# terms

id: SO:0000661
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000661 intron_attribute (obsolete SO:0000661)","termid":"SO:0000661"}


id: GO:0015245
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of fatty acids from one side of a membrane to the other. Fatty acids are aliphatic monocarboxylic acids liberated from naturally occurring fats and oils by hydrolysis.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transmembrane transporter activity","termid":"GO:0008028"},{"relation_name":"is_a","term_name":"lipid transmembrane transporter activity","termid":"GO:0170055"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"fatty acid transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-5627891","Reactome:R-HSA-9032323","GO:0015246","Reactome:R-HSA-9032315","Reactome:R-HSA-879585"],"synonyms":[{"name":"fatty acid transporter activity","type":"related"},{"name":"fatty acyl transporter activity","type":"exact"},{"name":"fatty-acyl group transporter activity","type":"broad"},{"name":"peroxisomal fatty acyl transporter","type":"narrow"}],"termid":"GO:0015245"}


id: PBO:0039032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ArfGAP with GTPase domain, ankyrin repeat and PH domain 9","termid":"PBO:0039032"}


id: GO:0060285
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell motility due to the motion of one or more eukaryotic cilia. A eukaryotic cilium is a specialized organelle that consists of a filiform extrusion of the cell surface. Each cilium is bounded by an extrusion of the cytoplasmic (plasma) membrane, and contains a regular longitudinal array of microtubules, anchored basally in a centriole.","definition_xrefs":["GOC:cilia","GOC:dgh","GOC:krc","GOC:mtg_cambridge_2013","GOC:dph","GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cilium or flagellum-dependent cell motility","termid":"GO:0001539"}],"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":"cilium-dependent cell motility","secondary_identifiers":["GO:0071974"],"synonyms":[{"name":"ciliary cell motility","type":"related"},{"name":"cilium cell motility","type":"exact"},{"name":"microtubule-based flagellar cell motility","type":"exact"}],"termid":"GO:0060285"}


id: PBO:0046077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 4A1 pseudogene 2","termid":"PBO:0046077"}


id: GO:0140024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of an endosome towards the plus end of a microtubule, mediated by motor proteins. This process begins with the attachment of an endosome to a microtubule, and ends when the endosome reaches its final destination.","definition_xrefs":["PMID:25706234","PMID:24803650"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plus-end-directed vesicle transport along microtubule","termid":"GO:0072383"}],"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"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"plus-end-directed endosome transport along mitotic spindle midzone microtubule","termid":"GO:0140024"}


id: MONDO:1010260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nephrolithiasis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urolithiasis, non-human animal","termid":"MONDO:1010267"},{"relation_name":"is_a","term_name":"renal disease, non-human animal","termid":"MONDO:1011909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nephrolithiasis, non-human animal","secondary_identifiers":["OMIA:000709"],"termid":"MONDO:1010260","xrefs":{"Monarch":{"xref_id":"1010260"}}}


id: PBO:0029151
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_paraquat","termid":"PBO:0029151"}


id: PBO:0043550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"collagen type IV alpha 1 chain","termid":"PBO:0043550"}


id: GO:0003920
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: IMP + NADP+ + NH4 = GMP + 2 H+ + NADPH.","definition_xrefs":["RHEA:17185","EC:1.7.1.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor","termid":"GO:0046857"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"GMP reductase activity","secondary_identifiers":["KEGG_REACTION:R01134","MetaCyc:GMP-REDUCT-RXN","Reactome:R-HSA-514604"],"synonyms":[{"name":"NADPH2:guanosine-5'-phosphate oxidoreductase (deaminating)","type":"related"},{"name":"NADPH:GMP oxidoreductase (deaminating) activity","type":"related"},{"name":"NADPH:guanosine-5'-phosphate oxidoreductase (deaminating) activity","type":"related"},{"name":"guanosine 5'-monophosphate oxidoreductase activity","type":"related"},{"name":"guanosine 5'-monophosphate reductase activity","type":"related"},{"name":"guanosine 5'-phosphate reductase activity","type":"related"},{"name":"guanosine monophosphate reductase activity","type":"related"},{"name":"guanylate reductase activity","type":"related"},{"name":"inosine-5'-phosphate:NADP+ oxidoreductase (aminating)","type":"related"}],"termid":"GO:0003920"}


id: PATO:0000737
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000737 functional value (obsolete PATO:0000737)","termid":"PATO:0000737"}


id: GO:0043719
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-octaprenyl-3-methyl-6-methoxy-1,4-benzoquinol + O2 + H+ = 2-octaprenyl-3-methyl-5-hydroxy-6-methoxy-1,4-benzoquinol + H2O.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-octaprenyl-3-methyl-6-methoxy-1,4-benzoquinol hydroxylase activity (obsolete GO:0043719)","termid":"GO:0043719"}


id: PBO:0056711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MEMO1 pseudogene 3","termid":"PBO:0056711"}


id: PBO:0073921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 16 member 10","termid":"PBO:0073921"}


id: GO:0097552
data:
  {"annotated_genes":["SJAG_05373"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81139],"is_not":false,"summary":null,"term":"GO:0097552"}]},"cv_name":"biological_process","definition":"The repair of a double-strand break in mitochondrial DNA in which the broken DNA molecule is repaired using homologous sequences.","definition_xrefs":["PMID:22214610","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"recombinational repair","termid":"GO:0000725"},{"relation_name":"is_a","term_name":"mitochondrial double-strand break repair","termid":"GO:0097551"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05373":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0008150","GO:0006310","GO:0006281","GO:0006259"],"is_obsolete":false,"name":"mitochondrial double-strand break repair via homologous recombination","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"mtDSB repair via homologous recombination","type":"exact"}],"termid":"GO:0097552","terms_by_termid":{"GO:0097552":null}}


id: MONDO:0008695
data:
  {"annotated_genes":["SJAG_01229","SJAG_16459"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87240,87241],"is_not":false,"summary":null,"term":"MONDO:0008695"}]},"cv_name":"mondo","definition":"Chorea-acanthocytosis (ChAc) is a form of neuroacanthocytosis and is characterized clinically by a Huntington disease-like phenotype with progressive neurological symptoms including movement disorders, psychiatric manifestations and cognitive disturbances.","definition_xrefs":["Orphanet:2388"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroacanthocytosis","termid":"MONDO:0016987"},{"relation_name":"is_a","term_name":"epidermal disease","termid":"MONDO:0019268"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01229":null,"SJAG_16459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0005244","MONDO:0005093","MONDO:0005559"],"is_obsolete":false,"name":"chorea-acanthocytosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NANDO:1200014","SCTID:66881004","UMLS:C0393576","ICD9:333.0","GARD:3956","MEDGEN:98277","OMIM:200150","DOID:0050766"],"synonyms":[{"name":"CHAC","type":"exact"},{"name":"CHOREOACANTHOCYTOSIS","type":"related"},{"name":"Chac","type":"exact"},{"name":"Levine-Critchley syndrome","type":"exact"},{"name":"acanthocytosis with neurologic disorder","type":"related"},{"name":"chorea acanthocytosis","type":"related"},{"name":"chorea-acanthocytosis","type":"exact"},{"name":"choreaacanthocytosis","type":"related"},{"name":"choreo-acanthocytosis","type":"exact"},{"name":"choreoacanthocytosis","type":"exact"},{"name":"neuroacanthocytosis","type":"related"}],"termid":"MONDO:0008695","terms_by_termid":{"MONDO:0008695":null},"xrefs":{"Monarch":{"xref_id":"0008695"}}}


id: MONDO:0019017
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome is characterized by bilateral shortening of the fifth fingers and fifth metacarpals. It has been described in several members of one family. Some members of the family also had spherocytosis and insulin resistance. Transmission is autosomal dominant.","definition_xrefs":["Orphanet:66518"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"diabetes mellitus","termid":"MONDO:0005015"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short fifth metacarpals-insulin resistance syndrome","secondary_identifiers":["UMLS:C4303621","GARD:18868","MEDGEN:929290"],"termid":"MONDO:0019017","xrefs":{"Monarch":{"xref_id":"0019017"}}}


id: MONDO:0010030
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune disorder in which immune cells attack and destroy the glands that produce tears and saliva. Sjögren syndrome is also associated with rheumatic disorders such as rheumatoid arthritis or systemic lupus erythematosus. The hallmark symptoms of Sjögren syndrome are dry mouth and dry eyes. In addition, Sjogren syndrome may cause skin, nose, and vaginal dryness. It also may affect other organs of the body including the kidneys, blood vessels, lungs, liver, pancreas, and brain","direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disorder of exocrine system","termid":"MONDO:0000586"},{"relation_name":"is_a","term_name":"salivary gland disorder","termid":"MONDO:0001142"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"disorder of lacrimal gland","termid":"MONDO:0024625"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005328"],"is_obsolete":false,"name":"Sjogren syndrome","secondary_identifiers":["SCTID:83901003","ICD9:710.2","MEDGEN:282890","NANDO:1200279","UMLS:C1527336","icd11.foundation:899463360","EFO:0000699","Orphanet:378","OMIM:270150","GARD:10252","ICD10CM:M35.0","MESH:D012859","DOID:12894","NANDO:1200280","NANDO:2200420","NCIT:C26883","Orphanet:289390"],"synonyms":[{"name":"Sjogren syndrome","type":"exact"},{"name":"Sjogren's syndrome","type":"related"},{"name":"Sjögren syndrome","type":"exact"},{"name":"Sjögren-Gougerot syndrome","type":"exact"},{"name":"primary Sjogren-Gougerot syndrome","type":"exact"},{"name":"primary Sjögren syndrome","type":"related"},{"name":"primary Sjögren-Gougerot syndrome","type":"exact"},{"name":"sicca syndrome","type":"exact"},{"name":"syndrome, Sjogren's","type":"exact"},{"name":"xerodermosteosis","type":"exact"}],"termid":"MONDO:0010030","xrefs":{"Monarch":{"xref_id":"0010030"}}}


id: PBO:0054875
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 2289","termid":"PBO:0054875"}


id: FYPO:0001054
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An inviable phenotype in which a cell enters mitosis when longer than wild type, and then septates to give rise to a cut phenotype. In a cut phenotype, a cell undergoes septation despite abnormal mitosis such that the septum physically divides the nucleus into two parts.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"inviable elongated vegetative cell","termid":"FYPO:0001490"},{"relation_name":"has_part","term_name":"cut with abnormal chromosome segregation","termid":"FYPO:0003165"},{"relation_name":"is_a","term_name":"inviable elongated vegetative cell","termid":"FYPO:0001490"},{"relation_name":"is_a","term_name":"cut with abnormal chromosome segregation","termid":"FYPO:0003165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"has_part","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"has_part","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"has_part","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000641","FYPO:0000032","FYPO:0001985","FYPO:0000631","FYPO:0000004","FYPO:0001320","FYPO:0000005","FYPO:0000337"],"is_obsolete":false,"name":"cut, elongated cell","synonyms":[{"name":"cut following delayed onset of mitosis","type":"exact"},{"name":"cut with mitotic catastrophe, elongated cell","type":"related"},{"name":"cut, elongated cell during mitotic cell cycle","type":"related"},{"name":"cut, elongated cell during vegetative growth","type":"exact"},{"name":"cut, long cell","type":"exact"},{"name":"elongated cut cell","type":"exact"},{"name":"mitotic catastrophe with cut, elongated cell","type":"related"},{"name":"septation following abnormal nuclear division, long cell","type":"exact"}],"termid":"FYPO:0001054"}


id: PBO:0034205
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-is_model_of","termid":"PBO:0034205"}


id: GO:1905180
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cardiac muscle tissue regeneration.","definition_xrefs":["GOC:TermGenie","GOC:rph","GO_REF:0000058","GOC:BHF","GOC:BHF_miRNA","PMID:23222520"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental growth","termid":"GO:0048639"},{"relation_name":"is_a","term_name":"regulation of cardiac muscle tissue regeneration","termid":"GO:1905178"},{"relation_name":"positively_regulates","term_name":"cardiac muscle tissue regeneration","termid":"GO:0061026"}],"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 cardiac muscle tissue regeneration","synonyms":[{"name":"activation of cardiac muscle tissue regeneration","type":"narrow"},{"name":"up regulation of cardiac muscle tissue regeneration","type":"exact"},{"name":"up-regulation of cardiac muscle tissue regeneration","type":"exact"},{"name":"upregulation of cardiac muscle tissue regeneration","type":"exact"}],"termid":"GO:1905180"}


id: PBO:0082551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Central kinetochore associated protein; mediates mitotic progression; interacts with several central kinetochore proteins and centromeric histone Cse4p; role in resistance to oxidative stress; similar to Slk19p; YBP2 has a paralog, YBP1, that arose from the whole genome duplication","termid":"PBO:0082551"}


id: PBO:0062367
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 A member 2 pseudogene","termid":"PBO:0062367"}


id: GO:0007559
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The breakdown of tissues; usually, if not always, accompanied by cell death, followed by the complete dissolution of dead tissue.","definition_xrefs":["GOC:dph","GOC:ma"],"gene_count":0,"genotype_count":0,"name":"obsolete histolysis (obsolete GO:0007559)","secondary_identifiers":["Wikipedia:Histolysis"],"termid":"GO:0007559"}


id: MOD:01282
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Other -","definition_xrefs":["PubMed:10825247","PubMed:15541752","Unimod:206#H"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acrolein addition +56","termid":"MOD:00557"},{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acrolein addition +56 - site H","synonyms":[{"name":"Acrolein addition +56","type":"related"},{"name":"Delta:H(4)C(3)O(1)","type":"related"}],"termid":"MOD:01282"}


id: PBO:0011423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor, zf-fungal binuclear cluster type","termid":"PBO:0011423"}


id: MONDO:0014089
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse palmoplantar keratoderma","termid":"MONDO:0017666"},{"relation_name":"is_a","term_name":"superficial corneal dystrophy","termid":"MONDO:0020212"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005093"],"is_obsolete":false,"name":"corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome","secondary_identifiers":["GARD:17525","MEDGEN:815206","OMIM:615225","OMIM:616964","Orphanet:352662","UMLS:C3808876"],"synonyms":[{"name":"CIDED","type":"related"},{"name":"MSPC","type":"exact"},{"name":"corneal intraepithelial dyskeratosis and ectodermal dysplasia","type":"related"},{"name":"corneal intraepithelial dyskeratosis and ectodermal dysplasia, formerly","type":"related"},{"name":"palmoplantar carcinoma, multiple self-healing","type":"exact"},{"name":"palmoplantar carcinoma, multiple self-healing; MSPC","type":"exact"}],"termid":"MONDO:0014089","xrefs":{"Monarch":{"xref_id":"0014089"}}}


id: MONDO:0800345
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial atrial fibrillation","termid":"MONDO:0018054"}],"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":"atrial fibrillation, familial, 17","secondary_identifiers":["MEDGEN:861997","UMLS:C4013560"],"synonyms":[{"name":"ATFB17","type":"exact"}],"termid":"MONDO:0800345","xrefs":{"Monarch":{"xref_id":"0800345"}}}


id: GO:0010823
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that decreases the frequency, rate or extent of a process involved in the formation, arrangement of constituent parts, or disassembly of a mitochondrion.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of mitochondrion organization (obsolete GO:0010823)","synonyms":[{"name":"negative regulation of mitochondrion organisation","type":"exact"}],"termid":"GO:0010823"}


id: PR:Q9HE08
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A methylthioribulose-1-phosphate dehydratase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00873","PRO:DNx","PANTHER:PTHR10640:SF2"],"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":"methylthioribulose-1-phosphate dehydratase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC20H4.05c","secondary_identifiers":["UniProtKB:Q9HE08"],"synonyms":[{"name":"MTRu-1-P dehydratase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-APIP","type":"exact"}],"termid":"PR:Q9HE08"}


id: MONDO:0002217
data:
  {"annotated_genes":["SJAG_04755","SJAG_05313"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89141,89142],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013224"}]},"cv_name":"mondo","definition":"A sarcoma that arises from the central nervous system.","definition_xrefs":["NCIT:C5153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system cancer","termid":"MONDO:0002714"},{"relation_name":"is_a","term_name":"soft tissue sarcoma","termid":"MONDO:0018078"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04755":null,"SJAG_05313":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"central nervous system sarcoma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:272444","UMLS:C1332892","DOID:2133"],"synonyms":[{"name":"CNS sarcoma","type":"exact"},{"name":"central nervous system sarcoma","type":"exact"},{"name":"sarcoma of CNS","type":"exact"},{"name":"sarcoma of central nervous system","type":"exact"},{"name":"sarcoma of the CNS","type":"exact"},{"name":"sarcoma of the central nervous system","type":"exact"}],"termid":"MONDO:0002217","terms_by_termid":{"MONDO:0013224":null},"xrefs":{"Monarch":{"xref_id":"0002217"}}}


id: MONDO:0000961
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign adipose tissue neoplasm located within the lumen of a bronchus. It is predominantly found in males and usually originates within the fatty tissue between bronchial cartilage. May cause irreversible pulmonary damage distally. Two-thirds of the tumors occur on the right side and most are located on the first three subdivisions of the tracheobronchial tree.","definition_xrefs":["NCIT:C5063"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lung benign neoplasm","termid":"MONDO:0002732"},{"relation_name":"is_a","term_name":"respiratory system benign neoplasm","termid":"MONDO:0000382"},{"relation_name":"is_a","term_name":"bronchial neoplasm","termid":"MONDO:0002807"},{"relation_name":"is_a","term_name":"lipoma","termid":"MONDO:0005106"},{"relation_name":"is_a","term_name":"benign soft tissue neoplasm","termid":"MONDO:0044335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endobronchial lipoma","secondary_identifiers":["MEDGEN:208874","UMLS:C0852937","DOID:10183"],"synonyms":[{"name":"endobronchial lipoma","type":"exact"}],"termid":"MONDO:0000961","xrefs":{"Monarch":{"xref_id":"0000961"}}}


id: MONDO:0007735
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital Horner syndrome is a rare neurological disorder characterized by relative pupillary miosis and blepharoptosis, evident at birth, caused by interruption of the oculosympathetic innervation at any point along the neural pathway from the hypothalamus to the orbit. Often additional symptoms, such as enophthalmos, facial anhidrosis, iris heterochromia, conjunctival congestion, transient hypotonia and/or pupillary dilation lag, may be present. Association with birth trauma, neoplasms or vascular malformations has been reported.","definition_xrefs":["Orphanet:91413"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Horner syndrome","termid":"MONDO:0001294"}],"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":"congenital Horner syndrome","secondary_identifiers":["HP:0006837","GARD:6670","MEDGEN:327111","MESH:C564178","OMIM:143000","UMLS:C1840475"],"synonyms":[{"name":"HORNER syndrome, congenital","type":"related"},{"name":"congenital Claude-Bernard-Horner syndrome","type":"exact"},{"name":"congenital Horner syndrome","type":"exact"},{"name":"congenital Horner syndrome (disease)","type":"exact"}],"termid":"MONDO:0007735","xrefs":{"Monarch":{"xref_id":"0007735"}}}


id: PBO:0091183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orf307","termid":"PBO:0091183"}


id: GO:0034644
data:
  {"annotated_genes":["SJAG_02182","SJAG_04190","SJAG_00272","SJAG_02818","SJAG_01648","SJAG_00208","SJAG_00814","SJAG_02334","SJAG_02199","SJAG_01010","SJAG_00863","SJAG_05197","SJAG_04877","SJAG_04150","SJAG_03898","SJAG_01262","SJAG_00729","SJAG_02828","SJAG_02200"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110951,104650,78623,97054],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904161"},{"annotations":[98936,107774,60816,67884,114689,77410,97835,71778,89826,66049,95472,69019,106052,66937,70507],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070914"}]},"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 an ultraviolet radiation (UV light) stimulus. Ultraviolet radiation is electromagnetic radiation with a wavelength in the range of 10 to 380 nanometers.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to UV","termid":"GO:0009411"},{"relation_name":"is_a","term_name":"cellular response to light stimulus","termid":"GO:0071482"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00208":null,"SJAG_00272":null,"SJAG_00729":null,"SJAG_00814":null,"SJAG_00863":null,"SJAG_01010":null,"SJAG_01262":null,"SJAG_01648":null,"SJAG_02182":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02334":null,"SJAG_02818":null,"SJAG_02828":null,"SJAG_03898":null,"SJAG_04150":null,"SJAG_04190":null,"SJAG_04877":null,"SJAG_05197":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 UV","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"cellular response to UV light stimulus","type":"exact"},{"name":"cellular response to UV radiation stimulus","type":"exact"},{"name":"cellular response to ultraviolet light stimulus","type":"exact"},{"name":"cellular response to ultraviolet radiation stimulus","type":"exact"}],"termid":"GO:0034644","terms_by_termid":{"GO:0070914":null,"GO:1904161":null}}


id: GO:0032529
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a microvillus on a follicle cell. A microvillus is a thin cylindrical membrane-covered projection on the surface of an animal cell containing a core bundle of actin filaments.","definition_xrefs":["GOC:sart","PMID:16507588"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microvillus organization","termid":"GO:0032528"}],"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":"follicle cell microvillus organization","synonyms":[{"name":"follicle cell microvillus organisation","type":"exact"},{"name":"follicle cell microvillus organization and biogenesis","type":"related"}],"termid":"GO:0032529"}


id: GO:1903145
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any actin filament that is part of a cell cortex of cell tip.","definition_xrefs":["GO_REF:0000064","PMID:20807799","PMID:24954052","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament","termid":"GO:0005884"},{"relation_name":"part_of","term_name":"cell cortex of cell tip","termid":"GO:0051285"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005938"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0015629"}],"interesting_parent_ids":["GO:0015629","GO:0005938","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"actin filament of cell cortex of cell tip","synonyms":[{"name":"actin filament of cell cortex of cell end","type":"exact"},{"name":"microfilament of cell cortex of cell end","type":"exact"},{"name":"microfilament of cell cortex of cell tip","type":"exact"}],"termid":"GO:1903145"}


id: PR:O42894
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An exosome complex component RRP46 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02536","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":"exosome complex component rrp46 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC115.01c","secondary_identifiers":["UniProtKB:O42894"],"synonyms":[{"name":"Spom972h-EXOSC5","type":"exact"},{"name":"ribosomal RNA-processing protein 46 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42894"}


id: GO:0008853
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the degradation of double-stranded DNA. It acts progressively in a 3' to 5' direction, releasing 5'-phosphomononucleotides.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete exodeoxyribonuclease III activity (obsolete GO:0008853)","termid":"GO:0008853"}


id: MONDO:1011174
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Osteochondrosis that occurs in pig.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrosis, non-human animal","termid":"MONDO:1010299"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteochondrosis, pig","secondary_identifiers":["OMIA:000750-9823"],"termid":"MONDO:1011174","xrefs":{"Monarch":{"xref_id":"1011174"}}}


id: MONDO:1012291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neonatal hepatitis, non-human animal","termid":"MONDO:1011779"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neonatal hepatitis, dog","secondary_identifiers":["OMIA:001094-9615"],"termid":"MONDO:1012291","xrefs":{"Monarch":{"xref_id":"1012291"}}}


id: PBO:0027886
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_histone_H4-K20_dimethylation","termid":"PBO:0027886"}


id: PBO:0044957
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dehydrogenase/reductase 4","termid":"PBO:0044957"}


id: GO:0036153
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Remodeling the acyl chains of triacylglycerol, through sequential deacylation and re-acylation reactions, to generate triacylglycerol containing different types of fatty acid acyl chains.","definition_xrefs":["GOC:mw","PMID:15364929"],"direct_ancestors":[{"relation_name":"is_a","term_name":"triglyceride metabolic process","termid":"GO:0006641"},{"relation_name":"is_a","term_name":"acylglycerol acyl-chain remodeling","termid":"GO:0036155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"triglyceride acyl-chain remodeling","synonyms":[{"name":"triacylglycerol acyl-chain remodeling","type":"exact"},{"name":"triglyceride acyl-chain remodelling","type":"exact"}],"termid":"GO:0036153"}


id: PBO:0049325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIA subunit 2","termid":"PBO:0049325"}


id: PBO:0070209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 137 pseudogene","termid":"PBO:0070209"}


id: PBO:0036438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RhoGAP, GTPase activating protein Rga5","termid":"PBO:0036438"}


id: GO:0050008
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: isopiperitenone = piperitenone.","definition_xrefs":["RHEA:21516"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, transposing C=C bonds","termid":"GO:0016863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"isopiperitenone delta-isomerase activity","secondary_identifiers":["KEGG_REACTION:R03782","MetaCyc:ISOPIPERITENONE-DELTA-ISOMERASE-RXN","EC:5.3.3.11"],"synonyms":[{"name":"isopiperitenone D-isomerase activity","type":"exact"},{"name":"isopiperitenone delta8-delta4-isomerase activity","type":"related"}],"termid":"GO:0050008"}


id: PBO:0063538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudopodium enriched atypical kinase 1","termid":"PBO:0063538"}


id: FYPO:0002826
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 gamma-tubulin complex assembly is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein complex assembly during vegetative growth","termid":"FYPO:0001215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal gamma-tubulin complex assembly","synonyms":[{"name":"normal gamma-tubulin complex assembly during mitotic cell cycle","type":"related"},{"name":"normal gamma-tubulin complex assembly during vegetative growth","type":"exact"}],"termid":"FYPO:0002826"}


id: PBO:0040534
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-1,3-galactosyltransferase 1","termid":"PBO:0040534"}


id: PBO:0051990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"janus kinase and microtubule interacting protein 2","termid":"PBO:0051990"}


id: MONDO:0009302
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Gonadal dysgenesis with multiple anomalies is an association syndrome described only once in two sisters aged 1 1/2 and 8 1/2 years. They had a 46,XY karyotype, cleft lip and palate, preauricular pits, and a 'squashed down' appearance because of a short columella and small nares. Other anomalies included broad hands and feet, and a hypermuscular appearance. Cardiac, renal, musculoskeletal, and ectodermal anomalies were also present. Ectodermal defects included 'punched out scalp defects' and unusual positioning of hair whorls. They also had short stature, streak gonads, and mild developmental delay. The mode of inheritance is most likely autosomal recessive.","definition_xrefs":["Orphanet:1770"],"direct_ancestors":[{"relation_name":"is_a","term_name":"46,XY disorder of sex development","termid":"MONDO:0020040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XY type gonadal dysgenesis-associated anomalies syndrome","secondary_identifiers":["MEDGEN:344696","GARD:2541","OMIM:233430","MESH:C565536","UMLS:C1856272"],"synonyms":[{"name":"gonadal dysgenesis XY type associated anomalies","type":"related"},{"name":"gonadal dysgenesis, 10Y type, with associated anomalies","type":"related"},{"name":"gonadal dysgenesis, XY type, with associated anomalies","type":"related"}],"termid":"MONDO:0009302","xrefs":{"Monarch":{"xref_id":"0009302"}}}


id: PBO:0047998
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fyn related Src family tyrosine kinase","termid":"PBO:0047998"}


id: MONDO:0016758
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microcephaly-brain defect-spasticity-hypernatremia syndrome is a rare congenital genetic syndrome with a central nervous system malformation as a major feature characterized by microcephaly, hypertonia, developmental delay and cognitive impairment, swallowing difficulty, hypernatremia, and hypoplasia of the frontal parts and fusion of the lateral ventricles on brain MRI. Only one familial case with three affected siblings reported and there have been no further descriptions in the literature since 1986.","definition_xrefs":["Orphanet:2523"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microcephaly-brain defect-spasticity-hypernatremia syndrome","secondary_identifiers":["MEDGEN:1668792","UMLS:C4749368","GARD:3607"],"synonyms":[{"name":"Franek-Bocker-Kahlen syndrome","type":"exact"},{"name":"microcephaly - brain defect - spasticity - hypernatremia","type":"related"},{"name":"microcephaly brain defect spasticity hypernatremia","type":"related"}],"termid":"MONDO:0016758","xrefs":{"Monarch":{"xref_id":"0016758"}}}


id: PBO:0108910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAFF interacting protein","termid":"PBO:0108910"}


id: MONDO:0002459
data:
  {"annotated_genes":["SJAG_03453","SJAG_01787","SJAG_00610"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013767"},{"annotations":[87602,87603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:8000024"}]},"cv_name":"mondo","definition":"A disease that has its basis in the disruption of type IV hypersensitivity.","definition_xrefs":["MONDO:patterns/basis_in_disruption_of_process"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypersensitivity reaction disease","termid":"MONDO:0000605"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null,"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"type IV hypersensitivity disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0020522","MEDGEN:9371","NCIT:C3115","DOID:2916"],"synonyms":[{"name":"DTH","type":"exact"},{"name":"delayed hypersensitivity reaction","type":"exact"},{"name":"delayed-type hypersensitivity","type":"exact"},{"name":"delayed-type hypersensitivity response","type":"exact"},{"name":"disorder of type IV hypersensitivity","type":"exact"},{"name":"hypersensitivity reaction type IV disease","type":"related"},{"name":"immunoproliferative disease","type":"related"},{"name":"type 4 hypersensitivity reaction","type":"exact"},{"name":"type IV hypersensitivity","type":"exact"},{"name":"type IV hypersensitivity reaction","type":"exact"}],"termid":"MONDO:0002459","terms_by_termid":{"MONDO:0013767":null,"MONDO:8000024":null},"xrefs":{"Monarch":{"xref_id":"0002459"}}}


id: PBO:0044499
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cystin 1","termid":"PBO:0044499"}


id: PR:O14242
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pyridoxine kinase 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":"pyridoxal kinase C6F6.11c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F6.11c","secondary_identifiers":["UniProtKB:O14242"],"synonyms":[{"name":"Spom972h-pdxK","type":"exact"}],"termid":"PR:O14242"}


id: PBO:0076714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor 20","termid":"PBO:0076714"}


id: PR:Q9UT86
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An anaphase-promoting complex subunit 11 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":"anaphase-promoting complex subunit 11 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC343.03","secondary_identifiers":["UniProtKB:Q9UT86"],"synonyms":[{"name":"20S cyclosome/APC complex protein apc11 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAC343.03","type":"related"},{"name":"Spom972h-ANAPC11","type":"exact"}],"termid":"PR:Q9UT86"}


id: MONDO:0008629
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":"urolithiasis, uric acid, autosomal dominant","secondary_identifiers":["OMIM:191700","MEDGEN:393068","DOID:0080654","UMLS:C2674049"],"synonyms":[{"name":"nephrolithiasis, uric acid, autosomal dominant","type":"related"},{"name":"urolithiasis, uric acid, autosomal dominant","type":"exact"}],"termid":"MONDO:0008629","xrefs":{"Monarch":{"xref_id":"0008629"}}}


id: PBO:0081176
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger FYVE-type containing 26","termid":"PBO:0081176"}


id: GO:1904328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of myofibroblast contraction.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:19239477"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament-based movement","termid":"GO:1903115"},{"relation_name":"regulates","term_name":"myofibroblast contraction","termid":"GO:1990764"}],"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 myofibroblast contraction","synonyms":[{"name":"regulation of MF contraction","type":"exact"},{"name":"regulation of MFB contraction","type":"exact"}],"termid":"GO:1904328"}


id: PBO:0109143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane integral protein involved in protein targeting to mitochondrion Ema19","termid":"PBO:0109143"}


id: GO:0015420
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: vitamin B12(out) + ATP + H2O = ADP + an vitamin B12(in) + H+ + phosphate. Vitamin B12 is alkylcob(III)alamin.","definition_xrefs":["GOC:pz","RHEA:17873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin transmembrane transporter activity","termid":"GO:0090482"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"ABC-type vitamin B12 transporter activity","secondary_identifiers":["Reactome:R-HSA-5223313","Reactome:R-HSA-5683325","MetaCyc:3.6.3.33-RXN","Reactome:R-HSA-9759206","GO:0015235","GO:0102023","EC:7.6.2.8","Reactome:R-HSA-3095901"],"synonyms":[{"name":"ATP-dependent cobalamin transmembrane transporter activity","type":"related"},{"name":"ATP-dependent vitamin B12 transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled cobalamin transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled vitamin B12 transmembrane transporter activity","type":"related"},{"name":"cobalamin ABC transporter","type":"exact"},{"name":"cobalamin porter activity","type":"broad"},{"name":"cobalamin transporter activity","type":"broad"},{"name":"cobalamin-transporting ATPase activity","type":"related"},{"name":"vitamin B12 ABC transporter activity","type":"exact"},{"name":"vitamin B12 porter activity","type":"broad"},{"name":"vitamin B12 transporter activity","type":"broad"},{"name":"vitamin B12-transporting ATPase activity","type":"broad"}],"termid":"GO:0015420"}


id: PBO:0047586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroblast growth factor receptor 3 pseudogene 6","termid":"PBO:0047586"}


id: GO:0021714
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the inferior olivary nucleus is generated and organized. The inferior olivary nucleus is a capsule-shaped structure in the ventral medulla located just lateral and dorsal to the medullary pyramids. Neurons in the inferior olivary nucleus are the source of climbing fiber input to the cerebellar cortex; these neurons have been implicated in various functions, such as learning and timing of movements.","definition_xrefs":["ISBN:0838580343","GOC:cls","GOC:dph","GOC:dgh","GOC:jid","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"medulla oblongata morphogenesis","termid":"GO:0021579"},{"relation_name":"part_of","term_name":"inferior olivary nucleus development","termid":"GO:0021713"}],"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":"inferior olivary nucleus morphogenesis","synonyms":[{"name":"inferior olive morphogenesis","type":"related"}],"termid":"GO:0021714"}


id: PBO:0058810
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7852","termid":"PBO:0058810"}


id: PBO:0076447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TAFA chemokine like family member 3","termid":"PBO:0076447"}


id: MONDO:0026167
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic neuromuscular disease (obsolete MONDO:0026167)","secondary_identifiers":["Orphanet:183497"],"termid":"MONDO:0026167","xrefs":{"Monarch":{"xref_id":"0026167"}}}


id: PBO:0046570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K member 12","termid":"PBO:0046570"}


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


id: GO:0048714
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of oligodendrocyte differentiation.","definition_xrefs":["GOC:vp","PMID:15139015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of glial cell differentiation","termid":"GO:0045687"},{"relation_name":"is_a","term_name":"regulation of oligodendrocyte differentiation","termid":"GO:0048713"},{"relation_name":"positively_regulates","term_name":"oligodendrocyte differentiation","termid":"GO:0048709"}],"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 oligodendrocyte differentiation","synonyms":[{"name":"activation of oligodendrocyte differentiation","type":"narrow"},{"name":"stimulation of oligodendrocyte differentiation","type":"narrow"},{"name":"up regulation of oligodendrocyte differentiation","type":"exact"},{"name":"up-regulation of oligodendrocyte differentiation","type":"exact"},{"name":"upregulation of oligodendrocyte differentiation","type":"exact"}],"termid":"GO:0048714"}


id: GO:0018783
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: deisopropyldeethylatrazine + H2O = 2-chloro-4-hydroxy-6-amino-1,3,5-triazine + NH3.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete deisopropyldeethylatrazine hydrolase activity (obsolete GO:0018783)","termid":"GO:0018783"}


id: GO:0072742
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a SAGA complex is transported to, or maintained in, a specific location in the transcription regulatory region of a gene.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex localization","termid":"GO:0031503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"SAGA complex localization to transcription regulatory region","synonyms":[{"name":"SAGA complex localization to promoter","type":"exact"},{"name":"SAGA complex recruitment","type":"exact"}],"termid":"GO:0072742"}


id: PBO:0069788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1074, pseudogene","termid":"PBO:0069788"}


id: MONDO:0800180
data:
  {"annotated_genes":["SJAG_04944"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"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"}]},"cv_name":"mondo","definition":"Any inherited porphyria in which the cause of the disease is monoallelic or biallelic variants in the CPOX gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited porphyria","termid":"MONDO:0019142"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04944":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0019142"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005093","MONDO:0019142"],"is_obsolete":false,"name":"CPOX-related hereditary coproporphyria","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0800180","terms_by_termid":{"MONDO:0007369":null,"MONDO:0030048":null},"xrefs":{"Monarch":{"xref_id":"0800180"}}}


id: PBO:0039108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AHNAK nucleoprotein","termid":"PBO:0039108"}


id: PBO:0089422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIM23 translocase complex subunit Tim44","termid":"PBO:0089422"}


id: PBO:0012220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteiasome complex subunit beta 4 (predicted)","termid":"PBO:0012220"}


id: PBO:0028681
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_attachment_of_spindle_microtubules_to_kinetochore","termid":"PBO:0028681"}


id: PBO:0011994
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBR ubiquitin ligase Ubr11","termid":"PBO:0011994"}


id: FYPO:0003234
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 methylation of lysine at position 9 of histone H3 at heterochromatin domains is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone H3-K9 methylation during vegetative growth","termid":"FYPO:0003232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal histone H3-K9 methylation at heterochromatin domain during vegetative growth","synonyms":[{"name":"normal histone H3 K9 methylation at heterochromatin domain during vegetative growth","type":"exact"},{"name":"normal histone H3-K9 methylation at HOOD during vegetative growth","type":"exact"},{"name":"normal histone H3-K9 methylation at heterochromatin domain during mitotic cell cycle","type":"related"},{"name":"normal histone H3K9me at heterochromatin domain during vegetative growth","type":"exact"},{"name":"normal histone lysine H3 K9 methylation at heterochromatin domain during vegetative growth","type":"exact"}],"termid":"FYPO:0003234"}


id: PBO:0011464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA methyltransferase, implicated in ribosome biogenesis (predicted)","termid":"PBO:0011464"}


id: GO:0042625
data:
  {"annotated_genes":["SJAG_01913","SJAG_05294","SJAG_02023","SJAG_00516","SJAG_03406","SJAG_00212","SJAG_01471","SJAG_01447","SJAG_01817","SJAG_04015","SJAG_04955","SJAG_02782","SJAG_01397","SJAG_00136"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[62724,61330,61864,63402,61084,65868,66567,69234,72953,80207,80260,81382,58525,62040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046961"}]},"cv_name":"molecular_function","definition":"Enables the transfer of an ion from one side of a membrane to the other, driven by the reaction: ATP + H2O = ADP + phosphate.","definition_xrefs":["GOC:jl","ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATPase-coupled transmembrane transporter activity","termid":"GO:0042626"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00136":null,"SJAG_00212":null,"SJAG_00516":null,"SJAG_01397":null,"SJAG_01447":null,"SJAG_01471":null,"SJAG_01817":null,"SJAG_01913":null,"SJAG_02023":null,"SJAG_02782":null,"SJAG_03406":null,"SJAG_04015":null,"SJAG_04955":null,"SJAG_05294":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"ATPase-coupled ion transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null},"synonyms":[{"name":"ATP-dependent ion transmembrane transporter activity","type":"exact"},{"name":"ATPase activity, coupled to transmembrane movement of ions","type":"exact"},{"name":"ATPase coupled ion transmembrane transporter activity","type":"exact"}],"termid":"GO:0042625","terms_by_termid":{"GO:0046961":null}}


id: PBO:0087959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transmembrane protein involved in forming Cvt and autophagic vesicles; cycles between the phagophore assembly site (PAS) and other cytosolic punctate structures, not found in autophagosomes; may be involved in membrane delivery to the PAS","termid":"PBO:0087959"}


id: MONDO:0013016
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Leukocyte adhesion deficiency type III (LAD-III) is a form of LAD characterized by both severe bacterial infections and a severe bleeding disorder.","definition_xrefs":["Orphanet:99844"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte adhesion deficiency","termid":"MONDO:0017570"},{"relation_name":"is_a","term_name":"autosomal recessive osteopetrosis","termid":"MONDO:0019026"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0006025","MONDO:0005328","MONDO:0005570"],"is_obsolete":false,"name":"leukocyte adhesion deficiency 3","secondary_identifiers":["MEDGEN:411605","DOID:0110912","GARD:16915","UMLS:C2748536","OMIM:612840","MESH:C567555"],"synonyms":[{"name":"FERMT3 leukocyte adhesion deficiency","type":"exact"},{"name":"IADD","type":"exact"},{"name":"LAD-III","type":"exact"},{"name":"LAD1 variant","type":"exact"},{"name":"LAD1V","type":"exact"},{"name":"LAD3","type":"exact"},{"name":"integrin Activation deficiency disease","type":"related"},{"name":"integrin activation deficiency disease","type":"exact"},{"name":"lad-1 variant","type":"exact"},{"name":"lad-III","type":"exact"},{"name":"leukocyte adhesion deficiency 1 variant","type":"exact"},{"name":"leukocyte adhesion deficiency 3","type":"exact"},{"name":"leukocyte adhesion deficiency caused by mutation in FERMT3","type":"exact"},{"name":"leukocyte adhesion deficiency type 3","type":"exact"},{"name":"leukocyte adhesion deficiency type III","type":"exact"},{"name":"leukocyte adhesion deficiency, type 3","type":"related"},{"name":"leukocyte adhesion deficiency, type III","type":"related"},{"name":"leukocyte adhesion deficiency-1 variant","type":"exact"}],"termid":"MONDO:0013016","xrefs":{"Monarch":{"xref_id":"0013016"}}}


id: PBO:0041905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cbl proto-oncogene","termid":"PBO:0041905"}


id: PBO:0000262
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5.3.4.1","termid":"PBO:0000262"}


id: PR:O13702
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A glycerol dehydrogenase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00898"],"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":"glycerol dehydrogenase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13F5.03c","secondary_identifiers":["UniProtKB:O13702"],"synonyms":[{"name":"GDH (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"GLDH (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gldA","type":"exact"}],"termid":"PR:O13702"}


id: PBO:0050241
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 19","termid":"PBO:0050241"}


id: PBO:0003621
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar membrane palmitoyltransferase Pfa5 (predicted)","termid":"PBO:0003621"}


id: GO:0141163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cAMP/PKA signal transduction.","definition_xrefs":["PMID:21585352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cAMP/PKA signal transduction","termid":"GO:0141161"},{"relation_name":"is_a","term_name":"positive regulation of intracellular signal transduction","termid":"GO:1902533"},{"relation_name":"positively_regulates","term_name":"cAMP/PKA signal transduction","termid":"GO:0141156"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of cAMP/PKA signal transduction","synonyms":[{"name":"positive regulation of cAMP/PKA signaling","type":"exact"}],"termid":"GO:0141163"}


id: PBO:0041885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cation channel sperm associated 3","termid":"PBO:0041885"}


id: GO:0043243
data:
  {"annotated_genes":["SJAG_05265","SJAG_03126","SJAG_02189","SJAG_04312","SJAG_02433","SJAG_02812"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99438],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901098"},{"annotations":[103671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031117"},{"annotations":[113819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904595"},{"annotations":[70302,78279,67842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045905"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein complex disassembly, the disaggregation of a protein complex into its constituent components.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein-containing complex disassembly","termid":"GO:0043244"},{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"positively_regulates","term_name":"protein-containing complex disassembly","termid":"GO:0032984"}],"gene_count":6,"genes_by_uniquename":{"SJAG_02189":null,"SJAG_02433":null,"SJAG_02812":null,"SJAG_03126":null,"SJAG_04312":null,"SJAG_05265":null},"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 protein-containing complex disassembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"synonyms":[{"name":"activation of protein complex disassembly","type":"narrow"},{"name":"positive regulation of protein complex disassembly","type":"related"},{"name":"stimulation of protein complex disassembly","type":"narrow"},{"name":"up regulation of protein complex disassembly","type":"exact"},{"name":"up-regulation of protein complex disassembly","type":"exact"},{"name":"upregulation of protein complex disassembly","type":"exact"}],"termid":"GO:0043243","terms_by_termid":{"GO:0031117":null,"GO:0045905":null,"GO:1901098":null,"GO:1904595":null}}


id: PBO:0034394
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-immediately_causally_upstream_of","termid":"PBO:0034394"}


id: GO:0061784
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of (1->4)-beta linkages of N-acetyl-D-glucosamine (GlcNAc) from peptidoglycan.","definition_xrefs":["GOC:dph","GOC:jh","PMID:22748813"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosaminidase activity","termid":"GO:0015929"},{"relation_name":"is_a","term_name":"peptidoglycan muralytic activity","termid":"GO:0061783"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016798","GO:0016787"],"is_obsolete":false,"name":"peptidoglycan N-acetylglucosaminidase activity","termid":"GO:0061784"}


id: SO:0002183
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that encodes a sense overlap long non-coding RNA.","direct_ancestors":[{"relation_name":"is_a","term_name":"lncRNA_gene","termid":"SO:0002127"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sense_overlap_lncRNA_gene","synonyms":[{"name":"sense overlap lncRNA gene","type":"exact"},{"name":"sense overlap ncRNA gene","type":"exact"},{"name":"sense_overlap_lncRNA_gene","type":"exact"}],"termid":"SO:0002183"}


id: GO:0035259
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a nuclear glucocorticoid receptor.","definition_xrefs":["GOC:bf"],"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: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":"nuclear glucocorticoid receptor binding","synonyms":[{"name":"glucocorticoid receptor binding","type":"broad"}],"termid":"GO:0035259"}


id: PBO:0047434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FCF1 pseudogene 5","termid":"PBO:0047434"}


id: PBO:0055109
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 2527","termid":"PBO:0055109"}


id: FYPO:0002037
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of an endodeoxyribonuclease activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal endodeoxyribonuclease activity","termid":"FYPO:0002036"},{"relation_name":"is_a","term_name":"decreased nuclease activity","termid":"FYPO:0004253"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000654","FYPO:0000002","FYPO:0000707","FYPO:0000652","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased endodeoxyribonuclease activity","synonyms":[{"name":"reduced endodeoxyribonuclease activity","type":"exact"}],"termid":"FYPO:0002037"}


id: MONDO:0030073
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A peroxisomal disease characterized by progressive episodic demyelination, sensorimotor polyneuropathy, and hearing loss that has material basis in heterozygous mutation in the ACOX1 gene on chromosome 17q25.1.","definition_xrefs":["DOID:0070516"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of defective peroxisome oxidative status","termid":"MONDO:0100306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019053"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0019053"],"is_obsolete":false,"name":"Mitchell syndrome","secondary_identifiers":["OMIM:618960","Orphanet:631248","MEDGEN:1714342","UMLS:C5394554"],"synonyms":[{"name":"ACOX1 upregulation","type":"exact"},{"name":"MITCH","type":"exact"},{"name":"Mitchell syndrome","type":"exact"}],"termid":"MONDO:0030073","xrefs":{"Monarch":{"xref_id":"0030073"}}}


id: FYPO:0005300
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the kinetochore of a chromosome is decreased during mitotic spindle assembly checkpoint signaling.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to kinetochore during mitotic M phase","termid":"FYPO:0005215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"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"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein localization to kinetochore during mitotic spindle assembly checkpoint signaling","synonyms":[{"name":"decreased protein localisation to kinetochore during mitotic spindle assembly checkpoint signalling","type":"exact"},{"name":"decreased protein localization to kinetochore during mitotic cell cycle spindle assembly checkpoint signaling","type":"exact"},{"name":"decreased protein localization to kinetochore during signal transduction involved in mitotic spindle assembly checkpoint","type":"exact"},{"name":"decreased protein localization to kinetochore during spindle assembly checkpoint signaling during mitotic cell cycle","type":"exact"},{"name":"defective protein recruitment to unattached kinetochores","type":"exact"},{"name":"reduced protein localization to kinetochore during mitotic spindle assembly checkpoint signaling","type":"exact"}],"termid":"FYPO:0005300"}


id: PBO:0028626
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_shmoo_tip","termid":"PBO:0028626"}


id: MONDO:0013142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary sensory and autonomic neuropathy type 2 in which the cause of the disease is a mutation in the RETREG1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary sensory and autonomic neuropathy type 2","termid":"MONDO:0019941"}],"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":"neuropathy, hereditary sensory and autonomic, type 2B","secondary_identifiers":["MEDGEN:413474","GARD:15618","OMIM:613115","UMLS:C2751092","DOID:0070150"],"synonyms":[{"name":"HSAN2B","type":"exact"},{"name":"RETREG1 hereditary sensory and autonomic neuropathy type 2","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy type 2 caused by mutation in RETREG1","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy type 2B","type":"related"},{"name":"hereditary sensory and autonomic neuropathy type IIB","type":"exact"},{"name":"neuropathy, hereditary sensory and autonomic, type 2B","type":"exact"},{"name":"neuropathy, hereditary sensory and autonomic, type IIB","type":"related"}],"termid":"MONDO:0013142","xrefs":{"Monarch":{"xref_id":"0013142"}}}


id: PBO:0016556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAR adaptor protein, human endophilin-A2 ortholog, implicated in endocytosis","termid":"PBO:0016556"}


id: GO:1902679
data:
  {"annotated_genes":["SJAG_01804","SJAG_03143","SJAG_01799","SJAG_02858","SJAG_02255","SJAG_00792","SJAG_00410","SJAG_04268","SJAG_03067","SJAG_02752","SJAG_01157","SJAG_00290","SJAG_01000","SJAG_00802","SJAG_04539","SJAG_04607","SJAG_01728","SJAG_04039","SJAG_04613","SJAG_00926","SJAG_01707","SJAG_04381","SJAG_03319","SJAG_01311","SJAG_00969","SJAG_01254","SJAG_02846","SJAG_02385","SJAG_04584","SJAG_00996","SJAG_01680","SJAG_00987","SJAG_03473","SJAG_00163","SJAG_04026","SJAG_00441","SJAG_02898","SJAG_02048","SJAG_04312","SJAG_02730","SJAG_02104","SJAG_00266","SJAG_02981","SJAG_00142","SJAG_05343","SJAG_00861","SJAG_04921","SJAG_03845","SJAG_03081","SJAG_01230","SJAG_04512","SJAG_01199","SJAG_04249","SJAG_00124","SJAG_02444"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109810],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060195"},{"annotations":[102893],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045892"},{"annotations":[75543,102819,74156,108083,108564,107737,95206,110413,112574,114832,71838,78497,93951,96455,78880,72272,92997,96539,119236,105777,75413,61783,58371,74964,75769,95553,110858,115690,81336,73622,93973,76042,95696,93069,82204,96040,89407,98104,100702,109812,113000,113947,116125,103670,106082,107641,95107,108332,110073,108584,77083,105376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000122"},{"annotations":[75528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016480"},{"annotations":[119798],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034244"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of RNA biosynthetic process.","definition_xrefs":["GO_REF:0000058","GO:jl","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of macromolecule biosynthetic process","termid":"GO:0010558"},{"relation_name":"is_a","term_name":"negative regulation of RNA metabolic process","termid":"GO:0051253"},{"relation_name":"is_a","term_name":"regulation of RNA biosynthetic process","termid":"GO:2001141"},{"relation_name":"negatively_regulates","term_name":"RNA biosynthetic process","termid":"GO:0032774"}],"gene_count":55,"genes_by_uniquename":{"SJAG_00124":null,"SJAG_00142":null,"SJAG_00163":null,"SJAG_00266":null,"SJAG_00290":null,"SJAG_00410":null,"SJAG_00441":null,"SJAG_00792":null,"SJAG_00802":null,"SJAG_00861":null,"SJAG_00926":null,"SJAG_00969":null,"SJAG_00987":null,"SJAG_00996":null,"SJAG_01000":null,"SJAG_01157":null,"SJAG_01199":null,"SJAG_01230":null,"SJAG_01254":null,"SJAG_01311":null,"SJAG_01680":null,"SJAG_01707":null,"SJAG_01728":null,"SJAG_01799":null,"SJAG_01804":null,"SJAG_02048":null,"SJAG_02104":null,"SJAG_02255":null,"SJAG_02385":null,"SJAG_02444":null,"SJAG_02730":null,"SJAG_02752":null,"SJAG_02846":null,"SJAG_02858":null,"SJAG_02898":null,"SJAG_02981":null,"SJAG_03067":null,"SJAG_03081":null,"SJAG_03143":null,"SJAG_03319":null,"SJAG_03473":null,"SJAG_03845":null,"SJAG_04026":null,"SJAG_04039":null,"SJAG_04249":null,"SJAG_04268":null,"SJAG_04312":null,"SJAG_04381":null,"SJAG_04512":null,"SJAG_04539":null,"SJAG_04584":null,"SJAG_04607":null,"SJAG_04613":null,"SJAG_04921":null,"SJAG_05343":null},"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 RNA biosynthetic process","references_by_uniquename":{"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"down regulation of RNA anabolism","type":"exact"},{"name":"down regulation of RNA biosynthesis","type":"exact"},{"name":"down regulation of RNA biosynthetic process","type":"exact"},{"name":"down regulation of RNA formation","type":"exact"},{"name":"down regulation of RNA synthesis","type":"exact"},{"name":"down-regulation of RNA anabolism","type":"exact"},{"name":"down-regulation of RNA biosynthesis","type":"exact"},{"name":"down-regulation of RNA biosynthetic process","type":"exact"},{"name":"down-regulation of RNA formation","type":"exact"},{"name":"down-regulation of RNA synthesis","type":"exact"},{"name":"downregulation of RNA anabolism","type":"exact"},{"name":"downregulation of RNA biosynthesis","type":"exact"},{"name":"downregulation of RNA biosynthetic process","type":"exact"},{"name":"downregulation of RNA formation","type":"exact"},{"name":"downregulation of RNA synthesis","type":"exact"},{"name":"inhibition of RNA anabolism","type":"narrow"},{"name":"inhibition of RNA biosynthesis","type":"narrow"},{"name":"inhibition of RNA biosynthetic process","type":"narrow"},{"name":"inhibition of RNA formation","type":"narrow"},{"name":"inhibition of RNA synthesis","type":"narrow"},{"name":"negative regulation of RNA anabolism","type":"exact"},{"name":"negative regulation of RNA biosynthesis","type":"exact"},{"name":"negative regulation of RNA formation","type":"exact"},{"name":"negative regulation of RNA synthesis","type":"exact"}],"termid":"GO:1902679","terms_by_termid":{"GO:0000122":null,"GO:0016480":null,"GO:0034244":null,"GO:0045892":null,"GO:0060195":null}}


id: GO:0017134
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a fibroblast growth factor.","definition_xrefs":["PMID:9806903"],"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:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"fibroblast growth factor binding","secondary_identifiers":["GO:0048606","GO:0048602","GO:0048603","GO:0048605","GO:0048604","GO:0048607"],"synonyms":[{"name":"FGF 1 binding","type":"narrow"},{"name":"FGF 2 binding","type":"narrow"},{"name":"FGF 3 binding","type":"narrow"},{"name":"FGF 4 binding","type":"narrow"},{"name":"FGF 5 binding","type":"narrow"},{"name":"FGF 6 binding","type":"narrow"},{"name":"FGF binding","type":"exact"},{"name":"fibroblast growth factor 1 binding","type":"narrow"},{"name":"fibroblast growth factor 2 binding","type":"narrow"},{"name":"fibroblast growth factor 3 binding","type":"narrow"},{"name":"fibroblast growth factor 4 binding","type":"narrow"},{"name":"fibroblast growth factor 5 binding","type":"narrow"},{"name":"fibroblast growth factor 6 binding","type":"narrow"}],"termid":"GO:0017134"}


id: PBO:0034425
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-localization_dependent_on_(obsolete_localization_dependent_on)","termid":"PBO:0034425"}


id: PBO:0067627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 799, pseudogene","termid":"PBO:0067627"}


id: MONDO:0700033
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy 13 in which the presence of an extra copy of chromosome 13 is present in all the cells of the organism.","definition_xrefs":["doi:10.1186/1753-6561-9-S1-A51"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trisomy 13","termid":"MONDO:0018068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005328"],"is_obsolete":false,"name":"complete trisomy 13","termid":"MONDO:0700033","xrefs":{"Monarch":{"xref_id":"0700033"}}}


id: MONDO:0005480
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory skin condition caused by direct contact between the skin and either an irritating substance or an allergen.","definition_xrefs":["NCIT:C26743"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dermatitis","termid":"MONDO:0002406"}],"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":"contact dermatitis","secondary_identifiers":["SCTID:40275004","MEDGEN:8329","ICD9:692.9","ICD9:692.89","DOID:2773","UMLS:C0011616","EFO:0005319","MESH:D003877"],"synonyms":[{"name":"contact dermatitis","type":"exact"},{"name":"contact dermatitis/eczema","type":"exact"},{"name":"contact eczema","type":"narrow"},{"name":"dermatitis venenata","type":"exact"},{"name":"dermatitis, venenata","type":"exact"}],"termid":"MONDO:0005480","xrefs":{"Monarch":{"xref_id":"0005480"}}}


id: PBO:0086918
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative zinc finger DNA binding transcription factor; contains two N-terminal C2H2 zinc fingers and C-terminal proline rich domain; overproduction impairs cell growth and induces expression of genes involved in monosaccharide catabolism and aldehyde metabolism; regulates expression of of Y' telomeric elements and subtelomeric COS genes; relocalizes to the cytosol in response to hypoxia; RGM1 has a paralog, USV1, that arose from the whole genome duplication","termid":"PBO:0086918"}


id: GO:1901726
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of histone deacetylase activity.","definition_xrefs":["GOC:rl","GOC:BHF","PMID:20497126","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of histone deacetylase activity (obsolete GO:1901726)","synonyms":[{"name":"down regulation of histone deacetylase activity","type":"exact"},{"name":"down-regulation of histone deacetylase activity","type":"exact"},{"name":"downregulation of histone deacetylase activity","type":"exact"},{"name":"inhibition of histone deacetylase activity","type":"narrow"}],"termid":"GO:1901726"}


id: PBO:0040070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin beta 1","termid":"PBO:0040070"}


id: GO:0042139
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"During meiosis, the aggregation, arrangement and bonding together of strand exchange proteins (recombinases) to form small, electron dense structures in association with meiotic chromosomes during leptotene and zygotene.","definition_xrefs":["PMID:9334324","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic recombination nodule assembly","termid":"GO:0007146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0006310"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006281"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0006281","GO:0006310","GO:0007049","GO:0065003","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"early meiotic recombination nodule assembly","termid":"GO:0042139"}


id: GO:0021787
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a branchiomotor neuron growth cone in the neural tube is directed to a specific target site in the neural tube in response to a repulsive chemical cue. Branchiomotor neurons are located in the hindbrain and innervate branchial arch-derived muscles that control jaw movements, facial expression, the larynx, and the pharynx.","definition_xrefs":["PMID:14699587","GO_REF:0000021","GOC:cls","GOC:dgh","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branchiomotor neuron axon guidance in neural tube","termid":"GO:0021786"},{"relation_name":"is_a","term_name":"chemorepulsion of branchiomotor axon","termid":"GO:0021793"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"chemorepulsion of branchiomotor neuron axon in neural tube","synonyms":[{"name":"negative chemotaxis of branchiomotor neuron axon in neural tube","type":"exact"}],"termid":"GO:0021787"}


id: GO:2001113
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 hepatocyte growth factor stimulus.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular response to growth factor stimulus","termid":"GO:0090288"},{"relation_name":"is_a","term_name":"regulation of cellular response to hepatocyte growth factor stimulus","termid":"GO:2001112"},{"relation_name":"negatively_regulates","term_name":"cellular response to hepatocyte growth factor stimulus","termid":"GO:0035729"}],"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 hepatocyte growth factor stimulus","synonyms":[{"name":"negative regulation of cellular response to HGF stimulus","type":"exact"}],"termid":"GO:2001113"}


id: PBO:0084373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lipoyl ligase; involved in the modification of mitochondrial enzymes by the attachment of lipoic acid groups","termid":"PBO:0084373"}


id: PBO:0043758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 8B, pseudogene","termid":"PBO:0043758"}


id: PBO:0091080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane organization protein, HVA22/TB2/DP1 family protein","termid":"PBO:0091080"}


id: PBO:0084673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial and cytoplasmic valyl-tRNA synthetase; human homolog VARS2 implicated in mitochondrial diseases, can partially complement yeast null mutant","termid":"PBO:0084673"}


id: PBO:0084659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondria-associated F-box protein; involved in maintenance of normal mitochondrial morphology; interacts with Skp1p through the F-box motif; preferentially localizes to the mother cell during budding","termid":"PBO:0084659"}


id: PBO:0089294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPOTS complex subunit, serine palmitoyltransferase activator Tsc3","termid":"PBO:0089294"}


id: PBO:0041528
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 16 open reading frame 90","termid":"PBO:0041528"}


id: MONDO:0019346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sialidosis type 1 (ST-1) is a very rare lysosomal storage disease, and is the normosomatic form of sialidosis, characterized by gait abnormalities, progressive visual loss, bilateral macular cherry red spots and myoclonic epilepsy and ataxia, that usually presents in the second to third decade of life.","definition_xrefs":["Orphanet:812"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"is_a","term_name":"sialidosis","termid":"MONDO:0017734"},{"relation_name":"is_a","term_name":"familial mucolipidosis","termid":"MONDO:0031422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"sialidosis type 1","secondary_identifiers":["SCTID:723675006","NANDO:2201191","UMLS:C0023806","GARD:7639","SCTID:34960006","NANDO:1200117","icd11.foundation:1154773192","MEDGEN:44174"],"synonyms":[{"name":"Normomorphic sialidosis","type":"exact"},{"name":"cherry red spot myoclonus syndrome","type":"related"},{"name":"cherry-red spot-myoclonus syndrome","type":"exact"},{"name":"lipomucopolysaccharidosis","type":"exact"},{"name":"myoclonus cherry red spot syndrome","type":"related"},{"name":"normosomatic sialidosis","type":"exact"},{"name":"sialidosis type I","type":"related"}],"termid":"MONDO:0019346","xrefs":{"Monarch":{"xref_id":"0019346"}}}


id: PBO:0079215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thiosulfate sulfurtransferase","termid":"PBO:0079215"}


id: GO:0005171
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an hepatocyte growth factor receptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor receptor binding","termid":"GO:0070851"}],"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:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"hepatocyte growth factor receptor binding","synonyms":[{"name":"HGF receptor binding","type":"exact"},{"name":"hepatocyte growth factor","type":"narrow"},{"name":"hepatocyte growth factor receptor ligand","type":"narrow"}],"termid":"GO:0005171"}


id: MONDO:0008510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Symphalangism with multiple anomalies of hands and feet is an exceedingly rare syndrome described in one family and characterized by proximal symphalangism and multiple hand and feet disorders (syndactyly, clinodactyly, hypoplasia of the thenar and hypothenar eminences, and a distinctive dermatoglyphic pattern). There have been no further descriptions in the literature since 1981.","definition_xrefs":["Orphanet:3246"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symphalangism","termid":"MONDO:0000151"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"symphalangism with multiple anomalies of hands and feet","secondary_identifiers":["GARD:5077","MEDGEN:348859","UMLS:C1861391","MESH:C566098","OMIM:185750","SCTID:732955001"],"synonyms":[{"name":"Learman syndrome","type":"exact"},{"name":"symphalangism with multiple anomalies of hands and feet","type":"exact"}],"termid":"MONDO:0008510","xrefs":{"Monarch":{"xref_id":"0008510"}}}


id: MONDO:0100264
data:
  {"annotated_genes":["SJAG_01165"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89040],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013936"},{"annotations":[89042],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013937"}]},"cv_name":"mondo","definition":"Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX10 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Zellweger spectrum disorders","termid":"MONDO:0019609"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01165":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0019053"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005066","MONDO:0019053","MONDO:0005559","MONDO:0005244"],"is_obsolete":false,"name":"peroxisome biogenesis disorder due to PEX10 defect","references_by_uniquename":{"PB_REF:0000006":null},"synonyms":[{"name":"PEX10 related Zellweger spectrum disorder","type":"exact"},{"name":"peroxisome biogenesis disorder due to PEX10 defect","type":"exact"}],"termid":"MONDO:0100264","terms_by_termid":{"MONDO:0013936":null,"MONDO:0013937":null},"xrefs":{"Monarch":{"xref_id":"0100264"}}}


id: MONDO:0004501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign, asymptomatic neoplasm that arises from the fallopian tube. The tumors are round and solitary and contain connective tissue and cystic structures lined by serous-type epithelium. The majority of cases are incidental findings during operation for an unrelated gynecologic disorder.","definition_xrefs":["NCIT:C40114"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fallopian tube serous adenofibroma","termid":"MONDO:0003461"},{"relation_name":"is_a","term_name":"cystadenofibroma","termid":"MONDO:0003464"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fallopian tube cystadenofibroma","secondary_identifiers":["DOID:8211","MEDGEN:273292","UMLS:C1517111"],"synonyms":[{"name":"cystadenofibroma of fallopian tube","type":"exact"},{"name":"fallopian tube cystadenofibroma","type":"exact"},{"name":"fallopian tube serous cystadenofibroma","type":"exact"}],"termid":"MONDO:0004501","xrefs":{"Monarch":{"xref_id":"0004501"}}}


id: PBO:0029318
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H2A_phosphorylation_at_subtelomere_during_mitotic_S_phase","termid":"PBO:0029318"}


id: GO:0075102
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism stops, prevents, or reduces the frequency, rate or extent of the symbiont MAP kinase-mediated signal transduction. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation by host of symbiont MAP kinase-mediated signal transduction (obsolete GO:0075102)","termid":"GO:0075102"}


id: FYPO:0003544
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the number of sites of double-strand breaks in DNA is greater than normal during a meiotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased number of double-strand break sites","termid":"FYPO:0003543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"name":"increased number of double-strand break sites during meiotic cell cycle","synonyms":[{"name":"accumulation of DNA damage foci during meiotic cell cycle","type":"related"},{"name":"accumulation of double-strand break sites during meiotic cell cycle","type":"exact"},{"name":"increased number of DNA damage foci during meiotic cell cycle","type":"related"},{"name":"increased number of double-strand break sites during meiosis","type":"related"},{"name":"increased number of meiotic double-strand break sites","type":"exact"},{"name":"increased number of meiotic double-strand breaks","type":"exact"}],"termid":"FYPO:0003544"}


id: GO:0042495
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a triacylated bacterial lipoprotein stimulus is received by a cell and converted into a molecular signal. Triacylated bacterial lipoproteins are lipopeptides of bacterial origin containing a nonprotein moiety consisting of three acyl groups.","definition_xrefs":["PMID:12077222","GOC:add","PMID:12524386","PMID:2757794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of bacterial lipopeptide","termid":"GO:0070340"},{"relation_name":"is_a","term_name":"response to triacyl bacterial lipopeptide","termid":"GO:0071725"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of triacyl bacterial lipopeptide","synonyms":[{"name":"detection of triacylated bacterial lipoprotein","type":"exact"},{"name":"perception of triacylated bacterial lipopeptide","type":"related"},{"name":"perception of triacylated bacterial lipoprotein","type":"related"}],"termid":"GO:0042495"}


id: GO:0090118
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A receptor-mediated endocytosis process involved in intracellular cholesterol transport.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:pr","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor-mediated endocytosis","termid":"GO:0006898"},{"relation_name":"is_a","term_name":"intracellular transport","termid":"GO:0046907"},{"relation_name":"part_of","term_name":"intracellular cholesterol transport","termid":"GO:0032367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"receptor-mediated endocytosis involved in cholesterol transport","synonyms":[{"name":"receptor-mediated endocytosis involved in intracellular cholesterol transport","type":"related"},{"name":"receptor-mediated endocytosis of LDL","type":"related"},{"name":"receptor-mediated endocytosis of low-density lipoprotein involved in cholesterol transport","type":"related"},{"name":"receptor-mediated endocytosis of low-density lipoprotein particle involved in cholesterol transport","type":"related"}],"termid":"GO:0090118"}


id: GO:0071261
data:
  {"annotated_genes":["SJAG_00959","SJAG_00064"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[99862,110151],"is_not":false,"summary":null,"term":"GO:0071261"}]},"cv_name":"cellular_component","definition":"A translocon complex that contains a core heterotrimer of alpha, beta and gamma subunits, and may contain additional proteins (translocon-associated proteins or TRAPs); in budding yeast the core proteins are Ssh1p, Sbh2p, and Sss1p. The Ssh1 translocon complex is involved in the cotranslational pathway of protein transport across the ER membrane, and recognizes proteins bearing strongly hydrophobic signal sequences.","definition_xrefs":["PMID:12134063","PMID:8612571","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translocon complex","termid":"GO:0071256"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00064":null,"SJAG_00959":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005789"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005789","GO:0005575","GO:0005737","GO:0005783"],"is_obsolete":false,"name":"Ssh1 translocon complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"Ssh1p-Sss1p-Sbh2p complex","type":"narrow"}],"termid":"GO:0071261","terms_by_termid":{"GO:0071261":null}}


id: PBO:0046384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EOLA1 divergent transcript","termid":"PBO:0046384"}


id: FYPO:0007448
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which autophagic degradation of the endoplasmic reticulum is normal (i.e. indistinguishable from wild type) when the cell is subject to nitrogen starvation.","definition_xrefs":["PMID:32735772","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process","termid":"FYPO:0000627"},{"relation_name":"is_a","term_name":"abnormal macroautophagy during nitrogen starvation","termid":"FYPO:0004670"},{"relation_name":"is_a","term_name":"abnormal reticulophagy","termid":"FYPO:0008083"}],"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:0000257"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000257"],"is_obsolete":false,"name":"normal reticulophagy during nitrogen starvation","synonyms":[{"name":"normal ER autophagy during nitrogen starvation","type":"exact"},{"name":"normal ER degradation during nitrogen starvation","type":"related"},{"name":"normal ER-phagy during nitrogen starvation","type":"exact"},{"name":"normal endoplasmic reticulum autophagy during nitrogen starvation","type":"exact"},{"name":"normal reticulophagy during nitrogen depletion","type":"exact"},{"name":"normal reticulophagy during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0007448"}


id: GO:1902201
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of bacterial-type flagellum-dependent cell motility.","definition_xrefs":["GOC:TermGenie","GOC:cilia","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of bacterial-type flagellum-dependent cell motility","termid":"GO:1902021"},{"relation_name":"is_a","term_name":"negative regulation of cell motility","termid":"GO:2000146"},{"relation_name":"negatively_regulates","term_name":"bacterial-type flagellum-dependent cell motility","termid":"GO:0071973"}],"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 bacterial-type flagellum-dependent cell motility","synonyms":[{"name":"down regulation of bacterial-type flagellar cell motility","type":"exact"},{"name":"down regulation of flagellin-based flagellar cell motility","type":"exact"},{"name":"down-regulation of bacterial-type flagellar cell motility","type":"exact"},{"name":"down-regulation of flagellin-based flagellar cell motility","type":"exact"},{"name":"downregulation of bacterial-type flagellar cell motility","type":"exact"},{"name":"downregulation of flagellin-based flagellar cell motility","type":"exact"},{"name":"inhibition of bacterial-type flagellar cell motility","type":"narrow"},{"name":"inhibition of flagellin-based flagellar cell motility","type":"exact"},{"name":"negative regulation of bacterial-type flagellar cell motility","type":"related"},{"name":"negative regulation of flagellin-based flagellar cell motility","type":"exact"}],"termid":"GO:1902201"}


id: MOD:00540
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a residue containing common isotopes to a 9x(13)C labeled residue.","definition_xrefs":["Unimod:184","PubMed:12716131"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(13)C labeled residue","termid":"MOD:00842"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"9x(13)C labeled residue","synonyms":[{"name":"13C(9) Silac label","type":"related"},{"name":"Label:13C(9)","type":"related"}],"termid":"MOD:00540"}


id: PBO:0050354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 57","termid":"PBO:0050354"}


id: PBO:0027428
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_number_of_converged_replication_forks","termid":"PBO:0027428"}


id: GO:0075523
data:
  {"annotated_genes":["SJAG_04546"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[67070],"is_not":false,"summary":null,"term":"GO:0075523"}]},"cv_name":"biological_process","definition":"A process which occurs during viral translation, which involves a translational recoding mechanism called programmed ribosomal frameshifting. This causes the ribosome to alter its reading of the mRNA to an a different open reading frame to produce alternate viral proteins.","definition_xrefs":["PMID:8852897","PMID:24825891","GOC:jl","GOC:ch","GOC:bf","VZ:860"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"},{"relation_name":"part_of","term_name":"viral translation","termid":"GO:0019081"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04546":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"viral translational frameshifting","references_by_uniquename":{"GO_REF:0000043":null},"synonyms":[{"name":"ribosomal frameshifting involved in viral translation","type":"exact"}],"termid":"GO:0075523","terms_by_termid":{"GO:0075523":null}}


id: MONDO:1012084
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tetragametic chimerism, non-human animal","termid":"MONDO:1011918"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetragametic chimerism, pig","secondary_identifiers":["OMIA:000393-9823"],"termid":"MONDO:1012084","xrefs":{"Monarch":{"xref_id":"1012084"}}}


id: GO:0032025
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 cobalt ion (Co2+) stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to metal ion","termid":"GO:0010038"}],"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 cobalt ion","termid":"GO:0032025"}


id: PBO:0041223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C1GALT1 pseudogene 3","termid":"PBO:0041223"}


id: PBO:0069033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 278, pseudogene","termid":"PBO:0069033"}


id: PATO:0001257
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Pink color having high brightness and moderate saturation.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pink","termid":"PATO:0000954"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"light deep pink","termid":"PATO:0001257"}


id: FYPO:0004284
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of oxanine DNA N-glycosylase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal oxanine DNA N-glycosylase activity","termid":"FYPO:0004283"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000661","FYPO:0000652","FYPO:0000654","FYPO:0001985"],"is_obsolete":false,"name":"decreased oxanine DNA N-glycosylase activity","synonyms":[{"name":"reduced oxanine DNA N-glycosylase activity","type":"exact"}],"termid":"FYPO:0004284"}


id: MONDO:0006285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from a pleomorphic adenoma in the major salivary glands. It usually originates in the parotid gland. Patients usually present with a history of a long-standing tumor mass which grew rapidly in the past few months. Patients with non-invasive or minimally invasive carcinoma have an excellent prognosis. In cases where there is invasion of the surrounding tissues, the clinical course is aggressive.","definition_xrefs":["NCIT:C5975"],"direct_ancestors":[{"relation_name":"is_a","term_name":"major salivary gland carcinoma","termid":"MONDO:0006284"},{"relation_name":"is_a","term_name":"salivary gland carcinoma ex pleomorphic adenoma","termid":"MONDO:0006403"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"major salivary gland carcinoma ex pleomorphic adenoma","secondary_identifiers":["MEDGEN:233655","UMLS:C1334550","EFO:1000345"],"synonyms":[{"name":"carcinoma ex pleomorphic adenoma of Major salivary gland","type":"exact"},{"name":"carcinoma ex pleomorphic adenoma of the Major salivary gland","type":"exact"},{"name":"major salivary gland carcinoma ex pleomorphic adenoma","type":"exact"},{"name":"major salivary gland salivary gland carcinoma ex pleomorphic adenoma","type":"exact"}],"termid":"MONDO:0006285","xrefs":{"Monarch":{"xref_id":"0006285"}}}


id: PBO:0055556
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 2992","termid":"PBO:0055556"}


id: PATO:0001587
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A variability of rate which is relatively high.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"variability of rate","termid":"PATO:0001586"},{"relation_name":"is_a","term_name":"increased process quality","termid":"PATO:0002304"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased variability of rate","synonyms":[{"name":"high variability of rate","type":"exact"}],"termid":"PATO:0001587"}


id: GO:0035761
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for the dorsal motor nucleus of the vagus nerve to attain its fully functional state.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure maturation","termid":"GO:0071695"},{"relation_name":"part_of","term_name":"dorsal motor nucleus of vagus nerve development","termid":"GO:0021744"}],"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":"dorsal motor nucleus of vagus nerve maturation","termid":"GO:0035761"}


id: GO:1904099
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein O-linked glycosylation.","definition_xrefs":["GO_REF:0000058","PMID:24509081","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of glycoprotein biosynthetic process","termid":"GO:0010561"},{"relation_name":"is_a","term_name":"regulation of protein O-linked glycosylation","termid":"GO:1904098"},{"relation_name":"negatively_regulates","term_name":"protein O-linked glycosylation","termid":"GO:0006493"}],"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 protein O-linked glycosylation","synonyms":[{"name":"down regulation of protein O-linked glycosylation","type":"exact"},{"name":"down regulation of protein amino acid O-linked glycosylation","type":"exact"},{"name":"down-regulation of protein O-linked glycosylation","type":"exact"},{"name":"down-regulation of protein amino acid O-linked glycosylation","type":"exact"},{"name":"downregulation of protein O-linked glycosylation","type":"exact"},{"name":"downregulation of protein amino acid O-linked glycosylation","type":"exact"},{"name":"inhibition of protein O-linked glycosylation","type":"narrow"},{"name":"inhibition of protein amino acid O-linked glycosylation","type":"narrow"},{"name":"negative regulation of protein amino acid O-linked glycosylation","type":"exact"}],"termid":"GO:1904099"}


id: PBO:0002102
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates rhp51","termid":"PBO:0002102"}


id: PBO:0047209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 220 member C, pseudogene","termid":"PBO:0047209"}


id: MONDO:0005116
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A systemic infection caused by the Gram-positive bacterium Tropheryma whipplei. It affects the small intestine resulting in malabsorption. Other sites or systems affected by the infection are the joints, central nervous system, and the cardiovascular system.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal disorder","termid":"MONDO:0005020"},{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"},{"relation_name":"is_a","term_name":"digestive system infectious disorder","termid":"MONDO:0043424"}],"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":"Whipple disease","secondary_identifiers":["GARD:7889","SCTID:41545003","MESH:D008061","ICD10CM:K90.81","UMLS:C0023788","MEDGEN:7347","MedDRA:10047931","icd11.foundation:1131038233","ICD10EXP:M14.8*","NCIT:C85228","Orphanet:3452","ICD10EXP:K90.8+","ICD9:040.2","DOID:8476","EFO:0000775","NORD:1850"],"synonyms":[{"name":"Tropheryma whippelii infection","type":"related"},{"name":"Tropheryma whipplei caused disease or disorder","type":"exact"},{"name":"Tropheryma whipplei disease or disorder","type":"exact"},{"name":"Tropheryma whipplei infectious disease","type":"exact"},{"name":"Whipple disease","type":"exact"},{"name":"Whipple's disease","type":"related"},{"name":"intestinal lipodystrophy","type":"exact"},{"name":"intestinal lipophagic granulomatosis","type":"exact"},{"name":"secondary non-tropical sprue","type":"exact"}],"termid":"MONDO:0005116","xrefs":{"Monarch":{"xref_id":"0005116"}}}


id: MONDO:0014380
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Colobomatous microphthalmia-rhizomelic dysplasia syndrome is a rare, genetic developmental defect during embryogenesis characterized by a range of developmental eye anomalies (including anophthalmia, microphthalmia, colobomas, microcornea, corectopia, cataract) and symmetric limb rhizomelia with short stature and contractures of large joints. Intellectual disability with autistic features, macrocephaly, dysmorphic features, urogenital anomalies (hypospadia, cryptorchidism), cutaneous syndactyly and precocious puberty may also be present.","definition_xrefs":["Orphanet:424099"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic microphthalmia","termid":"MONDO:0016073"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"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":"colobomatous microphthalmia-rhizomelic dysplasia syndrome","secondary_identifiers":["DOID:0111802","MEDGEN:862977","OMIM:615877","UMLS:C4014540","GARD:17707"],"synonyms":[{"name":"MCOPS14","type":"related"},{"name":"MCSKS","type":"related"},{"name":"microphthalmia and coloboma, with or without rhizomelic skeletal dysplasia","type":"related"},{"name":"microphthalmia or coloboma with or without rhizomelic skeletal dysplasia","type":"related"},{"name":"microphthalmia, syndromic 14","type":"related"},{"name":"microphthalmia, syndromic type 14","type":"exact"},{"name":"microphthalmia-coloboma-rhizomelic skeletal dysplasia","type":"exact"},{"name":"microphthalmia/coloboma and skeletal dysplasia syndrome","type":"related"}],"termid":"MONDO:0014380","xrefs":{"Monarch":{"xref_id":"0014380"}}}


id: PBO:0056708
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator of cell motility 1","termid":"PBO:0056708"}


id: PBO:0085711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in spore wall assembly; has similarity to 1,3-beta-D-glucan synthase catalytic subunits Fks1p and Gsc2p; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies","termid":"PBO:0085711"}


id: PBO:0073785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 5 member 5","termid":"PBO:0073785"}


id: GO:0052827
data:
  {"annotated_genes":["SJAG_00063"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990651"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: myo-inositol pentakisphosphate + H2O = myo-inositol tetrakisphosphate + phosphate.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol phosphate phosphatase activity","termid":"GO:0052745"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00063":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"inositol pentakisphosphate phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0052827","terms_by_termid":{"GO:1990651":null}}


id: PBO:0075020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 115-31","termid":"PBO:0075020"}


id: FYPO:0002834
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 chromatin silencing at centromeric regions is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin silencing at centromere","termid":"FYPO:0000146"},{"relation_name":"is_a","term_name":"decreased chromatin silencing","termid":"FYPO:0002353"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"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:0006551","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased chromatin silencing at centromere","synonyms":[{"name":"decreased chromatin silencing at centromere during mitotic cell cycle","type":"related"},{"name":"decreased chromatin silencing at centromere during vegetative growth","type":"exact"},{"name":"decreased heterochromatin silencing at centromere","type":"related"},{"name":"reduced chromatin silencing at centromere","type":"exact"}],"termid":"FYPO:0002834"}


id: PBO:0052686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 10","termid":"PBO:0052686"}


id: GO:1903527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of membrane tubulation.","definition_xrefs":["GOC:pm","GOC:TermGenie","GO_REF:0000058","PMID:18388313"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"is_a","term_name":"regulation of membrane tubulation","termid":"GO:1903525"},{"relation_name":"positively_regulates","term_name":"plasma membrane tubulation","termid":"GO:0097320"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"positive regulation of membrane tubulation","synonyms":[{"name":"activation of membrane tubulation","type":"narrow"},{"name":"activation of plasma membrane tubulation","type":"narrow"},{"name":"positive regulation of plasma membrane tubulation","type":"exact"},{"name":"up regulation of membrane tubulation","type":"exact"},{"name":"up regulation of plasma membrane tubulation","type":"exact"},{"name":"up-regulation of membrane tubulation","type":"exact"},{"name":"up-regulation of plasma membrane tubulation","type":"exact"},{"name":"upregulation of membrane tubulation","type":"exact"},{"name":"upregulation of plasma membrane tubulation","type":"exact"}],"termid":"GO:1903527"}


id: MONDO:0002374
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete parachordoma (obsolete MONDO:0002374)","termid":"MONDO:0002374","xrefs":{"Monarch":{"xref_id":"0002374"}}}


id: GO:1905197
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any endocannabinoid signaling pathway that is involved in retrograde trans-synaptic signaling by endocannabinoid.","definition_xrefs":["GO_REF:0000060","GOC:TermGenie","PMID:23040807"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocannabinoid signaling pathway involved in trans-synaptic signaling","termid":"GO:1905129"},{"relation_name":"part_of","term_name":"retrograde trans-synaptic signaling by endocannabinoid","termid":"GO:0098921"}],"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:0008150","GO:0023052"],"is_obsolete":false,"name":"endocannabinoid signaling pathway involved in retrograde trans-synaptic signaling","synonyms":[{"name":"endocannabinoid signalling pathway involved in retrograde trans-synaptic signaling by endocannabinoid","type":"exact"}],"termid":"GO:1905197"}


id: MONDO:0013428
data:
  {"annotated_genes":["SJAG_02394"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88699],"is_not":false,"summary":null,"term":"MONDO:0013428"}]},"cv_name":"mondo","definition":"Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Meier-Gorlin syndrome","termid":"MONDO:0016817"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02394":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"Meier-Gorlin syndrome 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C3151097","OMIM:613800","DOID:0080513","GARD:15708","MEDGEN:462447"],"synonyms":[{"name":"MGORS2","type":"related"},{"name":"Meier-GORLIN syndrome 2","type":"related"},{"name":"Meier-Gorlin syndrome 2","type":"exact"},{"name":"Meier-Gorlin syndrome caused by mutation in ORC4","type":"exact"},{"name":"Meier-Gorlin syndrome type 2","type":"exact"},{"name":"ORC4 Meier-Gorlin syndrome","type":"exact"}],"termid":"MONDO:0013428","terms_by_termid":{"MONDO:0013428":null},"xrefs":{"Monarch":{"xref_id":"0013428"}}}


id: PBO:0048055
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 4","termid":"PBO:0048055"}


id: PBO:0079292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin tyrosine ligase like 10","termid":"PBO:0079292"}


id: PBO:0056000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated","termid":"PBO:0056000"}


id: PBO:0110338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BBLN pseudogene 1","termid":"PBO:0110338"}


id: GO:0060641
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the epithelium of the mammary duct is destroyed in males.","definition_xrefs":["GOC:dph","PMID:12558599"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure regression","termid":"GO:0060033"},{"relation_name":"part_of","term_name":"mammary gland duct morphogenesis","termid":"GO:0060603"}],"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 duct regression in males","termid":"GO:0060641"}


id: PBO:0067043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 62, pseudogene","termid":"PBO:0067043"}


id: PBO:0077838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPBGL antisense RNA 1","termid":"PBO:0077838"}


id: PR:Q10309
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A phospholipid-transporting ATPase IIA that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00966","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":"phospholipid-transporting ATPase C6C3.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6C3.06c","secondary_identifiers":["UniProtKB:Q10309"],"synonyms":[{"name":"Spom972h-ATP9A","type":"exact"}],"termid":"PR:Q10309"}


id: PBO:0002768
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Noc2p-Noc3p complex subunit Noc2 family (predicted)","termid":"PBO:0002768"}


id: PBO:0078816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TROAP and PRPH antisense RNA 1","termid":"PBO:0078816"}


id: PBO:0053514
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 502","termid":"PBO:0053514"}


id: MONDO:1011272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease created by lentiviral transgenesis to create pigs with a deleterious mutation in the GUCY2D gene known to cause cone-rod dystrophy 6 in humans.","definition_xrefs":["OMIA:001929-9823"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cone-rod dystrophy, non-human animal","termid":"MONDO:1012582"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cone-rod dystrophy, GUCY2D-related, pig","synonyms":[{"name":"retinal atrophy - cone-rod dystrophy 6, pig","type":"related"}],"termid":"MONDO:1011272","xrefs":{"Monarch":{"xref_id":"1011272"}}}


id: MONDO:0020644
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare non-Hodgkin lymphoma that arises in and is confined to the lung at the time of diagnosis. Representative examples include bronchial mucosa-associated lymphoid tissue lymphoma and diffuse large B-cell lymphoma.","definition_xrefs":["NCIT:C5684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung lymphoma","termid":"MONDO:0003987"},{"relation_name":"is_a","term_name":"non-Hodgkin lymphoma","termid":"MONDO:0018908"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"lung non-Hodgkin lymphoma","secondary_identifiers":["UMLS:C1334453","MEDGEN:235267"],"synonyms":[{"name":"lung non-Hodgkin lymphoma","type":"exact"},{"name":"lung non-Hodgkin's lymphoma","type":"exact"},{"name":"non-Hodgkin lymphoma of lung","type":"exact"},{"name":"primary lung non-Hodgkin's lymphoma","type":"exact"}],"termid":"MONDO:0020644","xrefs":{"Monarch":{"xref_id":"0020644"}}}


id: PBO:0062997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidyl arginine deiminase 3","termid":"PBO:0062997"}


id: PBO:0090576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIM23 translocase complex subunit Tim23","termid":"PBO:0090576"}


id: GO:0033942
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of alpha-(1->4)-D-glucosidic linkage in 4-alpha-D-{(1->4)-alpha-D-glucanosyl}n trehalose to yield trehalose and alpha-(1->4)-D-glucan.","definition_xrefs":["EC:3.2.1.141"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0003674","GO:0016798","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"4-alpha-D-(1->4)-alpha-D-glucanotrehalose trehalohydrolase activity","secondary_identifiers":["MetaCyc:3.2.1.141-RXN"],"synonyms":[{"name":"4-alpha-D-{(1,4)-alpha-D-glucano}trehalose glucanohydrolase (trehalose-producing) activity","type":"related"},{"name":"4-alpha-D-{(1->4)-alpha-D-glucano}trehalose glucanohydrolase (trehalose-producing) activity","type":"related"},{"name":"malto-oligosyltrehalose trehalohydrolase activity","type":"related"},{"name":"maltooligosyl trehalose trehalohydrolase activity","type":"related"}],"termid":"GO:0033942"}


id: PBO:0075518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"speedy/RINGO cell cycle regulator family member A","termid":"PBO:0075518"}


id: MONDO:0003018
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete myotonic disease (obsolete MONDO:0003018)","termid":"MONDO:0003018","xrefs":{"Monarch":{"xref_id":"0003018"}}}


id: PBO:0080230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VKORC1 pseudogene 1","termid":"PBO:0080230"}


id: PBO:0089264
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase-promoting complex TPR lobe accessory factor subunit Hcn1/Apc12","termid":"PBO:0089264"}


id: PBO:0091316
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by A. thaliana AtSGP1","termid":"PBO:0091316"}


id: PBO:0031067
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,_without_cell_division,_with_normal_germ_tube_morphology","termid":"PBO:0031067"}


id: PBO:0070505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L6 pseudogene 4","termid":"PBO:0070505"}


id: PBO:0039133
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aminoacyl tRNA synthetase complex interacting multifunctional protein 2","termid":"PBO:0039133"}


id: PBO:0046041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 2 subunit gamma B","termid":"PBO:0046041"}


id: PBO:0015219
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae SEC14","termid":"PBO:0015219"}


id: MONDO:0013835
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any muscular dystrophy-dystroglycanopathy, type A in which the cause of the disease is a mutation in the ISPD gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type A","termid":"MONDO:0000171"},{"relation_name":"is_a","term_name":"myopathy caused by variation in CRPPA","termid":"MONDO:0100530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320","MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7","secondary_identifiers":["UMLS:C3553330","DOID:0111234","GARD:15829","MEDGEN:766244","OMIM:614643"],"synonyms":[{"name":"ISPD muscular dystrophy-dystroglycanopathy, type A","type":"exact"},{"name":"MDDGA7","type":"related"},{"name":"Walker-Warburg syndrome or muscle-eye-brain disease, ISPD-related","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy, type A caused by mutation in ISPD","type":"exact"}],"termid":"MONDO:0013835","xrefs":{"Monarch":{"xref_id":"0013835"}}}


id: FYPO:0006459
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which protein modification is abnormal during the meiotic cell cycle. All modifications may be affected, or only modifications of a certain type, or on specific proteins, or even specific sites within specific proteins.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein modification","termid":"FYPO:0002494"}],"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:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0002274","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein modification during meiotic cell cycle","termid":"FYPO:0006459"}


id: GO:0001650
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A structure found most metazoan nucleoli, but not usually found in lower eukaryotes; surrounded by the dense fibrillar component; the zone of transcription from multiple copies of the pre-rRNA genes is in the border region between these two structures.","definition_xrefs":["PMID:10754561"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"nucleolus","termid":"GO:0005730"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"part_of","termid":"GO:0005730"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0005730"],"is_obsolete":false,"name":"fibrillar center","synonyms":[{"name":"fibrillar centre","type":"exact"}],"termid":"GO:0001650"}


id: PBO:0045628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 4 like 40 (pseudogene)","termid":"PBO:0045628"}


id: FYPO:0005455
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which telomere assembly occurs at one or more chromosome ends generated by a double-strand break.","definition_xrefs":["PMID:17724078","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal telomere assembly","termid":"FYPO:0005454"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000641","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"telomere assembly at double-strand break site","synonyms":[{"name":"de novo telomere addition at double-strand break site","type":"exact"},{"name":"telomere assembly at double-strand break site during mitotic cell cycle","type":"related"},{"name":"telomere assembly at double-strand break site during vegetative growth","type":"exact"},{"name":"telomere formation at double-strand break site","type":"exact"}],"termid":"FYPO:0005455"}


id: PBO:0113046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chromatin segregase involved in DNA replication; ATPase activity, stimulated by S phase CDK-dependent phosphorylation, is coupled to nucleosome disassembly, promoting DNA replication; regulates cell-cycle-dependent histone gene expression; contains AAA+-ATPase domains and a non-canonical bromodomain; hexameric; relocalizes to the cytosol in response to hypoxia; human ortholog ATAD2 is a coregulator of oncogenic transcription factors and an oncogene overexpressed in cancers with poor prognosis","termid":"PBO:0113046"}


id: PBO:0048145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FXYD domain containing ion transport regulator 6 pseudogene 1","termid":"PBO:0048145"}


id: PBO:0000456
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein Nrd1","termid":"PBO:0000456"}


id: MONDO:0044636
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare hyperkinetic movement disorder (obsolete MONDO:0044636)","secondary_identifiers":["Orphanet:494457"],"termid":"MONDO:0044636","xrefs":{"Monarch":{"xref_id":"0044636"}}}


id: PBO:0043785
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carboxypeptidase D","termid":"PBO:0043785"}


id: GO:0102187
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4alpha-carboxy,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3beta-ol + NAD(1-) = 4alpha,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3-one + NADH(2-) + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 4alpha-carboxy,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3beta-ol dehydrogenase/C4-decarboxylase activity (obsolete GO:0102187)","termid":"GO:0102187"}


id: PBO:0111746
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-C3HC4 type (RING finger)","termid":"PBO:0111746"}


id: GO:0033716
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reactions: adenosine + 2 O2 = 9-riburonosyladenine + 2 hydrogen peroxide.","definition_xrefs":["EC:1.1.3.39","RHEA:15489"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor","termid":"GO:0016899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"nucleoside oxidase (hydrogen peroxide-forming) activity","secondary_identifiers":["MetaCyc:1.1.3.39-RXN"],"synonyms":[{"name":"nucleoside:oxygen 5'-oxidoreductase (hydrogen peroxide-forming) activity","type":"related"}],"termid":"GO:0033716"}


id: MONDO:0009363
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hydrocephaly-tall stature-joint laxity syndrome is a multiple congenital anomalies syndrome described in two sisters and characterized by the presence of hydrocephalus (onset in infancy), tall stature, joint laxity, and thoracolumbar kyphosis. There have been no further descriptions in the literature since 1989.","definition_xrefs":["Orphanet:2181"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrocephaly-tall stature-joint laxity syndrome","secondary_identifiers":["MESH:C535770","GARD:1666","UMLS:C1856051","MEDGEN:383828","SCTID:732926009","OMIM:236660"],"synonyms":[{"name":"Daish Hardman Lamont syndrome","type":"related"},{"name":"Daish-Hardman-Lamont syndrome","type":"exact"},{"name":"hydrocephalus, tall stature, JOINT laxity, and kyphoscoliosis","type":"related"},{"name":"hydrocephalus, tall stature, joint laxity and kyphoscoliosis","type":"related"},{"name":"hydrocephaly - tall stature - joint laxity","type":"related"}],"termid":"MONDO:0009363","xrefs":{"Monarch":{"xref_id":"0009363"}}}


id: MONDO:0022794
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A structural cytogenetic abnormality characterized by partial or complete loss of chromosome 8.","definition_xrefs":["NCIT:C36535"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"monosomy","termid":"MONDO:0020639"}],"gene_count":0,"genotype_count":0,"name":"obsolete chromosome 8 deletion (obsolete MONDO:0022794)","secondary_identifiers":["MESH:C537823"],"synonyms":[{"name":"Anomaly of chromosome pair 8","type":"related"},{"name":"Deletions of chromosome 8","type":"related"},{"name":"del(8)","type":"related"},{"name":"loss of chromosome 8","type":"related"}],"termid":"MONDO:0022794","xrefs":{"Monarch":{"xref_id":"0022794"}}}


id: MOD:00894
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"Natural or modified resiues with a mass of 128.058578 Da.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"residues isobaric at a resolution below 0.000001 Da","termid":"MOD:00569"},{"relation_name":"is_a","term_name":"residues isobaric at 128.0-128.1","termid":"MOD:00893"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"residues isobaric at 128.058578 Da","termid":"MOD:00894"}


id: GO:0030837
data:
  {"annotated_genes":["SJAG_01993","SJAG_01894","SJAG_02700","SJAG_00279"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77285,80885,81936,94138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051016"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of actin polymerization.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament polymerization","termid":"GO:0030833"},{"relation_name":"is_a","term_name":"negative regulation of protein polymerization","termid":"GO:0032272"},{"relation_name":"is_a","term_name":"negative regulation of cytoskeleton organization","termid":"GO:0051494"},{"relation_name":"is_a","term_name":"negative regulation of supramolecular fiber organization","termid":"GO:1902904"},{"relation_name":"negatively_regulates","term_name":"actin filament polymerization","termid":"GO:0030041"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00279":null,"SJAG_01894":null,"SJAG_01993":null,"SJAG_02700":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"negatively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"negatively_regulates","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0030036","GO:0044085","GO:0008150","GO:0007010","GO:0065003"],"is_obsolete":false,"name":"negative regulation of actin filament polymerization","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of actin filament polymerization","type":"exact"},{"name":"down-regulation of actin filament polymerization","type":"exact"},{"name":"downregulation of actin filament polymerization","type":"exact"},{"name":"inhibition of actin filament polymerization","type":"narrow"},{"name":"negative regulation of actin polymerization","type":"exact"},{"name":"negative regulation of actin polymerization and/or depolymerization","type":"broad"}],"termid":"GO:0030837","terms_by_termid":{"GO:0051016":null}}


id: PBO:0084144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High-affinity histidine permease; also involved in the transport of manganese ions","termid":"PBO:0084144"}


id: PBO:0078841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Pro (anticodon TGG) 3-5","termid":"PBO:0078841"}


id: PBO:0113115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Endoplasmic reticulum protein of unknown function; deletion confers resistance to fluconazole and to osmotic stress","termid":"PBO:0113115"}


id: FYPO:0006723
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 a protein that normally moves away from Cdr2 medial cortical node complexes during a cellular response to osmotic stress instead remains predominantly in the nodes.","definition_xrefs":["PMID:28924043","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein exit from Cdr2 medial cortical node complex during cellular response to osmotic stress","synonyms":[{"name":"decreased protein exit from Cdr2 medial cortical node complex during cellular response to osmotic stress during mitotic cell cycle","type":"related"},{"name":"decreased protein exit from Cdr2 medial cortical node complex during cellular response to osmotic stress during vegetative growth","type":"exact"}],"termid":"FYPO:0006723"}


id: MONDO:0100304
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any peroxisomal single enzyme/protein defect that has its basis in the disruption of bile acid aminotransferase.","definition_xrefs":["MONDO:patterns/inborn_metabolic_disrupts"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisomal single enzyme/protein defect","termid":"MONDO:0100257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019053"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0019053"],"is_obsolete":false,"name":"disorder of bile acid aminotransferase","synonyms":[{"name":"disorder of bile acid aminotransferase","type":"exact"}],"termid":"MONDO:0100304","xrefs":{"Monarch":{"xref_id":"0100304"}}}


id: PBO:0064124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase domain containing, cytoplasmic","termid":"PBO:0064124"}


id: PBO:0113466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the signal peptidase complex (SPC); SPC cleaves the signal sequence from proteins targeted to the endoplasmic reticulum (ER); regulates cellular levels of membrane proteins; homolog of the SPC12 subunit of mammalian signal peptidase complex; protein abundance increases in response to DNA replication stress","termid":"PBO:0113466"}


id: MONDO:0017402
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated arrhythmogenic right ventricular dysplasia","termid":"MONDO:0016342"}],"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":"familial isolated arrhythmogenic ventricular dysplasia, biventricular form","secondary_identifiers":["Orphanet:293899","UMLS:C5925016","MEDGEN:1864265","GARD:17346","DOID:0070535"],"synonyms":[{"name":"familial isolated arrhythmogenic ventricular cardiomyopathy, biventricular form","type":"exact"}],"termid":"MONDO:0017402","xrefs":{"Monarch":{"xref_id":"0017402"}}}


id: PBO:0086205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that associates with mitochondrial ribosome; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies; YDL027C is not an essential gene","termid":"PBO:0086205"}


id: PBO:0045795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EGF like repeats and discoidin domains 3","termid":"PBO:0045795"}


id: PBO:0082723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the RAM signaling network; is involved in regulation of Ace2p activity and cellular morphogenesis, interacts with protein kinase Cbk1p and also with Kic1p","termid":"PBO:0082723"}


id: MONDO:1011798
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forelimb-girdle muscular anomaly, non-human animal","secondary_identifiers":["OMIA:001442"],"termid":"MONDO:1011798","xrefs":{"Monarch":{"xref_id":"1011798"}}}


id: GO:1901925
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the movement of proteins from the cytoplasm into the nucleus, and that occurs as a response to the mitotic cell cycle spindle assembly checkpoint. In S. cerevisiae, this process involves inhibition of the karyopherin/importin Kap121p (also known as Pse1p), which acts as the specific nuclear import receptor for several proteins, including Glc7p. Glc7p functions in opposition to key spindle assembly checkpoint protein Aurora kinase (Ipl1p).","definition_xrefs":["GOC:dgf","GOC:TermGenie","PMID:23177738"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to mitotic cell cycle spindle assembly checkpoint signaling","termid":"GO:0072479"}],"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 protein import into nucleus during spindle assembly checkpoint","synonyms":[{"name":"KTIP","type":"related"},{"name":"Kap121p transport inhibitory pathway","type":"related"},{"name":"negative regulation of protein import into nucleus during mitotic cell cycle spindle assembly checkpoint","type":"exact"}],"termid":"GO:1901925"}


id: PBO:0031797
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_duration_of_mitotic_G2/M_phase_transition_(obsolete_FYPO:0000404)","termid":"PBO:0031797"}


id: MONDO:0007747
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"hereditary epidermal appendage anomaly","termid":"MONDO:0021026"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0006025"],"is_obsolete":false,"name":"isolated hyperchlorhidrosis","secondary_identifiers":["GARD:17984","ICD9:276.9","UMLS:C1840437","SCTID:709413001","MEDGEN:333560","OMIM:143860","Orphanet:542657","DOID:0111371"],"synonyms":[{"name":"hyperchlorhidrosis, isolated","type":"exact"},{"name":"isolated hyperchlorhidrosis","type":"exact"}],"termid":"MONDO:0007747","xrefs":{"Monarch":{"xref_id":"0007747"}}}


id: GO:0018646
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (1S,4R)-1-hydroxy-2-oxolimonene + NADPH + O2 = NADP+ + OH- + (3R)-3-isopropenyl-6-oxoheptanoate.","definition_xrefs":["UM-BBD_reactionID:r0736"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-hydroxy-2-oxolimonene 1,2-monooxygenase activity (obsolete GO:0018646)","termid":"GO:0018646"}


id: PBO:0035916
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_astral_microtubules","termid":"PBO:0035916"}


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


id: SO:0001200
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A negative_sense_RNA_viral_sequence is a ss_RNA_viral_sequence that is the sequence of a single stranded RNA virus that is complementary to mRNA and must be converted to positive sense RNA by RNA polymerase before translation.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ss_RNA_viral_sequence","termid":"SO:0001199"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negative_sense_ssRNA_viral_sequence","synonyms":[{"name":"negative sense single stranded RNA virus","type":"related"},{"name":"negative sense ssRNA viral sequence","type":"exact"}],"termid":"SO:0001200"}


id: GO:0044377
data:
  {"annotated_genes":["SJAG_04009","SJAG_05153"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[108891,110657],"is_not":false,"summary":null,"term":"GO:0044377"}]},"cv_name":"molecular_function","definition":"Binding to a specific upstream regulatory DNA sequence (transcription factor recognition sequence or binding site) located in cis relative to the transcription start site (i.e., on the same strand of DNA) of a gene transcribed by RNA polymerase II, and distorting the original structure of DNA, typically a straight helix, into a bend, or increasing the bend if the original structure was intrinsically bent due to its sequence.","definition_xrefs":["GOC:jl","GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II cis-regulatory region sequence-specific DNA binding","termid":"GO:0000978"},{"relation_name":"is_a","term_name":"sequence-specific DNA binding, bending","termid":"GO:0044374"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04009":null,"SJAG_05153":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:0000976"},{"rel_name":"is_a","termid":"GO:0003677"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0000976","GO:0003677"],"is_obsolete":false,"name":"RNA polymerase II cis-regulatory region sequence-specific DNA binding, bending","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"RNA polymerase II core promoter proximal region sequence-specific DNA binding, bending","type":"related"},{"name":"RNA polymerase II promoter proximal region sequence-specific DNA binding, bending","type":"related"},{"name":"RNA polymerase II proximal promoter region sequence-specific DNA binding, bending","type":"related"},{"name":"RNA polymerase II proximal promoter sequence-specific DNA binding, bending","type":"related"}],"termid":"GO:0044377","terms_by_termid":{"GO:0044377":null}}


id: MONDO:0008039
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tropical spastic paraparesis is a chronic systemic immune-mediated inflammatory myeloneuropathy, more frequently reported in women than in men, that usually presents in adulthood with slowly progressive spastic paraparesis of the lower limbs, bladder and bowel dysfunction, and sensory disturbances in the lower extremities (e.g. paresthesia and dysesthesia) and that is associated with a human T-cell lymphotropic virus type 1 (HTLV-1) infection.","definition_xrefs":["Orphanet:289326"],"direct_ancestors":[{"relation_name":"is_a","term_name":"human T-lymphotropic virus 1 infectious disease","termid":"MONDO:0005801"},{"relation_name":"is_a","term_name":"infectious disorder of the nervous system","termid":"MONDO:0020010"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tropical spastic paraparesis","secondary_identifiers":["ICD10CM:G04.1","UMLS:C0030481","GARD:8208","MESH:D015493","SCTID:714279000","EFO:0007527","NANDO:1200206","DOID:321","OMIM:159580","icd11.foundation:1043229589","MEDGEN:18298","MedDRA:10044696","ICD9:323.01"],"synonyms":[{"name":"HAM/TSP","type":"exact"},{"name":"HTLV-1 associated myelopathy/tropical spastic paraparesis","type":"related"},{"name":"HTLV-1-associated myelopathy/tropical spastic paraparesis","type":"exact"},{"name":"HTLV-associated myelopathy","type":"exact"},{"name":"Human T-cell leukaemia virus type 1 associated myelopathy/tropical spastic paraparesis","type":"related"},{"name":"Human T-cell leukemia virus type 1 associated myelopathy/tropical spastic paraparesis","type":"related"},{"name":"Human T-lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis","type":"exact"},{"name":"Human T-lymphotropic virus type-1-associated myelopathy/tropical spastic paraparesis","type":"exact"},{"name":"TSP","type":"exact"},{"name":"familial spastic paraparesis, HTLV-1-associated","type":"related"},{"name":"ham","type":"related"},{"name":"ham/TSP","type":"exact"},{"name":"myelopathy, HTLV-1-associated","type":"related"},{"name":"tropical spastic paralysis","type":"exact"},{"name":"tropical spastic paraparesis (formerly)","type":"related"},{"name":"tropical spastic paraplegia","type":"exact"}],"termid":"MONDO:0008039","xrefs":{"Monarch":{"xref_id":"0008039"}}}


id: GO:0033174
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The catalytic sector of the mitochondrial hydrogen-transporting ATP synthase; it comprises the catalytic core and central stalk, and is peripherally associated with the chloroplast thylakoid membrane when the entire ATP synthase is assembled. The chloroplast F0 domain contains three alpha, three beta, one gamma, one delta, and one epsilon subunits.","definition_xrefs":["GOC:pj","PMID:11032839","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete chloroplast proton-transporting ATP synthase complex, catalytic core CF(1) (obsolete GO:0033174)","synonyms":[{"name":"chloroplast proton-transporting F-type ATPase complex, catalytic core CF(1)","type":"exact"}],"termid":"GO:0033174"}


id: MONDO:0005658
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with astrovirus, causing gastroenteritis in human infants, calves, lambs, and piglets.","definition_xrefs":["MESH:D019350"],"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":"Astroviridae infectious disease","secondary_identifiers":["UMLS:C0376550","MEDGEN:84000"],"termid":"MONDO:0005658","xrefs":{"Monarch":{"xref_id":"0005658"}}}


id: FYPO:0009021
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is decreased relative to normal in a medium containing L-cysteine as the nitrogen source.","definition_xrefs":["PMID:34984977","PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased vegetative cell population growth","termid":"FYPO:0001355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003","FYPO:0005447","FYPO:0000139","FYPO:0002058","FYPO:0002060","FYPO:0002057"],"is_obsolete":false,"name":"decreased cell population growth on cysteine nitrogen source","synonyms":[{"name":"decreased growth on cysteine nitrogen source","type":"broad"},{"name":"decreased vegetative cell growth on cysteine nitrogen source","type":"exact"},{"name":"growth defect, slow growth with cysteine nitrogen source","type":"related"},{"name":"reduced cell growth on cysteine nitrogen source","type":"related"},{"name":"slow cell growth on cysteine nitrogen source","type":"narrow"}],"termid":"FYPO:0009021"}


id: PBO:0045029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DIS3L antisense RNA 1","termid":"PBO:0045029"}


id: MONDO:0008324
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":"pseudoarthrogryposis","secondary_identifiers":["MEDGEN:356790","OMIM:177300","UMLS:C1867485","MESH:C566753"],"synonyms":[{"name":"ankylosis at elbow and knee","type":"related"},{"name":"hereditary congenital rigidity of elbows and knees","type":"related"},{"name":"pseudoarthrogryposis","type":"exact"}],"termid":"MONDO:0008324","xrefs":{"Monarch":{"xref_id":"0008324"}}}


id: MONDO:0011344
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":"parotitis, juvenile recurrent","secondary_identifiers":["OMIM:603588","MESH:C566359","UMLS:C1863691","MEDGEN:350954"],"synonyms":[{"name":"parotitis, juvenile recurrent","type":"exact"}],"termid":"MONDO:0011344","xrefs":{"Monarch":{"xref_id":"0011344"}}}


id: GO:0160221
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway in which the signal is transmitted via the activation of Rho activity. Rho is a family of small (~21 kDa) signaling G proteins that include RhoA, Cdc42, and Rac1.","definition_xrefs":["PMID:33849392","PMID:10836144"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"}],"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:0008150","GO:0023052"],"is_obsolete":false,"name":"Rho-activating G protein-coupled receptor signaling pathway","termid":"GO:0160221"}


id: PBO:0070072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6atac small nuclear 29, pseudogene","termid":"PBO:0070072"}


id: GO:0043917
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-D-ribose 1,5-bisphosphate = D-ribulose 1,5-bisphosphate.","definition_xrefs":["RHEA:32243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"ribose 1,5-bisphosphate isomerase activity","secondary_identifiers":["EC:5.3.1.29","MetaCyc:RXN-8801"],"synonyms":[{"name":"ribose-1,5-bisphosphate isomerase activity","type":"exact"}],"termid":"GO:0043917"}


id: MONDO:0017287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A recently described mass-forming lesion that occurs in the pancreas, submandibular glands, lacrimal glands, lymph nodes, and hepatobiliary tract. It is characterized by the presence of marked tissue sclerosis and infiltration by numerous plasma cells. The plasma cells show immunohistochemical staining for IgG4 and the serum IgG4 levels are often increased.","definition_xrefs":["NCIT:C95992"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"}],"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":"immunoglobulin G4-related sclerosing disease","secondary_identifiers":["Orphanet:596448","icd11.foundation:99883782","MedDRA:10071569","MEDGEN:473761","Orphanet:284264","NANDO:1200924","UMLS:C3203653","GARD:12521","DOID:0080356","NANDO:1200923"],"synonyms":[{"name":"IgG4-RD","type":"exact"},{"name":"IgG4-associated disease","type":"related"},{"name":"IgG4-positive multiorgan lymphoproliferative syndrome","type":"related"},{"name":"IgG4-related autoimmune disease","type":"related"},{"name":"IgG4-related disease","type":"exact"},{"name":"IgG4-related sclerosing disease","type":"exact"},{"name":"IgG4-related systemic disease","type":"exact"},{"name":"IgG4-related systemic sclerosing disease","type":"related"},{"name":"IgG4-syndrome","type":"related"},{"name":"hyper-IgG4 disease","type":"related"},{"name":"immunoglobulin G4-related sclerosing disease","type":"exact"},{"name":"multifocal fibrosclerosis","type":"related"},{"name":"multifocal idiopathic fibrosclerosis","type":"related"},{"name":"systemic IgG4-related plasmacytic syndrome","type":"related"},{"name":"systemic IgG4-related sclerosing syndrome","type":"related"}],"termid":"MONDO:0017287","xrefs":{"Monarch":{"xref_id":"0017287"}}}


id: PBO:0048885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgin A6 family like 4","termid":"PBO:0048885"}


id: SO:0002202
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A repeat region that is prone to expansions and/or contractions.","direct_ancestors":[{"relation_name":"is_a","term_name":"tandem_repeat","termid":"SO:0000705"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"repeat_instability_region","synonyms":[{"name":"INSDC_feature:misc_feature","type":"broad"},{"name":"INSDC_note:repeat_instability_region","type":"exact"},{"name":"repeat instability region","type":"exact"}],"termid":"SO:0002202"}


id: GO:0006382
data:
  {"annotated_genes":["SJAG_04189","SJAG_00352","SJAG_04380"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75550,102931,59505],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002100"}]},"cv_name":"biological_process","definition":"The conversion of an adenosine residue to inosine in an RNA molecule by deamination.","definition_xrefs":["PMID:11092837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"base conversion or substitution editing","termid":"GO:0016553"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00352":null,"SJAG_04189":null,"SJAG_04380":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"adenosine to inosine editing","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-75064"],"termid":"GO:0006382","terms_by_termid":{"GO:0002100":null}}


id: GO:1901286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving iron-sulfur-molybdenum cofactor.","definition_xrefs":["GOC:TermGenie","UniPathway:UPA00782","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic process","termid":"GO:0008152"}],"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":"iron-sulfur-molybdenum cofactor metabolic process","synonyms":[{"name":"FeMo-co metabolic process","type":"exact"},{"name":"FeMo-co metabolism","type":"exact"},{"name":"iron-molybdenum cofactor metabolic process","type":"exact"},{"name":"iron-molybdenum cofactor metabolism","type":"exact"},{"name":"iron-sulfur-molybdenum cofactor metabolism","type":"exact"}],"termid":"GO:1901286"}


id: GO:1903355
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of distal tip cell migration.","definition_xrefs":["PMID:24968003","GO_REF:0000058","GOC:mm2","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell migration","termid":"GO:0030336"},{"relation_name":"is_a","term_name":"regulation of distal tip cell migration","termid":"GO:1903354"},{"relation_name":"negatively_regulates","term_name":"distal tip cell migration","termid":"GO:0097628"}],"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 distal tip cell migration","synonyms":[{"name":"down regulation of distal tip cell migration","type":"exact"},{"name":"down-regulation of distal tip cell migration","type":"exact"},{"name":"downregulation of distal tip cell migration","type":"exact"},{"name":"inhibition of distal tip cell migration","type":"narrow"}],"termid":"GO:1903355"}


id: MONDO:0003922
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma arising from the ovary. It is characterized by the presence of malignant epithelial cells with clear cytoplasm in a fibrotic stroma.","definition_xrefs":["NCIT:C40079"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian clear cell cancer","termid":"MONDO:0000548"}],"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 clear cell malignant adenofibroma","secondary_identifiers":["DOID:6554","UMLS:C2075522","MEDGEN:384483","ICDO:8313/3"],"synonyms":[{"name":"ovarian clear cell adenocarcinofibroma","type":"exact"},{"name":"ovarian clear cell malignant adenofibroma","type":"exact"}],"termid":"MONDO:0003922","xrefs":{"Monarch":{"xref_id":"0003922"}}}


id: GO:0008292
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of acetylcholine, the acetic acid ester of the organic base choline.","definition_xrefs":["GOC:jl","ISBN:0192800752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylcholine metabolic process","termid":"GO:0008291"},{"relation_name":"is_a","term_name":"acetate ester biosynthetic process","termid":"GO:1900620"}],"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":"acetylcholine biosynthetic process","synonyms":[{"name":"acetylcholine anabolism","type":"exact"},{"name":"acetylcholine biosynthesis","type":"exact"},{"name":"acetylcholine formation","type":"exact"},{"name":"acetylcholine synthesis","type":"exact"}],"termid":"GO:0008292"}


id: GO:1904819
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a parietal peritoneum over time, from its formation to the mature structure.","definition_xrefs":["GOC:dph","PMID:15840053","GO_REF:0000094","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"peritoneum development","termid":"GO:1904820"}],"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":"parietal peritoneum development","synonyms":[{"name":"peritoneal cavity lining development","type":"exact"}],"termid":"GO:1904819"}


id: PBO:0084623
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Methionine-S-sulfoxide reductase; involved in the response to oxidative stress; protects iron-sulfur clusters from oxidative inactivation along with MXR2; involved in the regulation of lifespan; reduced activity of human homolog implicated in Alzheimer disease","termid":"PBO:0084623"}


id: PBO:0018180
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin involved in ubiquitin-dependent endocytosis","termid":"PBO:0018180"}


id: PATO:0001819
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A morphological quality inhering in a bearer by virtue of the bearer's absence or closure of a normal body orifice or tubular passage.","definition_xrefs":["answers.com:answers.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"closed","termid":"PATO:0000608"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atretic","synonyms":[{"name":"atresia","type":"exact"}],"termid":"PATO:0001819"}


id: PBO:0001177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate-tRNA ligase (predicted)","termid":"PBO:0001177"}


id: PBO:0081655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 580","termid":"PBO:0081655"}


id: GO:0090120
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of cholesterol, cholest-5-en-3-beta-ol, or cholesterol-containing compounds, from the lysosome to the endoplasmic reticulum.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal transport","termid":"GO:0007041"},{"relation_name":"is_a","term_name":"vesicle-mediated transport","termid":"GO:0016192"},{"relation_name":"is_a","term_name":"intracellular cholesterol transport","termid":"GO:0032367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"lysosome to ER cholesterol transport","synonyms":[{"name":"lysosome to endoplasmic reticulum cholesterol transport","type":"exact"}],"termid":"GO:0090120"}


id: PBO:0056315
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase kinase kinase 2","termid":"PBO:0056315"}


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


id: PBO:0070423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribulose-5-phosphate-3-epimerase pseudogene 1","termid":"PBO:0070423"}


id: GO:0030948
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of vascular endothelial growth factor receptor signaling pathway activity.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"regulation of vascular endothelial growth factor receptor signaling pathway","termid":"GO:0030947"},{"relation_name":"is_a","term_name":"negative regulation of cellular response to growth factor stimulus","termid":"GO:0090288"},{"relation_name":"negatively_regulates","term_name":"vascular endothelial growth factor receptor signaling pathway","termid":"GO:0048010"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of vascular endothelial growth factor receptor signaling pathway","synonyms":[{"name":"down regulation of vascular endothelial growth factor receptor signaling pathway","type":"exact"},{"name":"down-regulation of vascular endothelial growth factor receptor signaling pathway","type":"exact"},{"name":"downregulation of vascular endothelial growth factor receptor signaling pathway","type":"exact"},{"name":"inhibition of vascular endothelial growth factor receptor signaling pathway","type":"narrow"},{"name":"negative regulation of VEGF receptor signaling pathway","type":"exact"},{"name":"negative regulation of VEGF receptor signalling pathway","type":"exact"},{"name":"negative regulation of vascular endothelial growth factor receptor signalling pathway","type":"exact"}],"termid":"GO:0030948"}


id: GO:0000336
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of DNA transposition.","definition_xrefs":["GOC:krc","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transposition, DNA-mediated (obsolete GO:0000336)","synonyms":[{"name":"activation of DNA transposition","type":"narrow"},{"name":"positive regulation of DNA transposition","type":"exact"},{"name":"stimulation of DNA transposition","type":"narrow"},{"name":"up regulation of DNA transposition","type":"exact"},{"name":"up-regulation of DNA transposition","type":"exact"},{"name":"upregulation of DNA transposition","type":"exact"}],"termid":"GO:0000336"}


id: PBO:0090523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial thiosulfate sulfurtransferase, involved in tRNA wobble position thiolation Tum1","termid":"PBO:0090523"}


id: PBO:0043340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytokine dependent hematopoietic cell linker","termid":"PBO:0043340"}


id: PR:O14199
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A UDP-N-acetylglucosamine transferase subunit ALG14 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00606","PRO:DNx","PANTHER:PTHR12154:SF0"],"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":"UDP-N-acetylglucosamine transferase subunit alg14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC5D6.06c","secondary_identifiers":["UniProtKB:O14199"],"synonyms":[{"name":"Spom972h-ALG14","type":"exact"},{"name":"asparagine-linked glycosylation protein 14 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14199"}


id: GO:0160274
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a white fat cell acquires specialized features of a beige adipocyte. Beige adipocytes reside within white adipose tissue and can be induced to produce heat in response to cold exposure or certain stimuli, resembling brown adipocytes.","definition_xrefs":["PMID:24439384"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fat cell differentiation","termid":"GO:0045444"}],"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":"beige fat cell differentiation","synonyms":[{"name":"brite fat cell differentiation","type":"exact"},{"name":"brown-in white fat cell differentiation","type":"exact"}],"termid":"GO:0160274"}


id: PBO:0002052
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human HSET","termid":"PBO:0002052"}


id: MONDO:0957921
data:
  {"annotated_genes":["SJAG_02701"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88040],"is_not":false,"summary":null,"term":"MONDO:0957921"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Cornelia de Lange syndrome","termid":"MONDO:0016033"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02701":null},"genotype_count":0,"is_obsolete":false,"name":"Cornelia de Lange syndrome 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620568","UMLS:C5882712","MEDGEN:1848930","DOID:0060970"],"termid":"MONDO:0957921","terms_by_termid":{"MONDO:0957921":null},"xrefs":{"Monarch":{"xref_id":"0957921"}}}


id: GO:0071152
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex formed by the association of the guanine nucleotide exchange factor synembrin with the alpha(q) subunit of a heterotrimeric G protein.","definition_xrefs":["PMID:12509430","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"part_of","term_name":"intracellular anatomical structure","termid":"GO:0005622"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"G-protein alpha(q)-synembrin complex","synonyms":[{"name":"Ric-8A G(q) alpha subunit complex","type":"narrow"}],"termid":"GO:0071152"}


id: PBO:0003323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial metalloendopeptidase (predicted)","termid":"PBO:0003323"}


id: PATO:0000385
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000385 hardness value (obsolete PATO:0000385)","termid":"PATO:0000385"}


id: GO:0060041
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the retina over time, from its formation to the mature structure. The retina is the innermost layer or coating at the back of the eyeball, which is sensitive to light and in which the optic nerve terminates.","definition_xrefs":["ISBN:0815340729","GOC:bf","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"camera-type eye development","termid":"GO:0043010"}],"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":"retina development in camera-type eye","secondary_identifiers":["GO:0002073"],"synonyms":[{"name":"retina development in camera-style eye","type":"exact"},{"name":"retinal development","type":"related"}],"termid":"GO:0060041"}


id: PBO:0078667
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (anticodon TTT) 3-2","termid":"PBO:0078667"}


id: GO:0038028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An insulin receptor signaling pathway in which the signal is transmitted via the phosphatidylinositol 3-kinase cascade.","definition_xrefs":["GOC:signaling","PMID:20696212","PMID:19322168","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete insulin receptor signaling pathway via phosphatidylinositol 3-kinase (obsolete GO:0038028)","synonyms":[{"name":"insulin receptor signaling pathway via PI3K cascade","type":"exact"},{"name":"insulin receptor signaling pathway via phosphatidylinositol 3-kinase cascade","type":"related"},{"name":"insulin receptor signaling via PI3K","type":"exact"},{"name":"insulin receptor signalling pathway via phosphatidylinositol 3-kinase cascade","type":"exact"}],"termid":"GO:0038028"}


id: GO:0042216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of phenanthrene, a tricyclic aromatic hydrocarbon.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenanthrene metabolic process","termid":"GO:0018955"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"},{"relation_name":"is_a","term_name":"hydrocarbon catabolic process","termid":"GO:0120253"}],"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":"phenanthrene catabolic process","secondary_identifiers":["UM-BBD_pathwayID:phe"],"synonyms":[{"name":"phenanthrene breakdown","type":"exact"},{"name":"phenanthrene catabolism","type":"exact"},{"name":"phenanthrene degradation","type":"exact"}],"termid":"GO:0042216"}


id: GO:0060929
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of cells to atrioventricular (AV) node cell fates and their capacity to differentiate into AV node cells.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac pacemaker cell fate commitment","termid":"GO:0060927"},{"relation_name":"part_of","term_name":"atrioventricular node cell differentiation","termid":"GO:0060922"}],"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":"atrioventricular node cell fate commitment","synonyms":[{"name":"AV node cell fate commitment","type":"exact"}],"termid":"GO:0060929"}


id: PBO:0077549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 256 pseudogene 2","termid":"PBO:0077549"}


id: PBO:0060964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFU1 iron-sulfur cluster scaffold pseudogene 1","termid":"PBO:0060964"}


id: PBO:0000876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fusion cytochrome c oxidase assembly protein Cox1101, mitochondrial ribosomal protein Rsm22 (predicted)","termid":"PBO:0000876"}


id: PBO:0113227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Myb-related transcription factor; involved in regulating basal and induced expression of genes of the purine and histidine biosynthesis pathways; controls cellular ATP levels; also involved in regulation of meiotic recombination at specific genes","termid":"PBO:0113227"}


id: PBO:0090628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GID complex subunit Gid9","termid":"PBO:0090628"}


id: PBO:0026783
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_DNA_synthesis_involved_in_mitotic_DNA_replication","termid":"PBO:0026783"}


id: PBO:0065616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTP4A2 pseudogene 2","termid":"PBO:0065616"}


id: GO:2001164
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of phosphorylation of RNA polymerase II C-terminal domain serine 2 residues.","definition_xrefs":["PMID:15149594"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of phosphorylation of RNA polymerase II C-terminal domain serine 2 residues (obsolete GO:2001164)","termid":"GO:2001164"}


id: MONDO:0005684
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of paralytic poliomyelitis affecting neurons of the medulla oblongata of the brain stem. Clinical features include impaired respiration, hypertension, alterations of vasomotor control, and dysphagia. Weakness and atrophy of the limbs and trunk due to spinal cord involvement is usually associated. (From Adams et al., Principles of Neurology, 6th ed, p765)","definition_xrefs":["MESH:D011052"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paralytic poliomyelitis","termid":"MONDO:0000341"},{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"bulbar polio","secondary_identifiers":["UMLS:C0032372","MEDGEN:45982","DOID:9786","ICD9:045.0"],"synonyms":[{"name":"bulbar polio","type":"exact"},{"name":"bulbar poliomyelitis","type":"exact"},{"name":"medullary involvement poliomyelitis","type":"related"},{"name":"polio, bulbar","type":"related"},{"name":"poliomyelitis, medullary involvement","type":"related"}],"termid":"MONDO:0005684","xrefs":{"Monarch":{"xref_id":"0005684"}}}


id: GO:0031990
data:
  {"annotated_genes":["SJAG_01584"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74922],"is_not":false,"summary":null,"term":"GO:0031990"}]},"cv_name":"biological_process","definition":"The directed movement of mRNA from the nucleus to the cytoplasm during a heat stimulus, a temperature stimulus above the optimal temperature for the organism; in particular, a process that enables an organism withstand exposure to temperatures that would otherwise lethally impair poly(A)+ mRNA-nucleus export.","definition_xrefs":["GOC:vw","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA export from nucleus","termid":"GO:0006406"},{"relation_name":"is_a","term_name":"cellular response to heat","termid":"GO:0034605"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01584":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006913"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006913","GO:0008150","GO:0010467","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"mRNA export from nucleus in response to heat stress","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"mRNA export from cell nucleus during heat stress","type":"exact"},{"name":"mRNA export from nucleus during heat stress","type":"related"}],"termid":"GO:0031990","terms_by_termid":{"GO:0031990":null}}


id: MONDO:0009408
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":"hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase","secondary_identifiers":["MEDGEN:383794","MESH:C565489","OMIM:240000","UMLS:C1855884"],"synonyms":[{"name":"hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase","type":"exact"}],"termid":"MONDO:0009408","xrefs":{"Monarch":{"xref_id":"0009408"}}}


id: PBO:0039340
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alsin Rho guanine nucleotide exchange factor ALS2","termid":"PBO:0039340"}


id: GO:1905931
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of vascular smooth muscle cell differentiation involved in phenotypic switching.","definition_xrefs":["GO_REF:0000058","GOC:BHF","GOC:rph","GOC:TermGenie","GOC:BHF_miRNA","PMID:25089138"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of vascular associated smooth muscle cell differentiation","termid":"GO:1905064"},{"relation_name":"is_a","term_name":"negative regulation of cell differentiation involved in phenotypic switching","termid":"GO:1905916"},{"relation_name":"is_a","term_name":"regulation of vascular associated smooth muscle cell differentiation involved in phenotypic switching","termid":"GO:1905930"},{"relation_name":"negatively_regulates","term_name":"vascular associated smooth muscle cell differentiation involved in phenotypic switching","termid":"GO:1905420"}],"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 vascular associated smooth muscle cell differentiation involved in phenotypic switching","synonyms":[{"name":"down regulation of VSMC differentiation involved in phenotypic dimorphism","type":"related"},{"name":"down regulation of VSMC differentiation involved in phenotypic switching","type":"exact"},{"name":"down regulation of vascular associated smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"down regulation of vascular associated smooth muscle cell differentiation involved in phenotypic switching","type":"exact"},{"name":"down regulation of vascular smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"down regulation of vascular smooth muscle cell differentiation involved in phenotypic switching","type":"exact"},{"name":"down-regulation of VSMC differentiation involved in phenotypic dimorphism","type":"related"},{"name":"down-regulation of VSMC differentiation involved in phenotypic switching","type":"exact"},{"name":"down-regulation of vascular associated smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"down-regulation of vascular associated smooth muscle cell differentiation involved in phenotypic switching","type":"exact"},{"name":"down-regulation of vascular smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"down-regulation of vascular smooth muscle cell differentiation involved in phenotypic switching","type":"exact"},{"name":"downregulation of VSMC differentiation involved in phenotypic dimorphism","type":"related"},{"name":"downregulation of VSMC differentiation involved in phenotypic switching","type":"exact"},{"name":"downregulation of vascular associated smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"downregulation of vascular associated smooth muscle cell differentiation involved in phenotypic switching","type":"exact"},{"name":"downregulation of vascular smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"downregulation of vascular smooth muscle cell differentiation involved in phenotypic switching","type":"exact"},{"name":"inhibition of VSMC differentiation involved in phenotypic dimorphism","type":"related"},{"name":"inhibition of VSMC differentiation involved in phenotypic switching","type":"narrow"},{"name":"inhibition of vascular associated smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"inhibition of vascular associated smooth muscle cell differentiation involved in phenotypic switching","type":"narrow"},{"name":"inhibition of vascular smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"inhibition of vascular smooth muscle cell differentiation involved in phenotypic switching","type":"narrow"},{"name":"negative regulation of VSMC differentiation involved in phenotypic dimorphism","type":"related"},{"name":"negative regulation of VSMC differentiation involved in phenotypic switching","type":"exact"},{"name":"negative regulation of vascular associated smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"negative regulation of vascular smooth muscle cell differentiation involved in phenotypic dimorphism","type":"related"},{"name":"negative regulation of vascular smooth muscle cell differentiation involved in phenotypic switching","type":"exact"}],"termid":"GO:1905931"}


id: GO:0061842
data:
  {"annotated_genes":["SJAG_02332","SJAG_04558","SJAG_03200","SJAG_01422","SJAG_05196","SJAG_01460"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[102422,113289,114702,91944,104643,105277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140480"}]},"cv_name":"biological_process","definition":"Any process in which the microtubule organizing center is transported to, and/or maintained in, a specific location within the cell.","definition_xrefs":["PMID:21281821"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"},{"relation_name":"is_a","term_name":"localization","termid":"GO:0051179"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01422":null,"SJAG_01460":null,"SJAG_02332":null,"SJAG_03200":null,"SJAG_04558":null,"SJAG_05196":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"microtubule organizing center localization","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"MTOC localization","type":"exact"},{"name":"MTOC polarity","type":"narrow"},{"name":"microtubule organizing center polarity","type":"narrow"}],"termid":"GO:0061842","terms_by_termid":{"GO:0140480":null}}


id: FYPO:0004950
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell is elongated, and the nucleus is longer than normal and undergoes oscillatory movement.","definition_xrefs":["PomBase:mah","PomBase:vw","PMID:16611238"],"direct_ancestors":[{"relation_name":"has_part","term_name":"elongated nucleus during vegetative growth","termid":"FYPO:0000832"},{"relation_name":"is_a","term_name":"elongated nucleus during vegetative growth","termid":"FYPO:0000832"},{"relation_name":"is_a","term_name":"elongated vegetative cell with oscillating nucleus","termid":"FYPO:0005002"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000005","FYPO:0002403","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"elongated vegetative cell with elongated oscillating nucleus","synonyms":[{"name":"elongated cell with elongated oscillating nucleus during vegetative growth","type":"exact"},{"name":"elongated vegetative cell with elongated oscillating nucleus during mitotic cell cycle","type":"related"}],"termid":"FYPO:0004950"}


id: FYPO:0009066
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of amorolfine than normal.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003","FYPO:0005447","FYPO:0002682","FYPO:0000139"],"is_obsolete":false,"name":"resistance to amorolfine","synonyms":[{"name":"resistance to amorolfine during mitotic cell cycle","type":"related"},{"name":"resistance to amorolfine during vegetative growth","type":"exact"},{"name":"resistant to amorolfine","type":"exact"}],"termid":"FYPO:0009066"}


id: MONDO:0007841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Small patella syndrome (SPS) is a very rare benign bone dysplasia affecting skeletal structures of the lower limb and the pelvis.","definition_xrefs":["Orphanet:1509"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coxopodopatellar syndrome","secondary_identifiers":["UMLS:C1840061","DOID:0111382","MESH:C535540","OMIM:147891","MEDGEN:333474","GARD:3030","SCTID:720752007","icd11.foundation:794154672"],"synonyms":[{"name":"Coxo-podo-patellar syndrome","type":"related"},{"name":"ICPPS","type":"related"},{"name":"SPS","type":"related"},{"name":"Scott-Taor syndrome","type":"exact"},{"name":"congenital coxa vara, patella aplasia and tarsal synostosis","type":"related"},{"name":"coxopodopatellar syndrome","type":"exact"},{"name":"ischiocoxopodopatellar syndrome","type":"related"},{"name":"ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension","type":"exact"},{"name":"ischiopatellar dysplasia","type":"exact"},{"name":"patella aplasia, coxa vara, tarsal synostosis","type":"related"},{"name":"small patella syndrome","type":"exact"}],"termid":"MONDO:0007841","xrefs":{"Monarch":{"xref_id":"0007841"}}}


id: MONDO:0014893
data:
  {"annotated_genes":["SJAG_01799"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87917],"is_not":false,"summary":null,"term":"MONDO:0014893"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01799":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"Okur-Chung neurodevelopmental syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:617062","UMLS:C4310739","MEDGEN:934706"],"synonyms":[{"name":"OCNDS","type":"exact"},{"name":"Okur-Chung neurodevelopmental syndrome","type":"exact"},{"name":"Okur-Chung neurodevelopmental syndrome; OCNDS","type":"exact"}],"termid":"MONDO:0014893","terms_by_termid":{"MONDO:0014893":null},"xrefs":{"Monarch":{"xref_id":"0014893"}}}


id: FYPO:0004582
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cell cycle arrest in response to nitrogen starvation occurs in G1 phase, but its occurrence is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cell cycle arrest in mitotic G1 phase during nitrogen starvation","termid":"FYPO:0001000"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0000257","FYPO:0000631"],"is_obsolete":false,"name":"increased cell cycle arrest in mitotic G1 phase in response to nitrogen starvation","synonyms":[{"name":"increased cell cycle arrest in mitotic G1 phase during cellular response to nitrogen starvation","type":"exact"},{"name":"increased cell cycle arrest in mitotic G1 phase in response to nitrogen depletion","type":"exact"},{"name":"increased cell cycle arrest in mitotic G1 phase in response to nitrogen deprivation","type":"exact"},{"name":"increased mitotic G1 arrest in response to nitrogen starvation","type":"exact"},{"name":"increased mitotic cell cycle arrest in G1 phase in response to nitrogen starvation","type":"exact"},{"name":"increased nitrogen deprivation-induced G1 arrest","type":"exact"}],"termid":"FYPO:0004582"}


id: PBO:0004060
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Suppressor Of Cdc2","termid":"PBO:0004060"}


id: GO:2000744
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of anterior head development.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of anterior head development","termid":"GO:2000742"},{"relation_name":"positively_regulates","term_name":"anterior head development","termid":"GO:0097065"}],"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 anterior head development","termid":"GO:2000744"}


id: MONDO:0006226
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low grade, indolent B-cell lymphoma, usually associated with Helicobacter pylori infection. Morphologically it is characterized by a dense mucosal atypical lymphocytic (centrocyte-like cell) infiltrate with often prominent lymphoepithelial lesions and plasmacytic differentiation. Approximately 40% of gastric MALT lymphomas carry the t(11;18)(q21;q21). Such cases are resistant to Helicobacter pylori therapy.","definition_xrefs":["NCIT:C5266"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spleen cancer","termid":"MONDO:0005966"},{"relation_name":"is_a","term_name":"MALT lymphoma","termid":"MONDO:0007650"},{"relation_name":"is_a","term_name":"hereditary gastric cancer","termid":"MONDO:0018502"},{"relation_name":"is_a","term_name":"gastric non-hodgkin lymphoma","termid":"MONDO:0042493"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005046","MONDO:0004335","MONDO:0005570"],"is_obsolete":false,"name":"gastric mucosa-associated lymphoid tissue lymphoma","secondary_identifiers":["UMLS:C1333782","EFO:1000274","MEDGEN:232547"],"synonyms":[{"name":"MALT lymphoma of stomach","type":"exact"},{"name":"MALT lymphoma of the stomach","type":"exact"},{"name":"MALToma of stomach","type":"exact"},{"name":"MALToma of the stomach","type":"exact"},{"name":"gastric MALT lymphoma","type":"exact"},{"name":"gastric MALToma","type":"exact"},{"name":"gastric mucosa-associated lymphoid tissue lymphoma","type":"exact"},{"name":"primary MALT lymphoma of stomach","type":"exact"},{"name":"primary MALT lymphoma of the stomach","type":"exact"},{"name":"primary gastric B-cell MALT lymphoma","type":"exact"},{"name":"primary gastric MALT lymphoma","type":"exact"},{"name":"stomach MALT lymphoma","type":"exact"}],"termid":"MONDO:0006226","xrefs":{"Monarch":{"xref_id":"0006226"}}}


id: MONDO:0007335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cleft lip with or without cleft palate mapped to chromosome 6p24.","definition_xrefs":["NCIT:C124838"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orofacial cleft","termid":"MONDO:0000358"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orofacial cleft 1","secondary_identifiers":["UMLS:C1861537","MEDGEN:349303","DOID:0080395","OMIM:119530","MESH:C566121"],"synonyms":[{"name":"OFC1","type":"exact"},{"name":"cleft Lip/palate, nonsyndromic","type":"related"},{"name":"cleft lip with or without cleft palate, nonsyndromic, 1","type":"related"},{"name":"orofacial cleft 1","type":"exact"},{"name":"orofacial cleft, nonsyndromic","type":"related"},{"name":"orofacial cleft-1","type":"exact"}],"termid":"MONDO:0007335","xrefs":{"Monarch":{"xref_id":"0007335"}}}


id: GO:0014857
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of skeletal muscle cell proliferation.","definition_xrefs":["GOC:ef","CL:0000188","GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell population proliferation","termid":"GO:0042127"},{"relation_name":"regulates","term_name":"skeletal muscle cell proliferation","termid":"GO:0014856"}],"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 skeletal muscle cell proliferation","termid":"GO:0014857"}


id: PATO:0000699
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000699 glutinous (obsolete PATO:0000699)","termid":"PATO:0000699"}


id: PBO:0051232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable (II)-30-21 (pseudogene)","termid":"PBO:0051232"}


id: GO:1903687
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of border follicle cell migration.","definition_xrefs":["PMID:18394891","GOC:TermGenie","GO_REF:0000058","GOC:als"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of epithelial cell migration","termid":"GO:0010633"},{"relation_name":"is_a","term_name":"regulation of border follicle cell migration","termid":"GO:1903684"},{"relation_name":"negatively_regulates","term_name":"border follicle cell migration","termid":"GO:0007298"}],"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 border follicle cell migration","synonyms":[{"name":"inhibition of border follicle cell migration","type":"narrow"}],"termid":"GO:1903687"}


id: PBO:0087064
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L31A; associates with karyopherin Sxm1p; loss of both Rpl31p and Rpl39p confers lethality; homologous to mammalian ribosomal protein L31, no bacterial homolog; RPL31A has a paralog, RPL31B, that arose from the whole genome duplication","termid":"PBO:0087064"}


id: PBO:0073811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC6A14 pseudogene 2","termid":"PBO:0073811"}


id: PBO:0111924
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CLTH domain","termid":"PBO:0111924"}


id: GO:0006142
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving pyrimidine nucleobases.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nucleobase-containing compound metabolic process","termid":"GO:0019219"},{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"regulates","term_name":"pyrimidine nucleobase metabolic process","termid":"GO:0006206"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"regulation of pyrimidine nucleobase metabolic process","synonyms":[{"name":"regulation of pyrimidine base metabolic process","type":"exact"},{"name":"regulation of pyrimidine base metabolism","type":"exact"}],"termid":"GO:0006142"}


id: GO:0016311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of removing one or more phosphoric (ester or anhydride) residues from a molecule.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphate-containing compound metabolic process","termid":"GO:0006796"}],"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":"dephosphorylation","secondary_identifiers":["Wikipedia:Dephosphorylation"],"termid":"GO:0016311"}


id: SO:0002209
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A contig composed of genomic DNA derived sequences.","definition_xrefs":["BCS:etrwz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"contig","termid":"SO:0000149"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genomic_DNA_contig","synonyms":[{"name":"gDNA contig","type":"exact"},{"name":"gDNA_contig","type":"exact"},{"name":"genomic DNA contig","type":"exact"}],"termid":"SO:0002209"}


id: MONDO:0004272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tuberculosis that involves the urinary bladder.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial urinary tract infection","termid":"MONDO:0005247"},{"relation_name":"is_a","term_name":"urogenital tuberculosis","termid":"MONDO:0006002"},{"relation_name":"is_a","term_name":"urinary bladder disorder","termid":"MONDO:0006026"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urinary bladder tuberculosis","secondary_identifiers":["MEDGEN:509075","ICD9:016.14","ICD9:016.10","ICD9:016.1","ICD10CM:A18.12","SCTID:32268008","DOID:754","UMLS:C0152793"],"synonyms":[{"name":"bladder tuberculosis","type":"related"},{"name":"bladder tuberculous","type":"exact"},{"name":"tuberculosis of bladder","type":"exact"},{"name":"tuberculosis of bladder, unspecified examination","type":"exact"},{"name":"tuberculous cystitis","type":"exact"},{"name":"urinary bladder tuberculosis","type":"exact"}],"termid":"MONDO:0004272","xrefs":{"Monarch":{"xref_id":"0004272"}}}


id: PBO:0031747
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_mitotic_centromeric_sister_chromatid_cohesion","termid":"PBO:0031747"}


id: PBO:0055923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 37 member A11, pseudogene","termid":"PBO:0055923"}


id: GO:0060930
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The commitment of cells to sinoatrial (SA) node cell fates and their capacity to differentiate into SA node cells. SA node cells are pacemaker cells that are found in the sinoatrial node.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac pacemaker cell fate commitment","termid":"GO:0060927"},{"relation_name":"part_of","term_name":"sinoatrial node cell differentiation","termid":"GO:0060921"}],"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":"sinoatrial node cell fate commitment","synonyms":[{"name":"SA node cell commitment","type":"exact"},{"name":"SAN cell commitment","type":"exact"},{"name":"sinus node cell commitment","type":"narrow"}],"termid":"GO:0060930"}


id: MONDO:0016266
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that involves the body of uterus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma","termid":"MONDO:0005096"},{"relation_name":"is_a","term_name":"uterine carcinoma","termid":"MONDO:0005213"},{"relation_name":"is_a","term_name":"uterine corpus cancer","termid":"MONDO:0006003"}],"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":"squamous cell carcinoma of the corpus uteri","secondary_identifiers":["GARD:20479","MEDGEN:1633992","Orphanet:213716","ICD10CM:C54.1","UMLS:C4707099"],"synonyms":[{"name":"body of uterus squamous cell carcinoma","type":"exact"},{"name":"endometrial squamous cell carcinoma","type":"related"}],"termid":"MONDO:0016266","xrefs":{"Monarch":{"xref_id":"0016266"}}}


id: GO:0004311
data:
  {"annotated_genes":["SJAG_00580","SJAG_03352"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[101415,111332],"is_not":false,"summary":null,"term":"GO:0004311"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (2E,6E)-farnesyl diphosphate + isopentenyl diphosphate = (2E,6E,10E)-geranylgeranyl diphosphate + diphosphate.","definition_xrefs":["RHEA:17653"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prenyl diphosphate synthase activity","termid":"GO:0120531"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00580":null,"SJAG_03352":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016765"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016765"],"is_obsolete":false,"name":"geranylgeranyl diphosphate synthase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R02061","MetaCyc:FARNESYLTRANSTRANSFERASE-RXN","EC:2.5.1.29"],"synonyms":[{"name":"farnesyltranstransferase activity","type":"exact"},{"name":"geranylgeranyl pyrophosphate synthase activity","type":"exact"},{"name":"geranylgeranyl pyrophosphate synthetase activity","type":"exact"},{"name":"geranylgeranyl-PP synthetase activity","type":"exact"},{"name":"geranylgeranyl-diphosphate synthase activity","type":"exact"},{"name":"trans,trans-farnesyl-diphosphate:isopentenyl-diphosphate farnesyltranstransferase activity","type":"related"}],"termid":"GO:0004311","terms_by_termid":{"GO:0004311":null}}


id: PBO:0071207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 48","termid":"PBO:0071207"}


id: PBO:0003853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase-promoting complex cullin family subunit Apc2","termid":"PBO:0003853"}


id: PBO:0069487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 754, pseudogene","termid":"PBO:0069487"}


id: PBO:0082253
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha subunit of translation initiation factor eIF2B; guanine-nucleotide exchange factor for eIF2; activity regulated by phosphorylated eIF2; positive regulator of GCN4 expression; mutations in human ortholog EIF2B2 cause fatal brain disease childhood ataxia with central nervous system hypomyelination (CACH); human ortholog EIF2B1 can complement yeast null mutant","termid":"PBO:0082253"}


id: GO:0097387
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Simple or compound process of epithelial glial cells with a spherical head that inserts into photoreceptor axons. Capitate projections have only been observed in Brachycera (flies).","definition_xrefs":["PMID:3098431","GOC:mc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell projection","termid":"GO:0097386"}],"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":"capitate projection","termid":"GO:0097387"}


id: PBO:0034656
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_DNA_recombination_frequency_at_subtelomere","termid":"PBO:0034656"}


id: PBO:0044746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 24","termid":"PBO:0044746"}


id: PBO:0087671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the Isw1a complex; Isw1a has nucleosome-stimulated ATPase activity and represses transcription initiation by specific positioning of a promoter proximal dinucleosome; promotes nucleosome shifts in the 5 prime direction; IOC3 has a paralog, ESC8, that arose from the whole genome duplication","termid":"PBO:0087671"}


id: PBO:0002237
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.7.-","termid":"PBO:0002237"}


id: MONDO:0004827
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare neoplasm arising from the distal third of the esophagus. Morphologically, it is characterized by the presence of fibrovascular cores covered by mature stratified squamous epithelium. Progression to squamous cell carcinoma is extremely rare.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous papilloma","termid":"MONDO:0001825"},{"relation_name":"is_a","term_name":"benign neoplasm of esophagus","termid":"MONDO:0021459"}],"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":"esophagus squamous cell papilloma","secondary_identifiers":["UMLS:C1333467","NCIT:C5344","DOID:959","MEDGEN:272592"],"synonyms":[{"name":"esophageal squamous papilloma","type":"exact"},{"name":"esophagus squamous cell papilloma","type":"exact"},{"name":"esophagus squamous papilloma","type":"exact"},{"name":"oesophagus squamous papilloma","type":"exact"},{"name":"squamous cell papilloma of esophagus","type":"exact"},{"name":"squamous cell papilloma of oesophagus","type":"exact"},{"name":"squamous cell papilloma of the esophagus","type":"exact"},{"name":"squamous cell papilloma of the oesophagus","type":"exact"}],"termid":"MONDO:0004827","xrefs":{"Monarch":{"xref_id":"0004827"}}}


id: PBO:0090226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S2","termid":"PBO:0090226"}


id: GO:0019878
data:
  {"annotated_genes":["SJAG_01630","SJAG_01574","SJAG_00869","SJAG_02388","SJAG_00502","SJAG_04688","SJAG_01061","SJAG_01955","SJAG_03312"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[65338,65995,71906,76772,77977,78412,79201,98180,115310],"is_not":false,"summary":null,"term":"GO:0019878"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of lysine by the aminoadipic pathway.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysine biosynthetic process","termid":"GO:0009085"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00502":null,"SJAG_00869":null,"SJAG_01061":null,"SJAG_01574":null,"SJAG_01630":null,"SJAG_01955":null,"SJAG_02388":null,"SJAG_03312":null,"SJAG_04688":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0006520","GO:0008150"],"is_obsolete":false,"name":"lysine biosynthetic process via aminoadipic acid","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"synonyms":[{"name":"lysine anabolism via aminoadipic acid","type":"exact"},{"name":"lysine biosynthesis, aminoadipic acid pathway","type":"exact"},{"name":"lysine biosynthesis, aminoadipic pathway","type":"exact"},{"name":"lysine biosynthetic process, aminoadipic acid pathway","type":"exact"},{"name":"lysine biosynthetic process, aminoadipic pathway","type":"exact"},{"name":"lysine formation via aminoadipic acid","type":"exact"},{"name":"lysine synthesis via aminoadipic acid","type":"exact"}],"termid":"GO:0019878","terms_by_termid":{"GO:0019878":null}}


id: PBO:0111313
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II 3' end processing-associated factor","termid":"PBO:0111313"}


id: PBO:0048589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gamma-glutamyltransferase light chain family member 3","termid":"PBO:0048589"}


id: PBO:0088341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin II essential light chain","termid":"PBO:0088341"}


id: PBO:0076362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SZT2 subunit of KICSTOR complex","termid":"PBO:0076362"}


id: MONDO:0004532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the auditory system","direct_ancestors":[{"relation_name":"is_a","term_name":"sensory system cancer","termid":"MONDO:0000649"},{"relation_name":"is_a","term_name":"auditory system disorder","termid":"MONDO:0002409"}],"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":"auditory system cancer","secondary_identifiers":["NCIT:C3000","DOID:833","MESH:D004428"],"synonyms":[{"name":"auditory system cancer","type":"exact"},{"name":"cancer of auditory system","type":"exact"},{"name":"malignant auditory system neoplasm","type":"exact"},{"name":"malignant neoplasm of auditory system","type":"exact"}],"termid":"MONDO:0004532","xrefs":{"Monarch":{"xref_id":"0004532"}}}


id: PR:P41390
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An amidophosphoribosyltransferase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02227","PANTHER:PTHR11907:SF0","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":"amidophosphoribosyltransferase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.08c","secondary_identifiers":["UniProtKB:P41390"],"synonyms":[{"name":"ATase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PPAT","type":"exact"},{"name":"glutamine phosphoribosylpyrophosphate amidotransferase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P41390"}


id: GO:0009824
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: AMP + dimethylallyl diphosphate = N(6)-(dimethylallyl)adenosine 5'-phosphate + diphosphate.","definition_xrefs":["RHEA:15285"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016765","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"AMP dimethylallyltransferase activity","secondary_identifiers":["KEGG_REACTION:R04038","EC:2.5.1.27","MetaCyc:RXN-4307"],"synonyms":[{"name":"2-isopentenyl-diphosphate:AMP 2-isopentenyltransferase activity","type":"exact"},{"name":"2-isopentenyl-diphosphate:AMP delta2-isopentenyltransferase activity","type":"exact"},{"name":"adenylate dimethylallyltransferase (AMP-dependent) activity","type":"exact"},{"name":"adenylate dimethylallyltransferase activity","type":"related"},{"name":"adenylate isopentenyltransferase activity","type":"broad"},{"name":"cytokinin synthase activity","type":"broad"},{"name":"dimethylallyl-diphosphate:AMP dimethylallyltransferase activity","type":"related"},{"name":"isopentenyltransferase activity","type":"broad"}],"termid":"GO:0009824"}


id: PBO:0031339
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_thiabendazole","termid":"PBO:0031339"}


id: PBO:0069688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 967, pseudogene","termid":"PBO:0069688"}


id: MONDO:0013712
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary pulmonary alveolar proteinosis in which the cause of the disease is a mutation in the CSF2RB gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary pulmonary alveolar proteinosis","termid":"MONDO:0012580"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"surfactant metabolism dysfunction, pulmonary, 5","secondary_identifiers":["UMLS:C3280574","OMIM:614370","GARD:15793","MEDGEN:482204"],"synonyms":[{"name":"CSF2RB hereditary pulmonary alveolar proteinosis","type":"exact"},{"name":"Csf2Rb deficiency","type":"related"},{"name":"Pap due to Csf2Rb deficiency","type":"related"},{"name":"SMDP5","type":"related"},{"name":"hereditary pulmonary alveolar proteinosis caused by mutation in CSF2RB","type":"exact"},{"name":"pulmonary alveolar proteinosis 5","type":"related"},{"name":"surfactant metabolism dysfunction, pulmonary, 5","type":"exact"},{"name":"surfactant metabolism dysfunction, pulmonary, type 5","type":"exact"}],"termid":"MONDO:0013712","xrefs":{"Monarch":{"xref_id":"0013712"}}}


id: MONDO:0024245
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"eccrine carcinoma","termid":"MONDO:0024240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005093"],"is_obsolete":false,"name":"ductal eccrine adenocarcinoma","secondary_identifiers":["MEDGEN:266048","SCTID:403939009","UMLS:C1260964","NCIT:C43345","DOID:5570"],"synonyms":[{"name":"anaplastic syringoma","type":"exact"},{"name":"ductal eccrine adenocarcinoma","type":"exact"},{"name":"ductal eccrine carcinoma","type":"exact"},{"name":"eccrine ductal carcinoma","type":"exact"},{"name":"eccrine ductal carcinoma (morphologic abnormality)","type":"related"},{"name":"eccrine ductal carcinoma of skin","type":"related"},{"name":"hidradenocarcinoma","type":"related"},{"name":"malignant acrospiroma","type":"exact"},{"name":"malignant hidradenoma","type":"related"},{"name":"primary mucoepidermoid cutaneous carcinoma","type":"related"},{"name":"sweat gland carcinoma of the hand","type":"narrow"}],"termid":"MONDO:0024245","xrefs":{"Monarch":{"xref_id":"0024245"}}}


id: MONDO:0003217
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ureter carcinoma (obsolete MONDO:0003217)","termid":"MONDO:0003217","xrefs":{"Monarch":{"xref_id":"0003217"}}}


id: PBO:0036408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved fungal protein DUF2410","termid":"PBO:0036408"}


id: PR:O42707
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC4F6.05c gene.","definition_xrefs":["UniProtKB:O42707","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":"L-type lectin-like domain-containing protein C4F6.05c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4F6.05c","synonyms":[{"name":"Spom972h-SPBC4F6.05c","type":"exact"}],"termid":"PR:O42707"}


id: GO:0032723
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of connective tissue growth factor production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cytokine production","termid":"GO:0001819"},{"relation_name":"is_a","term_name":"regulation of connective tissue growth factor production","termid":"GO:0032643"},{"relation_name":"positively_regulates","term_name":"connective tissue growth factor production","termid":"GO:0032601"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of connective tissue growth factor production","secondary_identifiers":["GO:0045422"],"synonyms":[{"name":"activation of connective tissue growth factor production","type":"narrow"},{"name":"positive regulation of CCN2 production","type":"exact"},{"name":"positive regulation of CTGF production","type":"exact"},{"name":"positive regulation of Fisp12 production","type":"exact"},{"name":"positive regulation of Hcs24 production","type":"exact"},{"name":"positive regulation of IGFBP8 production","type":"exact"},{"name":"positive regulation of connective tissue growth factor biosynthetic process","type":"narrow"},{"name":"positive regulation of hypertrophic chondrocyte-specific gene product 24 production","type":"exact"},{"name":"stimulation of connective tissue growth factor production","type":"narrow"},{"name":"up regulation of connective tissue growth factor production","type":"exact"},{"name":"up-regulation of connective tissue growth factor production","type":"exact"},{"name":"upregulation of connective tissue growth factor production","type":"exact"}],"termid":"GO:0032723"}


id: PBO:0108691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ArfGEF Spo7","termid":"PBO:0108691"}


id: GO:0060094
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of glycinergic synaptic transmission. Glycinergic synaptic transmission is the process of communication from a neuron to another neuron across a synapse using the neurotransmitter glycine.","definition_xrefs":["GOC:dph","GOC:dms"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of synaptic transmission","termid":"GO:0050806"},{"relation_name":"is_a","term_name":"regulation of synaptic transmission, glycinergic","termid":"GO:0060092"},{"relation_name":"positively_regulates","term_name":"synaptic transmission, glycinergic","termid":"GO:0060012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of synaptic transmission, glycinergic","synonyms":[{"name":"positive regulation of glycinergic synaptic transmission","type":"exact"}],"termid":"GO:0060094"}


id: PBO:0067905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 207","termid":"PBO:0067905"}


id: PBO:0048775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GDP-mannose pyrophosphorylase B","termid":"PBO:0048775"}


id: PBO:0046863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fumarylacetoacetate hydrolase domain containing 2A","termid":"PBO:0046863"}


id: PBO:0065314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 37","termid":"PBO:0065314"}


id: GO:0036020
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding an endolysosome. An endolysosome is a transient hybrid organelle formed by fusion of a late endosome with a lysosome.","definition_xrefs":["GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysosomal membrane","termid":"GO:0005765"},{"relation_name":"is_a","term_name":"endosome membrane","termid":"GO:0010008"},{"relation_name":"part_of","term_name":"endolysosome","termid":"GO:0036019"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005773"}],"interesting_parent_ids":["GO:0005773","GO:0005768","GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"endolysosome membrane","synonyms":[{"name":"endolysosomal membrane","type":"exact"}],"termid":"GO:0036020"}


id: MONDO:0033335
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic larynx anomaly (obsolete MONDO:0033335)","secondary_identifiers":["Orphanet:435609"],"termid":"MONDO:0033335","xrefs":{"Monarch":{"xref_id":"0033335"}}}


id: MONDO:0100330
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infectious disease that arises from reactivation of a virus from a latent phase to a lytic phase.","definition_xrefs":["PMID:21799704"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral infectious disease","termid":"MONDO:0005108"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disease arising from reactivation of latent virus","synonyms":[{"name":"latent infection","type":"exact"}],"termid":"MONDO:0100330","xrefs":{"Monarch":{"xref_id":"0100330"}}}


id: GO:0016740
data:
  {"annotated_genes":["SJAG_00559","SJAG_03029","SJAG_02085","SJAG_04282","SJAG_00114","SJAG_00580","SJAG_02222","SJAG_01070","SJAG_02519","SJAG_02288","SJAG_04337","SJAG_04059","SJAG_02468","SJAG_01474","SJAG_04882","SJAG_01654","SJAG_04777","SJAG_03869","SJAG_01444","SJAG_02804","SJAG_04881","SJAG_02660","SJAG_02842","SJAG_03213","SJAG_02299","SJAG_03367","SJAG_03753","SJAG_04865","SJAG_01193","SJAG_03618","SJAG_02954","SJAG_03580","SJAG_00582","SJAG_02415","SJAG_02885","SJAG_04309","SJAG_01566","SJAG_02506","SJAG_04161","SJAG_02887","SJAG_02281","SJAG_04186","SJAG_04535","SJAG_02627","SJAG_00943","SJAG_00508","SJAG_01814","SJAG_04434","SJAG_03825","SJAG_00300","SJAG_03540","SJAG_03250","SJAG_01058","SJAG_04206","SJAG_03932","SJAG_02022","SJAG_03878","SJAG_05979","SJAG_00337","SJAG_04233","SJAG_03831","SJAG_02725","SJAG_01776","SJAG_03970","SJAG_04106","SJAG_00341","SJAG_00173","SJAG_03188","SJAG_01352","SJAG_04622","SJAG_04734","SJAG_01899","SJAG_01582","SJAG_04735","SJAG_01360","SJAG_03630","SJAG_04394","SJAG_00661","SJAG_04425","SJAG_03163","SJAG_04268","SJAG_03016","SJAG_04952","SJAG_03048","SJAG_04041","SJAG_03352","SJAG_04312","SJAG_06603","SJAG_00020","SJAG_03061","SJAG_01787","SJAG_00519","SJAG_01356","SJAG_04130","SJAG_00598","SJAG_00747","SJAG_04461","SJAG_03985","SJAG_04993","SJAG_02350","SJAG_01713","SJAG_06284","SJAG_00827","SJAG_03154","SJAG_01368","SJAG_00402","SJAG_02773","SJAG_00256","SJAG_05200","SJAG_00169","SJAG_01571","SJAG_01863","SJAG_01561","SJAG_02719","SJAG_00946","SJAG_00610","SJAG_04401","SJAG_00815","SJAG_05285","SJAG_02858","SJAG_04571","SJAG_03764","SJAG_01434","SJAG_04700","SJAG_03657","SJAG_03901","SJAG_00956","SJAG_00611","SJAG_01799","SJAG_02426","SJAG_00832","SJAG_01825","SJAG_03311","SJAG_01885","SJAG_03006","SJAG_03174","SJAG_05693","SJAG_01900","SJAG_03305","SJAG_02658","SJAG_05239","SJAG_03557","SJAG_00209","SJAG_00797","SJAG_01021","SJAG_01359","SJAG_01019","SJAG_00727","SJAG_02841","SJAG_04728","SJAG_00102","SJAG_03877","SJAG_04131","SJAG_05018","SJAG_01718","SJAG_00068","SJAG_00331","SJAG_00004","SJAG_03587","SJAG_04495","SJAG_04465","SJAG_00021","SJAG_00619","SJAG_05274","SJAG_03318","SJAG_01805","SJAG_03160","SJAG_00895","SJAG_01531","SJAG_00876","SJAG_04435","SJAG_02521","SJAG_04678","SJAG_01958","SJAG_01373","SJAG_02791","SJAG_00903","SJAG_02058","SJAG_02290","SJAG_05277","SJAG_02168","SJAG_02305","SJAG_04756","SJAG_04915","SJAG_01313","SJAG_01972","SJAG_00458","SJAG_01935","SJAG_01233","SJAG_04883","SJAG_02654","SJAG_01264","SJAG_03056","SJAG_03900","SJAG_00769","SJAG_04165","SJAG_04127","SJAG_03333","SJAG_04149","SJAG_00993","SJAG_03322","SJAG_03529","SJAG_04052","SJAG_01047","SJAG_02319","SJAG_03136","SJAG_02421","SJAG_03289","SJAG_03854","SJAG_00208","SJAG_00855","SJAG_02360","SJAG_00999","SJAG_02104","SJAG_03811","SJAG_04053","SJAG_04709","SJAG_04537","SJAG_00718","SJAG_03336","SJAG_04276","SJAG_00238","SJAG_03773","SJAG_04783","SJAG_03906","SJAG_00224","SJAG_03660","SJAG_01383","SJAG_01253","SJAG_00649","SJAG_02575","SJAG_01146","SJAG_02653","SJAG_02736","SJAG_03005","SJAG_03257","SJAG_02817","SJAG_02908","SJAG_00635","SJAG_02498","SJAG_02821","SJAG_06309","SJAG_00533","SJAG_01212","SJAG_03017","SJAG_04792","SJAG_05236","SJAG_02467","SJAG_00486","SJAG_04619","SJAG_03162","SJAG_00683","SJAG_03173","SJAG_03921","SJAG_02429","SJAG_00509","SJAG_04182","SJAG_04317","SJAG_02042","SJAG_05327","SJAG_01592","SJAG_02808","SJAG_01239","SJAG_03409","SJAG_03961","SJAG_04287","SJAG_04972","SJAG_04334","SJAG_01826","SJAG_03292","SJAG_03115","SJAG_01425","SJAG_00963","SJAG_01376","SJAG_04126","SJAG_03713","SJAG_02165","SJAG_00255","SJAG_01593","SJAG_02471","SJAG_16460","SJAG_04688","SJAG_04499","SJAG_02347","SJAG_01535","SJAG_04878","SJAG_03362","SJAG_02417","SJAG_02760","SJAG_03384","SJAG_00257","SJAG_01040","SJAG_03386","SJAG_01443","SJAG_00218","SJAG_04305","SJAG_01724","SJAG_04507","SJAG_00964","SJAG_03810","SJAG_03896","SJAG_00779","SJAG_03506","SJAG_02985","SJAG_05181","SJAG_04877","SJAG_03067","SJAG_03708","SJAG_00119","SJAG_02038","SJAG_04408","SJAG_01491","SJAG_00358","SJAG_03592","SJAG_02746","SJAG_05334","SJAG_05323","SJAG_03761","SJAG_00495","SJAG_01791","SJAG_00286","SJAG_05340","SJAG_04736","SJAG_05228","SJAG_02796","SJAG_04178","SJAG_02082","SJAG_04231","SJAG_02769","SJAG_00496","SJAG_03913","SJAG_00097","SJAG_04849","SJAG_04751","SJAG_02624","SJAG_01311","SJAG_01957","SJAG_04642","SJAG_01043","SJAG_00866","SJAG_01251","SJAG_03181","SJAG_00633","SJAG_02913","SJAG_01176","SJAG_02723","SJAG_00506","SJAG_02024","SJAG_01766","SJAG_04453","SJAG_04680","SJAG_05022","SJAG_02637","SJAG_03914","SJAG_03066","SJAG_04994","SJAG_04693","SJAG_02183","SJAG_02692","SJAG_04699","SJAG_01837","SJAG_02600","SJAG_02491","SJAG_04612","SJAG_04568","SJAG_03860","SJAG_00435","SJAG_02371","SJAG_03656","SJAG_01276","SJAG_04049","SJAG_03129","SJAG_01204","SJAG_00676","SJAG_06383","SJAG_04468","SJAG_04119","SJAG_03175","SJAG_01271","SJAG_01042","SJAG_00427","SJAG_00605","SJAG_04946","SJAG_04481","SJAG_04574","SJAG_04760","SJAG_00293","SJAG_01536","SJAG_04628","SJAG_02923","SJAG_02901","SJAG_00731","SJAG_01619","SJAG_04761","SJAG_04597","SJAG_01269","SJAG_04966","SJAG_00690","SJAG_03613","SJAG_03548","SJAG_02713","SJAG_04573","SJAG_04184","SJAG_00395","SJAG_03934","SJAG_02950","SJAG_01942","SJAG_00413","SJAG_02126","SJAG_03501","SJAG_04113","SJAG_00890","SJAG_02163","SJAG_04970","SJAG_04906","SJAG_03486","SJAG_00111","SJAG_03087","SJAG_02668","SJAG_06592","SJAG_02169","SJAG_04551","SJAG_00246","SJAG_01877","SJAG_01855","SJAG_01937","SJAG_02583","SJAG_00334","SJAG_02070","SJAG_03438","SJAG_03531","SJAG_04713","SJAG_04451","SJAG_03609","SJAG_01854","SJAG_03887","SJAG_00244","SJAG_00816","SJAG_01922","SJAG_03014","SJAG_01979","SJAG_01562","SJAG_03376","SJAG_02603","SJAG_04770","SJAG_04681","SJAG_03799","SJAG_00825","SJAG_01704","SJAG_05330","SJAG_04107","SJAG_01363","SJAG_02916","SJAG_01082","SJAG_03790","SJAG_01946","SJAG_00596","SJAG_02249","SJAG_01148","SJAG_04145","SJAG_03553","SJAG_02099","SJAG_03949","SJAG_04457","SJAG_02680","SJAG_00875","SJAG_04627","SJAG_00931","SJAG_02685","SJAG_00604","SJAG_01974","SJAG_01618","SJAG_04980","SJAG_03701","SJAG_02851","SJAG_00881","SJAG_04189","SJAG_00378","SJAG_03555","SJAG_03798","SJAG_03457","SJAG_01865","SJAG_00039","SJAG_03946","SJAG_03475","SJAG_04095","SJAG_01859","SJAG_00442","SJAG_02873","SJAG_00933","SJAG_05304","SJAG_03987","SJAG_02726","SJAG_00694","SJAG_03789","SJAG_02386","SJAG_02420","SJAG_00638","SJAG_01079","SJAG_03755","SJAG_00426","SJAG_01679","SJAG_02271","SJAG_01772","SJAG_01402","SJAG_03578","SJAG_02903","SJAG_04552","SJAG_05012","SJAG_03209","SJAG_04990","SJAG_04261","SJAG_03191","SJAG_00437","SJAG_00636","SJAG_03306","SJAG_03883","SJAG_02712","SJAG_02296","SJAG_04354","SJAG_02596","SJAG_01000","SJAG_03672","SJAG_00704","SJAG_04280","SJAG_00561","SJAG_02309","SJAG_03953","SJAG_03356","SJAG_00499","SJAG_00295","SJAG_03055","SJAG_02756","SJAG_00381","SJAG_01500","SJAG_02896","SJAG_01164","SJAG_00812","SJAG_04857","SJAG_01918","SJAG_00252","SJAG_01314","SJAG_03487","SJAG_00469","SJAG_03288","SJAG_04316","SJAG_02973","SJAG_03871","SJAG_03149","SJAG_04486","SJAG_05197","SJAG_01181","SJAG_02705","SJAG_01637","SJAG_00399","SJAG_04320","SJAG_04747","SJAG_04030","SJAG_03880","SJAG_03968","SJAG_02990","SJAG_01950","SJAG_02996","SJAG_00179","SJAG_03537","SJAG_01084","SJAG_00075","SJAG_00714","SJAG_00845","SJAG_01426","SJAG_02408","SJAG_06634","SJAG_02652","SJAG_05225","SJAG_01054","SJAG_03387","SJAG_04483","SJAG_00886","SJAG_03881","SJAG_04181","SJAG_03972","SJAG_03659","SJAG_05231","SJAG_02818","SJAG_02064","SJAG_03615","SJAG_02940","SJAG_04323","SJAG_03554","SJAG_05264","SJAG_02523","SJAG_01765","SJAG_04791","SJAG_03035","SJAG_03144","SJAG_02488","SJAG_03563","SJAG_02392","SJAG_00673","SJAG_00695","SJAG_01018","SJAG_01112","SJAG_01375","SJAG_00500","SJAG_04469","SJAG_04039","SJAG_02178","SJAG_03421","SJAG_03082","SJAG_03167","SJAG_04866","SJAG_03057","SJAG_00150","SJAG_03468","SJAG_04516","SJAG_00475","SJAG_04631","SJAG_01507","SJAG_02868","SJAG_00129","SJAG_01080","SJAG_03709","SJAG_00996","SJAG_03150","SJAG_00183","SJAG_04159","SJAG_01835","SJAG_05413","SJAG_00394","SJAG_02592","SJAG_04089","SJAG_00084","SJAG_04657","SJAG_02342","SJAG_00814","SJAG_00554","SJAG_00637","SJAG_02383","SJAG_01028","SJAG_04868","SJAG_01680","SJAG_02972","SJAG_04288","SJAG_01992","SJAG_01587","SJAG_02370","SJAG_03141","SJAG_00188","SJAG_01575","SJAG_02308","SJAG_01533","SJAG_03312","SJAG_04236","SJAG_00186","SJAG_04085","SJAG_00364","SJAG_03775","SJAG_02321","SJAG_04034","SJAG_01165","SJAG_00924","SJAG_01192","SJAG_03935","SJAG_00819","SJAG_03112","SJAG_03180","SJAG_03434","SJAG_03332","SJAG_04429","SJAG_03324","SJAG_04600","SJAG_01427","SJAG_01288","SJAG_04894","SJAG_03720","SJAG_02838","SJAG_02102","SJAG_01955","SJAG_00678","SJAG_01299","SJAG_04232","SJAG_02889","SJAG_03228","SJAG_03602","SJAG_04821","SJAG_01482","SJAG_04658","SJAG_02158","SJAG_04845","SJAG_03008","SJAG_00325","SJAG_04988","SJAG_04319","SJAG_02720","SJAG_02659","SJAG_03302","SJAG_05290","SJAG_04151","SJAG_02878","SJAG_00552","SJAG_03102","SJAG_00153","SJAG_00865","SJAG_00356","SJAG_01261","SJAG_05016","SJAG_04655","SJAG_00722","SJAG_03863","SJAG_01661","SJAG_01075","SJAG_00168","SJAG_04263","SJAG_04923","SJAG_00342","SJAG_02101","SJAG_01302","SJAG_01290","SJAG_04934","SJAG_03967","SJAG_01089","SJAG_02918"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[59870],"is_not":false,"summary":null,"term":"GO:0016740"},{"annotations":[69267,58421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004337"},{"annotations":[76524,81752,115023,77582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003843"},{"annotations":[77601,72798,74740,76255],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042124"},{"annotations":[78567,91849,73404],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003841"},{"annotations":[78570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047184"},{"annotations":[105801],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106262"},{"annotations":[78253,73513,95039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004430"},{"annotations":[73300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016303"},{"annotations":[93665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052811"},{"annotations":[74381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000285"},{"annotations":[81398],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016308"},{"annotations":[70125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052909"},{"annotations":[74125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990883"},{"annotations":[69744,67997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090560"},{"annotations":[116049],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003846"},{"annotations":[70636],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003848"},{"annotations":[74281,78414,101199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047536"},{"annotations":[78892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003852"},{"annotations":[75872],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008425"},{"annotations":[80409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052907"},{"annotations":[66277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061542"},{"annotations":[116734],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120537"},{"annotations":[78664,79962],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003849"},{"annotations":[77075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016784"},{"annotations":[79407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003864"},{"annotations":[78680,58814],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004315"},{"annotations":[119325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004676"},{"annotations":[74063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003866"},{"annotations":[74744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046820"},{"annotations":[115868],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106344"},{"annotations":[57226],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034386"},{"annotations":[79121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008412"},{"annotations":[71704,80222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003870"},{"annotations":[116915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033857"},{"annotations":[65236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003871"},{"annotations":[80452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000906"},{"annotations":[76754,75099,82020,80558],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003873"},{"annotations":[79579],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003872"},{"annotations":[60356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004313"},{"annotations":[71959,60357],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004314"},{"annotations":[78529,77185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008775"},{"annotations":[77800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003984"},{"annotations":[74896],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003985"},{"annotations":[73165],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003991"},{"annotations":[58655],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016407"},{"annotations":[112382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016411"},{"annotations":[61725],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016746"},{"annotations":[80104,80744,77756,66661,77743,70916,73914,77733,58738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016747"},{"annotations":[75676],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003999"},{"annotations":[71734],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004001"},{"annotations":[77922],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004015"},{"annotations":[76695],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004020"},{"annotations":[62903],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070566"},{"annotations":[121440,121439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0097269"},{"annotations":[102879,80591,95159],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003825"},{"annotations":[100740,100599,100600,100597,100598,119922],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031278"},{"annotations":[79266,76424,81081,79755,76553,78717],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000026"},{"annotations":[112559,112565],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0001962"},{"annotations":[72373,75268,73158,80517,75096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047657"},{"annotations":[119655],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033840"},{"annotations":[71797,73749,82177],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000009"},{"annotations":[74169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004044"},{"annotations":[57987],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004047"},{"annotations":[73637,73841],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004017"},{"annotations":[67135],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004048"},{"annotations":[76120],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004059"},{"annotations":[73918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004057"},{"annotations":[73641],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004070"},{"annotations":[75343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004072"},{"annotations":[94727],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061651"},{"annotations":[80593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141046"},{"annotations":[73821,111622,112125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019776"},{"annotations":[80167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003879"},{"annotations":[99479,67820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004143"},{"annotations":[72432,89944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046404"},{"annotations":[95279],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051736"},{"annotations":[76570,72071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052929"},{"annotations":[98822],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141192"},{"annotations":[94578],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046941"},{"annotations":[81075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004076"},{"annotations":[117684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140752"},{"annotations":[73009,75685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004662"},{"annotations":[75019,118350,95376,76949],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004683"},{"annotations":[75090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004691"},{"annotations":[94857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043337"},{"annotations":[94858],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008808"},{"annotations":[106986],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030735"},{"annotations":[76569,72070],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052927"},{"annotations":[73002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008444"},{"annotations":[78415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003881"},{"annotations":[68748],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003882"},{"annotations":[76186,75978],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004100"},{"annotations":[69630],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004578"},{"annotations":[75256],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004103"},{"annotations":[71605],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004105"},{"annotations":[101281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036440"},{"annotations":[79223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051267"},{"annotations":[111762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141035"},{"annotations":[81832,97622,104218,81186,81299,107526,77960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004693"},{"annotations":[77031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003962"},{"annotations":[80607],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031071"},{"annotations":[111307,112359],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004124"},{"annotations":[111308],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141223"},{"annotations":[62215],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160205"},{"annotations":[94787,116781],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043771"},{"annotations":[78904],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004856"},{"annotations":[72184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017125"},{"annotations":[72577],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034038"},{"annotations":[72872,73141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004140"},{"annotations":[94874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004142"},{"annotations":[78800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004144"},{"annotations":[69401],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004697"},{"annotations":[92585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004699"},{"annotations":[89217,102445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004145"},{"annotations":[63490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004742"},{"annotations":[77570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004149"},{"annotations":[81533],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004156"},{"annotations":[59921],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141133"},{"annotations":[76175,73800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045547"},{"annotations":[97059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034061"},{"annotations":[72182,79714,75748,76573,104704,76821,78621,74986,104653,58593,79416,76599],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003887"},{"annotations":[80687,79834,66541,79167,77591,72131,103331,78701,77275,76921,77483,103371,77116,57201,76221,111629,114237,118315,118628,72803,75189,75896,111124,104359,104781,73035,117538,71839,106718,58859,75032,97697,107162,78280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003899"},{"annotations":[104866],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180041"},{"annotations":[93039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120563"},{"annotations":[117073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120564"},{"annotations":[99916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120565"},{"annotations":[78343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052925"},{"annotations":[63464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052926"},{"annotations":[61764],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052917"},{"annotations":[63463],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052918"},{"annotations":[82079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004168"},{"annotations":[81761],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042283"},{"annotations":[70726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106073"},{"annotations":[78964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042281"},{"annotations":[80996,78153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004579"},{"annotations":[59073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004582"},{"annotations":[68173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004581"},{"annotations":[71598,76682,78950],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004169"},{"annotations":[72777],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004798"},{"annotations":[119899],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120136"},{"annotations":[82042,78050],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034737"},{"annotations":[75257],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004305"},{"annotations":[77106],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004306"},{"annotations":[94875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004307"},{"annotations":[71680,76983,73878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004694"},{"annotations":[67785,79478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009922"},{"annotations":[58806,60348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004312"},{"annotations":[60359,58816],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004321"},{"annotations":[80331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003919"},{"annotations":[71955,77837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008865"},{"annotations":[79058],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004335"},{"annotations":[107594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047220"},{"annotations":[61421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004378"},{"annotations":[61422],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102704"},{"annotations":[78592],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004377"},{"annotations":[111332,101415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004311"},{"annotations":[71952,77834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004340"},{"annotations":[81696],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046316"},{"annotations":[72651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004343"},{"annotations":[78900],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032216"},{"annotations":[71783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004349"},{"annotations":[80088],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004360"},{"annotations":[110561],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016603"},{"annotations":[72589],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016756"},{"annotations":[78833,115731,80364,76428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004364"},{"annotations":[113843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106158"},{"annotations":[72288,71824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004366"},{"annotations":[80384],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004371"},{"annotations":[72289,71825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016287"},{"annotations":[75072,73812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004372"},{"annotations":[79877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004379"},{"annotations":[77669],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004385"},{"annotations":[77091,89245],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003923"},{"annotations":[62337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051730"},{"annotations":[95572],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052657"},{"annotations":[79620,70239],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009927"},{"annotations":[58150],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004400"},{"annotations":[66561],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004402"},{"annotations":[77238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008469"},{"annotations":[75770],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043998"},{"annotations":[118098,108458],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140995"},{"annotations":[112048,75030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990259"},{"annotations":[116363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072371"},{"annotations":[118073,120728],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140850"},{"annotations":[93227,92570],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036408"},{"annotations":[91868,79088],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032041"},{"annotations":[96164],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140851"},{"annotations":[93228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043993"},{"annotations":[97300],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140954"},{"annotations":[80343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046975"},{"annotations":[65322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140955"},{"annotations":[58335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062122"},{"annotations":[100782],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044016"},{"annotations":[106018],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141222"},{"annotations":[80342],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042800"},{"annotations":[59050],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140999"},{"annotations":[74321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032931"},{"annotations":[91869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140765"},{"annotations":[93229],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043992"},{"annotations":[79089,116286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046969"},{"annotations":[112344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140948"},{"annotations":[63751],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140949"},{"annotations":[112346],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140947"},{"annotations":[118547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035175"},{"annotations":[79983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072354"},{"annotations":[75772,100783],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010485"},{"annotations":[90244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043997"},{"annotations":[79090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046970"},{"annotations":[118884],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140943"},{"annotations":[90245],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043995"},{"annotations":[90246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043996"},{"annotations":[115383,78107,78246,72683],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042054"},{"annotations":[58810,69083,76771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008897"},{"annotations":[77976],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004410"},{"annotations":[71407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004413"},{"annotations":[78084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004414"},{"annotations":[66838],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004417"},{"annotations":[78104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004418"},{"annotations":[81862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004421"},{"annotations":[75670,75728,71802],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008902"},{"annotations":[77380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004422"},{"annotations":[77676],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000107"},{"annotations":[104123,89317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033164"},{"annotations":[58721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052723"},{"annotations":[99318],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045140"},{"annotations":[97547],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0103064"},{"annotations":[76523],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035299"},{"annotations":[72967,77257],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000824"},{"annotations":[72963,77253],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008440"},{"annotations":[100618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000823"},{"annotations":[119722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036455"},{"annotations":[62393,108589,105337,100673,110008],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016301"},{"annotations":[75555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016212"},{"annotations":[113090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004021"},{"annotations":[72616,79445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004069"},{"annotations":[90049],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047198"},{"annotations":[66640,74114],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004042"},{"annotations":[66639],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004358"},{"annotations":[75590],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052706"},{"annotations":[112287],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052656"},{"annotations":[112288],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052654"},{"annotations":[103714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160210"},{"annotations":[69492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061710"},{"annotations":[100162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004838"},{"annotations":[112289],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052655"},{"annotations":[76759],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016992"},{"annotations":[107068],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016979"},{"annotations":[72512],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033819"},{"annotations":[79952],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017118"},{"annotations":[72839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042171"},{"annotations":[77838,99815],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019158"},{"annotations":[104912,77166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004475"},{"annotations":[73630,80021,116648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051377"},{"annotations":[77208,97071],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000030"},{"annotations":[63818,76440,66633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004707"},{"annotations":[76169,78046,73280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004708"},{"annotations":[66269,89352,102723,70659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004709"},{"annotations":[102724],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008349"},{"annotations":[76746],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004478"},{"annotations":[79975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004479"},{"annotations":[92066,102846,70278],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008168"},{"annotations":[81913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004496"},{"annotations":[81187,78655],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061863"},{"annotations":[92271,95741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062152"},{"annotations":[74084],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004482"},{"annotations":[77230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004484"},{"annotations":[64711,59154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061711"},{"annotations":[64380,100495],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004577"},{"annotations":[104849,72181,64501,119122],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008080"},{"annotations":[75392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016410"},{"annotations":[79096,64968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071885"},{"annotations":[63236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003992"},{"annotations":[99288,93739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003951"},{"annotations":[93740,99289,98278],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042736"},{"annotations":[120275],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061654"},{"annotations":[76497,72551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000309"},{"annotations":[114949],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034317"},{"annotations":[76495],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004515"},{"annotations":[117964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050144"},{"annotations":[72776,77888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004550"},{"annotations":[62718],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016779"},{"annotations":[112360],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051009"},{"annotations":[77242,72711,63442],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008374"},{"annotations":[81329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004648"},{"annotations":[80146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004587"},{"annotations":[80232],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004585"},{"annotations":[75062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004588"},{"annotations":[81680],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004594"},{"annotations":[100784],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106226"},{"annotations":[100785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140065"},{"annotations":[97318,98299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102559"},{"annotations":[100786,93230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140064"},{"annotations":[81803,121078],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004605"},{"annotations":[57693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000773"},{"annotations":[79960],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004608"},{"annotations":[79209,94811,110425,113455,119104,94901],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017176"},{"annotations":[71702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004618"},{"annotations":[76306],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046027"},{"annotations":[71803,75671,75729],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008972"},{"annotations":[76045],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004631"},{"annotations":[79621,66853,58229],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000155"},{"annotations":[71661],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004643"},{"annotations":[73332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004644"},{"annotations":[91589],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016773"},{"annotations":[64789,78056,59632,80051,80738,70707,98074,70538],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990817"},{"annotations":[73268],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051731"},{"annotations":[116379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008976"},{"annotations":[78369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010420"},{"annotations":[81984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019702"},{"annotations":[77887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0018423"},{"annotations":[77172],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004671"},{"annotations":[73008,75272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004660"},{"annotations":[60204,111053,69728,72293],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004672"},{"annotations":[119041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008276"},{"annotations":[117208,105403],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120518"},{"annotations":[79102,75773],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990189"},{"annotations":[72836,81438,75926,73369,81779,76464,80726,74873,79637,73170,75665,81181,73075,79212,76993,73222,77975,117872,72910,73032,78241,79273,80765,81357,93957,73849,73806,72032,80317,80856,78099,115019,74328,75235,75561,78265,77868,73421,72676,77345,72180,77340,71834,79285,75724,79832,72932,78316,81385,81980,74791,76420,100248,63513,73380,81789,79030,68075,80668,81295,78839,75357,108229,75011,71870,76323,81975,78990,79450,74014,77123,75116,81883,74217,82174,67556,77875,81877,74041,78997,74437],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004674"},{"annotations":[110421,93555,100820],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004712"},{"annotations":[112038,80336,112837,72933,91472,72426,104762,93980,95703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004713"},{"annotations":[114524,102241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035242"},{"annotations":[102242,114525],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035241"},{"annotations":[69532,76775,74675,72790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019706"},{"annotations":[89467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0018064"},{"annotations":[64967,75299,78108,76778,118685,71770,79397,73766,80166],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016279"},{"annotations":[105814],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061733"},{"annotations":[119857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004596"},{"annotations":[91212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008999"},{"annotations":[79103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990190"},{"annotations":[80135],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008495"},{"annotations":[107326],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050225"},{"annotations":[80859],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004731"},{"annotations":[76969,79972],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008478"},{"annotations":[100847],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004740"},{"annotations":[81369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004743"},{"annotations":[102442],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046919"},{"annotations":[103229,75571,80702],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004663"},{"annotations":[74582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008531"},{"annotations":[112231,78173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004746"},{"annotations":[72978],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004747"},{"annotations":[75609,64433,74162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004749"},{"annotations":[118999],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004711"},{"annotations":[114950],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050262"},{"annotations":[114951],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061769"},{"annotations":[109877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990276"},{"annotations":[76751],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071164"},{"annotations":[114557],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008173"},{"annotations":[96193,99651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008353"},{"annotations":[110884,96152,97624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140834"},{"annotations":[96153,107885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140836"},{"annotations":[81585,81444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050265"},{"annotations":[73658],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003968"},{"annotations":[78941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016433"},{"annotations":[100215],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106142"},{"annotations":[59966],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000179"},{"annotations":[97436,80683],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009383"},{"annotations":[96721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070043"},{"annotations":[91446],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070039"},{"annotations":[77358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070037"},{"annotations":[77426,77671,80469],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008650"},{"annotations":[81343],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070042"},{"annotations":[75024,112050],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008649"},{"annotations":[57392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106388"},{"annotations":[60528,60587,63024,119042,93816,69023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008757"},{"annotations":[78079],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008898"},{"annotations":[79551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017061"},{"annotations":[78596,80660],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004758"},{"annotations":[77891],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009001"},{"annotations":[60424],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004765"},{"annotations":[110963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090486"},{"annotations":[76736],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004766"},{"annotations":[104581],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016768"},{"annotations":[99480],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008481"},{"annotations":[79847,80826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050291"},{"annotations":[78238],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051996"},{"annotations":[78242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003838"},{"annotations":[93256],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008260"},{"annotations":[68105],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004781"},{"annotations":[77418,106304],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061656"},{"annotations":[74239,106182,74258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061665"},{"annotations":[72413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003720"},{"annotations":[79954],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004788"},{"annotations":[78756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004789"},{"annotations":[111609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0018708"},{"annotations":[75938,118827,71534],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004792"},{"annotations":[81213],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004799"},{"annotations":[96498],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046547"},{"annotations":[74864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004801"},{"annotations":[97592],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008483"},{"annotations":[81417],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004802"},{"annotations":[69096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0050354"},{"annotations":[74200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106335"},{"annotations":[62838,114006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160107"},{"annotations":[99665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106339"},{"annotations":[80904,112006],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052735"},{"annotations":[107612,72333,81208],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016428"},{"annotations":[63961],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160102"},{"annotations":[61664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160104"},{"annotations":[68305],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052906"},{"annotations":[73334],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008176"},{"annotations":[67091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106340"},{"annotations":[58886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052905"},{"annotations":[68780],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030697"},{"annotations":[60991,99667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106050"},{"annotations":[75574],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000215"},{"annotations":[99884],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0102522"},{"annotations":[59018],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043399"},{"annotations":[74126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051392"},{"annotations":[72730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052381"},{"annotations":[75236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008193"},{"annotations":[96517,75427,74139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008175"},{"annotations":[97285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106261"},{"annotations":[64567],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141101"},{"annotations":[61368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061708"},{"annotations":[74348,97610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008479"},{"annotations":[96080,110255,107693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0103016"},{"annotations":[97011],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120048"},{"annotations":[75160,73054,89828,89985,104084,66412,79270,89611,118649,116135,79752,76097],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061631"},{"annotations":[63188,103131,113943,114678,81739,80903,77079,101210,70906,61906,78366,76026,64228,74903,95380,77111,116190,74489,111817,107073,119070,77369,115255,79173,92542,78064,111487,98599,108788,71019,57159,81265,66900,105229,73233,104850,89839,76029,80448,93356,118566,74702,75309,90126,89829,100351,105244,90452,109848,80522,73675,65630,91540,120318,76125,58673,106183,79943,79208,66953,73578,90800,92019,118565],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061630"},{"annotations":[115497,106712,93321,109028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061659"},{"annotations":[72863],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004842"},{"annotations":[76534],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034450"},{"annotations":[81285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003980"},{"annotations":[74344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008108"},{"annotations":[78345],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003977"},{"annotations":[77745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003975"},{"annotations":[82167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033862"},{"annotations":[89273,90267,116782,93790],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004845"},{"annotations":[80776,94788],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004849"},{"annotations":[73098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004851"},{"annotations":[74292,81919],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003983"},{"annotations":[95575],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000310"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a group, e.g. a methyl group, glycosyl group, acyl group, phosphorus-containing, or other groups, from one compound (generally regarded as the donor) to another compound (generally regarded as the acceptor). Transferase is the systematic name for any enzyme of EC class 2.","definition_xrefs":["EC:2.-.-.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity","termid":"GO:0003824"}],"gene_count":722,"genes_by_uniquename":{"SJAG_00004":null,"SJAG_00020":null,"SJAG_00021":null,"SJAG_00039":null,"SJAG_00068":null,"SJAG_00075":null,"SJAG_00084":null,"SJAG_00097":null,"SJAG_00102":null,"SJAG_00111":null,"SJAG_00114":null,"SJAG_00119":null,"SJAG_00129":null,"SJAG_00150":null,"SJAG_00153":null,"SJAG_00168":null,"SJAG_00169":null,"SJAG_00173":null,"SJAG_00179":null,"SJAG_00183":null,"SJAG_00186":null,"SJAG_00188":null,"SJAG_00208":null,"SJAG_00209":null,"SJAG_00218":null,"SJAG_00224":null,"SJAG_00238":null,"SJAG_00244":null,"SJAG_00246":null,"SJAG_00252":null,"SJAG_00255":null,"SJAG_00256":null,"SJAG_00257":null,"SJAG_00286":null,"SJAG_00293":null,"SJAG_00295":null,"SJAG_00300":null,"SJAG_00325":null,"SJAG_00331":null,"SJAG_00334":null,"SJAG_00337":null,"SJAG_00341":null,"SJAG_00342":null,"SJAG_00356":null,"SJAG_00358":null,"SJAG_00364":null,"SJAG_00378":null,"SJAG_00381":null,"SJAG_00394":null,"SJAG_00395":null,"SJAG_00399":null,"SJAG_00402":null,"SJAG_00413":null,"SJAG_00426":null,"SJAG_00427":null,"SJAG_00435":null,"SJAG_00437":null,"SJAG_00442":null,"SJAG_00458":null,"SJAG_00469":null,"SJAG_00475":null,"SJAG_00486":null,"SJAG_00495":null,"SJAG_00496":null,"SJAG_00499":null,"SJAG_00500":null,"SJAG_00506":null,"SJAG_00508":null,"SJAG_00509":null,"SJAG_00519":null,"SJAG_00533":null,"SJAG_00552":null,"SJAG_00554":null,"SJAG_00559":null,"SJAG_00561":null,"SJAG_00580":null,"SJAG_00582":null,"SJAG_00596":null,"SJAG_00598":null,"SJAG_00604":null,"SJAG_00605":null,"SJAG_00610":null,"SJAG_00611":null,"SJAG_00619":null,"SJAG_00633":null,"SJAG_00635":null,"SJAG_00636":null,"SJAG_00637":null,"SJAG_00638":null,"SJAG_00649":null,"SJAG_00661":null,"SJAG_00673":null,"SJAG_00676":null,"SJAG_00678":null,"SJAG_00683":null,"SJAG_00690":null,"SJAG_00694":null,"SJAG_00695":null,"SJAG_00704":null,"SJAG_00714":null,"SJAG_00718":null,"SJAG_00722":null,"SJAG_00727":null,"SJAG_00731":null,"SJAG_00747":null,"SJAG_00769":null,"SJAG_00779":null,"SJAG_00797":null,"SJAG_00812":null,"SJAG_00814":null,"SJAG_00815":null,"SJAG_00816":null,"SJAG_00819":null,"SJAG_00825":null,"SJAG_00827":null,"SJAG_00832":null,"SJAG_00845":null,"SJAG_00855":null,"SJAG_00865":null,"SJAG_00866":null,"SJAG_00875":null,"SJAG_00876":null,"SJAG_00881":null,"SJAG_00886":null,"SJAG_00890":null,"SJAG_00895":null,"SJAG_00903":null,"SJAG_00924":null,"SJAG_00931":null,"SJAG_00933":null,"SJAG_00943":null,"SJAG_00946":null,"SJAG_00956":null,"SJAG_00963":null,"SJAG_00964":null,"SJAG_00993":null,"SJAG_00996":null,"SJAG_00999":null,"SJAG_01000":null,"SJAG_01018":null,"SJAG_01019":null,"SJAG_01021":null,"SJAG_01028":null,"SJAG_01040":null,"SJAG_01042":null,"SJAG_01043":null,"SJAG_01047":null,"SJAG_01054":null,"SJAG_01058":null,"SJAG_01070":null,"SJAG_01075":null,"SJAG_01079":null,"SJAG_01080":null,"SJAG_01082":null,"SJAG_01084":null,"SJAG_01089":null,"SJAG_01112":null,"SJAG_01146":null,"SJAG_01148":null,"SJAG_01164":null,"SJAG_01165":null,"SJAG_01176":null,"SJAG_01181":null,"SJAG_01192":null,"SJAG_01193":null,"SJAG_01204":null,"SJAG_01212":null,"SJAG_01233":null,"SJAG_01239":null,"SJAG_01251":null,"SJAG_01253":null,"SJAG_01261":null,"SJAG_01264":null,"SJAG_01269":null,"SJAG_01271":null,"SJAG_01276":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01299":null,"SJAG_01302":null,"SJAG_01311":null,"SJAG_01313":null,"SJAG_01314":null,"SJAG_01352":null,"SJAG_01356":null,"SJAG_01359":null,"SJAG_01360":null,"SJAG_01363":null,"SJAG_01368":null,"SJAG_01373":null,"SJAG_01375":null,"SJAG_01376":null,"SJAG_01383":null,"SJAG_01402":null,"SJAG_01425":null,"SJAG_01426":null,"SJAG_01427":null,"SJAG_01434":null,"SJAG_01443":null,"SJAG_01444":null,"SJAG_01474":null,"SJAG_01482":null,"SJAG_01491":null,"SJAG_01500":null,"SJAG_01507":null,"SJAG_01531":null,"SJAG_01533":null,"SJAG_01535":null,"SJAG_01536":null,"SJAG_01561":null,"SJAG_01562":null,"SJAG_01566":null,"SJAG_01571":null,"SJAG_01575":null,"SJAG_01582":null,"SJAG_01587":null,"SJAG_01592":null,"SJAG_01593":null,"SJAG_01618":null,"SJAG_01619":null,"SJAG_01637":null,"SJAG_01654":null,"SJAG_01661":null,"SJAG_01679":null,"SJAG_01680":null,"SJAG_01704":null,"SJAG_01713":null,"SJAG_01718":null,"SJAG_01724":null,"SJAG_01765":null,"SJAG_01766":null,"SJAG_01772":null,"SJAG_01776":null,"SJAG_01787":null,"SJAG_01791":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_01814":null,"SJAG_01825":null,"SJAG_01826":null,"SJAG_01835":null,"SJAG_01837":null,"SJAG_01854":null,"SJAG_01855":null,"SJAG_01859":null,"SJAG_01863":null,"SJAG_01865":null,"SJAG_01877":null,"SJAG_01885":null,"SJAG_01899":null,"SJAG_01900":null,"SJAG_01918":null,"SJAG_01922":null,"SJAG_01935":null,"SJAG_01937":null,"SJAG_01942":null,"SJAG_01946":null,"SJAG_01950":null,"SJAG_01955":null,"SJAG_01957":null,"SJAG_01958":null,"SJAG_01972":null,"SJAG_01974":null,"SJAG_01979":null,"SJAG_01992":null,"SJAG_02022":null,"SJAG_02024":null,"SJAG_02038":null,"SJAG_02042":null,"SJAG_02058":null,"SJAG_02064":null,"SJAG_02070":null,"SJAG_02082":null,"SJAG_02085":null,"SJAG_02099":null,"SJAG_02101":null,"SJAG_02102":null,"SJAG_02104":null,"SJAG_02126":null,"SJAG_02158":null,"SJAG_02163":null,"SJAG_02165":null,"SJAG_02168":null,"SJAG_02169":null,"SJAG_02178":null,"SJAG_02183":null,"SJAG_02222":null,"SJAG_02249":null,"SJAG_02271":null,"SJAG_02281":null,"SJAG_02288":null,"SJAG_02290":null,"SJAG_02296":null,"SJAG_02299":null,"SJAG_02305":null,"SJAG_02308":null,"SJAG_02309":null,"SJAG_02319":null,"SJAG_02321":null,"SJAG_02342":null,"SJAG_02347":null,"SJAG_02350":null,"SJAG_02360":null,"SJAG_02370":null,"SJAG_02371":null,"SJAG_02383":null,"SJAG_02386":null,"SJAG_02392":null,"SJAG_02408":null,"SJAG_02415":null,"SJAG_02417":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_02426":null,"SJAG_02429":null,"SJAG_02467":null,"SJAG_02468":null,"SJAG_02471":null,"SJAG_02488":null,"SJAG_02491":null,"SJAG_02498":null,"SJAG_02506":null,"SJAG_02519":null,"SJAG_02521":null,"SJAG_02523":null,"SJAG_02575":null,"SJAG_02583":null,"SJAG_02592":null,"SJAG_02596":null,"SJAG_02600":null,"SJAG_02603":null,"SJAG_02624":null,"SJAG_02627":null,"SJAG_02637":null,"SJAG_02652":null,"SJAG_02653":null,"SJAG_02654":null,"SJAG_02658":null,"SJAG_02659":null,"SJAG_02660":null,"SJAG_02668":null,"SJAG_02680":null,"SJAG_02685":null,"SJAG_02692":null,"SJAG_02705":null,"SJAG_02712":null,"SJAG_02713":null,"SJAG_02719":null,"SJAG_02720":null,"SJAG_02723":null,"SJAG_02725":null,"SJAG_02726":null,"SJAG_02736":null,"SJAG_02746":null,"SJAG_02756":null,"SJAG_02760":null,"SJAG_02769":null,"SJAG_02773":null,"SJAG_02791":null,"SJAG_02796":null,"SJAG_02804":null,"SJAG_02808":null,"SJAG_02817":null,"SJAG_02818":null,"SJAG_02821":null,"SJAG_02838":null,"SJAG_02841":null,"SJAG_02842":null,"SJAG_02851":null,"SJAG_02858":null,"SJAG_02868":null,"SJAG_02873":null,"SJAG_02878":null,"SJAG_02885":null,"SJAG_02887":null,"SJAG_02889":null,"SJAG_02896":null,"SJAG_02901":null,"SJAG_02903":null,"SJAG_02908":null,"SJAG_02913":null,"SJAG_02916":null,"SJAG_02918":null,"SJAG_02923":null,"SJAG_02940":null,"SJAG_02950":null,"SJAG_02954":null,"SJAG_02972":null,"SJAG_02973":null,"SJAG_02985":null,"SJAG_02990":null,"SJAG_02996":null,"SJAG_03005":null,"SJAG_03006":null,"SJAG_03008":null,"SJAG_03014":null,"SJAG_03016":null,"SJAG_03017":null,"SJAG_03029":null,"SJAG_03035":null,"SJAG_03048":null,"SJAG_03055":null,"SJAG_03056":null,"SJAG_03057":null,"SJAG_03061":null,"SJAG_03066":null,"SJAG_03067":null,"SJAG_03082":null,"SJAG_03087":null,"SJAG_03102":null,"SJAG_03112":null,"SJAG_03115":null,"SJAG_03129":null,"SJAG_03136":null,"SJAG_03141":null,"SJAG_03144":null,"SJAG_03149":null,"SJAG_03150":null,"SJAG_03154":null,"SJAG_03160":null,"SJAG_03162":null,"SJAG_03163":null,"SJAG_03167":null,"SJAG_03173":null,"SJAG_03174":null,"SJAG_03175":null,"SJAG_03180":null,"SJAG_03181":null,"SJAG_03188":null,"SJAG_03191":null,"SJAG_03209":null,"SJAG_03213":null,"SJAG_03228":null,"SJAG_03250":null,"SJAG_03257":null,"SJAG_03288":null,"SJAG_03289":null,"SJAG_03292":null,"SJAG_03302":null,"SJAG_03305":null,"SJAG_03306":null,"SJAG_03311":null,"SJAG_03312":null,"SJAG_03318":null,"SJAG_03322":null,"SJAG_03324":null,"SJAG_03332":null,"SJAG_03333":null,"SJAG_03336":null,"SJAG_03352":null,"SJAG_03356":null,"SJAG_03362":null,"SJAG_03367":null,"SJAG_03376":null,"SJAG_03384":null,"SJAG_03386":null,"SJAG_03387":null,"SJAG_03409":null,"SJAG_03421":null,"SJAG_03434":null,"SJAG_03438":null,"SJAG_03457":null,"SJAG_03468":null,"SJAG_03475":null,"SJAG_03486":null,"SJAG_03487":null,"SJAG_03501":null,"SJAG_03506":null,"SJAG_03529":null,"SJAG_03531":null,"SJAG_03537":null,"SJAG_03540":null,"SJAG_03548":null,"SJAG_03553":null,"SJAG_03554":null,"SJAG_03555":null,"SJAG_03557":null,"SJAG_03563":null,"SJAG_03578":null,"SJAG_03580":null,"SJAG_03587":null,"SJAG_03592":null,"SJAG_03602":null,"SJAG_03609":null,"SJAG_03613":null,"SJAG_03615":null,"SJAG_03618":null,"SJAG_03630":null,"SJAG_03656":null,"SJAG_03657":null,"SJAG_03659":null,"SJAG_03660":null,"SJAG_03672":null,"SJAG_03701":null,"SJAG_03708":null,"SJAG_03709":null,"SJAG_03713":null,"SJAG_03720":null,"SJAG_03753":null,"SJAG_03755":null,"SJAG_03761":null,"SJAG_03764":null,"SJAG_03773":null,"SJAG_03775":null,"SJAG_03789":null,"SJAG_03790":null,"SJAG_03798":null,"SJAG_03799":null,"SJAG_03810":null,"SJAG_03811":null,"SJAG_03825":null,"SJAG_03831":null,"SJAG_03854":null,"SJAG_03860":null,"SJAG_03863":null,"SJAG_03869":null,"SJAG_03871":null,"SJAG_03877":null,"SJAG_03878":null,"SJAG_03880":null,"SJAG_03881":null,"SJAG_03883":null,"SJAG_03887":null,"SJAG_03896":null,"SJAG_03900":null,"SJAG_03901":null,"SJAG_03906":null,"SJAG_03913":null,"SJAG_03914":null,"SJAG_03921":null,"SJAG_03932":null,"SJAG_03934":null,"SJAG_03935":null,"SJAG_03946":null,"SJAG_03949":null,"SJAG_03953":null,"SJAG_03961":null,"SJAG_03967":null,"SJAG_03968":null,"SJAG_03970":null,"SJAG_03972":null,"SJAG_03985":null,"SJAG_03987":null,"SJAG_04030":null,"SJAG_04034":null,"SJAG_04039":null,"SJAG_04041":null,"SJAG_04049":null,"SJAG_04052":null,"SJAG_04053":null,"SJAG_04059":null,"SJAG_04085":null,"SJAG_04089":null,"SJAG_04095":null,"SJAG_04106":null,"SJAG_04107":null,"SJAG_04113":null,"SJAG_04119":null,"SJAG_04126":null,"SJAG_04127":null,"SJAG_04130":null,"SJAG_04131":null,"SJAG_04145":null,"SJAG_04149":null,"SJAG_04151":null,"SJAG_04159":null,"SJAG_04161":null,"SJAG_04165":null,"SJAG_04178":null,"SJAG_04181":null,"SJAG_04182":null,"SJAG_04184":null,"SJAG_04186":null,"SJAG_04189":null,"SJAG_04206":null,"SJAG_04231":null,"SJAG_04232":null,"SJAG_04233":null,"SJAG_04236":null,"SJAG_04261":null,"SJAG_04263":null,"SJAG_04268":null,"SJAG_04276":null,"SJAG_04280":null,"SJAG_04282":null,"SJAG_04287":null,"SJAG_04288":null,"SJAG_04305":null,"SJAG_04309":null,"SJAG_04312":null,"SJAG_04316":null,"SJAG_04317":null,"SJAG_04319":null,"SJAG_04320":null,"SJAG_04323":null,"SJAG_04334":null,"SJAG_04337":null,"SJAG_04354":null,"SJAG_04394":null,"SJAG_04401":null,"SJAG_04408":null,"SJAG_04425":null,"SJAG_04429":null,"SJAG_04434":null,"SJAG_04435":null,"SJAG_04451":null,"SJAG_04453":null,"SJAG_04457":null,"SJAG_04461":null,"SJAG_04465":null,"SJAG_04468":null,"SJAG_04469":null,"SJAG_04481":null,"SJAG_04483":null,"SJAG_04486":null,"SJAG_04495":null,"SJAG_04499":null,"SJAG_04507":null,"SJAG_04516":null,"SJAG_04535":null,"SJAG_04537":null,"SJAG_04551":null,"SJAG_04552":null,"SJAG_04568":null,"SJAG_04571":null,"SJAG_04573":null,"SJAG_04574":null,"SJAG_04597":null,"SJAG_04600":null,"SJAG_04612":null,"SJAG_04619":null,"SJAG_04622":null,"SJAG_04627":null,"SJAG_04628":null,"SJAG_04631":null,"SJAG_04642":null,"SJAG_04655":null,"SJAG_04657":null,"SJAG_04658":null,"SJAG_04678":null,"SJAG_04680":null,"SJAG_04681":null,"SJAG_04688":null,"SJAG_04693":null,"SJAG_04699":null,"SJAG_04700":null,"SJAG_04709":null,"SJAG_04713":null,"SJAG_04728":null,"SJAG_04734":null,"SJAG_04735":null,"SJAG_04736":null,"SJAG_04747":null,"SJAG_04751":null,"SJAG_04756":null,"SJAG_04760":null,"SJAG_04761":null,"SJAG_04770":null,"SJAG_04777":null,"SJAG_04783":null,"SJAG_04791":null,"SJAG_04792":null,"SJAG_04821":null,"SJAG_04845":null,"SJAG_04849":null,"SJAG_04857":null,"SJAG_04865":null,"SJAG_04866":null,"SJAG_04868":null,"SJAG_04877":null,"SJAG_04878":null,"SJAG_04881":null,"SJAG_04882":null,"SJAG_04883":null,"SJAG_04894":null,"SJAG_04906":null,"SJAG_04915":null,"SJAG_04923":null,"SJAG_04934":null,"SJAG_04946":null,"SJAG_04952":null,"SJAG_04966":null,"SJAG_04970":null,"SJAG_04972":null,"SJAG_04980":null,"SJAG_04988":null,"SJAG_04990":null,"SJAG_04993":null,"SJAG_04994":null,"SJAG_05012":null,"SJAG_05016":null,"SJAG_05018":null,"SJAG_05022":null,"SJAG_05181":null,"SJAG_05197":null,"SJAG_05200":null,"SJAG_05225":null,"SJAG_05228":null,"SJAG_05231":null,"SJAG_05236":null,"SJAG_05239":null,"SJAG_05264":null,"SJAG_05274":null,"SJAG_05277":null,"SJAG_05285":null,"SJAG_05290":null,"SJAG_05304":null,"SJAG_05323":null,"SJAG_05327":null,"SJAG_05330":null,"SJAG_05334":null,"SJAG_05340":null,"SJAG_05413":null,"SJAG_05693":null,"SJAG_05979":null,"SJAG_06284":null,"SJAG_06309":null,"SJAG_06383":null,"SJAG_06592":null,"SJAG_06603":null,"SJAG_06634":null,"SJAG_16460":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674"],"is_obsolete":false,"name":"transferase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:25318672":null,"PMID:29191091":null},"secondary_identifiers":["Reactome:R-HSA-8868783","Reactome:R-HSA-5333607","Reactome:R-HSA-5668414","Reactome:R-HSA-1483089","Reactome:R-HSA-1483186"],"termid":"GO:0016740","terms_by_termid":{"GO:0000009":null,"GO:0000026":null,"GO:0000030":null,"GO:0000107":null,"GO:0000155":null,"GO:0000179":null,"GO:0000215":null,"GO:0000285":null,"GO:0000309":null,"GO:0000310":null,"GO:0000773":null,"GO:0000823":null,"GO:0000824":null,"GO:0000906":null,"GO:0001962":null,"GO:0003720":null,"GO:0003825":null,"GO:0003838":null,"GO:0003841":null,"GO:0003843":null,"GO:0003846":null,"GO:0003848":null,"GO:0003849":null,"GO:0003852":null,"GO:0003864":null,"GO:0003866":null,"GO:0003870":null,"GO:0003871":null,"GO:0003872":null,"GO:0003873":null,"GO:0003879":null,"GO:0003881":null,"GO:0003882":null,"GO:0003887":null,"GO:0003899":null,"GO:0003919":null,"GO:0003923":null,"GO:0003951":null,"GO:0003962":null,"GO:0003968":null,"GO:0003975":null,"GO:0003977":null,"GO:0003980":null,"GO:0003983":null,"GO:0003984":null,"GO:0003985":null,"GO:0003991":null,"GO:0003992":null,"GO:0003999":null,"GO:0004001":null,"GO:0004015":null,"GO:0004017":null,"GO:0004020":null,"GO:0004021":null,"GO:0004042":null,"GO:0004044":null,"GO:0004047":null,"GO:0004048":null,"GO:0004057":null,"GO:0004059":null,"GO:0004069":null,"GO:0004070":null,"GO:0004072":null,"GO:0004076":null,"GO:0004100":null,"GO:0004103":null,"GO:0004105":null,"GO:0004124":null,"GO:0004140":null,"GO:0004142":null,"GO:0004143":null,"GO:0004144":null,"GO:0004145":null,"GO:0004149":null,"GO:0004156":null,"GO:0004168":null,"GO:0004169":null,"GO:0004305":null,"GO:0004306":null,"GO:0004307":null,"GO:0004311":null,"GO:0004312":null,"GO:0004313":null,"GO:0004314":null,"GO:0004315":null,"GO:0004321":null,"GO:0004335":null,"GO:0004337":null,"GO:0004340":null,"GO:0004343":null,"GO:0004349":null,"GO:0004358":null,"GO:0004360":null,"GO:0004364":null,"GO:0004366":null,"GO:0004371":null,"GO:0004372":null,"GO:0004377":null,"GO:0004378":null,"GO:0004379":null,"GO:0004385":null,"GO:0004400":null,"GO:0004402":null,"GO:0004410":null,"GO:0004413":null,"GO:0004414":null,"GO:0004417":null,"GO:0004418":null,"GO:0004421":null,"GO:0004422":null,"GO:0004430":null,"GO:0004475":null,"GO:0004478":null,"GO:0004479":null,"GO:0004482":null,"GO:0004484":null,"GO:0004496":null,"GO:0004515":null,"GO:0004550":null,"GO:0004577":null,"GO:0004578":null,"GO:0004579":null,"GO:0004581":null,"GO:0004582":null,"GO:0004585":null,"GO:0004587":null,"GO:0004588":null,"GO:0004594":null,"GO:0004596":null,"GO:0004605":null,"GO:0004608":null,"GO:0004618":null,"GO:0004631":null,"GO:0004643":null,"GO:0004644":null,"GO:0004648":null,"GO:0004660":null,"GO:0004662":null,"GO:0004663":null,"GO:0004671":null,"GO:0004672":null,"GO:0004674":null,"GO:0004676":null,"GO:0004683":null,"GO:0004691":null,"GO:0004693":null,"GO:0004694":null,"GO:0004697":null,"GO:0004699":null,"GO:0004707":null,"GO:0004708":null,"GO:0004709":null,"GO:0004711":null,"GO:0004712":null,"GO:0004713":null,"GO:0004731":null,"GO:0004740":null,"GO:0004742":null,"GO:0004743":null,"GO:0004746":null,"GO:0004747":null,"GO:0004749":null,"GO:0004758":null,"GO:0004765":null,"GO:0004766":null,"GO:0004781":null,"GO:0004788":null,"GO:0004789":null,"GO:0004792":null,"GO:0004798":null,"GO:0004799":null,"GO:0004801":null,"GO:0004802":null,"GO:0004838":null,"GO:0004842":null,"GO:0004845":null,"GO:0004849":null,"GO:0004851":null,"GO:0004856":null,"GO:0006743":null,"GO:0006744":null,"GO:0008080":null,"GO:0008108":null,"GO:0008168":null,"GO:0008173":null,"GO:0008175":null,"GO:0008176":null,"GO:0008193":null,"GO:0008260":null,"GO:0008276":null,"GO:0008349":null,"GO:0008353":null,"GO:0008374":null,"GO:0008412":null,"GO:0008425":null,"GO:0008440":null,"GO:0008444":null,"GO:0008469":null,"GO:0008478":null,"GO:0008479":null,"GO:0008481":null,"GO:0008483":null,"GO:0008495":null,"GO:0008531":null,"GO:0008649":null,"GO:0008650":null,"GO:0008654":null,"GO:0008757":null,"GO:0008775":null,"GO:0008808":null,"GO:0008865":null,"GO:0008897":null,"GO:0008898":null,"GO:0008902":null,"GO:0008972":null,"GO:0008976":null,"GO:0008999":null,"GO:0009001":null,"GO:0009383":null,"GO:0009922":null,"GO:0009927":null,"GO:0010420":null,"GO:0010485":null,"GO:0016212":null,"GO:0016279":null,"GO:0016287":null,"GO:0016301":null,"GO:0016303":null,"GO:0016308":null,"GO:0016407":null,"GO:0016410":null,"GO:0016411":null,"GO:0016428":null,"GO:0016433":null,"GO:0016603":null,"GO:0016740":null,"GO:0016746":null,"GO:0016747":null,"GO:0016756":null,"GO:0016768":null,"GO:0016773":null,"GO:0016779":null,"GO:0016784":null,"GO:0016979":null,"GO:0016992":null,"GO:0017061":null,"GO:0017118":null,"GO:0017125":null,"GO:0017176":null,"GO:0018064":null,"GO:0018423":null,"GO:0018708":null,"GO:0019158":null,"GO:0019702":null,"GO:0019706":null,"GO:0019776":null,"GO:0030697":null,"GO:0030735":null,"GO:0031071":null,"GO:0031278":null,"GO:0032041":null,"GO:0032216":null,"GO:0032931":null,"GO:0033164":null,"GO:0033819":null,"GO:0033840":null,"GO:0033857":null,"GO:0033862":null,"GO:0034038":null,"GO:0034061":null,"GO:0034317":null,"GO:0034386":null,"GO:0034450":null,"GO:0034737":null,"GO:0035175":null,"GO:0035241":null,"GO:0035242":null,"GO:0035299":null,"GO:0036408":null,"GO:0036440":null,"GO:0036455":null,"GO:0042054":null,"GO:0042124":null,"GO:0042171":null,"GO:0042281":null,"GO:0042283":null,"GO:0042736":null,"GO:0042800":null,"GO:0043337":null,"GO:0043399":null,"GO:0043771":null,"GO:0043992":null,"GO:0043993":null,"GO:0043995":null,"GO:0043996":null,"GO:0043997":null,"GO:0043998":null,"GO:0044016":null,"GO:0045140":null,"GO:0045547":null,"GO:0046027":null,"GO:0046316":null,"GO:0046404":null,"GO:0046547":null,"GO:0046820":null,"GO:0046919":null,"GO:0046941":null,"GO:0046969":null,"GO:0046970":null,"GO:0046975":null,"GO:0047184":null,"GO:0047198":null,"GO:0047220":null,"GO:0047536":null,"GO:0047657":null,"GO:0050144":null,"GO:0050225":null,"GO:0050262":null,"GO:0050265":null,"GO:0050291":null,"GO:0050354":null,"GO:0051009":null,"GO:0051267":null,"GO:0051377":null,"GO:0051392":null,"GO:0051730":null,"GO:0051731":null,"GO:0051736":null,"GO:0051996":null,"GO:0052381":null,"GO:0052654":null,"GO:0052655":null,"GO:0052656":null,"GO:0052657":null,"GO:0052706":null,"GO:0052723":null,"GO:0052735":null,"GO:0052811":null,"GO:0052905":null,"GO:0052906":null,"GO:0052907":null,"GO:0052909":null,"GO:0052917":null,"GO:0052918":null,"GO:0052925":null,"GO:0052926":null,"GO:0052927":null,"GO:0052929":null,"GO:0061542":null,"GO:0061630":null,"GO:0061631":null,"GO:0061651":null,"GO:0061654":null,"GO:0061656":null,"GO:0061659":null,"GO:0061665":null,"GO:0061708":null,"GO:0061710":null,"GO:0061711":null,"GO:0061733":null,"GO:0061769":null,"GO:0061863":null,"GO:0062122":null,"GO:0062152":null,"GO:0070037":null,"GO:0070039":null,"GO:0070042":null,"GO:0070043":null,"GO:0070566":null,"GO:0071164":null,"GO:0071885":null,"GO:0072354":null,"GO:0072371":null,"GO:0090486":null,"GO:0090560":null,"GO:0097269":null,"GO:0102522":null,"GO:0102559":null,"GO:0102704":null,"GO:0103016":null,"GO:0103064":null,"GO:0106050":null,"GO:0106073":null,"GO:0106142":null,"GO:0106158":null,"GO:0106226":null,"GO:0106261":null,"GO:0106262":null,"GO:0106335":null,"GO:0106339":null,"GO:0106340":null,"GO:0106344":null,"GO:0106388":null,"GO:0120048":null,"GO:0120136":null,"GO:0120518":null,"GO:0120537":null,"GO:0120563":null,"GO:0120564":null,"GO:0120565":null,"GO:0140064":null,"GO:0140065":null,"GO:0140752":null,"GO:0140765":null,"GO:0140834":null,"GO:0140836":null,"GO:0140850":null,"GO:0140851":null,"GO:0140943":null,"GO:0140947":null,"GO:0140948":null,"GO:0140949":null,"GO:0140954":null,"GO:0140955":null,"GO:0140995":null,"GO:0140999":null,"GO:0141035":null,"GO:0141046":null,"GO:0141101":null,"GO:0141133":null,"GO:0141192":null,"GO:0141222":null,"GO:0141223":null,"GO:0160102":null,"GO:0160104":null,"GO:0160107":null,"GO:0160205":null,"GO:0160210":null,"GO:0180041":null,"GO:1990189":null,"GO:1990190":null,"GO:1990259":null,"GO:1990276":null,"GO:1990817":null,"GO:1990883":null}}


id: PBO:0068349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 126","termid":"PBO:0068349"}


id: MOD:00323
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to L-lysine methyl ester.","definition_xrefs":["PubMed:11875433","RESID:AA0318","PubMed:10973948","Unimod:34#C-term"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monomethylated L-lysine","termid":"MOD:01683"},{"relation_name":"is_a","term_name":"alpha-carboxyl methylated residue","termid":"MOD:01689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"L-lysine methyl ester","synonyms":[{"name":"2,6-diaminohexanoic methyl ester","type":"exact"},{"name":"L-lysine methyl ester","type":"exact"},{"name":"MOD_RES Lysine methyl ester","type":"exact"},{"name":"Methyl","type":"related"},{"name":"Methylation","type":"related"},{"name":"OMeLys","type":"exact"},{"name":"alpha,epsilon-diaminocaproic methyl ester","type":"exact"},{"name":"methyl (S)-2,6-diaminohexanoate","type":"exact"},{"name":"methyl L-lysinate","type":"exact"},{"name":"methyl esterified L-lysine","type":"exact"}],"termid":"MOD:00323"}


id: MONDO:0018001
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vascular neoplasm","termid":"MONDO:0024296"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inverse Klippel-Trenaunay syndrome","secondary_identifiers":["UMLS:C5679859","GARD:21488","Orphanet:329324","MEDGEN:1830088"],"synonyms":[{"name":"cutaneous hemangioma with muscle or bone atrophy","type":"exact"},{"name":"inverse Klippel-Trénaunay syndrome","type":"related"}],"termid":"MONDO:0018001","xrefs":{"Monarch":{"xref_id":"0018001"}}}


id: GO:0061703
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an assemble of ASC dimers that is capable of inducing pyroptosis.","definition_xrefs":["PMID:17599095","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"pyroptosome complex","synonyms":[{"name":"ASC pyroptosome","type":"exact"}],"termid":"GO:0061703"}


id: GO:0120036
data:
  {"annotated_genes":["SJAG_02989","SJAG_04509","SJAG_02379","SJAG_01943","SJAG_01794","SJAG_03453","SJAG_02700","SJAG_00514","SJAG_01993","SJAG_01894","SJAG_02864"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90073,94327,100714,116184,100102,100795],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904600"},{"annotations":[113220,91685,95289,92659,89709],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1902917"}]},"cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of a plasma membrane bounded prolongation or process extending from a cell, e.g. a cilium or axon.","definition_xrefs":["GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell projection organization","termid":"GO:0030030"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00514":null,"SJAG_01794":null,"SJAG_01894":null,"SJAG_01943":null,"SJAG_01993":null,"SJAG_02379":null,"SJAG_02700":null,"SJAG_02864":null,"SJAG_02989":null,"SJAG_03453":null,"SJAG_04509":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"plasma membrane bounded cell projection organization","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0120036","terms_by_termid":{"GO:1902917":null,"GO:1904600":null}}


id: PBO:0027247
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_polyadenylated_25S_rRNA_level","termid":"PBO:0027247"}


id: PBO:0034601
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_iron_ion_binding","termid":"PBO:0034601"}


id: MONDO:0000914
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.","definition_xrefs":["PMID:10476042","PMID:8878478","DOID:0111035"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral arteriopathy with subcortical infarcts and leukoencephalopathy","termid":"MONDO:0007432"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1","secondary_identifiers":["MEDGEN:1634330","OMIM:125310","Orphanet:136","MESH:D046589","NCIT:C84606","SCTID:390936003","GARD:1049","MedDRA:10065551","NORD:883","icd11.foundation:1621899838","UMLS:C4551768"],"synonyms":[{"name":"CADASIL","type":"exact"},{"name":"CADASIL 1","type":"exact"},{"name":"CADASIL syndrome","type":"exact"},{"name":"CADASIL type 1","type":"exact"},{"name":"CADASIL1","type":"exact"},{"name":"CASIL","type":"exact"},{"name":"autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1","type":"exact"},{"name":"cerebral arteriopathy with subcortical infarcts and leukoencephalopathy","type":"related"},{"name":"cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1","type":"exact"},{"name":"cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1","type":"exact"},{"name":"cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy","type":"broad"},{"name":"dementia, hereditary multi-infarct type","type":"exact"},{"name":"familial vascular leukoencephalopathy","type":"related"},{"name":"hereditary multi-infarct dementia","type":"exact"}],"termid":"MONDO:0000914","xrefs":{"Monarch":{"xref_id":"0000914"}}}


id: GO:0036408
data:
  {"annotated_genes":["SJAG_02773","SJAG_02165"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[92570,93227],"is_not":false,"summary":null,"term":"GO:0036408"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + histone H3 L-lysine (position 14) = CoA + histone H3 N6-acetyl-L-lysine (position 14).","definition_xrefs":["PMID:21289066","GOC:vw","PMID:18552846","PMID:19056256"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 acetyltransferase activity","termid":"GO:0010484"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02165":null,"SJAG_02773":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0034212"}],"interesting_parent_ids":["GO:0003674","GO:0140096","GO:0016740","GO:0034212","GO:0003824","GO:0016746"],"is_obsolete":false,"name":"histone H3K14 acetyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"histone H3-K14 acetyltransferase activity","type":"exact"},{"name":"histone acetylase activity (H3-K14 specific)","type":"exact"},{"name":"histone acetyltransferase activity (H3-K14 specific)","type":"exact"},{"name":"histone lysine N-acetyltransferase activity (H3-K14 specific)","type":"exact"}],"termid":"GO:0036408","terms_by_termid":{"GO:0036408":null}}


id: PBO:0027519
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_duration_of_meiotic_interphase","termid":"PBO:0027519"}


id: PBO:0067620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 792, pseudogene","termid":"PBO:0067620"}


id: MONDO:0008290
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"porokeratosis of Mibelli","termid":"MONDO:0019141"}],"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":"porokeratosis 1, Mibelli type","secondary_identifiers":["GARD:15108","OMIM:175800"],"synonyms":[{"name":"POROK1","type":"exact"},{"name":"porokeratosis 1, MIBELLI type","type":"related"},{"name":"porokeratosis 1, multiple types","type":"related"},{"name":"porokeratosis of Mibelli","type":"related"}],"termid":"MONDO:0008290","xrefs":{"Monarch":{"xref_id":"0008290"}}}


id: GO:2000976
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any regulation of transcription from RNA polymerase II promoter that is involved in detection of glucose.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter involved in detection of glucose (obsolete GO:2000976)","synonyms":[{"name":"global transcription regulation from Pol II promoter involved in detection of glucose","type":"related"},{"name":"global transcription regulation from Pol II promoter involved in glucose detection","type":"related"},{"name":"global transcription regulation from Pol II promoter involved in glucose perception","type":"related"},{"name":"global transcription regulation from Pol II promoter involved in glucose sensing","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter involved in detection of glucose","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter involved in glucose detection","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter involved in glucose perception","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter involved in glucose sensing","type":"related"},{"name":"regulation of global transcription from Pol II promoter involved in detection of glucose","type":"related"},{"name":"regulation of global transcription from Pol II promoter involved in glucose detection","type":"related"},{"name":"regulation of global transcription from Pol II promoter involved in glucose perception","type":"related"},{"name":"regulation of global transcription from Pol II promoter involved in glucose sensing","type":"related"},{"name":"regulation of transcription from Pol II promoter involved in detection of glucose","type":"exact"},{"name":"regulation of transcription from Pol II promoter involved in glucose detection","type":"exact"},{"name":"regulation of transcription from Pol II promoter involved in glucose perception","type":"related"},{"name":"regulation of transcription from Pol II promoter involved in glucose sensing","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter involved in glucose detection","type":"exact"},{"name":"regulation of transcription from RNA polymerase II promoter involved in glucose perception","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter involved in glucose sensing","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter, global involved in detection of glucose","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter, global involved in glucose detection","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter, global involved in glucose perception","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter, global involved in glucose sensing","type":"related"}],"termid":"GO:2000976"}


id: PBO:0005309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U4/U6 x U5 tri-snRNP complex subunit Dim1","termid":"PBO:0005309"}


id: PBO:0078948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon TCG) 6-1","termid":"PBO:0078948"}


id: PBO:0036514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histidinol-phosphatase(predicted)","termid":"PBO:0036514"}


id: GO:1900046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of hemostasis.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological process","termid":"GO:0050789"},{"relation_name":"is_a","term_name":"regulation of body fluid levels","termid":"GO:0050878"},{"relation_name":"regulates","term_name":"hemostasis","termid":"GO:0007599"}],"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 hemostasis","termid":"GO:1900046"}


id: PBO:0042580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral dopamine neurotrophic factor","termid":"PBO:0042580"}


id: MONDO:1011301
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Auditory system disorder 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":"auditory system disorder, non-human animal","termid":"MONDO:1011301","xrefs":{"Monarch":{"xref_id":"1011301"}}}


id: MOD:00716
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-methionine residue to a methylated methionine, such as N-methyl-L-methionine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methylated residue","termid":"MOD:00427"},{"relation_name":"is_a","term_name":"modified L-methionine residue","termid":"MOD:00913"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"methylated methionine","synonyms":[{"name":"MeMet","type":"exact"}],"termid":"MOD:00716"}


id: MONDO:0021569
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Emery-Dreifuss muscular dystrophy inherited in an autosomal dominant pattern and caused by mutations in the LMNA gene.","definition_xrefs":["NCIT:C126745"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy, limb-girdle, autosomal dominant","termid":"MONDO:0015151"},{"relation_name":"is_a","term_name":"autosomal dominant Emery-Dreifuss muscular dystrophy","termid":"MONDO:0020336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005267","MONDO:0005336"],"is_obsolete":false,"name":"Emery-Dreifuss muscular dystrophy 2, autosomal dominant","secondary_identifiers":["OMIM:181350","DOID:0070247","MESH:C535898","MEDGEN:98048","OMIM:159001","Orphanet:264","UMLS:C0410190","ICD9:425.4","SCTID:240072005","GARD:10230","DOID:0110301","SCTID:718178006"],"synonyms":[{"name":"EDMD2","type":"exact"},{"name":"EMD2","type":"related"},{"name":"Emery-Dreifuss muscular dystrophy 2, autosomal dominant","type":"exact"},{"name":"Emery-Dreifuss muscular dystrophy, autosomal dominant","type":"related"},{"name":"Hauptmann-Thannhauser muscular dystrophy","type":"exact"},{"name":"LGMD1B","type":"exact"},{"name":"LMNA autosomal dominant limb-girdle muscular dystrophy","type":"exact"},{"name":"autosomal dominant limb-girdle muscular dystrophy caused by mutation in LMNA","type":"exact"},{"name":"autosomal dominant limb-girdle muscular dystrophy type 1B","type":"exact"},{"name":"benign scapuloperoneal muscular dystrophy with cardiomyopathy","type":"related"},{"name":"limb-girdle muscular dystrophy due to lamin A/C deficiency","type":"exact"},{"name":"limb-girdle muscular dystrophy type 1B","type":"related"},{"name":"muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant","type":"related"},{"name":"muscular dystrophy, limb-girdle type 1B","type":"exact"},{"name":"muscular dystrophy, limb-girdle, type 1B","type":"related"},{"name":"muscular dystrophy, proximal, type 1B","type":"related"},{"name":"proximal muscular dystrophy type 1B","type":"exact"},{"name":"scapuloilioperoneal atrophy with cardiopathy","type":"related"}],"termid":"MONDO:0021569","xrefs":{"Monarch":{"xref_id":"0021569"}}}


id: PBO:0028009
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_during_meiotic_cell_cycle","termid":"PBO:0028009"}


id: PBO:0048497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ganglioside induced differentiation associated protein 1","termid":"PBO:0048497"}


id: PBO:0047533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FYVE, RhoGEF and PH domain containing 5 pseudogene 1","termid":"PBO:0047533"}


id: PR:O43038
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- vps36 gene.","definition_xrefs":["UniProtKB:O43038","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":"vacuolar protein-sorting-associated protein 36 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3B9.09","synonyms":[{"name":"Spom972h-vps36","type":"exact"}],"termid":"PR:O43038"}


id: GO:0001543
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Disruption of theca cell layer releasing follicular fluid and/or the oocyte.","direct_ancestors":[{"relation_name":"is_a","term_name":"ovulation cycle process","termid":"GO:0022602"},{"relation_name":"part_of","term_name":"ovulation from ovarian follicle","termid":"GO:0001542"}],"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":"ovarian follicle rupture","termid":"GO:0001543"}


id: PBO:0087243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Serine protein phosphatase involved in formation of FAR complex; inhibits mitophagy by dephosphorylating Atg32p; required for glycogen accumulation; interacts with Tap42p, which binds to and regulates other protein phosphatases","termid":"PBO:0087243"}


id: PBO:0059903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND1 pseudogene 26","termid":"PBO:0059903"}


id: MONDO:0021440
data:
  {"annotated_genes":["SJAG_03453","SJAG_02855"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87115],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010621"},{"annotations":[88588],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044792"},{"annotations":[87667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008097"},{"annotations":[87246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009578"},{"annotations":[86807],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008093"}]},"cv_name":"mondo","definition":"A benign neoplasm that involves the zone of skin.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system benign neoplasm","termid":"MONDO:0000652"},{"relation_name":"is_a","term_name":"skin neoplasm","termid":"MONDO:0002531"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02855":null,"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"benign neoplasm of skin","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:216.9","MEDGEN:2197","ICD9:216.8","NCIT:C2896","SCTID:92384009","UMLS:C0004998"],"synonyms":[{"name":"benign cutaneous neoplasm","type":"exact"},{"name":"benign cutaneous tumor","type":"exact"},{"name":"benign cutaneous tumour","type":"exact"},{"name":"benign neoplasm of the skin","type":"exact"},{"name":"benign skin neoplasm","type":"exact"},{"name":"benign skin tumor","type":"exact"},{"name":"benign skin tumour","type":"exact"},{"name":"benign tumor of skin","type":"exact"},{"name":"benign tumor of the skin","type":"exact"},{"name":"benign tumour of skin","type":"exact"},{"name":"benign tumour of the skin","type":"exact"},{"name":"skin neoplasms, benign","type":"exact"},{"name":"zone of skin benign neoplasm","type":"exact"}],"termid":"MONDO:0021440","terms_by_termid":{"MONDO:0008093":null,"MONDO:0008097":null,"MONDO:0009578":null,"MONDO:0010621":null,"MONDO:0044792":null},"xrefs":{"Monarch":{"xref_id":"0021440"}}}


id: GO:0097708
data:
  {"annotated_genes":["SJAG_01783","SJAG_04598","SJAG_04343","SJAG_05207","SJAG_00072","SJAG_00314","SJAG_04616","SJAG_00181","SJAG_04359","SJAG_03663","SJAG_04505","SJAG_00173","SJAG_03137","SJAG_01772","SJAG_01030","SJAG_03536","SJAG_01379","SJAG_01236","SJAG_04517","SJAG_04349","SJAG_00900","SJAG_02429","SJAG_01088","SJAG_02805","SJAG_03123","SJAG_02852","SJAG_03783","SJAG_01633","SJAG_00380","SJAG_00767","SJAG_03465","SJAG_02432","SJAG_04047","SJAG_04643","SJAG_01025","SJAG_16459","SJAG_03511","SJAG_04609","SJAG_02349","SJAG_04592","SJAG_02789","SJAG_01382","SJAG_01448","SJAG_02315","SJAG_01112","SJAG_03429","SJAG_04021","SJAG_01415","SJAG_03385","SJAG_00204","SJAG_04822","SJAG_01939","SJAG_03005","SJAG_02234","SJAG_01748","SJAG_04196","SJAG_01876","SJAG_05344","SJAG_04391","SJAG_02160","SJAG_02833","SJAG_04966","SJAG_04931","SJAG_03504","SJAG_00557","SJAG_00821","SJAG_00521","SJAG_01135","SJAG_03848","SJAG_03976","SJAG_03131","SJAG_00152","SJAG_03404","SJAG_01600","SJAG_04338","SJAG_00916","SJAG_02539","SJAG_03891","SJAG_01488","SJAG_04329","SJAG_02120","SJAG_02453","SJAG_01508","SJAG_04902","SJAG_01281","SJAG_00777","SJAG_03963","SJAG_02012","SJAG_03915","SJAG_02049","SJAG_01571","SJAG_03403","SJAG_01309","SJAG_00108","SJAG_00800","SJAG_05209","SJAG_02241","SJAG_05030","SJAG_03368","SJAG_00971","SJAG_02584","SJAG_04629","SJAG_00379","SJAG_01991","SJAG_03146","SJAG_05303","SJAG_00299","SJAG_02443","SJAG_00416","SJAG_00287","SJAG_07012","SJAG_04112","SJAG_02587","SJAG_00785","SJAG_01285","SJAG_04886","SJAG_00114","SJAG_03153","SJAG_04023","SJAG_02100","SJAG_03467","SJAG_02655","SJAG_03250","SJAG_04509","SJAG_00104","SJAG_01927","SJAG_00906","SJAG_00328","SJAG_00638","SJAG_02264","SJAG_03889","SJAG_04513","SJAG_04618","SJAG_01642","SJAG_02282","SJAG_03907","SJAG_01167","SJAG_04070","SJAG_03270","SJAG_01645","SJAG_04402","SJAG_01598","SJAG_00171","SJAG_03488","SJAG_04936","SJAG_04489","SJAG_00339","SJAG_02516","SJAG_03892","SJAG_01189","SJAG_04912","SJAG_04565","SJAG_00357","SJAG_01324","SJAG_01367","SJAG_04275","SJAG_02902","SJAG_01229","SJAG_00092","SJAG_03347","SJAG_04474","SJAG_02177","SJAG_05345","SJAG_05194","SJAG_00669","SJAG_03072","SJAG_04024","SJAG_01039","SJAG_02750","SJAG_01981","SJAG_02811","SJAG_01809","SJAG_05013","SJAG_02525","SJAG_00632","SJAG_00192","SJAG_04740","SJAG_02240","SJAG_00284","SJAG_00301","SJAG_04552","SJAG_00430","SJAG_04002","SJAG_03933","SJAG_05210","SJAG_04978","SJAG_02482","SJAG_00677","SJAG_04219","SJAG_04837","SJAG_02839","SJAG_04569","SJAG_04358","SJAG_04644","SJAG_01242","SJAG_03558"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[110451],"is_not":false,"summary":null,"term":"GO:0097708"},{"annotations":[79369,114641,114853,62802],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030121"},{"annotations":[58661,80009,110173,76197],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030122"},{"annotations":[59068,66612],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030130"},{"annotations":[75567,81522],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030125"},{"annotations":[79488,102153,75371,94017,107544],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030136"},{"annotations":[68439,95995],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030665"},{"annotations":[81636,100264,72606,108958,65309,79764,75378,95040,80078],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030126"},{"annotations":[101334,115997,94954,93426],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030137"},{"annotations":[58242,64301],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030663"},{"annotations":[74747,76579,78843,73207,80200,97327,73085,76933,77378,78268],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030127"},{"annotations":[77397,71596,72764,120681,112592,76238,76401,78722,105090,94955,97428,78686,80980,118376,80554,93342,77458,74008],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030134"},{"annotations":[91987,120305,71023,73699,102126,118754],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033263"},{"annotations":[92387],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010009"},{"annotations":[76481,77104,71747,76615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031410"},{"annotations":[99203,59717],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030659"},{"annotations":[74831,76408,81839,104481,81792,101729,74855],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005769"},{"annotations":[101528,97712,82053],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031901"},{"annotations":[112536,79918,77719,95633,117327],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030139"},{"annotations":[101282,102008,79077,69152,73296,76900,114858,120765,101789,107462,66212,80913,79259,62750,105863,68653,111495,99556,102946,95854,81546,114643,75461,70955,63483,102034,98954,100411,114765,94437,120406,73124,78254,97760,73690,72236,79944,77391,108574,81383,96045,67317,116565,97594,75565,81520,104332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005768"},{"annotations":[103786,103798,74379,61405,81853,100499,79907],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010008"},{"annotations":[72188,77853,68773,102897,75633],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0012507"},{"annotations":[73902,89933],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000813"},{"annotations":[73866,80217,72665],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000814"},{"annotations":[77545,72771,77970,79469,72445,71874],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000815"},{"annotations":[75243,93311],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033565"},{"annotations":[117328,89698],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070382"},{"annotations":[73662,79048],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034044"},{"annotations":[80441,71696,98955,81378],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000938"},{"annotations":[96842,116857],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005798"},{"annotations":[76409,78928,101529,105881,110522,111483,76597,79029,72972,72757,72436,119413,81756,73511,73289,81793,113111,106911,100680],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005770"},{"annotations":[99448],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031906"},{"annotations":[102899,77849,89934,80215,93818,99475,101325],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031902"},{"annotations":[92813],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035658"},{"annotations":[107583,115164,71873,121292,72769,72443,77968,116307,77543,80988,77726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005771"},{"annotations":[121294,60925,63115],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032585"},{"annotations":[72793,104483,79241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0055037"},{"annotations":[102012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030140"},{"annotations":[121063,76411],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030133"},{"annotations":[73251,90475,104350,111671,76838,99117,91160,101578,100916,105193],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990071"},{"annotations":[76406],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097422"},{"annotations":[77048,100681],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034424"}]},"cv_name":"cellular_component","definition":"Any vesicle that is part of the intracellular region.","definition_xrefs":["GOC:vesicles"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle","termid":"GO:0031982"},{"relation_name":"is_a","term_name":"intracellular membrane-bounded organelle","termid":"GO:0043231"}],"gene_count":196,"genes_by_uniquename":{"SJAG_00072":null,"SJAG_00092":null,"SJAG_00104":null,"SJAG_00108":null,"SJAG_00114":null,"SJAG_00152":null,"SJAG_00171":null,"SJAG_00173":null,"SJAG_00181":null,"SJAG_00192":null,"SJAG_00204":null,"SJAG_00284":null,"SJAG_00287":null,"SJAG_00299":null,"SJAG_00301":null,"SJAG_00314":null,"SJAG_00328":null,"SJAG_00339":null,"SJAG_00357":null,"SJAG_00379":null,"SJAG_00380":null,"SJAG_00416":null,"SJAG_00430":null,"SJAG_00521":null,"SJAG_00557":null,"SJAG_00632":null,"SJAG_00638":null,"SJAG_00669":null,"SJAG_00677":null,"SJAG_00767":null,"SJAG_00777":null,"SJAG_00785":null,"SJAG_00800":null,"SJAG_00821":null,"SJAG_00900":null,"SJAG_00906":null,"SJAG_00916":null,"SJAG_00971":null,"SJAG_01025":null,"SJAG_01030":null,"SJAG_01039":null,"SJAG_01088":null,"SJAG_01112":null,"SJAG_01135":null,"SJAG_01167":null,"SJAG_01189":null,"SJAG_01229":null,"SJAG_01236":null,"SJAG_01242":null,"SJAG_01281":null,"SJAG_01285":null,"SJAG_01309":null,"SJAG_01324":null,"SJAG_01367":null,"SJAG_01379":null,"SJAG_01382":null,"SJAG_01415":null,"SJAG_01448":null,"SJAG_01488":null,"SJAG_01508":null,"SJAG_01571":null,"SJAG_01598":null,"SJAG_01600":null,"SJAG_01633":null,"SJAG_01642":null,"SJAG_01645":null,"SJAG_01748":null,"SJAG_01772":null,"SJAG_01783":null,"SJAG_01809":null,"SJAG_01876":null,"SJAG_01927":null,"SJAG_01939":null,"SJAG_01981":null,"SJAG_01991":null,"SJAG_02012":null,"SJAG_02049":null,"SJAG_02100":null,"SJAG_02120":null,"SJAG_02160":null,"SJAG_02177":null,"SJAG_02234":null,"SJAG_02240":null,"SJAG_02241":null,"SJAG_02264":null,"SJAG_02282":null,"SJAG_02315":null,"SJAG_02349":null,"SJAG_02429":null,"SJAG_02432":null,"SJAG_02443":null,"SJAG_02453":null,"SJAG_02482":null,"SJAG_02516":null,"SJAG_02525":null,"SJAG_02539":null,"SJAG_02584":null,"SJAG_02587":null,"SJAG_02655":null,"SJAG_02750":null,"SJAG_02789":null,"SJAG_02805":null,"SJAG_02811":null,"SJAG_02833":null,"SJAG_02839":null,"SJAG_02852":null,"SJAG_02902":null,"SJAG_03005":null,"SJAG_03072":null,"SJAG_03123":null,"SJAG_03131":null,"SJAG_03137":null,"SJAG_03146":null,"SJAG_03153":null,"SJAG_03250":null,"SJAG_03270":null,"SJAG_03347":null,"SJAG_03368":null,"SJAG_03385":null,"SJAG_03403":null,"SJAG_03404":null,"SJAG_03429":null,"SJAG_03465":null,"SJAG_03467":null,"SJAG_03488":null,"SJAG_03504":null,"SJAG_03511":null,"SJAG_03536":null,"SJAG_03558":null,"SJAG_03663":null,"SJAG_03783":null,"SJAG_03848":null,"SJAG_03889":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03907":null,"SJAG_03915":null,"SJAG_03933":null,"SJAG_03963":null,"SJAG_03976":null,"SJAG_04002":null,"SJAG_04021":null,"SJAG_04023":null,"SJAG_04024":null,"SJAG_04047":null,"SJAG_04070":null,"SJAG_04112":null,"SJAG_04196":null,"SJAG_04219":null,"SJAG_04275":null,"SJAG_04329":null,"SJAG_04338":null,"SJAG_04343":null,"SJAG_04349":null,"SJAG_04358":null,"SJAG_04359":null,"SJAG_04391":null,"SJAG_04402":null,"SJAG_04474":null,"SJAG_04489":null,"SJAG_04505":null,"SJAG_04509":null,"SJAG_04513":null,"SJAG_04517":null,"SJAG_04552":null,"SJAG_04565":null,"SJAG_04569":null,"SJAG_04592":null,"SJAG_04598":null,"SJAG_04609":null,"SJAG_04616":null,"SJAG_04618":null,"SJAG_04629":null,"SJAG_04643":null,"SJAG_04644":null,"SJAG_04740":null,"SJAG_04822":null,"SJAG_04837":null,"SJAG_04886":null,"SJAG_04902":null,"SJAG_04912":null,"SJAG_04931":null,"SJAG_04936":null,"SJAG_04966":null,"SJAG_04978":null,"SJAG_05013":null,"SJAG_05030":null,"SJAG_05194":null,"SJAG_05207":null,"SJAG_05209":null,"SJAG_05210":null,"SJAG_05303":null,"SJAG_05344":null,"SJAG_05345":null,"SJAG_07012":null,"SJAG_16459":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"intracellular vesicle","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000043":null,"GO_REF:0000044":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:30726171":null,"PMID:32109380":null},"termid":"GO:0097708","terms_by_termid":{"GO:0000813":null,"GO:0000814":null,"GO:0000815":null,"GO:0000938":null,"GO:0005768":null,"GO:0005769":null,"GO:0005770":null,"GO:0005771":null,"GO:0005798":null,"GO:0010008":null,"GO:0010009":null,"GO:0012507":null,"GO:0030121":null,"GO:0030122":null,"GO:0030125":null,"GO:0030126":null,"GO:0030127":null,"GO:0030130":null,"GO:0030133":null,"GO:0030134":null,"GO:0030136":null,"GO:0030137":null,"GO:0030139":null,"GO:0030140":null,"GO:0030659":null,"GO:0030663":null,"GO:0030665":null,"GO:0031410":null,"GO:0031901":null,"GO:0031902":null,"GO:0031906":null,"GO:0032585":null,"GO:0033263":null,"GO:0033565":null,"GO:0034044":null,"GO:0034424":null,"GO:0035658":null,"GO:0055037":null,"GO:0070382":null,"GO:0097422":null,"GO:0097708":null,"GO:1990071":null}}


id: PBO:0054132
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 1498","termid":"PBO:0054132"}


id: GO:0010025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of wax, which includes C16 and C18 fatty acids.","definition_xrefs":["ISBN:0943088399"],"direct_ancestors":[{"relation_name":"is_a","term_name":"wax metabolic process","termid":"GO:0010166"},{"relation_name":"is_a","term_name":"fatty acid derivative biosynthetic process","termid":"GO:1901570"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"wax biosynthetic process","secondary_identifiers":["Reactome:R-HSA-9640463","MetaCyc:PWY-282"],"synonyms":[{"name":"wax anabolism","type":"exact"},{"name":"wax biosynthesis","type":"exact"},{"name":"wax formation","type":"exact"},{"name":"wax synthesis","type":"exact"}],"termid":"GO:0010025"}


id: MONDO:0007754
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":"hyperhidrosis palmaris ET plantaris","secondary_identifiers":["MEDGEN:224808","UMLS:C1274743","MESH:C563185","OMIM:144110"],"synonyms":[{"name":"HYPRPP","type":"exact"},{"name":"hyperhidrosis palmaris ET plantaris","type":"exact"},{"name":"hyperhidrosis, primary palmar","type":"related"}],"termid":"MONDO:0007754","xrefs":{"Monarch":{"xref_id":"0007754"}}}


id: MOD:01698
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an amino group with a trimethylaminium group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trimethylated protonated-residue","termid":"MOD:00711"},{"relation_name":"is_a","term_name":"alpha-amino methylated residue","termid":"MOD:01460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"alpha-amino trimethylated protonated-residue","synonyms":[{"name":"N2Me3+Res","type":"exact"},{"name":"Trimethyl","type":"related"},{"name":"tri-Methylation","type":"related"}],"termid":"MOD:01698"}


id: GO:0005987
data:
  {"annotated_genes":["SJAG_04301"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78550],"is_not":false,"summary":null,"term":"GO:0005987"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of sucrose, the disaccharide fructofuranosyl-glucopyranoside.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sucrose metabolic process","termid":"GO:0005985"},{"relation_name":"is_a","term_name":"disaccharide catabolic process","termid":"GO:0046352"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04301":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"sucrose catabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"sucrose breakdown","type":"exact"},{"name":"sucrose catabolism","type":"exact"},{"name":"sucrose degradation","type":"exact"}],"termid":"GO:0005987","terms_by_termid":{"GO:0005987":null}}


id: PBO:0027828
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_positive_regulation_of_transcription_during_G0_phase","termid":"PBO:0027828"}


id: PBO:0046373
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ectonucleoside triphosphate diphosphohydrolase 8","termid":"PBO:0046373"}


id: FYPO:0005837
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which protein transport along microtubules to the cortex of the cell tip does not occur. Transport of all proteins or a specific protein may be affected.","definition_xrefs":["GO:0099110","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein transport along microtubule to cell tip cortex during vegetative growth","termid":"FYPO:0005832"},{"relation_name":"is_a","term_name":"abolished protein transport along microtubule to cell tip during vegetative growth","termid":"FYPO:0005836"},{"relation_name":"is_a","term_name":"abolished protein localization to cell cortex of cell tip during vegetative growth","termid":"FYPO:0006502"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"abolished protein transport along microtubule to cell tip cortex during vegetative growth","synonyms":[{"name":"abolished protein movement along microtubule to cell tip cortex during vegetative growth","type":"exact"},{"name":"abolished protein transport along microtubule to cell cortex of cell tip during vegetative growth","type":"exact"},{"name":"abolished protein transport along microtubule to cell tip cortex during mitotic cell cycle","type":"related"},{"name":"protein transport along microtubule to cell tip cortex abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0005837"}


id: PBO:0073273
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 9","termid":"PBO:0073273"}


id: MONDO:0011036
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Porencephaly-cerebellar hypoplasia-internal malformations syndrome is rare central nervous system malformation syndrome characterized by bilateral porencephaly, absence of the septum pellucidum and cerebellar hypoplasia with absent vermis. Additionally, dysmorphic facial features (hypertelorism, epicanthic folds, high arched palate, prominent metopic suture), macrocephaly, corneal clouding, situs inversus, tetralogy of Fallot, atrial septal defects and/or seizures have been observed.","definition_xrefs":["Orphanet:2941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"porencephaly-cerebellar hypoplasia-internal malformations syndrome","secondary_identifiers":["SCTID:763821001","UMLS:C1832472","MEDGEN:331296","GARD:4437","MESH:C536336","OMIM:601322"],"synonyms":[{"name":"Bonnemann Meinecke syndrome","type":"related"},{"name":"Bonnemann-Meinecke syndrome","type":"exact"},{"name":"porencephaly cerebellar hypoplasia internal malformations","type":"related"},{"name":"porencephaly, cerebellar hypoplasia, and internal malformations","type":"related"}],"termid":"MONDO:0011036","xrefs":{"Monarch":{"xref_id":"0011036"}}}


id: SO:0000918
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An edit to delete a uridine.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000918 delete_U (obsolete SO:0000918)","synonyms":[{"name":"delete U","type":"exact"}],"termid":"SO:0000918"}


id: FYPO:0000358
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which cells do not form mating projections.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cell shape","termid":"FYPO:0001126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000005","FYPO:0001985"],"is_obsolete":false,"name":"shmoo absent","synonyms":[{"name":"absent mating projection morphology","type":"exact"},{"name":"mating projection absent","type":"exact"},{"name":"mating projection morphology: absent","type":"related"}],"termid":"FYPO:0000358"}


id: GO:0099562
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process which maintains the organization and the arrangement of proteins in the presynaptic density.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of postsynaptic specialization structure","termid":"GO:0098880"}],"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":"maintenance of postsynaptic density structure","termid":"GO:0099562"}


id: PR:O74962
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A pantothenate kinase 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03694","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":"pantothenate kinase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4B4.01c","secondary_identifiers":["UniProtKB:O74962"],"synonyms":[{"name":"Spom972h-PANK3","type":"exact"},{"name":"pantothenic acid kinase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74962"}


id: PBO:0064084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PITH domain containing 1","termid":"PBO:0064084"}


id: MONDO:0850151
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymph node cancer that has material basis in abnormally proliferating cells derives from epithelial cells.","definition_xrefs":["DOID:0080618"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymph node cancer","termid":"MONDO:0001082"},{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"lymph node carcinoma","termid":"MONDO:0850151","xrefs":{"Monarch":{"xref_id":"0850151"}}}


id: MONDO:0019746
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cystinuria","termid":"MONDO:0009067"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"cystinuria type B","secondary_identifiers":["GARD:16828","Orphanet:93613","UMLS:C1857389","MEDGEN:347442","icd11.foundation:491796307"],"termid":"MONDO:0019746","xrefs":{"Monarch":{"xref_id":"0019746"}}}


id: PBO:0050657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein 90 alpha family class B member 7, pseudogene","termid":"PBO:0050657"}


id: GO:0098762
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"One of the distinct periods or stages into which the meiotic cell cycle is divided. Each phase is characterized by the occurrence of specific biochemical and morphological events.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cycle phase","termid":"GO:0022403"}],"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":"meiotic cell cycle phase","termid":"GO:0098762"}


id: FYPO:0005337
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which acetylation of lysine at positions 9 and 14 of histone H3 occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete increased histone H3-K9K14 acetylation during vegetative growth (obsolete FYPO:0005337)","synonyms":[{"name":"increased histone H3 K9K14 acetylation during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 and K14 acetylation during vegetative growth","type":"exact"},{"name":"increased histone H3-K9K14 acetylation during mitotic cell cycle","type":"related"},{"name":"increased histone lysine H3 K9K14 acetylation during vegetative growth","type":"exact"}],"termid":"FYPO:0005337"}


id: GO:1905135
data:
  {"annotated_genes":["SJAG_02779","SJAG_02780"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73529,80968],"is_not":false,"summary":null,"term":"GO:1905135"}]},"cv_name":"biological_process","definition":"The directed movement of biotin from outside of a cell, across the plasma membrane and into the cytosol.","definition_xrefs":["GOC:TermGenie","PMID:12557275","GO_REF:0000075"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biotin transport","termid":"GO:0015878"},{"relation_name":"is_a","term_name":"vitamin transmembrane transport","termid":"GO:0035461"},{"relation_name":"is_a","term_name":"import across plasma membrane","termid":"GO:0098739"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02779":null,"SJAG_02780":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0055085","GO:0006810"],"is_obsolete":false,"name":"biotin import across plasma membrane","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:1901689","GO:0044756"],"synonyms":[{"name":"biotin import","type":"related"},{"name":"biotin import into cell","type":"exact"}],"termid":"GO:1905135","terms_by_termid":{"GO:1905135":null}}


id: GO:0015909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a long-chain fatty acid into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. A long-chain fatty acid has an aliphatic tail containing 13 to 22 carbons.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid transport","termid":"GO:0015908"}],"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"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"long-chain fatty acid transport","secondary_identifiers":["Reactome:R-HSA-804914"],"termid":"GO:0015909"}


id: PBO:0013443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMARCAD1 family ATP-dependent DNA helicase Fft1 (predicted)","termid":"PBO:0013443"}


id: GO:0097235
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of fatty acid beta-oxidation by activating or increasing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:dgf","PMID:1899286"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of fatty acid beta-oxidation by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:0097235)","termid":"GO:0097235"}


id: GO:1903629
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of dUTP diphosphatase activity.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","PMID:1315924"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of dUTP diphosphatase activity (obsolete GO:1903629)","synonyms":[{"name":"activation of dUTP diphosphatase activity","type":"narrow"},{"name":"activation of dUTP nucleotidohydrolase activity","type":"narrow"},{"name":"activation of dUTP pyrophosphatase activity","type":"narrow"},{"name":"activation of dUTPase activity","type":"narrow"},{"name":"activation of deoxyuridine-triphosphatase activity","type":"narrow"},{"name":"activation of desoxyuridine 5'-triphosphatase activity","type":"narrow"},{"name":"activation of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"narrow"},{"name":"positive regulation of dUTP nucleotidohydrolase activity","type":"exact"},{"name":"positive regulation of dUTP pyrophosphatase activity","type":"exact"},{"name":"positive regulation of dUTPase activity","type":"exact"},{"name":"positive regulation of deoxyuridine-triphosphatase activity","type":"exact"},{"name":"positive regulation of desoxyuridine 5'-triphosphatase activity","type":"exact"},{"name":"positive regulation of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"exact"},{"name":"up regulation of dUTP diphosphatase activity","type":"exact"},{"name":"up regulation of dUTP nucleotidohydrolase activity","type":"exact"},{"name":"up regulation of dUTP pyrophosphatase activity","type":"exact"},{"name":"up regulation of dUTPase activity","type":"exact"},{"name":"up regulation of deoxyuridine-triphosphatase activity","type":"exact"},{"name":"up regulation of desoxyuridine 5'-triphosphatase activity","type":"exact"},{"name":"up regulation of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"exact"},{"name":"up-regulation of dUTP diphosphatase activity","type":"exact"},{"name":"up-regulation of dUTP nucleotidohydrolase activity","type":"exact"},{"name":"up-regulation of dUTP pyrophosphatase activity","type":"exact"},{"name":"up-regulation of dUTPase activity","type":"exact"},{"name":"up-regulation of deoxyuridine-triphosphatase activity","type":"exact"},{"name":"up-regulation of desoxyuridine 5'-triphosphatase activity","type":"exact"},{"name":"up-regulation of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"exact"},{"name":"upregulation of dUTP diphosphatase activity","type":"exact"},{"name":"upregulation of dUTP nucleotidohydrolase activity","type":"exact"},{"name":"upregulation of dUTP pyrophosphatase activity","type":"exact"},{"name":"upregulation of dUTPase activity","type":"exact"},{"name":"upregulation of deoxyuridine-triphosphatase activity","type":"exact"},{"name":"upregulation of desoxyuridine 5'-triphosphatase activity","type":"exact"},{"name":"upregulation of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"exact"}],"termid":"GO:1903629"}


id: PBO:0036139
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K9_methylation_during_vegetative_growth","termid":"PBO:0036139"}


id: PBO:0027751
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_nucleus","termid":"PBO:0027751"}


id: GO:1990112
data:
  {"annotated_genes":["SJAG_01074","SJAG_00188","SJAG_01134","SJAG_01497","SJAG_04384","SJAG_03345"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[71581,75275,78364,91072,105790,106647],"is_not":false,"summary":null,"term":"GO:1990112"}]},"cv_name":"cellular_component","definition":"A multiprotein complex that forms a stable complex with large ribosomal subunits (60S in eukaryotes and 50S in prokaryotes) containing stalled polypeptides and triggers their degradation (ribosomal quality control). In budding yeast, this complex includes Cdc48p, Rkr1p, Tae2p, Rqc1p, Npl4p and Ufd1p proteins.","definition_xrefs":["PMID:23178123","GOC:rb","PMID:23232563"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00188":null,"SJAG_01074":null,"SJAG_01134":null,"SJAG_01497":null,"SJAG_03345":null,"SJAG_04384":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"RQC complex","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"ribosome quality control complex","type":"exact"},{"name":"ribosome-bound quality control complex","type":"exact"}],"termid":"GO:1990112","terms_by_termid":{"GO:1990112":null}}


id: PBO:0089405
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translational activator, zf-CCHC type zinc finger protein","termid":"PBO:0089405"}


id: internal:misnomer
data:
  {"annotation_feature_type":"gene","cv_name":"synonym_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"misnomer","termid":"internal:misnomer"}


id: MONDO:0042370
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Yersinia infectious disease","termid":"MONDO:0007023"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Yersinia enterocolitica infectious disease","secondary_identifiers":["EFO:0009424","SCTID:80960004"],"synonyms":[{"name":"infection by Yersinia enterocolitica","type":"exact"},{"name":"infection caused by Yersinia enterocolitica","type":"related"}],"termid":"MONDO:0042370","xrefs":{"Monarch":{"xref_id":"0042370"}}}


id: MONDO:0003429
data:
  {"annotated_genes":["SJAG_03429"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009050"}]},"cv_name":"mondo","definition":"A hormone producing pituitary gland adenoma, associated with a hormonal syndrome.","definition_xrefs":["NCIT:C8388"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functioning pituitary gland neoplasm","termid":"MONDO:0003604"},{"relation_name":"is_a","term_name":"pituitary gland adenoma","termid":"MONDO:0006373"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03429":null},"genotype_count":0,"is_obsolete":false,"name":"functioning pituitary gland adenoma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0854486","GARD:21389","DOID:5395","MEDGEN:163135","Orphanet:314753"],"synonyms":[{"name":"endocrine active pituitary adenoma","type":"exact"},{"name":"functioning adenoma of pituitary","type":"exact"},{"name":"functioning adenoma of pituitary gland","type":"exact"},{"name":"functioning adenoma of the pituitary","type":"exact"},{"name":"functioning adenoma of the pituitary gland","type":"exact"},{"name":"functioning pituitary adenoma","type":"exact"},{"name":"functioning pituitary gland adenoma","type":"exact"},{"name":"functioning pituitary gland adenoma (benign)","type":"exact"},{"name":"secreting pituitary adenoma","type":"exact"},{"name":"secretory adenoma of pituitary","type":"exact"},{"name":"secretory adenoma of pituitary gland","type":"exact"},{"name":"secretory adenoma of the pituitary","type":"exact"},{"name":"secretory adenoma of the pituitary gland","type":"exact"},{"name":"secretory pituitary adenoma","type":"exact"},{"name":"secretory pituitary gland adenoma","type":"exact"}],"termid":"MONDO:0003429","terms_by_termid":{"MONDO:0009050":null},"xrefs":{"Monarch":{"xref_id":"0003429"}}}


id: MONDO:0044880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pancreatic exocrine neoplasm","termid":"MONDO:0021076"}],"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":"cystic tumor of the pancreas","secondary_identifiers":["NCIT:C200227","ONCOTREE:PACT"],"termid":"MONDO:0044880","xrefs":{"Monarch":{"xref_id":"0044880"}}}


id: GO:0086086
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transmembrane transfer of a potassium ion by a voltage-gated channel through the plasma membrane of an AV node cardiac muscle cell contributing to the repolarization phase of an action potential. A voltage-gated channel is a channel whose open state is dependent on the voltage across the membrane in which it is embedded.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel activity involved in cardiac muscle cell action potential repolarization","termid":"GO:0086008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"voltage-gated potassium channel activity involved in AV node cell action potential repolarization","synonyms":[{"name":"voltage-gated potassium channel activity involved in AV node cardiac muscle cell action potential repolarization","type":"exact"},{"name":"voltage-gated potassium channel activity involved in atrioventricular node cardiac muscle cell action potential","type":"exact"}],"termid":"GO:0086086"}


id: MONDO:1011436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Histiocytosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoid system disorder, non-human animal","termid":"MONDO:1011330"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histiocytosis, non-human animal","secondary_identifiers":["OMIA:000474"],"termid":"MONDO:1011436","xrefs":{"Monarch":{"xref_id":"1011436"}}}


id: MONDO:0000153
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital cardiac defect in which two heart vessels are reversed (transposed).","definition_xrefs":["NCIT:C84742"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital heart malformation","termid":"MONDO:0019512"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transposition of the great arteries","secondary_identifiers":["MEDGEN:21245","MESH:D014188","NANDO:2200258","icd11.foundation:429190257","GARD:7795","UMLS:C0040761","Orphanet:216675"],"synonyms":[{"name":"TGA","type":"exact"},{"name":"TGV","type":"exact"},{"name":"complete transposition","type":"exact"},{"name":"great vessels transposition","type":"exact"},{"name":"transposition of great vessels","type":"exact"},{"name":"transposition of the great vessels","type":"exact"}],"termid":"MONDO:0000153","xrefs":{"Monarch":{"xref_id":"0000153"}}}


id: PR:O74503
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spp27 gene.","definition_xrefs":["UniProtKB:O74503","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":"upstream activation factor subunit spp27 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC285.17","synonyms":[{"name":"Spom972h-spp27","type":"exact"},{"name":"p27 (Schizosaccharomyces pombe 972h-)","type":"broad"},{"name":"p30 (Schizosaccharomyces pombe 972h-)","type":"broad"},{"name":"upstream activation factor 27 KDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"upstream activation factor 30 KDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"upstream activation factor subunit uaf30 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74503"}


id: PBO:0119982
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 3148","termid":"PBO:0119982"}


id: PR:Q9Y7K1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A peptide methionine sulfoxide reductase MsrB that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02634"],"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 C216.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC216.04c","secondary_identifiers":["UniProtKB:Q9Y7K1"],"synonyms":[{"name":"Spom972h-msrB","type":"exact"}],"termid":"PR:Q9Y7K1"}


id: GO:0140169
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 3alpha-hydroxysteroid + NAD(P)+ = a 3-oxosteroid + NAD(P)H + H+.","definition_xrefs":["EC:1.1.1.357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0033764"}],"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:0003674","GO:0016491"],"is_obsolete":false,"name":"3-alpha-hydroxysteroid 3-dehydrogenase [NAD(P)+] activity","termid":"GO:0140169"}


id: MONDO:0030878
data:
  {"annotated_genes":["SJAG_01642"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87482],"is_not":false,"summary":null,"term":"MONDO:0030878"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01642":null},"genotype_count":0,"is_obsolete":false,"name":"Kaya-Barakat-Masson syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619125","MEDGEN:1725501","GARD:18537","UMLS:C5436856"],"synonyms":[{"name":"KABAMAS","type":"exact"}],"termid":"MONDO:0030878","terms_by_termid":{"MONDO:0030878":null},"xrefs":{"Monarch":{"xref_id":"0030878"}}}


id: PATO:0002090
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A morphology quality inhering in a tumour by virtue of the bearer's exhbiting the morphological characteristics of a glandular epithelial cell.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphology","termid":"PATO:0000051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adenomatous","termid":"PATO:0002090"}


id: GO:0042277
data:
  {"annotated_genes":["SJAG_01282","SJAG_00326","SJAG_01013","SJAG_03299","SJAG_01488","SJAG_02330","SJAG_01759","SJAG_00840","SJAG_04411","SJAG_03358","SJAG_01909","SJAG_00702","SJAG_02418","SJAG_02208","SJAG_01640","SJAG_03959","SJAG_04996","SJAG_03781","SJAG_03662","SJAG_03729","SJAG_02998","SJAG_03684","SJAG_01840","SJAG_00962"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57073,60536,77297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030942"},{"annotations":[115491],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045015"},{"annotations":[75176,75720,80896],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030943"},{"annotations":[78065,75401,76724,80418,74595,95804,97945,79657,75463,77322],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008139"},{"annotations":[75451],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005052"},{"annotations":[72392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005053"},{"annotations":[92241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033328"},{"annotations":[74956,118507,75365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005048"},{"annotations":[105887],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010209"}]},"cv_name":"molecular_function","definition":"Binding to a peptide, an organic compound comprising two or more amino acids linked by peptide bonds.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":24,"genes_by_uniquename":{"SJAG_00326":null,"SJAG_00702":null,"SJAG_00840":null,"SJAG_00962":null,"SJAG_01013":null,"SJAG_01282":null,"SJAG_01488":null,"SJAG_01640":null,"SJAG_01759":null,"SJAG_01840":null,"SJAG_01909":null,"SJAG_02208":null,"SJAG_02330":null,"SJAG_02418":null,"SJAG_02998":null,"SJAG_03299":null,"SJAG_03358":null,"SJAG_03662":null,"SJAG_03684":null,"SJAG_03729":null,"SJAG_03781":null,"SJAG_03959":null,"SJAG_04411":null,"SJAG_04996":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"peptide binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0042277","terms_by_termid":{"GO:0005048":null,"GO:0005052":null,"GO:0005053":null,"GO:0008139":null,"GO:0010209":null,"GO:0030942":null,"GO:0030943":null,"GO:0033328":null,"GO:0045015":null}}


id: FYPO:0002474
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 region of a chromosome at which a DNA double-strand break has occurred is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to double-strand break site","termid":"FYPO:0002473"},{"relation_name":"is_a","term_name":"decreased protein localization to chromosome during vegetative growth","termid":"FYPO:0002839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein localization to double-strand break site","synonyms":[{"name":"decreased protein localisation to double-strand break site","type":"exact"},{"name":"decreased protein localization to DSB site","type":"exact"},{"name":"decreased protein localization to double-strand break site during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to double-strand break site during vegetative growth","type":"exact"},{"name":"decreased protein localization to site of double-strand break","type":"exact"},{"name":"reduced protein localization to double-strand break site","type":"exact"}],"termid":"FYPO:0002474"}


