particular outcome (the effect).","definition_xrefs":["ISBN:0582227089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"learning","termid":"GO:0007612"}],"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":"associative learning","secondary_identifiers":["Wikipedia:Learning#Associative_learning"],"synonyms":[{"name":"Pavlovian conditioning","type":"exact"},{"name":"classical conditioning","type":"exact"},{"name":"conditional learning","type":"exact"},{"name":"conditional response","type":"exact"}],"termid":"GO:0008306"}


id: GO:0006132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete dihydrolipoylprotein reduction (obsolete GO:0006132)","synonyms":[{"name":"dihydrolipoylprotein reduction","type":"exact"}],"termid":"GO:0006132"}


id: PR:P0CT69
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl2002 gene.","definition_xrefs":["UniProtKB:P0CT69","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":"60S ribosomal protein L20-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26A3.04","synonyms":[{"name":"Spom972h-rpl2002","type":"exact"},{"name":"YL17 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P0CT69"}


id: GO:0070135
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving beta-1,2-linked oligomannosides, which are found in fungal cell wall phosphopeptidomannan and phospholipomannan.","definition_xrefs":["PMID:18234669","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannan metabolic process","termid":"GO:0010412"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0071554","GO:0008150","GO:0005975"],"is_obsolete":false,"name":"beta-1,2-oligomannoside metabolic process","synonyms":[{"name":"beta-1,2-oligomannoside metabolism","type":"exact"}],"termid":"GO:0070135"}


id: PBO:0064107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pejvakin","termid":"PBO:0064107"}


id: PBO:0086383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative ATP-dependent RNA helicase of the DEAD-box protein family; constituent of 66S pre-ribosomal particles; essential protein involved in ribosome biogenesis","termid":"PBO:0086383"}


id: GO:0036294
data:
  {"annotated_genes":["SJAG_00221","SJAG_03345","SJAG_01585","SJAG_00642","SJAG_04018","SJAG_01150"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118851,111698,103039,113566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071456"},{"annotations":[91077,118251],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1900039"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus reflecting a decline in the level of oxygen.","definition_xrefs":["GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to decreased oxygen levels","termid":"GO:0036293"},{"relation_name":"is_a","term_name":"cellular response to oxygen levels","termid":"GO:0071453"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00221":null,"SJAG_00642":null,"SJAG_01150":null,"SJAG_01585":null,"SJAG_03345":null,"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to decreased oxygen levels","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"cellular response to lowered oxygen levels","type":"exact"}],"termid":"GO:0036294","terms_by_termid":{"GO:0071456":null,"GO:1900039":null}}


id: PBO:0045353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DOP1 leucine zipper like protein B","termid":"PBO:0045353"}


id: MONDO:0054615
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 18","secondary_identifiers":["GARD:18402","DOID:0070165","MEDGEN:1617309","OMIM:617576","UMLS:C4539783"],"synonyms":[{"name":"SPGF18","type":"related"},{"name":"spermatogenic failure 18","type":"exact"}],"termid":"MONDO:0054615","xrefs":{"Monarch":{"xref_id":"0054615"}}}


id: GO:0005004
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a GPI-anchored ephrin to initiate a change in cell activity.","definition_xrefs":["GOC:mah","PMID:9530499"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ephrin receptor activity","termid":"GO:0005003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016301","GO:0004672","GO:0140096","GO:0038023"],"is_obsolete":false,"name":"GPI-linked ephrin receptor activity","synonyms":[{"name":"GPI-linked Eph receptor activity","type":"exact"}],"termid":"GO:0005004"}


id: MONDO:0859263
data:
  {"annotated_genes":["SJAG_01025","SJAG_02160"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88634,88635],"is_not":false,"summary":null,"term":"MONDO:0859263"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01025":null,"SJAG_02160":null},"genotype_count":0,"is_obsolete":false,"name":"developmental delay, impaired speech, and behavioral abnormalities, with or without seizures","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1811329","UMLS:C5575272","OMIM:619964"],"termid":"MONDO:0859263","terms_by_termid":{"MONDO:0859263":null},"xrefs":{"Monarch":{"xref_id":"0859263"}}}


id: PR:O14062
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps1201 gene.","definition_xrefs":["UniProtKB:O14062","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":"40S ribosomal protein S12-A (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC962.04","synonyms":[{"name":"Spom972h-rps1201","type":"exact"}],"termid":"PR:O14062"}


id: PBO:0061480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuregulin 1","termid":"PBO:0061480"}


id: MONDO:0018530
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare epithelial tumor of liver and intrahepatic biliary tract (obsolete MONDO:0018530)","secondary_identifiers":["Orphanet:424933"],"synonyms":[{"name":"rare epithelial tumor of liver and IBT","type":"exact"}],"termid":"MONDO:0018530","xrefs":{"Monarch":{"xref_id":"0018530"}}}


id: GO:2000687
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of rubidium ion transmembrane transporter activity.","definition_xrefs":["GOC:yaf"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of rubidium ion transmembrane transporter activity (obsolete GO:2000687)","synonyms":[{"name":"negative regulation of Rb+ transmembrane transporter activity","type":"exact"},{"name":"negative regulation of rubidium cation transmembrane transporter activity","type":"exact"},{"name":"negative regulation of rubidium transmembrane transporter activity","type":"related"}],"termid":"GO:2000687"}


id: PBO:0045648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox A pseudogene 6","termid":"PBO:0045648"}


id: PBO:0058286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4662a","termid":"PBO:0058286"}


id: PBO:0069908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1199, pseudogene","termid":"PBO:0069908"}


id: GO:0071202
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A voltage-gated potassium channel complex that contains the peptidase-related protein DPP10 associated with the channel via interaction with the Kv alpha subunit 4.3.","definition_xrefs":["PMID:15911355"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel complex","termid":"GO:0008076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0032991"],"is_obsolete":false,"name":"Kv4.3-DPP10 channel complex","secondary_identifiers":["CORUM:598"],"synonyms":[{"name":"Kv4.3-DPPY channel complex","type":"exact"}],"termid":"GO:0071202"}


id: MONDO:0001925
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"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 dystrophy in systemic or cerebroretinal lipidoses","secondary_identifiers":["UMLS:C0154861","SCTID:192788009","MEDGEN:1843490","ICD9:362.71","DOID:14253","SCTID:15059000"],"termid":"MONDO:0001925","xrefs":{"Monarch":{"xref_id":"0001925"}}}


id: PBO:0085606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in control of DNA replication; binds Rap1p C-terminus, telomeres, centromeres, replication origins; contributes to resection of DNA double strand breaks (DSBs); acts synergistically with Rif2p to help control telomere length and establish telomeric silencing; in addition to controlling DNA replication initiation, plays ongoing role after initiation and controls events at blocked replication forks","termid":"PBO:0085606"}


id: GO:0042531
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the introduction of a phosphate group to a tyrosine residue of a STAT (Signal Transducer and Activator of Transcription) protein.","definition_xrefs":["GOC:jl","PMID:11426647"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tyrosine phosphorylation of STAT protein","termid":"GO:0042509"},{"relation_name":"is_a","term_name":"positive regulation of peptidyl-tyrosine phosphorylation","termid":"GO:0050731"},{"relation_name":"positively_regulates","term_name":"tyrosine phosphorylation of STAT protein","termid":"GO:0007260"}],"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 tyrosine phosphorylation of STAT protein","secondary_identifiers":["GO:0042529","GO:0042526","GO:0042511","GO:0042517","GO:0042520","GO:0042523","GO:0042515"],"synonyms":[{"name":"activation of tyrosine phosphorylation of STAT protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"activation of tyrosine phosphorylation of Stat7 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"positive regulation of tyrosine phosphorylation of Stat7 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of STAT protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"stimulation of tyrosine phosphorylation of Stat7 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of STAT protein","type":"exact"},{"name":"up regulation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"up regulation of tyrosine phosphorylation of Stat7 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of STAT protein","type":"exact"},{"name":"up-regulation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"up-regulation of tyrosine phosphorylation of Stat7 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of STAT protein","type":"exact"},{"name":"upregulation of tyrosine phosphorylation of Stat1 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat2 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat3 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat4 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat5 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat6 protein","type":"narrow"},{"name":"upregulation of tyrosine phosphorylation of Stat7 protein","type":"narrow"}],"termid":"GO:0042531"}


id: PBO:0085841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and the nucleus; YDL129W is not an essential gene; relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0085841"}


id: RO:0002522
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x bounds the sequence of y iff the upstream-most part of x is upstream of or coincident with the upstream-most part of y, and the downstream-most part of x is downstream of or coincident with the downstream-most part of y","direct_ancestors":[{"relation_name":"is_a","term_name":"sequentially_related_to","termid":"RO:0002514"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bounds_sequence_of","termid":"RO:0002522"}


id: MONDO:0015508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hereditary parenchymatous liver disease (obsolete MONDO:0015508)","secondary_identifiers":["Orphanet:156604"],"synonyms":[{"name":"genetic parenchymatous liver disease","type":"exact"}],"termid":"MONDO:0015508","xrefs":{"Monarch":{"xref_id":"0015508"}}}


id: PBO:0068551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 2, pseudogene","termid":"PBO:0068551"}


id: GO:0030695
data:
  {"annotated_genes":["SJAG_01659","SJAG_02368","SJAG_04938","SJAG_02307","SJAG_00092","SJAG_04400","SJAG_02004","SJAG_04010","SJAG_04837","SJAG_05210","SJAG_02666","SJAG_02520","SJAG_03581","SJAG_00143","SJAG_02529","SJAG_00858","SJAG_02833","SJAG_00990","SJAG_04391","SJAG_01319","SJAG_04982","SJAG_04491","SJAG_04462","SJAG_03748","SJAG_02248","SJAG_00514","SJAG_02645","SJAG_04653","SJAG_03361","SJAG_03655","SJAG_02390","SJAG_04080","SJAG_04522","SJAG_01600","SJAG_02493","SJAG_04724","SJAG_01576","SJAG_02277","SJAG_00028","SJAG_02422","SJAG_01695","SJAG_04771","SJAG_00338","SJAG_04464","SJAG_02831","SJAG_02819","SJAG_04733","SJAG_02765","SJAG_03021","SJAG_01415","SJAG_01526","SJAG_00467","SJAG_03338","SJAG_03678","SJAG_01367","SJAG_03142","SJAG_00216","SJAG_00807","SJAG_03153","SJAG_05346","SJAG_03268","SJAG_03246","SJAG_03002","SJAG_00064","SJAG_02379","SJAG_04203","SJAG_00801","SJAG_00289","SJAG_04013","SJAG_01184","SJAG_02278","SJAG_01114","SJAG_05184","SJAG_03089","SJAG_01030","SJAG_03705","SJAG_01025","SJAG_01699","SJAG_00864","SJAG_03488","SJAG_02160","SJAG_02012","SJAG_04910","SJAG_01309","SJAG_06588","SJAG_01011","SJAG_04074","SJAG_00991","SJAG_04615","SJAG_02471","SJAG_02486","SJAG_00551","SJAG_02027","SJAG_03600","SJAG_03704","SJAG_02231","SJAG_04548","SJAG_00824","SJAG_04943","SJAG_04283","SJAG_02063","SJAG_03085","SJAG_02539","SJAG_04498","SJAG_01386","SJAG_01048","SJAG_04776","SJAG_04765"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72221,77742,92907,108512,117896],"is_not":false,"summary":null,"term":"GO:0030695"},{"annotations":[73759,70313],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005092"},{"annotations":[75285,80011,95145,81399,71850,89347,76744,80153,97687,98373,67705,67827,74907,75164,73363,72098,76664,60663,72979,77376,72642,80963,74645,67222,74535,69968,59025,66944,79350,70804,107120,66475,72570,71931,95137,72396,73282,74064,69468,79159,95787,79347,97918,78481,112813,116862,73581,71921,78522,78841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005096"},{"annotations":[118167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005095"},{"annotations":[74230,71761,75673,76407,77304,79946,96133,100922,110155,70913,75659,71718,92817,93010,66480,81245,72422,70183,82158,108831,57278,80746,93935,81856,57949,95858,57574,99540,99784,108250,117398,73180,94586,118364,65895,71535,73654,74096,67704,79192,80338,73741,75883,76912,61771,99123,62812,79916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005085"},{"annotations":[77870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005093"},{"annotations":[112653,77061],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005094"}]},"cv_name":"molecular_function","definition":"Binds to and modulates the activity of a GTPase.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside-triphosphatase regulator activity","termid":"GO:0060589"}],"gene_count":108,"genes_by_uniquename":{"SJAG_00028":null,"SJAG_00064":null,"SJAG_00092":null,"SJAG_00143":null,"SJAG_00216":null,"SJAG_00289":null,"SJAG_00338":null,"SJAG_00467":null,"SJAG_00514":null,"SJAG_00551":null,"SJAG_00801":null,"SJAG_00807":null,"SJAG_00824":null,"SJAG_00858":null,"SJAG_00864":null,"SJAG_00990":null,"SJAG_00991":null,"SJAG_01011":null,"SJAG_01025":null,"SJAG_01030":null,"SJAG_01048":null,"SJAG_01114":null,"SJAG_01184":null,"SJAG_01309":null,"SJAG_01319":null,"SJAG_01367":null,"SJAG_01386":null,"SJAG_01415":null,"SJAG_01526":null,"SJAG_01576":null,"SJAG_01600":null,"SJAG_01659":null,"SJAG_01695":null,"SJAG_01699":null,"SJAG_02004":null,"SJAG_02012":null,"SJAG_02027":null,"SJAG_02063":null,"SJAG_02160":null,"SJAG_02231":null,"SJAG_02248":null,"SJAG_02277":null,"SJAG_02278":null,"SJAG_02307":null,"SJAG_02368":null,"SJAG_02379":null,"SJAG_02390":null,"SJAG_02422":null,"SJAG_02471":null,"SJAG_02486":null,"SJAG_02493":null,"SJAG_02520":null,"SJAG_02529":null,"SJAG_02539":null,"SJAG_02645":null,"SJAG_02666":null,"SJAG_02765":null,"SJAG_02819":null,"SJAG_02831":null,"SJAG_02833":null,"SJAG_03002":null,"SJAG_03021":null,"SJAG_03085":null,"SJAG_03089":null,"SJAG_03142":null,"SJAG_03153":null,"SJAG_03246":null,"SJAG_03268":null,"SJAG_03338":null,"SJAG_03361":null,"SJAG_03488":null,"SJAG_03581":null,"SJAG_03600":null,"SJAG_03655":null,"SJAG_03678":null,"SJAG_03704":null,"SJAG_03705":null,"SJAG_03748":null,"SJAG_04010":null,"SJAG_04013":null,"SJAG_04074":null,"SJAG_04080":null,"SJAG_04203":null,"SJAG_04283":null,"SJAG_04391":null,"SJAG_04400":null,"SJAG_04462":null,"SJAG_04464":null,"SJAG_04491":null,"SJAG_04498":null,"SJAG_04522":null,"SJAG_04548":null,"SJAG_04615":null,"SJAG_04653":null,"SJAG_04724":null,"SJAG_04733":null,"SJAG_04765":null,"SJAG_04771":null,"SJAG_04776":null,"SJAG_04837":null,"SJAG_04910":null,"SJAG_04938":null,"SJAG_04943":null,"SJAG_04982":null,"SJAG_05184":null,"SJAG_05210":null,"SJAG_05346":null,"SJAG_06588":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0098772","GO:0003674","GO:0030234"],"is_obsolete":false,"name":"GTPase regulator activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0005083"],"synonyms":[{"name":"small GTPase regulator activity","type":"related"},{"name":"small GTPase regulatory/interacting protein activity","type":"related"}],"termid":"GO:0030695","terms_by_termid":{"GO:0005085":null,"GO:0005092":null,"GO:0005093":null,"GO:0005094":null,"GO:0005095":null,"GO:0005096":null,"GO:0030695":null}}


id: MONDO:0019955
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"6cm and approximately 1/3 have metastasized at the time of diagnosis. It often co-occurs with Zollinger-Ellison syndrome or multiple endocrine neoplasia type 1 (MEN 1).","definition_xrefs":["Orphanet:97261"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic neuroendocrine tumor","termid":"MONDO:0019954"}],"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":"GRFoma","secondary_identifiers":["UMLS:C0346406","icd11.foundation:1245945716","MEDGEN:577391","GARD:19356"],"synonyms":[{"name":"GRF tumor","type":"exact"},{"name":"GRF tumour","type":"exact"},{"name":"Growth hormone releasing factor tumor","type":"exact"},{"name":"Growth hormone releasing factor tumour","type":"exact"}],"termid":"MONDO:0019955","xrefs":{"Monarch":{"xref_id":"0019955"}}}


id: PR:O42897
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A 26S proteasome non-ATPase regulatory subunit 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10758:SF2","PRO:DNx","OMA:SCHPO02558"],"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":"26S proteasome regulatory subunit rpn3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC119.01","secondary_identifiers":["UniProtKB:O42897"],"synonyms":[{"name":"Spom972h-PSMD3","type":"exact"}],"termid":"PR:O42897"}


id: PBO:0088022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U1 snRNP protein involved in splicing; contains multiple tetriatricopeptide repeats","termid":"PBO:0088022"}


id: PBO:0055911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 34 pseudogene 2","termid":"PBO:0055911"}


id: MONDO:0010052
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any azoospermia in which the cause of the disease is a mutation in the SYCP3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 4","secondary_identifiers":["DOID:0070176","GARD:15235","MESH:C536875","MEDGEN:68568","OMIM:270960","UMLS:C0232981"],"synonyms":[{"name":"SPGF4","type":"related"},{"name":"SYCP3 azoospermia","type":"exact"},{"name":"arrest of spermatogenesis","type":"related"},{"name":"azoospermia caused by mutation in SYCP3","type":"exact"},{"name":"azoospermia due to Perturbations of meiosis","type":"related"},{"name":"azoospermia with maturation arrest","type":"related"},{"name":"pregnancy loss, recurrent, 4","type":"related"},{"name":"pregnancy loss, recurrent, susceptibility to, 4","type":"related"},{"name":"spermatogenesis arrest","type":"related"},{"name":"spermatogenic failure 4","type":"exact"},{"name":"spermatogenic failure type 4","type":"exact"}],"termid":"MONDO:0010052","xrefs":{"Monarch":{"xref_id":"0010052"}}}


id: PBO:0050237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 2 pseudogene 15","termid":"PBO:0050237"}


id: PBO:0027622
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_linear_element_morphology","termid":"PBO:0027622"}


id: PBO:0060218
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MX dynamin like GTPase 2","termid":"PBO:0060218"}


id: PR:O74926
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rbd2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74926"],"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":"rhomboid protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC790.03","synonyms":[{"name":"Spom972h-rbd2","type":"exact"}],"termid":"PR:O74926"}


id: MONDO:0002452
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from the prostate. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:C5544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"benign neoplasm of prostate","termid":"MONDO:0021510"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostate leiomyoma","secondary_identifiers":["DOID:2887","MEDGEN:233875","UMLS:C1335510"],"synonyms":[{"name":"leiomyoma of prostate","type":"exact"},{"name":"leiomyoma of prostate gland","type":"exact"},{"name":"leiomyoma of the prostate","type":"exact"},{"name":"prostate gland leiomyoma","type":"exact"},{"name":"prostate leiomyoma","type":"exact"},{"name":"prostatic leiomyoma","type":"exact"}],"termid":"MONDO:0002452","xrefs":{"Monarch":{"xref_id":"0002452"}}}


id: MONDO:0014922
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any myofibrillar myopathy in which the cause of the disease is a mutation in the KY gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myofibrillar myopathy","termid":"MONDO:0018943"}],"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":"myofibrillar myopathy 7","secondary_identifiers":["DOID:0080098","MEDGEN:934678","OMIM:617114","UMLS:C4310711"],"synonyms":[{"name":"KY myofibrillar myopathy (disease)","type":"exact"},{"name":"MFM7","type":"related"},{"name":"alpha-b crystalin-related fatal infantile hypertonic myofibrillar myopathy","type":"exact"},{"name":"myofibrillar myopathy (disease) caused by mutation in KY","type":"exact"},{"name":"myopathy, myofibrillar, 7","type":"exact"},{"name":"myopathy, myofibrillar, type 7","type":"exact"}],"termid":"MONDO:0014922","xrefs":{"Monarch":{"xref_id":"0014922"}}}


id: PBO:0050488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOXB cluster antisense RNA 3","termid":"PBO:0050488"}


id: MONDO:0009627
data:
  {"annotated_genes":["SJAG_03986","SJAG_04700","SJAG_04201","SJAG_02863","SJAG_04848","SJAG_04182","SJAG_00378","SJAG_06560","SJAG_04148","SJAG_01374"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030476"},{"annotations":[87704],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033006"},{"annotations":[87006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033007"},{"annotations":[87007],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033008"},{"annotations":[87009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033009"},{"annotations":[87866],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032691"},{"annotations":[87867],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032692"},{"annotations":[87869,87868],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032693"},{"annotations":[87824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030471"}]},"cv_name":"mondo","definition":"Galloway syndrome is characterized by the association of nephrotic syndrome and central nervous system anomalies.","definition_xrefs":["Orphanet:2065"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00378":null,"SJAG_01374":null,"SJAG_02863":null,"SJAG_03986":null,"SJAG_04148":null,"SJAG_04182":null,"SJAG_04201":null,"SJAG_04700":null,"SJAG_04848":null,"SJAG_06560":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Galloway-Mowat syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:251300","NANDO:1200713","MESH:C537548","NANDO:2200120","MEDGEN:167086","NORD:1171","SCTID:721297008","UMLS:C0795949","GARD:65","DOID:0080694","NCIT:C132195","NANDO:2201385"],"synonyms":[{"name":"GAMOS","type":"related"},{"name":"Galloway Mowat syndrome","type":"related"},{"name":"Galloway syndrome","type":"exact"},{"name":"Galloway-Mowat syndrome","type":"exact"},{"name":"cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities","type":"related"},{"name":"cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities","type":"related"},{"name":"hiatal hernia-microcephaly-nephrosis, Galloway type","type":"related"},{"name":"microcephaly nephrosis syndrome","type":"related"},{"name":"microcephaly, hiatal hernia and nephrotic syndrome","type":"exact"},{"name":"microcephaly, hiatal hernia, and nephrotic syndrome","type":"related"},{"name":"microcephaly-hiatus hernia-nephrotic syndrome","type":"exact"},{"name":"nephrosis neuronal dysmigration syndrome","type":"related"},{"name":"nephrosis-microcephaly syndrome","type":"exact"},{"name":"nephrosis-neuronal dysmigration syndrome","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 5","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 5, formerly","type":"related"}],"termid":"MONDO:0009627","terms_by_termid":{"MONDO:0030471":null,"MONDO:0030476":null,"MONDO:0032691":null,"MONDO:0032692":null,"MONDO:0032693":null,"MONDO:0033006":null,"MONDO:0033007":null,"MONDO:0033008":null,"MONDO:0033009":null},"xrefs":{"Monarch":{"xref_id":"0009627"}}}


id: GO:0033583
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The portion of the plasma membrane surrounding the rhabdomere.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell projection membrane","termid":"GO:0031253"},{"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"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"rhabdomere membrane","termid":"GO:0033583"}


id: PBO:0081992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and SCAN domain containing 22","termid":"PBO:0081992"}


id: MONDO:0016418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple system atrophy, cerebellar type (MSA-c) is a form of multiple system atrophy (MSA) with predominant cerebellar features (gait and limb ataxia, oculomotor dysfunction, and dysarthria).","definition_xrefs":["Orphanet:227510"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-hereditary degenerative ataxia (obsolete MONDO:0016592)","termid":"MONDO:0016592"},{"relation_name":"is_a","term_name":"multiple system atrophy","termid":"MONDO:0007803"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0021179"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0021179","MONDO:0005559"],"is_obsolete":false,"name":"multiple system atrophy, cerebellar type","secondary_identifiers":["GARD:20565","MEDGEN:1843304","NANDO:1200035","UMLS:C5554234","icd11.foundation:1585600114"],"synonyms":[{"name":"MSA, cerebellar type","type":"exact"},{"name":"MSA-c","type":"exact"},{"name":"sporadic OPCA type 1","type":"exact"},{"name":"sporadic olivopontocerebellar atrophy type 1","type":"exact"}],"termid":"MONDO:0016418","xrefs":{"Monarch":{"xref_id":"0016418"}}}


id: PBO:0056020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich single-pass membrane protein 1","termid":"PBO:0056020"}


id: PBQ:0000001
data:
  {"annotation_feature_type":"gene","cv_name":"pb_quiescence","definition":"A specialized resting state that cells enter in response to cues from the cell's environment. Quiescence is characterized by the absence of cell growth and division, by a reprogramming of global gene expression, and by changes characteristic of the organism and specific cell type. Depending on external conditions, quiescence may persist until cell death or cells may resume cell growth and division. In some cell types or under certain conditions, cellular metabolism may proceed.","definition_xrefs":["PomBase:jb","PomBase:mah"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell quiescence","synonyms":[{"name":"G0 phase","type":"related"},{"name":"cell cycle quiescence","type":"related"},{"name":"cellular quiescence","type":"exact"},{"name":"quiescence","type":"broad"}],"termid":"PBQ:0000001"}


id: GO:0030957
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to Tat, a viral transactivating regulatory protein from the human immunodeficiency virus, or the equivalent protein from another virus.","definition_xrefs":["PMID:9094689","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II-specific DNA-binding transcription factor binding","termid":"GO:0061629"}],"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"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"Tat protein binding","termid":"GO:0030957"}


id: PBO:0004718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit Srb7","termid":"PBO:0004718"}


id: PBO:0062008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily J member 2","termid":"PBO:0062008"}


id: GO:0071791
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to chemokine (C-C motif) ligand 5.","definition_xrefs":["GOC:amm","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-C chemokine binding","termid":"GO:0019957"}],"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"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"chemokine (C-C motif) ligand 5 binding","synonyms":[{"name":"CCL5 binding","type":"exact"},{"name":"RANTES binding","type":"exact"},{"name":"Regulated upon Activation, Normal T-cell Expressed, and Secreted binding","type":"exact"}],"termid":"GO:0071791"}


id: PBO:0077191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell leukemia homeobox 2","termid":"PBO:0077191"}


id: MONDO:0002197
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign neoplasm that arises from the vulva It is characterized by the presence of clusters of small glands lined by mucinous epithelial cells. Bartholin duct structures are not present.","definition_xrefs":["NCIT:C40301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vestibular gland benign neoplasm","termid":"MONDO:0000626"},{"relation_name":"is_a","term_name":"vulvar glandular neoplasm","termid":"MONDO:0002198"},{"relation_name":"is_a","term_name":"paraurethral gland neoplasm","termid":"MONDO:0002219"},{"relation_name":"is_a","term_name":"benign urethral neoplasm","termid":"MONDO:0004177"},{"relation_name":"is_a","term_name":"adenoma","termid":"MONDO:0004972"},{"relation_name":"is_a","term_name":"benign epithelial neoplasm","termid":"MONDO:0036976"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"minor vestibular glands adenoma","secondary_identifiers":["MEDGEN:267644","DOID:2075","UMLS:C1510791"],"synonyms":[{"name":"adenoma of minor vestibular glands","type":"exact"},{"name":"minor vestibular gland adenoma","type":"exact"}],"termid":"MONDO:0002197","xrefs":{"Monarch":{"xref_id":"0002197"}}}


id: GO:0033275
data:
  {"annotated_genes":["SJAG_00750"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[119505],"is_not":false,"summary":null,"term":"GO:0033275"}]},"cv_name":"biological_process","definition":"The sliding movement of actin thin filaments and myosin thick filaments past each other.","definition_xrefs":["GOC:pf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin-mediated cell contraction","termid":"GO:0070252"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00750":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"actin-myosin filament sliding","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"actin filament sliding","type":"related"}],"termid":"GO:0033275","terms_by_termid":{"GO:0033275":null}}


id: RO:0002331
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"c involved_in p if and only if c enables some process p', and p' is part of p","direct_ancestors":[{"relation_name":"is_a","term_name":"involved_in_or_involved_in_regulation_of","termid":"RO:0002431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"involved_in","termid":"RO:0002331"}


id: PBO:0004410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF55 family protein","termid":"PBO:0004410"}


id: GO:0046879
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of hormones, substances with a specific regulatory effect on a particular organ or group of cells.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone transport","termid":"GO:0009914"},{"relation_name":"is_a","term_name":"signal release","termid":"GO:0023061"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0023052","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"hormone secretion","termid":"GO:0046879"}


id: GO:0019741
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of pentacyclic triterpenoid compounds, terpenoids with six isoprene units and 5 carbon rings.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triterpenoid catabolic process","termid":"GO:0016105"},{"relation_name":"is_a","term_name":"pentacyclic triterpenoid metabolic process","termid":"GO:0019742"}],"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":"pentacyclic triterpenoid catabolic process","synonyms":[{"name":"pentacyclic triterpenoid breakdown","type":"exact"},{"name":"pentacyclic triterpenoid catabolism","type":"exact"},{"name":"pentacyclic triterpenoid degradation","type":"exact"}],"termid":"GO:0019741"}


id: SO:0100011
data:
  {"annotated_genes":["SJAG_01006","SJAG_04067","SJAG_04525","SJAG_00975","SJAG_02958","SJAG_03201","SJAG_02413","SJAG_02582","SJAG_01086","SJAG_04904","SJAG_00860","SJAG_01595","SJAG_01675","SJAG_01858","SJAG_03148","SJAG_02478","SJAG_00790","SJAG_05279","SJAG_00846","SJAG_01709","SJAG_01985","SJAG_03483","SJAG_00732","SJAG_01488","SJAG_02258","SJAG_04090","SJAG_02823","SJAG_00680","SJAG_00620","SJAG_02173","SJAG_00161","SJAG_01416","SJAG_06600","SJAG_04247","SJAG_04398","SJAG_01028","SJAG_01136","SJAG_00025","SJAG_02827","SJAG_04922","SJAG_00239","SJAG_01069","SJAG_05327","SJAG_00784","SJAG_04073","SJAG_03270","SJAG_02875","SJAG_01290","SJAG_03814","SJAG_04905","SJAG_01970","SJAG_02145","SJAG_04924","SJAG_01171","SJAG_04677","SJAG_05353","SJAG_03640","SJAG_01689","SJAG_02190","SJAG_04821","SJAG_03057","SJAG_00254","SJAG_04796","SJAG_04345","SJAG_04835","SJAG_01189","SJAG_00554","SJAG_02093","SJAG_04808","SJAG_04046","SJAG_01445","SJAG_01128","SJAG_05008","SJAG_02580","SJAG_04875","SJAG_05013","SJAG_02495","SJAG_02944","SJAG_00484","SJAG_00310","SJAG_01427","SJAG_02537","SJAG_03030","SJAG_03138","SJAG_00906","SJAG_00096","SJAG_04851","SJAG_04799","SJAG_02435","SJAG_01846","SJAG_02959","SJAG_00709","SJAG_03204","SJAG_01861","SJAG_05189","SJAG_04927","SJAG_04819","SJAG_00780","SJAG_05272","SJAG_00876","SJAG_03535","SJAG_01363","SJAG_02877","SJAG_02301","SJAG_03239","SJAG_04238","SJAG_04975","SJAG_04685","SJAG_00570","SJAG_02694","SJAG_02076","SJAG_05291","SJAG_03444","SJAG_00530","SJAG_02949","SJAG_01705","SJAG_00057","SJAG_03295","SJAG_04786","SJAG_01321","SJAG_00771","SJAG_00981","SJAG_04196","SJAG_01999","SJAG_00222","SJAG_02676","SJAG_00110","SJAG_04483","SJAG_03178","SJAG_00415","SJAG_00340","SJAG_01458","SJAG_01959","SJAG_03749","SJAG_03824","SJAG_05001","SJAG_01029","SJAG_00852","SJAG_01223","SJAG_02432","SJAG_04797","SJAG_00131","SJAG_02193","SJAG_02134","SJAG_02389","SJAG_03727","SJAG_02131","SJAG_01421","SJAG_02568","SJAG_02987","SJAG_00517","SJAG_03650","SJAG_01626","SJAG_04193","SJAG_04720","SJAG_04598","SJAG_03521","SJAG_00437","SJAG_00490","SJAG_00286","SJAG_00357","SJAG_04106","SJAG_01968","SJAG_00810","SJAG_02839","SJAG_02049","SJAG_04184","SJAG_04571","SJAG_04807","SJAG_00751","SJAG_02489","SJAG_00781","SJAG_03816","SJAG_00481","SJAG_04770","SJAG_04833","SJAG_04419","SJAG_02260","SJAG_04850","SJAG_01948","SJAG_04301","SJAG_00109","SJAG_01407","SJAG_04785","SJAG_01965","SJAG_03203","SJAG_03800","SJAG_03333","SJAG_04236","SJAG_00708","SJAG_00593","SJAG_01388","SJAG_01868","SJAG_01038","SJAG_03930","SJAG_03672","SJAG_04789","SJAG_02437","SJAG_02102","SJAG_04723","SJAG_05261","SJAG_16452","SJAG_03606","SJAG_03280","SJAG_00667","SJAG_06425","SJAG_04363","SJAG_01835","SJAG_01991","SJAG_02192","SJAG_00288","SJAG_00403","SJAG_04209","SJAG_03202","SJAG_02191","SJAG_04864","SJAG_03282","SJAG_03414","SJAG_04435","SJAG_00367","SJAG_00218","SJAG_02091","SJAG_03820","SJAG_04096","SJAG_01755","SJAG_04906"],"annotation_feature_type":"gene","cv_annotations":{"sequence":[{"annotations":[82482,82497,82420,82489,82405,82302,82319,82233,82260,82462,82264,82252,82329,82221,82281,82293,82355,82375,82398,82445,82451,82493,82343,82499,82226,82346,82315,82235,82386,82374,82432,82490,82500,82342,82220,82427,82238,82434,82291,82348,82206,82236,82521,82496,82256,82368,82397,82308,82430,82288,82457,82283,82341,82415,82336,82520,82218,82297,82334,82258,82228,82277,82314,82485,82292,82429,82487,82471,82217,82518,82447,82407,82274,82311,82402,82433,82458,82263,82310,82400,82399,82435,82242,82239,82328,82417,82250,82280,82359,82307,82523,82512,82464,82408,82325,82380,82449,82354,82395,82421,82287,82356,82461,82478,82479,82492,82423,82459,82448,82269,82282,82455,82227,82438,82313,82273,82517,82234,82278,82470,82205,82211,82514,82212,82253,82223,82222,82276,82300,82257,82391,82412,82488,82510,82422,82431,82296,82453,82498,82486,82290,82376,82249,82349,82298,82305,82266,82406,82460,82515,82208,82316,82320,82414,82262,82270,82299,82352,82452,82454,82463,82367,82312,82247,82358,82363,82357,82267,82531,82509,82337,82271,82468,82345,82424,82207,82322,82241,82491,82524,82330,82279,82214,82522,82403,82446,82511,82456,82495,82248,82378,82225,82401,82513,82369,82309,82219,82295,82251,82436,82494,82347,82529,82321,82306,82289,82360,82469,82419,82216,82519,82396,82379,82501,82366,82224,82265,82526,82246,82418,82261,82240,82335,82294,82382,82481],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"SO:0000418"}]},"cv_name":"sequence","definition":"The cleaved_peptide_region is the region of a peptide sequence that is cleaved during maturation.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_region","termid":"SO:0000839"},{"relation_name":"part_of","term_name":"immature_peptide_region","termid":"SO:0001063"}],"gene_count":226,"genes_by_uniquename":{"SJAG_00025":null,"SJAG_00057":null,"SJAG_00096":null,"SJAG_00109":null,"SJAG_00110":null,"SJAG_00131":null,"SJAG_00161":null,"SJAG_00218":null,"SJAG_00222":null,"SJAG_00239":null,"SJAG_00254":null,"SJAG_00286":null,"SJAG_00288":null,"SJAG_00310":null,"SJAG_00340":null,"SJAG_00357":null,"SJAG_00367":null,"SJAG_00403":null,"SJAG_00415":null,"SJAG_00437":null,"SJAG_00481":null,"SJAG_00484":null,"SJAG_00490":null,"SJAG_00517":null,"SJAG_00530":null,"SJAG_00554":null,"SJAG_00570":null,"SJAG_00593":null,"SJAG_00620":null,"SJAG_00667":null,"SJAG_00680":null,"SJAG_00708":null,"SJAG_00709":null,"SJAG_00732":null,"SJAG_00751":null,"SJAG_00771":null,"SJAG_00780":null,"SJAG_00781":null,"SJAG_00784":null,"SJAG_00790":null,"SJAG_00810":null,"SJAG_00846":null,"SJAG_00852":null,"SJAG_00860":null,"SJAG_00876":null,"SJAG_00906":null,"SJAG_00975":null,"SJAG_00981":null,"SJAG_01006":null,"SJAG_01028":null,"SJAG_01029":null,"SJAG_01038":null,"SJAG_01069":null,"SJAG_01086":null,"SJAG_01128":null,"SJAG_01136":null,"SJAG_01171":null,"SJAG_01189":null,"SJAG_01223":null,"SJAG_01290":null,"SJAG_01321":null,"SJAG_01363":null,"SJAG_01388":null,"SJAG_01407":null,"SJAG_01416":null,"SJAG_01421":null,"SJAG_01427":null,"SJAG_01445":null,"SJAG_01458":null,"SJAG_01488":null,"SJAG_01595":null,"SJAG_01626":null,"SJAG_01675":null,"SJAG_01689":null,"SJAG_01705":null,"SJAG_01709":null,"SJAG_01755":null,"SJAG_01835":null,"SJAG_01846":null,"SJAG_01858":null,"SJAG_01861":null,"SJAG_01868":null,"SJAG_01948":null,"SJAG_01959":null,"SJAG_01965":null,"SJAG_01968":null,"SJAG_01970":null,"SJAG_01985":null,"SJAG_01991":null,"SJAG_01999":null,"SJAG_02049":null,"SJAG_02076":null,"SJAG_02091":null,"SJAG_02093":null,"SJAG_02102":null,"SJAG_02131":null,"SJAG_02134":null,"SJAG_02145":null,"SJAG_02173":null,"SJAG_02190":null,"SJAG_02191":null,"SJAG_02192":null,"SJAG_02193":null,"SJAG_02258":null,"SJAG_02260":null,"SJAG_02301":null,"SJAG_02389":null,"SJAG_02413":null,"SJAG_02432":null,"SJAG_02435":null,"SJAG_02437":null,"SJAG_02478":null,"SJAG_02489":null,"SJAG_02495":null,"SJAG_02537":null,"SJAG_02568":null,"SJAG_02580":null,"SJAG_02582":null,"SJAG_02676":null,"SJAG_02694":null,"SJAG_02823":null,"SJAG_02827":null,"SJAG_02839":null,"SJAG_02875":null,"SJAG_02877":null,"SJAG_02944":null,"SJAG_02949":null,"SJAG_02958":null,"SJAG_02959":null,"SJAG_02987":null,"SJAG_03030":null,"SJAG_03057":null,"SJAG_03138":null,"SJAG_03148":null,"SJAG_03178":null,"SJAG_03201":null,"SJAG_03202":null,"SJAG_03203":null,"SJAG_03204":null,"SJAG_03239":null,"SJAG_03270":null,"SJAG_03280":null,"SJAG_03282":null,"SJAG_03295":null,"SJAG_03333":null,"SJAG_03414":null,"SJAG_03444":null,"SJAG_03483":null,"SJAG_03521":null,"SJAG_03535":null,"SJAG_03606":null,"SJAG_03640":null,"SJAG_03650":null,"SJAG_03672":null,"SJAG_03727":null,"SJAG_03749":null,"SJAG_03800":null,"SJAG_03814":null,"SJAG_03816":null,"SJAG_03820":null,"SJAG_03824":null,"SJAG_03930":null,"SJAG_04046":null,"SJAG_04067":null,"SJAG_04073":null,"SJAG_04090":null,"SJAG_04096":null,"SJAG_04106":null,"SJAG_04184":null,"SJAG_04193":null,"SJAG_04196":null,"SJAG_04209":null,"SJAG_04236":null,"SJAG_04238":null,"SJAG_04247":null,"SJAG_04301":null,"SJAG_04345":null,"SJAG_04363":null,"SJAG_04398":null,"SJAG_04419":null,"SJAG_04435":null,"SJAG_04483":null,"SJAG_04525":null,"SJAG_04571":null,"SJAG_04598":null,"SJAG_04677":null,"SJAG_04685":null,"SJAG_04720":null,"SJAG_04723":null,"SJAG_04770":null,"SJAG_04785":null,"SJAG_04786":null,"SJAG_04789":null,"SJAG_04796":null,"SJAG_04797":null,"SJAG_04799":null,"SJAG_04807":null,"SJAG_04808":null,"SJAG_04819":null,"SJAG_04821":null,"SJAG_04833":null,"SJAG_04835":null,"SJAG_04850":null,"SJAG_04851":null,"SJAG_04864":null,"SJAG_04875":null,"SJAG_04904":null,"SJAG_04905":null,"SJAG_04906":null,"SJAG_04922":null,"SJAG_04924":null,"SJAG_04927":null,"SJAG_04975":null,"SJAG_05001":null,"SJAG_05008":null,"SJAG_05013":null,"SJAG_05189":null,"SJAG_05261":null,"SJAG_05272":null,"SJAG_05279":null,"SJAG_05291":null,"SJAG_05327":null,"SJAG_05353":null,"SJAG_06425":null,"SJAG_06600":null,"SJAG_16452":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"cleaved_peptide_region","references_by_uniquename":{"PMID:36408920":null},"synonyms":[{"name":"cleaved peptide region","type":"exact"}],"termid":"SO:0100011","terms_by_termid":{"SO:0000418":null}}


id: PBO:0075440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPANX family member N5","termid":"PBO:0075440"}


id: GO:0051428
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a receptor for a peptide hormone.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone receptor binding","termid":"GO:0051427"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"peptide hormone receptor binding","synonyms":[{"name":"polypeptide hormone receptor binding","type":"exact"}],"termid":"GO:0051428"}


id: GO:0034514
data:
  {"annotated_genes":["SJAG_00564"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79436],"is_not":false,"summary":null,"term":"GO:0034514"}]},"cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of the presence of unfolded proteins in the mitochondrial matrix; results in transcriptional upregulation of nuclear genes encoding mitochondrial stress proteins.","definition_xrefs":["GOC:mah","PMID:17849004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to unfolded protein","termid":"GO:0034620"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00564":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mitochondrial unfolded protein response","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"mtUPR","type":"exact"}],"termid":"GO:0034514","terms_by_termid":{"GO:0034514":null}}


id: FYPO:0001658
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 import of valine into the cell is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal amino acid import during vegetative growth","termid":"FYPO:0001361"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abnormal valine import","synonyms":[{"name":"abnormal L-valine import","type":"exact"},{"name":"abnormal L-valine import across plasma membrane","type":"exact"},{"name":"abnormal valine import during mitotic cell cycle","type":"related"},{"name":"abnormal valine import during vegetative growth","type":"exact"},{"name":"abnormal valine import into cell","type":"exact"},{"name":"abnormal valine uptake","type":"exact"}],"termid":"FYPO:0001658"}


id: PBO:0029996
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-small_P-bodies_during_glucose_starvation","termid":"PBO:0029996"}


id: GO:0030965
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The transfer of electrons from NADH to the quinone pool that occurs during oxidative phosphorylation and results in the generation of a proton gradient, mediated by the enzyme known as NADH-quinone oxidoreductase.","definition_xrefs":["GOC:mah","GOC:sd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory electron transport chain","termid":"GO:0022904"},{"relation_name":"part_of","term_name":"plasma membrane ATP synthesis coupled electron transport","termid":"GO:0042774"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"plasma membrane electron transport, NADH to quinone","termid":"GO:0030965"}


id: PBO:0114948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FMN-dependent alpha-hydroxy acid dehydrogenase, probable lactate dehydrogenase","termid":"PBO:0114948"}


id: GO:0005854
data:
  {"annotated_genes":["SJAG_01733","SJAG_01641"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[65695,78832],"is_not":false,"summary":null,"term":"GO:0005854"}]},"cv_name":"cellular_component","definition":"A heterodimeric protein complex that can reversibly bind to ribosomes, and is located in direct proximity to newly synthesized polypeptide chains as they emerge from the ribosome.","definition_xrefs":["PMID:7568149","PMID:12475173"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01641":null,"SJAG_01733":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"nascent polypeptide-associated complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"synonyms":[{"name":"NAC","type":"exact"},{"name":"NACA","type":"exact"}],"termid":"GO:0005854","terms_by_termid":{"GO:0005854":null}}


id: FYECO:0000354
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which phleomycin 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":"+ phleomycin","termid":"FYECO:0000354"}


id: SO:0000082
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000082 processed_transcript_attribute (obsolete SO:0000082)","termid":"SO:0000082"}


id: MONDO:1012427
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy (limb-girdle), non-human animal","termid":"MONDO:1011803"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy (limb-girdle), domestic cat","secondary_identifiers":["OMIA:001621-9685"],"termid":"MONDO:1012427","xrefs":{"Monarch":{"xref_id":"1012427"}}}


id: GO:1902161
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cyclic nucleotide-gated ion channel activity.","definition_xrefs":["GOC:TermGenie","PMID:11420311"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of ion transmembrane transporter activity","termid":"GO:0032414"},{"relation_name":"is_a","term_name":"regulation of cyclic nucleotide-gated ion channel activity","termid":"GO:1902159"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"positive regulation of cyclic nucleotide-gated ion channel activity","synonyms":[{"name":"activation of cyclic nucleotide activated ion channel activity","type":"exact"},{"name":"activation of cyclic nucleotide gated ion channel activity","type":"exact"},{"name":"activation of cyclic nucleotide-activated ion channel activity","type":"exact"},{"name":"activation of cyclic nucleotide-gated ion channel activity","type":"narrow"},{"name":"positive regulation of cyclic nucleotide activated ion channel activity","type":"exact"},{"name":"positive regulation of cyclic nucleotide gated ion channel activity","type":"exact"},{"name":"positive regulation of cyclic nucleotide-activated ion channel activity","type":"exact"},{"name":"up regulation of cyclic nucleotide activated ion channel activity","type":"exact"},{"name":"up regulation of cyclic nucleotide gated ion channel activity","type":"exact"},{"name":"up regulation of cyclic nucleotide-activated ion channel activity","type":"exact"},{"name":"up regulation of cyclic nucleotide-gated ion channel activity","type":"exact"},{"name":"up-regulation of cyclic nucleotide activated ion channel activity","type":"exact"},{"name":"up-regulation of cyclic nucleotide gated ion channel activity","type":"exact"},{"name":"up-regulation of cyclic nucleotide-activated ion channel activity","type":"exact"},{"name":"up-regulation of cyclic nucleotide-gated ion channel activity","type":"exact"},{"name":"upregulation of cyclic nucleotide activated ion channel activity","type":"exact"},{"name":"upregulation of cyclic nucleotide gated ion channel activity","type":"exact"},{"name":"upregulation of cyclic nucleotide-activated ion channel activity","type":"exact"},{"name":"upregulation of cyclic nucleotide-gated ion channel activity","type":"exact"}],"termid":"GO:1902161"}


id: PBO:0058060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR4280 host gene","termid":"PBO:0058060"}


id: GO:0033890
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the exonucleolytic cleavage that removes extra residues from the 3'-terminus of tRNA to produce 5'-mononucleotides.","definition_xrefs":["EC:3.1.13.5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA exonuclease activity, producing 5'-phosphomonoesters","termid":"GO:0016896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0004527"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0004527","GO:0016787","GO:0003674","GO:0016788","GO:0140098","GO:0003824"],"is_obsolete":false,"name":"ribonuclease D activity","secondary_identifiers":["MetaCyc:3.1.13.5-RXN"],"synonyms":[{"name":"RNase D activity","type":"related"}],"termid":"GO:0033890"}


id: MONDO:0011934
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dermatofibrosarcoma protuberans (DFSP) is a rare infiltrating soft tissue sarcoma, generally of low grade malignancy, arising from the dermis of the skin and characteristically associated with a specific chromosomal translocation t(17;22).","definition_xrefs":["Orphanet:31112"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare skin tumor or hamartoma (obsolete MONDO:0019300)","termid":"MONDO:0019300"},{"relation_name":"is_a","term_name":"integumentary system cancer","termid":"MONDO:0000653"},{"relation_name":"is_a","term_name":"fibrosarcoma","termid":"MONDO:0005164"}],"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":"dermatofibrosarcoma protuberans","secondary_identifiers":["UMLS:C3693482","OMIM:607907","DOID:3507","NCIT:C4683","ICDO:8832/3","GARD:9569","MEDGEN:811326","MESH:D018223","SCTID:276799004","icd11.foundation:1579898301","MedDRA:10057070","ONCOTREE:DFSP"],"synonyms":[{"name":"DFSP","type":"exact"},{"name":"dermatofibrosarcoma","type":"exact"},{"name":"dermatofibrosarcoma protuberans","type":"exact"},{"name":"familial dermatofibrosarcoma protuberans (subtype)","type":"related"},{"name":"giant cell fibroblastoma","type":"related"},{"name":"metastatic dermatofibrosarcoma protuberans (subtype)","type":"related"}],"termid":"MONDO:0011934","xrefs":{"Monarch":{"xref_id":"0011934"}}}


id: PBO:0053079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lebercilin LCA5 like","termid":"PBO:0053079"}


id: GO:0043839
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a methyl group from S-adenosylmethionine (SAM) to the 1-phosphate group of lipid A.","definition_xrefs":["PMID:15994324"],"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:0016741"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016741","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"lipid A phosphate methyltransferase activity","synonyms":[{"name":"LmtA","type":"related"},{"name":"lipid A 1-phosphomethyltransferase activity","type":"exact"},{"name":"lipid A methyltransferase","type":"broad"},{"name":"lipid A phosphomethyltransferase activity","type":"exact"}],"termid":"GO:0043839"}


id: PBO:0038742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACTN1 divergent transcript","termid":"PBO:0038742"}


id: GO:0006936
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which force is generated within muscle tissue, resulting in a change in muscle geometry. Force generation involves a chemo-mechanical energy conversion step that is carried out by the actin/myosin complex activity, which generates force through ATP hydrolysis.","definition_xrefs":["GOC:mtg_muscle","GOC:ef","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle system process","termid":"GO:0003012"}],"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":"muscle contraction","secondary_identifiers":["Reactome:R-HSA-445355","Wikipedia:Muscle_contraction"],"termid":"GO:0006936"}


id: PBO:0059148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myeloperoxidase","termid":"PBO:0059148"}


id: PBO:0091646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alanine racemase Alr2","termid":"PBO:0091646"}


id: MONDO:1010228
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dandy-Walker syndrome that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental defect during embryogenesis, non-human animal","termid":"MONDO:1011310"},{"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":"Dandy-Walker syndrome, non-human animal","secondary_identifiers":["OMIA:000258"],"termid":"MONDO:1010228","xrefs":{"Monarch":{"xref_id":"1010228"}}}


id: GO:1902631
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of membrane hyperpolarization.","definition_xrefs":["GOC:TermGenie","PMID:23223304","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biological process","termid":"GO:0048519"},{"relation_name":"is_a","term_name":"regulation of membrane hyperpolarization","termid":"GO:1902630"},{"relation_name":"negatively_regulates","term_name":"membrane hyperpolarization","termid":"GO:0060081"}],"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 membrane hyperpolarization","synonyms":[{"name":"down regulation of membrane hyperpolarization","type":"exact"},{"name":"down-regulation of membrane hyperpolarization","type":"exact"},{"name":"downregulation of membrane hyperpolarization","type":"exact"},{"name":"inhibition of membrane hyperpolarization","type":"narrow"}],"termid":"GO:1902631"}


id: MONDO:0850470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diffuse large B-cell lymphoma that is categorized as MCD with high probability by the LymphGen algorithm. This is based on a combination of genetic features and MCD DLBCLs often, but do not always, have the most common hot spot mutation in MYD88 (L265P) and/or activating mutations in CD79B. This subgroup also commonly has mutations due to aberrant somatic hypermutation affecting PIM1 and/or ETV6, which can be coding or non-coding.","definition_xrefs":["DOID:0081066"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"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":"MCD diffuse large B-cell lymphoma","secondary_identifiers":["UMLS:C4725002","NCIT:C148394","MEDGEN:1669702"],"termid":"MONDO:0850470","xrefs":{"Monarch":{"xref_id":"0850470"}}}


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: GO:0047591
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-hydroxypentanoate + acetyl-CoA = 5-hydroxy-pentanoyl-CoA + acetate.","definition_xrefs":["EC:2.8.3.14","RHEA:23496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-transferase activity","termid":"GO:0008410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016782"},{"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:0003674","GO:0003824","GO:0016782","GO:0016740"],"is_obsolete":false,"name":"5-hydroxypentanoate CoA-transferase activity","secondary_identifiers":["MetaCyc:5-HYDROXYPENTANOATE-COA-TRANSFERASE-RXN","KEGG_REACTION:R04057"],"synonyms":[{"name":"5-hydroxyvalerate CoA-transferase activity","type":"related"},{"name":"5-hydroxyvalerate coenzyme A transferase activity","type":"related"},{"name":"acetyl-CoA:5-hydroxypentanoate CoA-transferase activity","type":"related"}],"termid":"GO:0047591"}


id: GO:0034271
data:
  {"annotated_genes":["SJAG_01876","SJAG_00114","SJAG_02699","SJAG_04552","SJAG_04860"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[73301,78516,79031,96438,113373],"is_not":false,"summary":null,"term":"GO:0034271"}]},"cv_name":"cellular_component","definition":"A class III phosphatidylinositol 3-kinase complex that is involved in autophagy. In budding yeast, this complex consists of Vps30p, Vps34p, Apg14p and Vps15p.","definition_xrefs":["GOC:ha","PMID:11157979","GOC:rb","PMID:16421251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylinositol 3-kinase complex, class III","termid":"GO:0035032"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_01876":null,"SJAG_02699":null,"SJAG_04552":null,"SJAG_04860":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"phosphatidylinositol 3-kinase complex, class III, type I","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"PtdIns-3-kinase complex I","type":"related"},{"name":"autophagy-specific phosphatidylinositol 3-kinase (PtdIns3K) complex","type":"exact"},{"name":"phosphatidylinositol 3-kinase complex I","type":"related"}],"termid":"GO:0034271","terms_by_termid":{"GO:0034271":null}}


id: PBO:0117413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zDHHC palmitoyltransferase 8","termid":"PBO:0117413"}


id: PBO:0078802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (GTT) 19-2","termid":"PBO:0078802"}


id: PBO:0038360
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-transports","termid":"PBO:0038360"}


id: PBO:0089291
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reticulon Rtn1","termid":"PBO:0089291"}


id: MOD:01110
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of an L-cysteine residue with a group derived from an isoprene polymer, such as a geranyl (C10), farnesyl (C15) or geranylgeranyl (C20).","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprenylated residue","termid":"MOD:00703"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"},{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905","MOD:01155"],"is_obsolete":false,"name":"isoprenylated cysteine","synonyms":[{"name":"IpCys","type":"exact"}],"termid":"MOD:01110"}


id: PBO:0027714
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_cell_division,_small_cell","termid":"PBO:0027714"}


id: PBO:0029523
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_swollen_septated_spheroid_vegetative_cell","termid":"PBO:0029523"}


id: PBO:0077151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TLC domain containing 2","termid":"PBO:0077151"}


id: MONDO:1011312
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disease related to transplantation that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disease related to transplantation, non-human animal","termid":"MONDO:1011312","xrefs":{"Monarch":{"xref_id":"1011312"}}}


id: GO:0016985
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the random hydrolysis of (1->4)-beta-D-mannosidic linkages in mannans, galactomannans, glucomannans, and galactoglucomannans.","definition_xrefs":["EC:3.2.1.78"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-mannosidase activity","termid":"GO:0004567"}],"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:0016798"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016798","GO:0016787"],"is_obsolete":false,"name":"mannan endo-1,4-beta-mannosidase activity","secondary_identifiers":["MetaCyc:3.2.1.78-RXN"],"synonyms":[{"name":"1,4-beta-D-mannan mannanohydrolase activity","type":"related"},{"name":"beta-1,4-mannan 4-mannanohydrolase activity","type":"related"},{"name":"beta-D-mannanase activity","type":"related"},{"name":"beta-mannanase B","type":"related"},{"name":"beta-mannanase activity","type":"broad"},{"name":"endo-1,4-beta-mannanase activity","type":"related"},{"name":"endo-1,4-mannanase activity","type":"broad"},{"name":"endo-beta-1,4-mannase activity","type":"related"},{"name":"endo-beta-mannanase activity","type":"broad"}],"termid":"GO:0016985"}


id: MONDO:0011268
data:
  {"annotated_genes":["SJAG_00516"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87926],"is_not":false,"summary":null,"term":"MONDO:0011268"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"renal tubular acidosis","termid":"MONDO:0001909"},{"relation_name":"is_a","term_name":"inherited renal tubular disease","termid":"MONDO:0015962"},{"relation_name":"is_a","term_name":"autosomal recessive distal renal tubular acidosis","termid":"MONDO:0018440"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00516":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005240","MONDO:0005066"],"is_obsolete":false,"name":"renal tubular acidosis, distal, 3, with or without sensorineural hearing loss","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:602722","GARD:15350","UMLS:C5399980","MEDGEN:1732975"],"synonyms":[{"name":"RTA, distal, autosomal recessive","type":"related"},{"name":"RTADR","type":"related"},{"name":"classical distal RTA","type":"exact"},{"name":"classical distal renal tubular acidosis","type":"exact"},{"name":"distal renal tubular acidosis 3, with or without sensorineural hearing loss","type":"exact"},{"name":"renal tubular acidosis, autosomal recessive with preserved hearing","type":"related"},{"name":"renal tubular acidosis, autosomal recessive, with preserved hearing","type":"related"},{"name":"renal tubular acidosis, distal, 3, with or without sensorineural hearing loss","type":"exact"},{"name":"renal tubular acidosis, distal, autosomal recessive","type":"exact"},{"name":"renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss","type":"related"},{"name":"renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss, included","type":"related"},{"name":"type 1 RTA","type":"exact"},{"name":"type 1 renal tubular acidosis","type":"exact"}],"termid":"MONDO:0011268","terms_by_termid":{"MONDO:0011268":null},"xrefs":{"Monarch":{"xref_id":"0011268"}}}


id: GO:0043047
data:
  {"annotated_genes":["SJAG_01677","SJAG_04245","SJAG_02194","SJAG_02362","SJAG_00939","SJAG_04863","SJAG_05214","SJAG_03855"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[64278,81966,82028,97886,109961,112223,113389],"is_not":false,"summary":null,"term":"GO:0043047"},{"annotations":[78796],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098505"}]},"cv_name":"molecular_function","definition":"Binding to single-stranded telomere-associated DNA.","definition_xrefs":["GOC:jl","ISBN:0321000382"],"direct_ancestors":[{"relation_name":"is_a","term_name":"telomeric DNA binding","termid":"GO:0042162"},{"relation_name":"is_a","term_name":"sequence-specific single stranded DNA binding","termid":"GO:0098847"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00939":null,"SJAG_01677":null,"SJAG_02194":null,"SJAG_02362":null,"SJAG_03855":null,"SJAG_04245":null,"SJAG_04863":null,"SJAG_05214":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003677"}],"interesting_parent_ids":["GO:0003677","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"single-stranded telomeric DNA binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"telomeric ssDNA binding","type":"exact"}],"termid":"GO:0043047","terms_by_termid":{"GO:0043047":null,"GO:0098505":null}}


id: GO:0047122
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: A + H2O + quinaldate = AH(2) + kynurenate.","definition_xrefs":["RHEA:16697","EC:1.3.99.18"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors","termid":"GO:0016627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"quinaldate 4-oxidoreductase activity","secondary_identifiers":["MetaCyc:1.3.99.18-RXN","KEGG_REACTION:R03687"],"synonyms":[{"name":"quinaldic acid 4-oxidoreductase activity","type":"related"},{"name":"quinoline-2-carboxylate:acceptor 4-oxidoreductase (hydroxylating)","type":"related"}],"termid":"GO:0047122"}


id: PBO:0082430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Blocked reading frame otherwise encoding L-serine dehydratase","termid":"PBO:0082430"}


id: PBO:0047154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 183 member E, pseudogene","termid":"PBO:0047154"}


id: PBO:0044360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 48","termid":"PBO:0044360"}


id: GO:0098003
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a virus tail.","definition_xrefs":["GOC:bm","VZ:3955"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"},{"relation_name":"part_of","term_name":"virion assembly","termid":"GO:0019068"}],"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 tail assembly","synonyms":[{"name":"bacteriophage tail assembly","type":"narrow"},{"name":"virus tail assembly","type":"exact"}],"termid":"GO:0098003"}


id: PBO:0090230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CBS and PB1 domain protein, conserved in fungi and plants, implicated in signalling Mug70","termid":"PBO:0090230"}


id: SO:1000041
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosome structure variation whereby a transposition occurred within a chromosome.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_part","term_name":"translocation","termid":"SO:0000199"},{"relation_name":"has_part","term_name":"duplication","termid":"SO:1000035"},{"relation_name":"is_a","term_name":"chromosomal_transposition","termid":"SO:0000453"},{"relation_name":"is_a","term_name":"intrachromosomal_duplication","termid":"SO:1000038"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intrachromosomal_transposition","synonyms":[{"name":"(Drosophila)Tp","type":"related"},{"name":"intrachromosomal transposition","type":"exact"}],"termid":"SO:1000041"}


id: FYPO:0005806
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 rate, or speed, of movement of one or more proteins within the plasma membrane of the lateral part of the cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:25837586"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein movement within plasma membrane during vegetative growth","termid":"FYPO:0005804"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal rate of protein movement within plasma membrane at cell side","synonyms":[{"name":"normal rate of protein movement within plasma membrane at cell side during mitotic cell cycle","type":"related"},{"name":"normal rate of protein movement within plasma membrane at cell side during vegetative growth","type":"exact"},{"name":"normal rate of protein movement within plasma membrane at lateral part of cell","type":"exact"}],"termid":"FYPO:0005806"}


id: MONDO:0859576
data:
  {"annotated_genes":["SJAG_03436"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87396],"is_not":false,"summary":null,"term":"MONDO:0859576"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mosaic variegated aneuploidy syndrome","termid":"MONDO:0000141"},{"relation_name":"is_a","term_name":"Atelis syndrome","termid":"MONDO:0859393"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03436":null},"genotype_count":0,"is_obsolete":false,"name":"Atelis syndrome 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5774282","MEDGEN:1824055","OMIM:620185"],"termid":"MONDO:0859576","terms_by_termid":{"MONDO:0859576":null},"xrefs":{"Monarch":{"xref_id":"0859576"}}}


id: PBO:0012254
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"octameric","termid":"PBO:0012254"}


id: MONDO:0005137
data:
  {"annotated_genes":["SJAG_00857","SJAG_04425","SJAG_04398","SJAG_01881","SJAG_05230","SJAG_01199","SJAG_04042","SJAG_04980","SJAG_03069","SJAG_04459"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88197],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014352"},{"annotations":[88832],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015005"},{"annotations":[88067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009666"},{"annotations":[87332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0006065"},{"annotations":[87032,87031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009354"},{"annotations":[87642],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009609"},{"annotations":[88473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010184"},{"annotations":[86988],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010961"},{"annotations":[87280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012407"}]},"cv_name":"mondo","definition":"Any condition related to a disturbance between proper intake and utilization of nourishment.","definition_xrefs":["NCIT:C26836"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"metabolic disease","termid":"MONDO:0005066"},{"relation_name":"excluded_subClassOf","term_name":"acquired metabolic disease","termid":"MONDO:0006504"},{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00857":null,"SJAG_01199":null,"SJAG_01881":null,"SJAG_03069":null,"SJAG_04042":null,"SJAG_04398":null,"SJAG_04425":null,"SJAG_04459":null,"SJAG_04980":null,"SJAG_05230":null},"genotype_count":0,"is_obsolete":false,"name":"nutritional disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D009748","DOID:374","ICD9:783.9","SCTID:2492009","UMLS:C3714509","MEDGEN:811347","EFO:0001069"],"synonyms":[{"name":"nutrition disease","type":"related"},{"name":"nutritional disorder","type":"exact"}],"termid":"MONDO:0005137","terms_by_termid":{"MONDO:0006065":null,"MONDO:0009354":null,"MONDO:0009609":null,"MONDO:0009666":null,"MONDO:0010184":null,"MONDO:0010961":null,"MONDO:0012407":null,"MONDO:0014352":null,"MONDO:0015005":null},"xrefs":{"Monarch":{"xref_id":"0005137"}}}


id: PBO:0017901
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by rat PEMT","termid":"PBO:0017901"}


id: GO:0016318
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which photoreceptors are arranged in ommatidia in the dorsal and ventral fields to be mirror images. The polarity is established in the imaginal discs concurrently with cell fate specification.","definition_xrefs":["PMID:10725247"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern specification process","termid":"GO:0007389"},{"relation_name":"part_of","term_name":"establishment of ommatidial planar polarity","termid":"GO:0042067"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"ommatidial rotation","termid":"GO:0016318"}


id: GO:0043332
data:
  {"annotated_genes":["SJAG_02351","SJAG_02169","SJAG_01017","SJAG_03453","SJAG_04100","SJAG_00700","SJAG_02700","SJAG_00667","SJAG_01888","SJAG_01732","SJAG_02718","SJAG_04982","SJAG_04901","SJAG_00514","SJAG_02222","SJAG_03596","SJAG_00677","SJAG_01993","SJAG_03145","SJAG_00938","SJAG_01943","SJAG_02486","SJAG_04703","SJAG_05285","SJAG_03444","SJAG_02228","SJAG_01794","SJAG_04509","SJAG_04887","SJAG_05001","SJAG_03646","SJAG_02924","SJAG_04723","SJAG_03011","SJAG_04001","SJAG_00279","SJAG_01215","SJAG_03357","SJAG_01171","SJAG_00870","SJAG_04781","SJAG_00185"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[71883,73922,75691,77309,78058,79530,80454,89700,92482,92528,94396,98677,99534,99728,100709,105072,107932,108692,108993,110689,110899,116181,117674],"is_not":false,"summary":null,"term":"GO:0043332"},{"annotations":[90089,95634,103761,101968,113168,118033,95828,109966,101366,94323,116481,121516,90906,92652,103762,97182,109905],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990819"},{"annotations":[98190,112041],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070867"}]},"cv_name":"cellular_component","definition":"The apex of the mating projection in unicellular fungi exposed to mating pheromone; site of polarized growth.","definition_xrefs":["GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"site of polarized growth","termid":"GO:0030427"},{"relation_name":"is_a","term_name":"cell tip","termid":"GO:0051286"},{"relation_name":"part_of","term_name":"mating projection","termid":"GO:0005937"}],"gene_count":42,"genes_by_uniquename":{"SJAG_00185":null,"SJAG_00279":null,"SJAG_00514":null,"SJAG_00667":null,"SJAG_00677":null,"SJAG_00700":null,"SJAG_00870":null,"SJAG_00938":null,"SJAG_01017":null,"SJAG_01171":null,"SJAG_01215":null,"SJAG_01732":null,"SJAG_01794":null,"SJAG_01888":null,"SJAG_01943":null,"SJAG_01993":null,"SJAG_02169":null,"SJAG_02222":null,"SJAG_02228":null,"SJAG_02351":null,"SJAG_02486":null,"SJAG_02700":null,"SJAG_02718":null,"SJAG_02924":null,"SJAG_03011":null,"SJAG_03145":null,"SJAG_03357":null,"SJAG_03444":null,"SJAG_03453":null,"SJAG_03596":null,"SJAG_03646":null,"SJAG_04001":null,"SJAG_04100":null,"SJAG_04509":null,"SJAG_04703":null,"SJAG_04723":null,"SJAG_04781":null,"SJAG_04887":null,"SJAG_04901":null,"SJAG_04982":null,"SJAG_05001":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"mating projection tip","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"PMID:36148799":null},"synonyms":[{"name":"conjugation tube tip","type":"narrow"},{"name":"shmoo tip","type":"narrow"}],"termid":"GO:0043332","terms_by_termid":{"GO:0043332":null,"GO:0070867":null,"GO:1990819":null}}


id: PBO:0079113
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA splicing endonuclease subunit 15 pseudogene 1","termid":"PBO:0079113"}


id: MONDO:0017930
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with increased bone density (obsolete MONDO:0019703)","termid":"MONDO:0019703"},{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mixed sclerosing bone dystrophy with extra-skeletal manifestations","secondary_identifiers":["GARD:21439","UMLS:C5191052","MEDGEN:1676501","Orphanet:324364"],"termid":"MONDO:0017930","xrefs":{"Monarch":{"xref_id":"0017930"}}}


id: GO:0080188
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A small RNA-based gene silencing process in which small interfering RNAs (siRNAs) guide DNA methylation to the siRNA-generating genomic loci and other loci that are homologous to the siRNAs for de novo DNA methylation. This results in a heterochromatin assembly, a chromatin conformation that is refractory to transcription. In general this process consists of three phases: biogenesis of siRNAs, scaffold RNA production, and the formation of the guiding complex that recruits de novo DNA methyltransferases to the target loci. Transposable elements are silenced by this mechanism.","definition_xrefs":["PMID:33031395","PMID:21420348"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA methylation-dependent constitutive heterochromatin formation","termid":"GO:0006346"},{"relation_name":"is_a","term_name":"siRNA-mediated heterochromatin formation","termid":"GO:0141194"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006325"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0006325"],"is_obsolete":false,"name":"gene silencing by siRNA-directed DNA methylation","synonyms":[{"name":"RNA-directed DNA methylation","type":"related"},{"name":"RdDM","type":"exact"},{"name":"gene silencing by RNA-directed DNA methylation","type":"related"}],"termid":"GO:0080188"}


id: PBO:0078224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 11-2","termid":"PBO:0078224"}


id: GO:0160185
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to and increases the activity of the enzyme phospholipase C.","definition_xrefs":["PMID:28130414"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipase activator activity","termid":"GO:0016004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140677"}],"interesting_parent_ids":["GO:0030234","GO:0003674","GO:0098772","GO:0140677"],"is_obsolete":false,"name":"phospholipase C activator activity","termid":"GO:0160185"}


id: PBO:0084062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase-activating protein (GAP) subunit of the Iml1p/SEACIT complex; SEACIT (Iml1p-Npr2p-Npr3p) is a subcomplex of the SEA complex, a coatomer-related complex that associates dynamically with the vacuole; Iml1p functions in the SEACIT complex as a GAP for the Rag family GTPase Gtr1p (EGOC subunit), resulting in the inhibition of TORC1 signaling in response to amino acid deprivation; the Iml1p/SEACIT complex is required for non-nitrogen-starvation (NNS)-induced autophagy","termid":"PBO:0084062"}


id: GO:0030331
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a nuclear estrogen receptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear receptor binding","termid":"GO:0016922"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"nuclear estrogen receptor binding","synonyms":[{"name":"estrogen receptor binding","type":"broad"}],"termid":"GO:0030331"}


id: MONDO:0008578
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":"toe, rotated fifth","secondary_identifiers":["MEDGEN:348254","OMIM:189150","UMLS:C1861060"],"synonyms":[{"name":"toe, rotated fifth","type":"exact"}],"termid":"MONDO:0008578","xrefs":{"Monarch":{"xref_id":"0008578"}}}


id: MONDO:0020417
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An anatomic abnormality that occurs during embryonic development, in which the aortic arch is right-sided.","definition_xrefs":["NCIT:C103917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aortic arch defects","termid":"MONDO:0015236"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"right aortic arch","secondary_identifiers":["GARD:19640","Orphanet:99081","icd11.foundation:769265824","UMLS:C0035615","MedDRA:10067407","SCTID:111321007","HP:0012020","MEDGEN:48474","ICD10CM:Q25.47"],"synonyms":[{"name":"right aortic arch","type":"exact"},{"name":"right aortic arch (disease)","type":"exact"}],"termid":"MONDO:0020417","xrefs":{"Monarch":{"xref_id":"0020417"}}}


id: GO:0061151
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by the binding of a member of the BMP (bone morphogenetic protein) family to its receptor on the surface of a target cell, which contributes to the segmentation of the renal system.","definition_xrefs":["GOC:yaf","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete BMP signaling pathway involved in renal system segmentation (obsolete GO:0061151)","synonyms":[{"name":"BMP signalling pathway involved in renal system segmentation","type":"exact"}],"termid":"GO:0061151"}


id: MONDO:0001707
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sarcoidosis affecting the tissues of the heart.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-familial restrictive cardiomyopathy","termid":"MONDO:0016345"},{"relation_name":"is_a","term_name":"sarcoidosis","termid":"MONDO:0019338"}],"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":"cardiac sarcoidosis","secondary_identifiers":["MEDGEN:140260","NCIT:C35589","SCTID:75403004","UMLS:C0392077","DOID:13405"],"synonyms":[{"name":"heart sarcoidosis","type":"exact"},{"name":"sarcoidosis of heart","type":"exact"}],"termid":"MONDO:0001707","xrefs":{"Monarch":{"xref_id":"0001707"}}}


id: PBO:0041866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase 12 (gene/pseudogene)","termid":"PBO:0041866"}


id: MONDO:0015596
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Non-herpetic acute limbic encephalitis is a rare neuroinflammatory/neuroautoimmune disease characterized by an acute (or subacute) onset of disturbance of consciousness (occasionally presenting as convulsions) and high fever, associated with cerebral lesions (on magnetic resonance imaging) that are restricted to the limbic system (particularly the hippocampi and amygdalae), in the absence of viral, bacterial, fungal, paraneoplastic and other disorders.","definition_xrefs":["Orphanet:163924"],"direct_ancestors":[{"relation_name":"is_a","term_name":"limbic encephalitis","termid":"MONDO:0015588"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-herpetic acute limbic encephalitis","secondary_identifiers":["UMLS:C4707262","MEDGEN:1646654","SCTID:764998005"],"termid":"MONDO:0015596","xrefs":{"Monarch":{"xref_id":"0015596"}}}


id: PBO:0004234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,2-mannosyltransferase Omh1","termid":"PBO:0004234"}


id: PBO:0040017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"armadillo repeat containing 6","termid":"PBO:0040017"}


id: FYPO:0000331
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 histone acetylation occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone acetylation during vegetative growth","termid":"FYPO:0000456"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0002274","FYPO:0002494"],"is_obsolete":false,"name":"decreased histone acetylation during vegetative growth","synonyms":[{"name":"decreased histone acetylation during mitotic cell cycle","type":"related"},{"name":"reduced histone acetylation during vegetative growth","type":"exact"}],"termid":"FYPO:0000331"}


id: PBO:0080742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XPA binding protein 2","termid":"PBO:0080742"}


id: PBO:0062923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P2Y receptor family member 10B, pseudogene","termid":"PBO:0062923"}


id: PBO:0077668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF receptor superfamily member 13C","termid":"PBO:0077668"}


id: PBO:0071238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 79","termid":"PBO:0071238"}


id: GO:0035045
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The gradual disintegration of the sperm plasma membrane following insemination. This process is seen in Drosophila after entry of the entire sperm, surrounded by its plasma membrane, into the egg.","definition_xrefs":["ISBN:0879694238","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane organization","termid":"GO:0007009"},{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"is_a","term_name":"membrane disassembly","termid":"GO:0030397"},{"relation_name":"part_of","term_name":"single fertilization","termid":"GO:0007338"}],"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":"sperm plasma membrane disassembly","synonyms":[{"name":"sperm plasma membrane breakdown","type":"exact"},{"name":"sperm plasma membrane catabolism","type":"exact"},{"name":"sperm plasma membrane degradation","type":"exact"}],"termid":"GO:0035045"}


id: PBO:0079568
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin B","termid":"PBO:0079568"}


id: GO:0008319
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 prenyl protein specific endopeptidase activity (obsolete GO:0008319)","synonyms":[{"name":"prenyl protein specific endopeptidase activity","type":"exact"}],"termid":"GO:0008319"}


id: PBO:0044426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 3 subfamily A member 52, pseudogene","termid":"PBO:0044426"}


id: GO:0021943
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of scaffolds from a radial glial cell. The scaffolds are used as a substrate for the radial migration of cells.","definition_xrefs":["GOC:jid","GOC:cls","GOC:dgh","GO_REF:0000021","GOC:dph","PMID:15157725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell morphogenesis","termid":"GO:0000902"},{"relation_name":"part_of","term_name":"hindbrain radial glia guided cell migration","termid":"GO:0021932"}],"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 radial glial scaffolds","synonyms":[{"name":"Bergmann fiber biosynthesis","type":"related"},{"name":"Bergmann fiber formation","type":"related"}],"termid":"GO:0021943"}


id: FYECO:0000039
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which P-factor was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"+ mating pheromone","termid":"FYECO:0000058"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ P-factor","synonyms":[{"name":"P factor added","type":"exact"}],"termid":"FYECO:0000039"}


id: PBO:0057092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 188","termid":"PBO:0057092"}


id: PR:Q12381
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pre-mRNA-processing factor 6 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11246:SF1","PRO:DNx","OMA:SCHPO03357"],"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":"pre-mRNA-splicing factor prp1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC6B1.07","secondary_identifiers":["UniProtKB:Q12381"],"synonyms":[{"name":"Spom972h-PRPF6","type":"exact"}],"termid":"PR:Q12381"}


id: PBO:0088890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine/serine/threonine phosphatase","termid":"PBO:0088890"}


id: PBO:0002831
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protease S. Pombe","termid":"PBO:0002831"}


id: GO:0060008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized structural and/or functional features of a Sertoli cell. A Sertoli cell is a supporting cell projecting inward from the basement membrane of seminiferous tubules.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"epithelial cell differentiation","termid":"GO:0030855"},{"relation_name":"part_of","term_name":"male gonad development","termid":"GO:0008584"}],"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":"Sertoli cell differentiation","termid":"GO:0060008"}


id: GO:0098700
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The active transport of neurotransmitters into a synaptic vesicle. This import is fuelled by an electrochemical gradient across the vesicle membrane, established by the action of proton pumps.","definition_xrefs":["GOC:bf","PMID:10099709","GOC:PARL","PMID:15217342","GOC:pad"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurotransmitter transport","termid":"GO:0006836"},{"relation_name":"is_a","term_name":"establishment of localization in cell","termid":"GO:0051649"},{"relation_name":"part_of","term_name":"synaptic vesicle cycle","termid":"GO:0099504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"neurotransmitter loading into synaptic vesicle","synonyms":[{"name":"neurotransmitter import into synaptic vesicle","type":"exact"},{"name":"neurotransmitter uptake into synaptic vesicle","type":"exact"},{"name":"synaptic vesicle neurotransmitter loading","type":"exact"}],"termid":"GO:0098700"}


id: MONDO:0100184
data:
  {"annotated_genes":["SJAG_03275"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007495"},{"annotations":[87205],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100186"}]},"cv_name":"mondo","definition":"A disease characterized by a deficiency in GTP cyclohydrolase I, which leads to a consequent reduction in BH4 and reduces the activity of three BH4-cofactor dependent enzymes - phenylalanine hydroxylase, tyrosine hydroxylase, and tryptophan hydroxylase. GTP cyclohydrolase I deficiency encompasses a spectrum of disease that includes autosomal dominant and autosomal recessive forms, with severity correlating with the residual enzyme activity. Individuals who are heterozygous for pathogenic variants in GCH1 have symptoms ranging from none (due to reduced penetrance) to dopa-responsive dystonia, which is the most common presentation in symptomatic cases, to rarer neurological presentations such as adult-onset \\\"benign\\\" parkinsonism, various types of focal dystonia, and symptoms simulating cerebral palsy or spastic paraplegia. Hyperphenylalaninemia is absent, and patients respond well to treatment with levodopa. Individuals who are homozygous or compound heterozygous for pathogenic variants in GCH1 typically present with hyperphenylalaninemia, often identified by newborn screening, and severe neurological features and due to very low or undetectable enzyme activity. Treatment with levodopa, BH4, and 5-hydroxytryptophan can improve the symptoms but does not prevent development of severe encephalopathy. Rare cases of GTP cyclohydrolase I deficiency with a phenotype that is intermediate in severity between dopa-responsive dystonia and the severe autosomal recessive form have also been described, supporting the existence a phenotypic spectrum of disease.","definition_xrefs":["PMID:20818608","PMID:22729819","PMID:18044725","PMID:19332422","PMID:29471552","PMID:9566389","PMID:9667588","PMID:19234759","PMID:20842687","PMID:18276179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tetrahydrobiopterin metabolic process disease","termid":"MONDO:0045014"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03275":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"GTP cyclohydrolase I deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:75683","UMLS:C0268467"],"synonyms":[{"name":"GTP cyclohydrolase I deficiency","type":"exact"},{"name":"GTP-cyclohydrolase I deficiency","type":"exact"}],"termid":"MONDO:0100184","terms_by_termid":{"MONDO:0007495":null,"MONDO:0100186":null},"xrefs":{"Monarch":{"xref_id":"0100184"}}}


id: PBO:0057653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1245b","termid":"PBO:0057653"}


id: PBO:0060863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIMA related kinase 6","termid":"PBO:0060863"}


id: SO:0002187
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An insertion of sequence from the HERV family of mobile elements with respect to a reference.","definition_xrefs":["NCBI:th"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"Endogenous_Retrovirus_LTR_retrotransposon","termid":"SO:0002268"},{"relation_name":"is_a","term_name":"mobile_element_insertion","termid":"SO:0001837"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HERV_insertion","synonyms":[{"name":"HERV insertion","type":"exact"}],"termid":"SO:0002187"}


id: GO:0021969
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the migration of an axon growth cone of a pyramidal cell that is part of the corticospinal tract is directed after exiting the internal capsule through the cerebral peduncle in response to a combination of attractive and repulsive cues.","definition_xrefs":["GOC:cls","GO_REF:0000021","GOC:dgh","GOC:dph","GOC:jid","PMID:9878731"],"direct_ancestors":[{"relation_name":"is_a","term_name":"axon guidance","termid":"GO:0007411"},{"relation_name":"part_of","term_name":"corticospinal neuron axon guidance","termid":"GO:0021966"}],"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":"corticospinal neuron axon guidance through the cerebral peduncle","synonyms":[{"name":"corticospinal neuron axon pathfinding through the cerebral peduncle","type":"exact"}],"termid":"GO:0021969"}


id: GO:0100019
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that regulates cAMP-mediated signaling.","definition_xrefs":["GOC:obol","GOC:cjm"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cAMP-mediated signaling by transcription from RNA polymerase II promoter (obsolete GO:0100019)","termid":"GO:0100019"}


id: PBO:0041161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basic transcription factor 3 pseudogene 16","termid":"PBO:0041161"}


id: GO:0140865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by interleukin-22 binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:34755534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"interleukin-22-mediated signaling pathway","synonyms":[{"name":"IL-22-mediated signaling pathway","type":"exact"},{"name":"interleukin-22-mediated signalling pathway","type":"exact"}],"termid":"GO:0140865"}


id: GO:0099043
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Formation of a macromolecular complex during clathrin-dependent endocytosis that connects the assembling clathrin coat to the proteins and/or lipoproteins to be transported in an endocytic vesicle. This complex includes a receptor and an adaptor protein that links the receptor to the clathrin coat.","definition_xrefs":["GOC:dos","GOC:lb","PMID:21779028","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin-coated vesicle cargo loading","termid":"GO:0035652"},{"relation_name":"part_of","term_name":"clathrin-dependent endocytosis","termid":"GO:0072583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0051179","GO:0016192","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"cargo loading involved in clathrin-dependent endocytosis","termid":"GO:0099043"}


id: MONDO:0009645
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chronic mucocutaneous candidiasis","termid":"MONDO:0015279"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"chronic mucocutaneous candidiasis due to monocyte chemotactic disorder","secondary_identifiers":["UMLS:C1854982","GARD:15203","MEDGEN:343238","MESH:C565371","OMIM:252250"],"synonyms":[{"name":"monocyte chemotactic disorder","type":"exact"}],"termid":"MONDO:0009645","xrefs":{"Monarch":{"xref_id":"0009645"}}}


id: PBO:0052560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kynurenine 3-monooxygenase","termid":"PBO:0052560"}


id: PBO:0070626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 like 1 pseudogene 10","termid":"PBO:0070626"}


id: PBO:0034388
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_pseudoparalogy_relationship_with","termid":"PBO:0034388"}


id: GO:2000655
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cellular response to testosterone stimulus.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of cellular response to testosterone stimulus","termid":"GO:2000654"},{"relation_name":"negatively_regulates","term_name":"cellular response to testosterone stimulus","termid":"GO:0071394"}],"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 cellular response to testosterone stimulus","termid":"GO:2000655"}


id: PBO:0079530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-yW synthesizing protein 5","termid":"PBO:0079530"}


id: PBO:0029117
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cell_cycle_process","termid":"PBO:0029117"}


id: GO:0099514
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of synaptic vesicles along cytoskeletal fibers such as microfilaments or microtubules within a cell, powered by molecular motors.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synaptic vesicle transport","termid":"GO:0048489"},{"relation_name":"is_a","term_name":"vesicle cytoskeletal trafficking","termid":"GO:0099518"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"synaptic vesicle cytoskeletal transport","termid":"GO:0099514"}


id: PBO:0040223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATE1 opposite strand, pseudogene","termid":"PBO:0040223"}


id: GO:1901256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of macrophage colony-stimulating factor production.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"macrophage colony-stimulating factor production","termid":"GO:0036301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of macrophage colony-stimulating factor production","synonyms":[{"name":"regulation of M-CSF production","type":"exact"}],"termid":"GO:1901256"}


id: PBO:0082780
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the SWR1 complex; complex exchanges histone variant H2AZ (Htz1p) for chromatin-bound histone H2A; protein abundance increases in response to DNA replication stress; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0082780"}


id: SO:0002364
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that codes for mitochondrial LSU rRNA.","direct_ancestors":[{"relation_name":"is_a","term_name":"mt_rRNA_gene","termid":"SO:0002363"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mt_LSU_rRNA_gene","synonyms":[{"name":"mitochondrial large subunit rRNA gene","type":"exact"},{"name":"rRNA 21S gene","type":"exact"},{"name":"rRNA_21S_gene","type":"exact"}],"termid":"SO:0002364"}


id: GO:0004397
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-histidine = urocanate + NH3.","definition_xrefs":["EC:4.3.1.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ammonia-lyase activity","termid":"GO:0016841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"histidine ammonia-lyase activity","secondary_identifiers":["MetaCyc:HISTIDINE-AMMONIA-LYASE-RXN","Reactome:R-HSA-70899","RHEA:21232"],"synonyms":[{"name":"L-histidine ammonia-lyase (urocanate-forming)","type":"related"},{"name":"L-histidine ammonia-lyase activity","type":"related"},{"name":"histidase activity","type":"related"},{"name":"histidinase activity","type":"related"},{"name":"histidine alpha-deaminase activity","type":"related"}],"termid":"GO:0004397"}


id: GO:0018109
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The phosphorylation of peptidyl-arginine to form omega-N-phospho-L-arginine.","definition_xrefs":["RESID:AA0222"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein phosphorylation","termid":"GO:0006468"},{"relation_name":"is_a","term_name":"peptidyl-arginine modification","termid":"GO:0018195"}],"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":"peptidyl-arginine phosphorylation","termid":"GO:0018109"}


id: PBO:0004609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Dbp2","termid":"PBO:0004609"}


id: PBO:0043946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crystallin beta A1","termid":"PBO:0043946"}


id: GO:1904529
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of actin filament binding.","definition_xrefs":["PMID:24520051","GOC:als","GOC:TermGenie","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of actin filament binding (obsolete GO:1904529)","synonyms":[{"name":"regulation of F-actin binding","type":"exact"},{"name":"regulation of actin cross-linking activity","type":"related"}],"termid":"GO:1904529"}


id: MONDO:0000690
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Preoccupations with appearance or self-image causing significant distress or impairment in important areas of functioning.","definition_xrefs":["MESH:D057215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatoform disorder","termid":"MONDO:0003117"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"body dysmorphic disorder","secondary_identifiers":["DOID:0060163","ICD10CM:F45.22","icd11.foundation:731724655","UMLS:C0005887","MEDGEN:2302","SCTID:83482000"],"synonyms":[{"name":"body dysmorphia","type":"exact"},{"name":"dysmorphic syndrome","type":"exact"},{"name":"dysmorphophobia","type":"exact"}],"termid":"MONDO:0000690","xrefs":{"Monarch":{"xref_id":"0000690"}}}


id: MONDO:0005187
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infectious process caused by the human herpesvirus 8. This infection is associated with Kaposi sarcoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human herpesvirus 8 infection","secondary_identifiers":["NCIT:C39291","UMLS:C1512508","EFO:0002612","MEDGEN:268211"],"synonyms":[{"name":"HHV8 infection","type":"exact"},{"name":"Human Herpes Virus 8 infection","type":"exact"},{"name":"Human Herpesvirus 8 infection","type":"exact"}],"termid":"MONDO:0005187","xrefs":{"Monarch":{"xref_id":"0005187"}}}


id: GO:0048796
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for a swim bladder to attain its fully functional state. The swim bladder is used by some fishes to maintain buoyancy and may function in addition as a sound producing organ, a sound receptor, and a respiratory organ.","definition_xrefs":["GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ maturation","termid":"GO:0048799"},{"relation_name":"part_of","term_name":"swim bladder development","termid":"GO:0048794"}],"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":"swim bladder maturation","synonyms":[{"name":"gas bladder maturation","type":"exact"}],"termid":"GO:0048796"}


id: GO:1900859
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of brevianamide F biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:di"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of brevianamide F biosynthetic process (obsolete GO:1900859)","synonyms":[{"name":"down regulation of brevianamide F biosynthetic process","type":"exact"},{"name":"down-regulation of brevianamide F biosynthetic process","type":"exact"},{"name":"downregulation of brevianamide F biosynthetic process","type":"exact"}],"termid":"GO:1900859"}


id: MONDO:0044314
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"retinitis pigmentosa 78","secondary_identifiers":["UMLS:C4479481","GARD:16229","MEDGEN:1378790","OMIM:617433"],"synonyms":[{"name":"RP78","type":"related"},{"name":"retinitis pigmentosa 78","type":"exact"}],"termid":"MONDO:0044314","xrefs":{"Monarch":{"xref_id":"0044314"}}}


id: PBO:0091760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pdc2-Repressed lncRNA, antisense to Mat1-Mi","termid":"PBO:0091760"}


id: PR:000085734
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3.3, initiator methionine removed form (Schizosaccharomyces pombe) that has been phosphorylated on Ser-10. UniProtKB:P10651, 2-136, Ser-11, MOD:00046.","definition_xrefs":["PomBase:VW","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fungal histone H3.3, initiator methionine removed form (Schizosaccharomyces pombe)","termid":"PR:000027598"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hht3/Phos(S10)","pombase_gene_id":"SPBC1105.11c","synonyms":[{"name":"PRO_0000221367, Ser-11, MOD:00046","type":"exact"},{"name":"PomBase_original_PRO_term_name: histone H3.3, initiator methionine removed phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-hht3/InitMet-/Phos:1","type":"exact"},{"name":"UniProtKB:P10651, 2-136, Ser-11, MOD:00046","type":"exact"},{"name":"hht3/Phos(S10)","type":"exact"}],"termid":"PR:000085734"}


id: PBO:0073644
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sialic acid binding Ig like lectin 31, pseudogene","termid":"PBO:0073644"}


id: GO:0061073
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the ciliary body generated and organized. The ciliary body is the circumferential tissue inside the eye composed of the ciliary muscle and ciliary processes.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"camera-type eye morphogenesis","termid":"GO:0048593"}],"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":"ciliary body morphogenesis","termid":"GO:0061073"}


id: PBO:0005201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinetochore protein Mis16","termid":"PBO:0005201"}


id: MONDO:0005871
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections caused by nematode larvae which never develop into the adult stage and migrate through various body tissues. They commonly infect the skin, eyes, and viscera in humans. Ancylostoma brasiliensis causes cutaneous larva migrans. Toxocara causes visceral larva migrans.","definition_xrefs":["MESH:D007815"],"direct_ancestors":[{"relation_name":"is_a","term_name":"helminthiasis","termid":"MONDO:0004664"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nematoda infectious disease","secondary_identifiers":["UMLS:C0027583","EFO:0007391","MEDGEN:45025","MONDO:0021556","MESH:D009349","SCTID:84706005"],"synonyms":[{"name":"Disease due to Nematoda","type":"related"},{"name":"Infection, Nematode","type":"related"},{"name":"Infections, Nematode","type":"related"},{"name":"Nematoda caused disease or disorder","type":"exact"},{"name":"Nematoda disease or disorder","type":"exact"},{"name":"Nematode Infection","type":"related"},{"name":"Nematode Infections","type":"related"},{"name":"Nematode infection","type":"related"},{"name":"Nematodiasis","type":"related"},{"name":"disease due to nematoda","type":"exact"},{"name":"nematode infection","type":"related"},{"name":"nematodiasis","type":"related"}],"termid":"MONDO:0005871","xrefs":{"Monarch":{"xref_id":"0005871"}}}


id: PBO:0062417
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 53 pseudogene","termid":"PBO:0062417"}


id: GO:0090238
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of arachidonic acid secretion, the controlled release of arachidonic acid from a cell or a tissue.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of icosanoid secretion","termid":"GO:0032305"},{"relation_name":"is_a","term_name":"regulation of arachidonate secretion","termid":"GO:0090237"},{"relation_name":"positively_regulates","term_name":"arachidonate secretion","termid":"GO:0050482"}],"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 arachidonate secretion","synonyms":[{"name":"positive regulation of arachidonic acid secretion","type":"exact"}],"termid":"GO:0090238"}


id: GO:0002436
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of immune complex clearance by monocytes or macrophages.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune complex clearance","termid":"GO:0002434"}],"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":"immune complex clearance by monocytes and macrophages","termid":"GO:0002436"}


id: PBO:0044698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 3 pseudogene 1","termid":"PBO:0044698"}


id: SO:0000079
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript that is dicistronic.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"dicistronic","termid":"SO:0000879"},{"relation_name":"is_a","term_name":"polycistronic_transcript","termid":"SO:0000078"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dicistronic_transcript","synonyms":[{"name":"dicistronic transcript","type":"exact"}],"termid":"SO:0000079"}


id: PBO:0031427
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_glycerol_dehydrogenase_activity","termid":"PBO:0031427"}


id: PBO:0054885
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 2299","termid":"PBO:0054885"}


id: MONDO:0008444
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":"spastic paraplegia, optic atrophy, and dementia","secondary_identifiers":["MESH:C566679","MEDGEN:356630","OMIM:182830","UMLS:C1866849"],"synonyms":[{"name":"spastic paraplegia, optic atrophy, and dementia","type":"exact"}],"termid":"MONDO:0008444","xrefs":{"Monarch":{"xref_id":"0008444"}}}


id: PR:000050491
data:
  {"annotation_feature_type":"gene","cv_name":"protein","direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"division mal foutue 1 protein (Schizosaccharomyces pombe)","pombase_gene_id":"SPCC4B3.15","termid":"PR:000050491"}


id: PBO:0029935
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,_multiple_cell_divisions,_spheroid_cell","termid":"PBO:0029935"}


id: FYPO:0003775
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of DNA recombination between cDNAs derived from transposon-encoded genes is decreased.","definition_xrefs":["PomBase:mah","PMID:10022921"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased DNA recombination","termid":"FYPO:0002712"}],"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":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased transposon-derived cDNA recombination","synonyms":[{"name":"decreased recombination of transposon-derived cDNAs","type":"exact"},{"name":"decreased transposon-derived cDNA recombination frequency","type":"exact"},{"name":"decreased transposon-derived cDNA recombination rate","type":"related"},{"name":"reduced transposon-derived cDNA recombination","type":"exact"}],"termid":"FYPO:0003775"}


id: GO:1900648
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of chanoclavine-I aldehyde biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chanoclavine-I aldehyde biosynthetic process","termid":"GO:1900646"},{"relation_name":"is_a","term_name":"positive regulation of ergot alkaloid biosynthetic process","termid":"GO:1900824"},{"relation_name":"positively_regulates","term_name":"chanoclavine-I aldehyde biosynthetic process","termid":"GO:1900569"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"positive regulation of chanoclavine-I aldehyde biosynthetic process","synonyms":[{"name":"activation of chanoclavine-I aldehyde biosynthesis","type":"exact"},{"name":"activation of chanoclavine-I aldehyde biosynthetic process","type":"narrow"},{"name":"activation of chanoclavine-I aldehyde formation","type":"exact"},{"name":"activation of chanoclavine-I aldehyde synthesis","type":"exact"},{"name":"positive regulation of chanoclavine-I aldehyde anabolism","type":"exact"},{"name":"positive regulation of chanoclavine-I aldehyde biosynthesis","type":"exact"},{"name":"positive regulation of chanoclavine-I aldehyde formation","type":"exact"},{"name":"activation of chanoclavine-I aldehyde anabolism","type":"exact"},{"name":"positive regulation of chanoclavine-I aldehyde synthesis","type":"exact"},{"name":"up regulation of chanoclavine-I aldehyde anabolism","type":"exact"},{"name":"up regulation of chanoclavine-I aldehyde biosynthesis","type":"exact"},{"name":"up regulation of chanoclavine-I aldehyde biosynthetic process","type":"exact"},{"name":"up regulation of chanoclavine-I aldehyde formation","type":"exact"},{"name":"up regulation of chanoclavine-I aldehyde synthesis","type":"exact"},{"name":"up-regulation of chanoclavine-I aldehyde anabolism","type":"exact"},{"name":"up-regulation of chanoclavine-I aldehyde biosynthesis","type":"exact"},{"name":"up-regulation of chanoclavine-I aldehyde biosynthetic process","type":"exact"},{"name":"up-regulation of chanoclavine-I aldehyde formation","type":"exact"},{"name":"up-regulation of chanoclavine-I aldehyde synthesis","type":"exact"},{"name":"upregulation of chanoclavine-I aldehyde anabolism","type":"exact"},{"name":"upregulation of chanoclavine-I aldehyde biosynthesis","type":"exact"},{"name":"upregulation of chanoclavine-I aldehyde biosynthetic process","type":"exact"},{"name":"upregulation of chanoclavine-I aldehyde formation","type":"exact"},{"name":"upregulation of chanoclavine-I aldehyde synthesis","type":"exact"}],"termid":"GO:1900648"}


id: MONDO:0009278
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency (obsolete MONDO:0009278)","secondary_identifiers":["NANDO:2200516"],"synonyms":[{"name":"SCHAD deficiency, formerly","type":"related"}],"termid":"MONDO:0009278","xrefs":{"Monarch":{"xref_id":"0009278"}}}


id: PBO:0056234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGI2 antisense RNA 1","termid":"PBO:0056234"}


id: PBO:0049507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A clustered histone 14","termid":"PBO:0049507"}


id: PBO:0066293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein Y-linked family 2 member U, pseudogene","termid":"PBO:0066293"}


id: GO:0055120
data:
  {"annotated_genes":["SJAG_02396"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[72119],"is_not":false,"summary":null,"term":"GO:0055120"}]},"cv_name":"cellular_component","definition":"A vinculin-containing myofibril attachment structure of striated muscle that connects sarcomeres to the extracellular matrix. In nematode body wall muscle, the dense body performs the dual role of Z-disk and costamere.","definition_xrefs":["PMID:17492481","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"contractile muscle fiber","termid":"GO:0043292"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02396":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"striated muscle dense body","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0055120","terms_by_termid":{"GO:0055120":null}}


id: SO:0001594
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant which causes a disruption of the translational reading frame, by shifting one base backward.","direct_ancestors":[{"relation_name":"is_a","term_name":"frameshift_variant","termid":"SO:0001589"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plus_1_frameshift_variant","synonyms":[{"name":"+1 frameshift variant","type":"exact"},{"name":"plus 1 frameshift variant","type":"exact"}],"termid":"SO:0001594"}


id: MONDO:0014513
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any nemaline myopathy in which the cause of the disease is a mutation in the LMOD3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"severe congenital nemaline myopathy","termid":"MONDO:0015735"},{"relation_name":"is_a","term_name":"typical nemaline myopathy","termid":"MONDO:0015737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"nemaline myopathy 10","secondary_identifiers":["OMIM:616165","GARD:16066","MEDGEN:863797","DOID:0110931","UMLS:C4015360"],"synonyms":[{"name":"LMOD3 nemaline myopathy","type":"exact"},{"name":"NEM10","type":"exact"},{"name":"nemaline myopathy 10","type":"exact"},{"name":"nemaline myopathy caused by mutation in LMOD3","type":"exact"},{"name":"nemaline myopathy type 10","type":"exact"}],"termid":"MONDO:0014513","xrefs":{"Monarch":{"xref_id":"0014513"}}}


id: PBO:0117206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane sulfite efflux transmembrane transporter Ssu1","termid":"PBO:0117206"}


id: PBO:0069571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 843, pseudogene","termid":"PBO:0069571"}


id: PBO:0050040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major histocompatibility complex, class II, DR beta 8 (pseudogene)","termid":"PBO:0050040"}


id: MONDO:1011857
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":"progressive cerebellar abiotrophy, non-human animal","secondary_identifiers":["OMIA:000826"],"termid":"MONDO:1011857","xrefs":{"Monarch":{"xref_id":"1011857"}}}


id: PR:Q10324
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sec3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10324"],"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 C17G8.12 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G8.12","synonyms":[{"name":"Spom972h-sec3","type":"exact"}],"termid":"PR:Q10324"}


id: PBO:0086374
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative aryl-alcohol dehydrogenase; similar to P. chrysosporium aryl-alcohol dehydrogenase; mutational analysis has not yet revealed a physiological role; AAD3 has a paralog, AAD15, that arose from a segmental duplication; members of the AAD gene family comprise three pairs (AAD3 + AAD15, AAD6/AAD16 + AAD4, AAD10 + AAD14) whose two genes are more related to one another than to other members of the family","termid":"PBO:0086374"}


id: GO:0006616
data:
  {"annotated_genes":["SJAG_00064","SJAG_00959","SJAG_02330","SJAG_02208","SJAG_04129","SJAG_03684"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74957,75366,77296,99865,104406,110154],"is_not":false,"summary":null,"term":"GO:0006616"}]},"cv_name":"biological_process","definition":"The process during cotranslational membrane targeting wherein proteins move across a membrane. SRP and its receptor initiate the transfer of the nascent chain across the endoplasmic reticulum (ER) membrane; they then dissociate from the chain, which is transferred to a set of transmembrane proteins, collectively called the translocon. Once the nascent chain translocon complex is assembled, the elongating chain passes directly from the large ribosomal subunit into the centers of the translocon, a protein-lined channel within the membrane. The growing chain is never exposed to the cytosol and does not fold until it reaches the ER lumen.","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein transmembrane transport","termid":"GO:0065002"},{"relation_name":"part_of","term_name":"SRP-dependent cotranslational protein targeting to membrane","termid":"GO:0006614"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00064":null,"SJAG_00959":null,"SJAG_02208":null,"SJAG_02330":null,"SJAG_03684":null,"SJAG_04129":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"part_of","termid":"GO:0006605"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150","GO:0055085","GO:0006605"],"is_obsolete":false,"name":"SRP-dependent cotranslational protein targeting to membrane, translocation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"ER translocation","type":"broad"},{"name":"SRP-dependent cotranslational membrane targeting, translocation","type":"exact"},{"name":"SRP-dependent cotranslational protein-membrane targeting, translocation","type":"exact"},{"name":"translocation during SRP-dependent cotranslational protein targeting to membrane","type":"exact"}],"termid":"GO:0006616","terms_by_termid":{"GO:0006616":null}}


id: MONDO:1012418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"anal furunculosis, non-human animal","termid":"MONDO:1011665"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anal furunculosis, dog","secondary_identifiers":["OMIA:001589-9615"],"termid":"MONDO:1012418","xrefs":{"Monarch":{"xref_id":"1012418"}}}


id: PBO:0069957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1250, pseudogene","termid":"PBO:0069957"}


id: PR:O74484
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A mannose-1-phosphate guanyltransferase beta that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR22572:SF15","OMA:SCHPO04907","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":"mannose-1-phosphate guanyltransferase beta (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1906.01","secondary_identifiers":["UniProtKB:O74484"],"synonyms":[{"name":"GDP-mannose pyrophosphorylase (Schizosaccharomyces pombe 972h-)","type":"broad"},{"name":"GTP-mannose-1-phosphate guanylyltransferase (Schizosaccharomyces pombe 972h-)","type":"broad"},{"name":"SPCC1906.01","type":"related"},{"name":"Spom972h-GMPPB","type":"exact"}],"termid":"PR:O74484"}


id: GO:0090728
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases brood size. Brood size is the number of progeny that survive embryogenesis and are cared for at one time.","definition_xrefs":["GOC:rz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological regulation","termid":"GO:0065007"}],"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 brood size","termid":"GO:0090728"}


id: PBO:0066983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 286","termid":"PBO:0066983"}


id: GO:0035419
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that initiates the activity of the inactive enzyme MAP kinase in the context of an innate immune response, a defense response mediated by germline encoded components that directly recognize components of potential pathogens.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of MAPK activity involved in innate immune response (obsolete GO:0035419)","termid":"GO:0035419"}


id: FYPO:0003460
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 trehalose measured in a cell is lower than normal when the cell is subject to oxidative stress.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased level of substance in cell during vegetative growth","termid":"FYPO:0001329"},{"relation_name":"is_a","term_name":"decreased cellular trehalose level","termid":"FYPO:0001447"}],"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:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased cellular trehalose level during cellular response to oxidative stress","synonyms":[{"name":"decreased cellular trehalose level during cellular response to oxidative stress during mitotic cell cycle","type":"related"},{"name":"decreased cellular trehalose level during oxidative stress response","type":"exact"},{"name":"decreased cellular trehalose level during vegetative growth and during cellular response to oxidative stress","type":"exact"},{"name":"decreased cellular trehalose level in response to oxidative stress","type":"exact"},{"name":"decreased trehalose accumulation during cellular response to oxidative stress","type":"related"},{"name":"reduced cellular trehalose level during cellular response to oxidative stress","type":"exact"}],"termid":"FYPO:0003460"}


id: PBO:0089695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar CorA family magnesium ion transmembrane transporter Mnr2","termid":"PBO:0089695"}


id: PBO:0064497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit A","termid":"PBO:0064497"}


id: PBO:0056540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MCF.2 cell line derived transforming sequence","termid":"PBO:0056540"}


id: GO:1900598
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of demethylkotanin.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary metabolite catabolic process","termid":"GO:0090487"},{"relation_name":"is_a","term_name":"demethylkotanin metabolic process","termid":"GO:1900597"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"demethylkotanin catabolic process","synonyms":[{"name":"demethylkotanin breakdown","type":"exact"},{"name":"demethylkotanin catabolism","type":"exact"},{"name":"demethylkotanin degradation","type":"exact"}],"termid":"GO:1900598"}


id: GO:0072016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a glomerular parietal epithelial cell over time, from its formation to the mature structure. Glomerular parietal epithelial cells are specialized epithelial cells that form tight junctions as a barrier to protein transport.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular epithelial cell development","termid":"GO:0072310"},{"relation_name":"part_of","term_name":"glomerular parietal epithelial cell differentiation","termid":"GO:0072139"}],"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":"glomerular parietal epithelial cell development","synonyms":[{"name":"Bowman's capsule development","type":"exact"}],"termid":"GO:0072016"}


id: MONDO:0003221
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sclerosing hemangioma (obsolete MONDO:0003221)","termid":"MONDO:0003221","xrefs":{"Monarch":{"xref_id":"0003221"}}}


id: GO:0140140
data:
  {"annotated_genes":["SJAG_00760"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117011],"is_not":false,"summary":null,"term":"GO:0140140"}]},"cv_name":"biological_process","definition":"The process in which a guanine nucleotide is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["GOC:vw","PMID:14998997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"guanine transmembrane transport","termid":"GO:1903716"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00760":null},"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:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"mitochondrial guanine nucleotide transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140140","terms_by_termid":{"GO:0140140":null}}


id: PR:Q9UUK3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An OTU domain-containing protein 6B 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":"ubiquitin thioesterase otu2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1952.03","secondary_identifiers":["UniProtKB:Q9UUK3"],"synonyms":[{"name":"OTU domain-containing protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAC1952.03","type":"related"},{"name":"Spom972h-OTUD6B","type":"exact"}],"termid":"PR:Q9UUK3"}


id: GO:0010672
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 as part of the meiotic cell cycle.","definition_xrefs":["GOC:tb","PMID:12161753","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter involved in meiotic cell cycle (obsolete GO:0010672)","synonyms":[{"name":"regulation of meiosis by regulation of transcription from RNA polymerase II promoter","type":"narrow"},{"name":"regulation of transcription from RNA polymerase II promoter, meiotic","type":"exact"}],"termid":"GO:0010672"}


id: GO:0009863
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals mediated by salicylic acid.","definition_xrefs":["GOC:jy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signal transduction","termid":"GO:0007165"},{"relation_name":"part_of","term_name":"cellular response to salicylic acid stimulus","termid":"GO:0071446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"salicylic acid mediated signaling pathway","synonyms":[{"name":"salicylic acid mediated signal transduction","type":"exact"},{"name":"salicylic acid mediated signalling pathway","type":"exact"},{"name":"salicylic acid-mediated signaling pathway","type":"exact"}],"termid":"GO:0009863"}


id: PBO:0000797
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"named from map position, met5","termid":"PBO:0000797"}


id: PBO:0046925
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 43 member A","termid":"PBO:0046925"}


id: PBO:0072337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 23","termid":"PBO:0072337"}


id: PBO:0052964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L1 cell adhesion molecule","termid":"PBO:0052964"}


id: MONDO:0013243
data:
  {"annotated_genes":["SJAG_02919","SJAG_04567","SJAG_03815"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88101,88102,88103],"is_not":false,"summary":null,"term":"MONDO:0013243"}]},"cv_name":"mondo","definition":"Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the HSPB3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"distal hereditary motor neuropathy type 2","termid":"MONDO:0015352"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02919":null,"SJAG_03815":null,"SJAG_04567":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005244","MONDO:0000426"],"is_obsolete":false,"name":"neuronopathy, distal hereditary motor, type 2C","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3150619","DOID:0111209","MEDGEN:461969","OMIM:613376","GARD:18264"],"synonyms":[{"name":"HMN 2C","type":"related"},{"name":"HMN2C","type":"related"},{"name":"HSPB3 neuronopathy, distal hereditary motor","type":"exact"},{"name":"neuronopathy, distal hereditary motor caused by mutation in HSPB3","type":"exact"},{"name":"neuronopathy, distal hereditary motor, type IIC","type":"related"},{"name":"neuropathy, distal hereditary motor, type 2C","type":"related"}],"termid":"MONDO:0013243","terms_by_termid":{"MONDO:0013243":null},"xrefs":{"Monarch":{"xref_id":"0013243"}}}


id: MONDO:0003065
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that arises from the ciliated respiratory mucosa that lines the nasal cavity. It results from the invagination and proliferation of epithelial cells in the underlying stroma. Clinical manifestations include nasal obstruction, epistaxis, and anosmia. It has the tendency to recur and extend to adjacent structures. Inverted papillomas are occasionally associated with the development or presence of carcinomas, usually squamous cell carcinomas.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nasal cavity neoplasm","termid":"MONDO:0004756"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nasal cavity inverting papilloma","secondary_identifiers":["NCIT:C8194","UMLS:C0280336","DOID:4633","MEDGEN:79106"],"synonyms":[{"name":"inverting papilloma of nasal cavity","type":"exact"},{"name":"inverting papilloma of the nasal cavity","type":"exact"},{"name":"nasal cavity Schneiderian papilloma, inverted type","type":"exact"},{"name":"nasal cavity inverted papilloma","type":"exact"}],"termid":"MONDO:0003065","xrefs":{"Monarch":{"xref_id":"0003065"}}}


id: MOD:00892
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to D-serine.","definition_xrefs":["PubMed:18025465","PubMed:6893271","RESID:AA0195#CYS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-serine","termid":"MOD:00891"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"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":"D-serine (Cys)","synonyms":[{"name":"(R)-2-amino-3-hydroxypropanoic acid","type":"exact"},{"name":"D-serine","type":"exact"},{"name":"MOD_RES D-serine (Cys)","type":"exact"}],"termid":"MOD:00892"}


id: GO:0060432
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any developmental process that results in the creation of defined areas or spaces within the lung, to which cells respond and eventually are instructed to differentiate.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern specification process","termid":"GO:0007389"},{"relation_name":"part_of","term_name":"lung development","termid":"GO:0030324"}],"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":"lung pattern specification process","termid":"GO:0060432"}


id: PBO:0109992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3, human RNF181 like, unknown biological role","termid":"PBO:0109992"}


id: GO:0071064
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphaE-beta7 integrin complex bound to E-cadherin.","definition_xrefs":["PMID:10837471"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005886"],"is_obsolete":false,"name":"alphaE-beta7 integrin-E-cadherin complex","synonyms":[{"name":"ITGAE-ITGB7-CDH1 complex","type":"narrow"}],"termid":"GO:0071064"}


id: MONDO:0024390
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete actinomycotic infectious disease (obsolete MONDO:0024390)","termid":"MONDO:0024390","xrefs":{"Monarch":{"xref_id":"0024390"}}}


id: PBO:0055598
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 3034","termid":"PBO:0055598"}


id: GO:0032250
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of adenosine into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of purine nucleoside transport","termid":"GO:0032247"},{"relation_name":"is_a","term_name":"regulation of adenosine transport","termid":"GO:0032249"},{"relation_name":"negatively_regulates","term_name":"adenosine transport","termid":"GO:0032238"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of adenosine transport","synonyms":[{"name":"down regulation of adenosine transport","type":"exact"},{"name":"down-regulation of adenosine transport","type":"exact"},{"name":"downregulation of adenosine transport","type":"exact"},{"name":"inhibition of adenosine transport","type":"narrow"}],"termid":"GO:0032250"}


id: PBO:0036554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variant C2 domain protein, human FAM102A and FAM102B ortholog","termid":"PBO:0036554"}


id: FYPO:0002838
data:
  {"alleles_by_uniquename":{"SJAG_01050:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01050","name":"nur1delta","uniquename":"SJAG_01050:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121312],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001132"}]},"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 a specific location on a chromosome is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"},{"relation_name":"is_a","term_name":"abnormal protein localization to chromosome","termid":"FYPO:0004996"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01050":null,"SJAG_01745":null,"SJAG_03892":null},"genotype_count":1,"genotypes_by_uniquename":{"nur1delta__vps4delta":{"display_name":"nur1delta vps4delta","display_uniquename":"nur1delta__vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_01050","SJAG_03892"],"name":"abnormal protein localization to chromosome during vegetative growth","references_by_uniquename":{"PMID:32109380":null},"synonyms":[{"name":"abnormal protein localisation to chromosome during vegetative growth","type":"exact"},{"name":"abnormal protein localization to chromosome during mitotic cell cycle","type":"related"}],"termid":"FYPO:0002838","terms_by_termid":{"FYPO:0001132":null,"FYPO_EXT:0000001":null}}


id: MONDO:0015773
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fibular dimelia-diplopodia syndrome is a rare developmental anomaly.","definition_xrefs":["Orphanet:1757"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibular dimelia-diplopodia syndrome","secondary_identifiers":["MEDGEN:929427","SCTID:720953006","UMLS:C4303758","GARD:18746"],"synonyms":[{"name":"leg duplication-mirror foot syndrome","type":"exact"}],"termid":"MONDO:0015773","xrefs":{"Monarch":{"xref_id":"0015773"}}}


id: PBO:0080384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS13B divergent transcript","termid":"PBO:0080384"}


id: MONDO:0018399
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare disorder with female infertility due to a congenital hypogonadotropic hypogonadism (obsolete MONDO:0018399)","termid":"MONDO:0018399","xrefs":{"Monarch":{"xref_id":"0018399"}}}


id: GO:1904313
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 methamphetamine hydrochloride stimulus.","definition_xrefs":["GO_REF:0000071","PMID:22174933","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to amine","termid":"GO:0014075"}],"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 methamphetamine hydrochloride","synonyms":[{"name":"response to methamphetamine HCL","type":"exact"}],"termid":"GO:1904313"}


id: GO:1905700
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of xenobiotic transmembrane export. A xenobiotic is a compound foreign to the organism exposed to it. It may be synthesized by another organism (like ampicilin) or it can be a synthetic chemical.","definition_xrefs":["GO_REF:0000058","PMID:15198509","GOC:krc","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of transmembrane transport","termid":"GO:0034763"},{"relation_name":"is_a","term_name":"regulation of xenobiotic detoxification by transmembrane export across the plasma membrane","termid":"GO:1905699"},{"relation_name":"is_a","term_name":"negative regulation of response to drug","termid":"GO:2001024"},{"relation_name":"negatively_regulates","term_name":"xenobiotic detoxification by transmembrane export across the plasma membrane","termid":"GO:1990961"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"negative regulation of xenobiotic detoxification by transmembrane export across the plasma membrane","synonyms":[{"name":"down regulation of drug transmembrane export","type":"narrow"},{"name":"down-regulation of drug transmembrane export","type":"narrow"},{"name":"downregulation of drug transmembrane export","type":"narrow"},{"name":"inhibition of drug transmembrane export","type":"narrow"},{"name":"negative regulation of drug transmembrane export","type":"narrow"},{"name":"negative regulation of xenobiotic transmembrane export","type":"narrow"}],"termid":"GO:1905700"}


id: PBO:0026645
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_oxidized_DNA_binding","termid":"PBO:0026645"}


id: PBO:0046136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 5A2","termid":"PBO:0046136"}


id: PBO:0067809
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 111","termid":"PBO:0067809"}


id: GO:0033648
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Organized structure of distinctive morphology and function, as found in host cells, bounded by a single or double lipid bilayer membrane and occurring within the cell. Includes the nucleus, mitochondria, plastids, vacuoles, and vesicles. Excludes the plasma membrane. 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 intracellular organelle","termid":"GO:0033647"}],"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 membrane-bounded organelle","synonyms":[{"name":"host intracellular membrane-enclosed organelle","type":"exact"}],"termid":"GO:0033648"}


id: MONDO:0004455
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital mesoblastic nephroma characterized by the presence of interlacing fascicles of fibroblastic cells, low mitotic activity, and collagen formation.","definition_xrefs":["NCIT:C39814"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital mesoblastic nephroma","termid":"MONDO:0017043"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0004992"],"is_obsolete":false,"name":"classic congenital mesoblastic nephroma","secondary_identifiers":["MEDGEN:273923","UMLS:C1516475","DOID:8083"],"synonyms":[{"name":"classic congenital mesoblastic nephroma","type":"exact"}],"termid":"MONDO:0004455","xrefs":{"Monarch":{"xref_id":"0004455"}}}


id: PBO:0031386
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_glucan_synthesis","termid":"PBO:0031386"}


id: MONDO:0008615
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":"tune deafness","secondary_identifiers":["UMLS:C1860646","MEDGEN:349862","MESH:C566019","OMIM:191200","ICD9:389.8","SCTID:55647004"],"synonyms":[{"name":"Dysmelodia","type":"related"},{"name":"amusia, congenital","type":"related"},{"name":"tone deafness","type":"related"},{"name":"tune deafness","type":"exact"}],"termid":"MONDO:0008615","xrefs":{"Monarch":{"xref_id":"0008615"}}}


id: PBO:0028467
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-misoriented_cytoplasmic_microtubules","termid":"PBO:0028467"}


id: PBO:0041887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cation channel sperm associated auxiliary subunit beta","termid":"PBO:0041887"}


id: MONDO:0018178
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dilatation of the intestinal lymphatic system usually caused by an obstruction in the intestinal wall. It may be congenital or acquired and is characterized by diarrhea; hypoproteinemia; peripheral and/or abdominal edema; and protein-losing enteropathies.","definition_xrefs":["MESH:D008201"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"}],"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":"intestinal lymphangiectasia","secondary_identifiers":["Orphanet:36204","NANDO:2200914","MedDRA:10025213","SCTID:197260007","MEDGEN:9828","GARD:12331","HP:0002593","ICD9:457.1","NANDO:2100256","UMLS:C0024215","icd11.foundation:1255239964"],"synonyms":[{"name":"intestinal lymphangiectasia","type":"exact"},{"name":"intestinal lymphangiectasia (disease)","type":"exact"}],"termid":"MONDO:0018178","xrefs":{"Monarch":{"xref_id":"0018178"}}}


id: PR:Q09866
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A WD repeat-containing protein mio that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00133","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 WD repeat-containing protein C12G12.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC12G12.01c","secondary_identifiers":["UniProtKB:Q09866"],"synonyms":[{"name":"Spom972h-MIOS","type":"exact"}],"termid":"PR:Q09866"}


id: GO:0052676
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-methylbutanol + NAD+ = 3-methylbutanal + NADH + H+. 3-methylbutanal is also known as isovaleraldehyde.","definition_xrefs":["KEGG_REACTION:R05685","RHEA:18529"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol dehydrogenase (NAD+) activity","termid":"GO:0004022"},{"relation_name":"is_a","term_name":"3-methylbutanal reductase [NAD(P)H] activity","termid":"GO:0046568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"3-methylbutanal reductase (NADH) activity","synonyms":[{"name":"3-methylbutanal reductase (NAD) activity","type":"exact"},{"name":"3-methylbutanol:NAD oxidoreductase activity","type":"exact"},{"name":"3-methylbutanol:NAD+ oxidoreductase activity","type":"related"},{"name":"3-methylbutyraldehyde reductase (NAD) activity","type":"exact"},{"name":"isoamyl alcohol oxidase (NAD) activity","type":"exact"}],"termid":"GO:0052676"}


id: PBO:0112997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-1,3-mannosyltransferase; integral membrane glycoprotein of Golgi complex, required for addition of alpha1,3-mannose linkages to N-linked and O-linked oligosaccharides; one of five S. cerevisiae proteins of MNN1 family; targeted to vacuole via AP-3 pathway","termid":"PBO:0112997"}


id: PBO:0088220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PLLLP motif protein","termid":"PBO:0088220"}


id: FYPO:0005763
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 replication fork pausing occurs to a greater extent than normal, including at sites where forks do not normally pause.","definition_xrefs":["PMID:25471935","PMID:27611590","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased rate of mitotic DNA replication elongation","termid":"FYPO:0003923"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0000293","FYPO:0000631"],"is_obsolete":false,"name":"increased replication fork pausing","synonyms":[{"name":"increased replication fork pausing during mitotic cell cycle","type":"related"},{"name":"increased replication fork pausing during vegetative growth","type":"exact"}],"termid":"FYPO:0005763"}


id: GO:0140105
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by interleukin-10 binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:11244051"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"}],"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":"interleukin-10-mediated signaling pathway","synonyms":[{"name":"IL-10-mediated signaling pathway","type":"exact"},{"name":"interleukin-10-mediated signalling pathway","type":"exact"}],"termid":"GO:0140105"}


id: GO:0032055
data:
  {"annotated_genes":["SJAG_00690","SJAG_02592","SJAG_01942","SJAG_00169","SJAG_00786","SJAG_03869"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117480,76982,101149,96179,71679,111520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990625"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate of translation as a result of a stimulus indicating the organism is under stress.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of translation","termid":"GO:0017148"},{"relation_name":"is_a","term_name":"regulation of translation in response to stress","termid":"GO:0043555"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00690":null,"SJAG_00786":null,"SJAG_01942":null,"SJAG_02592":null,"SJAG_03869":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of translation in response to stress","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of translation in response to stress","type":"exact"},{"name":"down-regulation of translation in response to stress","type":"exact"},{"name":"downregulation of translation in response to stress","type":"exact"},{"name":"inhibition of translation in response to stress","type":"narrow"}],"termid":"GO:0032055","terms_by_termid":{"GO:1990625":null}}


id: PBO:0091749
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"II:g.1950050_1950051insG","termid":"PBO:0091749"}


id: MONDO:0020492
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemimegalencephaly is a rare cerebral malformation characterized by overgrowth of all or part of a cerebral hemisphere, often with ipsilateral severe cortical dysplasia or dysgenesis, white matter hypertrophy and dilated lateral ventricle, presenting in early infancy with progressive hemiparesis, severe psychomotor retardation and intractable seizures. Hemimegalencephaly may be an isolated finding or associated with other syndromes such as angioosteohypertrophic syndrome, epidermal nevus syndrome and Ito hypomelanosis. Management includes seizure control by antiepileptic medications and early hemispherectomy.","definition_xrefs":["Orphanet:99802"],"direct_ancestors":[{"relation_name":"is_a","term_name":"overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes","termid":"MONDO:0100283"}],"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":"hemimegalencephaly","secondary_identifiers":["GARD:2637","SCTID:253170008","MESH:D065705","UMLS:C0431391","NCIT:C177779","ICD9:742.4","MEDGEN:140910","NANDO:1200563","icd11.foundation:961229160","NORD:1220"],"synonyms":[{"name":"macrencephaly","type":"related"},{"name":"unilateral megalencephaly","type":"exact"}],"termid":"MONDO:0020492","xrefs":{"Monarch":{"xref_id":"0020492"}}}


id: GO:0000749
data:
  {"annotated_genes":["SJAG_03340","SJAG_01718","SJAG_00990","SJAG_01345","SJAG_03209","SJAG_00993","SJAG_02923","SJAG_01978"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107350],"is_not":false,"summary":null,"term":"GO:0000749"},{"annotations":[65842,95136,108110,98858,98201,91048],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071507"},{"annotations":[72448],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000750"}]},"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 pheromone stimulus that positively regulates the process of conjugation with cellular fusion. An example of this process is found in Saccharomyces cerevisiae.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to pheromone","termid":"GO:0071444"},{"relation_name":"positively_regulates","term_name":"conjugation with cellular fusion","termid":"GO:0000747"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00990":null,"SJAG_00993":null,"SJAG_01345":null,"SJAG_01718":null,"SJAG_01978":null,"SJAG_02923":null,"SJAG_03209":null,"SJAG_03340":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0000747"},{"rel_name":"positively_regulates","termid":"GO:0000747"}],"interesting_parent_ids":["GO:0000747","GO:0008150"],"is_obsolete":false,"name":"response to pheromone triggering conjugation with cellular fusion","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0030434","GO:0007328"],"synonyms":[{"name":"response to pheromone during conjugation with cellular fusion","type":"related"}],"termid":"GO:0000749","terms_by_termid":{"GO:0000749":null,"GO:0000750":null,"GO:0071507":null}}


id: FYPO:0004735
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 medial cortical nodes is abolished, and the protein is present in the cytoplasm instead.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to medial cortical node","termid":"FYPO:0003919"},{"relation_name":"is_a","term_name":"abolished protein localization to medial cortex, with protein mislocalized to cytoplasm, during vegetative growth","termid":"FYPO:0007027"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"abolished protein localization to medial cortical node, with protein mislocalized to cytoplasm","synonyms":[{"name":"abolished protein localisation to medial cortical node, with protein mislocalised to cytoplasm","type":"exact"},{"name":"abolished protein localization to cortical medial dot, with protein mislocalized to cytoplasm","type":"exact"},{"name":"abolished protein localization to cytokinetic nodes, with protein mislocalized to cytoplasm","type":"related"},{"name":"abolished protein localization to medial cortical node, with protein mislocalized to cytoplasm, during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to medial cortical node, with protein mislocalized to cytoplasm, during vegetative growth","type":"exact"},{"name":"abolished protein localization to medial cortical nodes, with protein mislocalized to cytoplasm","type":"exact"},{"name":"abolished protein recruitment to medial cortical node, with protein mislocalized to cytoplasm","type":"related"},{"name":"protein localization to medial cortical node abolished, with protein mislocalized to cytoplasm","type":"exact"}],"termid":"FYPO:0004735"}


id: GO:0160072
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The binding activity of a molecule that brings together an ubiquitin ligase and an ubiquitin ligase-substrate adaptor, permitting those molecules to function in a coordinated way.","definition_xrefs":["PMID:27664236"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-macromolecule adaptor activity","termid":"GO:0030674"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0003674","GO:0060090","GO:0030674"],"is_obsolete":false,"name":"ubiquitin ligase complex scaffold activity","synonyms":[{"name":"core protein activity for the CUL-RING ubiquitin ligase complex","type":"narrow"},{"name":"core protein activity for the Cullin-RING ubiquitin ligase complex","type":"narrow"}],"termid":"GO:0160072"}


id: PBO:0036286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy associated protein Atg14","termid":"PBO:0036286"}


id: GO:0031894
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a V1A vasopressin receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vasopressin receptor binding","termid":"GO:0031893"}],"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:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"V1A vasopressin receptor binding","synonyms":[{"name":"V1A vasopressin receptor ligand","type":"narrow"}],"termid":"GO:0031894"}


id: GO:0048153
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of S100 alpha protein. S100 is a small calcium and zinc binding protein produced in astrocytes that is implicated in Alzheimer's disease, Down Syndrome and ALS.","definition_xrefs":["GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete S100 alpha biosynthetic process (obsolete GO:0048153)","synonyms":[{"name":"S100 alpha anabolism","type":"exact"},{"name":"S100 alpha biosynthesis","type":"exact"},{"name":"S100 alpha formation","type":"exact"},{"name":"S100 alpha synthesis","type":"exact"}],"termid":"GO:0048153"}


id: PBO:0047151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 182 member B","termid":"PBO:0047151"}


id: MONDO:0020520
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Adult pulmonary Langerhans Cell Histiocytosis (PLCH) is a rare histiocytic lung disease characterized by the accumulation of Langerhans and other inflammatory cells in the small airways, resulting in the formation of nodular inflammatory lesions.","definition_xrefs":["Orphanet:99874"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Langerhans cell histiocytosis specific to adulthood","termid":"MONDO:0017029"},{"relation_name":"is_a","term_name":"eosinophilic granuloma","termid":"MONDO:0020517"}],"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":"adult pulmonary Langerhans cell histiocytosis","secondary_identifiers":["NCIT:C142833","SCTID:328611000119105","UMLS:C3161104","icd11.foundation:792398738","MEDGEN:853967","ICD10CM:J84.82"],"synonyms":[{"name":"PLCH","type":"exact"},{"name":"pulmonary Langerhans cell histiocytosis","type":"exact"},{"name":"pulmonary eosinophilic granuloma","type":"exact"},{"name":"pulmonary histiocytosis X","type":"exact"}],"termid":"MONDO:0020520","xrefs":{"Monarch":{"xref_id":"0020520"}}}


id: PBO:0087479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of chromatin assembly factor I (CAF-1); chromatin assembly by CAF-1 affects multiple processes including silencing at telomeres, mating type loci, and rDNA; maintenance of kinetochore structure; deactivation of DNA damage checkpoint after DNA repair; chromatin dynamics during transcription; and repression of divergent noncoding transcription; Msi1p localizes to nucleus and cytoplasm and independently regulates the RAS/cAMP pathway via sequestration of Npr1p kinase","termid":"PBO:0087479"}


id: PBO:0045178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member B1","termid":"PBO:0045178"}


id: GO:0044498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant modulation of the force with which blood travels through the circulatory system of the bitten/stung organism.","definition_xrefs":["PMID:19837656","GOC:jl","GOC:fj"],"gene_count":0,"genotype_count":0,"name":"obsolete venom-mediated perturbation of blood pressure in another organism (obsolete GO:0044498)","synonyms":[{"name":"envenomation resulting in modulation of blood pressure in another organism","type":"exact"},{"name":"envenomation resulting in modulation of blood pressure in other organism","type":"exact"},{"name":"envenomation resulting in regulation of blood pressure in other organism","type":"exact"}],"termid":"GO:0044498"}


id: PBO:0087152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA endoribonuclease involved in perinuclear mRNP quality control; involved in perinuclear mRNP quality control via the turnover of aberrant, unprocessed pre-mRNAs; interacts with subunits of THO/TREX, TREX-2, and RNA polymerase II; contains a PIN (PilT N terminus) domain","termid":"PBO:0087152"}


id: GO:0060818
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Compensating for the two-fold variation in X-chromosome:autosome ratios between sexes by a global inactivation of all, or most of, the genes on the paternal X-chromosome in the XX sex by genomic imprinting.","definition_xrefs":["GOC:tb","PMID:16789828","GOC:sdb_2009","PMID:18425126","PMID:23578369","GOC:dph","PMID:11743158"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dosage compensation by inactivation of X chromosome","termid":"GO:0009048"},{"relation_name":"is_a","term_name":"genomic imprinting","termid":"GO:0071514"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0006325","GO:0008150"],"is_obsolete":false,"name":"inactivation of paternal X chromosome by genomic imprinting","synonyms":[{"name":"iXCI","type":"related"},{"name":"inactivation of paternal X chromosome by genetic imprinting","type":"related"}],"termid":"GO:0060818"}


id: GO:0031404
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a chloride ion (Cl-).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"chloride ion binding","synonyms":[{"name":"Cl- ion binding","type":"exact"},{"name":"chloride binding","type":"exact"}],"termid":"GO:0031404"}


id: GO:0038085
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a vascular endothelial growth factor.","definition_xrefs":["PMID:17470632"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor binding","termid":"GO:0019838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"vascular endothelial growth factor binding","synonyms":[{"name":"VEGF binding","type":"exact"}],"termid":"GO:0038085"}


id: FYPO:0003191
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 microtubules does not occur, and the protein is instead visible in one or a few foci or dots in the cytoplasm, during interphase of the mitotic cell cycle.","definition_xrefs":["PMID:18799626","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule cytoskeleton during vegetative growth","termid":"FYPO:0000931"}],"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":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abolished protein localization to microtubule during mitotic interphase, with protein mislocalized to cytoplasmic foci","synonyms":[{"name":"abolished protein localisation to microtubule during mitotic interphase, with protein mislocalised to cytoplasmic foci","type":"exact"},{"name":"protein localization to microtubule abolished during interphase, with protein mislocalized to cytoplasmic foci, during vegetative growth","type":"exact"},{"name":"protein localization to microtubule abolished during mitotic interphase, with protein mislocalized to cytoplasmic foci","type":"exact"}],"termid":"FYPO:0003191"}


id: PBO:0017810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pig-U, Gab1 (predicted)","termid":"PBO:0017810"}


id: MONDO:0008469
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare primary bone dysplasia disorder characterized by congenital hypotrichosis associated with rhizomelic short stature (more pronounced in upper limbs than lower limbs), limited hip abduction and mild genu varum. Flared and irregular metaphyses, delayed and irregular epiphiseal ossification and pear-shaped vertebral bodies are characteristic radiologic findings.","definition_xrefs":["Orphanet:168443"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"},{"relation_name":"is_a","term_name":"spondyloepimetaphyseal dysplasia","termid":"MONDO:0100510"}],"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":"spondyloepimetaphyseal dysplasia-hypotrichosis syndrome","secondary_identifiers":["UMLS:C1866728","MESH:C535783","GARD:10101","MEDGEN:357120","OMIM:183849"],"synonyms":[{"name":"Whyte Petersen McAlister syndrome","type":"related"},{"name":"Whyte syndrome","type":"related"},{"name":"spondyloepimetaphyseal dysplasia with hypotrichosis","type":"related"}],"termid":"MONDO:0008469","xrefs":{"Monarch":{"xref_id":"0008469"}}}


id: MONDO:0044748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease of cattle caused by parasitization of the red blood cells by bacteria of the genus ANAPLASMA.","definition_xrefs":["MESH:D000712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cattle disease","termid":"MONDO:0024913"},{"relation_name":"is_a","term_name":"Anaplasmataceae infectious disease, non-human animal","termid":"MONDO:0700113"},{"relation_name":"is_a","term_name":"tick-borne infectious disease, non-human animal","termid":"MONDO:0700201"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaplasmosis in cattle","synonyms":[{"name":"Anaplasmoses","type":"related"}],"termid":"MONDO:0044748","xrefs":{"Monarch":{"xref_id":"0044748"}}}


id: GO:0070906
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: aspartate(out) + alanine(in) = aspartate(in) + alanine(out).","definition_xrefs":["GOC:dh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid transmembrane transporter activity","termid":"GO:0005310"},{"relation_name":"is_a","term_name":"antiporter activity","termid":"GO:0015297"},{"relation_name":"is_a","term_name":"C4-dicarboxylate transmembrane transporter activity","termid":"GO:0015556"},{"relation_name":"is_a","term_name":"alanine transmembrane transporter activity","termid":"GO:0022858"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"aspartate:alanine antiporter activity","secondary_identifiers":["RHEA:33139"],"synonyms":[{"name":"aspartate-alanine antiporter activity","type":"exact"},{"name":"aspartate/alanine antiporter activity","type":"exact"}],"termid":"GO:0070906"}


id: PBO:0084293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Intracellular beta-1,3-endoglucanase; expression is induced during sporulation; may have a role in cortical actin cytoskeleton assembly; protein abundance increases in response to DNA replication stress","termid":"PBO:0084293"}


id: GO:0008051
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A complex that possesses farnesyl-diphosphate farnesyl transferase activity.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete farnesyl-diphosphate farnesyl transferase complex (obsolete GO:0008051)","synonyms":[{"name":"farnesyl-diphosphate farnesyl transferase complex","type":"exact"}],"termid":"GO:0008051"}


id: GO:1903157
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any iron ion transmembrane transporter activity that is involved in iron ion import into cell.","definition_xrefs":["GO_REF:0000061","GOC:TermGenie","GOC:dos","ISBN:0-8249-3695-6"],"gene_count":0,"genotype_count":0,"name":"obsolete iron ion transmembrane transporter activity involved in iron ion import into cell (obsolete GO:1903157)","synonyms":[{"name":"iron ion transmembrane transporter activity involved in iron import into cell","type":"related"},{"name":"iron ion transmembrane transporter activity involved in iron ion import into cell","type":"exact"},{"name":"iron transporter activity involved in iron import into cell","type":"related"},{"name":"iron transporter activity involved in iron ion import into cell","type":"exact"},{"name":"multicopper ferroxidase iron transport mediator activity involved in iron import into cell","type":"related"},{"name":"multicopper ferroxidase iron transport mediator activity involved in iron ion import into cell","type":"related"},{"name":"transmembrane iron ion permease activity involved in iron import into cell","type":"related"},{"name":"transmembrane iron ion permease activity involved in iron ion import into cell","type":"exact"},{"name":"transmembrane iron permease activity involved in iron import into cell","type":"related"},{"name":"transmembrane iron permease activity involved in iron ion import into cell","type":"exact"},{"name":"zinc, iron permease activity involved in iron import into cell","type":"related"},{"name":"zinc, iron permease activity involved in iron ion import into cell","type":"related"}],"termid":"GO:1903157"}


id: GO:0140880
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of terrein, a fungal metabolite with ecological, antimicrobial, antiproliferative, and antioxidative activities.","definition_xrefs":["PMID:24816227"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mycotoxin biosynthetic process","termid":"GO:0043386"},{"relation_name":"is_a","term_name":"polyol biosynthetic process","termid":"GO:0046173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0019748"],"is_obsolete":false,"name":"terrein biosynthetic process","synonyms":[{"name":"terrein anabolism","type":"exact"},{"name":"terrein biosynthesis","type":"exact"},{"name":"terrein formation","type":"exact"},{"name":"terrein synthesis","type":"exact"}],"termid":"GO:0140880"}


id: PBO:0003405
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein intermediate chain Dic1","termid":"PBO:0003405"}


id: MONDO:0011760
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Scheie syndrome is the mildest form of mucopolysaccharidosis type 1 (MPS1), a rare lysosomal storage disease, characterized by skeletal deformities and a delay in motor development.","definition_xrefs":["Orphanet:93474"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucopolysaccharidosis type 1","termid":"MONDO:0001586"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"lysosomal storage disease with skeletal involvement","termid":"MONDO:0800088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0002561","MONDO:0005328","MONDO:0005066"],"is_obsolete":false,"name":"Scheie syndrome","secondary_identifiers":["SCTID:73123008","OMIM:607016","GARD:12561","DOID:0060222","MEDGEN:6453","NCIT:C61265","NANDO:1200095","NANDO:2201169","UMLS:C0026708"],"synonyms":[{"name":"MPS I S","type":"exact"},{"name":"MPS V","type":"related"},{"name":"MPS V, formerly","type":"related"},{"name":"MPS1-S","type":"related"},{"name":"MPS1S","type":"exact"},{"name":"MPS5, formerly","type":"related"},{"name":"MPSIS","type":"exact"},{"name":"Scheie syndrome","type":"exact"},{"name":"mucopolysaccharidosis Is","type":"related"},{"name":"mucopolysaccharidosis type 1S","type":"exact"},{"name":"mucopolysaccharidosis type IS","type":"exact"},{"name":"mucopolysaccharidosis type V","type":"exact"},{"name":"mucopolysaccharidosis type V, formerly","type":"related"}],"termid":"MONDO:0011760","xrefs":{"Monarch":{"xref_id":"0011760"}}}


id: PBO:0066034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAN pseudogene 3","termid":"PBO:0066034"}


id: PBO:0071674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L37 pseudogene 6","termid":"PBO:0071674"}


id: PBO:0000205
data:
  {"annotation_feature_type":"gene","cv_name":"m_f_g","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleocytoplasmic shuttling protein","termid":"PBO:0000205"}


id: PBO:0043989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colony stimulating factor 3","termid":"PBO:0043989"}


id: GO:0052704
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The pathway resulting in the formation of ergothioneine from histidine via a set of steps in which gamma-glutamyl-hercynylcysteine sulfoxide is formed as an intermediate.","definition_xrefs":["PMID:5484456","PMID:4276459"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ergothioneine biosynthetic process","termid":"GO:0052699"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0006790","GO:0044281"],"is_obsolete":false,"name":"ergothioneine biosynthesis from histidine via gamma-glutamyl-hercynylcysteine sulfoxide","secondary_identifiers":["Wikipedia:Ergothioneine"],"synonyms":[{"name":"ergothioneine biosynthesis from histidine via N-alpha,N-alpha,N-alpha-trimethyl-L-histidine","type":"broad"}],"termid":"GO:0052704"}


id: PBO:0030537
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_processing","termid":"PBO:0030537"}


id: PBO:0044400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 2 subfamily C member 61, pseudogene","termid":"PBO:0044400"}


id: GO:0034940
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 5-oxo-4,5-dihydropyrrole-2-carboxylate + 2 H2O = 2-oxoglutarate + NH3.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 5-oxo-4,5-dihydropyrrole-2-carboxylate amidase activity (obsolete GO:0034940)","termid":"GO:0034940"}


id: PBO:0012299
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"human LYAR homolog","termid":"PBO:0012299"}


id: MONDO:0010675
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy","termid":"MONDO:0020121"}],"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":"muscular dystrophy, cardiac type","secondary_identifiers":["OMIM:309930","UMLS:C1442927","MESH:C563247","MEDGEN:254845"],"synonyms":[{"name":"muscular dystrophy, cardiac type","type":"exact"}],"termid":"MONDO:0010675","xrefs":{"Monarch":{"xref_id":"0010675"}}}


id: GO:1990827
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an enzyme that catalyzes the removal of an amino group from a substrate, producing ammonia (NH3).","definition_xrefs":["PMID:9792439"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"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:0003674","GO:0005515"],"is_obsolete":false,"name":"deaminase binding","termid":"GO:1990827"}


id: GO:1903869
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of methylenetetrahydrofolate reductase (NAD(P)H) activity.","definition_xrefs":["GOC:TermGenie","PMID:24769206","GO_REF:0000059","GOC:rph","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of methylenetetrahydrofolate reductase (NAD(P)H) activity (obsolete GO:1903869)","synonyms":[{"name":"down regulation of 5,10-CH(2)-H(4)folate reductase activity","type":"exact"},{"name":"down regulation of 5,10-CH2-H4folate reductase activity","type":"exact"},{"name":"down regulation of 5,10-methylenetetrahydrofolate reductase (FADH(2)) activity","type":"related"},{"name":"down regulation of 5,10-methylenetetrahydrofolate reductase (FADH) activity","type":"exact"},{"name":"down regulation of 5,10-methylenetetrahydrofolate reductase (FADH2) activity","type":"exact"},{"name":"down regulation of 5,10-methylenetetrahydrofolate reductase (NADPH) activity","type":"exact"},{"name":"down regulation of 5,10-methylenetetrahydropteroylglutamate reductase activity","type":"exact"},{"name":"down regulation of 5-methyltetrahydrofolate:(acceptor) oxidoreductase activity","type":"exact"},{"name":"down regulation of 5-methyltetrahydrofolate:NAD oxidoreductase activity","type":"exact"},{"name":"down regulation of 5-methyltetrahydrofolate:NAD(+) oxidoreductase activity","type":"exact"},{"name":"down regulation of 5-methyltetrahydrofolate:NAD(P)+ oxidoreductase activity","type":"exact"},{"name":"down regulation of 5-methyltetrahydrofolate:NAD+ oxidoreductase activity","type":"exact"},{"name":"down regulation of 5-methyltetrahydrofolate:NADP(+) oxidoreductase activity","type":"exact"},{"name":"down regulation of 5-methyltetrahydrofolate:NADP+ oxidoreductase activity","type":"exact"},{"name":"down regulation of MetF","type":"related"},{"name":"down regulation of N5,10-methylenetetrahydrofolate reductase activity","type":"exact"},{"name":"down regulation of N5,N10-methylenetetrahydrofolate reductase activity","type":"exact"},{"name":"down regulation of methylenetetrahydrofolate (reduced nicotinamide adenine dinucleotide phosphate) reductase activity","type":"exact"},{"name":"down regulation of methylenetetrahydrofolate (reduced riboflavin adenine dinucleotide) reductase activity","type":"related"},{"name":"down regulation of methylenetetrahydrofolate reductase (NAD(P)H) activity","type":"exact"},{"name":"down regulation of methylenetetrahydrofolate reductase (NADPH(2)) activity","type":"exact"},{"name":"down regulation of methylenetetrahydrofolate reductase (NADPH2)","type":"exact"},{"name":"down regulation of methylenetetrahydrofolate reductase [NAD(P)H]","type":"related"},{"name":"down-regulation of 5,10-CH(2)-H(4)folate reductase activity","type":"exact"},{"name":"down-regulation of 5,10-CH2-H4folate reductase activity","type":"exact"},{"name":"down-regulation of 5,10-methylenetetrahydrofolate reductase (FADH(2)) activity","type":"related"},{"name":"down-regulation of 5,10-methylenetetrahydrofolate reductase (FADH) activity","type":"exact"},{"name":"down-regulation of 5,10-methylenetetrahydrofolate reductase (FADH2) activity","type":"exact"},{"name":"down-regulation of 5,10-methylenetetrahydrofolate reductase (NADPH) activity","type":"exact"},{"name":"down-regulation of 5,10-methylenetetrahydropteroylglutamate reductase activity","type":"exact"},{"name":"down-regulation of 5-methyltetrahydrofolate:(acceptor) oxidoreductase activity","type":"exact"},{"name":"down-regulation of 5-methyltetrahydrofolate:NAD oxidoreductase activity","type":"exact"},{"name":"down-regulation of 5-methyltetrahydrofolate:NAD(+) oxidoreductase activity","type":"exact"},{"name":"down-regulation of 5-methyltetrahydrofolate:NAD(P)+ oxidoreductase activity","type":"exact"},{"name":"down-regulation of 5-methyltetrahydrofolate:NAD+ oxidoreductase activity","type":"exact"},{"name":"down-regulation of 5-methyltetrahydrofolate:NADP(+) oxidoreductase activity","type":"exact"},{"name":"down-regulation of 5-methyltetrahydrofolate:NADP+ oxidoreductase activity","type":"exact"},{"name":"down-regulation of MetF","type":"related"},{"name":"down-regulation of N5,10-methylenetetrahydrofolate reductase activity","type":"exact"},{"name":"down-regulation of N5,N10-methylenetetrahydrofolate reductase activity","type":"exact"},{"name":"down-regulation of methylenetetrahydrofolate (reduced nicotinamide adenine dinucleotide phosphate) reductase activity","type":"exact"},{"name":"down-regulation of methylenetetrahydrofolate (reduced riboflavin adenine dinucleotide) reductase activity","type":"related"},{"name":"down-regulation of methylenetetrahydrofolate reductase (NAD(P)H) activity","type":"exact"},{"name":"down-regulation of methylenetetrahydrofolate reductase (NADPH(2)) activity","type":"exact"},{"name":"down-regulation of methylenetetrahydrofolate reductase (NADPH2)","type":"exact"},{"name":"down-regulation of methylenetetrahydrofolate reductase [NAD(P)H]","type":"related"},{"name":"downregulation of 5,10-CH(2)-H(4)folate reductase activity","type":"exact"},{"name":"downregulation of 5,10-CH2-H4folate reductase activity","type":"exact"},{"name":"downregulation of 5,10-methylenetetrahydrofolate reductase (FADH(2)) activity","type":"related"},{"name":"downregulation of 5,10-methylenetetrahydrofolate reductase (FADH) activity","type":"exact"},{"name":"downregulation of 5,10-methylenetetrahydrofolate reductase (FADH2) activity","type":"exact"},{"name":"downregulation of 5,10-methylenetetrahydrofolate reductase (NADPH) activity","type":"exact"},{"name":"downregulation of 5,10-methylenetetrahydropteroylglutamate reductase activity","type":"exact"},{"name":"downregulation of 5-methyltetrahydrofolate:(acceptor) oxidoreductase activity","type":"exact"},{"name":"downregulation of 5-methyltetrahydrofolate:NAD oxidoreductase activity","type":"exact"},{"name":"downregulation of 5-methyltetrahydrofolate:NAD(+) oxidoreductase activity","type":"exact"},{"name":"downregulation of 5-methyltetrahydrofolate:NAD(P)+ oxidoreductase activity","type":"exact"},{"name":"downregulation of 5-methyltetrahydrofolate:NAD+ oxidoreductase activity","type":"exact"},{"name":"downregulation of 5-methyltetrahydrofolate:NADP(+) oxidoreductase activity","type":"exact"},{"name":"downregulation of 5-methyltetrahydrofolate:NADP+ oxidoreductase activity","type":"exact"},{"name":"downregulation of MetF","type":"related"},{"name":"downregulation of N5,10-methylenetetrahydrofolate reductase activity","type":"exact"},{"name":"downregulation of N5,N10-methylenetetrahydrofolate reductase activity","type":"exact"},{"name":"downregulation of methylenetetrahydrofolate (reduced nicotinamide adenine dinucleotide phosphate) reductase activity","type":"exact"},{"name":"downregulation of methylenetetrahydrofolate (reduced riboflavin adenine dinucleotide) reductase activity","type":"related"},{"name":"downregulation of methylenetetrahydrofolate reductase (NAD(P)H) activity","type":"exact"},{"name":"downregulation of methylenetetrahydrofolate reductase (NADPH(2)) activity","type":"exact"},{"name":"downregulation of methylenetetrahydrofolate reductase (NADPH2)","type":"exact"},{"name":"downregulation of methylenetetrahydrofolate reductase [NAD(P)H]","type":"related"},{"name":"inhibition of 5,10-CH(2)-H(4)folate reductase activity","type":"narrow"},{"name":"inhibition of 5,10-CH2-H4folate reductase activity","type":"narrow"},{"name":"inhibition of 5,10-methylenetetrahydrofolate reductase (FADH(2)) activity","type":"related"},{"name":"inhibition of 5,10-methylenetetrahydrofolate reductase (FADH) activity","type":"narrow"},{"name":"inhibition of 5,10-methylenetetrahydrofolate reductase (FADH2) activity","type":"narrow"},{"name":"inhibition of 5,10-methylenetetrahydrofolate reductase (NADPH) activity","type":"narrow"},{"name":"inhibition of 5,10-methylenetetrahydropteroylglutamate reductase activity","type":"narrow"},{"name":"inhibition of 5-methyltetrahydrofolate:(acceptor) oxidoreductase activity","type":"narrow"},{"name":"inhibition of 5-methyltetrahydrofolate:NAD oxidoreductase activity","type":"narrow"},{"name":"inhibition of 5-methyltetrahydrofolate:NAD(+) oxidoreductase activity","type":"narrow"},{"name":"inhibition of 5-methyltetrahydrofolate:NAD(P)+ oxidoreductase activity","type":"narrow"},{"name":"inhibition of 5-methyltetrahydrofolate:NAD+ oxidoreductase activity","type":"narrow"},{"name":"inhibition of 5-methyltetrahydrofolate:NADP(+) oxidoreductase activity","type":"narrow"},{"name":"inhibition of 5-methyltetrahydrofolate:NADP+ oxidoreductase activity","type":"narrow"},{"name":"inhibition of MetF","type":"related"},{"name":"inhibition of N5,10-methylenetetrahydrofolate reductase activity","type":"narrow"},{"name":"inhibition of N5,N10-methylenetetrahydrofolate reductase activity","type":"narrow"},{"name":"inhibition of methylenetetrahydrofolate (reduced nicotinamide adenine dinucleotide phosphate) reductase activity","type":"narrow"},{"name":"inhibition of methylenetetrahydrofolate (reduced riboflavin adenine dinucleotide) reductase activity","type":"related"},{"name":"inhibition of methylenetetrahydrofolate reductase (NAD(P)H) activity","type":"narrow"},{"name":"inhibition of methylenetetrahydrofolate reductase (NADPH(2)) activity","type":"narrow"},{"name":"inhibition of methylenetetrahydrofolate reductase (NADPH2)","type":"narrow"},{"name":"inhibition of methylenetetrahydrofolate reductase [NAD(P)H]","type":"related"},{"name":"negative regulation of 5,10-CH(2)-H(4)folate reductase activity","type":"exact"},{"name":"negative regulation of 5,10-CH2-H4folate reductase activity","type":"exact"},{"name":"negative regulation of 5,10-methylenetetrahydrofolate reductase (FADH(2)) activity","type":"related"},{"name":"negative regulation of 5,10-methylenetetrahydrofolate reductase (FADH) activity","type":"exact"},{"name":"negative regulation of 5,10-methylenetetrahydrofolate reductase (FADH2) activity","type":"exact"},{"name":"negative regulation of 5,10-methylenetetrahydrofolate reductase (NADPH) activity","type":"exact"},{"name":"negative regulation of 5,10-methylenetetrahydropteroylglutamate reductase activity","type":"exact"},{"name":"negative regulation of 5-methyltetrahydrofolate:(acceptor) oxidoreductase activity","type":"exact"},{"name":"negative regulation of 5-methyltetrahydrofolate:NAD oxidoreductase activity","type":"exact"},{"name":"negative regulation of 5-methyltetrahydrofolate:NAD(+) oxidoreductase activity","type":"exact"},{"name":"negative regulation of 5-methyltetrahydrofolate:NAD(P)+ oxidoreductase activity","type":"exact"},{"name":"negative regulation of 5-methyltetrahydrofolate:NAD+ oxidoreductase activity","type":"exact"},{"name":"negative regulation of 5-methyltetrahydrofolate:NADP(+) oxidoreductase activity","type":"exact"},{"name":"negative regulation of 5-methyltetrahydrofolate:NADP+ oxidoreductase activity","type":"exact"},{"name":"negative regulation of MetF","type":"related"},{"name":"negative regulation of N5,10-methylenetetrahydrofolate reductase activity","type":"exact"},{"name":"negative regulation of N5,N10-methylenetetrahydrofolate reductase activity","type":"exact"},{"name":"negative regulation of methylenetetrahydrofolate (reduced nicotinamide adenine dinucleotide phosphate) reductase activity","type":"exact"},{"name":"negative regulation of methylenetetrahydrofolate (reduced riboflavin adenine dinucleotide) reductase activity","type":"related"},{"name":"negative regulation of methylenetetrahydrofolate reductase (NADPH(2)) activity","type":"exact"},{"name":"negative regulation of methylenetetrahydrofolate reductase (NADPH2)","type":"exact"},{"name":"negative regulation of methylenetetrahydrofolate reductase [NAD(P)H]","type":"related"}],"termid":"GO:1903869"}


id: GO:1900983
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving vindoline.","definition_xrefs":["GOC:TermGenie","GOC:yaf","PMID:23864440"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terpenoid indole alkaloid metabolic process","termid":"GO:0046447"},{"relation_name":"is_a","term_name":"acetate ester metabolic process","termid":"GO:1900619"},{"relation_name":"is_a","term_name":"tertiary alcohol metabolic process","termid":"GO:1902644"}],"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":"vindoline metabolic process","synonyms":[{"name":"vindoline metabolism","type":"exact"}],"termid":"GO:1900983"}


id: PBO:0058767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6891","termid":"PBO:0058767"}


id: PBO:0036061
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_localization_to_eMTOC_during_vegetative_growth","termid":"PBO:0036061"}


id: SO:0001755
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A SL2_acceptor_site which appends the SL10 RNA leader sequence to the 5' end of an mRNA. SL10 acceptor sites occur in genes in internal segments of polycistronic transcripts.","definition_xrefs":["SO:nlw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SL2_acceptor_site","termid":"SO:0000709"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SL10_acceptor_site","synonyms":[{"name":"SL10 acceptor site","type":"exact"}],"termid":"SO:0001755"}


id: MONDO:0012542
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"psoriasis, susceptibility to","termid":"MONDO:0100171"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psoriasis 8, susceptibility to","secondary_identifiers":["UMLS:C1853143","OMIM:610707","DOID:0111288","MEDGEN:377839"],"synonyms":[{"name":"PSORS8","type":"exact"},{"name":"psoriasis 8, susceptibility to","type":"exact"},{"name":"psoriasis susceptibility 8","type":"exact"}],"termid":"MONDO:0012542","xrefs":{"Monarch":{"xref_id":"0012542"}}}


id: PBO:0058867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 9900","termid":"PBO:0058867"}


id: PBO:0004843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-B homolog Cbh2","termid":"PBO:0004843"}


id: PBO:0072565
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome binding protein 1","termid":"PBO:0072565"}


id: PBO:0052091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch repeat and BTB domain containing 8","termid":"PBO:0052091"}


id: PBO:0041412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 7 open reading frame 25","termid":"PBO:0041412"}


id: PBO:0045005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"damage induced long noncoding RNA","termid":"PBO:0045005"}


id: PBO:0016065
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin-related endocytic adaptor Any2 (predicted)","termid":"PBO:0016065"}


id: MONDO:1010498
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrial fibrillation that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrial fibrillation, non-human animal","termid":"MONDO:1010024"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atrial fibrillation, dog","secondary_identifiers":["OMIA:001181-9615"],"termid":"MONDO:1010498","xrefs":{"Monarch":{"xref_id":"1010498"}}}


id: PBO:0046269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane protein complex subunit 8","termid":"PBO:0046269"}


id: PBO:0049411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanylate cyclase 1 soluble subunit beta 2 (pseudogene)","termid":"PBO:0049411"}


id: SO:0001932
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A terminal region of DNA sequence where the end of the region is not blunt ended and the exposed single strand terminates at the 5' end.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"restriction_enzyme_single_strand_overhang","termid":"SO:0001695"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restriction_enzyme_five_prime_single_strand_overhang","synonyms":[{"name":"restriction enzyme five prime single strand overhang","type":"exact"}],"termid":"SO:0001932"}


id: FYPO:0001383
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of DNA measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell","termid":"FYPO:0001076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal DNA content","termid":"FYPO:0001383"}


id: PBO:0053348
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 237","termid":"PBO:0053348"}


id: PBO:0088144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar SNARE protein; functions with Vam3p in vacuolar protein trafficking; has an N-terminal PX domain (phosphoinositide-binding module) that binds PtdIns-3-P and mediates membrane binding; SNAP-25 homolog; protein abundance increases in response to DNA replication stress","termid":"PBO:0088144"}


id: PBO:0079449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor suppressor candidate 1","termid":"PBO:0079449"}


id: MONDO:0004306
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A high grade malignant bone-forming mesenchymal neoplasm that produces osteoid and occurs in childhood. It arises from the medullary portion of the bone. It affects the long bones, and most commonly, the distal femur, proximal tibia, and proximal humerus. Pain with or without a palpable mass is the most common clinical presentation. It usually has an aggressive growth and may metastasize through the hematogenous route. The lung is the most frequent site of metastasis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pediatric osteosarcoma","termid":"MONDO:0002623"},{"relation_name":"is_a","term_name":"conventional osteosarcoma","termid":"MONDO:0002631"}],"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":"childhood intracortical osteosarcoma","secondary_identifiers":["MEDGEN:232350","DOID:7612","NCIT:C6590","UMLS:C1332974"],"synonyms":[{"name":"childhood conventional osteosarcoma","type":"exact"},{"name":"childhood intracortical osteosarcoma","type":"exact"}],"termid":"MONDO:0004306","xrefs":{"Monarch":{"xref_id":"0004306"}}}


id: PBO:0005400
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.5.1.29","termid":"PBO:0005400"}


id: PBO:0119294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"farnesyltranstransferase subunit Erg20","termid":"PBO:0119294"}


id: PBO:0067540
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 685, pseudogene","termid":"PBO:0067540"}


id: MONDO:0700024
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder in which chromosome 19 is affected.","definition_xrefs":["MONDO:patterns/chromosome_type"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal anomaly","termid":"MONDO:0020049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 19 disorder","termid":"MONDO:0700024","xrefs":{"Monarch":{"xref_id":"0700024"}}}


id: FYPO:0004975
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 depolymerization (i.e. removal of tubulin dimers) of microtubules extending behind a moving spindle pole body occurs at a lower rate, or speed, than normal.","definition_xrefs":["PMID:16611238","PomBase:mah","GO:0036078"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased rate of microtubule depolymerization during vegetative growth","termid":"FYPO:0000903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000054","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"decreased rate of microtubule depolymerization behind moving spindle pole body","synonyms":[{"name":"decreased microtubule shrinkage behind moving spindle pole body","type":"related"},{"name":"decreased rate of backward-extending microtubule depolymerization","type":"exact"},{"name":"decreased rate of microtubule catastrophe behind moving spindle pole body","type":"related"},{"name":"decreased rate of microtubule depolymerisation behind moving spindle pole body","type":"exact"},{"name":"decreased rate of microtubule depolymerization behind moving SPB","type":"exact"},{"name":"decreased rate of microtubule depolymerization behind moving spindle pole body during mitotic cell cycle","type":"related"},{"name":"decreased rate of microtubule depolymerization behind moving spindle pole body during vegetative growth","type":"exact"},{"name":"increased microtubule stability behind moving spindle pole body","type":"related"},{"name":"increased stability of backwards-extending microtubules","type":"related"},{"name":"reduced rate of microtubule depolymerization behind moving spindle pole body","type":"exact"}],"termid":"FYPO:0004975"}


id: GO:0016896
data:
  {"annotated_genes":["SJAG_01798","SJAG_00966","SJAG_06586","SJAG_04824","SJAG_02275","SJAG_01822","SJAG_04369","SJAG_04153","SJAG_03132","SJAG_03276","SJAG_01836","SJAG_03876","SJAG_00401","SJAG_02540","SJAG_04006","SJAG_04587","SJAG_00081","SJAG_04818","SJAG_02993","SJAG_04084","SJAG_03745","SJAG_00841","SJAG_04519","SJAG_04407"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[67868,100760,106232,81454,76331,71671,107100,120190,72366,91796,105491,81199,103909,63799],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000175"},{"annotations":[75240,79648,71732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004534"},{"annotations":[116293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008859"},{"annotations":[118469,79202,80541,75985,109622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004535"},{"annotations":[70118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990838"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of ester linkages within ribonucleic acids by removing nucleotide residues from the 3' or 5' end to yield 5' phosphomonoesters.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA exonuclease activity","termid":"GO:0004532"}],"gene_count":24,"genes_by_uniquename":{"SJAG_00081":null,"SJAG_00401":null,"SJAG_00841":null,"SJAG_00966":null,"SJAG_01798":null,"SJAG_01822":null,"SJAG_01836":null,"SJAG_02275":null,"SJAG_02540":null,"SJAG_02993":null,"SJAG_03132":null,"SJAG_03276":null,"SJAG_03745":null,"SJAG_03876":null,"SJAG_04006":null,"SJAG_04084":null,"SJAG_04153":null,"SJAG_04369":null,"SJAG_04407":null,"SJAG_04519":null,"SJAG_04587":null,"SJAG_04818":null,"SJAG_04824":null,"SJAG_06586":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004527"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0004527","GO:0016787","GO:0016788","GO:0140098"],"is_obsolete":false,"name":"RNA exonuclease activity, producing 5'-phosphomonoesters","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"secondary_identifiers":["EC:3.1.13.-","Reactome:R-HSA-429860"],"synonyms":[{"name":"exoribonuclease activity, producing 5' phosphomonoesters","type":"exact"},{"name":"exoribonuclease activity, producing 5'-phosphomonoesters","type":"exact"}],"termid":"GO:0016896","terms_by_termid":{"GO:0000175":null,"GO:0004534":null,"GO:0004535":null,"GO:0008859":null,"GO:1990838":null}}


id: GO:0089721
data:
  {"annotated_genes":["SJAG_01960","SJAG_00276"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78355,95154],"is_not":false,"summary":null,"term":"GO:0089721"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a phosphoenolpyruvate from one side of a membrane to the other.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transmembrane transporter activity","termid":"GO:0008028"},{"relation_name":"is_a","term_name":"organophosphate ester transmembrane transporter activity","termid":"GO:0015605"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00276":null,"SJAG_01960":null},"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":"phosphoenolpyruvate transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0089721","terms_by_termid":{"GO:0089721":null}}


id: MONDO:0003808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An osteosarcoma arising from the mediastinum.","definition_xrefs":["NCIT:C6615"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extraosseous osteosarcoma","termid":"MONDO:0002621"},{"relation_name":"is_a","term_name":"mediastinum sarcoma","termid":"MONDO:0002852"}],"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":"mediastinal extraskeletal osteosarcoma","secondary_identifiers":["MEDGEN:235314","UMLS:C1334675","DOID:6208"],"synonyms":[{"name":"mediastinal extraskeletal osteosarcoma","type":"exact"},{"name":"mediastinal osteogenic sarcoma","type":"exact"},{"name":"mediastinal osteosarcoma","type":"exact"},{"name":"mediastinum osteosarcoma (disease)","type":"exact"},{"name":"osteogenic sarcoma of mediastinum","type":"exact"},{"name":"osteogenic sarcoma of the mediastinum","type":"exact"},{"name":"osteosarcoma of mediastinum","type":"exact"},{"name":"osteosarcoma of the mediastinum","type":"exact"}],"termid":"MONDO:0003808","xrefs":{"Monarch":{"xref_id":"0003808"}}}


id: GO:0009932
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Growth that occurs specifically at the tip of a cell.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unidimensional cell growth","termid":"GO:0009826"}],"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":"cell tip growth","termid":"GO:0009932"}


id: GO:0061883
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A clathrin-mediated endocytosis process whereby yolk proteins are internalized and trafficked through the endocytic pathway for yolk deposition.","definition_xrefs":["PMID:26265702"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin-dependent endocytosis","termid":"GO:0072583"},{"relation_name":"part_of","term_name":"vitellogenesis","termid":"GO:0007296"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0051179","GO:0016192","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"clathrin-dependent endocytosis involved in vitellogenesis","synonyms":[{"name":"clathrin-dependent endocytosis involved in yolk formation","type":"exact"}],"termid":"GO:0061883"}


id: PBO:0091792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GEF Muk1","termid":"PBO:0091792"}


id: PBO:0091486
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glcoside Hydrolase family Sixteen","termid":"PBO:0091486"}


id: GO:0039659
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces the activity of the host TBK1-IKBKE-DDX3 complex.","definition_xrefs":["VZ:719"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host TBK1-IKBKE-DDX3 complex activity (obsolete GO:0039659)","synonyms":[{"name":"inhibition of host TBK1-IKBKE-DDX3 complex by virus","type":"exact"},{"name":"suppression by virus of host TBK1-IKKE-DDX3 complex activity","type":"exact"}],"termid":"GO:0039659"}


id: PBO:0056075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lymphocyte antigen 6 family member G6E (pseudogene)","termid":"PBO:0056075"}


id: MONDO:0004353
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-invasive, papillary epithelial neoplasm that arises from the epithelium of the extrahepatic bile ducts.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bile duct papillary neoplasm","termid":"MONDO:0003455"}],"gene_count":0,"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":"extrahepatic biliary papillomatosis","secondary_identifiers":["UMLS:C1333511","MEDGEN:232484","NCIT:C7124","DOID:7752"],"synonyms":[{"name":"extrahepatic bile duct papillary neoplasm","type":"exact"},{"name":"extrahepatic bile duct papillomatosis","type":"exact"},{"name":"extrahepatic biliary papillomatosis","type":"exact"}],"termid":"MONDO:0004353","xrefs":{"Monarch":{"xref_id":"0004353"}}}


id: GO:2000757
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of peptidyl-lysine acetylation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein acetylation","termid":"GO:1901984"},{"relation_name":"is_a","term_name":"regulation of peptidyl-lysine acetylation","termid":"GO:2000756"},{"relation_name":"negatively_regulates","term_name":"peptidyl-lysine acetylation","termid":"GO:0018394"}],"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 peptidyl-lysine acetylation","termid":"GO:2000757"}


id: MONDO:0030935
data:
  {"annotated_genes":["SJAG_07005"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87368],"is_not":false,"summary":null,"term":"MONDO:0030935"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex II deficiency, nuclear type","termid":"MONDO:0031230"}],"gene_count":1,"genes_by_uniquename":{"SJAG_07005":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005336","MONDO:0004069"],"is_obsolete":false,"name":"mitochondrial complex 2 deficiency, nuclear type 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16429","MEDGEN:1742371","UMLS:C5436933","OMIM:619166"],"synonyms":[{"name":"MC2DN2","type":"exact"},{"name":"mitochondrial complex 2 deficiency, nuclear type 2","type":"exact"},{"name":"mitochondrial complex II deficiency, nuclear type 2","type":"exact"}],"termid":"MONDO:0030935","terms_by_termid":{"MONDO:0030935":null},"xrefs":{"Monarch":{"xref_id":"0030935"}}}


id: GO:0060611
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the mammary gland fat over time, from its formation to the mature structure. The mammary fat is an adipose structure in the gland that is invaded by the mammary ducts.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adipose tissue development","termid":"GO:0060612"},{"relation_name":"part_of","term_name":"mammary gland development","termid":"GO:0030879"}],"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":"mammary gland fat development","termid":"GO:0060611"}


id: PBO:0060508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NSF attachment protein alpha","termid":"PBO:0060508"}


id: MONDO:0016200
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase (obsolete MONDO:0016200)","secondary_identifiers":["Orphanet:209203"],"synonyms":[{"name":"qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase type -","type":"exact"}],"termid":"MONDO:0016200","xrefs":{"Monarch":{"xref_id":"0016200"}}}


id: GO:0031763
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a galanin receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide receptor binding","termid":"GO:0071855"}],"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"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"galanin receptor binding","synonyms":[{"name":"galanin receptor ligand","type":"narrow"}],"termid":"GO:0031763"}


id: GO:0098816
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that leads to a temporary increase in postsynaptic potential due to the flow of positively charged ions into the postsynaptic cell, induced by the spontaneous release of a single vesicle of an excitatory neurotransmitter into the synapse.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"excitatory postsynaptic potential","termid":"GO:0060079"}],"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":"mini excitatory postsynaptic potential","termid":"GO:0098816"}


id: GO:0003997
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 2,3-saturated acyl-CoA + O2 = a (2E)-enoyl-CoA + H2O2.","definition_xrefs":["RHEA:38959"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor","termid":"GO:0016634"}],"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:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"acyl-CoA oxidase activity","secondary_identifiers":["Reactome:R-HSA-390256","EC:1.3.3.6","Reactome:R-HSA-192335","MetaCyc:RXN-11026","Reactome:R-HSA-2066787","Reactome:R-HSA-193369"],"synonyms":[{"name":"acyl coenzyme A oxidase activity","type":"related"},{"name":"acyl-CoA:oxygen 2-oxidoreductase activity","type":"related"},{"name":"fatty acyl-CoA oxidase activity","type":"related"},{"name":"fatty acyl-coenzyme A oxidase activity","type":"related"}],"termid":"GO:0003997"}


id: MONDO:0044723
data:
  {"annotated_genes":["SJAG_00737","SJAG_03258"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88811,88812],"is_not":false,"summary":null,"term":"MONDO:0044723"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"3-methylglutaconic aciduria","termid":"MONDO:0017359"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00737":null,"SJAG_03258":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"3-methylglutaconic aciduria type 8","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070000","GARD:22050","OMIM:617248","Orphanet:505208","UMLS:C4310650","MEDGEN:934617"],"synonyms":[{"name":"3-Methylglutaconic aciduria, type 8","type":"related"},{"name":"3-methylglutaconic aciduria type VIII","type":"related"},{"name":"3-methylglutaconic aciduria type VIII, MGCA8","type":"exact"},{"name":"3-methylglutaconic aciduria, type VIII","type":"exact"},{"name":"3-methylglutaconic aciduria, type VIII; MGCA8","type":"exact"},{"name":"MGA8","type":"exact"},{"name":"MGCA8","type":"exact"}],"termid":"MONDO:0044723","terms_by_termid":{"MONDO:0044723":null},"xrefs":{"Monarch":{"xref_id":"0044723"}}}


id: GO:0052358
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 glucan 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 glucan (obsolete GO:0052358)","termid":"GO:0052358"}


id: GO:0044174
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A membrane-bounded organelle that carries materials newly ingested by endocytosis. It passes many of the materials to host cell lysosomes for degradation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host intracellular membrane-bounded organelle","termid":"GO:0033648"},{"relation_name":"is_a","term_name":"host cell cytoplasm part","termid":"GO:0033655"}],"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 cell endosome","synonyms":[{"name":"host endosome","type":"exact"}],"termid":"GO:0044174"}


id: GO:0008085
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete phototransduction, visible light, light adaptation (obsolete GO:0008085)","synonyms":[{"name":"phototransduction, visible light, light adaptation","type":"exact"}],"termid":"GO:0008085"}


id: PBO:0028779
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_telomere_during_vegetative_growth","termid":"PBO:0028779"}


id: PBO:0075190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide G pseudogene 2","termid":"PBO:0075190"}


id: PBO:0039853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGAP19-SLIT1 readthrough (NMD candidate)","termid":"PBO:0039853"}


id: GO:0009913
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of an epidermal cell, any of the cells making up the epidermis.","definition_xrefs":["GOC:mtg_sensu","GOC:dph","GOC:go_curators","GOC:sdb_2009","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell differentiation","termid":"GO:0030855"},{"relation_name":"part_of","term_name":"epidermis development","termid":"GO:0008544"}],"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":"epidermal cell differentiation","secondary_identifiers":["GO:0043355"],"synonyms":[{"name":"hypodermal cell differentiation","type":"related"}],"termid":"GO:0009913"}


id: PBO:0027059
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_Congo_Red","termid":"PBO:0027059"}


id: PBO:0029749
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cytosolic_calcium_level","termid":"PBO:0029749"}


id: PBO:0061683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin 133","termid":"PBO:0061683"}


id: MONDO:0007703
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete heart, malformation of (obsolete MONDO:0007703)","termid":"MONDO:0007703","xrefs":{"Monarch":{"xref_id":"0007703"}}}


id: PBO:0050171
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 27","termid":"PBO:0050171"}


id: PR:O43063
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A proteasome subunit beta type-6 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03572","PANTHER:PTHR11599:SF4","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":"proteasome subunit beta type-1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4C3.10c","secondary_identifiers":["UniProtKB:O43063"],"synonyms":[{"name":"Spom972h-PSMB6","type":"exact"}],"termid":"PR:O43063"}


id: GO:0008773
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UTP + (protein-PII) = diphosphate + uridylyl-(protein-PII).","definition_xrefs":["EC:2.7.7.59"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uridylyltransferase activity","termid":"GO:0070569"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016779"},{"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:0016779","GO:0140096","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"[protein-PII] uridylyltransferase activity","secondary_identifiers":["MetaCyc:URITRANS-RXN","RHEA:13673"],"synonyms":[{"name":"PII uridylyl-transferase activity","type":"related"},{"name":"UTP:[protein-PII] uridylyltransferase activity","type":"exact"},{"name":"UTP:protein-PII uridylyltransferase activity","type":"related"},{"name":"protein-PII uridylyltransferase activity","type":"related"},{"name":"uridyl removing enzyme","type":"related"},{"name":"uridylyl removing enzyme activity","type":"broad"}],"termid":"GO:0008773"}


id: MONDO:0016138
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete malignant lymphoma with peripheral neuropathy (obsolete MONDO:0016138)","secondary_identifiers":["Orphanet:207046"],"termid":"MONDO:0016138","xrefs":{"Monarch":{"xref_id":"0016138"}}}


id: PBO:0083228
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 with YCR047C; identified by gene-trapping, microarray expression analysis, and genome-wide homology searching","termid":"PBO:0083228"}


id: PBO:0031446
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_double-strand_break_repair_during_vegetative_growth","termid":"PBO:0031446"}


id: PBO:0044836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 124","termid":"PBO:0044836"}


id: PBO:0088638
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 Taf4","termid":"PBO:0088638"}


id: PBO:0040681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain enriched myelin associated protein 1","termid":"PBO:0040681"}


id: PBO:0070037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1334, pseudogene","termid":"PBO:0070037"}


id: PBO:0109842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPATA31 subfamily H member 1","termid":"PBO:0109842"}


id: GO:0050734
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a hydroxycinnamoyl group to an acceptor molecule.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016746"}],"interesting_parent_ids":["GO:0003674","GO:0016746","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"hydroxycinnamoyltransferase activity","termid":"GO:0050734"}


id: GO:0045321
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A change in morphology and behavior of a leukocyte resulting from exposure to a specific antigen, mitogen, cytokine, cellular ligand, or soluble factor.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell activation","termid":"GO:0001775"},{"relation_name":"is_a","term_name":"immune system process","termid":"GO:0002376"}],"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":"leukocyte activation","secondary_identifiers":["Wikipedia:Immunologic_activation"],"synonyms":[{"name":"immune cell activation","type":"exact"},{"name":"leucocyte activation","type":"exact"}],"termid":"GO:0045321"}


id: PBO:0049450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GXYLT1 pseudogene 4","termid":"PBO:0049450"}


id: MONDO:0030692
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency 95","secondary_identifiers":["UMLS:C5676929","MEDGEN:1802205","OMIM:619773"],"synonyms":[{"name":"IMD95","type":"exact"},{"name":"immunodeficiency 95","type":"exact"}],"termid":"MONDO:0030692","xrefs":{"Monarch":{"xref_id":"0030692"}}}


id: PBO:0059240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L11 pseudogene 3","termid":"PBO:0059240"}


id: PBO:0078106
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trafficking protein particle complex subunit 13","termid":"PBO:0078106"}


id: MONDO:0024881
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm that arises from a pre-existing lower grade lesion, or as a result of a primary lesion that has spread to secondary sites, or due to a complication of a cancer treatment.","definition_xrefs":["NCIT:C4968"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"},{"relation_name":"is_a","term_name":"secondary neoplasm","termid":"MONDO:0024882"}],"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":"secondary malignant neoplasm","secondary_identifiers":["UMLS:C3266877","MEDGEN:473807","EFO:0009812","ICD9:198.89","SCTID:128462008","ICD9:199.1"],"synonyms":[{"name":"secondary cancer","type":"exact"},{"name":"secondary malignancy","type":"exact"},{"name":"secondary malignant neoplasm","type":"exact"}],"termid":"MONDO:0024881","xrefs":{"Monarch":{"xref_id":"0024881"}}}


id: MONDO:0006083
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete anaplastic large cell lymphoma, ALK-negative (obsolete MONDO:0006083)","termid":"MONDO:0006083","xrefs":{"Monarch":{"xref_id":"0006083"}}}


id: PBO:0046431
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epoxide hydrolase 1","termid":"PBO:0046431"}


id: MONDO:0859286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures","secondary_identifiers":["UMLS:C5774213","MEDGEN:1823986","OMIM:620029","DOID:0070536"],"termid":"MONDO:0859286","xrefs":{"Monarch":{"xref_id":"0859286"}}}


id: PBO:0082468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Calmodulin; Ca2+ binding protein that regulates Ca2+ independent processes (mitosis, bud growth, actin organization, endocytosis, etc.) and Ca2+ dependent processes (stress-activated pathways), targets include Nuf1p, Myo2p and calcineurin; binds to the Hog1p MAPK in response to hyperosmotic stress; potentiates membrane tubulation and constriction mediated by the Rvs161p-Rvs167p complex; human CALM1 or CALM2 functionally complement repression induced inviability","termid":"PBO:0082468"}


id: MONDO:1011523
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hemophilia A that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemophilia A, non-human animal","termid":"MONDO:1011408"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemophilia A, horse","secondary_identifiers":["OMIA:000437-9796"],"termid":"MONDO:1011523","xrefs":{"Monarch":{"xref_id":"1011523"}}}


id: FYPO:0004021
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells form polar microtubules that are longer than normal. Polar microtubules are the spindle microtubules that come from each pole and overlap at the spindle midzone.","definition_xrefs":["GO:0005827","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long microtubules","termid":"FYPO:0000055"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0002399"],"is_obsolete":false,"name":"long polar microtubules","synonyms":[{"name":"elongated polar microtubules","type":"exact"},{"name":"long polar microtubules during mitotic cell cycle","type":"related"},{"name":"long polar microtubules during vegetative growth","type":"exact"}],"termid":"FYPO:0004021"}


id: MONDO:0043653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lesion caused by type 1 or type 2 herpes simplex virus, typically involving the oralfacial region.","definition_xrefs":["NCIT:C34695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"herpes simplex infectious disease","termid":"MONDO:0004609"},{"relation_name":"is_a","term_name":"lip disorder","termid":"MONDO:0004748"},{"relation_name":"is_a","term_name":"disease arising from reactivation of latent virus","termid":"MONDO:0100330"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"herpes labialis","secondary_identifiers":["MESH:D006560","SCTID:1475003","MEDGEN:5533","UMLS:C0019345"],"synonyms":[{"name":"Herpes simplex, labial","type":"related"},{"name":"Sore, cold","type":"related"},{"name":"Sores, cold","type":"related"},{"name":"blister, fever","type":"related"},{"name":"blisters, fever","type":"related"},{"name":"cold sore","type":"exact"},{"name":"cold sores","type":"exact"},{"name":"fever blister","type":"related"},{"name":"fever blisters","type":"related"},{"name":"herpes labialis","type":"exact"},{"name":"herpes simplex labialis","type":"related"},{"name":"labial Herpes simplex","type":"related"}],"termid":"MONDO:0043653","xrefs":{"Monarch":{"xref_id":"0043653"}}}


id: GO:0106267
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (3-chloro-2,4,6-trihydroxyphenyl)hexan-1-one + chloride + FADH2 + O2 = (3,5-dichloro-2,4,6-trihydroxyphenyl)hexan-1-one + FAD + 2 H2O.","definition_xrefs":["RHEA:64360","PMID:20231486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"3,5 dichloro-THPH synthase activity","termid":"GO:0106267"}


id: GO:0060953
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of cells to cardiac glial cell fates and their capacity to differentiate into cardiac glial cells.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell fate commitment","termid":"GO:0021781"},{"relation_name":"is_a","term_name":"cardiac cell fate commitment","termid":"GO:0060911"},{"relation_name":"part_of","term_name":"cardiac glial cell differentiation","termid":"GO:0060950"}],"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":"cardiac glial cell fate commitment","termid":"GO:0060953"}


id: PBO:0038935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alcohol dehydrogenase 1C (class I), gamma polypeptide","termid":"PBO:0038935"}


id: GO:0042579
data:
  {"annotated_genes":["SJAG_03781","SJAG_02693","SJAG_03166","SJAG_04823","SJAG_00706","SJAG_00947","SJAG_03324","SJAG_02630","SJAG_02496","SJAG_01165","SJAG_03671","SJAG_04763","SJAG_04146","SJAG_02619","SJAG_03091","SJAG_03493","SJAG_00114","SJAG_01474","SJAG_01685","SJAG_02384","SJAG_04299","SJAG_03440","SJAG_04315","SJAG_04467","SJAG_05950","SJAG_00326","SJAG_03464","SJAG_02997","SJAG_00891","SJAG_02247","SJAG_04428","SJAG_00702","SJAG_03715","SJAG_02848"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[61604,120169,107134,113700,116605,117622,72393],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005782"},{"annotations":[59366,100385,77617,75449,80239,79504,92238,108523,117623,98769,75057,72419,81409,120044,73481,82100,79872,117160,77261],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0005778"},{"annotations":[73297,78025,111463,71988,115793,81544,76043,74131,75359,101662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005777"}]},"cv_name":"cellular_component","definition":"Cytoplasmic organelles, spherical or oval in shape, that are bounded by a single membrane and contain oxidative enzymes, especially those utilizing hydrogen peroxide (H2O2).","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membrane-bounded organelle","termid":"GO:0043231"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":34,"genes_by_uniquename":{"SJAG_00114":null,"SJAG_00326":null,"SJAG_00702":null,"SJAG_00706":null,"SJAG_00891":null,"SJAG_00947":null,"SJAG_01165":null,"SJAG_01474":null,"SJAG_01685":null,"SJAG_02247":null,"SJAG_02384":null,"SJAG_02496":null,"SJAG_02619":null,"SJAG_02630":null,"SJAG_02693":null,"SJAG_02848":null,"SJAG_02997":null,"SJAG_03091":null,"SJAG_03166":null,"SJAG_03324":null,"SJAG_03440":null,"SJAG_03464":null,"SJAG_03493":null,"SJAG_03671":null,"SJAG_03715":null,"SJAG_03781":null,"SJAG_04146":null,"SJAG_04299":null,"SJAG_04315":null,"SJAG_04428":null,"SJAG_04467":null,"SJAG_04763":null,"SJAG_04823":null,"SJAG_05950":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"microbody","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000044":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Microbody"],"termid":"GO:0042579","terms_by_termid":{"GO:0005777":null,"GO:0005778":null,"GO:0005782":null}}


id: PBO:0060662
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal calcium sensor 1","termid":"PBO:0060662"}


id: GO:1902494
data:
  {"annotated_genes":["SJAG_01956","SJAG_02469","SJAG_03193","SJAG_03627","SJAG_04756","SJAG_03651","SJAG_00080","SJAG_02329","SJAG_04932","SJAG_01711","SJAG_01720","SJAG_04420","SJAG_03385","SJAG_02773","SJAG_02107","SJAG_04357","SJAG_01006","SJAG_00738","SJAG_03114","SJAG_03952","SJAG_00392","SJAG_01490","SJAG_00412","SJAG_00656","SJAG_03218","SJAG_01392","SJAG_03371","SJAG_00119","SJAG_00823","SJAG_04969","SJAG_03672","SJAG_02374","SJAG_05329","SJAG_01436","SJAG_03626","SJAG_03234","SJAG_02317","SJAG_02502","SJAG_04614","SJAG_01471","SJAG_03454","SJAG_00182","SJAG_01521","SJAG_00341","SJAG_01801","SJAG_04859","SJAG_03328","SJAG_00735","SJAG_02404","SJAG_02165","SJAG_03841","SJAG_01876","SJAG_00087","SJAG_02686","SJAG_01149","SJAG_06309","SJAG_04754","SJAG_03535","SJAG_03956","SJAG_01862","SJAG_00939","SJAG_00581","SJAG_05025","SJAG_02768","SJAG_04142","SJAG_03940","SJAG_00184","SJAG_00814","SJAG_00045","SJAG_01349","SJAG_02397","SJAG_02844","SJAG_00783","SJAG_02369","SJAG_00461","SJAG_04540","SJAG_04087","SJAG_00691","SJAG_00369","SJAG_05282","SJAG_03898","SJAG_01230","SJAG_02299","SJAG_05192","SJAG_03962","SJAG_00113","SJAG_04179","SJAG_02778","SJAG_01456","SJAG_00414","SJAG_04095","SJAG_03858","SJAG_00457","SJAG_03925","SJAG_05032","SJAG_02162","SJAG_01657","SJAG_05274","SJAG_01044","SJAG_00819","SJAG_04898","SJAG_07011","SJAG_01207","SJAG_03802","SJAG_01245","SJAG_02289","SJAG_03761","SJAG_04189","SJAG_07003","SJAG_00411","SJAG_00604","SJAG_04150","SJAG_02564","SJAG_02766","SJAG_02990","SJAG_00596","SJAG_01151","SJAG_01581","SJAG_02444","SJAG_03126","SJAG_02589","SJAG_03587","SJAG_03029","SJAG_01214","SJAG_04755","SJAG_02685","SJAG_03406","SJAG_01671","SJAG_02385","SJAG_02900","SJAG_04477","SJAG_00758","SJAG_05316","SJAG_03230","SJAG_01572","SJAG_00306","SJAG_04882","SJAG_00506","SJAG_02809","SJAG_MIT13","SJAG_01573","SJAG_04552","SJAG_00534","SJAG_00880","SJAG_03618","SJAG_03255","SJAG_02901","SJAG_03160","SJAG_01236","SJAG_04097","SJAG_03681","SJAG_02206","SJAG_03417","SJAG_00615","SJAG_00322","SJAG_02504","SJAG_04732","SJAG_00911","SJAG_04486","SJAG_01077","SJAG_00739","SJAG_00600","SJAG_03628","SJAG_00033","SJAG_02172","SJAG_00272","SJAG_06449","SJAG_04576","SJAG_04175","SJAG_01128","SJAG_02466","SJAG_02981","SJAG_04568","SJAG_04306","SJAG_03954","SJAG_00872","SJAG_04582","SJAG_04389","SJAG_00554","SJAG_01886","SJAG_02275","SJAG_00421","SJAG_02386","SJAG_01531","SJAG_00512","SJAG_03575","SJAG_03151","SJAG_03737","SJAG_01332","SJAG_05978","SJAG_02197","SJAG_02536","SJAG_02360","SJAG_03290","SJAG_05348","SJAG_02057","SJAG_01063","SJAG_04232","SJAG_04229","SJAG_02163","SJAG_03353","SJAG_04638","SJAG_03591","SJAG_01823","SJAG_01857","SJAG_03261","SJAG_04661","SJAG_03033","SJAG_03921","SJAG_01808","SJAG_01540","SJAG_04497","SJAG_03982","SJAG_02066","SJAG_03118","SJAG_00438","SJAG_04934","SJAG_00146","SJAG_02665","SJAG_00498","SJAG_03555","SJAG_03356","SJAG_00712","SJAG_03668","SJAG_01599","SJAG_01489","SJAG_01611","SJAG_03796","SJAG_02183","SJAG_04816","SJAG_03494","SJAG_00605","SJAG_04106","SJAG_00192","SJAG_04520","SJAG_01710","SJAG_03292","SJAG_03685","SJAG_06383","SJAG_05236","SJAG_03035","SJAG_03421","SJAG_01351","SJAG_00186","SJAG_03045","SJAG_02869","SJAG_04178","SJAG_01716","SJAG_00619","SJAG_04280","SJAG_01577","SJAG_01203","SJAG_02286","SJAG_01763","SJAG_00638","SJAG_00976","SJAG_03900","SJAG_02262","SJAG_02918","SJAG_04933","SJAG_01187","SJAG_00320","SJAG_02541","SJAG_03061","SJAG_02527","SJAG_00778","SJAG_04550","SJAG_02722","SJAG_03066","SJAG_02908","SJAG_01016","SJAG_03602","SJAG_01131","SJAG_00746","SJAG_01794","SJAG_02846","SJAG_03931","SJAG_02703","SJAG_03144","SJAG_00260","SJAG_00741","SJAG_05294","SJAG_02023","SJAG_02994","SJAG_01259","SJAG_04368","SJAG_02629","SJAG_03884","SJAG_02305","SJAG_00924","SJAG_05224","SJAG_03302","SJAG_01238","SJAG_01544","SJAG_02044","SJAG_03867","SJAG_03070","SJAG_02303","SJAG_02627","SJAG_00078","SJAG_05560","SJAG_04675","SJAG_02600","SJAG_03579","SJAG_02186","SJAG_04408","SJAG_00641","SJAG_01190","SJAG_00441","SJAG_00514","SJAG_04923","SJAG_00128","SJAG_03163","SJAG_02561","SJAG_01551","SJAG_04770","SJAG_04122","SJAG_04677","SJAG_03561","SJAG_01750","SJAG_01475","SJAG_02721","SJAG_02464","SJAG_01276","SJAG_03641","SJAG_04758","SJAG_01260","SJAG_04968","SJAG_00571","SJAG_03949","SJAG_00676","SJAG_03680","SJAG_03677","SJAG_03285","SJAG_01533","SJAG_00516","SJAG_03601","SJAG_00458","SJAG_03839","SJAG_03490","SJAG_00378","SJAG_04989","SJAG_02822","SJAG_02447","SJAG_04665","SJAG_04654","SJAG_04084","SJAG_00901","SJAG_04451","SJAG_00766","SJAG_01110","SJAG_03576","SJAG_02158","SJAG_00836","SJAG_02818","SJAG_01447","SJAG_01159","SJAG_04994","SJAG_03495","SJAG_01585","SJAG_MIT37","SJAG_04704","SJAG_00666","SJAG_01637","SJAG_01455","SJAG_01819","SJAG_02663","SJAG_03525","SJAG_03115","SJAG_03862","SJAG_04182","SJAG_04026","SJAG_03787","SJAG_00995","SJAG_00150","SJAG_02105","SJAG_03036","SJAG_04484","SJAG_03064","SJAG_02782","SJAG_02804","SJAG_04853","SJAG_02174","SJAG_03350","SJAG_00136","SJAG_02304","SJAG_03431","SJAG_02506","SJAG_03844","SJAG_01658","SJAG_01431","SJAG_00566","SJAG_00762","SJAG_00153","SJAG_04818","SJAG_03289","SJAG_01870","SJAG_00352","SJAG_00868","SJAG_04144","SJAG_00769","SJAG_03345","SJAG_07006","SJAG_00639","SJAG_02308","SJAG_03695","SJAG_04355","SJAG_01524","SJAG_03638","SJAG_03181","SJAG_00532","SJAG_01662","SJAG_04030","SJAG_00934","SJAG_01427","SJAG_04641","SJAG_04917","SJAG_01865","SJAG_05629","SJAG_04107","SJAG_01009","SJAG_05240","SJAG_02658","SJAG_02562","SJAG_03130","SJAG_01587","SJAG_MIT09","SJAG_04274","SJAG_03813","SJAG_04619","SJAG_03333","SJAG_02041","SJAG_00579","SJAG_01301","SJAG_02003","SJAG_04396","SJAG_00754","SJAG_05020","SJAG_00460","SJAG_02646","SJAG_00139","SJAG_00854","SJAG_00755","SJAG_03789","SJAG_00894","SJAG_04127","SJAG_02598","SJAG_01111","SJAG_02948","SJAG_00915","SJAG_00142","SJAG_01302","SJAG_00743","SJAG_00295","SJAG_01910","SJAG_00859","SJAG_00212","SJAG_03500","SJAG_02101","SJAG_01008","SJAG_01562","SJAG_03436","SJAG_02505","SJAG_00262","SJAG_02319","SJAG_04860","SJAG_03920","SJAG_01068","SJAG_01906","SJAG_02571","SJAG_00602","SJAG_04824","SJAG_01378","SJAG_00559","SJAG_03631","SJAG_03081","SJAG_01389","SJAG_04783","SJAG_02726","SJAG_05017","SJAG_00439","SJAG_04252","SJAG_03776","SJAG_00147","SJAG_00643","SJAG_03215","SJAG_04888","SJAG_04907","SJAG_03702","SJAG_01693","SJAG_03145","SJAG_04541","SJAG_02653","SJAG_05219","SJAG_00985","SJAG_04970","SJAG_03578","SJAG_03206","SJAG_04181","SJAG_01370","SJAG_06425","SJAG_00584","SJAG_04151","SJAG_05197","SJAG_02222","SJAG_01472","SJAG_01678","SJAG_03501","SJAG_05323","SJAG_04335","SJAG_04088","SJAG_00816","SJAG_00910","SJAG_04131","SJAG_04596","SJAG_00611","SJAG_02637","SJAG_03468","SJAG_04815","SJAG_05979","SJAG_04509","SJAG_01480","SJAG_02547","SJAG_00988","SJAG_01288","SJAG_00100","SJAG_00623","SJAG_03107","SJAG_03179","SJAG_04230","SJAG_02039","SJAG_04586","SJAG_00114","SJAG_01817","SJAG_00808","SJAG_02545","SJAG_01465","SJAG_01069","SJAG_03861","SJAG_03403","SJAG_03711","SJAG_04894","SJAG_02542","SJAG_02500","SJAG_04015","SJAG_01179","SJAG_01799","SJAG_01313","SJAG_00446","SJAG_03006","SJAG_04434","SJAG_00349","SJAG_01401","SJAG_04201","SJAG_04090","SJAG_07007","SJAG_04971","SJAG_05012","SJAG_00159","SJAG_02233","SJAG_02591","SJAG_01617","SJAG_04140","SJAG_00955","SJAG_MIT15","SJAG_03793","SJAG_02871","SJAG_02070","SJAG_03752","SJAG_03408","SJAG_01315","SJAG_00866","SJAG_02398","SJAG_03809","SJAG_03792","SJAG_02651","SJAG_04161","SJAG_03048","SJAG_01652","SJAG_04890","SJAG_02439","SJAG_01776","SJAG_00727","SJAG_03453","SJAG_00545","SJAG_01826","SJAG_02119","SJAG_01191","SJAG_00133","SJAG_01884","SJAG_03728","SJAG_04153","SJAG_00552","SJAG_00873","SJAG_02872","SJAG_00845","SJAG_01453","SJAG_03321","SJAG_02063","SJAG_06382","SJAG_02863","SJAG_04318","SJAG_04062","SJAG_04559","SJAG_03801","SJAG_02553","SJAG_02667","SJAG_00293","SJAG_MIT03","SJAG_MIT20","SJAG_00071","SJAG_02895","SJAG_03014","SJAG_06613","SJAG_01926","SJAG_01234","SJAG_02785","SJAG_01014","SJAG_00601","SJAG_00187","SJAG_04972","SJAG_00973","SJAG_01051","SJAG_03015","SJAG_04213","SJAG_03758","SJAG_04205","SJAG_00896","SJAG_04005","SJAG_01698","SJAG_02441","SJAG_04321","SJAG_05285","SJAG_00542","SJAG_04612","SJAG_01385","SJAG_02583","SJAG_04119","SJAG_00731","SJAG_03599","SJAG_04574","SJAG_00229","SJAG_03985","SJAG_01197","SJAG_02706","SJAG_01253","SJAG_01327","SJAG_01397","SJAG_00116","SJAG_00083","SJAG_02549","SJAG_02182","SJAG_02237","SJAG_02992","SJAG_04821","SJAG_01646","SJAG_06635","SJAG_05297","SJAG_06560","SJAG_04384","SJAG_04572","SJAG_00440","SJAG_02082","SJAG_04848","SJAG_00129","SJAG_03280","SJAG_02753","SJAG_02798","SJAG_03441","SJAG_04613","SJAG_02279","SJAG_04877","SJAG_04879","SJAG_01270","SJAG_00831","SJAG_03460","SJAG_04309","SJAG_01369","SJAG_04312","SJAG_01213","SJAG_01022","SJAG_01325","SJAG_05235","SJAG_03967","SJAG_01134","SJAG_03694","SJAG_00756","SJAG_05239","SJAG_00966","SJAG_00400","SJAG_03425","SJAG_04955","SJAG_00213","SJAG_00846","SJAG_05027","SJAG_01504","SJAG_02687","SJAG_01818","SJAG_05313","SJAG_05278","SJAG_04680","SJAG_01804","SJAG_04186","SJAG_01610","SJAG_04199","SJAG_04916","SJAG_02903","SJAG_03037","SJAG_04502","SJAG_00095","SJAG_00091","SJAG_03311","SJAG_16453","SJAG_01010","SJAG_01709","SJAG_00526","SJAG_01274","SJAG_04793","SJAG_02867","SJAG_04694","SJAG_02837","SJAG_03648","SJAG_04631","SJAG_05204","SJAG_00637","SJAG_03093","SJAG_02913","SJAG_02254","SJAG_01622","SJAG_03932","SJAG_02843","SJAG_02396","SJAG_04881","SJAG_01058","SJAG_02776","SJAG_04397","SJAG_03745","SJAG_02341","SJAG_04211","SJAG_MIT04","SJAG_03811","SJAG_01056","SJAG_02699","SJAG_01444","SJAG_01713","SJAG_02458","SJAG_02170","SJAG_02725","SJAG_03219","SJAG_03496","SJAG_04117","SJAG_00435","SJAG_00885","SJAG_04977","SJAG_04085","SJAG_04452","SJAG_03351","SJAG_03944","SJAG_00651","SJAG_02920","SJAG_01913","SJAG_04035","SJAG_00729","SJAG_04852","SJAG_01765","SJAG_02879","SJAG_04261","SJAG_02927","SJAG_03699","SJAG_02006","SJAG_01355","SJAG_01623","SJAG_04006","SJAG_02808","SJAG_03810","SJAG_00283","SJAG_01629"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[65201,63726,104457,70938,60627],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000148"},{"annotations":[107077,111552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120513"},{"annotations":[79581],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005945"},{"annotations":[77481,77803],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005948"},{"annotations":[76987,72132,76600,74688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005658"},{"annotations":[113363,77832,80592,81642,75686,81071,76212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005946"},{"annotations":[72478,79890,78472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017101"},{"annotations":[73721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031250"},{"annotations":[75714,80735,67515,71822,74779,81693,65539,80844,96982,72599,74900,72368,58113,78320,79563,80124,80870,82131],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005680"},{"annotations":[116518,105316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005950"},{"annotations":[74308,72604,74018,119668,81463],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990316"},{"annotations":[73822],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034274"},{"annotations":[76244,82038,59533,79360],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031429"},{"annotations":[73006,75684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005953"},{"annotations":[81305,74795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005955"},{"annotations":[72715,75089],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005952"},{"annotations":[108350,72111],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005951"},{"annotations":[73809,79432,110078,75847,73548,77629,77823,89586,115316,118738,78445,73674,77249,81062,77784,77436,75829,71615,77220,72121,72166,94500,109476,80639,72213,73983,80645,74875,78862,75640,79399,74234,79876,81107,114731,80064,72150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071013"},{"annotations":[105507,106348,89688,95280,92645,91667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071521"},{"annotations":[80382,74265,68492,78002,72832],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016593"},{"annotations":[100236,100810,117861,105302],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110115"},{"annotations":[120689,96155,98536,112329,115839,119555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043494"},{"annotations":[81223,97615,112763],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070692"},{"annotations":[76657],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031463"},{"annotations":[77952,92720,98494,92672,72587,107169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0080008"},{"annotations":[71740],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031464"},{"annotations":[81257,81069,77691,99305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035361"},{"annotations":[91061],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031461"},{"annotations":[107520,104166,106146,76716,80026,72287,71930,78466,73248,90028,108089,75809,110195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000307"},{"annotations":[67427,67236,92797,79100,81496],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005868"},{"annotations":[76328,77985,79425,74180,73060,73355,74946,76814,76063,117738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000177"},{"annotations":[69232,101853],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904564"},{"annotations":[107687,79277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002144"},{"annotations":[77205,113885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031431"},{"annotations":[73801,76176],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904423"},{"annotations":[72734,104647,78622,76823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043625"},{"annotations":[120053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033203"},{"annotations":[81962,118182,101760],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032807"},{"annotations":[98242,105588,108552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033185"},{"annotations":[102119,113806,120088],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990567"},{"annotations":[118248,72868,90797,66041,109843,114672],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044695"},{"annotations":[101272,73113,80486,100093,81180],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000408"},{"annotations":[114683,78851,74393,66048,79536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031391"},{"annotations":[73932,74069,79902,59007,81518,66351],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033588"},{"annotations":[111994,76610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031211"},{"annotations":[115422,111785,109178,117263],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008622"},{"annotations":[98035,80724],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035657"},{"annotations":[58811,74004],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005835"},{"annotations":[63801],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005760"},{"annotations":[90106,80779,79114,72727,82125,81735,116113],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034657"},{"annotations":[80163,78490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017177"},{"annotations":[79181,80491],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017109"},{"annotations":[80122,97310],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903600"},{"annotations":[73536,76883,120276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030956"},{"annotations":[98825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036087"},{"annotations":[75915,79793,89228,57985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005960"},{"annotations":[79383,117994],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990529"},{"annotations":[93037,91368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120097"},{"annotations":[94809,72689,79210,58590,110423,94899],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000506"},{"annotations":[76290,76288,77092,72552,72312],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042765"},{"annotations":[78185,74273],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990131"},{"annotations":[65541],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070823"},{"annotations":[115606,93646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032478"},{"annotations":[108329,77039,75949,82141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005834"},{"annotations":[79463,79679],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033573"},{"annotations":[90241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000123"},{"annotations":[76080,81051],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048476"},{"annotations":[107126,111412,119021,105788,91070,106645,109508],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000836"},{"annotations":[95199,73052,72969,76404],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033503"},{"annotations":[61755,90683,103380,73507,95817,58017,74371,89614,115001,117259,78030,73386,71639,68162,73907,110898,74663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031011"},{"annotations":[78000,75486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070916"},{"annotations":[93512,65711,120433,96774],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090730"},{"annotations":[77614],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005745"},{"annotations":[71795],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000136"},{"annotations":[71489,89310,60008,119918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140497"},{"annotations":[94999,94772,104929,65117,108712,111526,115732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099128"},{"annotations":[89219,79168],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034245"},{"annotations":[78574,81709],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042720"},{"annotations":[107408,115046],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017087"},{"annotations":[92563,107138,106252,101489],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036410"},{"annotations":[78291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990304"},{"annotations":[72657,71768,79101,77706],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031415"},{"annotations":[79675,72384],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031416"},{"annotations":[68428,74119,76984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031417"},{"annotations":[111575,114604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071595"},{"annotations":[109759,95764,108347,107139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033100"},{"annotations":[79602],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990467"},{"annotations":[81894,74664,78031,94184,105855,75411,81766,110903,79171,80817,69738,108709,80028,100773,75536,74711,106543],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035267"},{"annotations":[74179,76327,76813,79424,73354,74945,73059,77984,102854,117302,75181,72356,76062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000176"},{"annotations":[71871,73659,119842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031380"},{"annotations":[99586,110919,96158,92413,106696,112167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043224"},{"annotations":[72917,61025,117252,64547,106381,117164,73150,101303,120472,73486,92898],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005655"},{"annotations":[71754,81160,120095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031588"},{"annotations":[64158,80995,76167,65965,77084,80624,101850],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008250"},{"annotations":[71969,73494,65188,108570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045252"},{"annotations":[110875,110718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070691"},{"annotations":[79453,80542,71982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031251"},{"annotations":[89545,81854,111836,115417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070772"},{"annotations":[79443,80782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009328"},{"annotations":[73301,96438,78516,79031,113373],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034271"},{"annotations":[73302,107541,79032,78517],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034272"},{"annotations":[72142,71585,78742],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000015"},{"annotations":[112180],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000502"},{"annotations":[76899,73653,71543,74250,74787,77303,80143],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0019773"},{"annotations":[65359,71170,57546,61897,57354,62386,64470],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0019774"},{"annotations":[75445,79747,81596,74869,79862,78642,80192,80929,81313],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008540"},{"annotations":[117016,75962,78205,100764,62007,70517,72994,74518,75989,81240,79900,63275],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008541"},{"annotations":[73007,75271],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005965"},{"annotations":[97073,120158],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009365"},{"annotations":[79855,77763,75925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005956"},{"annotations":[74368,109241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030289"},{"annotations":[94792],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000164"},{"annotations":[66097,72844,63628,77577,79993,106322,73456],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000159"},{"annotations":[117342,119811],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008287"},{"annotations":[66217,117706,65176,79561,65487,120950,120944,120955,105498,96661,68603,68387,71920,109738,58107,74479,60393],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045259"},{"annotations":[70814,99511,118447],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072357"},{"annotations":[76345,89232,74450,96820,75085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045254"},{"annotations":[81283,75570,80701],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005968"},{"annotations":[78869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097505"},{"annotations":[96693,97823,72169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031422"},{"annotations":[90628,76365,78554,77750],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045273"},{"annotations":[77424,62513,75502,73916,119549,105897,77506,115259,120938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045275"},{"annotations":[120933,120963,75991,69434,117320,62547,110125,73579,120911,116088],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045277"},{"annotations":[69161],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009349"},{"annotations":[61013,72084,81987],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032299"},{"annotations":[117254,107484,61024,117166,64546,98602,75336,107483,92899,81176,73485,77795,72958],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000172"},{"annotations":[78208,109089],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005971"},{"annotations":[64434,60554,62483],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002189"},{"annotations":[80380,120064,119050,120438,73414,105935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120330"},{"annotations":[69191,58456,104357,72806,77485,78706,79238,77592,117386,78284,76277,75898,106715,116076,71841,77278,76925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005736"},{"annotations":[76222,72402,78282,78704,114706,76923,72804,74469,75033,77276,80688,79836,77117],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0005665"},{"annotations":[72869,76740,57205,72805,75897,81415,81553,118626,75190,64236,78599,71840,76924,78283,73037,78705,77277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005666"},{"annotations":[64515,63732,82008,96453,108582,116094,77694,77885,77566,80718,90921,61573,79084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033698"},{"annotations":[77567,96454,106546,79883,112323,80438,116004,61574,80719,76528,82009,108583,79085,90922,95052,64516,116095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070210"},{"annotations":[74457,63731,78336,95591,74710,97264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032221"},{"annotations":[114985,81391,75430,72339,59098,81528,89471,94108,97707,74715,67724,89969,95819,95962],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016586"},{"annotations":[63998,73308,118144,75704,80622,93221,75535,77313,75250,67721,78911,90306,62732,105185,58160,72680,113602,78454,119428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000124"},{"annotations":[104692,61262,90376,97357,82092,75810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019005"},{"annotations":[105099,119439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990520"},{"annotations":[74834,107364,80659,98714,107820,95362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017059"},{"annotations":[92521,75688,73025,77237,80252,73631,111193,117568],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048188"},{"annotations":[106007,80887,80437,95053,68393],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034967"},{"annotations":[115147,113959,73400,109997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070824"},{"annotations":[75644,66921,69370,62662],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005787"},{"annotations":[110921,112170],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017117"},{"annotations":[64000,58587],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046695"},{"annotations":[113341,76135,76179,74241,89855,119724,71965,77013],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030915"},{"annotations":[77072,116833],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009361"},{"annotations":[71917,119341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009337"},{"annotations":[77299,99570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031510"},{"annotations":[91408,98024],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106068"},{"annotations":[93351,98499,111810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033768"},{"annotations":[89472,109279,116869,71638,73072,97708,95944,78788,114986,79421,74428,78092],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016514"},{"annotations":[100777,71831,74662,81765,94185,116574,115175,78697,75410,115004,119314,109716,98462,100048,110906,78029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000812"},{"annotations":[72411],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000333"},{"annotations":[92444,97635,114739,71377,109874,71644,110372,108175,117727,118259,116795,109957],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005697"},{"annotations":[73786,80395],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005672"},{"annotations":[69632,77314,76699,78584,60015,75389,76181,58180,72379,105435,97392,71636,82082,78455,119429,73107],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005669"},{"annotations":[71895,77901],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005673"},{"annotations":[71637,80946,82197],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005674"},{"annotations":[93985,72104,80463,77905,110823,71878,116687,76126],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0005675"},{"annotations":[61470,67369,77961],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070985"},{"annotations":[70105,70394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990234"},{"annotations":[75889,76679],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031515"},{"annotations":[105957,77141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043528"},{"annotations":[117577,59465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106143"},{"annotations":[75682,61127,80709,73202],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000214"},{"annotations":[102930,106057],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052718"},{"annotations":[79233,75213,72594,79671,62643],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071006"},{"annotations":[79234,73792,79672,79710,81086],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071007"},{"annotations":[118647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031371"},{"annotations":[76024,118613,103295,75318,91152,112886,114840,76123,72351,75909,106419,117509,118709,109060,78695,76964,63735,101449,79206],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000151"},{"annotations":[80527],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990861"},{"annotations":[76571,100152,105391],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043541"},{"annotations":[59570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035550"},{"annotations":[93868,105729,97465,101764,97646,91973,62725],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000220"},{"annotations":[89849,72954,61085,111718,120607,104492,98426,100730],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000221"},{"annotations":[79419,104700],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016035"}]},"cv_name":"cellular_component","definition":"A protein complex which is capable of catalytic activity.","definition_xrefs":["GOC:bhm","PMID:8077207","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":777,"genes_by_uniquename":{"SJAG_00033":null,"SJAG_00045":null,"SJAG_00071":null,"SJAG_00078":null,"SJAG_00080":null,"SJAG_00083":null,"SJAG_00087":null,"SJAG_00091":null,"SJAG_00095":null,"SJAG_00100":null,"SJAG_00113":null,"SJAG_00114":null,"SJAG_00116":null,"SJAG_00119":null,"SJAG_00128":null,"SJAG_00129":null,"SJAG_00133":null,"SJAG_00136":null,"SJAG_00139":null,"SJAG_00142":null,"SJAG_00146":null,"SJAG_00147":null,"SJAG_00150":null,"SJAG_00153":null,"SJAG_00159":null,"SJAG_00182":null,"SJAG_00184":null,"SJAG_00186":null,"SJAG_00187":null,"SJAG_00192":null,"SJAG_00212":null,"SJAG_00213":null,"SJAG_00229":null,"SJAG_00260":null,"SJAG_00262":null,"SJAG_00272":null,"SJAG_00283":null,"SJAG_00293":null,"SJAG_00295":null,"SJAG_00306":null,"SJAG_00320":null,"SJAG_00322":null,"SJAG_00341":null,"SJAG_00349":null,"SJAG_00352":null,"SJAG_00369":null,"SJAG_00378":null,"SJAG_00392":null,"SJAG_00400":null,"SJAG_00411":null,"SJAG_00412":null,"SJAG_00414":null,"SJAG_00421":null,"SJAG_00435":null,"SJAG_00438":null,"SJAG_00439":null,"SJAG_00440":null,"SJAG_00441":null,"SJAG_00446":null,"SJAG_00457":null,"SJAG_00458":null,"SJAG_00460":null,"SJAG_00461":null,"SJAG_00498":null,"SJAG_00506":null,"SJAG_00512":null,"SJAG_00514":null,"SJAG_00516":null,"SJAG_00526":null,"SJAG_00532":null,"SJAG_00534":null,"SJAG_00542":null,"SJAG_00545":null,"SJAG_00552":null,"SJAG_00554":null,"SJAG_00559":null,"SJAG_00566":null,"SJAG_00571":null,"SJAG_00579":null,"SJAG_00581":null,"SJAG_00584":null,"SJAG_00596":null,"SJAG_00600":null,"SJAG_00601":null,"SJAG_00602":null,"SJAG_00604":null,"SJAG_00605":null,"SJAG_00611":null,"SJAG_00615":null,"SJAG_00619":null,"SJAG_00623":null,"SJAG_00637":null,"SJAG_00638":null,"SJAG_00639":null,"SJAG_00641":null,"SJAG_00643":null,"SJAG_00651":null,"SJAG_00656":null,"SJAG_00666":null,"SJAG_00676":null,"SJAG_00691":null,"SJAG_00712":null,"SJAG_00727":null,"SJAG_00729":null,"SJAG_00731":null,"SJAG_00735":null,"SJAG_00738":null,"SJAG_00739":null,"SJAG_00741":null,"SJAG_00743":null,"SJAG_00746":null,"SJAG_00754":null,"SJAG_00755":null,"SJAG_00756":null,"SJAG_00758":null,"SJAG_00762":null,"SJAG_00766":null,"SJAG_00769":null,"SJAG_00778":null,"SJAG_00783":null,"SJAG_00808":null,"SJAG_00814":null,"SJAG_00816":null,"SJAG_00819":null,"SJAG_00823":null,"SJAG_00831":null,"SJAG_00836":null,"SJAG_00845":null,"SJAG_00846":null,"SJAG_00854":null,"SJAG_00859":null,"SJAG_00866":null,"SJAG_00868":null,"SJAG_00872":null,"SJAG_00873":null,"SJAG_00880":null,"SJAG_00885":null,"SJAG_00894":null,"SJAG_00896":null,"SJAG_00901":null,"SJAG_00910":null,"SJAG_00911":null,"SJAG_00915":null,"SJAG_00924":null,"SJAG_00934":null,"SJAG_00939":null,"SJAG_00955":null,"SJAG_00966":null,"SJAG_00973":null,"SJAG_00976":null,"SJAG_00985":null,"SJAG_00988":null,"SJAG_00995":null,"SJAG_01006":null,"SJAG_01008":null,"SJAG_01009":null,"SJAG_01010":null,"SJAG_01014":null,"SJAG_01016":null,"SJAG_01022":null,"SJAG_01044":null,"SJAG_01051":null,"SJAG_01056":null,"SJAG_01058":null,"SJAG_01063":null,"SJAG_01068":null,"SJAG_01069":null,"SJAG_01077":null,"SJAG_01110":null,"SJAG_01111":null,"SJAG_01128":null,"SJAG_01131":null,"SJAG_01134":null,"SJAG_01149":null,"SJAG_01151":null,"SJAG_01159":null,"SJAG_01179":null,"SJAG_01187":null,"SJAG_01190":null,"SJAG_01191":null,"SJAG_01197":null,"SJAG_01203":null,"SJAG_01207":null,"SJAG_01213":null,"SJAG_01214":null,"SJAG_01230":null,"SJAG_01234":null,"SJAG_01236":null,"SJAG_01238":null,"SJAG_01245":null,"SJAG_01253":null,"SJAG_01259":null,"SJAG_01260":null,"SJAG_01270":null,"SJAG_01274":null,"SJAG_01276":null,"SJAG_01288":null,"SJAG_01301":null,"SJAG_01302":null,"SJAG_01313":null,"SJAG_01315":null,"SJAG_01325":null,"SJAG_01327":null,"SJAG_01332":null,"SJAG_01349":null,"SJAG_01351":null,"SJAG_01355":null,"SJAG_01369":null,"SJAG_01370":null,"SJAG_01378":null,"SJAG_01385":null,"SJAG_01389":null,"SJAG_01392":null,"SJAG_01397":null,"SJAG_01401":null,"SJAG_01427":null,"SJAG_01431":null,"SJAG_01436":null,"SJAG_01444":null,"SJAG_01447":null,"SJAG_01453":null,"SJAG_01455":null,"SJAG_01456":null,"SJAG_01465":null,"SJAG_01471":null,"SJAG_01472":null,"SJAG_01475":null,"SJAG_01480":null,"SJAG_01489":null,"SJAG_01490":null,"SJAG_01504":null,"SJAG_01521":null,"SJAG_01524":null,"SJAG_01531":null,"SJAG_01533":null,"SJAG_01540":null,"SJAG_01544":null,"SJAG_01551":null,"SJAG_01562":null,"SJAG_01572":null,"SJAG_01573":null,"SJAG_01577":null,"SJAG_01581":null,"SJAG_01585":null,"SJAG_01587":null,"SJAG_01599":null,"SJAG_01610":null,"SJAG_01611":null,"SJAG_01617":null,"SJAG_01622":null,"SJAG_01623":null,"SJAG_01629":null,"SJAG_01637":null,"SJAG_01646":null,"SJAG_01652":null,"SJAG_01657":null,"SJAG_01658":null,"SJAG_01662":null,"SJAG_01671":null,"SJAG_01678":null,"SJAG_01693":null,"SJAG_01698":null,"SJAG_01709":null,"SJAG_01710":null,"SJAG_01711":null,"SJAG_01713":null,"SJAG_01716":null,"SJAG_01720":null,"SJAG_01750":null,"SJAG_01763":null,"SJAG_01765":null,"SJAG_01776":null,"SJAG_01794":null,"SJAG_01799":null,"SJAG_01801":null,"SJAG_01804":null,"SJAG_01808":null,"SJAG_01817":null,"SJAG_01818":null,"SJAG_01819":null,"SJAG_01823":null,"SJAG_01826":null,"SJAG_01857":null,"SJAG_01862":null,"SJAG_01865":null,"SJAG_01870":null,"SJAG_01876":null,"SJAG_01884":null,"SJAG_01886":null,"SJAG_01906":null,"SJAG_01910":null,"SJAG_01913":null,"SJAG_01926":null,"SJAG_01956":null,"SJAG_02003":null,"SJAG_02006":null,"SJAG_02023":null,"SJAG_02039":null,"SJAG_02041":null,"SJAG_02044":null,"SJAG_02057":null,"SJAG_02063":null,"SJAG_02066":null,"SJAG_02070":null,"SJAG_02082":null,"SJAG_02101":null,"SJAG_02105":null,"SJAG_02107":null,"SJAG_02119":null,"SJAG_02158":null,"SJAG_02162":null,"SJAG_02163":null,"SJAG_02165":null,"SJAG_02170":null,"SJAG_02172":null,"SJAG_02174":null,"SJAG_02182":null,"SJAG_02183":null,"SJAG_02186":null,"SJAG_02197":null,"SJAG_02206":null,"SJAG_02222":null,"SJAG_02233":null,"SJAG_02237":null,"SJAG_02254":null,"SJAG_02262":null,"SJAG_02275":null,"SJAG_02279":null,"SJAG_02286":null,"SJAG_02289":null,"SJAG_02299":null,"SJAG_02303":null,"SJAG_02304":null,"SJAG_02305":null,"SJAG_02308":null,"SJAG_02317":null,"SJAG_02319":null,"SJAG_02329":null,"SJAG_02341":null,"SJAG_02360":null,"SJAG_02369":null,"SJAG_02374":null,"SJAG_02385":null,"SJAG_02386":null,"SJAG_02396":null,"SJAG_02397":null,"SJAG_02398":null,"SJAG_02404":null,"SJAG_02439":null,"SJAG_02441":null,"SJAG_02444":null,"SJAG_02447":null,"SJAG_02458":null,"SJAG_02464":null,"SJAG_02466":null,"SJAG_02469":null,"SJAG_02500":null,"SJAG_02502":null,"SJAG_02504":null,"SJAG_02505":null,"SJAG_02506":null,"SJAG_02527":null,"SJAG_02536":null,"SJAG_02541":null,"SJAG_02542":null,"SJAG_02545":null,"SJAG_02547":null,"SJAG_02549":null,"SJAG_02553":null,"SJAG_02561":null,"SJAG_02562":null,"SJAG_02564":null,"SJAG_02571":null,"SJAG_02583":null,"SJAG_02589":null,"SJAG_02591":null,"SJAG_02598":null,"SJAG_02600":null,"SJAG_02627":null,"SJAG_02629":null,"SJAG_02637":null,"SJAG_02646":null,"SJAG_02651":null,"SJAG_02653":null,"SJAG_02658":null,"SJAG_02663":null,"SJAG_02665":null,"SJAG_02667":null,"SJAG_02685":null,"SJAG_02686":null,"SJAG_02687":null,"SJAG_02699":null,"SJAG_02703":null,"SJAG_02706":null,"SJAG_02721":null,"SJAG_02722":null,"SJAG_02725":null,"SJAG_02726":null,"SJAG_02753":null,"SJAG_02766":null,"SJAG_02768":null,"SJAG_02773":null,"SJAG_02776":null,"SJAG_02778":null,"SJAG_02782":null,"SJAG_02785":null,"SJAG_02798":null,"SJAG_02804":null,"SJAG_02808":null,"SJAG_02809":null,"SJAG_02818":null,"SJAG_02822":null,"SJAG_02837":null,"SJAG_02843":null,"SJAG_02844":null,"SJAG_02846":null,"SJAG_02863":null,"SJAG_02867":null,"SJAG_02869":null,"SJAG_02871":null,"SJAG_02872":null,"SJAG_02879":null,"SJAG_02895":null,"SJAG_02900":null,"SJAG_02901":null,"SJAG_02903":null,"SJAG_02908":null,"SJAG_02913":null,"SJAG_02918":null,"SJAG_02920":null,"SJAG_02927":null,"SJAG_02948":null,"SJAG_02981":null,"SJAG_02990":null,"SJAG_02992":null,"SJAG_02994":null,"SJAG_03006":null,"SJAG_03014":null,"SJAG_03015":null,"SJAG_03029":null,"SJAG_03033":null,"SJAG_03035":null,"SJAG_03036":null,"SJAG_03037":null,"SJAG_03045":null,"SJAG_03048":null,"SJAG_03061":null,"SJAG_03064":null,"SJAG_03066":null,"SJAG_03070":null,"SJAG_03081":null,"SJAG_03093":null,"SJAG_03107":null,"SJAG_03114":null,"SJAG_03115":null,"SJAG_03118":null,"SJAG_03126":null,"SJAG_03130":null,"SJAG_03144":null,"SJAG_03145":null,"SJAG_03151":null,"SJAG_03160":null,"SJAG_03163":null,"SJAG_03179":null,"SJAG_03181":null,"SJAG_03193":null,"SJAG_03206":null,"SJAG_03215":null,"SJAG_03218":null,"SJAG_03219":null,"SJAG_03230":null,"SJAG_03234":null,"SJAG_03255":null,"SJAG_03261":null,"SJAG_03280":null,"SJAG_03285":null,"SJAG_03289":null,"SJAG_03290":null,"SJAG_03292":null,"SJAG_03302":null,"SJAG_03311":null,"SJAG_03321":null,"SJAG_03328":null,"SJAG_03333":null,"SJAG_03345":null,"SJAG_03350":null,"SJAG_03351":null,"SJAG_03353":null,"SJAG_03356":null,"SJAG_03371":null,"SJAG_03385":null,"SJAG_03403":null,"SJAG_03406":null,"SJAG_03408":null,"SJAG_03417":null,"SJAG_03421":null,"SJAG_03425":null,"SJAG_03431":null,"SJAG_03436":null,"SJAG_03441":null,"SJAG_03453":null,"SJAG_03454":null,"SJAG_03460":null,"SJAG_03468":null,"SJAG_03490":null,"SJAG_03494":null,"SJAG_03495":null,"SJAG_03496":null,"SJAG_03500":null,"SJAG_03501":null,"SJAG_03525":null,"SJAG_03535":null,"SJAG_03555":null,"SJAG_03561":null,"SJAG_03575":null,"SJAG_03576":null,"SJAG_03578":null,"SJAG_03579":null,"SJAG_03587":null,"SJAG_03591":null,"SJAG_03599":null,"SJAG_03601":null,"SJAG_03602":null,"SJAG_03618":null,"SJAG_03626":null,"SJAG_03627":null,"SJAG_03628":null,"SJAG_03631":null,"SJAG_03638":null,"SJAG_03641":null,"SJAG_03648":null,"SJAG_03651":null,"SJAG_03668":null,"SJAG_03672":null,"SJAG_03677":null,"SJAG_03680":null,"SJAG_03681":null,"SJAG_03685":null,"SJAG_03694":null,"SJAG_03695":null,"SJAG_03699":null,"SJAG_03702":null,"SJAG_03711":null,"SJAG_03728":null,"SJAG_03737":null,"SJAG_03745":null,"SJAG_03752":null,"SJAG_03758":null,"SJAG_03761":null,"SJAG_03776":null,"SJAG_03787":null,"SJAG_03789":null,"SJAG_03792":null,"SJAG_03793":null,"SJAG_03796":null,"SJAG_03801":null,"SJAG_03802":null,"SJAG_03809":null,"SJAG_03810":null,"SJAG_03811":null,"SJAG_03813":null,"SJAG_03839":null,"SJAG_03841":null,"SJAG_03844":null,"SJAG_03858":null,"SJAG_03861":null,"SJAG_03862":null,"SJAG_03867":null,"SJAG_03884":null,"SJAG_03898":null,"SJAG_03900":null,"SJAG_03920":null,"SJAG_03921":null,"SJAG_03925":null,"SJAG_03931":null,"SJAG_03932":null,"SJAG_03940":null,"SJAG_03944":null,"SJAG_03949":null,"SJAG_03952":null,"SJAG_03954":null,"SJAG_03956":null,"SJAG_03962":null,"SJAG_03967":null,"SJAG_03982":null,"SJAG_03985":null,"SJAG_04005":null,"SJAG_04006":null,"SJAG_04015":null,"SJAG_04026":null,"SJAG_04030":null,"SJAG_04035":null,"SJAG_04062":null,"SJAG_04084":null,"SJAG_04085":null,"SJAG_04087":null,"SJAG_04088":null,"SJAG_04090":null,"SJAG_04095":null,"SJAG_04097":null,"SJAG_04106":null,"SJAG_04107":null,"SJAG_04117":null,"SJAG_04119":null,"SJAG_04122":null,"SJAG_04127":null,"SJAG_04131":null,"SJAG_04140":null,"SJAG_04142":null,"SJAG_04144":null,"SJAG_04150":null,"SJAG_04151":null,"SJAG_04153":null,"SJAG_04161":null,"SJAG_04175":null,"SJAG_04178":null,"SJAG_04179":null,"SJAG_04181":null,"SJAG_04182":null,"SJAG_04186":null,"SJAG_04189":null,"SJAG_04199":null,"SJAG_04201":null,"SJAG_04205":null,"SJAG_04211":null,"SJAG_04213":null,"SJAG_04229":null,"SJAG_04230":null,"SJAG_04232":null,"SJAG_04252":null,"SJAG_04261":null,"SJAG_04274":null,"SJAG_04280":null,"SJAG_04306":null,"SJAG_04309":null,"SJAG_04312":null,"SJAG_04318":null,"SJAG_04321":null,"SJAG_04335":null,"SJAG_04355":null,"SJAG_04357":null,"SJAG_04368":null,"SJAG_04384":null,"SJAG_04389":null,"SJAG_04396":null,"SJAG_04397":null,"SJAG_04408":null,"SJAG_04420":null,"SJAG_04434":null,"SJAG_04451":null,"SJAG_04452":null,"SJAG_04477":null,"SJAG_04484":null,"SJAG_04486":null,"SJAG_04497":null,"SJAG_04502":null,"SJAG_04509":null,"SJAG_04520":null,"SJAG_04540":null,"SJAG_04541":null,"SJAG_04550":null,"SJAG_04552":null,"SJAG_04559":null,"SJAG_04568":null,"SJAG_04572":null,"SJAG_04574":null,"SJAG_04576":null,"SJAG_04582":null,"SJAG_04586":null,"SJAG_04596":null,"SJAG_04612":null,"SJAG_04613":null,"SJAG_04614":null,"SJAG_04619":null,"SJAG_04631":null,"SJAG_04638":null,"SJAG_04641":null,"SJAG_04654":null,"SJAG_04661":null,"SJAG_04665":null,"SJAG_04675":null,"SJAG_04677":null,"SJAG_04680":null,"SJAG_04694":null,"SJAG_04704":null,"SJAG_04732":null,"SJAG_04754":null,"SJAG_04755":null,"SJAG_04756":null,"SJAG_04758":null,"SJAG_04770":null,"SJAG_04783":null,"SJAG_04793":null,"SJAG_04815":null,"SJAG_04816":null,"SJAG_04818":null,"SJAG_04821":null,"SJAG_04824":null,"SJAG_04848":null,"SJAG_04852":null,"SJAG_04853":null,"SJAG_04859":null,"SJAG_04860":null,"SJAG_04877":null,"SJAG_04879":null,"SJAG_04881":null,"SJAG_04882":null,"SJAG_04888":null,"SJAG_04890":null,"SJAG_04894":null,"SJAG_04898":null,"SJAG_04907":null,"SJAG_04916":null,"SJAG_04917":null,"SJAG_04923":null,"SJAG_04932":null,"SJAG_04933":null,"SJAG_04934":null,"SJAG_04955":null,"SJAG_04968":null,"SJAG_04969":null,"SJAG_04970":null,"SJAG_04971":null,"SJAG_04972":null,"SJAG_04977":null,"SJAG_04989":null,"SJAG_04994":null,"SJAG_05012":null,"SJAG_05017":null,"SJAG_05020":null,"SJAG_05025":null,"SJAG_05027":null,"SJAG_05032":null,"SJAG_05192":null,"SJAG_05197":null,"SJAG_05204":null,"SJAG_05219":null,"SJAG_05224":null,"SJAG_05235":null,"SJAG_05236":null,"SJAG_05239":null,"SJAG_05240":null,"SJAG_05274":null,"SJAG_05278":null,"SJAG_05282":null,"SJAG_05285":null,"SJAG_05294":null,"SJAG_05297":null,"SJAG_05313":null,"SJAG_05316":null,"SJAG_05323":null,"SJAG_05329":null,"SJAG_05348":null,"SJAG_05560":null,"SJAG_05629":null,"SJAG_05978":null,"SJAG_05979":null,"SJAG_06309":null,"SJAG_06382":null,"SJAG_06383":null,"SJAG_06425":null,"SJAG_06449":null,"SJAG_06560":null,"SJAG_06613":null,"SJAG_06635":null,"SJAG_07003":null,"SJAG_07006":null,"SJAG_07007":null,"SJAG_07011":null,"SJAG_16453":null,"SJAG_MIT03":null,"SJAG_MIT04":null,"SJAG_MIT09":null,"SJAG_MIT13":null,"SJAG_MIT15":null,"SJAG_MIT20":null,"SJAG_MIT37":null},"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":"catalytic complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"enzyme complex","type":"exact"}],"termid":"GO:1902494","terms_by_termid":{"GO:0000015":null,"GO:0000123":null,"GO:0000124":null,"GO:0000136":null,"GO:0000148":null,"GO:0000151":null,"GO:0000159":null,"GO:0000164":null,"GO:0000172":null,"GO:0000176":null,"GO:0000177":null,"GO:0000214":null,"GO:0000220":null,"GO:0000221":null,"GO:0000307":null,"GO:0000333":null,"GO:0000408":null,"GO:0000502":null,"GO:0000506":null,"GO:0000812":null,"GO:0000836":null,"GO:0002144":null,"GO:0002189":null,"GO:0005655":null,"GO:0005658":null,"GO:0005665":null,"GO:0005666":null,"GO:0005669":null,"GO:0005672":null,"GO:0005673":null,"GO:0005674":null,"GO:0005675":null,"GO:0005680":null,"GO:0005697":null,"GO:0005736":null,"GO:0005745":null,"GO:0005760":null,"GO:0005787":null,"GO:0005834":null,"GO:0005835":null,"GO:0005868":null,"GO:0005945":null,"GO:0005946":null,"GO:0005948":null,"GO:0005950":null,"GO:0005951":null,"GO:0005952":null,"GO:0005953":null,"GO:0005955":null,"GO:0005956":null,"GO:0005960":null,"GO:0005965":null,"GO:0005968":null,"GO:0005971":null,"GO:0008250":null,"GO:0008287":null,"GO:0008540":null,"GO:0008541":null,"GO:0008622":null,"GO:0009328":null,"GO:0009337":null,"GO:0009349":null,"GO:0009361":null,"GO:0009365":null,"GO:0016035":null,"GO:0016514":null,"GO:0016586":null,"GO:0016593":null,"GO:0017059":null,"GO:0017087":null,"GO:0017101":null,"GO:0017109":null,"GO:0017117":null,"GO:0017177":null,"GO:0019005":null,"GO:0019773":null,"GO:0019774":null,"GO:0030289":null,"GO:0030915":null,"GO:0030956":null,"GO:0031011":null,"GO:0031211":null,"GO:0031250":null,"GO:0031251":null,"GO:0031371":null,"GO:0031380":null,"GO:0031391":null,"GO:0031415":null,"GO:0031416":null,"GO:0031417":null,"GO:0031422":null,"GO:0031429":null,"GO:0031431":null,"GO:0031461":null,"GO:0031463":null,"GO:0031464":null,"GO:0031510":null,"GO:0031515":null,"GO:0031588":null,"GO:0032221":null,"GO:0032299":null,"GO:0032478":null,"GO:0032807":null,"GO:0033100":null,"GO:0033185":null,"GO:0033203":null,"GO:0033503":null,"GO:0033573":null,"GO:0033588":null,"GO:0033698":null,"GO:0033768":null,"GO:0034245":null,"GO:0034271":null,"GO:0034272":null,"GO:0034274":null,"GO:0034657":null,"GO:0034967":null,"GO:0035267":null,"GO:0035361":null,"GO:0035550":null,"GO:0035657":null,"GO:0036087":null,"GO:0036410":null,"GO:0042720":null,"GO:0042765":null,"GO:0043224":null,"GO:0043494":null,"GO:0043528":null,"GO:0043541":null,"GO:0043625":null,"GO:0044695":null,"GO:0045252":null,"GO:0045254":null,"GO:0045259":null,"GO:0045273":null,"GO:0045275":null,"GO:0045277":null,"GO:0046695":null,"GO:0048188":null,"GO:0048476":null,"GO:0052718":null,"GO:0070210":null,"GO:0070691":null,"GO:0070692":null,"GO:0070772":null,"GO:0070823":null,"GO:0070824":null,"GO:0070916":null,"GO:0070985":null,"GO:0071006":null,"GO:0071007":null,"GO:0071013":null,"GO:0071521":null,"GO:0071595":null,"GO:0072357":null,"GO:0080008":null,"GO:0090730":null,"GO:0097505":null,"GO:0099128":null,"GO:0106068":null,"GO:0106143":null,"GO:0110115":null,"GO:0120097":null,"GO:0120330":null,"GO:0120513":null,"GO:0140497":null,"GO:1903600":null,"GO:1904423":null,"GO:1904564":null,"GO:1990131":null,"GO:1990234":null,"GO:1990304":null,"GO:1990316":null,"GO:1990467":null,"GO:1990520":null,"GO:1990529":null,"GO:1990567":null,"GO:1990861":null}}


id: PBO:0046930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 47 member D, pseudogene","termid":"PBO:0046930"}


id: PBO:0031209
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-premature_activation_of_bipolar_cell_growth","termid":"PBO:0031209"}


id: PBO:0004279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-PARP type","termid":"PBO:0004279"}


id: PBO:0002008
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L11 (predicted)","termid":"PBO:0002008"}


id: GO:0002538
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The synthesis or release of products of arachidonic acid metabolism following a stimulus as part of an inflammatory response, resulting in an increase in their intracellular or extracellular levels.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"production of molecular mediator involved in inflammatory response","termid":"GO:0002532"}],"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":"arachidonate metabolite production involved in inflammatory response","synonyms":[{"name":"arachidonic acid metabolite production involved in acute inflammatory response","type":"broad"},{"name":"arachidonic acid metabolite production involved in inflammatory response","type":"exact"},{"name":"production of arachidonic acid metabolites involved in acute inflammatory response","type":"broad"},{"name":"production of arachidonic acid metabolites involved in inflammatory response","type":"exact"}],"termid":"GO:0002538"}


id: PBO:0067806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 108","termid":"PBO:0067806"}


id: MONDO:1011983
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tapetal degeneration, non-human animal","secondary_identifiers":["OMIA:000980"],"termid":"MONDO:1011983","xrefs":{"Monarch":{"xref_id":"1011983"}}}


id: MONDO:0020787
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypomagnesemia, seizures, and intellectual disability","termid":"MONDO:0014631"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005240"],"is_obsolete":false,"name":"hypomagnesemia, seizures, and intellectual disability 1","secondary_identifiers":["MEDGEN:906582","UMLS:C4225333","OMIM:616418"],"synonyms":[{"name":"HOMGSMR1","type":"related"},{"name":"HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 1","type":"related"},{"name":"hypomagnesemia, seizures, and mental retardation","type":"broad"}],"termid":"MONDO:0020787","xrefs":{"Monarch":{"xref_id":"0020787"}}}


id: PBO:0064461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase alpha 2, accessory subunit","termid":"PBO:0064461"}


id: MONDO:1011258
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Retinitis pigmentosa that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa, non-human animal","termid":"MONDO:1010334"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinitis pigmentosa, pig","secondary_identifiers":["OMIA:001413-9823"],"termid":"MONDO:1011258","xrefs":{"Monarch":{"xref_id":"1011258"}}}


id: MONDO:0035433
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete calpain-3-related limb-girdle muscular dystrophy D4 (obsolete MONDO:0035433)","secondary_identifiers":["GARD:22272"],"termid":"MONDO:0035433","xrefs":{"Monarch":{"xref_id":"0035433"}}}


id: PBO:0016899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microtubule binding protein Mcp1","termid":"PBO:0016899"}


id: GO:0036491
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of translation initiation, as a result of endoplasmic reticulum stress.","definition_xrefs":["PMID:14676213","GOC:PARL","GOC:bf","PMID:16835242"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of translation in response to endoplasmic reticulum stress","termid":"GO:0036490"},{"relation_name":"is_a","term_name":"regulation of translational initiation in response to stress","termid":"GO:0043558"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of translation initiation in response to endoplasmic reticulum stress","synonyms":[{"name":"regulation of translation initiation in response to ER stress","type":"exact"}],"termid":"GO:0036491"}


id: MOD:01016
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DeltaMass","termid":"MOD:00947"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"t-butyloxycarbonyl","synonyms":[{"name":"tBoc","type":"exact"}],"termid":"MOD:01016"}


id: FYPO:0001954
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 import of calcium ions into a cell occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal calcium import","termid":"FYPO:0001953"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"decreased calcium import","synonyms":[{"name":"decreased calcium import during mitotic cell cycle","type":"related"},{"name":"decreased calcium import during vegetative growth","type":"exact"},{"name":"decreased calcium import into cell","type":"exact"},{"name":"decreased calcium ion import","type":"exact"},{"name":"decreased calcium ion import across plasma membrane","type":"exact"},{"name":"decreased calcium uptake","type":"exact"},{"name":"decreased calcium uptake into intracellular compartments","type":"related"},{"name":"decreased cellular calcium import","type":"exact"},{"name":"reduced calcium import","type":"exact"}],"termid":"FYPO:0001954"}


id: PATO:0001677
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An efficiency quality inhering in a bearer by virtue of the bearer's lacking efficiency.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"efficiency","termid":"PATO:0001029"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inefficient","termid":"PATO:0001677"}


id: GO:1902446
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of shade avoidance.","definition_xrefs":["PMID:23763263","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to red or far red light","termid":"GO:2000030"},{"relation_name":"regulates","term_name":"shade avoidance","termid":"GO:0009641"}],"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 shade avoidance","termid":"GO:1902446"}


id: PBO:0111749
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E3","termid":"PBO:0111749"}


id: PBO:0027536
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_ATP-dependent_5'-3'_DNA_helicase_activity","termid":"PBO:0027536"}


id: GO:0016625
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which an aldehyde or ketone (oxo) group acts as a hydrogen or electron donor and reduces an iron-sulfur protein.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors","termid":"GO:0016903"}],"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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, iron-sulfur protein as acceptor","secondary_identifiers":["EC:1.2.7.-"],"synonyms":[{"name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, iron-sulphur protein as acceptor","type":"exact"}],"termid":"GO:0016625"}


id: MONDO:0001317
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"keratoconjunctivitis","termid":"MONDO:0004768"}],"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":"phlyctenulosis","secondary_identifiers":["SCTID:67895005","DOID:11581","ICD10CM:H16.25","UMLS:C0155080","ICD9:370.31","MEDGEN:509775"],"synonyms":[{"name":"Phlyctenular keratoconjunctivitis","type":"exact"},{"name":"strumous ophthalmia","type":"exact"}],"termid":"MONDO:0001317","xrefs":{"Monarch":{"xref_id":"0001317"}}}


id: MONDO:0030524
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mucopolysaccharidosis","termid":"MONDO:0019249"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002561"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066","MONDO:0002561"],"is_obsolete":false,"name":"mucopolysaccharidosis, type 10","secondary_identifiers":["MEDGEN:1794274","Orphanet:662216","UMLS:C5562064","OMIM:619698"],"synonyms":[{"name":"MPS10","type":"exact"}],"termid":"MONDO:0030524","xrefs":{"Monarch":{"xref_id":"0030524"}}}


id: MONDO:0018491
data:
  {"annotated_genes":["SJAG_02313","SJAG_02791"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87262],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009736"},{"annotations":[88680],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014466"},{"annotations":[88722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011152"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurometabolic disorder due to serine deficiency","termid":"MONDO:0018162"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02313":null,"SJAG_02791":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"3-phosphoglycerate dehydrogenase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:663158","UMLS:C0580190","icd11.foundation:460538363","ICD9:270.7","SCTID:303098002","Orphanet:422519"],"termid":"MONDO:0018491","terms_by_termid":{"MONDO:0009736":null,"MONDO:0011152":null,"MONDO:0014466":null},"xrefs":{"Monarch":{"xref_id":"0018491"}}}


id: PBO:0109262
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secretory calcium-binding phosphoprotein proline-glutamine rich 1","termid":"PBO:0109262"}


id: PBO:0074286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLIT and NTRK like family member 1","termid":"PBO:0074286"}


id: GO:0031668
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an extracellular stimulus.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete cellular response to extracellular stimulus (obsolete GO:0031668)","termid":"GO:0031668"}


id: PBO:0061564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5' nucleotidase, ecto-like, pseudogene","termid":"PBO:0061564"}


id: PBO:0043279
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain family 4 member C","termid":"PBO:0043279"}


id: GO:0034880
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: citrazinate + H2O = 2,3,6-trihydroxyisonicotinate + 2 H+ + 2 e-.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete citrazinate dehydrogenase activity (obsolete GO:0034880)","termid":"GO:0034880"}


id: GO:0034890
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: endosulfan diol = endosulfan ether + H2O.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete endosulfan diol hydrolyase (cyclizing) activity (obsolete GO:0034890)","termid":"GO:0034890"}


id: PBO:0073137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEC22 homolog A, vesicle trafficking protein","termid":"PBO:0073137"}


id: PBO:0075479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPATA31 subfamily A member 7","termid":"PBO:0075479"}


id: PBO:0064020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 54","termid":"PBO:0064020"}


id: FYPO:0003032
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of RNA measured in a cell when the cell is subject to glucose starvation is lower than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level","termid":"FYPO:0000826"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased RNA level during glucose starvation","synonyms":[{"name":"decreased RNA accumulation during glucose starvation","type":"related"},{"name":"decreased RNA level during cellular response to glucose starvation","type":"exact"},{"name":"decreased RNA level during glucose depletion","type":"exact"},{"name":"decreased RNA level during glucose deprivation","type":"exact"},{"name":"decreased RNA level during glucose limitation","type":"related"},{"name":"decreased transcript level during glucose starvation","type":"exact"},{"name":"reduced RNA level during glucose starvation","type":"exact"}],"termid":"FYPO:0003032"}


id: GO:0006940
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of smooth muscle contraction.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle contraction","termid":"GO:0006937"},{"relation_name":"regulates","term_name":"smooth muscle contraction","termid":"GO:0006939"}],"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 smooth muscle contraction","termid":"GO:0006940"}


id: PBO:0083260
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; not conserved in closely related Saccharomyces species","termid":"PBO:0083260"}


id: PBO:0002940
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.3.1.76","termid":"PBO:0002940"}


id: GO:0050341
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: thymine + 2-oxoglutarate + O2 = 5-hydroxymethyluracil + succinate + CO2.","definition_xrefs":["EC:1.14.11.6","MetaCyc:THYMINE-DIOXYGENASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate-dependent dioxygenase activity","termid":"GO:0016706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"thymine dioxygenase activity","secondary_identifiers":["RHEA:10316"],"synonyms":[{"name":"5-hydroxy-methyluracil dioxygenase activity","type":"related"},{"name":"5-hydroxymethyluracil oxygenase activity","type":"related"},{"name":"thymine 7-hydroxylase activity","type":"related"},{"name":"thymine,2-oxoglutarate dioxygenase activity","type":"related"},{"name":"thymine,2-oxoglutarate:oxygen oxidoreductase (7-hydroxylating)","type":"related"}],"termid":"GO:0050341"}


id: PR:Q9P7M5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An H/ACA ribonucleoprotein complex subunit 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13305:SF0","OMA:SCHPO00663","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":"H/ACA ribonucleoprotein complex subunit 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP27G11.13c","secondary_identifiers":["UniProtKB:Q9P7M5"],"synonyms":[{"name":"Spom972h-NOP10","type":"exact"},{"name":"nucleolar protein 10 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"nucleolar protein family A member 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"snoRNP protein nop10 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P7M5"}


id: PBO:0002390
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol phoshorylceramide synthase regulatory subunit Kei1 (predicted)","termid":"PBO:0002390"}


id: PBO:0083062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dihydrolipoyl transsuccinylase; component of the mitochondrial alpha-ketoglutarate dehydrogenase complex, which catalyzes the oxidative decarboxylation of alpha-ketoglutarate to succinyl-CoA in the TCA cycle; phosphorylated","termid":"PBO:0083062"}


id: PBO:0076753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"teratocarcinoma-derived growth factor 1 pseudogene 3","termid":"PBO:0076753"}


id: PBO:0044924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diacylglycerol kinase alpha","termid":"PBO:0044924"}


id: PATO:0001585
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality inhering in a bearer by virtue of the bearer's disposition to transmit of an entity through a medium.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality","termid":"PATO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conductivity","termid":"PATO:0001585"}


id: PBO:0014571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfate transmembrane transporter (predicted)","termid":"PBO:0014571"}


id: PBO:0076970
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transglutaminase 1","termid":"PBO:0076970"}


id: PBO:0073466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sideroflexin 2","termid":"PBO:0073466"}


id: PBO:0026957
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rate_of_microtubule_depolymerization_ahead_of_moving_spindle_pole_body","termid":"PBO:0026957"}


id: PBO:0109458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADP binding superfamily, involved in heme catabolism","termid":"PBO:0109458"}


id: MONDO:0008715
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital malformation syndrome characterized by the association of facial and skeletal anomalies with severe intellectual deficit and occasional genitourinary anomalies.","definition_xrefs":["Orphanet:1784"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acrofacial dysostosis","termid":"MONDO:0018237"}],"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":"acrofrontofacionasal dysostosis","secondary_identifiers":["GARD:484","UMLS:C1860118","DOID:0060226","icd11.foundation:700995487","MEDGEN:349729","SCTID:720408003"],"synonyms":[{"name":"AFFN dysostosis","type":"exact"},{"name":"Affn dysostosis 1","type":"narrow"},{"name":"Richieri-Costa-Colletto syndrome","type":"exact"},{"name":"acro fronto facio nasal dysostosis","type":"related"},{"name":"acrofrontofacionasal dysostosis 1","type":"narrow"},{"name":"acrofrontofacionasal dysostosis syndrome","type":"related"},{"name":"acrofrontofacionasal dysostosis type 1","type":"narrow"},{"name":"cleft Lip/palate with frontonasal dysostosis and postaxial polysyndactyly","type":"related"},{"name":"polysyndactyly, postaxial, frontonasal dysostosis and cleft lip/palate","type":"related"},{"name":"polysyndactyly, postaxial, frontonasal dysostosis, and cleft Lip/palate","type":"related"}],"termid":"MONDO:0008715","xrefs":{"Monarch":{"xref_id":"0008715"}}}


id: PBO:0048070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferritin heavy chain 1 pseudogene 21","termid":"PBO:0048070"}


id: MONDO:0005211
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma that arises from the ovary and is characterized by the presence of malignant epithelial cells that, in well differentiated tumors, resemble the epithelium of the fallopian tube or, in poorly differentiated tumors, show anaplastic features and marked nuclear atypia.","definition_xrefs":["NCIT:C7550"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian adenocarcinoma","termid":"MONDO:0002752"},{"relation_name":"is_a","term_name":"serous adenocarcinoma","termid":"MONDO:0005278"},{"relation_name":"is_a","term_name":"malignant ovarian serous tumor","termid":"MONDO:0024885"}],"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":"ovarian serous adenocarcinoma","secondary_identifiers":["DOID:5744","DOID:0050933","MEDGEN:233278","ONCOTREE:SOC","UMLS:C1335177","EFO:0002917"],"synonyms":[{"name":"malignant ovarian serous tumour","type":"related"},{"name":"ovarian serous adenocarcinoma","type":"exact"},{"name":"ovarian serous carcinoma","type":"exact"},{"name":"ovary serous adenocarcinoma","type":"exact"},{"name":"serous adenocarcinoma of ovary","type":"exact"},{"name":"serous adenocarcinoma of the ovary","type":"exact"},{"name":"serous carcinoma of ovary","type":"exact"},{"name":"serous carcinoma of the ovary","type":"exact"},{"name":"serous ovarian cancer","type":"related"}],"termid":"MONDO:0005211","xrefs":{"Monarch":{"xref_id":"0005211"}}}


id: PBO:0066971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 273","termid":"PBO:0066971"}


id: MONDO:1011131
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrophic rhinitis that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrophic rhinitis, non-human animal","termid":"MONDO:1010285"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atrophic rhinitis, pig","secondary_identifiers":["OMIA:000091-9823"],"termid":"MONDO:1011131","xrefs":{"Monarch":{"xref_id":"1011131"}}}


id: PBO:0051996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"junction adhesion molecule like","termid":"PBO:0051996"}


id: GO:0019463
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of glycine into other compounds, including creatine.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete glycine catabolic process to creatine (obsolete GO:0019463)","synonyms":[{"name":"glycine breakdown to creatine","type":"exact"},{"name":"glycine degradation to creatine","type":"exact"}],"termid":"GO:0019463"}


id: GO:0015648
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the directed movement of lipid-linked peptidoglycans into, out of or within a cell, or between cells.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidoglycan transmembrane transporter activity","termid":"GO:0015647"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"lipid-linked peptidoglycan transporter activity","synonyms":[{"name":"lipid-linked murein transporter activity","type":"exact"}],"termid":"GO:0015648"}


id: PBO:0041575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 21 open reading frame 62","termid":"PBO:0041575"}


id: MONDO:0015306
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lemierre syndrome is a rare, potentially lethal, oropharyngeal infectious disease occurring in immunocompetent adolescents and young adults that is mainly due to Fusobacterium necrophorum and that is characterized by septic thrombophlebitis of the internal jugular vein that leads to septic, usually pulmonary, embolism, associated with ENT (ear, nose, and throat) infection that manifests with fever, neck pain, and tonsillopharyngitis.","definition_xrefs":["Orphanet:137839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"commensal bacterial infectious disease","termid":"MONDO:0000315"},{"relation_name":"is_a","term_name":"bacterial infectious disease with sepsis","termid":"MONDO:0005229"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lemierre syndrome","secondary_identifiers":["DOID:11337","SCTID:52542005","MEDGEN:6541","ICD9:040.3","UMLS:C0027537","MESH:D057831","GARD:6882","MedDRA:10065552"],"synonyms":[{"name":"Lemierre postanginal sepsis","type":"exact"},{"name":"Lemierre syndrome","type":"exact"},{"name":"Lemierre's syndrome","type":"related"},{"name":"acute sore throat","type":"related"},{"name":"human necrobacillosis","type":"exact"},{"name":"necrobacillosis","type":"related"},{"name":"oropharyngeal infection leading to secondary septic thrombophlebitis of the internal jugular vein","type":"related"},{"name":"postanginal sepsis","type":"exact"},{"name":"postanginal sepsis secondary to orophyngeal infection","type":"exact"},{"name":"septic phlebitis of the internal jugular vein","type":"exact"}],"termid":"MONDO:0015306","xrefs":{"Monarch":{"xref_id":"0015306"}}}


id: GO:1904220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of serine C-palmitoyltransferase activity.","definition_xrefs":["GO_REF:0000059","GOC:BHF","GOC:rl","GOC:TermGenie","PMID:16120614"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transferase activity","termid":"GO:0051338"}],"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 serine C-palmitoyltransferase activity","synonyms":[{"name":"regulation of 3-oxosphinganine synthetase activity","type":"exact"},{"name":"regulation of SPT","type":"related"},{"name":"regulation of acyl-CoA:serine C-2 acyltransferase decarboxylating","type":"related"},{"name":"regulation of palmitoyl-CoA:L-serine C-palmitoyltransferase (decarboxylating) activity","type":"exact"},{"name":"regulation of serine palmitoyltransferase","type":"broad"}],"termid":"GO:1904220"}


id: FYPO:0001346
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype that affects any DNA metabolic process in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA metabolism phenotype","termid":"FYPO:0000293"},{"relation_name":"is_a","term_name":"nucleic acid metabolism phenotype during vegetative growth","termid":"FYPO:0001347"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000293"],"is_obsolete":false,"name":"DNA metabolism phenotype during vegetative growth","synonyms":[{"name":"DNA metabolism phenotype during mitotic cell cycle","type":"related"},{"name":"fission yeast DNA metabolism phenotype during vegetative growth","type":"exact"}],"termid":"FYPO:0001346"}


id: PR:O94288
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A nucleolar complex protein 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR14428:SF5","OMA:SCHPO03754","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":"nucleolar complex-associated protein 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC887.03c","secondary_identifiers":["UniProtKB:O94288"],"synonyms":[{"name":"Spom972h-NOC3L","type":"exact"}],"termid":"PR:O94288"}


id: PBO:0113341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function involved in regulating assembly of Gid4p into the GID E3 ligase complex; interacts with GID complex components; involved in actin patch formation; computationally predicted to be involved in fructose-1,6-bisphosphatase (Fbp1p) degradation; non-essential gene","termid":"PBO:0113341"}


id: MOD:01899
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-arginine residue and an L-cysteine residue to form arginine thiazole-4-carboxylic acid.","definition_xrefs":["PubMed:21568297","RESID:AA0570","PubMed:21950656"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thiazole/thiazoline ring crosslinked residues","termid":"MOD:01420"},{"relation_name":"is_a","term_name":"didehydrogenated residue","termid":"MOD:01888"},{"relation_name":"is_a","term_name":"crosslinked L-arginine residue","termid":"MOD:02041"}],"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":"L-arginine thiazole-4-carboxylic acid","synonyms":[{"name":"2-[(1S)-1-amino-4-([diaminomethylidene]amino)butyl]-1,3-thiazole-4-carboxylic acid","type":"exact"},{"name":"CROSSLNK Thiazole-4-carboxylic acid (Arg-Cys)","type":"exact"},{"name":"L-arginine thiazole-4-carboxylic acid","type":"exact"}],"termid":"MOD:01899"}


id: MONDO:0021515
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the ethmoid sinus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system benign neoplasm","termid":"MONDO:0000382"},{"relation_name":"is_a","term_name":"bone benign neoplasm","termid":"MONDO:0000631"},{"relation_name":"is_a","term_name":"sensory organ benign neoplasm","termid":"MONDO:0000633"},{"relation_name":"is_a","term_name":"ethmoidal sinus neoplasm","termid":"MONDO:0001764"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of ethmoidal sinus","secondary_identifiers":["ICD9:212.0","SCTID:92093000","UMLS:C0345670","NCIT:C4417","MEDGEN:91050"],"synonyms":[{"name":"benign ethmoid sinus neoplasm","type":"exact"},{"name":"benign ethmoid sinus tumor","type":"exact"},{"name":"benign ethmoid sinus tumour","type":"exact"},{"name":"benign ethmoidal sinus neoplasm","type":"exact"},{"name":"benign ethmoidal sinus tumor","type":"exact"},{"name":"benign ethmoidal sinus tumour","type":"exact"},{"name":"benign neoplasm of ethmoid sinus","type":"exact"},{"name":"benign neoplasm of the ethmoid sinus","type":"exact"},{"name":"benign neoplasm of the ethmoidal sinus","type":"exact"},{"name":"benign tumor of ethmoid sinus","type":"exact"},{"name":"benign tumor of ethmoidal sinus","type":"exact"},{"name":"benign tumor of the ethmoid sinus","type":"exact"},{"name":"benign tumor of the ethmoidal sinus","type":"exact"},{"name":"benign tumour of ethmoid sinus","type":"exact"},{"name":"benign tumour of ethmoidal sinus","type":"exact"},{"name":"benign tumour of the ethmoid sinus","type":"exact"},{"name":"benign tumour of the ethmoidal sinus","type":"exact"},{"name":"ethmoid sinus benign neoplasm","type":"exact"}],"termid":"MONDO:0021515","xrefs":{"Monarch":{"xref_id":"0021515"}}}


