# terms

id: MONDO:0018278
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"},{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy","termid":"MONDO:0018276"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005066","MONDO:0005336","MONDO:0024322"],"is_obsolete":false,"name":"congenital muscular dystrophy with intellectual disability","secondary_identifiers":["UMLS:C5190846","Orphanet:370968","GARD:17606","MEDGEN:1683413"],"synonyms":[{"name":"CMD with intellectual disability","type":"exact"},{"name":"CMD-MR","type":"exact"}],"termid":"MONDO:0018278","xrefs":{"Monarch":{"xref_id":"0018278"}}}


id: PBO:0073248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"septin 2","termid":"PBO:0073248"}


id: MONDO:0016233
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare lymphatic system malformation (obsolete MONDO:0016233)","secondary_identifiers":["Orphanet:211255","NANDO:1200881"],"termid":"MONDO:0016233","xrefs":{"Monarch":{"xref_id":"0016233"}}}


id: PBO:0070461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L4 pseudogene 4","termid":"PBO:0070461"}


id: PBO:0079591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 D3 pseudogene 3","termid":"PBO:0079591"}


id: PBO:0086867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative serine/threonine protein kinase; regulates spermine uptake; involved in polyamine transport; possible mitochondrial protein; PTK1 has a paralog, PTK2, that arose from the whole genome duplication","termid":"PBO:0086867"}


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: FYPO:0001516
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 mercury ions than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0001985","FYPO:0002682","FYPO:0005447","FYPO:0000003"],"is_obsolete":false,"name":"resistance to mercury","synonyms":[{"name":"resistance to mercury during mitotic cell cycle","type":"related"},{"name":"resistance to mercury during vegetative growth","type":"exact"},{"name":"resistance to mercury ion","type":"exact"},{"name":"resistance to mercury ions","type":"exact"},{"name":"resistant to mercury","type":"exact"}],"termid":"FYPO:0001516"}


id: MONDO:0020649
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma that arises from the penis. It is characterized by a papillary growth pattern, hyperkeratosis and parakeratosis. Koilocytotic atypia is present. Human papillomavirus types 16 and 6 have been identified in some cases.","definition_xrefs":["NCIT:C6981"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary carcinoma of the penis","termid":"MONDO:0004433"},{"relation_name":"is_a","term_name":"human papillomavirus-related penile squamous cell carcinoma","termid":"MONDO:0020656"}],"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":"warty carcinoma of the penis","secondary_identifiers":["UMLS:C1337009","ONCOTREE:WPSCC","MEDGEN:234997"],"synonyms":[{"name":"condylomatous carcinoma of penis","type":"exact"},{"name":"condylomatous carcinoma of the penis","type":"exact"},{"name":"condylomatous penile squamous cell carcinoma","type":"exact"},{"name":"condylomatous squamous cell carcinoma of penis","type":"exact"},{"name":"condylomatous squamous cell carcinoma of the penis","type":"exact"},{"name":"squamous cell carcinoma of penis, condylomatous type","type":"exact"},{"name":"squamous cell carcinoma of penis, warty type","type":"exact"},{"name":"squamous cell carcinoma of the penis, condylomatous type","type":"exact"},{"name":"squamous cell carcinoma of the penis, warty type","type":"exact"},{"name":"warty carcinoma of penis","type":"exact"},{"name":"warty carcinoma of the penis","type":"exact"},{"name":"warty penile squamous cell carcinoma","type":"exact"},{"name":"warty squamous cell carcinoma of penis","type":"exact"},{"name":"warty squamous cell carcinoma of the penis","type":"exact"}],"termid":"MONDO:0020649","xrefs":{"Monarch":{"xref_id":"0020649"}}}


id: PBO:0060178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metaxin 2","termid":"PBO:0060178"}


id: PBO:0043655
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COPI coat complex subunit zeta 1","termid":"PBO:0043655"}


id: GO:1903053
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of extracellular matrix organization.","definition_xrefs":["GO_REF:0000058","GOC:rl","GOC:BHF","GOC:TermGenie","PMID:22357537"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"extracellular matrix organization","termid":"GO:0030198"}],"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 extracellular matrix organization","synonyms":[{"name":"regulation of extracellular matrix organisation","type":"exact"},{"name":"regulation of extracellular matrix organization and biogenesis","type":"related"}],"termid":"GO:1903053"}


id: GO:1903193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of sesquarterpene.","definition_xrefs":["PMID:21627333","GOC:mengo_curators","GO_REF:0000068","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terpene biosynthetic process","termid":"GO:0046246"},{"relation_name":"is_a","term_name":"sesquarterpene metabolic process","termid":"GO:1903192"}],"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":"sesquarterpene biosynthetic process","synonyms":[{"name":"sesquarterpene anabolism","type":"exact"},{"name":"sesquarterpene biosynthesis","type":"exact"},{"name":"sesquarterpene formation","type":"exact"},{"name":"sesquarterpene synthesis","type":"exact"}],"termid":"GO:1903193"}


id: MONDO:0018845
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Focal myositis is a rare inflammatory myopathy characterized by a localized swelling of skeletal muscle that is usually located in the lower extremities.","definition_xrefs":["Orphanet:48918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired idiopathic inflammatory myopathy","termid":"MONDO:0020122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"focal myositis","secondary_identifiers":["SCTID:240119009","UMLS:C0409988","MEDGEN:592748","ICD9:729.1","icd11.foundation:708931518","GARD:18837"],"synonyms":[{"name":"focal nodular myositis","type":"exact"},{"name":"inflammatory pseudotumor of skeletal muscle","type":"exact"}],"termid":"MONDO:0018845","xrefs":{"Monarch":{"xref_id":"0018845"}}}


id: GO:0047779
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + citrate + CoA = (3S)-citryl-CoA + ADP + H+ + phosphate.","definition_xrefs":["RHEA:21472","EC:6.2.1.18"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-thiol ligase activity","termid":"GO:0016878"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"citrate-CoA ligase activity","secondary_identifiers":["KEGG_REACTION:R01322","MetaCyc:CITRATE--COA-LIGASE-RXN"],"synonyms":[{"name":"citrate thiokinase activity","type":"related"},{"name":"citrate:CoA ligase (ADP-forming)","type":"related"},{"name":"citrate:CoA ligase activity","type":"related"},{"name":"citryl-CoA synthetase activity","type":"related"}],"termid":"GO:0047779"}


id: MONDO:0019172
data:
  {"annotated_genes":["SJAG_03677"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89034],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014937"}]},"cv_name":"mondo","definition":"Aniridia is a congenital ocular malformation characterized by the complete or partial absence of the iris. It can be isolated or part of a syndrome (isolated and syndromic aniridia).","definition_xrefs":["Orphanet:77"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iris disorder","termid":"MONDO:0002289"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03677":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"aniridia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D015783","SCTID:69278003","NCIT:C84563","DOID:12271","ICD9:743.45","icd11.foundation:970699895","NANDO:1201001","UMLS:C0003076","MedDRA:10002532","MEDGEN:1941"],"synonyms":[{"name":"aplasia of iris","type":"exact"}],"termid":"MONDO:0019172","terms_by_termid":{"MONDO:0014937":null},"xrefs":{"Monarch":{"xref_id":"0019172"}}}


id: PBO:0002535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pex19 protein (predicted)","termid":"PBO:0002535"}


id: MONDO:0043678
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder consisting of the presence a chromosome rearrangement in which a segment has been turned through 180 degrees (inverted), and inserted back into its original location on the chromosome.","definition_xrefs":["NCIT:C6827"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosomal disorder","termid":"MONDO:0019040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome inversion disorder","secondary_identifiers":["MEDGEN:7145","MESH:D007446","UMLS:C0021943"],"synonyms":[{"name":"Inversions, chromosomal","type":"related"},{"name":"Inversions, chromosome","type":"related"},{"name":"chromosomal Inversions","type":"related"},{"name":"chromosomal inversion","type":"related"},{"name":"chromosome Inversions","type":"related"},{"name":"inv","type":"related"},{"name":"inversion","type":"related"},{"name":"inversion, chromosomal","type":"related"},{"name":"inversion, chromosome","type":"related"},{"name":"inverted chromosome","type":"related"}],"termid":"MONDO:0043678","xrefs":{"Monarch":{"xref_id":"0043678"}}}


id: PBO:0054784
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 2197","termid":"PBO:0054784"}


id: GO:0045267
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The hexamer that possesses the catalytic activity of the mitochondrial hydrogen-transporting ATP synthase.","definition_xrefs":["PMID:10838056"],"gene_count":0,"genotype_count":0,"name":"obsolete proton-transporting ATP synthase, catalytic core (obsolete GO:0045267)","synonyms":[{"name":"hydrogen-transporting ATP synthase, catalytic core","type":"exact"}],"termid":"GO:0045267"}


id: MONDO:0002601
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-seminomatous germ cell tumor characterized by the presence of various tissues which correspond to the different germinal layers (endoderm, mesoderm, and ectoderm). It occurs in the testis, ovary, and extragonadal sites including central nervous system, mediastinum, lung, and stomach. According to the level of differentiation of the tissues which comprise the tumor, teratomas are classified as mature or immature. Mature teratomas are composed of well differentiated, adult-type tissues. Immature teratomas are composed of immature, fetal-type tissues. Testicular teratomas in children follow a benign clinical course. Mature ovarian teratomas without a fetal-type component have an excellent outcome. The prognosis of immature ovarian teratomas is related to the grade and stage of the tumor.","definition_xrefs":["NCIT:C3403"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete germ cell and embryonal cancer (obsolete MONDO:0002510)","termid":"MONDO:0002510"},{"relation_name":"is_a","term_name":"nongerminomatous germ cell tumor","termid":"MONDO:0021656"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"teratoma","secondary_identifiers":["MEDGEN:21097","DOID:3307","ONCOTREE:TT","MESH:D013724","ICDO:9080/1","SCTID:36591000119102","UMLS:C0039538"],"synonyms":[{"name":"teratoma","type":"exact"}],"termid":"MONDO:0002601","xrefs":{"Monarch":{"xref_id":"0002601"}}}


id: PBO:0057388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548BC","termid":"PBO:0057388"}


id: MONDO:0045044
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease or disorder that involves the ligament.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder","termid":"MONDO:0002081"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ligament disorder","secondary_identifiers":["MEDGEN:538235","SCTID:60492000","UMLS:C0263976"],"synonyms":[{"name":"disease of ligament","type":"exact"},{"name":"disease or disorder of ligament","type":"exact"},{"name":"disorder of ligament","type":"exact"},{"name":"ligament disease or disorder","type":"exact"}],"termid":"MONDO:0045044","xrefs":{"Monarch":{"xref_id":"0045044"}}}


id: PBO:0070869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L15","termid":"PBO:0070869"}


id: MONDO:0859304
data:
  {"annotated_genes":["SJAG_01806"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87618],"is_not":false,"summary":null,"term":"MONDO:0859304"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01806":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5774240","OMIM:620089","MEDGEN:1824013"],"termid":"MONDO:0859304","terms_by_termid":{"MONDO:0859304":null},"xrefs":{"Monarch":{"xref_id":"0859304"}}}


id: GO:0030465
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete autophagic death (sensu Fungi) (obsolete GO:0030465)","synonyms":[{"name":"autophagic death (sensu Fungi)","type":"exact"}],"termid":"GO:0030465"}


id: GO:0072028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the nephron are generated and organized. A nephron is the functional unit of the kidney.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"kidney morphogenesis","termid":"GO:0060993"},{"relation_name":"part_of","term_name":"nephron development","termid":"GO:0072006"}],"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":"nephron morphogenesis","termid":"GO:0072028"}


id: GO:1902667
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of axon guidance.","definition_xrefs":["GO_REF:0000058","GOC:hjd","GOC:TermGenie","PMID:23006775"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neuron projection development","termid":"GO:0010975"},{"relation_name":"is_a","term_name":"regulation of chemotaxis","termid":"GO:0050920"},{"relation_name":"regulates","term_name":"axon guidance","termid":"GO:0007411"}],"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 axon guidance","synonyms":[{"name":"regulation of axon chemotaxis","type":"related"},{"name":"regulation of axon growth cone guidance","type":"narrow"},{"name":"regulation of axon pathfinding","type":"exact"}],"termid":"GO:1902667"}


id: PBO:0086913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative Y' element ATP-dependent helicase; YLL066C is not an essential gene","termid":"PBO:0086913"}


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


id: PBO:0053337
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 200","termid":"PBO:0053337"}


id: PBO:0071356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 15","termid":"PBO:0071356"}


id: PBO:0048371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GAR1 ribonucleoprotein","termid":"PBO:0048371"}


id: GO:0008531
data:
  {"annotated_genes":["SJAG_04845"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74606],"is_not":false,"summary":null,"term":"GO:0008531"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + riboflavin = ADP + FMN + 2 H+.","definition_xrefs":["EC:2.7.1.26","RHEA:14357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04845":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016301","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"riboflavin kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:RIBOFLAVINKIN-RXN","KEGG_REACTION:R00549","Reactome:R-HSA-196964"],"synonyms":[{"name":"ATP:riboflavin 5'-phosphotransferase activity","type":"related"},{"name":"FK","type":"related"},{"name":"flavokinase activity","type":"related"},{"name":"riboflavin kinase (phosphorylating)","type":"related"},{"name":"riboflavine kinase activity","type":"related"}],"termid":"GO:0008531","terms_by_termid":{"GO:0008531":null}}


id: PBO:0003895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongator complex subunit Iki1 (predicted)","termid":"PBO:0003895"}


id: MONDO:0013508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myopia","termid":"MONDO:0001384"}],"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":"myopia 19, autosomal dominant","secondary_identifiers":["UMLS:C3151410","MEDGEN:462760","OMIM:613969"],"synonyms":[{"name":"MYP19","type":"exact"},{"name":"myopia 19, autosomal dominant","type":"exact"}],"termid":"MONDO:0013508","xrefs":{"Monarch":{"xref_id":"0013508"}}}


id: PR:Q9UUK3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An OTU domain-containing protein 6B that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin thioesterase otu2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1952.03","secondary_identifiers":["UniProtKB:Q9UUK3"],"synonyms":[{"name":"OTU domain-containing protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPAC1952.03","type":"related"},{"name":"Spom972h-OTUD6B","type":"exact"}],"termid":"PR:Q9UUK3"}


id: MONDO:0003445
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenoma that arises from the extrahepatic bile ducts. It is classified as papillary, tubular, or tubulopapillary.","definition_xrefs":["NCIT:C5857"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bile duct adenoma","termid":"MONDO:0006108"},{"relation_name":"is_a","term_name":"extrahepatic bile duct neoplasm","termid":"MONDO:0021385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"extrahepatic bile duct adenoma","secondary_identifiers":["MEDGEN:233098","DOID:5438","UMLS:C1331534"],"synonyms":[{"name":"adenoma of extrahepatic bile duct","type":"exact"},{"name":"adenoma of the extrahepatic bile duct","type":"exact"},{"name":"extrahepatic bile duct adenoma","type":"exact"}],"termid":"MONDO:0003445","xrefs":{"Monarch":{"xref_id":"0003445"}}}


id: PBO:0087632
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the EGO/GSE complex; the vacuolar/endosomal membrane associated EGO/GSE complex regulates exit from rapamycin-induced growth arrest, stimulating microautophagy and sorting of Gap1p from the endosome to the plasma membrane; essential for the integrity and function of EGO; gene exhibits synthetic genetic interaction with MSS4","termid":"PBO:0087632"}


id: GO:0150078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of neuroinflammatory response.","definition_xrefs":["GOC:bc","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of inflammatory response","termid":"GO:0050729"},{"relation_name":"is_a","term_name":"regulation of neuroinflammatory response","termid":"GO:0150077"},{"relation_name":"positively_regulates","term_name":"neuroinflammatory response","termid":"GO:0150076"}],"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 neuroinflammatory response","termid":"GO:0150078"}


id: GO:0060563
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which epiblast cells acquire specialized features of neuroepithelial cells.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"columnar/cuboidal epithelial cell differentiation","termid":"GO:0002065"}],"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":"neuroepithelial cell differentiation","termid":"GO:0060563"}


id: GO:0045209
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Leptomycin B-sensitive movement of a MAPK phosphatase from the nucleus to the cytoplasm.","definition_xrefs":["GOC:ebc"],"gene_count":0,"genotype_count":0,"name":"obsolete MAPK phosphatase export from nucleus, leptomycin B sensitive (obsolete GO:0045209)","synonyms":[{"name":"MAPK phosphatase export from cell nucleus, leptomycin B sensitive","type":"exact"},{"name":"MAPK phosphatase export out of nucleus, leptomycin B sensitive","type":"exact"},{"name":"MAPK phosphatase transport from nucleus to cytoplasm, leptomycin B sensitive","type":"exact"},{"name":"MAPK phosphatase-nucleus export, leptomycin B sensitive","type":"exact"},{"name":"leptomycin B-sensitive MAPK phosphatase export out of nucleus","type":"exact"},{"name":"leptomycin B-sensitive MAPK phosphatase transport from nucleus to cytoplasm","type":"exact"},{"name":"leptomycin B-sensitive MAPK phosphatase-nucleus export","type":"exact"}],"termid":"GO:0045209"}


id: PBO:0039914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho guanine nucleotide exchange factor 12","termid":"PBO:0039914"}


id: FYPO:0002351
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 stress granule disassembly is abnormal.","definition_xrefs":["PMID:21098141","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular component assembly during vegetative growth","termid":"FYPO:0001354"},{"relation_name":"is_a","term_name":"abnormal protein complex organization during vegetative growth","termid":"FYPO:0007402"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal stress granule disassembly","synonyms":[{"name":"abnormal cytoplasmic stress granule disassembly","type":"exact"},{"name":"abnormal stress granule disassembly during mitotic cell cycle","type":"related"},{"name":"abnormal stress granule disassembly during vegetative growth","type":"exact"}],"termid":"FYPO:0002351"}


id: PBO:0081103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZEB2 antisense RNA 1","termid":"PBO:0081103"}


id: PBO:0088386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER protein disulfide isomerase","termid":"PBO:0088386"}


id: PBO:0066192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBM12B antisense RNA 1","termid":"PBO:0066192"}


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


id: FYPO:0000855
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 nucleosome positioning in regions of heterochromatin is abnormal. Nucleosome positioning is the ordering of successions of nucleosomes into regular arrays so that nucleosomes are positioned at defined distances from one another.","definition_xrefs":["PomBase:mah","GO:0016584"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nucleosome positioning","termid":"FYPO:0000853"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000641","FYPO:0000002"],"is_obsolete":false,"name":"abnormal nucleosome positioning in heterochromatin","synonyms":[{"name":"abnormal nucleosome occupancy in heterochromatin","type":"related"},{"name":"abnormal nucleosome positioning in heterochromatin during mitotic cell cycle","type":"related"},{"name":"abnormal nucleosome positioning in heterochromatin during vegetative growth","type":"exact"},{"name":"abnormal nucleosome spacing in heterochromatin","type":"exact"}],"termid":"FYPO:0000855"}


id: PBO:0089271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-type ATPase V1 subunit D","termid":"PBO:0089271"}


id: PBO:0035812
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H2A_phosphorylation_at_tRNA_genes_during_vegetative_growth","termid":"PBO:0035812"}


id: GO:0004261
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of peptide bonds. Specificity similar to chymotrypsin C.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cathepsin G activity (obsolete GO:0004261)","synonyms":[{"name":"cathepsin G activity","type":"exact"},{"name":"chymotrypsin-like proteinase activity","type":"related"},{"name":"neutral proteinase activity","type":"related"}],"termid":"GO:0004261"}


id: PBO:0057906
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3609","termid":"PBO:0057906"}


id: GO:0001093
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a general RNA polymerase II transcription factor of the TFIIB class, one of the factors involved in formation of the preinitiation complex (PIC) by RNA polymerase II.","definition_xrefs":["PMID:16858867","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II general transcription initiation factor binding","termid":"GO:0001091"}],"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:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"TFIIB-class transcription factor binding","termid":"GO:0001093"}


id: PBO:0091187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase F0 subunit 6","termid":"PBO:0091187"}


id: PBO:0083367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; overlaps the verified ORF KAP95/YLR347C","termid":"PBO:0083367"}


id: PBO:0072419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 24","termid":"PBO:0072419"}


id: PBO:0058875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 10226","termid":"PBO:0058875"}


id: MONDO:0007692
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hairy ears (obsolete MONDO:0007692)","secondary_identifiers":["SCTID:89000008","MESH:C562484","OMIM:139500"],"synonyms":[{"name":"hairy ears","type":"exact"},{"name":"hypertrichosis pinnae auris","type":"related"}],"termid":"MONDO:0007692","xrefs":{"Monarch":{"xref_id":"0007692"}}}


id: PBO:0040796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"basic helix-loop-helix family member a9","termid":"PBO:0040796"}


id: PBO:0087287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Signal transducing MEK kinase; involved in pheromone response and pseudohyphal/invasive growth pathways where it phosphorylates Ste7p, and the high osmolarity response pathway, via phosphorylation of Pbs2p; regulated by Ste20p and Ste50p; protein abundance increases in response to DNA replication stress","termid":"PBO:0087287"}


id: MONDO:0859332
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complex cortical dysplasia with other brain malformations","termid":"MONDO:0000904"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cortical dysplasia, complex, with other brain malformations 11","secondary_identifiers":["MEDGEN:1824043","UMLS:C5774270","OMIM:620156"],"termid":"MONDO:0859332","xrefs":{"Monarch":{"xref_id":"0859332"}}}


id: GO:2000456
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of T-helper 17 cell extravasation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of CD8-positive, alpha-beta T cell extravasation","termid":"GO:2000450"},{"relation_name":"is_a","term_name":"regulation of T-helper 17 cell extravasation","termid":"GO:2000455"},{"relation_name":"negatively_regulates","term_name":"T-helper 17 cell extravasation","termid":"GO:0035699"}],"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 T-helper 17 cell extravasation","termid":"GO:2000456"}


id: GO:0000972
data:
  {"annotated_genes":["SJAG_00298","SJAG_04379","SJAG_02757","SJAG_03299","SJAG_01374","SJAG_03986","SJAG_04148","SJAG_04347"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75514,76904,78485,82211],"is_not":false,"summary":null,"term":"GO:0000972"},{"annotations":[77355,71644,72153,76131],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000973"}]},"cv_name":"biological_process","definition":"The chromosome organization process in which the DNA sequence containing a gene transcribed by RNA polymerase II is maintained in a specific location at the nuclear periphery. In S. cerevisiae, this process involves cis-acting DNA sequences such as the TATA box and upstream activating sequence (UAS) elements, trans-acting transcriptional activators, and also the 3'-UTR of the transcript.","definition_xrefs":["GOC:krc","PMID:18614049"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome organization","termid":"GO:0051276"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00298":null,"SJAG_01374":null,"SJAG_02757":null,"SJAG_03299":null,"SJAG_03986":null,"SJAG_04148":null,"SJAG_04347":null,"SJAG_04379":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"transcription-dependent tethering of RNA polymerase II gene DNA at nuclear periphery","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0000972","terms_by_termid":{"GO:0000972":null,"GO:0000973":null}}


id: MONDO:0015159
data:
  {"annotated_genes":["SJAG_01253","SJAG_03353","SJAG_04619","SJAG_02447","SJAG_01181","SJAG_04110","SJAG_03635","SJAG_02846","SJAG_01926","SJAG_02701","SJAG_02165","SJAG_04038","SJAG_02723","SJAG_03286","SJAG_03067","SJAG_04934","SJAG_04822","SJAG_00993","SJAG_01507","SJAG_03997","SJAG_04825","SJAG_01076","SJAG_03603","SJAG_01540","SJAG_00739","SJAG_05206","SJAG_04429","SJAG_01416","SJAG_01286","SJAG_03597","SJAG_00861","SJAG_02571","SJAG_04509","SJAG_00229","SJAG_03418","SJAG_04396","SJAG_04681","SJAG_05019","SJAG_02774","SJAG_04881","SJAG_02978","SJAG_04165","SJAG_00312","SJAG_05229","SJAG_02254","SJAG_02401","SJAG_00379","SJAG_03066","SJAG_00112","SJAG_00992","SJAG_03024","SJAG_03698","SJAG_04938","SJAG_02342","SJAG_03681","SJAG_04074","SJAG_01111","SJAG_02256","SJAG_03145","SJAG_02238","SJAG_01465","SJAG_05313","SJAG_00414","SJAG_00156","SJAG_00846","SJAG_01831","SJAG_00441","SJAG_01232","SJAG_03453","SJAG_04755","SJAG_03292","SJAG_00796","SJAG_03934","SJAG_00321","SJAG_01653","SJAG_04917","SJAG_05194","SJAG_01806","SJAG_02024","SJAG_03576","SJAG_04213","SJAG_02791","SJAG_04980","SJAG_01067","SJAG_03120","SJAG_01712","SJAG_03664","SJAG_01472","SJAG_01804","SJAG_04003","SJAG_02313","SJAG_02589"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012099"},{"annotations":[86834],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014700"},{"annotations":[87267],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014558"},{"annotations":[87113],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014601"},{"annotations":[88296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013812"},{"annotations":[88777],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010477"},{"annotations":[88376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011365"},{"annotations":[87408],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008879"},{"annotations":[86843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014112"},{"annotations":[86845,86846,86844],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014113"},{"annotations":[86850,86849,86851],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014114"},{"annotations":[87230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014529"},{"annotations":[87100],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044701"},{"annotations":[87007],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010221"},{"annotations":[87995,87996,87997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013256"},{"annotations":[87813],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007617"},{"annotations":[88548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032912"},{"annotations":[87453],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014838"},{"annotations":[87947,87946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032702"},{"annotations":[87121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014609"},{"annotations":[87316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012399"},{"annotations":[88632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011402"},{"annotations":[87379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007387"},{"annotations":[88894],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010370"},{"annotations":[87519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012555"},{"annotations":[87984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013864"},{"annotations":[88091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957921"},{"annotations":[87022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009026"},{"annotations":[87954],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0034106"},{"annotations":[88843],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032808"},{"annotations":[87756],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013578"},{"annotations":[89060],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044646"},{"annotations":[88784],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007621"},{"annotations":[88247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011640"},{"annotations":[86913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060627"},{"annotations":[87109,87110],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014602"},{"annotations":[88805],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032787"},{"annotations":[87727,87726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0026763"},{"annotations":[88854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030886"},{"annotations":[87116],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014605"},{"annotations":[87749],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024567"},{"annotations":[88553],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044319"},{"annotations":[88121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013819"},{"annotations":[88122,88123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013820"},{"annotations":[88124,88125],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013821"},{"annotations":[87215,87216],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030912"},{"annotations":[88465],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014336"},{"annotations":[88071,88072],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011053"},{"annotations":[89116],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009622"},{"annotations":[87670,87671],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009479"},{"annotations":[87713],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007843"},{"annotations":[88750],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010465"},{"annotations":[87330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009514"},{"annotations":[87844,87845],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014716"},{"annotations":[87737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014757"},{"annotations":[87808],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012516"},{"annotations":[87492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014273"},{"annotations":[88684],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015012"},{"annotations":[87798],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013563"},{"annotations":[88749],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010466"},{"annotations":[87793],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014165"},{"annotations":[87313],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009736"},{"annotations":[88732],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014466"},{"annotations":[87358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060502"},{"annotations":[86885],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009485"},{"annotations":[87729,87730],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014751"},{"annotations":[87375],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011213"},{"annotations":[87108,87107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060568"},{"annotations":[87959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014886"},{"annotations":[87644],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014238"},{"annotations":[87193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054636"},{"annotations":[89085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010035"},{"annotations":[88733],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010574"},{"annotations":[88920,88919,88921],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010355"},{"annotations":[88517],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010286"},{"annotations":[87462],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014848"},{"annotations":[87952],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014881"},{"annotations":[87473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014296"},{"annotations":[88003],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009910"},{"annotations":[87439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008684"},{"annotations":[87090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010485"},{"annotations":[86870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010655"},{"annotations":[87983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010306"},{"annotations":[87141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010496"},{"annotations":[89035,89036],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014936"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome","termid":"MONDO:0019042"}],"gene_count":92,"genes_by_uniquename":{"SJAG_00112":null,"SJAG_00156":null,"SJAG_00229":null,"SJAG_00312":null,"SJAG_00321":null,"SJAG_00379":null,"SJAG_00414":null,"SJAG_00441":null,"SJAG_00739":null,"SJAG_00796":null,"SJAG_00846":null,"SJAG_00861":null,"SJAG_00992":null,"SJAG_00993":null,"SJAG_01067":null,"SJAG_01076":null,"SJAG_01111":null,"SJAG_01181":null,"SJAG_01232":null,"SJAG_01253":null,"SJAG_01286":null,"SJAG_01416":null,"SJAG_01465":null,"SJAG_01472":null,"SJAG_01507":null,"SJAG_01540":null,"SJAG_01653":null,"SJAG_01712":null,"SJAG_01804":null,"SJAG_01806":null,"SJAG_01831":null,"SJAG_01926":null,"SJAG_02024":null,"SJAG_02165":null,"SJAG_02238":null,"SJAG_02254":null,"SJAG_02256":null,"SJAG_02313":null,"SJAG_02342":null,"SJAG_02401":null,"SJAG_02447":null,"SJAG_02571":null,"SJAG_02589":null,"SJAG_02701":null,"SJAG_02723":null,"SJAG_02774":null,"SJAG_02791":null,"SJAG_02846":null,"SJAG_02978":null,"SJAG_03024":null,"SJAG_03066":null,"SJAG_03067":null,"SJAG_03120":null,"SJAG_03145":null,"SJAG_03286":null,"SJAG_03292":null,"SJAG_03353":null,"SJAG_03418":null,"SJAG_03453":null,"SJAG_03576":null,"SJAG_03597":null,"SJAG_03603":null,"SJAG_03635":null,"SJAG_03664":null,"SJAG_03681":null,"SJAG_03698":null,"SJAG_03934":null,"SJAG_03997":null,"SJAG_04003":null,"SJAG_04038":null,"SJAG_04074":null,"SJAG_04110":null,"SJAG_04165":null,"SJAG_04213":null,"SJAG_04396":null,"SJAG_04429":null,"SJAG_04509":null,"SJAG_04619":null,"SJAG_04681":null,"SJAG_04755":null,"SJAG_04822":null,"SJAG_04825":null,"SJAG_04881":null,"SJAG_04917":null,"SJAG_04934":null,"SJAG_04938":null,"SJAG_04980":null,"SJAG_05019":null,"SJAG_05194":null,"SJAG_05206":null,"SJAG_05229":null,"SJAG_05313":null},"genotype_count":0,"is_obsolete":false,"name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:19832","MEDGEN:1826158","Orphanet:102283","UMLS:C5680372"],"synonyms":[{"name":"MCA/MR","type":"exact"},{"name":"multiple congenital anomalies-intellectual disability with or without dysmorphism","type":"exact"},{"name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","type":"exact"}],"termid":"MONDO:0015159","terms_by_termid":{"MONDO:0007387":null,"MONDO:0007617":null,"MONDO:0007621":null,"MONDO:0007843":null,"MONDO:0008684":null,"MONDO:0008879":null,"MONDO:0009026":null,"MONDO:0009479":null,"MONDO:0009485":null,"MONDO:0009514":null,"MONDO:0009622":null,"MONDO:0009736":null,"MONDO:0009910":null,"MONDO:0010035":null,"MONDO:0010221":null,"MONDO:0010286":null,"MONDO:0010306":null,"MONDO:0010355":null,"MONDO:0010370":null,"MONDO:0010465":null,"MONDO:0010466":null,"MONDO:0010477":null,"MONDO:0010485":null,"MONDO:0010496":null,"MONDO:0010574":null,"MONDO:0010655":null,"MONDO:0011053":null,"MONDO:0011213":null,"MONDO:0011365":null,"MONDO:0011402":null,"MONDO:0011640":null,"MONDO:0012099":null,"MONDO:0012399":null,"MONDO:0012516":null,"MONDO:0012555":null,"MONDO:0013256":null,"MONDO:0013563":null,"MONDO:0013578":null,"MONDO:0013812":null,"MONDO:0013819":null,"MONDO:0013820":null,"MONDO:0013821":null,"MONDO:0013864":null,"MONDO:0014112":null,"MONDO:0014113":null,"MONDO:0014114":null,"MONDO:0014165":null,"MONDO:0014238":null,"MONDO:0014273":null,"MONDO:0014296":null,"MONDO:0014336":null,"MONDO:0014466":null,"MONDO:0014529":null,"MONDO:0014558":null,"MONDO:0014601":null,"MONDO:0014602":null,"MONDO:0014605":null,"MONDO:0014609":null,"MONDO:0014700":null,"MONDO:0014716":null,"MONDO:0014751":null,"MONDO:0014757":null,"MONDO:0014838":null,"MONDO:0014848":null,"MONDO:0014881":null,"MONDO:0014886":null,"MONDO:0014936":null,"MONDO:0015012":null,"MONDO:0024567":null,"MONDO:0026763":null,"MONDO:0030886":null,"MONDO:0030912":null,"MONDO:0032702":null,"MONDO:0032787":null,"MONDO:0032808":null,"MONDO:0032912":null,"MONDO:0034106":null,"MONDO:0044319":null,"MONDO:0044646":null,"MONDO:0044701":null,"MONDO:0054636":null,"MONDO:0060502":null,"MONDO:0060568":null,"MONDO:0060627":null,"MONDO:0957921":null},"xrefs":{"Monarch":{"xref_id":"0015159"}}}


id: GO:0048511
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process pertinent to the generation and maintenance of rhythms in the physiology of an organism.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological_process","termid":"GO:0008150"}],"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":"rhythmic process","synonyms":[{"name":"rhythm","type":"related"}],"termid":"GO:0048511"}


id: PR:O94363
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GTP-binding protein Rheb that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02469","PANTHER:PTHR24070:SF274"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTP-binding protein rhb1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC428.16c","secondary_identifiers":["UniProtKB:O94363"],"synonyms":[{"name":"GTP-binding protein Rheb homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-RHEB","type":"exact"}],"termid":"PR:O94363"}


id: PBO:0058003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3926-2","termid":"PBO:0058003"}


id: PATO:0001590
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's coinciding spatially, partially or wholly with another entity.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"overlap with","synonyms":[{"name":"overlap","type":"exact"}],"termid":"PATO:0001590"}


id: SO:0001044
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A nuclear pseudogene of either coding or non-coding mitochondria derived sequence.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non_processed_pseudogene","termid":"SO:0001760"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear_mt_pseudogene","secondary_identifiers":["http://en.wikipedia.org/wiki/Numt"],"synonyms":[{"name":"NUMT","type":"exact"},{"name":"nuclear mitochondrial pseudogene","type":"exact"},{"name":"nuclear mt pseudogene","type":"exact"}],"termid":"SO:0001044"}


id: MONDO:0000058
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete melanoma, cutaneous malignant (obsolete MONDO:0000058)","termid":"MONDO:0000058","xrefs":{"Monarch":{"xref_id":"0000058"}}}


id: GO:0002657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of tolerance induction to nonself antigen.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of tolerance induction dependent upon immune response","termid":"GO:0002654"},{"relation_name":"is_a","term_name":"regulation of tolerance induction to nonself antigen","termid":"GO:0002655"},{"relation_name":"positively_regulates","term_name":"tolerance induction to nonself antigen","termid":"GO:0002462"}],"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 tolerance induction to nonself antigen","synonyms":[{"name":"activation of tolerance induction to nonself antigen","type":"narrow"},{"name":"stimulation of tolerance induction to nonself antigen","type":"narrow"},{"name":"up regulation of tolerance induction to nonself antigen","type":"exact"},{"name":"up-regulation of tolerance induction to nonself antigen","type":"exact"},{"name":"upregulation of tolerance induction to nonself antigen","type":"exact"}],"termid":"GO:0002657"}


id: MONDO:0006774
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Three or more consecutive spontaneous abortions.","definition_xrefs":["MESH:D000026"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive system disorder","termid":"MONDO:0005039"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"habitual spontaneous abortion","secondary_identifiers":["MEDGEN:1259","SCTID:102878001","UMLS:C0000809","MedDRA:10062935","EFO:1000954"],"termid":"MONDO:0006774","xrefs":{"Monarch":{"xref_id":"0006774"}}}


id: PBO:0108562
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mmi1 And Mei2-associated RNA","termid":"PBO:0108562"}


id: MONDO:1010223
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Prostate cancer that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive system disorder, non-human animal","termid":"MONDO:1011354"},{"relation_name":"is_a","term_name":"cancer, non-human animal","termid":"MONDO:1011828"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostate cancer, non-human animal","secondary_identifiers":["OMIA:002335"],"termid":"MONDO:1010223","xrefs":{"Monarch":{"xref_id":"1010223"}}}


id: GO:1901231
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of non-canonical Wnt signaling pathway via JNK cascade.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of non-canonical Wnt signaling pathway via JNK cascade (obsolete GO:1901231)","synonyms":[{"name":"activation of non-canonical Wnt receptor signaling pathway via JNK cascade","type":"narrow"},{"name":"activation of non-canonical Wnt receptor signalling pathway via JNK cascade","type":"narrow"},{"name":"positive regulation of non-canonical Wnt receptor signaling pathway via JNK cascade","type":"exact"},{"name":"positive regulation of non-canonical Wnt receptor signalling pathway via JNK cascade","type":"exact"},{"name":"positive regulation of non-canonical Wnt-activated signaling pathway via JNK cascade","type":"exact"},{"name":"up regulation of non-canonical Wnt receptor signaling pathway via JNK cascade","type":"exact"},{"name":"up regulation of non-canonical Wnt receptor signalling pathway via JNK cascade","type":"exact"},{"name":"up-regulation of non-canonical Wnt receptor signaling pathway via JNK cascade","type":"exact"},{"name":"up-regulation of non-canonical Wnt receptor signalling pathway via JNK cascade","type":"exact"},{"name":"upregulation of non-canonical Wnt receptor signaling pathway via JNK cascade","type":"exact"},{"name":"upregulation of non-canonical Wnt receptor signalling pathway via JNK cascade","type":"exact"}],"termid":"GO:1901231"}


id: GO:0008780
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-3-hydroxytetradecanoyl-[acyl-carrier protein] + UDP-N-acetylglucosamine = [acyl-carrier protein] + UDP-3-O-(3-hydroxytetradecanoyl)-N-acetylglucosamine.","definition_xrefs":["EC:2.3.1.129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acyltransferase activity","termid":"GO:0008374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016746","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"acyl-[acyl-carrier-protein]-UDP-N-acetylglucosamine O-acyltransferase activity","secondary_identifiers":["RHEA:13925","MetaCyc:UDPNACETYLGLUCOSAMACYLTRANS-RXN"],"synonyms":[{"name":"(R)-3-hydroxytetradecanoyl-acyl-carrier-protein:UDP-N-acetylglucosamine 3-O-(3-hydroxytetradecanoyl)transferase activity","type":"related"},{"name":"UDP-N-acetylglucosamine acyltransferase activity","type":"related"},{"name":"acyl-ACP-UDP-N-acetylglucosamine O-acyltransferase activity","type":"exact"},{"name":"acyl-[acyl-carrier protein]-UDP-N-acetylglucosamine O-acyltransferase activity","type":"exact"},{"name":"acyl-acyl-carrier-protein-UDP-N-acetylglucosamine O-acyltransferase","type":"broad"},{"name":"uridine diphosphoacetylglucosamine acyltransferase activity","type":"related"}],"termid":"GO:0008780"}


id: PBO:0063533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDZ and pleckstrin homology domains 1, pseudogene","termid":"PBO:0063533"}


id: PBO:0083775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential nuclear protein; constituent of 66S pre-ribosomal particles; required for maturation of 25S and 5.8S rRNAs; required for maintenance of M1 satellite double-stranded RNA of the L-A virus","termid":"PBO:0083775"}


id: MONDO:0000267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cryptogenic organizing pneumonia (obsolete MONDO:0000267)","termid":"MONDO:0000267","xrefs":{"Monarch":{"xref_id":"0000267"}}}


id: GO:0046553
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-malate + NAD+ = CO2 + NADH + pyruvate.","definition_xrefs":["RHEA:18365"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malate dehydrogenase activity","termid":"GO:0016615"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"D-malate dehydrogenase (decarboxylating) (NAD+) activity","secondary_identifiers":["KEGG_REACTION:R00215","MetaCyc:1.1.1.83-RXN","EC:1.1.1.83"],"synonyms":[{"name":"(R)-malate:NAD+ oxidoreductase (decarboxylating)","type":"related"},{"name":"D-malate dehydrogenase activity","type":"related"},{"name":"D-malic enzyme","type":"related"},{"name":"bifunctional L(+)-tartrate dehydrogenase-D(+)-malate (decarboxylating)","type":"related"}],"termid":"GO:0046553"}


id: GO:0070163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the regulated release of adiponectin from a cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hormone secretion","termid":"GO:0046883"},{"relation_name":"is_a","term_name":"regulation of protein secretion","termid":"GO:0050708"},{"relation_name":"regulates","term_name":"adiponectin secretion","termid":"GO:0070162"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of adiponectin secretion","termid":"GO:0070163"}


id: FYPO:0000629
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which programmed cell death by apoptosis is abnormal. Apoptosis is a form of cell death characterized by rounding-up of the cell, retraction of pseudopodes, reduction of cellular volume (pyknosis), chromatin condensation, nuclear fragmentation (karyorrhexis), plasma membrane blebbing and fragmentation of the cell into apoptotic bodies.","definition_xrefs":["PomBase:mah","GO:0006915"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process","termid":"FYPO:0000628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal apoptotic process","synonyms":[{"name":"abnormal apoptosis","type":"narrow"}],"termid":"FYPO:0000629"}


id: PBO:0004979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"28S ribosomal RNA","termid":"PBO:0004979"}


id: GO:0043188
data:
  {"annotated_genes":["SJAG_01290","SJAG_01835"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[58676,65204],"is_not":false,"summary":null,"term":"GO:0043188"}]},"cv_name":"cellular_component","definition":"The cell wall material that surrounds the septum in fungal cells.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"fungal-type cell wall","termid":"GO:0009277"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01290":null,"SJAG_01835":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005618"}],"interesting_parent_ids":["GO:0005618","GO:0005575"],"is_obsolete":false,"name":"cell septum edging","references_by_uniquename":{"GO_REF:0000117":null},"termid":"GO:0043188","terms_by_termid":{"GO:0043188":null}}


id: MONDO:0000653
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the integumental system","direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"}],"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":"integumentary system cancer","secondary_identifiers":["DOID:0060122"],"synonyms":[{"name":"cancer of integumental system","type":"exact"},{"name":"integumental system cancer","type":"exact"},{"name":"malignant integumental system neoplasm","type":"exact"},{"name":"malignant neoplasm of integumental system","type":"exact"}],"termid":"MONDO:0000653","xrefs":{"Monarch":{"xref_id":"0000653"}}}


id: MONDO:0017272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autosomal ichthyosis syndrome with prominent neurologics signs (obsolete MONDO:0017272)","secondary_identifiers":["Orphanet:281238"],"synonyms":[{"name":"autosomal ichthyosis syndrome with prominent neurologic signs","type":"related"}],"termid":"MONDO:0017272","xrefs":{"Monarch":{"xref_id":"0017272"}}}


id: GO:0035627
data:
  {"annotated_genes":["SJAG_03690","SJAG_01437","SJAG_00176","SJAG_00355","SJAG_04413","SJAG_01116"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74527,75068,119542,75504,111612,75969],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035621"}]},"cv_name":"biological_process","definition":"The directed movement of ceramides into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Ceramides are a class of lipid composed of sphingosine linked to a fatty acid.","definition_xrefs":["GOC:bf","GOC:sart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid transport","termid":"GO:0006869"},{"relation_name":"is_a","term_name":"amide transport","termid":"GO:0042886"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00176":null,"SJAG_00355":null,"SJAG_01116":null,"SJAG_01437":null,"SJAG_03690":null,"SJAG_04413":null},"genotype_count":0,"interesting_parent_details":[{"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:0006810"],"is_obsolete":false,"name":"ceramide transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9845576"],"termid":"GO:0035627","terms_by_termid":{"GO:0035621":null}}


id: PBO:0088407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi zinc importer, CDF family, Cis4","termid":"PBO:0088407"}


id: PBO:0038561
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABI family member 3","termid":"PBO:0038561"}


id: GO:0160226
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An oligosaccharyltransferase complex that contains STT3A as the catalytic subunit.","definition_xrefs":["PMID:31831667","PMID:39509507"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharyltransferase complex","termid":"GO:0008250"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005783"},{"rel_name":"part_of","termid":"GO:0005789"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005783","GO:0032991","GO:0005789"],"is_obsolete":false,"name":"oligosaccharyltransferase complex A","synonyms":[{"name":"OST-A","type":"exact"}],"termid":"GO:0160226"}


id: PBO:0091419
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human ELOVL7","termid":"PBO:0091419"}


id: MONDO:0009857
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent Mullerian duct syndrome (PMDS) is a rare disorder of sex development (DSD) characterized by the persistence of Müllerian derivatives, the uterus and/or fallopian tubes, in otherwise normally virilized boys.","definition_xrefs":["Orphanet:2856"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudohermaphroditism","termid":"MONDO:0005518"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent Mullerian duct syndrome","secondary_identifiers":["MESH:C536665","ICD9:752.89","OMIM:261550","GARD:8435","icd11.foundation:697796373","MEDGEN:342367","UMLS:C1849930","NCIT:C120188","SCTID:702358005","DOID:0050791"],"synonyms":[{"name":"PMDS","type":"exact"},{"name":"female genital ducts in otherwise normal Male","type":"related"},{"name":"female genital ducts in otherwise normal male","type":"related"},{"name":"hernia uteri inguinale","type":"related"},{"name":"persistent MULLERIAN duct syndrome, types I and II","type":"related"},{"name":"persistent Muellerian duct syndrome","type":"exact"},{"name":"persistent Mullerian derivatives","type":"exact"},{"name":"persistent Mullerian duct syndrome","type":"exact"},{"name":"persistent Müllerian derivatives","type":"exact"},{"name":"persistent Müllerian duct syndrome","type":"related"},{"name":"persistent mullerian duct syndrome, type I","type":"exact"},{"name":"persistent mullerian duct syndrome, type II","type":"exact"},{"name":"persistent mullerian duct syndrome, types 1 and 2","type":"related"},{"name":"persistent oviduct syndrome","type":"related"},{"name":"pseudohermaphroditism, Male internal","type":"related"}],"termid":"MONDO:0009857","xrefs":{"Monarch":{"xref_id":"0009857"}}}


id: PATO:0001571
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A size quality inhering in a bearer by virtue of the bearer's being made wider or larger in all dimensions.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased size","termid":"PATO:0000586"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dilated","termid":"PATO:0001571"}


id: PBO:0015212
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homomeric(2)","termid":"PBO:0015212"}


id: PATO:0000151
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000151 relative texture (obsolete PATO:0000151)","termid":"PATO:0000151"}


id: PBO:0029127
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_vacuole_fusion","termid":"PBO:0029127"}


id: PBO:0002198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ethanolamine-phosphate cytidylyltransferase (predicted)","termid":"PBO:0002198"}


id: GO:0140461
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The organization of chromatin into heterochromatin at the subtelomeric region of a chromosome.","definition_xrefs":["PMID:26744419"],"gene_count":0,"genotype_count":0,"name":"obsolete subtelomeric heterochromatin organization (obsolete GO:0140461)","termid":"GO:0140461"}


id: PBO:0051521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 1 receptor type 2","termid":"PBO:0051521"}


id: PBO:0057601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 938","termid":"PBO:0057601"}


id: GO:0070248
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of natural killer cell death by apoptotic process.","definition_xrefs":["GOC:add","ISBN:0781765196","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lymphocyte apoptotic process","termid":"GO:0070229"},{"relation_name":"is_a","term_name":"regulation of natural killer cell apoptotic process","termid":"GO:0070247"},{"relation_name":"negatively_regulates","term_name":"natural killer cell apoptotic process","termid":"GO:0070246"}],"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 natural killer cell apoptotic process","synonyms":[{"name":"down regulation of natural killer cell apoptosis","type":"exact"},{"name":"down-regulation of natural killer cell apoptosis","type":"exact"},{"name":"downregulation of natural killer cell apoptosis","type":"exact"},{"name":"inhibition of natural killer cell apoptosis","type":"narrow"},{"name":"negative regulation of NK cell apoptosis","type":"exact"},{"name":"negative regulation of natural killer cell apoptosis","type":"narrow"}],"termid":"GO:0070248"}


id: MONDO:0957588
data:
  {"annotated_genes":["SJAG_02116"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88230],"is_not":false,"summary":null,"term":"MONDO:0957588"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02116":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620494","UMLS:C5882686","MEDGEN:1847194"],"termid":"MONDO:0957588","terms_by_termid":{"MONDO:0957588":null},"xrefs":{"Monarch":{"xref_id":"0957588"}}}


id: PBO:0047266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 246 member A","termid":"PBO:0047266"}


id: GO:0031589
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of a cell to the underlying substrate via adhesion molecules.","definition_xrefs":["GOC:pf","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell adhesion","termid":"GO:0007155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"cell-substrate adhesion","termid":"GO:0031589"}


id: MONDO:0020379
data:
  {"annotated_genes":["SJAG_02919","SJAG_04567","SJAG_03815"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88768,88770,88769],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013411"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset partial cataract","termid":"MONDO:0020377"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02919":null,"SJAG_03815":null,"SJAG_04567":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"early-onset zonular cataract","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1842642","GARD:1898","UMLS:C5681642","Orphanet:98995","MESH:C535342"],"termid":"MONDO:0020379","terms_by_termid":{"MONDO:0013411":null},"xrefs":{"Monarch":{"xref_id":"0020379"}}}


id: FYPO:0004230
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins is normal (i.e. indistinguishable from wild type) during a cellular response to ultraviolet light.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein phosphorylation during vegetative growth","termid":"FYPO:0000776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0001320"],"is_obsolete":false,"name":"normal protein phosphorylation during cellular response to UV","synonyms":[{"name":"normal protein phosphorylation during cellular response to UV during mitotic cell cycle","type":"related"},{"name":"normal protein phosphorylation during cellular response to UV during vegetative growth","type":"exact"},{"name":"normal protein phosphorylation during cellular response to ultraviolet light","type":"related"}],"termid":"FYPO:0004230"}


id: PBO:0068027
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 332","termid":"PBO:0068027"}


id: PBO:0048377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"golgi associated RAB2 interactor family member 2","termid":"PBO:0048377"}


id: PBO:0059558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 1B","termid":"PBO:0059558"}


id: PBO:0056778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase like 27","termid":"PBO:0056778"}


id: PBO:0039052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiogenic factor with G-patch and FHA domains 1 pseudogene 1","termid":"PBO:0039052"}


id: GO:2000804
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of termination of RNA polymerase II transcription, poly(A)-coupled.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of termination of RNA polymerase II transcription","termid":"GO:1904594"},{"relation_name":"regulates","term_name":"termination of RNA polymerase II transcription, poly(A)-coupled","termid":"GO:0030846"}],"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 termination of RNA polymerase II transcription, poly(A)-coupled","synonyms":[{"name":"regulation of termination of RNA polymerase II transcription, polyadenylation-coupled","type":"related"},{"name":"regulation of transcription termination from Pol II promoter, RNA polymerase(A) coupled","type":"related"},{"name":"regulation of transcription termination from Pol II promoter, poly(A) coupled","type":"related"}],"termid":"GO:2000804"}


id: GO:0042428
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving serotonin (5-hydroxytryptamine), a monoamine neurotransmitter occurring in the peripheral and central nervous systems, also having hormonal properties.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound metabolic process","termid":"GO:0018958"},{"relation_name":"is_a","term_name":"indole-containing compound metabolic process","termid":"GO:0042430"},{"relation_name":"is_a","term_name":"ammonium ion metabolic process","termid":"GO:0097164"},{"relation_name":"is_a","term_name":"primary amino compound metabolic process","termid":"GO:1901160"}],"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":"serotonin metabolic process","synonyms":[{"name":"serotonin metabolism","type":"exact"}],"termid":"GO:0042428"}


id: SO:1000048
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosomal translocation with two breaks; two chromosome segments have simply been exchanged.","definition_xrefs":["FB:reference_manual"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosomal_translocation","termid":"SO:1000044"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reciprocal_chromosomal_translocation","synonyms":[{"name":"reciprocal chromosomal translocation","type":"exact"}],"termid":"SO:1000048"}


id: PBO:0068977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 221, pseudogene","termid":"PBO:0068977"}


id: MONDO:1012300
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"displaced abomasum, non-human animal","termid":"MONDO:1011663"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"displaced abomasum, sheep","secondary_identifiers":["OMIA:001119-9940"],"termid":"MONDO:1012300","xrefs":{"Monarch":{"xref_id":"1012300"}}}


id: GO:0035391
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The maintenance of chromatin in a transcriptionally silent state such as heterochromatin at silent mating-type loci.","definition_xrefs":["GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete maintenance of chromatin silencing at silent mating-type cassette (obsolete GO:0035391)","termid":"GO:0035391"}


id: GO:0043906
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of misacylated Ala-tRNA(Pro).","definition_xrefs":["PMID:14663147","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoacyl-tRNA deacylase activity","termid":"GO:0002161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140101","GO:0003674","GO:0140098","GO:0003824"],"is_obsolete":false,"name":"Ala-tRNA(Pro) deacylase activity","synonyms":[{"name":"Ala-tRNAPro hydrolase activity","type":"exact"}],"termid":"GO:0043906"}


id: PBO:0012853
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TWo Spored","termid":"PBO:0012853"}


id: MONDO:0000193
data:
  {"annotated_genes":["SJAG_02148","SJAG_02696"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87400,87401],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011503"}]},"cv_name":"mondo","definition":"A disorder in which there is a failure to regenerate the active glucocorticoid cortisol from cortisone via 11beta-HSD1. The resulting lack of cortisol regeneration stimulates ACTH-mediated adrenal hyperandrogenism, with males manifesting in childhood with precocious pseudopuberty and females presenting in adolescence and early adulthood with hirsutism, oligoamenorrhea, and infertility.","definition_xrefs":["PMID:21325058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited lipid metabolism disorder","termid":"MONDO:0002525"},{"relation_name":"is_a","term_name":"reproductive system disorder","termid":"MONDO:0005039"},{"relation_name":"is_a","term_name":"adrenogenital syndrome","termid":"MONDO:0015898"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02148":null,"SJAG_02696":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"cortisone reductase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:9882","ICD9:277.6","SCTID:124138004","UMLS:C1291245","MEDGEN:266223","MESH:C536447","Orphanet:168588","DOID:0090139","OMIMPS:604931"],"synonyms":[{"name":"11-alpha beta-hydroxysteroid dehydrogenase type I deficiency of","type":"related"},{"name":"11-beta-hydroxysteroid dehydrogenase deficiency type 1","type":"exact"},{"name":"CORTRD","type":"exact"},{"name":"HSD 11B1 deficiency","type":"narrow"},{"name":"deficiency of (R)-20-hydroxysteroid dehydrogenase","type":"exact"},{"name":"deficiency of cortisone reductase","type":"exact"},{"name":"hyperandrogenism due to cortisone reductase deficiency","type":"exact"}],"termid":"MONDO:0000193","terms_by_termid":{"MONDO:0011503":null},"xrefs":{"Monarch":{"xref_id":"0000193"}}}


id: FYPO:0006590
data:
  {"alleles_by_uniquename":{"SJAG_01745:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01745","name":"lem2delta","uniquename":"SJAG_01745:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0003657"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a protein that is not normally found in the endoplasmic reticulum is observed there.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalized protein","termid":"FYPO:0003452"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01050":null,"SJAG_01745":null},"genotype_count":1,"genotypes_by_uniquename":{"lem2delta":{"display_name":"lem2delta","display_uniquename":"lem2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01745:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"protein mislocalized to endoplasmic reticulum","references_by_uniquename":{"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_01745"],"single_locus_genotype_uniquenames":["lem2delta"],"synonyms":[{"name":"ectopic protein localization to endoplasmic reticulum","type":"exact"},{"name":"protein mislocalised to endoplasmic reticulum","type":"exact"},{"name":"protein mislocalized to ER","type":"exact"}],"termid":"FYPO:0006590","terms_by_termid":{"FYECO:0000137":null,"FYPO:0003657":null,"FYPO_EXT:0000001":null}}


id: GO:0050311
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: hydrogen sulfide + 3 oxidized ferredoxin + 3 H2O = sulfite + 3 reduced ferredoxin.","definition_xrefs":["EC:1.8.7.1","MetaCyc:SULFITE-REDUCTASE-FERREDOXIN-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, iron-sulfur protein as acceptor","termid":"GO:0016673"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"sulfite reductase (ferredoxin) activity","secondary_identifiers":["RHEA:23132"],"synonyms":[{"name":"ferredoxin-sulfite reductase activity","type":"related"},{"name":"hydrogen-sulfide:ferredoxin oxidoreductase activity","type":"related"},{"name":"sulphite reductase (ferredoxin) activity","type":"exact"}],"termid":"GO:0050311"}


id: PBO:0059134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MPHOSPH10 pseudogene 1","termid":"PBO:0059134"}


id: PBO:0045947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongation factor Tu GTP binding domain containing 2","termid":"PBO:0045947"}


id: GO:0042058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of epidermal growth factor receptor signaling pathway activity.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ERBB signaling pathway","termid":"GO:1901184"},{"relation_name":"regulates","term_name":"epidermal growth factor receptor signaling pathway","termid":"GO:0007173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of epidermal growth factor receptor signaling pathway","synonyms":[{"name":"regulation of EGF receptor signaling pathway","type":"exact"},{"name":"regulation of EGF receptor signalling pathway","type":"exact"},{"name":"regulation of EGFR signaling pathway","type":"exact"}],"termid":"GO:0042058"}


id: MONDO:0017507
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Congenital absence/hypoplasia of thumb, bilateral is a rare developmental defect during embryogenesis characterized by bilateral underdevelopment of the thumbs, ranging from a slight decrease in thumb size to complete absence of the thumbs. This anomaly counts for 20-60% of thumb hypoplasias.","definition_xrefs":["Orphanet:295112"],"gene_count":0,"genotype_count":0,"name":"obsolete congenital absence/hypoplasia of thumb, bilateral (obsolete MONDO:0017507)","synonyms":[{"name":"thumb hypodactyly, bilateral","type":"exact"},{"name":"thumb oligodactyly, bilateral","type":"exact"}],"termid":"MONDO:0017507","xrefs":{"Monarch":{"xref_id":"0017507"}}}


id: PBO:0061958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily A member 14","termid":"PBO:0061958"}


id: PBO:0046099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 4B pseudogene 2","termid":"PBO:0046099"}


id: GO:0071966
data:
  {"annotated_genes":["SJAG_05285","SJAG_00424","SJAG_03646","SJAG_03587","SJAG_00218","SJAG_02278","SJAG_04483","SJAG_01028","SJAG_01290","SJAG_01288","SJAG_00610","SJAG_03123","SJAG_04236","SJAG_04771","SJAG_05001","SJAG_04864","SJAG_03057","SJAG_04184","SJAG_01171","SJAG_00876","SJAG_01835","SJAG_04327","SJAG_02192","SJAG_02916","SJAG_01453","SJAG_02222","SJAG_04666"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74286,108666],"is_not":false,"summary":null,"term":"GO:0071966"},{"annotations":[96363],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034413"},{"annotations":[74763],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034412"},{"annotations":[72388,75119,75291,80560,73177],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070600"},{"annotations":[108074,77638,72818,76285,115173,74766,117841,93490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071970"},{"annotations":[80008,104588],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070880"},{"annotations":[97014,103889,110047,103888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070879"},{"annotations":[94313,89378],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140748"},{"annotations":[96850,94319,91318,104796],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0070610"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving the polysaccharides which make up the fungal-type cell wall.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell wall polysaccharide metabolic process","termid":"GO:0010383"},{"relation_name":"part_of","term_name":"fungal-type cell wall organization or biogenesis","termid":"GO:0071852"}],"gene_count":27,"genes_by_uniquename":{"SJAG_00218":null,"SJAG_00424":null,"SJAG_00610":null,"SJAG_00876":null,"SJAG_01028":null,"SJAG_01171":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01453":null,"SJAG_01835":null,"SJAG_02192":null,"SJAG_02222":null,"SJAG_02278":null,"SJAG_02916":null,"SJAG_03057":null,"SJAG_03123":null,"SJAG_03587":null,"SJAG_03646":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04327":null,"SJAG_04483":null,"SJAG_04666":null,"SJAG_04771":null,"SJAG_04864":null,"SJAG_05001":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0005975","GO:0071554","GO:0008150"],"is_obsolete":false,"name":"fungal-type cell wall polysaccharide metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0071966","terms_by_termid":{"GO:0034412":null,"GO:0034413":null,"GO:0070600":null,"GO:0070610":null,"GO:0070879":null,"GO:0070880":null,"GO:0071966":null,"GO:0071970":null,"GO:0140748":null}}


id: PBO:0070110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 24 pseudogene","termid":"PBO:0070110"}


id: MONDO:0021456
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the sternum.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thoracic benign neoplasm","termid":"MONDO:0000634"},{"relation_name":"is_a","term_name":"musculoskeletal system benign neoplasm","termid":"MONDO:0000636"},{"relation_name":"is_a","term_name":"sternal neoplasm","termid":"MONDO:0021578"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of sternum","secondary_identifiers":["SCTID:92410006","MEDGEN:87573","UMLS:C0347312","NCIT:C8416"],"synonyms":[{"name":"benign neoplasm of the sternum","type":"exact"},{"name":"benign sternal neoplasm","type":"exact"},{"name":"benign sternal tumor","type":"exact"},{"name":"benign sternal tumour","type":"exact"},{"name":"benign tumor of sternum","type":"exact"},{"name":"benign tumor of the sternum","type":"exact"},{"name":"benign tumour of sternum","type":"exact"},{"name":"benign tumour of the sternum","type":"exact"},{"name":"sternum benign neoplasm","type":"exact"}],"termid":"MONDO:0021456","xrefs":{"Monarch":{"xref_id":"0021456"}}}


id: PBO:0056904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIF4G domain containing","termid":"PBO:0056904"}


id: PBO:0041464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 10 open reading frame 105","termid":"PBO:0041464"}


id: MONDO:0013161
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive limb-girdle muscular dystrophy type 2O (LGMD2O) is a form of limb-girdle muscular dystrophy characterized by an onset in childhood or adolescence of rapidly progressive proximal limb muscle weakness (particularly affecting the neck, hip girdle, and shoulder abductors), hypertrophy in the calves and quadriceps, ankle contractures, and myopia.","definition_xrefs":["Orphanet:206564"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type C","termid":"MONDO:0000173"},{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"},{"relation_name":"is_a","term_name":"myopathy caused by variation in POMGNT1","termid":"MONDO:0700068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0024322","MONDO:0002320","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"autosomal recessive limb-girdle muscular dystrophy type 2O","secondary_identifiers":["DOID:0110292","GARD:12540","OMIM:613157","MEDGEN:461767","UMLS:C3150417"],"synonyms":[{"name":"LGMD-POMGNT1 related","type":"exact"},{"name":"LGMD2O","type":"exact"},{"name":"MDDGC3","type":"exact"},{"name":"POMGNT1 autosomal recessive limb-girdle muscular dystrophy","type":"exact"},{"name":"autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMGNT1","type":"exact"},{"name":"limb-girdle muscular dystrophy type 2O","type":"related"},{"name":"muscular dystrophy, limb-girdle, type 2O","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy (limb-girdle) type C3","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT1-related","type":"related"}],"termid":"MONDO:0013161","xrefs":{"Monarch":{"xref_id":"0013161"}}}


id: GO:0032082
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops or reduces the rate of type III restriction endodeoxyribonuclease activity.","definition_xrefs":["GOC:tb","GOC:mah","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of type III site-specific deoxyribonuclease activity (obsolete GO:0032082)","synonyms":[{"name":"down regulation of type III restriction endodeoxyribonuclease activity","type":"exact"},{"name":"down-regulation of type III restriction endodeoxyribonuclease activity","type":"exact"},{"name":"downregulation of type III restriction endodeoxyribonuclease activity","type":"exact"},{"name":"inhibition of type III restriction endodeoxyribonuclease activity","type":"narrow"},{"name":"negative regulation of type III restriction endodeoxyribonuclease activity","type":"exact"},{"name":"type III restriction endodeoxyribonuclease inhibitor","type":"related"},{"name":"type III restriction enzyme inhibitor","type":"related"}],"termid":"GO:0032082"}


id: PBO:0074622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 21","termid":"PBO:0074622"}


id: PBO:0077309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 45B","termid":"PBO:0077309"}


id: MONDO:0001356
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Anemia caused by low iron intake, inefficient iron absorption in the gastrointestinal tract, or chronic blood loss.","definition_xrefs":["NCIT:C84484"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypochromic microcytic anemia","termid":"MONDO:0000387"},{"relation_name":"is_a","term_name":"nutritional deficiency disease","termid":"MONDO:0006873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"iron deficiency anemia","secondary_identifiers":["DOID:11758","ICD9:280.9","MEDGEN:57668","SCTID:87522002","MESH:D018798","UMLS:C0162316","ICD9:280.8"],"synonyms":[{"name":"iron-deficiency anaemia","type":"exact"},{"name":"iron-deficiency anemia","type":"exact"}],"termid":"MONDO:0001356","xrefs":{"Monarch":{"xref_id":"0001356"}}}


id: MONDO:0100105
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive disorder resulting from fragility of cerebral vessels causing an increased risk of intracranial bleeding. The resultant phenotype is highly variable depending on timing and location of the intracranial bleed. Some patients may have onset in utero or early infancy, with subsequent global developmental delay, spasticity, and porencephaly on brain imaging. Other patients may have normal or mildly delayed development with sudden onset of intracranial hemorrhage causing acute neurologic deterioration.","definition_xrefs":["OMIM:618360"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial porencephaly","termid":"MONDO:0020496"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain small vessel disease 3","secondary_identifiers":["MEDGEN:1677948","UMLS:C5193053","DOID:0112315"],"synonyms":[{"name":"BSVD3","type":"exact"}],"termid":"MONDO:0100105","xrefs":{"Monarch":{"xref_id":"0100105"}}}


id: FYPO:0000321
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A mixed population phenotype in which all cells in a population are inviable, and the population includes a mixture of ungerminated spores and germinated spores that fail to divide.","definition_xrefs":["PomBase:jh","PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable mixed population including spores and undivided germinated spores (obsolete FYPO:0000321)","termid":"FYPO:0000321"}


id: PBO:0063593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal biogenesis factor 6","termid":"PBO:0063593"}


id: PBO:0083596
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame unlikely to encode a functional protein; deletion adversely affects sporulation; deletion mutant exhibits synthetic phenotype under expression of mutant huntingtin fragment, but gene does not have human ortholog","termid":"PBO:0083596"}


id: GO:0043969
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H2B by the addition of an acetyl group.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H2B acetylation (obsolete GO:0043969)","termid":"GO:0043969"}


id: MONDO:0020229
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete cerebral disease with cataract (obsolete MONDO:0020229)","secondary_identifiers":["Orphanet:98645"],"termid":"MONDO:0020229","xrefs":{"Monarch":{"xref_id":"0020229"}}}


id: MONDO:0032797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"myopathy, congenital, with tremor","secondary_identifiers":["MEDGEN:1684886","DOID:0081348","OMIM:618524","UMLS:C5231401"],"synonyms":[{"name":"MYOPATHY, CONGENITAL, WITH TREMOR","type":"related"},{"name":"MYOTREM","type":"related"},{"name":"Myogenic Tremor","type":"related"}],"termid":"MONDO:0032797","xrefs":{"Monarch":{"xref_id":"0032797"}}}


id: PBO:0058009
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3936","termid":"PBO:0058009"}


id: PBO:0003469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chitin synthase homolog Chs2","termid":"PBO:0003469"}


id: PBO:0017006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"antibiotic biosynthesis monooxygenase-like domain (predicted)","termid":"PBO:0017006"}


id: GO:0031084
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex required for the biogenesis of specialized organelles of the endosomal-lysosomal system, such as melanosomes and platelet dense granules. The human complex contains the Hps3, Hps5, and Hps6 proteins; the mouse complex contains ru2 and ru.","definition_xrefs":["PMID:12548288","PMID:14718540","PMID:15031569"],"direct_ancestors":[{"relation_name":"is_a","term_name":"BLOC complex","termid":"GO:0031082"}],"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":"BLOC-2 complex","termid":"GO:0031084"}


id: SO:0001605
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant within a CDS resulting in the gain of an amino acid to the resulting polypeptide.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_sequence_variant","termid":"SO:0001603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino_acid_insertion","synonyms":[{"name":"amino acid insertion","type":"exact"}],"termid":"SO:0001605"}


id: GO:0102947
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + (+)-delta-cadinene + NADPH + O2 = 8-hydroxy-(+)-delta-cadinene + NADP + H2O.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"(+)-delta-cadinene-8-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-9045"],"termid":"GO:0102947"}


id: GO:0071326
data:
  {"annotated_genes":["SJAG_01754","SJAG_00472","SJAG_04026","SJAG_01254","SJAG_00574","SJAG_04312","SJAG_02444","SJAG_01699","SJAG_03081"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108818,111000,96123,111511,117554,118587,108468,103793,107872],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0010619"}]},"cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a monosaccharide stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to monosaccharide","termid":"GO:0034284"},{"relation_name":"is_a","term_name":"cellular response to carbohydrate stimulus","termid":"GO:0071322"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00472":null,"SJAG_00574":null,"SJAG_01254":null,"SJAG_01699":null,"SJAG_01754":null,"SJAG_02444":null,"SJAG_03081":null,"SJAG_04026":null,"SJAG_04312":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 monosaccharide stimulus","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0071326","terms_by_termid":{"GO:0010619":null}}


id: PBO:0067580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 737, pseudogene","termid":"PBO:0067580"}


id: FYPO:0007097
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which actin fusion focus assembly takes place in one or more abnormal locations. An actin fusion focus normally forms during mating at the site where the two cells will fuse. Ectopic fusion foci often form near actin cortical patches, and may also have abnormal composition.","definition_xrefs":["PMID:31495586","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal actin fusion focus assembly","termid":"FYPO:0006108"}],"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:0004803"},{"rel_name":"is_a","termid":"FYPO:0000301"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000301","FYPO:0001985","FYPO:0004803","FYPO:0005447"],"is_obsolete":false,"name":"ectopic actin fusion focus assembly","synonyms":[{"name":"ectopic actin fusion focus formation","type":"exact"},{"name":"mislocalized actin fusion focus assembly","type":"exact"}],"termid":"FYPO:0007097"}


id: MONDO:0007526
data:
  {"annotated_genes":["SJAG_00222","SJAG_00183"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012873"},{"annotations":[87869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014139"}]},"cv_name":"mondo","definition":"A form of Ehlers-Danlos syndrome characterized by a premature aging with sparse hair, macrocephaly, loose elastic skin, failure to thrive, joint laxity, psychomotor retardation, hypotonia, and defective wound healing with atrophic scars.","definition_xrefs":["Orphanet:75496"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00183":null,"SJAG_00222":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"Ehlers-Danlos syndrome, spondylodysplastic type","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0050802","SCTID:720861000","MESH:C536201","GARD:9991"],"synonyms":[{"name":"B4GALT7-CDG","type":"exact"},{"name":"EDS, progeroid type","type":"exact"},{"name":"EDSSPD1","type":"narrow"},{"name":"Ehlers-Danlos syndrome progeroid type","type":"exact"},{"name":"Ehlers-Danlos syndrome with short stature and limb anomalies","type":"narrow"},{"name":"Ehlers-Danlos syndrome, progeroid type","type":"related"},{"name":"Ehlers-Danlos syndrome, progeroid type (former)","type":"related"},{"name":"Ehlers-Danlos syndrome, spondylodysplastic type, 1","type":"narrow"},{"name":"PDS","type":"exact"},{"name":"Pds, defective biosynthesis of","type":"narrow"},{"name":"XGPT deficiency","type":"narrow"},{"name":"defective biosynthesis of proteodermatan sulfate","type":"exact"},{"name":"defective biosynthesis of proteodermatan sulphate","type":"exact"},{"name":"dermatan sulfate proteoglycan","type":"narrow"},{"name":"dermatan sulphate proteoglycan","type":"narrow"},{"name":"galactosyltransferase 1 deficiency","type":"narrow"},{"name":"galactosyltransferase I deficiency","type":"exact"},{"name":"proteodermatan sulfate, defective biosynthesis of","type":"narrow"},{"name":"spondylodysplastic Ehlers-Danlos syndrome","type":"related"},{"name":"xylosylprotein 4-beta-galactosyltransferase deficiency","type":"narrow"}],"termid":"MONDO:0007526","terms_by_termid":{"MONDO:0012873":null,"MONDO:0014139":null},"xrefs":{"Monarch":{"xref_id":"0007526"}}}


id: PBO:0054683
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 2091","termid":"PBO:0054683"}


id: MONDO:0016042
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Late-onset isolated ACTH deficiency is a rare, acquired, pituitary hormone deficiency characterized by secondary adrenal insufficiency, with normal secretion of anterior pituitary hormones, except for ACTH. Patients present with weakness, fatigue, weight loss, anorexia, vomiting/nausea, hypoglycemia, and abnormally low serum ACTH and cortisol levels. Association with autoimmune disease such as Hashimoto's thyroiditis has been described.","definition_xrefs":["Orphanet:199299"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired pituitary hormone deficiency","termid":"MONDO:0019832"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"late-onset isolated ACTH deficiency","secondary_identifiers":["icd11.foundation:1651831896","MEDGEN:1651973","UMLS:C4751433","GARD:20331"],"termid":"MONDO:0016042","xrefs":{"Monarch":{"xref_id":"0016042"}}}


id: MONDO:0060596
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with dysmorphic facies and distal limb anomalies","secondary_identifiers":["GARD:18513","MEDGEN:1627464","OMIM:617755","UMLS:C4540327","DOID:0070514"],"synonyms":[{"name":"NEDDFL","type":"related"},{"name":"neurodevelopmental disorder with dysmorphic facies and distal limb anomalies","type":"exact"}],"termid":"MONDO:0060596","xrefs":{"Monarch":{"xref_id":"0060596"}}}


id: PBO:0039946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AT-rich interaction domain 5A","termid":"PBO:0039946"}


id: PBO:0085161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleotide excision repair (NER) protein; binds damaged DNA during NER; binds DNA in an ATP-dependent manner (with Rad7p) during NER; required for NER of non-transcribed chromatin; subunit of Nucleotide Excision Repair Factor 4 (NEF4) and the Elongin-Cullin-Socs (ECS) ligase complex","termid":"PBO:0085161"}


id: PBO:0070782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 12","termid":"PBO:0070782"}


id: GO:0005251
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a potassium ion by a delayed rectifying voltage-gated channel. A delayed rectifying current-voltage relation is one where channel activation kinetics are time-dependent, and inactivation is slow.","definition_xrefs":["GOC:mah","PMID:11343411","PMID:2462513"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel activity","termid":"GO:0005249"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"delayed rectifier potassium channel activity","secondary_identifiers":["Reactome:R-HSA-5577050","Reactome:R-HSA-5577237"],"termid":"GO:0005251"}


id: GO:0061846
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region of the neuronal cytoplasm located in dendritic spines.","definition_xrefs":["PMID:15673667"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendrite cytoplasm","termid":"GO:0032839"},{"relation_name":"part_of","term_name":"dendritic spine","termid":"GO:0043197"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737"],"is_obsolete":false,"name":"dendritic spine cytoplasm","termid":"GO:0061846"}


id: GO:0015821
data:
  {"annotated_genes":["SJAG_00991"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95224],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1905626"}]},"cv_name":"biological_process","definition":"The directed movement of methionine, 2-amino-4-(methylthio)butanoic acid, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur amino acid transport","termid":"GO:0000101"},{"relation_name":"is_a","term_name":"amino acid transport","termid":"GO:0006865"},{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00991":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"methionine transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"L-methionine transport","type":"narrow"}],"termid":"GO:0015821","terms_by_termid":{"GO:1905626":null}}


id: MONDO:0002305
data:
  {"annotated_genes":["SJAG_01466","SJAG_03712"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89145,89146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008559"}]},"cv_name":"mondo","definition":"A condition characterized by an abnormally high level of thrombi. Causes include thrombotic thrombocytopenic purpura, disseminated intravascular coagulation, bone marrow disorders, and antiphospholipid antibody syndrome.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood coagulation disease","termid":"MONDO:0001531"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01466":null,"SJAG_03712":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"thrombophilia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:2452","icd11.foundation:1733531851","MESH:D019851","NCIT:C84479","UMLS:C0398623","EFO:0009315","MEDGEN:98306","Orphanet:64738","ICD9:286.9","SCTID:234467004"],"synonyms":[{"name":"excessive blood clotting","type":"exact"},{"name":"hypercoagulability","type":"exact"},{"name":"hypercoagulability state","type":"exact"},{"name":"hypercoagulable","type":"exact"}],"termid":"MONDO:0002305","terms_by_termid":{"MONDO:0008559":null},"xrefs":{"Monarch":{"xref_id":"0002305"}}}


id: MONDO:0020507
data:
  {"annotated_genes":["SJAG_03678"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88171],"is_not":false,"summary":null,"term":"MONDO:0020507"}]},"cv_name":"mondo","definition":"Any leukoencephalopathy with vanishing white matter in which the cause of the disease is a variation in the EIF2B1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukoencephalopathy with vanishing white matter","termid":"MONDO:0800448"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03678":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"leukoencephalopathy with vanishing white matter 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:16919","UMLS:C5779972","DOID:0070374","OMIM:603896","Orphanet:99854","MEDGEN:1830482"],"synonyms":[{"name":"CACH","type":"exact"},{"name":"Cree leukoencephalopathy","type":"related"},{"name":"childhood ataxia with central nervous system hypomyelinization","type":"exact"},{"name":"vanishing white matter leukodystrophy","type":"exact"}],"termid":"MONDO:0020507","terms_by_termid":{"MONDO:0020507":null},"xrefs":{"Monarch":{"xref_id":"0020507"}}}


id: GO:0043004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The selective interaction of Cystic Fibrosis Transmembrane conductance Regulator (CFTR) protein with specific molecules in the cytoplasm, thereby inhibiting its transport to the cell membrane.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete cytoplasmic sequestering of CFTR protein (obsolete GO:0043004)","synonyms":[{"name":"cytoplasmic retention of CFTR (cystic fibrosis transmembrane conductance regulator) protein","type":"exact"},{"name":"cytoplasmic sequestering of cystic fibrosis transmembrane conductance regulator protein","type":"exact"},{"name":"cytoplasmic sequestration of CFTR (cystic fibrosis transmembrane conductance regulator protein)","type":"exact"},{"name":"cytoplasmic storage of CFTR (cystic fibrosis transmembrane conductance regulator) protein","type":"exact"},{"name":"maintenance of CFTR protein location in cytoplasm","type":"exact"},{"name":"retention of CFTR (cystic fibrosis transmembrane conductance regulator) protein in cytoplasm","type":"exact"},{"name":"sequestering of CFTR (cystic fibrosis transmembrane conductance regulator protein) in cytoplasm","type":"exact"},{"name":"sequestration of CFTR (cystic fibrosis transmembrane conductance regulator protein) in cytoplasm","type":"exact"},{"name":"storage of CFTR (cystic fibrosis transmembrane conductance regulator) protein in cytoplasm","type":"exact"}],"termid":"GO:0043004"}


id: GO:1904414
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cardiac ventricle development.","definition_xrefs":["GO_REF:0000058","PMID:19590510","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of cardiac ventricle development","termid":"GO:1904412"},{"relation_name":"positively_regulates","term_name":"cardiac ventricle development","termid":"GO:0003231"}],"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 ventricle development","synonyms":[{"name":"activation of cardiac ventricle development","type":"narrow"},{"name":"up regulation of cardiac ventricle development","type":"exact"},{"name":"up-regulation of cardiac ventricle development","type":"exact"},{"name":"upregulation of cardiac ventricle development","type":"exact"}],"termid":"GO:1904414"}


id: GO:0099617
data:
  {"annotated_genes":["SJAG_01806","SJAG_00438","SJAG_03282","SJAG_03925","SJAG_MIT09","SJAG_02564","SJAG_04122","SJAG_02105","SJAG_07003","SJAG_MIT15","SJAG_MIT37","SJAG_03114","SJAG_00077","SJAG_02598","SJAG_00797","SJAG_00542","SJAG_00915","SJAG_05204","SJAG_00852","SJAG_01249","SJAG_00985","SJAG_00133","SJAG_00836"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[91005,91372,91834,94743,95170,95709,95761,96752,98166,103761,104981,105598,105624,106974,109782,109874,110772,117865,121110,121116,121121],"is_not":false,"summary":null,"term":"GO:0099617"},{"annotations":[105709,102391],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099616"}]},"cv_name":"cellular_component","definition":"The side (leaflet) of the mitochondrial inner membrane that faces the matrix.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lumenal side of membrane","termid":"GO:0098576"},{"relation_name":"part_of","term_name":"mitochondrial inner membrane","termid":"GO:0005743"}],"gene_count":23,"genes_by_uniquename":{"SJAG_00077":null,"SJAG_00133":null,"SJAG_00438":null,"SJAG_00542":null,"SJAG_00797":null,"SJAG_00836":null,"SJAG_00852":null,"SJAG_00915":null,"SJAG_00985":null,"SJAG_01249":null,"SJAG_01806":null,"SJAG_02105":null,"SJAG_02564":null,"SJAG_02598":null,"SJAG_03114":null,"SJAG_03282":null,"SJAG_03925":null,"SJAG_04122":null,"SJAG_05204":null,"SJAG_07003":null,"SJAG_MIT09":null,"SJAG_MIT15":null,"SJAG_MIT37":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005739"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005739","GO:0005737"],"is_obsolete":false,"name":"matrix side of mitochondrial inner membrane","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0099617","terms_by_termid":{"GO:0099616":null,"GO:0099617":null}}


id: GO:0043634
data:
  {"annotated_genes":["SJAG_16455","SJAG_01176","SJAG_03984"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78088,101543,115277],"is_not":false,"summary":null,"term":"GO:0043634"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a noncoding RNA (ncRNA) molecule, initiated by the enzymatic addition of a sequence of adenylyl residues (polyadenylation) at the 3' end the target ncRNA.","definition_xrefs":["GOC:jl","GOC:dgf","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyadenylation-dependent RNA catabolic process","termid":"GO:0043633"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01176":null,"SJAG_03984":null,"SJAG_16455":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"polyadenylation-dependent ncRNA catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"poly(A)-dependent ncRNA catabolic process","type":"related"}],"termid":"GO:0043634","terms_by_termid":{"GO:0043634":null}}


id: PBO:0058710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6838","termid":"PBO:0058710"}


id: FYPO:0003116
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to plumbagin. Cells stop growing (and may die) at a concentration of plumbagin that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003","FYPO:0005447","FYPO:0002683","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to plumbagin","synonyms":[{"name":"hypersensitive to plumbagin","type":"exact"},{"name":"sensitive to plumbagin during mitotic cell cycle","type":"related"},{"name":"sensitive to plumbagin during vegetative growth","type":"exact"}],"termid":"FYPO:0003116"}


id: PBO:0051602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 25","termid":"PBO:0051602"}


id: PBO:0076612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 30","termid":"PBO:0076612"}


id: PBO:0080837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Y-box binding protein 1 pseudogene 1","termid":"PBO:0080837"}


id: PBO:0091547
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae SPT15","termid":"PBO:0091547"}


id: MONDO:0013703
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0006025"],"is_obsolete":false,"name":"intellectual disability, autosomal recessive 33","secondary_identifiers":["MEDGEN:482169","UMLS:C3280539","DOID:0081194","GARD:22556","OMIM:614341"],"synonyms":[{"name":"MRT33","type":"exact"},{"name":"intellectual disability, autosomal recessive 33","type":"exact"},{"name":"mental retardation, autosomal recessive 33","type":"related"}],"termid":"MONDO:0013703","xrefs":{"Monarch":{"xref_id":"0013703"}}}


id: PBO:0075448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermatogenesis associated 2 like","termid":"PBO:0075448"}


id: GO:0015079
data:
  {"annotated_genes":["SJAG_02883","SJAG_03401","SJAG_01353","SJAG_04616","SJAG_04167"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72423,73983],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140107"},{"annotations":[114358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008900"},{"annotations":[75178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015379"},{"annotations":[81846],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015386"}]},"cv_name":"molecular_function","definition":"Enables the transfer of potassium ions (K+) from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metal ion transmembrane transporter activity","termid":"GO:0046873"}],"gene_count":5,"genes_by_uniquename":{"SJAG_01353":null,"SJAG_02883":null,"SJAG_03401":null,"SJAG_04167":null,"SJAG_04616":null},"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:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"potassium ion transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0015388","GO:0022817"],"synonyms":[{"name":"potassium transporter activity","type":"exact"},{"name":"potassium uptake permease activity","type":"related"},{"name":"potassium uptake transmembrane transporter activity","type":"related"}],"termid":"GO:0015079","terms_by_termid":{"GO:0008900":null,"GO:0015379":null,"GO:0015386":null,"GO:0140107":null}}


id: FYPO:0004222
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which trimethylation of lysine at position 20 of histone H4 is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone methylation during vegetative growth","termid":"FYPO:0000861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal histone H4-K20 trimethylation during vegetative growth","synonyms":[{"name":"normal histone H4 K20 trimethylation during vegetative growth","type":"exact"},{"name":"normal histone H4-K20 trimethylation during mitotic cell cycle","type":"related"},{"name":"normal histone H4K20me3 during vegetative growth","type":"exact"},{"name":"normal histone lysine H4 K20 trimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0004222"}


id: PBO:0027629
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_histone_H3_in_cell","termid":"PBO:0027629"}


id: PBO:0040996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bolA family member 3 pseudogene 1","termid":"PBO:0040996"}


id: MONDO:0010496
data:
  {"annotated_genes":["SJAG_00992"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87141],"is_not":false,"summary":null,"term":"MONDO:0010496"}]},"cv_name":"mondo","definition":"X-linked intellectual disability-short stature-overweight syndrome is a multiple congenital anomalies syndrome characterized by borderline to severe intellectual disability, speech delay, short stature, elevated body mass index, a pattern of truncal obesity (reported in older males), and variable neurologic features (e.g. hypotonia, tremors, gait disturbances, behavioral problems, and seizure disorders). Less common manifestations include microcephaly, microorchidism and/or microphallus. Dysmorphic features have been reported in some patients but no consistent pattern has been noted.","definition_xrefs":["Orphanet:457240"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00992":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"X-linked intellectual disability-short stature-overweight syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112056","GARD:17800","MEDGEN:901885","UMLS:C0796218","OMIM:300957"],"synonyms":[{"name":"MRX12","type":"related"},{"name":"intellectual developmental disorder, X-linked 12, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked 12","type":"related"},{"name":"intellectual disability, X-linked 35","type":"related"},{"name":"intellectual disability, X-linked type 12","type":"exact"},{"name":"mental retardation, X-linked 12","type":"related"},{"name":"mental retardation, X-linked 35","type":"related"},{"name":"mental retardation, X-linked type 12","type":"exact"}],"termid":"MONDO:0010496","terms_by_termid":{"MONDO:0010496":null},"xrefs":{"Monarch":{"xref_id":"0010496"}}}


id: PR:Q9P3A9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- utp8 gene.","definition_xrefs":["UniProtKB:Q9P3A9","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C1565.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1565.05","synonyms":[{"name":"Spom972h-utp8","type":"exact"}],"termid":"PR:Q9P3A9"}


id: MONDO:0020852
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 31","secondary_identifiers":["DOID:0111922","MEDGEN:1648419","UMLS:C4748234","OMIM:618112"],"synonyms":[{"name":"SPGF31","type":"exact"},{"name":"spermatogenic failure 31","type":"exact"}],"termid":"MONDO:0020852","xrefs":{"Monarch":{"xref_id":"0020852"}}}


id: GO:0031989
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway initiated by a bombesin binding to its receptor, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:mah"],"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":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"bombesin receptor signaling pathway","synonyms":[{"name":"bombesin receptor signalling pathway","type":"exact"}],"termid":"GO:0031989"}


id: PBO:0066044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAP1B like (pseudogene)","termid":"PBO:0066044"}


id: MONDO:0033546
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"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":"neurodegeneration, infantile-onset, biotin-responsive","secondary_identifiers":["MEDGEN:1771692","OMIM:618973","UMLS:C5436520"],"synonyms":[{"name":"NERIB","type":"exact"},{"name":"SMVT deficiency","type":"exact"},{"name":"sodium-dependent multivitamin transporter deficiency","type":"exact"}],"termid":"MONDO:0033546","xrefs":{"Monarch":{"xref_id":"0033546"}}}


id: GO:0102829
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2 verbascose = ajugose + stachyose.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete ajugose synthase activity (obsolete GO:0102829)","termid":"GO:0102829"}


id: PBO:0083549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps uncharacterized ORF YER067W","termid":"PBO:0083549"}


id: GO:0097476
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a spinal cord motor neuron from one site to another. A spinal cord motor neuron is a motor neuron that passes from the spinal cord toward or to a muscle and conducts an impulse that causes movement.","definition_xrefs":["CL:0011001","GOC:yaf","PMID:20711475"],"direct_ancestors":[{"relation_name":"is_a","term_name":"motor neuron migration","termid":"GO:0097475"}],"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":"spinal cord motor neuron migration","termid":"GO:0097476"}


id: GO:0044197
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a Rel Homology Domain (RHD) of a protein. The RHD is found in a family of eukaryotic transcription factors, which includes NF-kappaB, Dorsal, Relish and NFAT.","definition_xrefs":["InterPro:IPR011539","Wikipedia:Rel_homology_domain"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"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:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"Rel homology domain binding","synonyms":[{"name":"RHD binding","type":"exact"}],"termid":"GO:0044197"}


id: GO:0018531
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-6-hydroxynicotine + H2O + O2 = 6-hydroxypseudooxynicotine + H2O2.","definition_xrefs":["EC:1.5.3.5","RHEA:11880"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydroxy-nicotine oxidase activity","termid":"GO:0019116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"(S)-6-hydroxynicotine oxidase activity","secondary_identifiers":["KEGG_REACTION:R03202","MetaCyc:S-6-HYDROXYNICOTINE-OXIDASE-RXN","UM-BBD_reactionID:r0478"],"synonyms":[{"name":"(S)-6-hydroxynicotine:oxygen oxidoreductase activity","type":"related"},{"name":"6-hydroxy-L-nicotine oxidase activity","type":"exact"},{"name":"6-hydroxy-L-nicotine:oxygen oxidoreductase activity","type":"related"},{"name":"L-6-hydroxynicotine oxidase activity","type":"exact"}],"termid":"GO:0018531"}


id: GO:0097434
data:
  {"annotated_genes":["SJAG_01406"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103606],"is_not":false,"summary":null,"term":"GO:0097434"}]},"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: succinate(out) + H+(out) = succinate(in) + H+(in).","definition_xrefs":["PMID:1293882","GOC:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"succinate transmembrane transporter activity","termid":"GO:0015141"},{"relation_name":"is_a","term_name":"solute:proton symporter activity","termid":"GO:0015295"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01406":null},"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":"succinate:proton symporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:29303"],"synonyms":[{"name":"succinate:hydrogen symporter activity","type":"exact"}],"termid":"GO:0097434","terms_by_termid":{"GO:0097434":null}}


id: GO:0005007
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a fibroblast growth factor receptor ligand and transmitting the signal across the plasma membrane to initiate a change in cell activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane receptor protein tyrosine kinase activity","termid":"GO:0004714"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0038023","GO:0016301","GO:0004672","GO:0140096","GO:0016740"],"is_obsolete":false,"name":"fibroblast growth factor receptor activity","synonyms":[{"name":"FGF receptor activity","type":"exact"},{"name":"FGF-activated receptor activity","type":"exact"},{"name":"FGFR","type":"exact"},{"name":"fibroblast growth factor-activated receptor activity","type":"exact"}],"termid":"GO:0005007"}


id: MONDO:0016241
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare neurodevelopmental disorder characterized by recurrent episodes of hemiplegia and paroxysmal disturbances associated with persistent developmental delay and cognitive impairment.","definition_xrefs":["Orphanet:2131"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemiplegia","termid":"MONDO:0001170"},{"relation_name":"is_a","term_name":"alternating hemiplegia","termid":"MONDO:0016210"},{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"alternating hemiplegia of childhood","secondary_identifiers":["MESH:C536589","NANDO:2200357","NANDO:1200525","DOID:0050635","icd11.foundation:301329822","GARD:11","UMLS:C0338488","OMIMPS:104290","SCTID:230466004","MEDGEN:90925","NORD:758","NANDO:2100239","NANDO:2200883","NANDO:1200403","NCIT:C35261"],"synonyms":[{"name":"AHC","type":"exact"},{"name":"adrenal hypoplasia congenita","type":"exact"},{"name":"alternating hemiplegia","type":"related"},{"name":"alternating hemiplegia of childhood","type":"exact"},{"name":"alternating hemiplegia syndrome","type":"related"},{"name":"childhood alternating hemiplegia","type":"exact"},{"name":"congenital adrenal Hypoplasia","type":"exact"},{"name":"congenital adrenal gland hypoplasia","type":"exact"},{"name":"paediatric alternating hemiplegia","type":"exact"},{"name":"pediatric alternating hemiplegia","type":"exact"}],"termid":"MONDO:0016241","xrefs":{"Monarch":{"xref_id":"0016241"}}}


id: PBO:0001330
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cells can become independent of the essential calnexin","termid":"PBO:0001330"}


id: PBO:0081618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 547","termid":"PBO:0081618"}


id: PBO:0082718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the Paf1 complex; which associates with RNA polymerase II and is involved in histone methylation; plays a role in regulating Ty1 transposition; involved in transcription elongation as demonstrated by the G-less-based run-on (GLRO) assay","termid":"PBO:0082718"}


id: GO:0097140
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex consisting of BIM and BCL-xl, members of the Bcl-2 family of anti- and proapoptotic regulators.","definition_xrefs":["GOC:so","PMID:14634621"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bcl-2 family protein complex","termid":"GO:0097136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"BIM-BCL-xl complex","termid":"GO:0097140"}


id: GO:0031173
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of otoliths during embryogenesis with completion in early postembryonic development. Formation occurs by precipitation of specific crystal forms of calcium carbonate around an organic core of extracellular matrix proteins. Otoconia (otoliths) are small (~10 micron) dense extracellular particles present in the otolith end organs of the vertebrate inner ear.","definition_xrefs":["GOC:dsf","PMID:15581873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"otolith mineralization","termid":"GO:0045299"}],"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":"otolith mineralization completed early in development","synonyms":[{"name":"otoconia mineralization","type":"exact"},{"name":"otoconium mineralization","type":"exact"}],"termid":"GO:0031173"}


id: PBO:0028127
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_valinomycin","termid":"PBO:0028127"}


id: GO:0015165
data:
  {"annotated_genes":["SJAG_00434","SJAG_04162","SJAG_04697","SJAG_01177"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90240,76620,77770],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005459"},{"annotations":[77771],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005460"},{"annotations":[79361],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005462"},{"annotations":[79362],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005464"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a pyrimidine nucleotide-sugar from one side of a membrane to the other. Pyrimidine nucleotide-sugars are pyrimidine nucleotides in glycosidic linkage with a monosaccharide or monosaccharide derivative.","definition_xrefs":["GOC:ai","GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar transmembrane transporter activity","termid":"GO:0005338"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00434":null,"SJAG_01177":null,"SJAG_04162":null,"SJAG_04697":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"pyrimidine nucleotide-sugar transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0015165","terms_by_termid":{"GO:0005459":null,"GO:0005460":null,"GO:0005462":null,"GO:0005464":null}}


id: GO:0050778
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the immune response, the immunological reaction of an organism to an immunogenic stimulus.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of immune system process","termid":"GO:0002684"},{"relation_name":"is_a","term_name":"positive regulation of response to stimulus","termid":"GO:0048584"},{"relation_name":"is_a","term_name":"regulation of immune response","termid":"GO:0050776"},{"relation_name":"positively_regulates","term_name":"immune response","termid":"GO:0006955"}],"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 immune response","synonyms":[{"name":"stimulation of immune response","type":"narrow"},{"name":"up regulation of immune response","type":"exact"},{"name":"up-regulation of immune response","type":"exact"},{"name":"upregulation of immune response","type":"exact"}],"termid":"GO:0050778"}


id: PBO:0078270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 6-1","termid":"PBO:0078270"}


id: MONDO:0007705
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hemolytic anemia","termid":"MONDO:0003664"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"Heinz body anemia","secondary_identifiers":["HP:0005511","MedDRA:10002058","UMLS:C0700299","MEDGEN:148583","Orphanet:178330","MESH:C563030","OMIM:140700","DOID:0111363"],"synonyms":[{"name":"Heinz body anemias","type":"related"},{"name":"Heinz body anemias, alpha-","type":"exact"}],"termid":"MONDO:0007705","xrefs":{"Monarch":{"xref_id":"0007705"}}}


id: FYPO:0005524
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 nucleosome occupancy is lower than normal in the central core of the centromeric regions. Nucleosome occupancy measures the tendency for DNA in a given region to be packaged into nucleosomes.","definition_xrefs":["PMID:22990236","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased nucleosome occupancy","termid":"FYPO:0004491"}],"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:0000641"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased nucleosome occupancy at centromere central core","synonyms":[{"name":"decreased nucleosome occupancy at centromere central core during mitotic cell cycle","type":"related"},{"name":"decreased nucleosome occupancy at centromere central core during vegetative growth","type":"exact"},{"name":"decreased nucleosome occupancy in centromere central core","type":"exact"},{"name":"reduced nucleosome occupancy at centromere central core","type":"exact"}],"termid":"FYPO:0005524"}


id: PBO:0083282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; not conserved in closely related Saccharomyces species; partially overlaps the verified essential gene RRP14","termid":"PBO:0083282"}


id: GO:0004776
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: GTP + succinate + CoA = GDP + succinyl-CoA + phosphate.","definition_xrefs":["RHEA:22120"],"direct_ancestors":[{"relation_name":"is_a","term_name":"succinate-CoA ligase activity","termid":"GO:0004774"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0016874","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"succinate-CoA ligase (GDP-forming) activity","secondary_identifiers":["EC:6.2.1.4","KEGG_REACTION:R00432","MetaCyc:SUCCINATE--COA-LIGASE-GDP-FORMING-RXN","Reactome:R-HSA-71775"],"synonyms":[{"name":"succinate:CoA ligase (GDP-forming) activity","type":"related"},{"name":"succinyl CoA synthetase activity","type":"related"},{"name":"succinyl coenzyme A synthetase","type":"broad"},{"name":"succinyl coenzyme A synthetase (GDP-forming) activity","type":"related"},{"name":"succinyl coenzyme A synthetase (guanosine diphosphate-forming) activity","type":"related"},{"name":"succinyl-CoA synthetase (GDP-forming) activity","type":"related"}],"termid":"GO:0004776"}


id: GO:0098756
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 an interleukin-21 stimulus.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cytokine","termid":"GO:0034097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to interleukin-21","synonyms":[{"name":"response to IL-21","type":"exact"}],"termid":"GO:0098756"}


id: PBO:0065808
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB3B, member RAS oncogene family","termid":"PBO:0065808"}


id: PBO:0054951
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 2365","termid":"PBO:0054951"}


id: RO:0001020
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A relation between a material entity and a condition (a phenotype or disease) of a host, in which the material entity is not part of the host, and is considered harmless to non-allergic hosts, and the condition results in pathological processes that include an abnormally strong immune response against the material entity.","direct_ancestors":[{"relation_name":"is_a","term_name":"causes_or_contributes_to_condition","termid":"RO:0003302"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_allergic_trigger_for","termid":"RO:0001020"}


id: PBO:0001067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk9 (predicted)","termid":"PBO:0001067"}


id: MONDO:0018125
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Focal epilepsy-intellectual disability-cerebro-cerebellar malformation is a rare, genetic neurological disorder characterized by early infantile-onset of seizures, borderline to moderate intellectual disability, cerebellar features including dysarthria and ataxia and cerebellar atrophy and cortical thickening observed on MRI imaging. Seizures are typically focal (with prominent eye blinking, facial and limb jerking), precipitated by fever and often commence with an oral sensory aura (anesthetized tongue sensation). When not properly controlled by anti-epileptic medication, weekly frequency and persistence into adult life is observed.","definition_xrefs":["Orphanet:352587"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monogenic epilepsy","termid":"MONDO:0015653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"focal epilepsy-intellectual disability-cerebro-cerebellar malformation","secondary_identifiers":["GARD:21522","MEDGEN:1640999","UMLS:C4707306"],"synonyms":[{"name":"focal epilepsy-intellectual disability-dysarthria-ataxia syndrome","type":"exact"}],"termid":"MONDO:0018125","xrefs":{"Monarch":{"xref_id":"0018125"}}}


id: PBO:0017682
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABC transmembrane transporter Pdr1","termid":"PBO:0017682"}


id: GO:0021675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a nerve over time, from its formation to the mature structure.","definition_xrefs":["GO_REF:0000021","GOC:cls","GOC:dgh","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"nervous system development","termid":"GO:0007399"}],"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":"nerve development","termid":"GO:0021675"}


id: PBO:0082227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-arrestin, ubiquitin ligase adaptor for Rsp5p; regulates starvation- and substrate-induced Ub-dependent endocytosis of select plasma membrane localized amino acid transporters; substrate of Rsp5p-mediated Lys63-polyubiquitination and Ubp2-mediated deubiquitination; promoter contains several Gcn4p binding sites required for induction in response to starvation via Gcn4p and the general amino acid control pathway; ECM21 has a paralog, CSR2, that arose from the whole genome duplication","termid":"PBO:0082227"}


id: GO:1903131
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a mononuclear cell.","definition_xrefs":["PMID:24759906","GOC:TermGenie","CL:0000842","GO_REF:0000086"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte differentiation","termid":"GO:0002521"}],"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":"mononuclear cell differentiation","termid":"GO:1903131"}


id: PR:000024934
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A ubiquitin ligase complex composed of two subunits of Schizosaccharomyces pombe E3 ubiquitin-protein ligase dma1.","definition_xrefs":["PRO:DAN","PMID:22669973"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dma1 homodimer (Schizosaccharomyces pombe)","pombase_gene_id":"SPAC17G8.10c","termid":"PR:000024934"}


id: GO:0032747
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of interleukin-23 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 interleukin-23 production","termid":"GO:0032667"},{"relation_name":"positively_regulates","term_name":"interleukin-23 production","termid":"GO:0032627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of interleukin-23 production","secondary_identifiers":["GO:0045398"],"synonyms":[{"name":"activation of interleukin-23 production","type":"narrow"},{"name":"positive regulation of IL-23 production","type":"exact"},{"name":"positive regulation of interleukin-23 biosynthetic process","type":"narrow"},{"name":"stimulation of interleukin-23 production","type":"narrow"},{"name":"up regulation of interleukin-23 production","type":"exact"},{"name":"up-regulation of interleukin-23 production","type":"exact"},{"name":"upregulation of interleukin-23 production","type":"exact"}],"termid":"GO:0032747"}


id: GO:0032118
data:
  {"annotated_genes":["SJAG_00368","SJAG_04143","SJAG_03073"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103380,108562,113227],"is_not":false,"summary":null,"term":"GO:0032118"}]},"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 the horsetail-astral array, a structure of astral microtubules that emanates from the spindle pole body during meiosis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule cytoskeleton organization","termid":"GO:0000226"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"dynein-driven meiotic oscillatory nuclear movement","termid":"GO:0030989"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00368":null,"SJAG_03073":null,"SJAG_04143":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"is_a","termid":"GO:0000226"},{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0000226","GO:0007010","GO:0140013","GO:0008150","GO:0006810","GO:0007049"],"is_obsolete":false,"name":"horsetail-astral microtubule organization","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"horsetail-astral microtubule array organization","type":"exact"},{"name":"horsetail-astral microtubule organisation","type":"exact"},{"name":"horsetail-astral microtubule organization and biogenesis","type":"related"}],"termid":"GO:0032118","terms_by_termid":{"GO:0032118":null}}


id: MONDO:0956989
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An EWSERI-negative small round cell tumor that is characterized by a recurrent translocation involving the CIC gene on chromosome 19 and either DUX4 gene on chromosome 4 or DUX4L gene on chromosome 10. The translocation results in either CIC-DUX4, t(4;19)(q35;q13) or CIC-DUX4L, t(10;19)(q26;q13) fusions.","definition_xrefs":["DOID:0081250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"EWSR1-negative small round cell tumor","termid":"MONDO:0858921"}],"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":"CIC-rearranged sarcoma","secondary_identifiers":["NCIT:C120224","UMLS:C3899764","MEDGEN:859358"],"termid":"MONDO:0956989","xrefs":{"Monarch":{"xref_id":"0956989"}}}


id: PBO:0081813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 736 pseudogene 6, Y-linked","termid":"PBO:0081813"}


id: FYPO:0005642
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which homologous chromosome biorientation is abnormal during meiosis, with chromosomes that are not correctly oriented with the kinetochores facing outwards. Homologous chromosome biorientation is the process in which the sister centromeres of one chromosome attach to microtubules that emanate from the same spindle pole, ensuring that homologous maternal and paternal chromosomes are pulled in opposite directions at anaphase of meiosis I.","definition_xrefs":["PMID:21920317","PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic homologous chromosome biorientation","termid":"FYPO:0003177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abnormal meiotic homologous chromosome biorientation with abnormal kinetochore orientation","synonyms":[{"name":"abnormal homologous chromosome biorientation with abnormal kinetochore orientation during meiosis","type":"exact"},{"name":"abnormal homologous chromosome orientation involved in meiotic metaphase I plate congression with abnormal kinetochore orientation","type":"exact"},{"name":"abnormal meiotic homologous chromosome biorientation with abnormal kinetochore position","type":"exact"}],"termid":"FYPO:0005642"}


id: PBO:0117095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTGER3 antisense RNA 1","termid":"PBO:0117095"}


id: PBO:0066826
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 125","termid":"PBO:0066826"}


id: MONDO:0012973
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory bowel disease that has material basis in variation in the chromosome region 12q15.","definition_xrefs":["DOID:0110901","PMID:19122664"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory bowel disease","termid":"MONDO:0005265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"inflammatory bowel disease 26","secondary_identifiers":["UMLS:C2675249","MESH:C567217","OMIM:612639","MEDGEN:382561"],"synonyms":[{"name":"IBD26","type":"exact"},{"name":"inflammatory bowel disease 26","type":"exact"},{"name":"inflammatory bowel disease type 26","type":"exact"}],"termid":"MONDO:0012973","xrefs":{"Monarch":{"xref_id":"0012973"}}}


id: PBO:0027613
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-branched,_elongated,_septated_cell","termid":"PBO:0027613"}


id: PR:O74836
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl101 gene.","definition_xrefs":["UniProtKB:O74836","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L1-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1183.08c","synonyms":[{"name":"L10a (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rpl101","type":"exact"}],"termid":"PR:O74836"}


id: MOD:00116
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-diacylglycerol-L-cysteine.","definition_xrefs":["RESID:AA0107","PubMed:9056182","PubMed:10896212","Unimod:377#C","PubMed:4575979"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"},{"relation_name":"is_a","term_name":"lipoconjugated residue","termid":"MOD:01155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"},{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905","MOD:01155"],"is_obsolete":false,"name":"S-diacylglycerol-L-cysteine","synonyms":[{"name":"(2R)-2-amino-3-[(2S)-2-((9Z)-9-octadecenoyloxy)-3-(hexadecanoyloxy)propyl]sulfanylpropanoic acid","type":"exact"},{"name":"2-amino-3-[(S)-2-((Z)-9-octadecenoyloxy)-3-(hexadecanoyloxy)propyl]thiopropanoic acid","type":"exact"},{"name":"Diacylglycerol","type":"related"},{"name":"LIPID S-diacylglycerol cysteine","type":"exact"},{"name":"S-(1-2'-oleoyl-3'-palmitoyl-glycerol)cysteine","type":"exact"},{"name":"S-(2',3'-diacylglycerol)-L-cysteine","type":"exact"},{"name":"S-diacylglycerol-L-cysteine","type":"exact"},{"name":"SAcyl2GlyceroCys","type":"exact"},{"name":"diacylglycerol","type":"related"}],"termid":"MOD:00116"}


id: PATO:0000056
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An organismal quality inhering in a bearer by virtue of the bearer's disposition to synthesize a particular organic compound required for its growth.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Trophic_level"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organismal quality","termid":"PATO:0001995"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trophic quality","synonyms":[{"name":"nutritional quality","type":"related"}],"termid":"PATO:0000056"}


id: PBO:0076480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane anterior posterior transformation 1","termid":"PBO:0076480"}


id: PBO:0072829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SANT and BTB domain regulator of CSR","termid":"PBO:0072829"}


id: PBO:0035705
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_arginase_activity","termid":"PBO:0035705"}


id: PBO:0029825
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_curved_elongated_vegetative_cell_population_(obsolete_FYPO:0002412)","termid":"PBO:0029825"}


id: FYPO:0006377
data:
  {"alleles_by_uniquename":{"SJAG_01745:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01745","name":"lem2delta","uniquename":"SJAG_01745:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0003657"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the endoplasmic reticulum is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization","termid":"FYPO:0001370"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01050":null,"SJAG_01745":null},"genotype_count":1,"genotypes_by_uniquename":{"lem2delta":{"display_name":"lem2delta","display_uniquename":"lem2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01745:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000138","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abnormal protein localization to endoplasmic reticulum","references_by_uniquename":{"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_01745"],"single_locus_genotype_uniquenames":["lem2delta"],"synonyms":[{"name":"abnormal protein localisation to endoplasmic reticulum","type":"exact"},{"name":"abnormal protein localization to ER","type":"exact"}],"termid":"FYPO:0006377","terms_by_termid":{"FYECO:0000137":null,"FYPO:0003657":null,"FYPO_EXT:0000001":null}}


id: PBO:0062947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proliferation-associated 2G4 pseudogene 5","termid":"PBO:0062947"}


id: PBO:0072915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scavenger receptor class A member 5","termid":"PBO:0072915"}


id: PBO:0027942
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_chromatin_at_RNA_polymerase_II-regulated_genes_during_vegetative_growth","termid":"PBO:0027942"}


id: GO:0033126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of GTP, guanosine triphosphate.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of GTP catabolic process (obsolete GO:0033126)","synonyms":[{"name":"positive regulation of GTP breakdown","type":"exact"},{"name":"positive regulation of GTP catabolism","type":"exact"},{"name":"positive regulation of GTP degradation","type":"exact"}],"termid":"GO:0033126"}


id: PBO:0073894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC12A9 antisense RNA 1","termid":"PBO:0073894"}


id: PBO:0043674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coronin 1B","termid":"PBO:0043674"}


id: MONDO:0013437
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the PDE6A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"},{"relation_name":"is_a","term_name":"PDE6A-related retinopathy","termid":"MONDO:0700224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005328","MONDO:0004736"],"is_obsolete":false,"name":"retinitis pigmentosa 43","secondary_identifiers":["MEDGEN:462489","GARD:15716","OMIM:613810","DOID:0110379","UMLS:C3151139","ICD10CM:H35.5"],"synonyms":[{"name":"PDE6A retinitis pigmentosa","type":"exact"},{"name":"RP43","type":"exact"},{"name":"retinitis pigmentosa 43","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in PDE6A","type":"exact"},{"name":"retinitis pigmentosa type 43","type":"exact"}],"termid":"MONDO:0013437","xrefs":{"Monarch":{"xref_id":"0013437"}}}


id: GO:0070013
data:
  {"annotated_genes":["SJAG_04768","SJAG_04054","SJAG_00172","SJAG_02104","SJAG_04084","SJAG_07011","SJAG_00245","SJAG_01282","SJAG_02762","SJAG_00483","SJAG_02608","SJAG_01719","SJAG_07005","SJAG_05338","SJAG_03156","SJAG_02469","SJAG_01753","SJAG_01610","SJAG_02372","SJAG_03636","SJAG_00288","SJAG_00830","SJAG_00207","SJAG_05307","SJAG_03877","SJAG_04995","SJAG_00941","SJAG_04824","SJAG_02244","SJAG_03804","SJAG_00728","SJAG_03719","SJAG_02424","SJAG_02813","SJAG_03752","SJAG_02835","SJAG_04160","SJAG_01797","SJAG_01140","SJAG_01604","SJAG_01677","SJAG_02952","SJAG_01436","SJAG_02274","SJAG_01347","SJAG_04017","SJAG_04993","SJAG_02071","SJAG_00294","SJAG_03425","SJAG_02560","SJAG_04477","SJAG_03051","SJAG_03402","SJAG_01431","SJAG_00764","SJAG_04274","SJAG_01303","SJAG_01577","SJAG_04379","SJAG_03568","SJAG_00611","SJAG_01234","SJAG_04823","SJAG_04303","SJAG_00746","SJAG_03709","SJAG_00995","SJAG_01761","SJAG_01818","SJAG_04006","SJAG_03578","SJAG_03694","SJAG_02359","SJAG_05187","SJAG_01180","SJAG_01708","SJAG_03724","SJAG_02101","SJAG_01230","SJAG_04610","SJAG_01926","SJAG_02829","SJAG_00512","SJAG_02413","SJAG_00540","SJAG_01045","SJAG_00142","SJAG_00456","SJAG_00231","SJAG_04004","SJAG_04010","SJAG_03103","SJAG_02100","SJAG_01122","SJAG_04840","SJAG_01821","SJAG_02911","SJAG_01368","SJAG_01417","SJAG_02070","SJAG_01325","SJAG_02836","SJAG_01387","SJAG_04310","SJAG_05232","SJAG_03919","SJAG_02214","SJAG_00202","SJAG_01498","SJAG_04818","SJAG_02900","SJAG_00088","SJAG_02724","SJAG_03976","SJAG_00758","SJAG_00863","SJAG_04244","SJAG_02432","SJAG_02690","SJAG_01377","SJAG_03898","SJAG_02248","SJAG_03022","SJAG_01752","SJAG_00896","SJAG_01839","SJAG_00833","SJAG_04128","SJAG_00882","SJAG_03451","SJAG_02303","SJAG_03700","SJAG_00689","SJAG_00697","SJAG_04918","SJAG_04395","SJAG_00584","SJAG_03020","SJAG_00695","SJAG_02901","SJAG_04366","SJAG_00947","SJAG_03900","SJAG_00894","SJAG_02164","SJAG_03033","SJAG_03176","SJAG_04492","SJAG_04420","SJAG_01877","SJAG_02360","SJAG_00410","SJAG_02546","SJAG_04308","SJAG_02283","SJAG_00163","SJAG_03125","SJAG_00706","SJAG_03916","SJAG_00868","SJAG_02682","SJAG_02475","SJAG_03255","SJAG_04180","SJAG_04436","SJAG_02736","SJAG_04680","SJAG_01446","SJAG_04389","SJAG_03584","SJAG_04062","SJAG_01765","SJAG_03923","SJAG_05248","SJAG_04788","SJAG_03438","SJAG_00255","SJAG_03583","SJAG_03155","SJAG_02610","SJAG_00095","SJAG_03927","SJAG_04817","SJAG_01868","SJAG_03956","SJAG_00145","SJAG_01419","SJAG_03053","SJAG_01149","SJAG_06022","SJAG_02991","SJAG_04785","SJAG_04635","SJAG_03638","SJAG_02235","SJAG_00358","SJAG_01153","SJAG_03649","SJAG_05218","SJAG_03252","SJAG_02094","SJAG_01494","SJAG_03844","SJAG_03036","SJAG_03199","SJAG_04009","SJAG_02812","SJAG_01128","SJAG_01670","SJAG_01615","SJAG_06253","SJAG_03299","SJAG_04473","SJAG_01518","SJAG_01275","SJAG_02652","SJAG_02644","SJAG_04889","SJAG_02098","SJAG_06440","SJAG_02187","SJAG_03413","SJAG_03840","SJAG_02607","SJAG_03780","SJAG_04897","SJAG_02821","SJAG_03234","SJAG_01684","SJAG_02541","SJAG_03685","SJAG_03654","SJAG_00714","SJAG_02653","SJAG_02229","SJAG_02627","SJAG_04508","SJAG_04856","SJAG_02879","SJAG_00644","SJAG_04959","SJAG_03666","SJAG_02723","SJAG_00986","SJAG_02077","SJAG_00617","SJAG_02433","SJAG_03008","SJAG_00400","SJAG_04284","SJAG_00616","SJAG_00703","SJAG_04353","SJAG_02535","SJAG_00799","SJAG_04748","SJAG_00564","SJAG_04601","SJAG_03847","SJAG_03495","SJAG_01807","SJAG_04791","SJAG_04069","SJAG_00814","SJAG_04493","SJAG_00272","SJAG_02073","SJAG_05560","SJAG_04862","SJAG_00403","SJAG_03662","SJAG_04195","SJAG_04933","SJAG_03430","SJAG_01476","SJAG_03449","SJAG_03459","SJAG_02495","SJAG_01551","SJAG_05237","SJAG_01213","SJAG_02393","SJAG_01565","SJAG_01468","SJAG_03901","SJAG_03080","SJAG_04367","SJAG_01630","SJAG_04688","SJAG_00961","SJAG_05321","SJAG_00945","SJAG_05190","SJAG_01176","SJAG_03181","SJAG_03846","SJAG_03967","SJAG_04164","SJAG_01745","SJAG_02990","SJAG_03627","SJAG_04056","SJAG_04599","SJAG_01712","SJAG_04094","SJAG_01823","SJAG_01882","SJAG_02549","SJAG_01811","SJAG_02409","SJAG_03874","SJAG_03458","SJAG_04377","SJAG_00701","SJAG_04289","SJAG_03441","SJAG_03617","SJAG_02571","SJAG_02871","SJAG_05276","SJAG_03964","SJAG_01413","SJAG_00751","SJAG_04911","SJAG_03040","SJAG_04378","SJAG_04738","SJAG_05186","SJAG_02872","SJAG_01444","SJAG_01201","SJAG_02981","SJAG_03014","SJAG_01574","SJAG_04641","SJAG_03567","SJAG_04527","SJAG_02300","SJAG_04019","SJAG_01915","SJAG_00349","SJAG_07002","SJAG_01111","SJAG_03839","SJAG_03843","SJAG_00458","SJAG_00083","SJAG_03232","SJAG_03722","SJAG_05193","SJAG_02377","SJAG_03128","SJAG_03163","SJAG_00749","SJAG_01560","SJAG_00468","SJAG_01088","SJAG_03867","SJAG_01624","SJAG_04656","SJAG_00635","SJAG_02548","SJAG_00060","SJAG_04106","SJAG_02846","SJAG_03832","SJAG_00139","SJAG_04917","SJAG_04210","SJAG_02170","SJAG_02397","SJAG_01909","SJAG_01358","SJAG_00936","SJAG_02341","SJAG_03539","SJAG_04838","SJAG_02417","SJAG_04571","SJAG_04064","SJAG_03586","SJAG_00790","SJAG_00364","SJAG_02287","SJAG_03099","SJAG_02238","SJAG_04046","SJAG_03593","SJAG_02174","SJAG_04118","SJAG_02754","SJAG_03303","SJAG_04893","SJAG_00756","SJAG_01895","SJAG_16455","SJAG_00441","SJAG_00323","SJAG_02043","SJAG_00741","SJAG_00841","SJAG_01575","SJAG_04940","SJAG_02306","SJAG_03569","SJAG_03290","SJAG_04528","SJAG_01820","SJAG_02524","SJAG_00844","SJAG_02466","SJAG_00170","SJAG_01352","SJAG_03479","SJAG_02777","SJAG_01013","SJAG_01853","SJAG_04411","SJAG_01662","SJAG_01191","SJAG_00657","SJAG_00883","SJAG_00813","SJAG_00702","SJAG_04753","SJAG_04663","SJAG_MIT05","SJAG_01503","SJAG_03957","SJAG_01169","SJAG_03603","SJAG_03468","SJAG_03535","SJAG_00949","SJAG_04396","SJAG_01369","SJAG_06135","SJAG_01777","SJAG_03289","SJAG_04494","SJAG_01049","SJAG_02189","SJAG_03411","SJAG_03433","SJAG_03221","SJAG_01407","SJAG_03550","SJAG_02749","SJAG_01391","SJAG_04894","SJAG_01207","SJAG_05216","SJAG_03321","SJAG_04145","SJAG_00731","SJAG_00692","SJAG_01922","SJAG_04152","SJAG_03028","SJAG_02790","SJAG_03985","SJAG_03322","SJAG_03107","SJAG_01727","SJAG_04671","SJAG_01272","SJAG_05020","SJAG_02299","SJAG_03217","SJAG_01988","SJAG_00798","SJAG_01606","SJAG_03222","SJAG_01420","SJAG_03786","SJAG_00653","SJAG_03179","SJAG_00921","SJAG_00962","SJAG_01410","SJAG_00884","SJAG_02702","SJAG_00253","SJAG_00943","SJAG_00628","SJAG_05270","SJAG_00327","SJAG_01262","SJAG_00168","SJAG_00230","SJAG_00159","SJAG_04321","SJAG_02530","SJAG_04539","SJAG_02458","SJAG_00735","SJAG_06635","SJAG_00944","SJAG_01548","SJAG_03431","SJAG_03585","SJAG_00889","SJAG_00311","SJAG_00634","SJAG_03984","SJAG_03090","SJAG_02768","SJAG_03426","SJAG_03104","SJAG_03025","SJAG_00668","SJAG_00888","SJAG_00259","SJAG_04478","SJAG_04576","SJAG_16456","SJAG_04863","SJAG_01250","SJAG_04414","SJAG_05197","SJAG_00582","SJAG_MIT07","SJAG_01591","SJAG_02621","SJAG_01465","SJAG_04208","SJAG_00562","SJAG_01907","SJAG_03789","SJAG_01132","SJAG_03266","SJAG_04574","SJAG_02046","SJAG_00840","SJAG_04950","SJAG_01597","SJAG_01374","SJAG_02553","SJAG_01996","SJAG_03855","SJAG_00854","SJAG_01185","SJAG_04899","SJAG_02585","SJAG_01623","SJAG_04149","SJAG_02253","SJAG_06586","SJAG_03872","SJAG_03211","SJAG_00181","SJAG_00930","SJAG_04014","SJAG_04979","SJAG_03959","SJAG_00086","SJAG_00344","SJAG_02207","SJAG_00399","SJAG_04654","SJAG_01611","SJAG_04030","SJAG_05398","SJAG_03161","SJAG_04758","SJAG_00572","SJAG_01327","SJAG_00315","SJAG_02998","SJAG_00148","SJAG_00796","SJAG_04977","SJAG_02074","SJAG_01521","SJAG_02744","SJAG_02396","SJAG_03159","SJAG_01019","SJAG_02217","SJAG_02899","SJAG_03861","SJAG_04638","SJAG_03551","SJAG_02747","SJAG_02057","SJAG_04305","SJAG_03618","SJAG_02667","SJAG_02818","SJAG_01767","SJAG_02547","SJAG_00659","SJAG_04285","SJAG_01203","SJAG_00687","SJAG_01903","SJAG_03745","SJAG_00341","SJAG_04766","SJAG_01804","SJAG_01473","SJAG_03884","SJAG_00166","SJAG_03118","SJAG_00077","SJAG_02186","SJAG_04339","SJAG_01004","SJAG_04533","SJAG_03410","SJAG_00153","SJAG_03144","SJAG_04524","SJAG_00965","SJAG_04140","SJAG_02281","SJAG_04669","SJAG_05244","SJAG_04614","SJAG_04142","SJAG_00744","SJAG_03574","SJAG_05261","SJAG_01674","SJAG_03532","SJAG_00369","SJAG_02721","SJAG_02778","SJAG_02097","SJAG_04989","SJAG_01509","SJAG_03097","SJAG_00119","SJAG_04432","SJAG_04368","SJAG_02250","SJAG_03180","SJAG_01764","SJAG_00396","SJAG_04039","SJAG_04877","SJAG_01354","SJAG_04213","SJAG_03796","SJAG_00220","SJAG_03424","SJAG_04754","SJAG_01632","SJAG_01005","SJAG_03836","SJAG_05573","SJAG_02506","SJAG_07009","SJAG_02922","SJAG_04562","SJAG_04560","SJAG_03454","SJAG_04994","SJAG_00326","SJAG_05192","SJAG_04173","SJAG_01605","SJAG_00497","SJAG_04033","SJAG_00530","SJAG_00872","SJAG_04397","SJAG_03230","SJAG_01867","SJAG_02908","SJAG_01296","SJAG_04281","SJAG_02119","SJAG_03026","SJAG_02394","SJAG_02656","SJAG_01710","SJAG_01936","SJAG_02841","SJAG_02210","SJAG_02500","SJAG_00480","SJAG_04409","SJAG_02428","SJAG_03689","SJAG_04108","SJAG_02606","SJAG_00769","SJAG_00901","SJAG_05331","SJAG_04261","SJAG_00082","SJAG_02025","SJAG_01083","SJAG_02800","SJAG_01517","SJAG_00513","SJAG_04645","SJAG_00729","SJAG_00646","SJAG_01182","SJAG_00271","SJAG_00939","SJAG_04148","SJAG_03127","SJAG_00286","SJAG_00897","SJAG_00857","SJAG_01698","SJAG_04272","SJAG_04341","SJAG_03906","SJAG_02067","SJAG_00196","SJAG_05239","SJAG_02294","SJAG_00636","SJAG_04670","SJAG_02527","SJAG_01592","SJAG_02318","SJAG_01762","SJAG_00047","SJAG_01475","SJAG_04324","SJAG_04153","SJAG_03460","SJAG_02870","SJAG_01147","SJAG_03016","SJAG_04141","SJAG_02856","SJAG_00618","SJAG_02451","SJAG_02496","SJAG_00421","SJAG_01478","SJAG_02830","SJAG_04330","SJAG_02490","SJAG_03563","SJAG_01808","SJAG_03297","SJAG_03713","SJAG_02758","SJAG_02917","SJAG_02825","SJAG_00984","SJAG_02630","SJAG_01226","SJAG_01125","SJAG_05295","SJAG_03952","SJAG_04346","SJAG_01375","SJAG_03070","SJAG_05320","SJAG_00879","SJAG_00363","SJAG_02226","SJAG_03182","SJAG_03285","SJAG_00306","SJAG_00968","SJAG_05333","SJAG_03461","SJAG_00696","SJAG_04879","SJAG_04530","SJAG_04400","SJAG_00045","SJAG_02680","SJAG_01280","SJAG_01454","SJAG_00583","SJAG_00532","SJAG_00132","SJAG_01047","SJAG_02887","SJAG_02427","SJAG_03061","SJAG_01110","SJAG_00860","SJAG_02236","SJAG_02037","SJAG_00105","SJAG_03971","SJAG_00838","SJAG_00100","SJAG_04083","SJAG_02979","SJAG_04306","SJAG_04767","SJAG_00455","SJAG_05253","SJAG_01799","SJAG_04596","SJAG_03961","SJAG_04257","SJAG_02891","SJAG_04929","SJAG_00958","SJAG_01580","SJAG_02771","SJAG_01647","SJAG_03418","SJAG_03473","SJAG_04216","SJAG_04457","SJAG_03674","SJAG_02172","SJAG_04355","SJAG_03042","SJAG_01540","SJAG_03068","SJAG_00887","SJAG_00782","SJAG_02242","SJAG_02662","SJAG_00934","SJAG_04256","SJAG_03065","SJAG_04582","SJAG_04008","SJAG_03466","SJAG_03730","SJAG_00581","SJAG_00449","SJAG_MIT06","SJAG_00955","SJAG_04916","SJAG_00269","SJAG_02464","SJAG_01713","SJAG_03579","SJAG_00103","SJAG_04098","SJAG_01010","SJAG_04650","SJAG_03897","SJAG_00373","SJAG_04852","SJAG_03939","SJAG_02416","SJAG_02615","SJAG_00629","SJAG_04992","SJAG_04224","SJAG_02156","SJAG_05180","SJAG_02622","SJAG_03206","SJAG_01330","SJAG_02508","SJAG_04081","SJAG_03145","SJAG_02544","SJAG_04116","SJAG_00107","SJAG_00097","SJAG_01016","SJAG_03393","SJAG_04097","SJAG_01463","SJAG_06110","SJAG_02499","SJAG_00932","SJAG_03341","SJAG_04312","SJAG_01650","SJAG_02201","SJAG_04491","SJAG_01193","SJAG_02759","SJAG_04186","SJAG_02977","SJAG_00576","SJAG_03728","SJAG_01734","SJAG_02038","SJAG_01562","SJAG_00538","SJAG_04974","SJAG_02592","SJAG_02661","SJAG_01151","SJAG_03982","SJAG_00471","SJAG_03641","SJAG_02439","SJAG_03905","SJAG_03554","SJAG_00523","SJAG_02720","SJAG_00722","SJAG_03954","SJAG_05679","SJAG_00116","SJAG_00054","SJAG_00874","SJAG_03946","SJAG_01267","SJAG_00178","SJAG_03284","SJAG_04150","SJAG_02182","SJAG_01313","SJAG_00566","SJAG_03608","SJAG_04559","SJAG_04190","SJAG_03419","SJAG_02681","SJAG_05008","SJAG_00502","SJAG_03071","SJAG_03862","SJAG_02324","SJAG_04336","SJAG_04936","SJAG_00873","SJAG_02198","SJAG_04424","SJAG_02775","SJAG_00150","SJAG_02536","SJAG_00536","SJAG_04689","SJAG_01174","SJAG_04919","SJAG_02798","SJAG_01813","SJAG_04207","SJAG_00198","SJAG_05282","SJAG_02526","SJAG_02329","SJAG_02353","SJAG_01084","SJAG_04547","SJAG_03680","SJAG_02875","SJAG_00186","SJAG_01520","SJAG_02335","SJAG_02382","SJAG_03888","SJAG_04908","SJAG_05301","SJAG_04490","SJAG_01949","SJAG_00420","SJAG_02385","SJAG_02658","SJAG_04183","SJAG_01238","SJAG_03931","SJAG_04575","SJAG_02348","SJAG_06613","SJAG_03192","SJAG_02452","SJAG_01323","SJAG_01495","SJAG_04351","SJAG_00772","SJAG_02643","SJAG_03077","SJAG_00748","SJAG_02209","SJAG_01067","SJAG_03481","SJAG_00886","SJAG_01829","SJAG_02267","SJAG_03588","SJAG_01365"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[74712,72148,77019,76628],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005658"},{"annotations":[59457,82089,76272,79399],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031429"},{"annotations":[97946,117135],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0015030"},{"annotations":[80426,78037,68486,74289,72850],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016593"},{"annotations":[74745,75672,80722],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030896"},{"annotations":[113294,100057,106243,89345,94123],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071920"},{"annotations":[115996,120857,119719,96240,98645,112473],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043494"},{"annotations":[92799,82018,76878,77559,80615],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000794"},{"annotations":[94982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099021"},{"annotations":[81270,97711,112909],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070692"},{"annotations":[76851,78658,72752,104772],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043625"},{"annotations":[90696],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001651"},{"annotations":[78982,118269,82080],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005662"},{"annotations":[113639,58553,115180,57179,113382,61742,78801,115573,109804,110024,67319,80058,61800,63601,95829,73751,75546],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031261"},{"annotations":[74061,74719],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032044"},{"annotations":[78177,64637],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070449"},{"annotations":[104873,80895,115776,94227,90483,94201,120564,115666,112985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005788"},{"annotations":[111929,117422,115574,109316],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008622"},{"annotations":[79255,73180],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0035101"},{"annotations":[99766,70298,117872,115314,95810,89334,103607,107719,116189,116463,99556,72597],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000328"},{"annotations":[63757],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005760"},{"annotations":[72117,81765,81147,82047],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000811"},{"annotations":[77631,104124,119665],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005796"},{"annotations":[65508],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070823"},{"annotations":[111042,117418,68154,89666,74687,71654,73529,61692,74395,103505,115152,78065,95901,57927,73931,73406,90744],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031011"},{"annotations":[99558],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031906"},{"annotations":[111635,113126,96656,93358,106841,117558,92214,90935,111543],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030998"},{"annotations":[107904,104822,104841,121084,90461,121093,64585,101228,121092],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000262"},{"annotations":[70942,102008,66403,61635,99054,79739,102093,71828,68348,96878,109453,62069,78506,80494,80102,62575,108834,63521,78854,90193,59762,96338,96260,78222,104157,109143,119082],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005758"},{"annotations":[90527,118288,94678,58404],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0042719"},{"annotations":[78395,112770,81039,118284,74827,79907,72522,81653,81199,110207,114732,113102,107671,79075,72964,77160,82230,98519,110058,99884,114229,73909,74566,81517,73579,74232,80218,115459,68355,108728,71379,99905,110157,79935,76588,116611,79671,77390,111832,78424,116729,118175,119949,105631],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005762"},{"annotations":[103835,117881,118064,119762,58663,107609,120079,97049,79912,113232,103476,96570,105579,96561,98054,108175,115035,107550,98276,104830,97482,103403,109168,80203,66850,90921,71779,74139,106724,103227,108087,109087,68917,113290,103872,110453,70285,95081,98596,110353,90855,112427,99245,80943,90540,105879,78651,117698,112067,100005,110609,97697,76177,120445,114875,100090,104573,106663,114860,117308,120336,59903,98579,114681,102620,92563,97156,79905,120091,59597,100880,95612,98379,105055,68477,72408,73186,76339,100182,100624,101175,110120,90260,98925,76188,119422,115260,80676,79967,93462,97848,98324,118578,92880,115024,58233,79881,57222,63970,96159,99546,113811,119878,89586,109465,116447,99592,73036,105724,89272,111448,103855,108851,68589,120040,96355,96421,98768,110297,115895,94194,115886,58322,113766,104621,100098,115966,96377,102802,106222,104211,114864,97412,109188,99233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005759"},{"annotations":[114071,90195,103238,77514,106097,97655,112116],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0042645"},{"annotations":[115197,107545],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0017087"},{"annotations":[91835],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005761"},{"annotations":[91809,99909,105028,110322,96086,99908,74129,75881,110062,110568,112658,93972,74361,98551,108369,112124,117613,118034,112376,105952,77503,120117,74993,108003,75929,70907,80136,78333,97837,104257,96395,114367],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005763"},{"annotations":[80161,77765,82004],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034457"},{"annotations":[76164,111246,77634,113464,92672,114763,76076],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016604"},{"annotations":[65407,93652,102517,108584,89730,95771,112543,70459,108037,112169,104133,97067,98152,108159,81166],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000228"},{"annotations":[70502,79572,78884,74414,78249,114835],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043599"},{"annotations":[76088,78019,75205,72372,76355,79463,102973,117461,73079,74969,73374,74203,76841],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000176"},{"annotations":[95333,120146,106247,93755,113298,89350,94127,109424],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990251"},{"annotations":[69980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031981"},{"annotations":[81337,57433],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016363"},{"annotations":[80548,71722,62095,76807,75545,81316],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005664"},{"annotations":[75739,91293,108125,93820,103830,107342,116909,118000,95290,92829,111952,61945,101763,116475,117533,118059,105889,95324,118480,117848,105324,105549,119448,111847,112322,62130,90879,98315,108286,79647,72008,112417,99715,110095,115041,116760,95058,77846,92965,93611,96885,109237,110676,113145,64006,106300,108100,97669,110448,113192,91639,92301,95878,102663,101762],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034399"},{"annotations":[112553,57177,113642,75544,67318,58551,115183,61799,73433,61741,63600,113385,105265,110027,109807],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005656"},{"annotations":[117423,109317,110028,97917,104823,113643,115575,67317,75631,106167,96734,94880,61740,109808,113386,114747,79290,115184,92322,99242,115163,105931,94449,102546,106098,92543,101346,105266,57176,96978,101229,58550,109700,120222,111930,113268,61798,63599,113902],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043596"},{"annotations":[114516],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0043601"},{"annotations":[97230,108615,94255,100475,109764,104852],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030874"},{"annotations":[117411,92972,120640,101416,117323,73170,60959,106513,72937,73508,64509],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005655"},{"annotations":[74145,114104,98302,91925,93538,109203,110994,98377,106891,116482,107691,93520,76522,74873,100558,119456,74633,81489,81923,96792,100711,106249,92910,118950,74084,117372,121508,102974,77121,73002,74968,107221,89793,111561,107711,95590,106052,110305,74592,113207,99890,108681,76087,62194,103623,107615,115392,78018,92747,76118,80735,108682,110306,115000,91798,118366,73408,93988,74585,116567,116951,74624,79868,74599,75370,67447,107614,72311,113683,99791,101539,105998,115270,116542,121360,76899,81003,90185,89944,81775,102168,117902,106369,106051,71806,97541,93115,96220,89552,111109,115326,116740,118247,117373,104520,75268,107591,114023,114905,70065,72552,75917,94542,78335,115549,97713,72136,105315,109658,116122,78821,76997,102415,79313,115440,65216,92673,98957,73765,89867,102404,113215,114024,118451,115679,75529,96020,74831,107637,119254,121359,94897,105617,101102,97026,80514,90659,98030,102339,97027,107366,113194,115441,81677,78209,115439,101387,103806,118899,75725,98591,103439,77214,73493,119685,79863,78644,92911,119457,119170,78087,108776,119633,119684,79998,113346,99804,115589,117185,100559,116027,117462,74581,82185,78180,107437,79027,91823,61675,106808,121035,113944,118606,99417,78917,80962,74514,95178,97633,100771,102530,108889,109425,98171,114517,74437,92909,72480,69468,117088,72712,80081,79747,110149,118220,116368,94792,120054,119801,112968,120004,74678,93768,93254,72645,109248,109338,108311,80444,77847,105607,72358,112470,115901,118384,119674,79284,102579,112633,113896,108585,107692,80049,73669,80726,71703,81045,104109,108777,72123,75616,78976,110511,114051,97918,97950,74171,116541,96793,74574,107367,72615,114686,114705,89457,90741,90438,107636,72371,108135,109969,92708,115872,93287,106079,77690,101332,81958,101660,102408,111533,59999,114886,74517,92821,72339,114298,104843,81355,111079,118884,73348,116568,118574,74001,72106,98419,79419,78167,78842,116558,58538,97333,80328,89609,76065],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005730"},{"annotations":[75316,77377,110788,110338,64035,74390,60469,76754,81957,102547,110581,111578,103444,107086,82154,106099,77537,111652,71245,113195,91465,65215,104274,101799,72099,119977,113700,81671,106168,106756,108219,103790,81321,78470,121239,92660,75427,74632,81625,91871,77521,90360,105489],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005654"},{"annotations":[111019,110862],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070691"},{"annotations":[75784,72846,78497,101168,105229,113799],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001405"},{"annotations":[77984,75448,76611],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070545"},{"annotations":[94988],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099020"},{"annotations":[120605],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097356"},{"annotations":[117782,116764,61540,120337,72411,107269,113849],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005782"},{"annotations":[73158,78655,73479,81550,75364],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034388"},{"annotations":[117294,101206,121383,103110],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030875"},{"annotations":[82170,101284,80041],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031298"},{"annotations":[114212,93158,120127],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030958"},{"annotations":[76957,78742,76305,104482,58366,78319,71857,77313,117545,106848,79277,77627,116233,72824,69186,77520,75924],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005736"},{"annotations":[81666,77501,81033],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070860"},{"annotations":[97487],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000120"},{"annotations":[95066,80969,107238,73852],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000500"},{"annotations":[74493,72822,77311,75057,76955,76250,72420,80732,114857,78740,79877,77149,78317],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005665"},{"annotations":[80762,77601,82059,77729,90984,96545,61509,108720,116251,64476,79123,63687,77920],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033698"},{"annotations":[76556,61510,116161,79124,90985,96546,79926,108721,106679,77602,116252,80482,64477,95132,82060,112467,80763],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070210"},{"annotations":[78371,74481,95673,74734,97360,63686],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032221"},{"annotations":[73653,73045,77270,111337,80295,75714,117727,92590],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0048188"},{"annotations":[95133,80481,106135,68386,80932],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034967"},{"annotations":[114108,73420,110137,115299],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070824"},{"annotations":[67759,61047],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0033557"},{"annotations":[60367,101867,115194],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032783"},{"annotations":[109631,62558],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032798"},{"annotations":[89795,112288],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034974"},{"annotations":[119478,75434,94264,111050,116733,78733,100889,81816,100158,74686,78064,115155,98571,109854,115327,71847],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000812"},{"annotations":[112563,74673,91115,93938,78123,94530],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034455"},{"annotations":[76577,80437],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008023"},{"annotations":[73808,80439],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005672"},{"annotations":[71651,76727,73127,119593,97488,58090,105563,76209,78491,77349,72395,75413,59940,78620,69630,82133],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005669"},{"annotations":[71911,77936],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005673"},{"annotations":[80993,71652,82248],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005674"},{"annotations":[110967,116846,77940,76152,72120,94063,71894,80507],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005675"},{"annotations":[67348,77996,61406],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070985"},{"annotations":[76361,77799,79897,80351,95632],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034456"}]},"cv_name":"cellular_component","definition":"An organelle lumen that is part of an intracellular organelle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle lumen","termid":"GO:0043233"},{"relation_name":"part_of","term_name":"intracellular organelle","termid":"GO:0043229"}],"gene_count":978,"genes_by_uniquename":{"SJAG_00045":null,"SJAG_00047":null,"SJAG_00054":null,"SJAG_00060":null,"SJAG_00077":null,"SJAG_00082":null,"SJAG_00083":null,"SJAG_00086":null,"SJAG_00088":null,"SJAG_00095":null,"SJAG_00097":null,"SJAG_00100":null,"SJAG_00103":null,"SJAG_00105":null,"SJAG_00107":null,"SJAG_00116":null,"SJAG_00119":null,"SJAG_00132":null,"SJAG_00139":null,"SJAG_00142":null,"SJAG_00145":null,"SJAG_00148":null,"SJAG_00150":null,"SJAG_00153":null,"SJAG_00159":null,"SJAG_00163":null,"SJAG_00166":null,"SJAG_00168":null,"SJAG_00170":null,"SJAG_00172":null,"SJAG_00178":null,"SJAG_00181":null,"SJAG_00186":null,"SJAG_00196":null,"SJAG_00198":null,"SJAG_00202":null,"SJAG_00207":null,"SJAG_00220":null,"SJAG_00230":null,"SJAG_00231":null,"SJAG_00245":null,"SJAG_00253":null,"SJAG_00255":null,"SJAG_00259":null,"SJAG_00269":null,"SJAG_00271":null,"SJAG_00272":null,"SJAG_00286":null,"SJAG_00288":null,"SJAG_00294":null,"SJAG_00306":null,"SJAG_00311":null,"SJAG_00315":null,"SJAG_00323":null,"SJAG_00326":null,"SJAG_00327":null,"SJAG_00341":null,"SJAG_00344":null,"SJAG_00349":null,"SJAG_00358":null,"SJAG_00363":null,"SJAG_00364":null,"SJAG_00369":null,"SJAG_00373":null,"SJAG_00396":null,"SJAG_00399":null,"SJAG_00400":null,"SJAG_00403":null,"SJAG_00410":null,"SJAG_00420":null,"SJAG_00421":null,"SJAG_00441":null,"SJAG_00449":null,"SJAG_00455":null,"SJAG_00456":null,"SJAG_00458":null,"SJAG_00468":null,"SJAG_00471":null,"SJAG_00480":null,"SJAG_00483":null,"SJAG_00497":null,"SJAG_00502":null,"SJAG_00512":null,"SJAG_00513":null,"SJAG_00523":null,"SJAG_00530":null,"SJAG_00532":null,"SJAG_00536":null,"SJAG_00538":null,"SJAG_00540":null,"SJAG_00562":null,"SJAG_00564":null,"SJAG_00566":null,"SJAG_00572":null,"SJAG_00576":null,"SJAG_00581":null,"SJAG_00582":null,"SJAG_00583":null,"SJAG_00584":null,"SJAG_00611":null,"SJAG_00616":null,"SJAG_00617":null,"SJAG_00618":null,"SJAG_00628":null,"SJAG_00629":null,"SJAG_00634":null,"SJAG_00635":null,"SJAG_00636":null,"SJAG_00644":null,"SJAG_00646":null,"SJAG_00653":null,"SJAG_00657":null,"SJAG_00659":null,"SJAG_00668":null,"SJAG_00687":null,"SJAG_00689":null,"SJAG_00692":null,"SJAG_00695":null,"SJAG_00696":null,"SJAG_00697":null,"SJAG_00701":null,"SJAG_00702":null,"SJAG_00703":null,"SJAG_00706":null,"SJAG_00714":null,"SJAG_00722":null,"SJAG_00728":null,"SJAG_00729":null,"SJAG_00731":null,"SJAG_00735":null,"SJAG_00741":null,"SJAG_00744":null,"SJAG_00746":null,"SJAG_00748":null,"SJAG_00749":null,"SJAG_00751":null,"SJAG_00756":null,"SJAG_00758":null,"SJAG_00764":null,"SJAG_00769":null,"SJAG_00772":null,"SJAG_00782":null,"SJAG_00790":null,"SJAG_00796":null,"SJAG_00798":null,"SJAG_00799":null,"SJAG_00813":null,"SJAG_00814":null,"SJAG_00830":null,"SJAG_00833":null,"SJAG_00838":null,"SJAG_00840":null,"SJAG_00841":null,"SJAG_00844":null,"SJAG_00854":null,"SJAG_00857":null,"SJAG_00860":null,"SJAG_00863":null,"SJAG_00868":null,"SJAG_00872":null,"SJAG_00873":null,"SJAG_00874":null,"SJAG_00879":null,"SJAG_00882":null,"SJAG_00883":null,"SJAG_00884":null,"SJAG_00886":null,"SJAG_00887":null,"SJAG_00888":null,"SJAG_00889":null,"SJAG_00894":null,"SJAG_00896":null,"SJAG_00897":null,"SJAG_00901":null,"SJAG_00921":null,"SJAG_00930":null,"SJAG_00932":null,"SJAG_00934":null,"SJAG_00936":null,"SJAG_00939":null,"SJAG_00941":null,"SJAG_00943":null,"SJAG_00944":null,"SJAG_00945":null,"SJAG_00947":null,"SJAG_00949":null,"SJAG_00955":null,"SJAG_00958":null,"SJAG_00961":null,"SJAG_00962":null,"SJAG_00965":null,"SJAG_00968":null,"SJAG_00984":null,"SJAG_00986":null,"SJAG_00995":null,"SJAG_01004":null,"SJAG_01005":null,"SJAG_01010":null,"SJAG_01013":null,"SJAG_01016":null,"SJAG_01019":null,"SJAG_01045":null,"SJAG_01047":null,"SJAG_01049":null,"SJAG_01067":null,"SJAG_01083":null,"SJAG_01084":null,"SJAG_01088":null,"SJAG_01110":null,"SJAG_01111":null,"SJAG_01122":null,"SJAG_01125":null,"SJAG_01128":null,"SJAG_01132":null,"SJAG_01140":null,"SJAG_01147":null,"SJAG_01149":null,"SJAG_01151":null,"SJAG_01153":null,"SJAG_01169":null,"SJAG_01174":null,"SJAG_01176":null,"SJAG_01180":null,"SJAG_01182":null,"SJAG_01185":null,"SJAG_01191":null,"SJAG_01193":null,"SJAG_01201":null,"SJAG_01203":null,"SJAG_01207":null,"SJAG_01213":null,"SJAG_01226":null,"SJAG_01230":null,"SJAG_01234":null,"SJAG_01238":null,"SJAG_01250":null,"SJAG_01262":null,"SJAG_01267":null,"SJAG_01272":null,"SJAG_01275":null,"SJAG_01280":null,"SJAG_01282":null,"SJAG_01296":null,"SJAG_01303":null,"SJAG_01313":null,"SJAG_01323":null,"SJAG_01325":null,"SJAG_01327":null,"SJAG_01330":null,"SJAG_01347":null,"SJAG_01352":null,"SJAG_01354":null,"SJAG_01358":null,"SJAG_01365":null,"SJAG_01368":null,"SJAG_01369":null,"SJAG_01374":null,"SJAG_01375":null,"SJAG_01377":null,"SJAG_01387":null,"SJAG_01391":null,"SJAG_01407":null,"SJAG_01410":null,"SJAG_01413":null,"SJAG_01417":null,"SJAG_01419":null,"SJAG_01420":null,"SJAG_01431":null,"SJAG_01436":null,"SJAG_01444":null,"SJAG_01446":null,"SJAG_01454":null,"SJAG_01463":null,"SJAG_01465":null,"SJAG_01468":null,"SJAG_01473":null,"SJAG_01475":null,"SJAG_01476":null,"SJAG_01478":null,"SJAG_01494":null,"SJAG_01495":null,"SJAG_01498":null,"SJAG_01503":null,"SJAG_01509":null,"SJAG_01517":null,"SJAG_01518":null,"SJAG_01520":null,"SJAG_01521":null,"SJAG_01540":null,"SJAG_01548":null,"SJAG_01551":null,"SJAG_01560":null,"SJAG_01562":null,"SJAG_01565":null,"SJAG_01574":null,"SJAG_01575":null,"SJAG_01577":null,"SJAG_01580":null,"SJAG_01591":null,"SJAG_01592":null,"SJAG_01597":null,"SJAG_01604":null,"SJAG_01605":null,"SJAG_01606":null,"SJAG_01610":null,"SJAG_01611":null,"SJAG_01615":null,"SJAG_01623":null,"SJAG_01624":null,"SJAG_01630":null,"SJAG_01632":null,"SJAG_01647":null,"SJAG_01650":null,"SJAG_01662":null,"SJAG_01670":null,"SJAG_01674":null,"SJAG_01677":null,"SJAG_01684":null,"SJAG_01698":null,"SJAG_01708":null,"SJAG_01710":null,"SJAG_01712":null,"SJAG_01713":null,"SJAG_01719":null,"SJAG_01727":null,"SJAG_01734":null,"SJAG_01745":null,"SJAG_01752":null,"SJAG_01753":null,"SJAG_01761":null,"SJAG_01762":null,"SJAG_01764":null,"SJAG_01765":null,"SJAG_01767":null,"SJAG_01777":null,"SJAG_01797":null,"SJAG_01799":null,"SJAG_01804":null,"SJAG_01807":null,"SJAG_01808":null,"SJAG_01811":null,"SJAG_01813":null,"SJAG_01818":null,"SJAG_01820":null,"SJAG_01821":null,"SJAG_01823":null,"SJAG_01829":null,"SJAG_01839":null,"SJAG_01853":null,"SJAG_01867":null,"SJAG_01868":null,"SJAG_01877":null,"SJAG_01882":null,"SJAG_01895":null,"SJAG_01903":null,"SJAG_01907":null,"SJAG_01909":null,"SJAG_01915":null,"SJAG_01922":null,"SJAG_01926":null,"SJAG_01936":null,"SJAG_01949":null,"SJAG_01988":null,"SJAG_01996":null,"SJAG_02025":null,"SJAG_02037":null,"SJAG_02038":null,"SJAG_02043":null,"SJAG_02046":null,"SJAG_02057":null,"SJAG_02067":null,"SJAG_02070":null,"SJAG_02071":null,"SJAG_02073":null,"SJAG_02074":null,"SJAG_02077":null,"SJAG_02094":null,"SJAG_02097":null,"SJAG_02098":null,"SJAG_02100":null,"SJAG_02101":null,"SJAG_02104":null,"SJAG_02119":null,"SJAG_02156":null,"SJAG_02164":null,"SJAG_02170":null,"SJAG_02172":null,"SJAG_02174":null,"SJAG_02182":null,"SJAG_02186":null,"SJAG_02187":null,"SJAG_02189":null,"SJAG_02198":null,"SJAG_02201":null,"SJAG_02207":null,"SJAG_02209":null,"SJAG_02210":null,"SJAG_02214":null,"SJAG_02217":null,"SJAG_02226":null,"SJAG_02229":null,"SJAG_02235":null,"SJAG_02236":null,"SJAG_02238":null,"SJAG_02242":null,"SJAG_02244":null,"SJAG_02248":null,"SJAG_02250":null,"SJAG_02253":null,"SJAG_02267":null,"SJAG_02274":null,"SJAG_02281":null,"SJAG_02283":null,"SJAG_02287":null,"SJAG_02294":null,"SJAG_02299":null,"SJAG_02300":null,"SJAG_02303":null,"SJAG_02306":null,"SJAG_02318":null,"SJAG_02324":null,"SJAG_02329":null,"SJAG_02335":null,"SJAG_02341":null,"SJAG_02348":null,"SJAG_02353":null,"SJAG_02359":null,"SJAG_02360":null,"SJAG_02372":null,"SJAG_02377":null,"SJAG_02382":null,"SJAG_02385":null,"SJAG_02393":null,"SJAG_02394":null,"SJAG_02396":null,"SJAG_02397":null,"SJAG_02409":null,"SJAG_02413":null,"SJAG_02416":null,"SJAG_02417":null,"SJAG_02424":null,"SJAG_02427":null,"SJAG_02428":null,"SJAG_02432":null,"SJAG_02433":null,"SJAG_02439":null,"SJAG_02451":null,"SJAG_02452":null,"SJAG_02458":null,"SJAG_02464":null,"SJAG_02466":null,"SJAG_02469":null,"SJAG_02475":null,"SJAG_02490":null,"SJAG_02495":null,"SJAG_02496":null,"SJAG_02499":null,"SJAG_02500":null,"SJAG_02506":null,"SJAG_02508":null,"SJAG_02524":null,"SJAG_02526":null,"SJAG_02527":null,"SJAG_02530":null,"SJAG_02535":null,"SJAG_02536":null,"SJAG_02541":null,"SJAG_02544":null,"SJAG_02546":null,"SJAG_02547":null,"SJAG_02548":null,"SJAG_02549":null,"SJAG_02553":null,"SJAG_02560":null,"SJAG_02571":null,"SJAG_02585":null,"SJAG_02592":null,"SJAG_02606":null,"SJAG_02607":null,"SJAG_02608":null,"SJAG_02610":null,"SJAG_02615":null,"SJAG_02621":null,"SJAG_02622":null,"SJAG_02627":null,"SJAG_02630":null,"SJAG_02643":null,"SJAG_02644":null,"SJAG_02652":null,"SJAG_02653":null,"SJAG_02656":null,"SJAG_02658":null,"SJAG_02661":null,"SJAG_02662":null,"SJAG_02667":null,"SJAG_02680":null,"SJAG_02681":null,"SJAG_02682":null,"SJAG_02690":null,"SJAG_02702":null,"SJAG_02720":null,"SJAG_02721":null,"SJAG_02723":null,"SJAG_02724":null,"SJAG_02736":null,"SJAG_02744":null,"SJAG_02747":null,"SJAG_02749":null,"SJAG_02754":null,"SJAG_02758":null,"SJAG_02759":null,"SJAG_02762":null,"SJAG_02768":null,"SJAG_02771":null,"SJAG_02775":null,"SJAG_02777":null,"SJAG_02778":null,"SJAG_02790":null,"SJAG_02798":null,"SJAG_02800":null,"SJAG_02812":null,"SJAG_02813":null,"SJAG_02818":null,"SJAG_02821":null,"SJAG_02825":null,"SJAG_02829":null,"SJAG_02830":null,"SJAG_02835":null,"SJAG_02836":null,"SJAG_02841":null,"SJAG_02846":null,"SJAG_02856":null,"SJAG_02870":null,"SJAG_02871":null,"SJAG_02872":null,"SJAG_02875":null,"SJAG_02879":null,"SJAG_02887":null,"SJAG_02891":null,"SJAG_02899":null,"SJAG_02900":null,"SJAG_02901":null,"SJAG_02908":null,"SJAG_02911":null,"SJAG_02917":null,"SJAG_02922":null,"SJAG_02952":null,"SJAG_02977":null,"SJAG_02979":null,"SJAG_02981":null,"SJAG_02990":null,"SJAG_02991":null,"SJAG_02998":null,"SJAG_03008":null,"SJAG_03014":null,"SJAG_03016":null,"SJAG_03020":null,"SJAG_03022":null,"SJAG_03025":null,"SJAG_03026":null,"SJAG_03028":null,"SJAG_03033":null,"SJAG_03036":null,"SJAG_03040":null,"SJAG_03042":null,"SJAG_03051":null,"SJAG_03053":null,"SJAG_03061":null,"SJAG_03065":null,"SJAG_03068":null,"SJAG_03070":null,"SJAG_03071":null,"SJAG_03077":null,"SJAG_03080":null,"SJAG_03090":null,"SJAG_03097":null,"SJAG_03099":null,"SJAG_03103":null,"SJAG_03104":null,"SJAG_03107":null,"SJAG_03118":null,"SJAG_03125":null,"SJAG_03127":null,"SJAG_03128":null,"SJAG_03144":null,"SJAG_03145":null,"SJAG_03155":null,"SJAG_03156":null,"SJAG_03159":null,"SJAG_03161":null,"SJAG_03163":null,"SJAG_03176":null,"SJAG_03179":null,"SJAG_03180":null,"SJAG_03181":null,"SJAG_03182":null,"SJAG_03192":null,"SJAG_03199":null,"SJAG_03206":null,"SJAG_03211":null,"SJAG_03217":null,"SJAG_03221":null,"SJAG_03222":null,"SJAG_03230":null,"SJAG_03232":null,"SJAG_03234":null,"SJAG_03252":null,"SJAG_03255":null,"SJAG_03266":null,"SJAG_03284":null,"SJAG_03285":null,"SJAG_03289":null,"SJAG_03290":null,"SJAG_03297":null,"SJAG_03299":null,"SJAG_03303":null,"SJAG_03321":null,"SJAG_03322":null,"SJAG_03341":null,"SJAG_03393":null,"SJAG_03402":null,"SJAG_03410":null,"SJAG_03411":null,"SJAG_03413":null,"SJAG_03418":null,"SJAG_03419":null,"SJAG_03424":null,"SJAG_03425":null,"SJAG_03426":null,"SJAG_03430":null,"SJAG_03431":null,"SJAG_03433":null,"SJAG_03438":null,"SJAG_03441":null,"SJAG_03449":null,"SJAG_03451":null,"SJAG_03454":null,"SJAG_03458":null,"SJAG_03459":null,"SJAG_03460":null,"SJAG_03461":null,"SJAG_03466":null,"SJAG_03468":null,"SJAG_03473":null,"SJAG_03479":null,"SJAG_03481":null,"SJAG_03495":null,"SJAG_03532":null,"SJAG_03535":null,"SJAG_03539":null,"SJAG_03550":null,"SJAG_03551":null,"SJAG_03554":null,"SJAG_03563":null,"SJAG_03567":null,"SJAG_03568":null,"SJAG_03569":null,"SJAG_03574":null,"SJAG_03578":null,"SJAG_03579":null,"SJAG_03583":null,"SJAG_03584":null,"SJAG_03585":null,"SJAG_03586":null,"SJAG_03588":null,"SJAG_03593":null,"SJAG_03603":null,"SJAG_03608":null,"SJAG_03617":null,"SJAG_03618":null,"SJAG_03627":null,"SJAG_03636":null,"SJAG_03638":null,"SJAG_03641":null,"SJAG_03649":null,"SJAG_03654":null,"SJAG_03662":null,"SJAG_03666":null,"SJAG_03674":null,"SJAG_03680":null,"SJAG_03685":null,"SJAG_03689":null,"SJAG_03694":null,"SJAG_03700":null,"SJAG_03709":null,"SJAG_03713":null,"SJAG_03719":null,"SJAG_03722":null,"SJAG_03724":null,"SJAG_03728":null,"SJAG_03730":null,"SJAG_03745":null,"SJAG_03752":null,"SJAG_03780":null,"SJAG_03786":null,"SJAG_03789":null,"SJAG_03796":null,"SJAG_03804":null,"SJAG_03832":null,"SJAG_03836":null,"SJAG_03839":null,"SJAG_03840":null,"SJAG_03843":null,"SJAG_03844":null,"SJAG_03846":null,"SJAG_03847":null,"SJAG_03855":null,"SJAG_03861":null,"SJAG_03862":null,"SJAG_03867":null,"SJAG_03872":null,"SJAG_03874":null,"SJAG_03877":null,"SJAG_03884":null,"SJAG_03888":null,"SJAG_03897":null,"SJAG_03898":null,"SJAG_03900":null,"SJAG_03901":null,"SJAG_03905":null,"SJAG_03906":null,"SJAG_03916":null,"SJAG_03919":null,"SJAG_03923":null,"SJAG_03927":null,"SJAG_03931":null,"SJAG_03939":null,"SJAG_03946":null,"SJAG_03952":null,"SJAG_03954":null,"SJAG_03956":null,"SJAG_03957":null,"SJAG_03959":null,"SJAG_03961":null,"SJAG_03964":null,"SJAG_03967":null,"SJAG_03971":null,"SJAG_03976":null,"SJAG_03982":null,"SJAG_03984":null,"SJAG_03985":null,"SJAG_04004":null,"SJAG_04006":null,"SJAG_04008":null,"SJAG_04009":null,"SJAG_04010":null,"SJAG_04014":null,"SJAG_04017":null,"SJAG_04019":null,"SJAG_04030":null,"SJAG_04033":null,"SJAG_04039":null,"SJAG_04046":null,"SJAG_04054":null,"SJAG_04056":null,"SJAG_04062":null,"SJAG_04064":null,"SJAG_04069":null,"SJAG_04081":null,"SJAG_04083":null,"SJAG_04084":null,"SJAG_04094":null,"SJAG_04097":null,"SJAG_04098":null,"SJAG_04106":null,"SJAG_04108":null,"SJAG_04116":null,"SJAG_04118":null,"SJAG_04128":null,"SJAG_04140":null,"SJAG_04141":null,"SJAG_04142":null,"SJAG_04145":null,"SJAG_04148":null,"SJAG_04149":null,"SJAG_04150":null,"SJAG_04152":null,"SJAG_04153":null,"SJAG_04160":null,"SJAG_04164":null,"SJAG_04173":null,"SJAG_04180":null,"SJAG_04183":null,"SJAG_04186":null,"SJAG_04190":null,"SJAG_04195":null,"SJAG_04207":null,"SJAG_04208":null,"SJAG_04210":null,"SJAG_04213":null,"SJAG_04216":null,"SJAG_04224":null,"SJAG_04244":null,"SJAG_04256":null,"SJAG_04257":null,"SJAG_04261":null,"SJAG_04272":null,"SJAG_04274":null,"SJAG_04281":null,"SJAG_04284":null,"SJAG_04285":null,"SJAG_04289":null,"SJAG_04303":null,"SJAG_04305":null,"SJAG_04306":null,"SJAG_04308":null,"SJAG_04310":null,"SJAG_04312":null,"SJAG_04321":null,"SJAG_04324":null,"SJAG_04330":null,"SJAG_04336":null,"SJAG_04339":null,"SJAG_04341":null,"SJAG_04346":null,"SJAG_04351":null,"SJAG_04353":null,"SJAG_04355":null,"SJAG_04366":null,"SJAG_04367":null,"SJAG_04368":null,"SJAG_04377":null,"SJAG_04378":null,"SJAG_04379":null,"SJAG_04389":null,"SJAG_04395":null,"SJAG_04396":null,"SJAG_04397":null,"SJAG_04400":null,"SJAG_04409":null,"SJAG_04411":null,"SJAG_04414":null,"SJAG_04420":null,"SJAG_04424":null,"SJAG_04432":null,"SJAG_04436":null,"SJAG_04457":null,"SJAG_04473":null,"SJAG_04477":null,"SJAG_04478":null,"SJAG_04490":null,"SJAG_04491":null,"SJAG_04492":null,"SJAG_04493":null,"SJAG_04494":null,"SJAG_04508":null,"SJAG_04524":null,"SJAG_04527":null,"SJAG_04528":null,"SJAG_04530":null,"SJAG_04533":null,"SJAG_04539":null,"SJAG_04547":null,"SJAG_04559":null,"SJAG_04560":null,"SJAG_04562":null,"SJAG_04571":null,"SJAG_04574":null,"SJAG_04575":null,"SJAG_04576":null,"SJAG_04582":null,"SJAG_04596":null,"SJAG_04599":null,"SJAG_04601":null,"SJAG_04610":null,"SJAG_04614":null,"SJAG_04635":null,"SJAG_04638":null,"SJAG_04641":null,"SJAG_04645":null,"SJAG_04650":null,"SJAG_04654":null,"SJAG_04656":null,"SJAG_04663":null,"SJAG_04669":null,"SJAG_04670":null,"SJAG_04671":null,"SJAG_04680":null,"SJAG_04688":null,"SJAG_04689":null,"SJAG_04738":null,"SJAG_04748":null,"SJAG_04753":null,"SJAG_04754":null,"SJAG_04758":null,"SJAG_04766":null,"SJAG_04767":null,"SJAG_04768":null,"SJAG_04785":null,"SJAG_04788":null,"SJAG_04791":null,"SJAG_04817":null,"SJAG_04818":null,"SJAG_04823":null,"SJAG_04824":null,"SJAG_04838":null,"SJAG_04840":null,"SJAG_04852":null,"SJAG_04856":null,"SJAG_04862":null,"SJAG_04863":null,"SJAG_04877":null,"SJAG_04879":null,"SJAG_04889":null,"SJAG_04893":null,"SJAG_04894":null,"SJAG_04897":null,"SJAG_04899":null,"SJAG_04908":null,"SJAG_04911":null,"SJAG_04916":null,"SJAG_04917":null,"SJAG_04918":null,"SJAG_04919":null,"SJAG_04929":null,"SJAG_04933":null,"SJAG_04936":null,"SJAG_04940":null,"SJAG_04950":null,"SJAG_04959":null,"SJAG_04974":null,"SJAG_04977":null,"SJAG_04979":null,"SJAG_04989":null,"SJAG_04992":null,"SJAG_04993":null,"SJAG_04994":null,"SJAG_04995":null,"SJAG_05008":null,"SJAG_05020":null,"SJAG_05180":null,"SJAG_05186":null,"SJAG_05187":null,"SJAG_05190":null,"SJAG_05192":null,"SJAG_05193":null,"SJAG_05197":null,"SJAG_05216":null,"SJAG_05218":null,"SJAG_05232":null,"SJAG_05237":null,"SJAG_05239":null,"SJAG_05244":null,"SJAG_05248":null,"SJAG_05253":null,"SJAG_05261":null,"SJAG_05270":null,"SJAG_05276":null,"SJAG_05282":null,"SJAG_05295":null,"SJAG_05301":null,"SJAG_05307":null,"SJAG_05320":null,"SJAG_05321":null,"SJAG_05331":null,"SJAG_05333":null,"SJAG_05338":null,"SJAG_05398":null,"SJAG_05560":null,"SJAG_05573":null,"SJAG_05679":null,"SJAG_06022":null,"SJAG_06110":null,"SJAG_06135":null,"SJAG_06253":null,"SJAG_06440":null,"SJAG_06586":null,"SJAG_06613":null,"SJAG_06635":null,"SJAG_07002":null,"SJAG_07005":null,"SJAG_07009":null,"SJAG_07011":null,"SJAG_16455":null,"SJAG_16456":null,"SJAG_MIT05":null,"SJAG_MIT06":null,"SJAG_MIT07":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"intracellular organelle lumen","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000024":null,"GO_REF:0000033":null,"GO_REF:0000044":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"GO_REF:0000117":null,"PMID:21802294":null,"PMID:23786411":null,"PMID:24184107":null,"PMID:26774782":null},"termid":"GO:0070013","terms_by_termid":{"GO:0000120":null,"GO:0000176":null,"GO:0000228":null,"GO:0000262":null,"GO:0000328":null,"GO:0000500":null,"GO:0000794":null,"GO:0000811":null,"GO:0000812":null,"GO:0001405":null,"GO:0001651":null,"GO:0005654":null,"GO:0005655":null,"GO:0005656":null,"GO:0005658":null,"GO:0005662":null,"GO:0005664":null,"GO:0005665":null,"GO:0005669":null,"GO:0005672":null,"GO:0005673":null,"GO:0005674":null,"GO:0005675":null,"GO:0005730":null,"GO:0005736":null,"GO:0005758":null,"GO:0005759":null,"GO:0005760":null,"GO:0005761":null,"GO:0005762":null,"GO:0005763":null,"GO:0005782":null,"GO:0005788":null,"GO:0005796":null,"GO:0008023":null,"GO:0008622":null,"GO:0015030":null,"GO:0016363":null,"GO:0016593":null,"GO:0016604":null,"GO:0017087":null,"GO:0030874":null,"GO:0030875":null,"GO:0030896":null,"GO:0030958":null,"GO:0030998":null,"GO:0031011":null,"GO:0031261":null,"GO:0031298":null,"GO:0031429":null,"GO:0031906":null,"GO:0031981":null,"GO:0032044":null,"GO:0032221":null,"GO:0032783":null,"GO:0032798":null,"GO:0033557":null,"GO:0033698":null,"GO:0034388":null,"GO:0034399":null,"GO:0034455":null,"GO:0034456":null,"GO:0034457":null,"GO:0034967":null,"GO:0034974":null,"GO:0035101":null,"GO:0042645":null,"GO:0042719":null,"GO:0043494":null,"GO:0043596":null,"GO:0043599":null,"GO:0043601":null,"GO:0043625":null,"GO:0048188":null,"GO:0070210":null,"GO:0070449":null,"GO:0070545":null,"GO:0070691":null,"GO:0070692":null,"GO:0070823":null,"GO:0070824":null,"GO:0070860":null,"GO:0070985":null,"GO:0071920":null,"GO:0097356":null,"GO:0099020":null,"GO:0099021":null,"GO:1990251":null}}


id: PBO:0003577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIIH complex subunit Tfb4","termid":"PBO:0003577"}


id: PBO:0081508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 415","termid":"PBO:0081508"}


id: GO:0055008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of cardiac muscle tissue are generated and organized.","definition_xrefs":["GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle tissue morphogenesis","termid":"GO:0060415"},{"relation_name":"part_of","term_name":"heart morphogenesis","termid":"GO:0003007"},{"relation_name":"part_of","term_name":"cardiac muscle tissue development","termid":"GO:0048738"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cardiac muscle tissue morphogenesis","synonyms":[{"name":"heart muscle morphogenesis","type":"exact"},{"name":"myocardium morphogenesis","type":"broad"}],"termid":"GO:0055008"}


id: PBO:0087024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L11B; expressed at half the level of Rpl11Ap; involved in ribosomal assembly; depletion causes degradation of 60S proteins and RNA; homologous to mammalian ribosomal protein L11 and bacterial L5; RPL11B has a paralog, RPL11A, that arose from the whole genome duplication","termid":"PBO:0087024"}


id: MONDO:0021455
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the neck.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign neoplasm","termid":"MONDO:0005165"},{"relation_name":"is_a","term_name":"neoplasm of neck","termid":"MONDO:0021351"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of neck","secondary_identifiers":["UMLS:C0684815","NCIT:C4884","SCTID:92246000","ICD9:229.8","MEDGEN:195775"],"synonyms":[{"name":"benign neck neoplasm","type":"exact"},{"name":"benign neck tumor","type":"exact"},{"name":"benign neck tumour","type":"exact"},{"name":"benign neoplasm of the neck","type":"exact"},{"name":"benign tumor of neck","type":"exact"},{"name":"benign tumor of the neck","type":"exact"},{"name":"benign tumour of neck","type":"exact"},{"name":"benign tumour of the neck","type":"exact"},{"name":"neck benign neoplasm","type":"exact"}],"termid":"MONDO:0021455","xrefs":{"Monarch":{"xref_id":"0021455"}}}


id: GO:1901212
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cardiac chamber formation.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cardiac chamber formation","termid":"GO:1901210"},{"relation_name":"is_a","term_name":"positive regulation of cardiac chamber morphogenesis","termid":"GO:1901221"},{"relation_name":"positively_regulates","term_name":"cardiac chamber formation","termid":"GO:0003207"}],"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 chamber formation","synonyms":[{"name":"activation of cardiac chamber formation","type":"narrow"},{"name":"activation of heart chamber formation","type":"exact"},{"name":"positive regulation of heart chamber formation","type":"exact"},{"name":"up regulation of cardiac chamber formation","type":"exact"},{"name":"up regulation of heart chamber formation","type":"exact"},{"name":"up-regulation of cardiac chamber formation","type":"exact"},{"name":"up-regulation of heart chamber formation","type":"exact"},{"name":"upregulation of cardiac chamber formation","type":"exact"},{"name":"upregulation of heart chamber formation","type":"exact"}],"termid":"GO:1901212"}


id: MONDO:0044346
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An disease or disorder caused by infection with Echinococcus granulosus.","definition_xrefs":["MONDO:patterns/specific_infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"echinococcosis","termid":"MONDO:0005738"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"echinococcus granulosus infectious disease","secondary_identifiers":["SCTID:75006000","ICD9:122.4","MEDGEN:508866","UMLS:C0152068","ICD9:122.3"],"synonyms":[{"name":"Echinococcus granulosus caused disease or disorder","type":"exact"},{"name":"Echinococcus granulosus disease or disorder","type":"exact"},{"name":"Echinococcus granulosus infectious disease","type":"exact"},{"name":"echinococcus granulosus infection","type":"exact"},{"name":"echinococcus granulosus infectious disease","type":"exact"},{"name":"unilocular hydatid disease","type":"related"}],"termid":"MONDO:0044346","xrefs":{"Monarch":{"xref_id":"0044346"}}}


id: MONDO:0009053
data:
  {"annotated_genes":["SJAG_00660","SJAG_03457"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89099,89100],"is_not":false,"summary":null,"term":"MONDO:0009053"}]},"cv_name":"mondo","definition":"ALDH18A1-related De Barsy syndrome combines intellectual deficit, bilateral cataracts, and skin and joint hyperlaxity.","definition_xrefs":["Orphanet:35664"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"de Barsy syndrome","termid":"MONDO:0017569"},{"relation_name":"is_a","term_name":"P5CS deficiency","termid":"MONDO:0100126"},{"relation_name":"is_a","term_name":"inherited cutis laxa","termid":"MONDO:0100237"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00660":null,"SJAG_03457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019303"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736","MONDO:0019303","MONDO:0006025"],"is_obsolete":false,"name":"ALDH18A1-related de Barsy syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1720006","SCTID:59252009","UMLS:C5234852","OMIM:219150","GARD:16638","DOID:0070132","ICD9:371.89"],"synonyms":[{"name":"ARCL3A","type":"exact"},{"name":"De Barsy syndrome A","type":"exact"},{"name":"De Barsy syndrome a","type":"related"},{"name":"Delta-1-pyrroline 5-carboxylate synthetase deficiency","type":"exact"},{"name":"P5CS deficiency","type":"broad"},{"name":"autosomal recessive cutis laxa type IIIA","type":"related"},{"name":"cutis laxa, autosomal recessive, type 3A","type":"related"},{"name":"cutis laxa, autosomal recessive, type IIIA","type":"related"},{"name":"cutis laxa, corneal clouding, and intellectual disability","type":"related"},{"name":"cutis laxa, corneal clouding, and mental retardation","type":"related"},{"name":"neurocutaneous syndrome, Bicknell type","type":"exact"},{"name":"progeroid syndrome of De Barsy","type":"related"}],"termid":"MONDO:0009053","terms_by_termid":{"MONDO:0009053":null},"xrefs":{"Monarch":{"xref_id":"0009053"}}}


id: PBO:0070797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 27","termid":"PBO:0070797"}


id: GO:1990967
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a toxin into, out of or within a cell, or between cells where two or more organisms of the same or different species are involved.","definition_xrefs":["GOC:bf","GOC:PARL","PMID:18191792","PMID:22042847"],"gene_count":0,"genotype_count":0,"name":"obsolete multi-organism toxin transport (obsolete GO:1990967)","synonyms":[{"name":"typhoid toxin transport","type":"narrow"}],"termid":"GO:1990967"}


id: PBO:0113352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for nuclear retention of unspliced pre-mRNAs; required along with Mlp1p and Pml1p; anchored to the nuclear pore complex through an interaction between its bimodular nuclear basket-interaction domain (NuBaID) and Mlp1p and Mlp2p; localizes to the nuclear basket enables linkage between subpopulations of Mlp1p; associates with the subset of nuclear pores farthest from the nucleolus; homologous to human ZC3HC1, a NuBaID containing protein","termid":"PBO:0113352"}


id: FYPO:0004304
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a phosphatase 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 phosphatase activity","termid":"FYPO:0004302"}],"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:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000654","FYPO:0001985","FYPO:0000661","FYPO:0000652"],"is_obsolete":false,"name":"decreased phosphatase activity","synonyms":[{"name":"reduced phosphatase activity","type":"exact"}],"termid":"FYPO:0004304"}


id: PBO:0003559
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paroxysmal nocturnal haemoglobinuri","termid":"PBO:0003559"}


id: PBO:0058651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6780a","termid":"PBO:0058651"}


id: PBO:0018075
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae DCP1","termid":"PBO:0018075"}


id: PBO:0075760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/arginine repetitive matrix 1 pseudogene 2","termid":"PBO:0075760"}


id: PBO:0058366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4738","termid":"PBO:0058366"}


id: GO:0061980
data:
  {"annotated_genes":["SJAG_02621","SJAG_03042","SJAG_04061"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[114220,90651,120141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035197"}]},"cv_name":"molecular_function","definition":"Binding to a small regulatory RNA, a short RNA (usually 50-200 nt long) that is either independently transcribed or processed from a longer RNA by an RNAse enzyme.","definition_xrefs":["PMID:23475961","PMID:14622403"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA binding","termid":"GO:0003723"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02621":null,"SJAG_03042":null,"SJAG_04061":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003723","GO:0003674"],"is_obsolete":false,"name":"regulatory RNA binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061980","terms_by_termid":{"GO:0035197":null}}


id: GO:0033570
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of transferrin from one side of a membrane to the other.","definition_xrefs":["GOC:mlg"],"gene_count":0,"genotype_count":0,"name":"obsolete transferrin transmembrane transporter activity (obsolete GO:0033570)","termid":"GO:0033570"}


id: PBO:0084968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAD-dependent arabinose dehydrogenase; involved in biosynthesis of dehydro-D-arabinono-1,4-lactone; similar to plant L-galactose dehydrogenase","termid":"PBO:0084968"}


id: MONDO:0010361
data:
  {"annotated_genes":["SJAG_00845","SJAG_02878"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88908,88909],"is_not":false,"summary":null,"term":"MONDO:0010361"}]},"cv_name":"mondo","definition":"Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the PAK3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic X-linked intellectual disability","termid":"MONDO:0019181"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00845":null,"SJAG_02878":null},"genotype_count":0,"is_obsolete":false,"name":"intellectual disability, X-linked 30","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112051","GARD:22682","MEDGEN:163235","UMLS:C0796237","OMIM:300558"],"synonyms":[{"name":"MRX30","type":"related"},{"name":"PAK3 non-syndromic X-linked intellectual disability","type":"exact"},{"name":"intellectual developmental disorder, X-linked 30, X-linked recessive","type":"exact"},{"name":"intellectual disability, X-linked 30","type":"exact"},{"name":"intellectual disability, X-linked 47","type":"related"},{"name":"intellectual disability, X-linked type 30","type":"exact"},{"name":"mental retardation, X-linked 30","type":"related"},{"name":"mental retardation, X-linked 47","type":"related"},{"name":"mental retardation, X-linked type 30","type":"exact"},{"name":"non-syndromic X-linked intellectual disability caused by mutation in PAK3","type":"exact"}],"termid":"MONDO:0010361","terms_by_termid":{"MONDO:0010361":null},"xrefs":{"Monarch":{"xref_id":"0010361"}}}


id: PBO:0086626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and the nucleus; overexpression causes a cell cycle delay or arrest; YML053C is not an essential gene","termid":"PBO:0086626"}


id: GO:0043457
data:
  {"annotated_genes":["SJAG_00698","SJAG_02433","SJAG_02592","SJAG_01062"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111682,96273,99550,113883],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903715"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular respiration, the enzymatic release of energy from organic compounds.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of generation of precursor metabolites and energy","termid":"GO:0043467"},{"relation_name":"regulates","term_name":"cellular respiration","termid":"GO:0045333"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00698":null,"SJAG_01062":null,"SJAG_02433":null,"SJAG_02592":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0008150","GO:0006091"],"is_obsolete":false,"name":"regulation of cellular respiration","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0043457","terms_by_termid":{"GO:1903715":null}}


id: PBO:0058353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4726","termid":"PBO:0058353"}


id: PBO:0038645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA thioesterase 13","termid":"PBO:0038645"}


id: FYPO:0006021
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 distribution of a protein localized to chromatin along the length of genes that can be transcribed by RNA polymerase II is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:28366642","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin at RNA polymerase II-transcribed genes during vegetative growth","termid":"FYPO:0007536"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312","FYPO:0000138"],"is_obsolete":false,"name":"normal protein distribution along RNA polymerase II-transcribed genes","synonyms":[{"name":"normal protein distribution across RNA polymerase II-transcribed genes","type":"exact"},{"name":"normal protein distribution along RNA polymerase II-regulated genes","type":"exact"},{"name":"normal protein distribution along RNA polymerase II-transcribed genes during mitotic cell cycle","type":"related"},{"name":"normal protein distribution along RNA polymerase II-transcribed genes during vegetative growth","type":"exact"},{"name":"normal protein distribution in chromatin along RNA polymerase II-transcribed genes","type":"exact"},{"name":"normal protein localization to chromatin along RNA polymerase II-transcribed genes","type":"exact"}],"termid":"FYPO:0006021"}


id: GO:0014037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a Schwann cell. Schwann cells are found in the peripheral nervous system, where they insulate neurons and axons, and regulate the environment in which neurons function.","definition_xrefs":["GOC:ef"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell differentiation","termid":"GO:0010001"},{"relation_name":"part_of","term_name":"peripheral nervous system development","termid":"GO:0007422"}],"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":"Schwann cell differentiation","termid":"GO:0014037"}


id: MONDO:0019370
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"female reproductive system disorder","termid":"MONDO:0002263"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vulvovaginal gingival syndrome","secondary_identifiers":["MEDGEN:848586","Orphanet:83453","SCTID:707250009","UMLS:C3873472","icd11.foundation:997964040","GARD:19037"],"termid":"MONDO:0019370","xrefs":{"Monarch":{"xref_id":"0019370"}}}


id: PR:000050507
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A septum-promoting GTP-binding protein 1 (Schizosaccharomyces pombe) that is non-covalently bound to GTP.","definition_xrefs":["PMID:9420333","PomBase:VW","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septum-promoting GTP-binding protein 1 (Schizosaccharomyces pombe)","termid":"PR:000050506"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spg1/GTP+","pombase_gene_id":"SPAC1565.06c","synonyms":[{"name":"PomBase_original_PRO_term_name: septum-promoting GTP-binding protein 1, GTP-bound form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-spg1/GTP+","type":"exact"},{"name":"spg1/GTP+","type":"exact"}],"termid":"PR:000050507"}


id: MONDO:0021244
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the submandibular gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"submandibular gland disorder","termid":"MONDO:0001597"},{"relation_name":"is_a","term_name":"neoplasm of major salivary gland","termid":"MONDO:0021368"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"submandibular gland neoplasm","secondary_identifiers":["UMLS:C0038558","EFO:1001853","MEDGEN:20986","MESH:D013365","NCIT:C3393","SCTID:254464000"],"synonyms":[{"name":"neoplasm of submandibular gland","type":"exact"},{"name":"neoplasm of the submandibular gland","type":"exact"},{"name":"submandibular gland neoplasm (disease)","type":"exact"},{"name":"submandibular gland tumor","type":"exact"},{"name":"submandibular gland tumour","type":"exact"},{"name":"tumor of submandibular gland","type":"exact"},{"name":"tumor of the submandibular gland","type":"exact"},{"name":"tumour of submandibular gland","type":"exact"},{"name":"tumour of the submandibular gland","type":"exact"}],"termid":"MONDO:0021244","xrefs":{"Monarch":{"xref_id":"0021244"}}}


id: PBO:0085906
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; may interact with ribosomes, based on co-purification experiments; authentic, non-tagged protein is detected in purified mitochondria in high-throughput studies; potential orthologs found in other fungi","termid":"PBO:0085906"}


id: PBO:0072126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 3","termid":"PBO:0072126"}


id: PBO:0077865
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tropomyosin 3 pseudogene 6","termid":"PBO:0077865"}


id: PBO:0075082
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 132","termid":"PBO:0075082"}


id: SO:0000655
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An RNA transcript that does not encode for a protein rather the RNA molecule is the gene product.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mature_transcript","termid":"SO:0000233"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ncRNA","secondary_identifiers":["http://www.gencodegenes.org/gencode_biotypes.html","http://en.wikipedia.org/wiki/NcRNA"],"synonyms":[{"name":"INSDC_qualifier:other","type":"broad"},{"name":"known_ncrna","type":"exact"},{"name":"noncoding RNA","type":"exact"}],"termid":"SO:0000655"}


id: MONDO:0013078
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing type 1 diabetes mellitus that has material basis in mutation of the locus at chromosome 10q23.31.","definition_xrefs":["DOID:0110761","PMID:19430480","MONDO:patterns/inherited_susceptibility"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"type 1 diabetes mellitus","termid":"MONDO:0005147"},{"relation_name":"is_a","term_name":"diabetes mellitus, insulin-dependent, X-linked, susceptibility to","termid":"MONDO:0010255"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"type 1 diabetes mellitus 24","secondary_identifiers":["UMLS:C2751697","MESH:C567818","OMIM:613006","MEDGEN:442792"],"synonyms":[{"name":"IDDM24","type":"exact"},{"name":"diabetes mellitus, insulin-dependent, 24","type":"related"},{"name":"insulin-dependent diabetes mellitus 24","type":"exact"}],"termid":"MONDO:0013078","xrefs":{"Monarch":{"xref_id":"0013078"}}}


id: PBO:0054663
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 2069","termid":"PBO:0054663"}


id: GO:0033591
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 an L-ascorbic acid (vitamin C) stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to vitamin","termid":"GO:0033273"},{"relation_name":"is_a","term_name":"response to monosaccharide","termid":"GO:0034284"}],"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 L-ascorbic acid","synonyms":[{"name":"response to L-ascorbate","type":"exact"},{"name":"response to ascorbic acid","type":"broad"},{"name":"response to vitamin C","type":"exact"}],"termid":"GO:0033591"}


id: FYPO:0002221
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of progression through the anaphase of meiosis II is longer than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased duration of meiotic cell cycle phase","termid":"FYPO:0002220"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000631","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased duration of meiotic anaphase II","synonyms":[{"name":"delayed meiotic anaphase II progression","type":"related"},{"name":"increased duration of meiotic anaphase II progression","type":"exact"},{"name":"prolonged meiotic anaphase II","type":"exact"}],"termid":"FYPO:0002221"}


id: PBO:0042190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin D2","termid":"PBO:0042190"}


id: PBO:0044242
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cutA divalent cation tolerance like, pseudogene","termid":"PBO:0044242"}


id: MONDO:0000998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete parotid disease (obsolete MONDO:0000998)","termid":"MONDO:0000998","xrefs":{"Monarch":{"xref_id":"0000998"}}}


id: MONDO:0009198
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare skin disorder characterized by erythrodermic, peeling skin from birth with no obvious nail or hair-shaft abnormalities and other associated anomalies including diarrhea, failure to thrive and severe hypoalbuminaemia resistant to correction by enteral or intravenous supplementation. An autosomal recessive mode of inheritance is highly probable. The prognosis is poor and infants die in the first months of life. There have been no further descriptions in the literature since 1992.","definition_xrefs":["Orphanet:1954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"congenital lethal erythroderma","secondary_identifiers":["GARD:2192","UMLS:C1856898","MESH:C535513","MEDGEN:384008","OMIM:227090","SCTID:722391005"],"synonyms":[{"name":"congenital exfoliative erythroderma resistant to treatment","type":"related"},{"name":"erythroderma lethal congenital","type":"related"},{"name":"erythroderma, lethal congenital","type":"related"},{"name":"lethal congenital erythroderma","type":"related"}],"termid":"MONDO:0009198","xrefs":{"Monarch":{"xref_id":"0009198"}}}


id: PBO:0027245
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_polyadenylated_5.8S_rRNA_level","termid":"PBO:0027245"}


id: PBO:0111882
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch repeat protein","termid":"PBO:0111882"}


id: GO:0018929
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving methyl fluoride, fluorine-substituted methane, a gaseous halogenated hydrocarbon that has been investigated as an inhibitor of methanotrophy and nitrification in soils.","definition_xrefs":["UM-BBD_pathwayID:mf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"halogenated hydrocarbon metabolic process","termid":"GO:0042197"},{"relation_name":"is_a","term_name":"organofluorine metabolic process","termid":"GO:0090346"}],"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":"methyl fluoride metabolic process","synonyms":[{"name":"methyl fluoride metabolism","type":"exact"}],"termid":"GO:0018929"}


id: MONDO:0019024
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare entity characterized by localized but destructive growth of a tumor consisting of highly atypical, immature mast cells.(WHO, 2001)","definition_xrefs":["NCIT:C9348"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system cancer","termid":"MONDO:0000621"},{"relation_name":"is_a","term_name":"sarcoma","termid":"MONDO:0005089"},{"relation_name":"is_a","term_name":"mastocytosis","termid":"MONDO:0007950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004992","MONDO:0005570"],"is_obsolete":false,"name":"mast cell sarcoma","secondary_identifiers":["icd11.foundation:233404891","ICDO:9740/3","MEDGEN:11322","ONCOTREE:MCSL","SCTID:118615008","Orphanet:66661","UMLS:C0036221","GARD:18870","icd11.foundation:1993363632","DOID:355","MESH:D012515","EFO:1000364","ICD9:202.6"],"synonyms":[{"name":"MCS","type":"exact"},{"name":"MCSL","type":"related"},{"name":"mast cell sarcoma","type":"exact"},{"name":"mast-cell sarcoma","type":"exact"},{"name":"sarcoma of mast cell","type":"exact"}],"termid":"MONDO:0019024","xrefs":{"Monarch":{"xref_id":"0019024"}}}


id: GO:0050983
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions resulting in the formation of deoxyhypusine from spermidine by the enzyme [eIF-5A]-deoxyhypusine synthase. The reaction occurs in four steps: 1. spermidine + NAD+ = dehydrospermidine + NADH + H+; 2. dehydrospermidine + [enzyme]-lysine = 1,3-diaminopropane + [enzyme]-lysine-N6=CH(CH2)3NH2; 3. [enzyme]-lysine-N6=CH(CH2)3NH2 = [eIF-5A]-lysine-N6=CH(CH2)3NH2; 4. [eIF-5A]-lysine-N6=CH(CH2)3NH2 + NADH + H+ = [eIF-5A]-deoxyhypusine + NAD+.","definition_xrefs":["MetaCyc:1.1.1.249-RXN"],"gene_count":0,"genotype_count":0,"name":"obsolete deoxyhypusine biosynthetic process from spermidine (obsolete GO:0050983)","synonyms":[{"name":"deoxyhypusine anabolism from spermidine, using deoxyhypusine synthase","type":"exact"},{"name":"deoxyhypusine biosynthesis from spermidine, using deoxyhypusine synthase","type":"exact"},{"name":"deoxyhypusine biosynthetic process from spermidine, using deoxyhypusine synthase","type":"exact"},{"name":"deoxyhypusine formation from spermidine, using deoxyhypusine synthase","type":"exact"},{"name":"spermidine breakdown to deoxyhypusine, using deoxyhypusine synthase","type":"exact"},{"name":"spermidine catabolic process to deoxyhypusine, using deoxyhypusine synthase","type":"exact"},{"name":"spermidine degradation to deoxyhypusine, using deoxyhypusine synthase","type":"exact"}],"termid":"GO:0050983"}


id: PBO:0060363
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myomesin 2","termid":"PBO:0060363"}


id: PBO:0073236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenophosphate synthetase 1","termid":"PBO:0073236"}


id: FYPO:0005911
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the repair of double-strand breaks formed as part of meiotic recombination begins later than normal.","definition_xrefs":["PMID:19023408","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic recombination double-strand break repair","termid":"FYPO:0005139"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000298","FYPO:0000631","FYPO:0000293","FYPO:0001985"],"is_obsolete":false,"name":"delayed onset of meiotic recombination double-strand break repair","synonyms":[{"name":"delayed meiotic recombination double-strand break repair","type":"exact"},{"name":"delayed onset of DSB repair involved in reciprocal meiotic recombination","type":"exact"},{"name":"delayed onset of double-strand break repair during meiotic recombination","type":"exact"},{"name":"delayed onset of double-strand break repair involved in reciprocal meiotic recombination","type":"exact"},{"name":"delayed onset of meiotic DNA double-strand break repair","type":"exact"}],"termid":"FYPO:0005911"}


id: GO:0043143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which proteins and protein complexes involved in translation are transported to, or maintained in, a specific location.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of translation","termid":"GO:0006417"},{"relation_name":"is_a","term_name":"protein localization","termid":"GO:0008104"},{"relation_name":"part_of","term_name":"translation","termid":"GO:0006412"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0051179"],"is_obsolete":false,"name":"regulation of translation by machinery localization","synonyms":[{"name":"establishment and maintenance of translational machinery localization","type":"exact"},{"name":"establishment and maintenance of translational protein localization","type":"exact"},{"name":"regulation of translation by machinery localisation","type":"exact"},{"name":"translational machinery localization","type":"exact"},{"name":"translational protein localization","type":"exact"}],"termid":"GO:0043143"}


id: MONDO:1011652
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cardiovascular disorder, non-human animal","termid":"MONDO:1011306"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitral valve dysplasia, non-human animal","secondary_identifiers":["OMIA:002521"],"termid":"MONDO:1011652","xrefs":{"Monarch":{"xref_id":"1011652"}}}


id: PBO:0049379
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTF3C2 antisense RNA 1","termid":"PBO:0049379"}


id: GO:0061620
data:
  {"annotated_genes":["SJAG_02796","SJAG_02009","SJAG_03903","SJAG_00839","SJAG_06621","SJAG_03373","SJAG_02945","SJAG_03828","SJAG_00461","SJAG_03660","SJAG_00027","SJAG_00605","SJAG_04334","SJAG_04192","SJAG_01310","SJAG_06622","SJAG_02107","SJAG_02135","SJAG_02369","SJAG_04495"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99918,107790,111385,118372,105331,74198,79623,96431,107419,111382,105589,100189,111386,111384,107421,111381,107420,111383,111387,107791],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061621"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a carbohydrate into pyruvate, occurring through a glucose-6-phosphate intermediate, with the concomitant production of a small amount of ATP.","definition_xrefs":["ISBN:0201090910","GOC:dph","ISBN:0879010479"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolytic process through fructose-6-phosphate","termid":"GO:0061615"}],"gene_count":20,"genes_by_uniquename":{"SJAG_00027":null,"SJAG_00461":null,"SJAG_00605":null,"SJAG_00839":null,"SJAG_01310":null,"SJAG_02009":null,"SJAG_02107":null,"SJAG_02135":null,"SJAG_02369":null,"SJAG_02796":null,"SJAG_02945":null,"SJAG_03373":null,"SJAG_03660":null,"SJAG_03828":null,"SJAG_03903":null,"SJAG_04192":null,"SJAG_04334":null,"SJAG_04495":null,"SJAG_06621":null,"SJAG_06622":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0005975","GO:0006091","GO:0055086"],"is_obsolete":false,"name":"glycolytic process through glucose-6-phosphate","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0061620","terms_by_termid":{"GO:0061621":null}}


id: MONDO:0000495
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A behavior disorder characterized by a persistent pattern of defiant, disobedient, and hostile behavior towards authority figures, manifested by a frequent loss of temper, arguing, becoming angry or vindictive, or other negativistic behaviors.","definition_xrefs":["NCIT:C92565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"specific developmental disorder","termid":"MONDO:0000592"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oppositional defiant disorder","secondary_identifiers":["DOID:0050856","SCTID:18941000","ICD9:313.81","icd11.foundation:1487528823","MESH:D019958","UMLS:C0029121","HP:0010865","MEDGEN:18178"],"synonyms":[{"name":"oppositional defiant disorder","type":"exact"},{"name":"oppositional defiant disorder (disease)","type":"exact"}],"termid":"MONDO:0000495","xrefs":{"Monarch":{"xref_id":"0000495"}}}


id: PBO:0078935
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon CCT) 3-1","termid":"PBO:0078935"}


id: PBO:0047756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"folate hydrolase 1","termid":"PBO:0047756"}


id: GO:0018874
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving benzoate, the anion of benzoic acid (benzenecarboxylic acid), a fungistatic compound widely used as a food preservative; it is conjugated to glycine in the liver and excreted as hippuric acid.","definition_xrefs":["ISBN:0721662544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"},{"relation_name":"is_a","term_name":"benzene-containing compound metabolic process","termid":"GO:0042537"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"benzoate metabolic process","secondary_identifiers":["UM-BBD_pathwayID:benz2"],"synonyms":[{"name":"benzoate metabolism","type":"exact"}],"termid":"GO:0018874"}


id: PBO:0116816
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F10 antisense RNA 2","termid":"PBO:0116816"}


id: SO:0001631
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant located 5' of a gene.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intergenic_variant","termid":"SO:0001628"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"upstream_gene_variant","secondary_identifiers":["http://snpeff.sourceforge.net/SnpEff_manual.html","http:www.ensembl.org/info/genome/variation/predicted_data.html#consequences"],"synonyms":[{"name":"ANNOVAR:upstream","type":"related"},{"name":"Jannovar:upstream_gene_variant","type":"exact"},{"name":"VEP:upstream_gene_variant","type":"exact"},{"name":"snpEff:UPSTREAM","type":"exact"},{"name":"upstream gene variant","type":"exact"}],"termid":"SO:0001631"}


id: GO:1900291
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of galactotriose transport.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"galactotriose transport","termid":"GO:2001093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of galactotriose transport","termid":"GO:1900291"}


id: GO:1904097
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of acid phosphatase activity.","definition_xrefs":["PMID:8132635","GO_REF:0000088","GOC:bhm","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase complex","termid":"GO:1903293"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"acid phosphatase complex","termid":"GO:1904097"}


id: MONDO:0003360
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive malignant smooth muscle neoplasm, arising from the small intestine. It is characterized by a proliferation of neoplastic spindle cells.","definition_xrefs":["NCIT:C7085"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small intestinal sarcoma","termid":"MONDO:0003361"},{"relation_name":"is_a","term_name":"leiomyosarcoma","termid":"MONDO:0005058"},{"relation_name":"is_a","term_name":"mesenchymal tumor of small intestine","termid":"MONDO:0018506"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"small intestine leiomyosarcoma","secondary_identifiers":["GARD:19852","SCTID:716651004","MEDGEN:183086","Orphanet:104076","UMLS:C0920305","DOID:5271"],"synonyms":[{"name":"leiomyosarcoma of small bowel","type":"exact"},{"name":"leiomyosarcoma of small intestine","type":"exact"},{"name":"leiomyosarcoma of the small bowel","type":"exact"},{"name":"leiomyosarcoma of the small intestine","type":"exact"},{"name":"small bowel leiomyosarcoma","type":"exact"},{"name":"small intestinal leiomyosarcoma","type":"exact"},{"name":"small intestine leiomyosarcoma","type":"exact"},{"name":"smooth muscle connective tissue tumor","type":"related"},{"name":"smooth muscle connective tissue tumour","type":"related"}],"termid":"MONDO:0003360","xrefs":{"Monarch":{"xref_id":"0003360"}}}


id: PBO:0051947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inositol-trisphosphate 3-kinase A","termid":"PBO:0051947"}


id: MONDO:0005860
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0005860 (obsolete MONDO:0005860)","termid":"MONDO:0005860","xrefs":{"Monarch":{"xref_id":"0005860"}}}


id: MONDO:0001374
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymal cell neoplasm that affects the urinary bladder.","definition_xrefs":["NCIT:C4669"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urinary bladder cancer","termid":"MONDO:0001187"},{"relation_name":"is_a","term_name":"soft tissue sarcoma","termid":"MONDO:0018078"}],"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":"bladder sarcoma","secondary_identifiers":["SCTID:278046008","UMLS:C0349666","MEDGEN:87612","DOID:11812"],"synonyms":[{"name":"bladder sarcoma","type":"exact"},{"name":"sarcoma of bladder","type":"exact"},{"name":"sarcoma of the bladder","type":"exact"},{"name":"sarcoma of the urinary bladder","type":"exact"},{"name":"sarcoma of urinary bladder","type":"exact"},{"name":"urinary bladder sarcoma","type":"exact"}],"termid":"MONDO:0001374","xrefs":{"Monarch":{"xref_id":"0001374"}}}


id: GO:0008530
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Combining with an extracellular peptide to initiate a change in cell activity.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete exogenous peptide receptor activity (obsolete GO:0008530)","synonyms":[{"name":"exogenous peptide receptor activity","type":"exact"}],"termid":"GO:0008530"}


id: PBO:0043251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"claudin 10","termid":"PBO:0043251"}


id: PATO:0002275
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color pattern quality inhering in a bearer by virtue of the bearer's color pattern in which light and dark colors (for example white and black) are codistributed to create a visual impression.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color pattern","termid":"PATO:0000019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high contrast color pattern","termid":"PATO:0002275"}


id: PBO:0043432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CNIH3 antisense RNA 1","termid":"PBO:0043432"}


id: GO:0086041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a potassium ion by a voltage-gated channel through the plasma membrane of an SA node cardiac muscle cell contributing to the depolarization 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:BHF","GOC:mtg_cardiac_conduct_nov11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"voltage-gated potassium channel activity","termid":"GO:0005249"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"voltage-gated potassium channel activity involved in SA node cell action potential depolarization","synonyms":[{"name":"voltage-gated potassium channel activity involved in SAN cell action potential depolarization","type":"exact"},{"name":"voltage-gated potassium channel activity involved in sinoatrial node cell action potential depolarization","type":"exact"},{"name":"voltage-gated potassium channel activity involved in sinus node cell action potential depolarization","type":"narrow"}],"termid":"GO:0086041"}


id: PBO:0084360
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-homoserine-O-acetyltransferase; catalyzes the conversion of homoserine to O-acetyl homoserine which is the first step of the methionine biosynthetic pathway","termid":"PBO:0084360"}


id: GO:0001059
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The synthesis of RNA from a DNA template by RNA polymerase IV, originating at a Pol IV-specific promoter.","definition_xrefs":["PMID:19110459","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription","termid":"GO:0006351"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006351","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"transcription by RNA polymerase IV","synonyms":[{"name":"transcription from RNA pol IV promoter","type":"exact"},{"name":"transcription from RNA polymerase IV promoter","type":"exact"}],"termid":"GO:0001059"}


id: GO:1903879
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to 11beta-hydroxyprogesterone.","definition_xrefs":["GOC:TermGenie","GO_REF:0000067","GOC:mr","PMID:10802282"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid binding","termid":"GO:0005496"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0008289","GO:0003674"],"is_obsolete":false,"name":"11beta-hydroxyprogesterone binding","termid":"GO:1903879"}


id: PBO:0044560
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deleted in azoospermia 1","termid":"PBO:0044560"}


id: PR:O14134
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- elf1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14134"],"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":"mRNA export factor elf1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC3C7.08c","synonyms":[{"name":"Spom972h-elf1","type":"exact"}],"termid":"PR:O14134"}


id: MONDO:0018303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete generalized isolated dystonia (obsolete MONDO:0018303)","termid":"MONDO:0018303","xrefs":{"Monarch":{"xref_id":"0018303"}}}


id: PR:P78920
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nap2 gene.","definition_xrefs":["UniProtKB:P78920","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":"nucleosome assembly protein C2D10.11C (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2D10.11c","synonyms":[{"name":"Spom972h-nap2","type":"exact"}],"termid":"PR:P78920"}


id: GO:0032717
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of interleukin-8 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of interleukin-8 production","termid":"GO:0032677"},{"relation_name":"negatively_regulates","term_name":"interleukin-8 production","termid":"GO:0032637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of interleukin-8 production","secondary_identifiers":["GO:0045415","GO:2000483"],"synonyms":[{"name":"down regulation of interleukin-8 production","type":"exact"},{"name":"down-regulation of interleukin-8 production","type":"exact"},{"name":"downregulation of interleukin-8 production","type":"exact"},{"name":"inhibition of interleukin-8 production","type":"narrow"},{"name":"negative regulation of IL-8 production","type":"exact"},{"name":"negative regulation of interleukin-8 biosynthetic process","type":"narrow"},{"name":"negative regulation of interleukin-8 secretion","type":"narrow"}],"termid":"GO:0032717"}


id: GO:0002256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of the kinin cascade.","definition_xrefs":["GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of acute inflammatory response","termid":"GO:0002673"},{"relation_name":"is_a","term_name":"regulation of protein activation cascade","termid":"GO:2000257"},{"relation_name":"regulates","term_name":"kinin cascade","termid":"GO:0002254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0051604"}],"interesting_parent_ids":["GO:0008150","GO:0051604","GO:0010467"],"is_obsolete":false,"name":"regulation of kinin cascade","termid":"GO:0002256"}


id: MONDO:0003929
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplastic process characterized by the presence of multiple vestibular papillomas in the vulva.","definition_xrefs":["NCIT:C40290"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vestibular papilloma","termid":"MONDO:0002194"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vestibular micropapillomatosis","secondary_identifiers":["DOID:6569","UMLS:C1519982","MEDGEN:275589"],"synonyms":[{"name":"micropapillomatosis labialis","type":"exact"},{"name":"vestibular micropapillomatosis","type":"exact"}],"termid":"MONDO:0003929","xrefs":{"Monarch":{"xref_id":"0003929"}}}


id: PBO:0003479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper chaperone Atx1","termid":"PBO:0003479"}


id: PBO:0066329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RCAN2 divergent transcript","termid":"PBO:0066329"}


id: PBO:0086200
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; green fluorescent protein (GFP)-fusion protein localizes to the mitochondrion; null mutation results in a decrease in plasma membrane electron transport","termid":"PBO:0086200"}


id: GO:0048212
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which Golgi vesicle coat proteins are depolymerized, and released for reuse.","definition_xrefs":["ISBN:0716731363","PMID:10219233","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle uncoating","termid":"GO:0072319"},{"relation_name":"part_of","term_name":"Golgi vesicle transport","termid":"GO:0048193"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"Golgi vesicle uncoating","synonyms":[{"name":"Golgi vesicle coat depolymerization","type":"exact"},{"name":"Golgi vesicle coat protein depolymerization","type":"exact"},{"name":"Golgi-derived vesicle uncoating","type":"exact"},{"name":"dictyosome vesicle coat depolymerization","type":"narrow"}],"termid":"GO:0048212"}


id: GO:0034945
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2,6-dimethyl-5-methylene-3-oxo-heptanoyl-CoA + CoASH = 3-isopropylbut-3-enoyl-CoA + propanoyl-CoA.","definition_xrefs":["UM-BBD_reactionID:r0987"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,6-dimethyl-5-methylene-3-oxo-heptanoyl-CoA C-acetyltransferase activity (obsolete GO:0034945)","termid":"GO:0034945"}


id: PR:O59718
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nem1 gene.","definition_xrefs":["UniProtKB:O59718","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":"nuclear envelope morphology protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3B8.10c","synonyms":[{"name":"Spom972h-nem1","type":"exact"}],"termid":"PR:O59718"}


id: GO:0044295
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The migrating motile tip of a growing nerve cell axon.","definition_xrefs":["NIF_Subcellular:sao203987954","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth cone","termid":"GO:0030426"}],"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":"axonal growth cone","secondary_identifiers":["NIF_Subcellular:sao1594955670"],"synonyms":[{"name":"axon growth cone","type":"exact"}],"termid":"GO:0044295"}


id: GO:0102533
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: genkwanin + S-adenosyl-L-methionine = apigenin 4',7-dimethyl ether + S-adenosyl-L-homocysteine.","definition_xrefs":["RHEA:73263"],"direct_ancestors":[{"relation_name":"is_a","term_name":"methyltransferase activity","termid":"GO:0008168"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"genkwanin 4'-O-methyltransferase activity","secondary_identifiers":["MetaCyc:RXN-14750"],"termid":"GO:0102533"}


id: PBO:0011124
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Warsaw breakage syndrome","termid":"PBO:0011124"}


id: PBO:0042930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cingulin","termid":"PBO:0042930"}


id: PBO:0062783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ORAI calcium release-activated calcium modulator 1","termid":"PBO:0062783"}


id: GO:0100061
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription factor catabolic process process that negatively regulates SREBP signaling pathway.","definition_xrefs":["GOC:cjm","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of SREBP signaling pathway by transcription factor catabolic process (obsolete GO:0100061)","termid":"GO:0100061"}


id: FYPO:0005600
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the size, shape, or structure of one or more chromosomes is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component","termid":"FYPO:0000287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal chromosome morphology","termid":"FYPO:0005600"}


id: PBO:0055891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 10","termid":"PBO:0055891"}


id: PBO:0042338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD70 molecule","termid":"PBO:0042338"}


id: FYPO:0008061
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of the serine residue at position 5 within one or more copies of the heptapeptide repeat (YSPTSPS) of the C-terminal domain of RNA polymerase II does not occur.","definition_xrefs":["PMID:1902677"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal RNA polymerase II C-terminal domain phosphorylation","termid":"FYPO:0007410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0002274","FYPO:0002494"],"is_obsolete":false,"name":"abolished phosphorylation of RNA polymerase II C-terminal domain serine 5 residues during vegetative growth","termid":"FYPO:0008061"}


id: GO:0046644
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of gamma-delta T cell activation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gamma-delta T cell activation","termid":"GO:0046643"},{"relation_name":"is_a","term_name":"negative regulation of T cell activation","termid":"GO:0050868"},{"relation_name":"negatively_regulates","term_name":"gamma-delta T cell activation","termid":"GO:0046629"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of gamma-delta T cell activation","synonyms":[{"name":"down regulation of gamma-delta T cell activation","type":"exact"},{"name":"down-regulation of gamma-delta T cell activation","type":"exact"},{"name":"downregulation of gamma-delta T cell activation","type":"exact"},{"name":"inhibition of gamma-delta T cell activation","type":"narrow"},{"name":"negative regulation of gamma-delta T lymphocyte activation","type":"exact"},{"name":"negative regulation of gamma-delta T-cell activation","type":"exact"},{"name":"negative regulation of gamma-delta T-lymphocyte activation","type":"exact"}],"termid":"GO:0046644"}


id: GO:0042048
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The behavior of an organism in response to an odor.","definition_xrefs":["GOC:pr","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemosensory behavior","termid":"GO:0007635"}],"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":"olfactory behavior","synonyms":[{"name":"behavioral response to scent","type":"exact"},{"name":"behavioral response to smell","type":"exact"},{"name":"behavioural response to odour","type":"exact"},{"name":"behavioural response to scent","type":"exact"},{"name":"behavioural response to smell","type":"exact"},{"name":"olfactory behaviour","type":"exact"}],"termid":"GO:0042048"}


id: GO:0015377
data:
  {"annotated_genes":["SJAG_03401"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015379"}]},"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: cation(out) + Cl-(out) = cation(in) + Cl-(in).","definition_xrefs":["PMID:31747317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chloride transmembrane transporter activity","termid":"GO:0015108"},{"relation_name":"is_a","term_name":"monoatomic anion:monoatomic cation symporter activity","termid":"GO:0015296"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03401":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:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"chloride:monoatomic cation symporter activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["TC:2.A.30"],"synonyms":[{"name":"cation:chloride cotransporter activity","type":"broad"},{"name":"cation:chloride symporter activity","type":"broad"}],"termid":"GO:0015377","terms_by_termid":{"GO:0015379":null}}


id: GO:0030961
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The hydroxylation of peptidyl-arginine to form peptidyl-hydroxyarginine.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-arginine modification","termid":"GO:0018195"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"peptidyl-arginine hydroxylation","termid":"GO:0030961"}


id: PBO:0039263
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldehyde dehydrogenase 8 family member A1","termid":"PBO:0039263"}


id: PR:O42643
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP-dependent RNA helicase DHX8 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00486","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":"pre-mRNA-splicing factor ATP-dependent RNA helicase prp22 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC10F6.02c","secondary_identifiers":["UniProtKB:O42643"],"synonyms":[{"name":"Spom972h-DHX8","type":"exact"}],"termid":"PR:O42643"}


id: GO:0018071
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: NAD(P)+ + L-cysteine = nicotinamide + N2-(ADP-D-ribosyl)-L-cysteine.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete NAD(P)-cysteine ADP-ribosyltransferase activity (obsolete GO:0018071)","termid":"GO:0018071"}


id: GO:0099170
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process, acting in the postsynapse that results in modulation of chemical synaptic transmission.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation of chemical synaptic transmission","termid":"GO:0050804"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"postsynaptic modulation of chemical synaptic transmission","termid":"GO:0099170"}


id: PBO:0071488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 29","termid":"PBO:0071488"}


id: PBO:0081401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF248 antisense RNA 1","termid":"PBO:0081401"}


id: PBO:0081070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger DHHC-type palmitoyltransferase 3","termid":"PBO:0081070"}


id: MONDO:0700122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any BAFopathy in which the cause of the disease is a mutation in the PBRM1 gene.","definition_xrefs":["MONDO:patterns/OMIM_disease_series_by_gene","PMID:30580808"],"direct_ancestors":[{"relation_name":"is_a","term_name":"BAFopathy","termid":"MONDO:0700120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PBRM1-related BAFopathy","termid":"MONDO:0700122","xrefs":{"Monarch":{"xref_id":"0700122"}}}


id: GO:0051712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the killing by an organism of cells in another organism.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell killing","termid":"GO:0031343"},{"relation_name":"is_a","term_name":"positive regulation of programmed cell death","termid":"GO:0043068"},{"relation_name":"is_a","term_name":"regulation of killing of cells of another organism","termid":"GO:0051709"},{"relation_name":"positively_regulates","term_name":"killing of cells of another organism","termid":"GO:0031640"}],"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 killing of cells of another organism","secondary_identifiers":["GO:0052529","GO:0052518","GO:0052501","GO:0052330","GO:0052388"],"synonyms":[{"name":"activation by organism of apoptotic programmed cell death in other organism during symbiotic interaction","type":"related"},{"name":"activation of killing of cells of another organism","type":"narrow"},{"name":"enhancement of other organism programmed cell death by organism","type":"related"},{"name":"positive regulation of killing of cells of other organism","type":"exact"},{"name":"stimulation of killing of cells of another organism","type":"narrow"},{"name":"up regulation of killing of cells of another organism","type":"exact"},{"name":"up-regulation of killing of cells of another organism","type":"exact"},{"name":"upregulation of killing of cells of another organism","type":"exact"}],"termid":"GO:0051712"}


id: PBO:0075567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Spi-C transcription factor","termid":"PBO:0075567"}


id: PBO:0071350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 8","termid":"PBO:0071350"}


id: PBO:0051971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interacts with SUPT6H, CTD assembly factor 1","termid":"PBO:0051971"}


id: MONDO:0005461
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma arising from the uterine body cavity. This is the most frequent malignant tumor affecting the uterine body, and is linked to estrogen therapy. Most patients present with uterine bleeding and are over age 40 at the time of diagnosis. The prognosis depends on the stage of the tumor, the depth of the uterine wall invasion, and the histologic subtype. Endometrioid adenocarcinoma is the most frequently seen morphologic variant of endometrial adenocarcinoma.","definition_xrefs":["NCIT:C7359"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endometrial carcinoma","termid":"MONDO:0002447"},{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"}],"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":"endometrium adenocarcinoma","secondary_identifiers":["UMLS:C1153706","EFO:0005232","NCIT:C6287","DOID:2870","MEDGEN:218862"],"synonyms":[{"name":"adenocarcinoma of endometrium","type":"exact"},{"name":"adenocarcinoma of the endometrium","type":"exact"},{"name":"adenocarcinoma of uterus","type":"exact"},{"name":"adenocarcinoma, endometrial, malignant","type":"exact"},{"name":"endometrial adenoacanthoma","type":"exact"},{"name":"endometrial adenocarcinoma","type":"exact"},{"name":"endometrial endometrioid adenocarcinoma","type":"related"},{"name":"endometrial endometrioid adenocarcinoma with squamous differentiation","type":"exact"},{"name":"endometrioid adenoma or carcinoma","type":"exact"},{"name":"endometrioid adenoma or carcinoma NOS (morphologic abnormality)","type":"exact"},{"name":"endometrioid adenomas and carcinomas","type":"exact"},{"name":"endometrioid adenomas and carcinomas (morphologic abnormality)","type":"exact"},{"name":"endometrioid carcinoma of endometrium","type":"broad"},{"name":"endometrium adenocarcinoma","type":"exact"}],"termid":"MONDO:0005461","xrefs":{"Monarch":{"xref_id":"0005461"}}}


id: GO:0051073
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: adenosylcobinamide-GDP + alpha-ribazole = GMP + adenosylcobalamin.","definition_xrefs":["MetaCyc:COBALAMINSYN-RXN","EC:2.7.8.26"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, for other substituted phosphate groups","termid":"GO:0016780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016780"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016780","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"adenosylcobinamide-GDP ribazoletransferase activity","secondary_identifiers":["RHEA:16049"],"synonyms":[{"name":"CobS","type":"related"},{"name":"adenosylcobinamide-GDP:alpha-ribazole ribazoletransferase activity","type":"related"},{"name":"cobalamin (5'-phosphate) synthase activity","type":"related"},{"name":"cobalamin synthase activity","type":"exact"},{"name":"cobalamin-5'-phosphate synthase activity","type":"related"}],"termid":"GO:0051073"}


id: MONDO:0700023
data:
  {"annotated_genes":["SJAG_01286"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011402"}]},"cv_name":"mondo","definition":"Chromosomal disorder in which chromosome 16 is affected.","definition_xrefs":["MONDO:patterns/chromosome_type"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal anomaly","termid":"MONDO:0020049"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01286":null},"genotype_count":0,"is_obsolete":false,"name":"chromosome 16 disorder","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0700023","terms_by_termid":{"MONDO:0011402":null},"xrefs":{"Monarch":{"xref_id":"0700023"}}}


id: PBO:0039306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alkB homolog 1, histone H2A dioxygenase","termid":"PBO:0039306"}


id: PR:O36031
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- hit1 gene.","definition_xrefs":["UniProtKB:O36031","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized zinc-finger protein C4F10.19c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4F10.19c","synonyms":[{"name":"Spom972h-hit1","type":"exact"}],"termid":"PR:O36031"}


id: PBO:0087112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosome-associated chaperone; zuotin functions in ribosome biogenesis and as a chaperone for nascent polypeptide chains in partnership with Ssz1p and SSb1/2; contains a DnaJ domain and functions as a J-protein partner for Ssb1p and Ssb2p; human gene DNAJC2 can partially complement yeast zuo1 null mutant","termid":"PBO:0087112"}


id: PATO:0000296
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000296 speed value (obsolete PATO:0000296)","termid":"PATO:0000296"}


id: FYPO:0000118
data:
  {"alleles_by_uniquename":{"SJAG_00118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00118","name":"mid2delta","uniquename":"SJAG_00118:allele-1"},"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121278],"is_not":false,"summary":null,"term":"FYPO:0000118"}],"single_locus_phenotype":[{"annotations":[121267,121268],"is_not":false,"summary":null,"term":"FYPO:0000118"}]},"cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle characterized by the presence of more than one septum in a cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"is_a","term_name":"septated vegetative cell","termid":"FYPO:0002342"},{"relation_name":"is_a","term_name":"multiseptate cell","termid":"FYPO:0004295"},{"relation_name":"output_of","term_name":"abnormal cytokinesis during vegetative growth","termid":"FYPO:0000032"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00118":null,"SJAG_01143":null},"genotype_count":3,"genotypes_by_uniquename":{"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__mid2delta":{"display_name":"mid1delta mid2delta","display_uniquename":"mid1delta__mid2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_00118:allele-1","expression":"Null"}]}]},"mid2delta":{"display_name":"mid2delta","display_uniquename":"mid2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00118:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000631","FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000032"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_00118","SJAG_01143"],"name":"multiseptate vegetative cell","references_by_uniquename":{"PMID:25866389":null},"single_locus_annotated_genes":["SJAG_00118","SJAG_01143"],"single_locus_genotype_uniquenames":["mid2delta","mid1delta"],"synonyms":[{"name":"multiseptate during mitotic cell cycle","type":"related"},{"name":"multiseptate during vegetative growth","type":"exact"},{"name":"septation defects, multiple septa during vegetative growth","type":"exact"}],"termid":"FYPO:0000118","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0000118":null}}


id: PBO:0087155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA helicase in the DEAD-box family; necessary for prespliceosome formation, bridges U1 and U2 snRNPs and enables stable U2 snRNP association with intron RNA","termid":"PBO:0087155"}


id: GO:0048390
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the intermediate mesoderm are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesoderm morphogenesis","termid":"GO:0048332"},{"relation_name":"part_of","term_name":"intermediate mesoderm development","termid":"GO:0048389"}],"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":"intermediate mesoderm morphogenesis","termid":"GO:0048390"}


id: MONDO:0018616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Central serous chorioretinopathy is a disease that causes fluid to build up under the retina, the back part of the inner eye that sends sight information to the brain. The fluid leaks from thechoroid (theblood vessel layer under the retina). The cause of this condition is unknown but stress can be a risk factor. Signs and symptoms include dim and blurred blind spot in the center of vision, distortion of straight linesand seeingobjectsas smaller or farther away. Many cases of central serous chorioretinopathy improve without treatment after 1-2 months. Laser treatment may be an option for other individuals.","direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"}],"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":"central serous chorioretinopathy","secondary_identifiers":["GARD:200","icd11.foundation:1623925689","MESH:D056833","NCIT:C115124","ICD9:362.41","Orphanet:443079","UMLS:C0730328","SCTID:312956001","MEDGEN:147591"],"synonyms":[{"name":"CSC","type":"exact"},{"name":"CSCR","type":"exact"},{"name":"central serous chorioretinopathy after bone marrow transplantation","type":"related"},{"name":"central serous choroidopathy","type":"related"},{"name":"central serous retinopathy","type":"exact"}],"termid":"MONDO:0018616","xrefs":{"Monarch":{"xref_id":"0018616"}}}


id: PBO:0071462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 3","termid":"PBO:0071462"}


id: FYPO:0006711
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, does not occur during a cellular response to a pH above 7.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein phosphorylation during vegetative growth","termid":"FYPO:0002033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0002494"],"is_obsolete":false,"name":"abolished protein phosphorylation during cellular response to alkaline pH","synonyms":[{"name":"abolished protein phosphorylation during cellular response to alkaline pH during mitotic cell cycle","type":"related"},{"name":"abolished protein phosphorylation during cellular response to alkaline pH during vegetative growth","type":"exact"},{"name":"abolished protein phosphorylation during cellular response to high pH","type":"exact"},{"name":"abolished protein phosphorylation in high pH","type":"related"},{"name":"protein phosphorylation abolished during cellular response to alkaline pH","type":"exact"}],"termid":"FYPO:0006711"}


id: MONDO:0022647
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardiomelic syndrome stratton Koehler type","termid":"MONDO:0022647","xrefs":{"Monarch":{"xref_id":"0022647"}}}


id: PBO:0048754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerate kinase","termid":"PBO:0048754"}


id: GO:0034050
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell death resulting from activation of endogenous cellular processes after interaction with a symbiont (defined as the smaller of two, or more, organisms engaged in symbiosis, a close interaction encompassing mutualism through parasitism). This can be triggered by direct interaction with the organism, for example, contact with penetrating hyphae of a fungus; or an indirect interaction such as symbiont-secreted molecules.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"programmed cell death","termid":"GO:0012501"},{"relation_name":"is_a","term_name":"defense response to symbiont","termid":"GO:0140546"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-induced defense-related programmed cell death","synonyms":[{"name":"host programmed cell death induced by symbiont","type":"exact"},{"name":"programmed cell death induced by symbiont","type":"exact"}],"termid":"GO:0034050"}


id: MONDO:0015894
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of hyperthyroidism that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare hyperthyroidism (obsolete MONDO:0015894)","secondary_identifiers":["Orphanet:181399"],"synonyms":[{"name":"rare hyperthyroidism","type":"exact"}],"termid":"MONDO:0015894","xrefs":{"Monarch":{"xref_id":"0015894"}}}


id: MONDO:0850071
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"developmental delay-immunodeficiency-leukoencephalopathy-hypohomocysteinemia syndrome","secondary_identifiers":["GARD:22468","MEDGEN:1842938","Orphanet:619979","UMLS:C5681830"],"termid":"MONDO:0850071","xrefs":{"Monarch":{"xref_id":"0850071"}}}


id: FYPO:0005907
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 nucleus is normal (i.e. indistinguishable from wild type) during a cellular response to heat.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to nucleus during vegetative growth","termid":"FYPO:0000838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001312","FYPO:0001320","FYPO:0000257","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to nucleus during cellular response to heat","synonyms":[{"name":"normal protein localisation to nucleus during cellular response to heat","type":"exact"},{"name":"normal protein localization to nucleus during cellular response to heat during mitotic cell cycle","type":"related"},{"name":"normal protein localization to nucleus during cellular response to heat during vegetative growth","type":"exact"}],"termid":"FYPO:0005907"}


id: MONDO:0014310
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome is a rare, genetic, hereditary poikiloderma syndrome characterized by early-onset poikiloderma (mainly on the face), hypotrichosis, hypohidrosis, muscle and tendon contractures with varus foot deformity, progressive proximal and distal muscle weakness in all extremities, and progressive pulmonary fibrosis. Mild lymphedema of the extremities, growth retardation, liver impairment, exocrine pancreatic insufficiency and hematologic abnormalities are additional variable features.","definition_xrefs":["Orphanet:221043"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"},{"relation_name":"is_a","term_name":"hereditary poikiloderma","termid":"MONDO:0016382"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"hereditary sclerosing poikiloderma with tendon and pulmonary involvement","secondary_identifiers":["OMIM:615704","GARD:13218","MEDGEN:816655","UMLS:C3810325","icd11.foundation:1585528459"],"synonyms":[{"name":"POIKTMP","type":"related"},{"name":"POIKTMP syndrome","type":"exact"},{"name":"hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis","type":"related"},{"name":"hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome","type":"related"},{"name":"poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis","type":"related"},{"name":"poikiloderma, hereditary sclerosing, with tendon and pulmonary involvement","type":"related"}],"termid":"MONDO:0014310","xrefs":{"Monarch":{"xref_id":"0014310"}}}


id: PBO:0073487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SGO1 antisense RNA 1","termid":"PBO:0073487"}


id: GO:0002370
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that contributes to cytokine production by a natural killer cell.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"natural killer cell mediated immunity","termid":"GO:0002228"},{"relation_name":"is_a","term_name":"cytokine production involved in immune response","termid":"GO:0002367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"natural killer cell cytokine production","synonyms":[{"name":"NK cell cytokine production","type":"exact"}],"termid":"GO:0002370"}


id: PBO:0089404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA (uridine) methyltransferase Trm9","termid":"PBO:0089404"}


id: PBO:0043406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CKLF like MARVEL transmembrane domain containing 3","termid":"PBO:0043406"}


id: GO:0072713
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a thiabendazole stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to thiabendazole","termid":"GO:0072712"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"}],"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":"cellular response to thiabendazole","synonyms":[{"name":"cellular response to TBZ","type":"exact"}],"termid":"GO:0072713"}


id: GO:0140570
data:
  {"annotated_genes":["SJAG_04203"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[76455],"is_not":false,"summary":null,"term":"GO:0140570"}]},"cv_name":"biological_process","definition":"The removal of a mislocalized protein from the mitochondrial outer membrane.","definition_xrefs":["PMID:32973005"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extraction of mislocalized protein from membrane","termid":"GO:0140568"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04203":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"extraction of mislocalized protein from mitochondrial outer membrane","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"extraction of mislocalized protein from outer mitochondrion membrane","type":"exact"}],"termid":"GO:0140570","terms_by_termid":{"GO:0140570":null}}


id: PBO:0043408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CKLF like MARVEL transmembrane domain containing 5","termid":"PBO:0043408"}


id: GO:0005107
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete GPI-linked ephrin (obsolete GO:0005107)","synonyms":[{"name":"GPI-linked ephrin","type":"exact"}],"termid":"GO:0005107"}


id: GO:0010294
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (+)-abscisate + UDP-D-glucose = abscisic acid glucose ester + UDP.","definition_xrefs":["DOI:10.1016/j.tetasy.2004.11.062"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016757","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"abscisic acid glucosyltransferase activity","secondary_identifiers":["RHEA:31031","MetaCyc:RXN-8155"],"termid":"GO:0010294"}


id: PBO:0086485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative nucleotide sugar transporter; has similarity to Vrg4p","termid":"PBO:0086485"}


id: MONDO:0020133
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic central nervous system malformation (obsolete MONDO:0015219)","termid":"MONDO:0015219"}],"gene_count":0,"genotype_count":0,"name":"obsolete posterior fossa malformation (obsolete MONDO:0020133)","secondary_identifiers":["Orphanet:98519"],"termid":"MONDO:0020133","xrefs":{"Monarch":{"xref_id":"0020133"}}}


id: MONDO:0016958
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosome 7q duplication is a chromosome abnormality that occurs when there is an extra copy of genetic material on the long arm (q) of chromosome 7. The severity of the condition and the signs and symptoms depend on the size and location of the duplication and which genes are involved. Features that often occur in people with chromosome 7q duplication include developmental delay, intellectual disability, behavioral problems and distinctive facial features. Most cases are not inherited, but people can pass the duplication on to their children. Treatment is based on the signs and symptoms present in each person.","definition_xrefs":["GARD:0005357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of chromosome 7","termid":"MONDO:0016928"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial duplication of the long arm of chromosome 7","secondary_identifiers":["UMLS:C0795821","MEDGEN:208637","Orphanet:262887","icd11.foundation:462724513","MESH:C537821","GARD:5357"],"synonyms":[{"name":"7q duplication","type":"related"},{"name":"7q trisomy","type":"related"},{"name":"Duplication 7q","type":"related"},{"name":"chromosome 7q duplication","type":"related"},{"name":"partial duplication of chromosome 7q","type":"exact"},{"name":"partial duplication of the long arm of chromosome type 7","type":"exact"},{"name":"partial trisomy 7q","type":"related"},{"name":"partial trisomy of chromosome 7q","type":"exact"},{"name":"partial trisomy of the long arm of chromosome 7","type":"exact"},{"name":"trisomy 7q","type":"related"}],"termid":"MONDO:0016958","xrefs":{"Monarch":{"xref_id":"0016958"}}}


id: FYPO:0006531
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype which protein degradation begins later than normal during one or both meiotic nuclear divisions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein degradation","termid":"FYPO:0002275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0002274","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"delayed onset of protein degradation during meiosis","synonyms":[{"name":"delayed onset of protein breakdown during meiosis","type":"exact"},{"name":"delayed onset of protein catabolic process during meiosis","type":"exact"},{"name":"delayed onset of protein catabolism during meiosis","type":"exact"},{"name":"delayed onset of protein degradation during meiotic nuclear division","type":"exact"},{"name":"delayed protein degradation during meiosis","type":"exact"}],"termid":"FYPO:0006531"}


id: PBO:0027295
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-elongated_tetranucleate_vegetative_cell","termid":"PBO:0027295"}


id: PBO:0074788
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 9","termid":"PBO:0074788"}


id: MONDO:0013033
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any spastic quadriplegia in which the cause of the disease is a mutation in the KANK1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spastic quadriplegic cerebral palsy","termid":"MONDO:0016215"},{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"cerebral palsy, spastic quadriplegic, 2","secondary_identifiers":["GARD:18309","OMIM:612900","UMLS:C2752061","MEDGEN:442880","MESH:C567867","DOID:0081360"],"synonyms":[{"name":"CPSQ2","type":"related"},{"name":"KANK1 spastic quadriplegia","type":"exact"},{"name":"cerebral palsy, spastic quadriplegic, 2","type":"exact"},{"name":"cerebral palsy, spastic quadriplegic, type 2","type":"exact"},{"name":"spastic quadriplegia caused by mutation in KANK1","type":"exact"}],"termid":"MONDO:0013033","xrefs":{"Monarch":{"xref_id":"0013033"}}}


id: PBO:0074084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 26 member 1","termid":"PBO:0074084"}


id: MONDO:0001629
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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":"Jaccoud syndrome","secondary_identifiers":["DOID:13080","SCTID:84801008","ICD9:714.4","UMLS:C0152084","MEDGEN:508877"],"synonyms":[{"name":"Jaccoud syndrome","type":"exact"},{"name":"Jaccoud's syndrome","type":"exact"}],"termid":"MONDO:0001629","xrefs":{"Monarch":{"xref_id":"0001629"}}}


id: PBO:0077963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ala (anticodon AGC) 16-1","termid":"PBO:0077963"}


id: SO:0001523
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute of a duplication, which is an insertion which derives from, or is identical in sequence to, nucleotides present at a known location in the genome.","direct_ancestors":[{"relation_name":"is_a","term_name":"alteration_attribute","termid":"SO:0001508"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"duplication_attribute","synonyms":[{"name":"duplication attribute","type":"related"}],"termid":"SO:0001523"}


id: PBO:0071161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a","termid":"PBO:0071161"}


id: FYPO:0003659
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 all or part of the mating-type region is duplicated or deleted upon mating type switching.","definition_xrefs":["PMID:8290356","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating type switching","termid":"FYPO:0000468"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000293","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abnormal mating type switching resulting in duplication or deletion in mating-type region","synonyms":[{"name":"abnormal mating type switching resulting in duplication or deletion in mating-type region during mitotic cell cycle","type":"related"},{"name":"abnormal mating type switching resulting in duplication or deletion in mating-type region during vegetative growth","type":"exact"}],"termid":"FYPO:0003659"}


id: GO:0106126
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a reservosome.","definition_xrefs":["GOC:ach","PMID:19288526","PMID:21818313","PMID:15521631","PMID:18452191","PMID:22425988","PMID:12204365"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"reservosome","termid":"GO:0106123"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005773"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005773"],"is_obsolete":false,"name":"reservosome membrane","termid":"GO:0106126"}


id: PBO:0084038
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPI-anchored cell wall protein of unknown function; induced in response to cell wall damaging agents and by mutations in genes involved in cell wall biogenesis; sequence similarity to YBR162C/TOS1, a covalently bound cell wall protein; protein abundance increases in response to DNA replication stress","termid":"PBO:0084038"}


id: PBO:0066061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rap guanine nucleotide exchange factor 5","termid":"PBO:0066061"}


id: MONDO:0020571
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epidemic louse-borne typhus","termid":"MONDO:0019362"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"relapsing epidemic typhus","secondary_identifiers":["MEDGEN:1826151","GARD:19726","Orphanet:99991","UMLS:C5681812"],"termid":"MONDO:0020571","xrefs":{"Monarch":{"xref_id":"0020571"}}}


id: MONDO:0968947
data:
  {"annotated_genes":["SJAG_04936"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89026],"is_not":false,"summary":null,"term":"MONDO:0968947"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04936":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder plus optic atrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620784","UMLS:C5935605","MEDGEN:1859522"],"termid":"MONDO:0968947","terms_by_termid":{"MONDO:0968947":null},"xrefs":{"Monarch":{"xref_id":"0968947"}}}


id: MONDO:0859374
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"hearing loss, autosomal recessive 120","secondary_identifiers":["UMLS:C5774309","MEDGEN:1824082","OMIM:620238"],"synonyms":[{"name":"deafness, autosomal recessive 120","type":"narrow"}],"termid":"MONDO:0859374","xrefs":{"Monarch":{"xref_id":"0859374"}}}


id: FYPO:0007924
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to a combination of potassium chloride and sodium dodecyl sulfate. Cells stop growing (and may die) at concentrations of potassium chloride and sodium dodecyl sulfate that allow wild type cells to grow.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0002683","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"sensitive to potassium chloride and sodium dodecyl sulfate","termid":"FYPO:0007924"}


id: GO:0002318
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a precursor cell type acquires the specialized features of a myeloid progenitor cell. Myeloid progenitor cells include progenitor cells for any of the myeloid lineages.","definition_xrefs":["PMID:16551264","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hematopoietic progenitor cell differentiation","termid":"GO:0002244"}],"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":"myeloid progenitor cell differentiation","termid":"GO:0002318"}


id: PBO:0041387
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 5 open reading frame 46","termid":"PBO:0041387"}


id: PBO:0076289
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synapsin II","termid":"PBO:0076289"}


id: GO:0003335
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the corneocyte over time, from its formation to the mature structure. A corneocyte is the last stage of development of a keratinocyte where the keratinocyte flattens, loses its nucleus and eventually delaminates from the epidermis.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell development","termid":"GO:0048468"},{"relation_name":"part_of","term_name":"keratinocyte development","termid":"GO:0003334"}],"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":"corneocyte development","termid":"GO:0003335"}


id: GO:2001277
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of L-leucine biosynthetic process.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"negative regulation of amino acid biosynthetic process","termid":"GO:2000283"},{"relation_name":"is_a","term_name":"regulation of L-leucine biosynthetic process","termid":"GO:2001276"},{"relation_name":"negatively_regulates","term_name":"L-leucine biosynthetic process","termid":"GO:0009098"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006520"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"negative regulation of L-leucine biosynthetic process","synonyms":[{"name":"negative regulation of L-leucine anabolism","type":"exact"},{"name":"negative regulation of L-leucine biosynthesis","type":"exact"},{"name":"negative regulation of L-leucine formation","type":"exact"},{"name":"negative regulation of L-leucine synthesis","type":"exact"},{"name":"negative regulation of leucine biosynthetic process","type":"broad"}],"termid":"GO:2001277"}


id: GO:0005833
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An iron-containing, oxygen carrying complex. In vertebrates it is made up of two pairs of associated globin polypeptide chains, each chain carrying a noncovalently bound heme prosthetic group.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cytosol","termid":"GO:0005829"}],"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:0005829"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005737","GO:0005829"],"is_obsolete":false,"name":"hemoglobin complex","synonyms":[{"name":"haemoglobin complex","type":"exact"}],"termid":"GO:0005833"}


id: PBO:0051097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy constant mu","termid":"PBO:0051097"}


id: PBO:0082188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alcohol dehydrogenase isoenzyme type IV; dimeric enzyme demonstrated to be zinc-dependent despite sequence similarity to iron-activated alcohol dehydrogenases; transcription is induced in response to zinc deficiency","termid":"PBO:0082188"}


id: PBO:0059142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MPHOSPH10 pseudogene 9","termid":"PBO:0059142"}


id: MONDO:0004117
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive neuroendocrine carcinoma arising from the ampulla of Vater and the periampullary region. Morphologically, it is characterized by the presence of small malignant cells, necrosis, and a high mitotic rate. Signs and symptoms include jaundice, abdominal pain, anorexia, nausea, vomiting, and weight loss.","definition_xrefs":["NCIT:C6655"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small cell carcinoma","termid":"MONDO:0000402"},{"relation_name":"is_a","term_name":"liver neuroendocrine carcinoma","termid":"MONDO:0015072"},{"relation_name":"is_a","term_name":"carcinoma of the ampulla of vater","termid":"MONDO:0017590"},{"relation_name":"is_a","term_name":"duodenal neuroendocrine neoplasm","termid":"MONDO:0024500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"ampulla of vater small cell neuroendocrine carcinoma","secondary_identifiers":["DOID:7136","MEDGEN:233974","UMLS:C1332250"],"synonyms":[{"name":"ampulla of Vater small cell NEC","type":"exact"},{"name":"ampulla of Vater small cell carcinoma","type":"exact"},{"name":"ampulla of Vater small cell neuroendocrine carcinoma","type":"exact"},{"name":"ampullary small cell carcinoma","type":"exact"},{"name":"hepatopancreatic ampulla small cell carcinoma","type":"exact"},{"name":"small cell neuroendocrine carcinoma of the ampullary region","type":"exact"}],"termid":"MONDO:0004117","xrefs":{"Monarch":{"xref_id":"0004117"}}}


id: PBO:0042657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEA cell adhesion molecule 6","termid":"PBO:0042657"}


id: PBO:0084736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial intermembrane space protein; forms a complex with Tim13p that delivers a subset of hydrophobic proteins to the TIM22 complex for inner membrane insertion; homolog of human TIMM8A, implicated in Mohr-Tranebjaerg syndrome, also known as deafness-dystonia-optic neuronopathy (DDON) syndrome; human TIMM8A can complement yeast null mutant","termid":"PBO:0084736"}


id: MONDO:0006386
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, serous adenocarcinoma that diffusely involves the pelvic peritoneum seen predominantly in elderly postmenopausal women. Exclusion of serous carcinoma arising from the ovary and fimbrial end of fallopian tube is required to diagnose the above entity.","definition_xrefs":["doi:10.4103/2278-0513.157944"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peritoneal serous adenocarcinoma","termid":"MONDO:0003195"},{"relation_name":"is_a","term_name":"primary peritoneal carcinoma","termid":"MONDO:0015686"}],"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":"primary peritoneal serous adenocarcinoma","secondary_identifiers":["MEDGEN:269517","NCIT:C40023","UMLS:C1514429","EFO:1000494"],"synonyms":[{"name":"primary peritoneal serous adenocarcinoma","type":"exact"}],"termid":"MONDO:0006386","xrefs":{"Monarch":{"xref_id":"0006386"}}}


id: PBO:0080669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WAP four-disulfide core domain 21, pseudogene","termid":"PBO:0080669"}


id: RO:0002323
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A mereological relationship or a topological relationship","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mereotopologically_related_to","termid":"RO:0002323"}


id: PBO:0001328
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxin 13 (predicted)","termid":"PBO:0001328"}


id: MONDO:0003214
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma with apocrine differentiation arising from the sweat glands. It presents as single or multiple nodular lesions which may be ulcerated or hemorrhagic and is usually in the axilla and less often in the anogenital region. It grows in the dermis and infiltrates subcutaneous tissues. It is characterized by the presence of large cells with abundant eosinophilic cytoplasm and large often vesicular nuclei. Most cases are slow growing tumors and have a prolonged course.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apocrine sweat gland cancer","termid":"MONDO:0003215"},{"relation_name":"is_a","term_name":"sweat gland carcinoma","termid":"MONDO:0005524"}],"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":"apocrine adenocarcinoma","secondary_identifiers":["DOID:4933","ICDO:8401/3","MEDGEN:569650","UMLS:C0334346","NCIT:C4169"],"synonyms":[{"name":"apocrine adenocarcinoma (morphologic abnormality)","type":"exact"},{"name":"apocrine carcinoma","type":"exact"},{"name":"apocrine gland adenocarcinoma","type":"exact"},{"name":"apocrine gland carcinoma","type":"exact"},{"name":"carcinoma of apocrine gland","type":"exact"},{"name":"carcinoma of the apocrine gland","type":"exact"}],"termid":"MONDO:0003214","xrefs":{"Monarch":{"xref_id":"0003214"}}}


id: MONDO:0700005
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease characteristic in which the disease has an uncertain or unknown cause.","direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic vs non-idiopathic","termid":"MONDO:0700004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"idiopathic","secondary_identifiers":["icd11.foundation:894194405"],"termid":"MONDO:0700005","xrefs":{"Monarch":{"xref_id":"0700005"}}}


id: PBO:0017075
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structures of acceptor stem and anticodon/intron loop of substrate tRNA crucial for RNaseP activity","termid":"PBO:0017075"}


id: FYPO:0004083
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein measured in a cell is normal (i.e. indistinguishable from wild type). Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell","termid":"FYPO:0001076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal protein level","synonyms":[{"name":"protein/peptide accumulation: normal","type":"related"}],"termid":"FYPO:0004083"}


id: PR:O74748
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trs8502 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74748"],"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":"transport protein particle subunit trs85-2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1734.07c","synonyms":[{"name":"Spom972h-trs8502","type":"exact"},{"name":"TRAPP subunit trs85-2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74748"}


id: GO:0102972
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A12 + 2-oxoglutarate + O2 = gibberellin A110 + succinate + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A12,2-oxoglutarate:oxygen oxidoreductase activity (gibberellin A110-forming) (obsolete GO:0102972)","termid":"GO:0102972"}


id: MONDO:1012194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"occipital dysplasia, non-human animal","termid":"MONDO:1011949"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"occipital dysplasia, dog","secondary_identifiers":["OMIA:000732-9615"],"termid":"MONDO:1012194","xrefs":{"Monarch":{"xref_id":"1012194"}}}


id: PBO:0076571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TBC1 domain family member 3L","termid":"PBO:0076571"}


id: GO:0001887
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving compounds that contain selenium, such as selenocysteine.","definition_xrefs":["PMID:12730456"],"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":"selenium compound metabolic process","secondary_identifiers":["Reactome:R-HSA-2408552","Reactome:R-HSA-2408550","Reactome:R-HSA-5263617","Reactome:R-HSA-2408508","Reactome:R-HSA-2408499"],"synonyms":[{"name":"selenium compound metabolism","type":"exact"},{"name":"selenium metabolic process","type":"exact"},{"name":"selenium metabolism","type":"exact"}],"termid":"GO:0001887"}


id: GO:0039647
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which a virus stops, prevents, or reduces the frequency, rate or extent of host poly(A)-binding protein (PABP) activity. PABP binds to the poly(A) tail of mRNA to facilitate translation.","definition_xrefs":["UniProtKB-KW:KW-1101"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host poly(A)-binding protein activity (obsolete GO:0039647)","synonyms":[{"name":"inhibition of host poly(A)-binding protein by virus","type":"exact"},{"name":"suppression by virus of host PABP activity","type":"exact"}],"termid":"GO:0039647"}


id: PR:P0CT72
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl803 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P0CT72"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L2-C (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC839.04","synonyms":[{"name":"K37 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"K5 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"KD4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rpl803","type":"exact"}],"termid":"PR:P0CT72"}


id: PBO:0053972
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 1283","termid":"PBO:0053972"}


id: PBO:0056825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major facilitator superfamily domain containing 14C, pseudogene","termid":"PBO:0056825"}


id: MONDO:0020084
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lymphoproliferative disease associated with primary immune disease (obsolete MONDO:0020084)","secondary_identifiers":["Orphanet:98291"],"termid":"MONDO:0020084","xrefs":{"Monarch":{"xref_id":"0020084"}}}


id: SO:0000575
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region that can be transcribed into a small cytoplasmic RNA (scRNA).","direct_ancestors":[{"relation_name":"is_a","term_name":"non_protein_coding","termid":"SO:0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scRNA_encoding","synonyms":[{"name":"scRNA encoding","type":"exact"}],"termid":"SO:0000575"}


id: PBO:0087462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of a kinetochore-microtubule binding complex; complex bridges centromeric heterochromatin and kinetochore MAPs and motors; required for sister chromatid bi-orientation and kinetochore binding of SAC components; complex also includes Kre28p; modified by sumoylation","termid":"PBO:0087462"}


id: GO:1900008
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of extrachromosomal rDNA circle accumulation involved in replicative cell aging.","definition_xrefs":["PMID:15020466","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of extrachromosomal rDNA circle accumulation involved in replicative cell aging (obsolete GO:1900008)","synonyms":[{"name":"down regulation of extrachromosomal rDNA circle accumulation during replicative cell ageing","type":"related"},{"name":"down regulation of extrachromosomal rDNA circle accumulation during replicative cell aging","type":"related"},{"name":"down regulation of extrachromosomal rDNA circle accumulation involved in replicative cell aging","type":"related"},{"name":"down regulation of extrachromosomal ribosomal DNA circle accumulation during replicative cell aging","type":"related"},{"name":"negative regulation of extrachromosomal rDNA circle accumulation during replicative cell ageing","type":"related"},{"name":"negative regulation of extrachromosomal rDNA circle accumulation during replicative cell aging","type":"related"},{"name":"negative regulation of extrachromosomal ribosomal DNA circle accumulation during replicative cell aging","type":"related"}],"termid":"GO:1900008"}


id: PBO:0084930
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA-binding protein of the PUF family; binds to specific mRNAs, often in the 3' UTR; has broad specificity and binds to more than 1000 mRNAs (16% of the transcriptome); recruits the CCR4-NOT deadenylase complex to mRNAs along with Dhh1p and Dcp1p to promote deadenylation, decapping, and decay; also interacts with the Caf20p translational initiation repressor, affecting its mRNA target specificity","termid":"PBO:0084930"}


id: PBO:0080103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UTP14C small subunit processome component","termid":"PBO:0080103"}


id: PBO:0087665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the inner nuclear membrane Asi ubiquitin ligase complex; the Asi complex targets both misfolded proteins of the inner nuclear membrane-associated degradation (INMAD) pathway and inner for ubiquitin-mediated degradation; acts with Asi1p and Asi3p to ensure the fidelity of SPS-sensor signaling by targeting latent unprocessed forms of Stp1p and Stp2p, maintaining the repressed state of gene expression in the absence of inducing amino acids","termid":"PBO:0087665"}


id: MONDO:0015699
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"complement deficiency","termid":"MONDO:0003832"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency due to a classical component pathway complement deficiency","secondary_identifiers":["UMLS:C0398750","MEDGEN:585054","Orphanet:169147","icd11.foundation:327609494","GARD:15025"],"synonyms":[{"name":"immunodeficiency due to C1, C4, or C2 component complement deficiency","type":"exact"},{"name":"immunodeficiency due to a C1, C4, or C2 component complement deficiency","type":"exact"},{"name":"immunodeficiency due to an early component of complement deficiency","type":"exact"}],"termid":"MONDO:0015699","xrefs":{"Monarch":{"xref_id":"0015699"}}}


id: FYPO:0006676
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 transcription occurs to a lower extent than normal during a cellular response to hydroxyurea. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased transcription during vegetative growth","termid":"FYPO:0000781"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000294","FYPO:0001320","FYPO:0006551","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased transcription during cellular response to hydroxyurea","synonyms":[{"name":"decreased transcription during cellular response to HU","type":"exact"},{"name":"decreased transcription during cellular response to hydroxyurea during mitotic cell cycle","type":"related"},{"name":"decreased transcription during cellular response to hydroxyurea during vegetative growth","type":"exact"},{"name":"decreased transcription in response to HU","type":"exact"},{"name":"decreased transcription in response to hydroxyurea","type":"exact"},{"name":"reduced transcription during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0006676"}


id: MONDO:0022824
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital craniosynostosis maternal hyperthyroiditis","termid":"MONDO:0022824","xrefs":{"Monarch":{"xref_id":"0022824"}}}


id: PBO:0114088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F1-FO ATP synthase peripheral stalk subunit d","termid":"PBO:0114088"}


id: PBO:0058700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6828","termid":"PBO:0058700"}


id: GO:0046364
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of monosaccharides, polyhydric alcohols containing either an aldehyde or a keto group and between three to ten or more carbon atoms.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monosaccharide metabolic process","termid":"GO:0005996"},{"relation_name":"is_a","term_name":"carbohydrate biosynthetic process","termid":"GO:0016051"},{"relation_name":"is_a","term_name":"small molecule biosynthetic process","termid":"GO:0044283"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"monosaccharide biosynthetic process","synonyms":[{"name":"monosaccharide anabolism","type":"exact"},{"name":"monosaccharide biosynthesis","type":"exact"},{"name":"monosaccharide formation","type":"exact"},{"name":"monosaccharide synthesis","type":"exact"}],"termid":"GO:0046364"}


id: GO:0090494
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of dopamine into a cell.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dopamine transport","termid":"GO:0015872"},{"relation_name":"is_a","term_name":"catecholamine uptake","termid":"GO:0090493"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"dopamine uptake","termid":"GO:0090494"}


id: PR:000041369
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3-like centromeric protein cnp1 that is encoded in the genome of Schizosaccharomyces pombe.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"core histone (Schizosaccharomyces pombe)","termid":"PR:000041293"},{"relation_name":"is_a","term_name":"histone H3-like centromeric protein cnp1","termid":"PR:000041443"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3-like centromeric protein cnp1 (Schizosaccharomyces pombe)","pombase_gene_id":"SPBC1105.17","synonyms":[{"name":"CENP-A homolog (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-cnp1","type":"exact"},{"name":"centromere protein 1 (Schizosaccharomyces pombe)","type":"exact"}],"termid":"PR:000041369"}


id: PBO:0079484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin 2","termid":"PBO:0079484"}


id: MONDO:0002488
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant epithelial neoplasm that arises anywhere in the ductal system of the breast. This category includes intraductal papilloma, intraductal papillary carcinoma, ductal hyperplasia with or without atypia, and ductal carcinoma in situ.","definition_xrefs":["NCIT:C36083"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast neoplasm","termid":"MONDO:0021100"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intraductal breast neoplasm","secondary_identifiers":["DOID:3013","MEDGEN:184927","UMLS:C0948967"],"synonyms":[{"name":"intraductal breast neoplasm","type":"exact"}],"termid":"MONDO:0002488","xrefs":{"Monarch":{"xref_id":"0002488"}}}


id: GO:0060329
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The actin filament-based movement by which cytoplasmic actin filaments slide past one another resulting in a contraction that propels the cell in the direction that has been defined as the rear of the cell.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic actin-based contraction involved in cell motility","termid":"GO:0060327"}],"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":"cytoplasmic actin-based contraction involved in rearward cell motility","synonyms":[{"name":"cytoplasmic actin-based contraction involved in rearward cell locomotion","type":"related"}],"termid":"GO:0060329"}


id: PBO:0065883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB33A, member RAS oncogene family","termid":"PBO:0065883"}


id: PBO:0050095
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 5","termid":"PBO:0050095"}


id: PBO:0049112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 174","termid":"PBO:0049112"}


id: FYPO:0000242
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cells grow normally (i.e. indistinguishably from wild type) in a medium containing ammonia as the nitrogen source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0002058","FYPO:0000257","FYPO:0000139","FYPO:0000003","FYPO:0002057","FYPO:0002060"],"is_obsolete":false,"name":"normal growth on ammonia nitrogen source","synonyms":[{"name":"growth defect, normal growth with ammonia nitrogen source","type":"related"},{"name":"normal cell population growth on ammonia nitrogen source","type":"exact"},{"name":"normal vegetative cell population growth on ammonia nitrogen source","type":"exact"}],"termid":"FYPO:0000242"}


id: PBO:0040209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASXL transcriptional regulator 2","termid":"PBO:0040209"}


id: GO:0021600
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the abducens nerve. This process pertains to the physical shaping of a rudimentary structure. The motor function of the abducens nerve is to contract the lateral rectus which results in abduction of the eye.","definition_xrefs":["GOC:dgh","ISBN:0838580343","GO_REF:0000021","GOC:dph","GOC:jid","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve structural organization","termid":"GO:0021604"},{"relation_name":"part_of","term_name":"abducens nerve morphogenesis","termid":"GO:0021598"}],"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":"abducens nerve structural organization","synonyms":[{"name":"CN VI structural organization","type":"related"},{"name":"abducens nerve structural organisation","type":"exact"}],"termid":"GO:0021600"}


id: GO:0045263
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. All non-F1 subunits of a hydrogen-transporting ATP synthase, including integral and peripheral membrane proteins.","definition_xrefs":["PMID:10838056"],"gene_count":0,"genotype_count":0,"name":"obsolete proton-transporting ATP synthase complex, coupling factor F(o) (obsolete GO:0045263)","synonyms":[{"name":"hydrogen-transporting ATP synthase complex, coupling factor F(o)","type":"exact"},{"name":"hydrogen-transporting ATP synthase, F0 sector","type":"exact"},{"name":"hydrogen-transporting ATP synthase, coupling factor CF(0)","type":"narrow"},{"name":"proton-transporting ATP synthase complex, coupling factor F(0)","type":"exact"}],"termid":"GO:0045263"}


id: PBO:0000143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nifs homolog, possible cysteine desulfurase","termid":"PBO:0000143"}


id: PBO:0090952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"folliculin-interacting protein, BFC/FNIP-Folliculin complex subunit subunit Fnp1","termid":"PBO:0090952"}


id: MONDO:0044265
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tooth size (obsolete MONDO:0044265)","secondary_identifiers":["OMIM:314240"],"synonyms":[{"name":"tooth size","type":"related"}],"termid":"MONDO:0044265","xrefs":{"Monarch":{"xref_id":"0044265"}}}


id: FYPO:0005636
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein from kinetochores to the spindle begins later than normal during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:21920317"],"direct_ancestors":[{"relation_name":"is_a","term_name":"delayed onset of protein localization to spindle during meiosis I","termid":"FYPO:0005635"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"delayed onset of protein localization from kinetochore to spindle during meiosis I","synonyms":[{"name":"delayed onset of protein localisation from kinetochore to spindle during meiosis I","type":"exact"},{"name":"delayed onset of protein localization from kinetochore to meiosis I spindle","type":"exact"},{"name":"delayed onset of protein localization from kinetochore to meiotic spindle during meiosis I","type":"exact"},{"name":"delayed onset of protein localization from kinetochore to spindle during first meiotic nuclear division","type":"exact"},{"name":"delayed onset of protein movement from kinetochore to spindle during meiosis I","type":"related"},{"name":"delayed protein localization from kinetochore to spindle during meiosis I","type":"exact"},{"name":"delayed protein localization to meiotic spindle from kinetochore during meiosis I","type":"exact"}],"termid":"FYPO:0005636"}


id: PBO:0072864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAM and SH3 domain containing 1","termid":"PBO:0072864"}


id: GO:2000397
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ubiquitin-dependent endocytosis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endocytosis","termid":"GO:0045807"},{"relation_name":"is_a","term_name":"positive regulation of protein transport","termid":"GO:0051222"},{"relation_name":"is_a","term_name":"regulation of ubiquitin-dependent endocytosis","termid":"GO:2000395"},{"relation_name":"positively_regulates","term_name":"ubiquitin-dependent endocytosis","termid":"GO:0070086"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0016192"},{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of ubiquitin-dependent endocytosis","synonyms":[{"name":"positive regulation of ubiquitin-mediated endocytosis","type":"exact"}],"termid":"GO:2000397"}


id: PBO:0056980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 29c","termid":"PBO:0056980"}


id: PBO:0066782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 80","termid":"PBO:0066782"}


id: FYPO:0001808
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the import of adenine into the cell occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal adenine import","termid":"FYPO:0001807"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased adenine import","synonyms":[{"name":"decreased adenine import across plasma membrane","type":"exact"},{"name":"decreased adenine import during mitotic cell cycle","type":"related"},{"name":"decreased adenine import during vegetative growth","type":"exact"},{"name":"decreased adenine import into cell","type":"exact"},{"name":"decreased adenine uptake","type":"exact"},{"name":"reduced adenine import","type":"exact"}],"termid":"FYPO:0001808"}


id: MONDO:0009242
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Brittle cornea syndrome is a form of Ehlers-Danlos syndrome characterized by a severe ocular manifestations due to extreme corneal thinning and fragility with rupture in the absence of significant trauma, and progression to blindness. Extraocular manifestations comprise deafness, developmental hip dysplasia, and joint hypermobility.","definition_xrefs":["Orphanet:90354"],"direct_ancestors":[{"relation_name":"is_a","term_name":"corneal disorder","termid":"MONDO:0000942"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0006025"],"is_obsolete":false,"name":"brittle cornea syndrome","secondary_identifiers":["SCTID:719096006","GARD:1019","OMIMPS:229200","DOID:14775","MESH:C536198"],"synonyms":[{"name":"BCS1","type":"related"},{"name":"EDS VIB (formerly)","type":"related"},{"name":"Ehlers-Danlos syndrome type 6B (formerly)","type":"related"},{"name":"Ehlers-Danlos syndrome type 6b","type":"related"},{"name":"brittle cornea syndrome","type":"exact"},{"name":"brittle cornea syndrome 1","type":"related"},{"name":"brittle cornea syndrome 2","type":"narrow"},{"name":"brittle cornea syndrome type 1","type":"exact"},{"name":"kyphoscoliosis type","type":"exact"},{"name":"type VIB Ehlers-Danlos syndrome","type":"exact"}],"termid":"MONDO:0009242","xrefs":{"Monarch":{"xref_id":"0009242"}}}


id: MONDO:1012866
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypercholesterolemia that occurs in rabbits due to a mutation in the PCSK9 gene created by genetic engineering or gene editing.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"hyperlipidemia, non-human animal","termid":"MONDO:1012975"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypercholesterolemia, PCSK9-related, rabbit","secondary_identifiers":["OMIA:002329-9986"],"synonyms":[{"name":"hypercholesterolaemia, PCSK9-related, rabbit","type":"exact"}],"termid":"MONDO:1012866","xrefs":{"Monarch":{"xref_id":"1012866"}}}


id: PBO:0043168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cartilage intermediate layer protein","termid":"PBO:0043168"}


id: GO:0034447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a very-low-density lipoprotein particle is removed from the blood via receptor-mediated endocytosis and its constituent parts degraded.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma lipoprotein particle clearance","termid":"GO:0034381"}],"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":"very-low-density lipoprotein particle clearance","secondary_identifiers":["Reactome:R-HSA-8964046"],"synonyms":[{"name":"VLDL clearance","type":"exact"}],"termid":"GO:0034447"}


id: PBO:0081688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 609","termid":"PBO:0081688"}


id: PBO:0017410
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-instance_of","termid":"PBO:0017410"}


id: MONDO:0020551
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hydatidiform mole (obsolete MONDO:0020551)","termid":"MONDO:0020551","xrefs":{"Monarch":{"xref_id":"0020551"}}}


id: PBO:0081136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZFP30 zinc finger protein","termid":"PBO:0081136"}


id: PBO:0042058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 121","termid":"PBO:0042058"}


id: MONDO:0003233
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A relatively common disorder characterized by a fairly specific pattern of tremors which are most prominent in the upper extremities and neck, inducing titubations of the head. The tremor is usually mild, but when severe may be disabling. An autosomal dominant pattern of inheritance may occur in some families (i.e., familial tremor). (Mov Disord 1988;13(1):5-10)","definition_xrefs":["MESH:D020329"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"essential tremor","secondary_identifiers":["ICD10CM:G25.0","ICD9:333.1","SCTID:609558009","OMIMPS:190300","Orphanet:862","EFO:0003108","MEDGEN:78725","DOID:4990","UMLS:C0270736"],"synonyms":[{"name":"benign essential tremor","type":"exact"},{"name":"essential hereditary tremor","type":"narrow"},{"name":"shaky hand syndrome","type":"exact"},{"name":"tremor, hereditary essential","type":"narrow"}],"termid":"MONDO:0003233","xrefs":{"Monarch":{"xref_id":"0003233"}}}


id: FYPO:0006511
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which cells form telomeres that are shorter than normal during G0 phase. Normally, telomere length is stable in G0, whereas telomere sequences can be lost in mutants.","definition_xrefs":["PomBase:mah","PMID:29167439"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal telomere length","termid":"FYPO:0006509"},{"relation_name":"is_a","term_name":"abnormal telomere morphology during G0","termid":"FYPO:0007413"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000641","FYPO:0000293","FYPO:0001985"],"is_obsolete":false,"name":"shortened telomeres during G0","synonyms":[{"name":"decreased telomere length during G0","type":"related"},{"name":"loss of telomeric sequence during G0","type":"exact"},{"name":"loss of telomeric sequence during quiescence","type":"exact"},{"name":"reduced telomere length during G0","type":"exact"},{"name":"short telomeres during G0","type":"exact"},{"name":"shortened telomeres during cell quiescence","type":"exact"},{"name":"shortened telomeres during quiescence","type":"exact"}],"termid":"FYPO:0006511"}


id: GO:1904985
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of quinolinate biosynthetic process.","definition_xrefs":["PMID:12140278","PMID:19843166","GOC:bf","GO_REF:0000058","GOC:PARL","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"regulation of quinolinate biosynthetic process","termid":"GO:1904984"},{"relation_name":"negatively_regulates","term_name":"quinolinate biosynthetic process","termid":"GO:0019805"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"negative regulation of quinolinate biosynthetic process","synonyms":[{"name":"down regulation of quinolinate anabolism","type":"exact"},{"name":"down regulation of quinolinate biosynthesis","type":"exact"},{"name":"down regulation of quinolinate biosynthetic process","type":"exact"},{"name":"down regulation of quinolinate formation","type":"exact"},{"name":"down regulation of quinolinate synthesis","type":"exact"},{"name":"down-regulation of quinolinate anabolism","type":"exact"},{"name":"down-regulation of quinolinate biosynthesis","type":"exact"},{"name":"down-regulation of quinolinate biosynthetic process","type":"exact"},{"name":"down-regulation of quinolinate formation","type":"exact"},{"name":"down-regulation of quinolinate synthesis","type":"exact"},{"name":"downregulation of quinolinate anabolism","type":"exact"},{"name":"downregulation of quinolinate biosynthesis","type":"exact"},{"name":"downregulation of quinolinate biosynthetic process","type":"exact"},{"name":"downregulation of quinolinate formation","type":"exact"},{"name":"downregulation of quinolinate synthesis","type":"exact"},{"name":"inhibition of quinolinate anabolism","type":"narrow"},{"name":"inhibition of quinolinate biosynthesis","type":"narrow"},{"name":"inhibition of quinolinate biosynthetic process","type":"narrow"},{"name":"inhibition of quinolinate formation","type":"narrow"},{"name":"inhibition of quinolinate synthesis","type":"narrow"},{"name":"negative regulation of quinolinate anabolism","type":"exact"},{"name":"negative regulation of quinolinate biosynthesis","type":"exact"},{"name":"negative regulation of quinolinate formation","type":"exact"},{"name":"negative regulation of quinolinate synthesis","type":"exact"}],"termid":"GO:1904985"}


id: GO:0016132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of brassinosteroids, any of a group of steroid derivatives that occur at very low concentrations in plant tissues and may have hormone-like effects.","definition_xrefs":["ISBN:0192801023"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phytosteroid biosynthetic process","termid":"GO:0016129"},{"relation_name":"is_a","term_name":"brassinosteroid metabolic process","termid":"GO:0016131"}],"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":"brassinosteroid biosynthetic process","synonyms":[{"name":"brassinosteroid anabolism","type":"exact"},{"name":"brassinosteroid biosynthesis","type":"exact"},{"name":"brassinosteroid formation","type":"exact"},{"name":"brassinosteroid synthesis","type":"exact"}],"termid":"GO:0016132"}


id: PBO:0088066
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-specific protease; cleaves ubiquitin from ubiquitinated proteins; present in the nucleus and cytoplasm","termid":"PBO:0088066"}


id: PBO:0002603
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.4.3.5","termid":"PBO:0002603"}


id: PBO:0058436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5000","termid":"PBO:0058436"}


id: PBO:0028162
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_ATP_binding","termid":"PBO:0028162"}


id: MONDO:0007771
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial progressive hyperpigmentation","termid":"MONDO:0013648"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"hyperpigmentation with or without hypopigmentation, familial progressive","secondary_identifiers":["MEDGEN:333550","DOID:0111373","GARD:18073","OMIM:145250","UMLS:C1840392"],"synonyms":[{"name":"FPHH","type":"related"},{"name":"hyperpigmentation with or without hypopigmentation","type":"exact"},{"name":"hyperpigmentation with or without hypopigmentation, familial progressive","type":"exact"},{"name":"hyperpigmentation, familial progressive, 2","type":"related"},{"name":"hyperpigmentation, familial progressive, 2, formerly","type":"related"},{"name":"macules, hereditary congenital hypopigmented and hyperpigmented","type":"exact"},{"name":"melanosis universalis hereditaria","type":"related"},{"name":"melanosis, universal","type":"exact"}],"termid":"MONDO:0007771","xrefs":{"Monarch":{"xref_id":"0007771"}}}


id: GO:1902219
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of intrinsic apoptotic signaling pathway in response to osmotic stress.","definition_xrefs":["GOC:rl","GOC:mtg_apoptosis","GOC:BHF","GOC:TermGenie","PMID:14569084"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intrinsic apoptotic signaling pathway in response to osmotic stress","termid":"GO:1902218"},{"relation_name":"is_a","term_name":"negative regulation of intrinsic apoptotic signaling pathway","termid":"GO:2001243"},{"relation_name":"negatively_regulates","term_name":"intrinsic apoptotic signaling pathway in response to osmotic stress","termid":"GO:0008627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of intrinsic apoptotic signaling pathway in response to osmotic stress","synonyms":[{"name":"down regulation of intrinsic apoptotic signaling pathway in response to osmotic stress","type":"exact"},{"name":"down-regulation of intrinsic apoptotic signaling pathway in response to osmotic stress","type":"exact"},{"name":"downregulation of intrinsic apoptotic signaling pathway in response to osmotic stress","type":"exact"},{"name":"inhibition of intrinsic apoptotic signaling pathway in response to osmotic stress","type":"narrow"}],"termid":"GO:1902219"}


id: RO:0002092
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","direct_ancestors":[{"relation_name":"is_a","term_name":"ends_during","termid":"RO:0002093"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"happens_during","termid":"RO:0002092"}


id: PATO:0001332
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A morphology quality inhering in a bearer by virtue of the bearer's lack of distinct morphology.","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":"amorphous","termid":"PATO:0001332"}


id: PATO:0000321
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A color consisting of red and blue hues.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Magenta"],"direct_ancestors":[{"relation_name":"is_a","term_name":"color","termid":"PATO:0000014"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"magenta","termid":"PATO:0000321"}


id: PBO:0067788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 90","termid":"PBO:0067788"}


id: MONDO:0014344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital heart defects, multiple types in which the cause of the disease is a mutation in the NR2F2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital heart defects, multiple types","termid":"MONDO:0000119"},{"relation_name":"is_a","term_name":"familial atrioventricular septal defect","termid":"MONDO:0020290"}],"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":"congenital heart defects, multiple types, 4","secondary_identifiers":["MEDGEN:862747","OMIM:615779","UMLS:C4014310"],"synonyms":[{"name":"CHTD4","type":"related"},{"name":"NR2F2 congenital heart defects, multiple types","type":"exact"},{"name":"congenital heart defects, multiple types caused by mutation in NR2F2","type":"exact"},{"name":"congenital heart defects, multiple types, 4","type":"exact"}],"termid":"MONDO:0014344","xrefs":{"Monarch":{"xref_id":"0014344"}}}


id: PR:Q10269
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- are1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10269"],"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":"sterol O-acyltransferase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13G7.05","synonyms":[{"name":"Spom972h-are1","type":"exact"},{"name":"sterol-ester synthase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10269"}


id: GO:0140498
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex with alpha-(1->6)-mannosyltransferase activity, located in the cis Golgi membrane; adds mannan to N-linked glycans on proteins as part of the priming and elongation of alpha 1,6-linked Man backbone. In S. cerevisiae, contains Mnn9p and Van1p.","definition_xrefs":["PMID:9430634"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannan polymerase complex","termid":"GO:0000136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005794"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005794","GO:0005737"],"is_obsolete":false,"name":"mannan polymerase I complex","termid":"GO:0140498"}


