# terms

id: PBO:0063767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PHEX antisense RNA 1","termid":"PBO:0063767"}


id: MONDO:0009774
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A major birth defect representing the severe end of the spectrum of the exstrophy-epispadias complex (EEC) characterized by omphalocele, exstrophy, imperforate anus and spinal defects (also referred to as the OEIS complex), often associated with other malformations.","definition_xrefs":["Orphanet:93929"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"exstrophy-epispadias complex","termid":"MONDO:0017919"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"cloacal exstrophy","secondary_identifiers":["NANDO:1200910","ICD9:759.89","MedDRA:10067424","GARD:4080","HP:0010475","NANDO:2200950","SCTID:20815007","MEDGEN:83377","UMLS:C0345217","NANDO:2200951","icd11.foundation:2004612103","DOID:0080175","MESH:C537748","NANDO:1200909"],"synonyms":[{"name":"OEIS complex","type":"related"},{"name":"OEIS syndrome","type":"related"},{"name":"cloacal exstrophy","type":"exact"},{"name":"cloacal exstrophy (disease)","type":"exact"},{"name":"cloacal exstrophy sequence","type":"related"},{"name":"omphalocele - cloacal exstrophy - imperforate anus - spinal defect","type":"related"},{"name":"omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects","type":"related"},{"name":"omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects complex","type":"related"},{"name":"omphalocele-cloacal exstrophy-imperforate anus-spinal defect syndrome","type":"exact"},{"name":"omphalocele-exstrophy-imperforate anus-spinal defects","type":"related"}],"termid":"MONDO:0009774","xrefs":{"Monarch":{"xref_id":"0009774"}}}


id: PBO:0061841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoglycin","termid":"PBO:0061841"}


id: SO:0000920
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An edit to insert a cytidine.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000920 insert_C (obsolete SO:0000920)","synonyms":[{"name":"insert C","type":"exact"}],"termid":"SO:0000920"}


id: MONDO:0008670
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Waardenburg syndrome type 1 (WS1) is a subtype of Waardenburg syndrome (WS), disorder characterized by congenital deafness, minor defects in structures arising from neural crest resulting in pigmentation anomalies of eyes, hair, and skin, in combination with dystopia canthorum.","definition_xrefs":["Orphanet:894"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Waardenburg syndrome","termid":"MONDO:0018094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Waardenburg syndrome type 1","secondary_identifiers":["UMLS:C1847800","OMIM:193500","icd11.foundation:547536187","ICD10CM:E70.3","DOID:0110948","GARD:5519","NCIT:C75008","MEDGEN:376211"],"synonyms":[{"name":"WS1","type":"exact"},{"name":"Waardenburg syndrome type 1","type":"exact"},{"name":"Waardenburg syndrome type I","type":"exact"},{"name":"Waardenburg syndrome with dystopia canthorum","type":"related"},{"name":"Waardenburg syndrome, type 1","type":"related"},{"name":"Waardenburg's syndrome type 1","type":"related"}],"termid":"MONDO:0008670","xrefs":{"Monarch":{"xref_id":"0008670"}}}


id: PBO:0079617
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 L2 (pseudogene)","termid":"PBO:0079617"}


id: PBO:0088193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zinc finger transcription factor; contains a Zn(2)-Cys(6) binuclear cluster domain, positively regulates transcription of URA1, URA3, URA4, and URA10, which are involved in de novo pyrimidine biosynthesis, in response to pyrimidine starvation; activity may be modulated by interaction with Tup1p","termid":"PBO:0088193"}


id: MONDO:1010689
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"AA amyloidosis that occurs in Sumatran tiger.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AA amyloidosis, non-human animal","termid":"MONDO:1010092"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AA amyloidosis, Sumatran tiger","secondary_identifiers":["OMIA:000038-9695"],"termid":"MONDO:1010689","xrefs":{"Monarch":{"xref_id":"1010689"}}}


id: PBO:0058147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4443","termid":"PBO:0058147"}


id: GO:0045840
data:
  {"annotated_genes":["SJAG_00666","SJAG_03048","SJAG_02498","SJAG_04259","SJAG_02336","SJAG_03126","SJAG_01297","SJAG_02169","SJAG_03681","SJAG_04573","SJAG_04968","SJAG_02451","SJAG_01805","SJAG_03353","SJAG_01679","SJAG_00883"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115034,112911,98782,113401,89932,106393,111101,103069,107405],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902426"},{"annotations":[93399],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[113402,93000,96890,99325,113903,101564,101291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045842"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of mitosis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic nuclear division","termid":"GO:0007088"},{"relation_name":"is_a","term_name":"positive regulation of nuclear division","termid":"GO:0051785"},{"relation_name":"is_a","term_name":"positive regulation of cell cycle process","termid":"GO:0090068"},{"relation_name":"positively_regulates","term_name":"mitotic nuclear division","termid":"GO:0140014"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00666":null,"SJAG_00883":null,"SJAG_01297":null,"SJAG_01679":null,"SJAG_01805":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02451":null,"SJAG_02498":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04259":null,"SJAG_04573":null,"SJAG_04968":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"positive regulation of mitotic nuclear division","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of mitosis","type":"narrow"},{"name":"mitogenic activity","type":"narrow"},{"name":"positive regulation of mitosis","type":"exact"},{"name":"stimulation of mitosis","type":"narrow"},{"name":"up regulation of mitosis","type":"exact"},{"name":"up-regulation of mitosis","type":"exact"},{"name":"upregulation of mitosis","type":"exact"}],"termid":"GO:0045840","terms_by_termid":{"GO:0045842":null,"GO:0140499":null,"GO:1902426":null}}


id: MONDO:0800425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coronary artery disease, severe, susceptibility to","secondary_identifiers":["UMLS:C1862591","MEDGEN:349546"],"termid":"MONDO:0800425","xrefs":{"Monarch":{"xref_id":"0800425"}}}


id: GO:1901682
data:
  {"annotated_genes":["SJAG_03652","SJAG_04673","SJAG_01589","SJAG_04325","SJAG_04295","SJAG_00835","SJAG_00671","SJAG_01890","SJAG_02779","SJAG_03452","SJAG_02962","SJAG_02463","SJAG_01941","SJAG_03334","SJAG_02780","SJAG_01660","SJAG_03577"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[100542],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046964"},{"annotations":[100543],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902557"},{"annotations":[105861],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008521"},{"annotations":[71172,91262],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015225"},{"annotations":[90039],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015228"},{"annotations":[118132,112824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033229"},{"annotations":[112270,94722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034634"},{"annotations":[99864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034216"},{"annotations":[101789,87480],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000095"},{"annotations":[109271],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008271"},{"annotations":[99533,115756,109272,87628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015116"},{"annotations":[102816],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090422"},{"annotations":[89359,89360],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015234"},{"annotations":[87629],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015117"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a sulfur compound from one side of a membrane to the other.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00671":null,"SJAG_00835":null,"SJAG_01589":null,"SJAG_01660":null,"SJAG_01890":null,"SJAG_01941":null,"SJAG_02463":null,"SJAG_02779":null,"SJAG_02780":null,"SJAG_02962":null,"SJAG_03334":null,"SJAG_03452":null,"SJAG_03577":null,"SJAG_03652":null,"SJAG_04295":null,"SJAG_04325":null,"SJAG_04673":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"sulfur compound transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"sulfur molecular entity transmembrane transporter activity","type":"exact"}],"termid":"GO:1901682","terms_by_termid":{"GO:0000095":null,"GO:0008271":null,"GO:0008521":null,"GO:0015116":null,"GO:0015117":null,"GO:0015225":null,"GO:0015228":null,"GO:0015234":null,"GO:0033229":null,"GO:0034216":null,"GO:0034634":null,"GO:0046964":null,"GO:0090422":null,"GO:1902557":null}}


id: GO:0031833
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 7 serotonin receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled serotonin receptor binding","termid":"GO:0031821"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"type 7 serotonin receptor binding","synonyms":[{"name":"5-hydroxytryptamine 7 receptor binding","type":"exact"},{"name":"type 7 serotonin receptor ligand","type":"narrow"}],"termid":"GO:0031833"}


id: PBO:0000521
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 Rad15","termid":"PBO:0000521"}


id: PBO:0032712
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_error-free_translesion_synthesis_of_cyclobutane_pyrimidine_dimers","termid":"PBO:0032712"}


id: GO:0052145
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of a motile cell or organism on or near its host organism towards a lower level of a physical stimulus involved in energy generation, such as light, oxygen, and oxidizable substrates. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete negative energy taxis on or near host (obsolete GO:0052145)","termid":"GO:0052145"}


id: PBO:0005467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteinase B inhibitor Pbi2 (predicted)","termid":"PBO:0005467"}


id: GO:0001068
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a RNA region within the transcript that regulates the transcription of a gene, cistron, or operon.","definition_xrefs":["GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulatory region RNA binding","termid":"GO:0001069"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003723","GO:0003674"],"is_obsolete":false,"name":"transcription regulatory region RNA binding","termid":"GO:0001068"}


id: PBO:0034673
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_break-induced_loss_of_heterozygosity_via_chromosomal_translocation","termid":"PBO:0034673"}


id: MONDO:0008397
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aplasia of the lacrimal and salivary glands (ALSG) is a rare autosomal dominant disorder characterized by aplasia, atresia or hypoplasia of the lacrimal and salivary glands leading to varying features since infancy such as recurrent eye infections, irritable eyes, epiphora, xerostomia, dental caries, dental erosion and oral inflammation.","definition_xrefs":["Orphanet:86815"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aplasia of lacrimal and salivary glands","secondary_identifiers":["icd11.foundation:539255304","OMIM:180920","SCTID:715656004","UMLS:C0158667","GARD:16759","DOID:0111549","MEDGEN:57641"],"synonyms":[{"name":"ALSG","type":"exact"},{"name":"aplasia of lacrimal and salivary glands","type":"exact"},{"name":"congenital absence of lacrimal puncta and salivary glands","type":"exact"},{"name":"parotid aplasia or hypoplasia","type":"related"},{"name":"salivary glands, absence of","type":"related"},{"name":"salivary glands, absence of, include","type":"related"}],"termid":"MONDO:0008397","xrefs":{"Monarch":{"xref_id":"0008397"}}}


id: PBO:0058310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4683","termid":"PBO:0058310"}


id: GO:0032941
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The controlled release of a substance by a tissue.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"is_a","term_name":"secretion","termid":"GO:0046903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"secretion by tissue","synonyms":[{"name":"expulsion of gland contents","type":"related"},{"name":"tissue secretion","type":"exact"}],"termid":"GO:0032941"}


id: GO:1901816
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving beta-zeacarotene.","definition_xrefs":["GOC:yaf","UniPathway:UPA00805","GOC:TermGenie","PMID:3710717"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotenoid metabolic process","termid":"GO:0016116"},{"relation_name":"is_a","term_name":"carotene metabolic process","termid":"GO:0016119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"beta-zeacarotene metabolic process","synonyms":[{"name":"beta-zeacarotene metabolism","type":"exact"}],"termid":"GO:1901816"}


id: PBO:0082567
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Chaperone that facilitates the assembly of cytochrome c oxidase; integral to the mitochondrial inner membrane; interacts with a subcomplex of subunits VII, VIIa, and VIII (Cox7p, Cox9p, and Cox8p) but not with the holoenzyme","termid":"PBO:0082567"}


id: PBO:0089985
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-1,3-galactosyltransferase Otg2","termid":"PBO:0089985"}


id: MONDO:0018601
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"bone disorder","termid":"MONDO:0005381"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome","secondary_identifiers":["Orphanet:440354","MEDGEN:1801714","GARD:21838","UMLS:C5680056"],"termid":"MONDO:0018601","xrefs":{"Monarch":{"xref_id":"0018601"}}}


id: FYECO:0000328
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"LNB medium is a Low Nutrient medium containing yeast nitrogen base without amino acids, glucose, salts and vitamins.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LNB glucose medium","termid":"FYECO:0000328"}


id: GO:0102363
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: isoscopoletin + S-adenosyl-L-methionine = scoparone + S-adenosyl-L-homocysteine + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete isoscopoletin-O-methyltransferase activity (obsolete GO:0102363)","termid":"GO:0102363"}


id: PBO:0082167
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adhesion subunit of a-agglutinin of a-cells; C-terminal sequence acts as a ligand for alpha-agglutinin (Sag1p) during agglutination, modified with O-linked oligomannosyl chains, linked to anchorage subunit Aga1p via two disulfide bonds","termid":"PBO:0082167"}


id: GO:0042216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of phenanthrene, a tricyclic aromatic hydrocarbon.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenanthrene metabolic process","termid":"GO:0018955"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"},{"relation_name":"is_a","term_name":"hydrocarbon catabolic process","termid":"GO:0120253"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"phenanthrene catabolic process","secondary_identifiers":["UM-BBD_pathwayID:phe"],"synonyms":[{"name":"phenanthrene breakdown","type":"exact"},{"name":"phenanthrene catabolism","type":"exact"},{"name":"phenanthrene degradation","type":"exact"}],"termid":"GO:0042216"}


id: PBO:0069790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1076, pseudogene","termid":"PBO:0069790"}


id: GO:0048373
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into a lateral mesoderm cell regardless of its environment; upon determination, the cell fate cannot be reversed.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesodermal cell fate determination","termid":"GO:0007500"},{"relation_name":"part_of","term_name":"lateral mesodermal cell fate commitment","termid":"GO:0048372"}],"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":"lateral mesodermal cell fate determination","synonyms":[{"name":"lateral mesoderm cell fate determination","type":"exact"},{"name":"lateral plate mesoderm cell fate determination","type":"exact"},{"name":"lateral plate mesodermal cell fate determination","type":"exact"}],"termid":"GO:0048373"}


id: PBO:0081201
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZKSCAN2 divergent transcript","termid":"PBO:0081201"}


id: PBO:0018006
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdc6 does not bind directly to Pcn1 (PCNA)","termid":"PBO:0018006"}


id: PR:P41831
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC4A8.14 gene.","definition_xrefs":["UniProtKB:P41831","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":"ribose-phosphate pyrophosphokinase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4A8.14","synonyms":[{"name":"Spom972h-SPAC4A8.14","type":"exact"},{"name":"phosphoribosyl pyrophosphate synthase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P41831"}


id: PBO:0013053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U2 snRNP-associated protein Sap130","termid":"PBO:0013053"}


id: MONDO:0018371
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"distal myopathy","termid":"MONDO:0018949"}],"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":"nebulin-related early-onset distal myopathy","secondary_identifiers":["GARD:21656","Orphanet:399103","MEDGEN:1677937","UMLS:C5190827"],"synonyms":[{"name":"distal nebulin myopathy","type":"related"}],"termid":"MONDO:0018371","xrefs":{"Monarch":{"xref_id":"0018371"}}}


id: PBO:0088356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-acetyltransferase","termid":"PBO:0088356"}


id: GO:0052438
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism modulates the frequency, rate or extent of callose deposition by the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of defense-related symbiont callose deposition (obsolete GO:0052438)","synonyms":[{"name":"modulation by organism of defense-related symbiont callose deposition","type":"exact"}],"termid":"GO:0052438"}


id: MONDO:0020202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete conjunctival lymphangiectasia (obsolete MONDO:0020202)","secondary_identifiers":["ICD9:372.89","Orphanet:98614","SCTID:231871007"],"termid":"MONDO:0020202","xrefs":{"Monarch":{"xref_id":"0020202"}}}


id: FYPO:0005364
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the rate, or speed, of kinetochore sliding, i.e. the movement of a kinetochore along spindle microtubules, during mitotic chromosome recapture is decreased.","definition_xrefs":["PMID:18256284","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic metaphase chromosome recapture","termid":"FYPO:0005362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001320","FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000641","FYPO:0000337"],"is_obsolete":false,"name":"decreased rate of kinetochore sliding during chromosome recapture","synonyms":[{"name":"decreased rate of chromosome migration during chromosome recapture","type":"exact"},{"name":"decreased rate of chromosome movement during chromosome recapture","type":"exact"},{"name":"decreased rate of kinetochore migration during chromosome recapture","type":"exact"},{"name":"decreased rate of kinetochore sliding along kinetochore microtubule towards spindle pole body during chromosome recapture","type":"exact"},{"name":"decreased rate of kinetochore sliding during chromosome recapture during mitosis","type":"exact"},{"name":"decreased rate of kinetochore sliding during chromosome recapture during vegetative growth","type":"exact"},{"name":"decreased rate of kinetochore sliding during kinetochore retrieval","type":"exact"},{"name":"decreased rate of kinetochore sliding during kinetochore retrieval in mitotic metaphase","type":"exact"},{"name":"decreased rate of kinetochore sliding during metaphase chromosome retrieval to the spindle pole body","type":"exact"},{"name":"decreased rate of kinetochore sliding during mitotic metaphase chromosome recapture","type":"exact"},{"name":"decreased rate of kinetochore sliding during sister kinetochore recapture","type":"exact"},{"name":"decreased rate of kinetochore sliding towards SPB during chromosome recapture","type":"exact"},{"name":"decreased rate of kinetochore sliding towards spindle pole body during chromosome recapture","type":"exact"},{"name":"reduced rate of kinetochore sliding during chromosome recapture","type":"exact"}],"termid":"FYPO:0005364"}


id: MONDO:0016651
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Maternal uniparental disomy of chromosome 1 is an uniparental disomy of maternal origin that most likely does not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only mother is a carrier.","definition_xrefs":["Orphanet:251009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 1 disorder","termid":"MONDO:0700008"},{"relation_name":"is_a","term_name":"uniparental disomy","termid":"MONDO:0700086"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"maternal uniparental disomy of chromosome 1","secondary_identifiers":["icd11.foundation:351448323","UMLS:C4749302","MEDGEN:1665577","GARD:20689"],"synonyms":[{"name":"UPD(1)mat","type":"exact"},{"name":"maternal uniparental disomy of chromosome type 1","type":"exact"}],"termid":"MONDO:0016651","xrefs":{"Monarch":{"xref_id":"0016651"}}}


id: GO:0019477
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-lysine, the L-enantiomer of (S)-2,6-diaminohexanoic acid.","definition_xrefs":["GOC:jsg","GOC:mah","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lysine catabolic process","termid":"GO:0006554"},{"relation_name":"is_a","term_name":"aspartate family amino acid catabolic process","termid":"GO:0009068"},{"relation_name":"is_a","term_name":"L-lysine metabolic process","termid":"GO:0046440"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044248"}],"interesting_parent_ids":["GO:0006520","GO:0044248","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"L-lysine catabolic process","synonyms":[{"name":"L-lysine breakdown","type":"exact"},{"name":"L-lysine catabolism","type":"exact"},{"name":"L-lysine degradation","type":"exact"}],"termid":"GO:0019477"}


id: PBO:0081894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 845","termid":"PBO:0081894"}


id: PBO:0003211
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RFC-like complex subunit Ctf18","termid":"PBO:0003211"}


id: MONDO:0010162
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tyrosinemia type 3 is an inborn error of tyrosine metabolism characterized by mild hypertyrosinemia and increased urinary excretion of 4-hydroxyphenylpyruvate, 4-hydroxyphenyllactate and 4-hydroxyphenylacetate.","definition_xrefs":["Orphanet:69723"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tyrosinemia","termid":"MONDO:0004741"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"tyrosinemia type III","secondary_identifiers":["DOID:0050727","OMIM:276710","NANDO:1200790","ICD9:270.2","MEDGEN:78694","SCTID:415764005","UMLS:C0268623","GARD:10332","MedDRA:10069461","NANDO:2200470"],"synonyms":[{"name":"4-Hydroxyphenylpyruvate dioxygenase deficiency","type":"related"},{"name":"4-Hydroxyphenylpyruvic acid oxidase deficiency","type":"related"},{"name":"4-alpha hydroxyphenylpyruvate dioxygenase deficiency","type":"related"},{"name":"4-alpha hydroxyphenylpyruvic acid oxidase deficiency","type":"related"},{"name":"TYRSN3","type":"related"},{"name":"tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency","type":"exact"},{"name":"tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency","type":"exact"},{"name":"tyrosinemia due to HPD deficiency","type":"exact"},{"name":"tyrosinemia type 3","type":"related"},{"name":"tyrosinemia type III","type":"exact"},{"name":"tyrosinemia, type 3","type":"related"},{"name":"tyrosinemia, type III","type":"related"}],"termid":"MONDO:0010162","xrefs":{"Monarch":{"xref_id":"0010162"}}}


id: PATO:0000078
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality of a single process inhering in a bearer by virtue of the bearer's movement or variation characterized by the regular recurrence or alternation of different quantities or conditions.","definition_xrefs":["answers.com:answers.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"temporal distribution quality","termid":"PATO:0002323"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rhythm quality","termid":"PATO:0000078"}


id: GO:0033537
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ajugose, the hexasaccharide beta-D-fructofuranosyl alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranoside, by a pathway in which galactinol:raffinose galactosyltransferase catalyzes chain elongation by transferring the alpha-galactosyl residue of galactinol to the oligosaccharide.","definition_xrefs":["GOC:mah","MetaCyc:PWY-5342"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ajugose biosynthetic process","termid":"GO:0033536"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"ajugose biosynthetic process using galactinol:raffinose galactosyltransferase","synonyms":[{"name":"ajugose anabolism using galactinol:raffinose galactosyltransferase","type":"exact"},{"name":"ajugose biosynthesis using galactinol:raffinose galactosyltransferase","type":"exact"},{"name":"ajugose formation using galactinol:raffinose galactosyltransferase","type":"exact"},{"name":"ajugose synthesis using galactinol:raffinose galactosyltransferase","type":"exact"}],"termid":"GO:0033537"}


id: PBO:0039419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"angiopoietin 2","termid":"PBO:0039419"}


id: GO:0051895
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of focal adhesion assembly, the establishment and maturation of focal adhesions.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell-matrix adhesion","termid":"GO:0001953"},{"relation_name":"is_a","term_name":"regulation of focal adhesion assembly","termid":"GO:0051893"},{"relation_name":"is_a","term_name":"negative regulation of cell-substrate junction organization","termid":"GO:0150118"},{"relation_name":"is_a","term_name":"negative regulation of cell junction assembly","termid":"GO:1901889"},{"relation_name":"negatively_regulates","term_name":"focal adhesion assembly","termid":"GO:0048041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of focal adhesion assembly","synonyms":[{"name":"down regulation of focal adhesion formation","type":"exact"},{"name":"down-regulation of focal adhesion formation","type":"exact"},{"name":"downregulation of focal adhesion formation","type":"exact"},{"name":"inhibition of focal adhesion formation","type":"narrow"}],"termid":"GO:0051895"}


id: PBO:0055023
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 2438","termid":"PBO:0055023"}


id: GO:0097718
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a disordered domain of a protein.","definition_xrefs":["GOC:gg","PMID:11746698"],"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:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"disordered domain specific binding","synonyms":[{"name":"disordered protein domain specific binding","type":"related"}],"termid":"GO:0097718"}


id: GO:1900604
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of tensidol A.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"},{"relation_name":"is_a","term_name":"secondary metabolite catabolic process","termid":"GO:0090487"},{"relation_name":"is_a","term_name":"tensidol A metabolic process","termid":"GO:1900603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"tensidol A catabolic process","synonyms":[{"name":"tensidol A breakdown","type":"exact"},{"name":"tensidol A catabolism","type":"exact"},{"name":"tensidol A degradation","type":"exact"}],"termid":"GO:1900604"}


id: GO:1905324
data:
  {"annotated_genes":["SJAG_01378","SJAG_03685","SJAG_00939"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98918,107275,115082],"is_not":false,"summary":null,"term":"GO:1905324"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a telomere-telomerase complex.","definition_xrefs":["GO_REF:0000079","PMID:26305931","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-DNA complex assembly","termid":"GO:0065004"},{"relation_name":"part_of","term_name":"telomere organization","termid":"GO:0032200"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00939":null,"SJAG_01378":null,"SJAG_03685":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032200"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0032200","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"telomere-telomerase complex assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"telomere-telomerase complex formation","type":"exact"}],"termid":"GO:1905324","terms_by_termid":{"GO:1905324":null}}


id: PBO:0086288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein with a role in copper homeostasis; possible role in vacuolar sorting and processing of secretory proteins; null mutants are hypersensitive to sortin2","termid":"PBO:0086288"}


id: GO:1904920
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of MAPK cascade involved in axon regeneration.","definition_xrefs":["GOC:kmv","GO_REF:0000058","GOC:TermGenie","PMID:20203177"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of MAPK cascade involved in axon regeneration (obsolete GO:1904920)","synonyms":[{"name":"regulation of ERK/MAPK cascade involved in axon regeneration","type":"narrow"},{"name":"regulation of MAP kinase cascade involved in axon regeneration","type":"exact"},{"name":"regulation of MAP kinase kinase kinase cascade involved in axon regeneration","type":"exact"},{"name":"regulation of MAPK signal transduction involved in axon regeneration","type":"exact"},{"name":"regulation of MAPK signaling involved in axon regeneration","type":"related"},{"name":"regulation of MAPK signalling involved in axon regeneration","type":"related"},{"name":"regulation of MAPKKK cascade during sporulation involved in axon regeneration","type":"narrow"},{"name":"regulation of MAPKKK cascade involved in axon regeneration","type":"exact"},{"name":"regulation of mitogen-activated protein kinase cascade involved in axon regeneration","type":"exact"}],"termid":"GO:1904920"}


id: PBO:0085881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; interacts with both the Reg1p/Glc7p phosphatase and the Snf1p kinase; forms cytoplasmic foci upon DNA replication stress","termid":"PBO:0085881"}


id: MONDO:0012292
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"T-B+ severe combined immunodeficiency","termid":"MONDO:0044200"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hepatitis C virus, susceptibility to","secondary_identifiers":["MEDGEN:322657","OMIM:609532","UMLS:C1835407"],"synonyms":[{"name":"HCV, resistance to","type":"related"},{"name":"HCV, susceptibility to","type":"related"},{"name":"Hepatitis C Virus infection, response to therapy of","type":"related"},{"name":"Hepatitis C Virus, resistance to","type":"related"},{"name":"hepatitis C virus, response to therapy of","type":"exact"},{"name":"hepatitis C virus, susceptibility to","type":"exact"}],"termid":"MONDO:0012292","xrefs":{"Monarch":{"xref_id":"0012292"}}}


id: FYPO:0002483
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetatively growing cell is inviable, has an abnormally low volume, and tapers at one end to a diameter smaller than the other. The cell diameter at the narrow end is smaller than that of a wild-type cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable small vegetative cell","termid":"FYPO:0000951"},{"relation_name":"is_a","term_name":"inviable tapered vegetative cell","termid":"FYPO:0002111"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0000004","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"inviable small tapered vegetative cell","synonyms":[{"name":"inviable small bottle-shaped vegetative cell","type":"exact"},{"name":"inviable small bottle-shaped vegetative cell during mitotic cell cycle","type":"related"},{"name":"inviable small bottle/skittle vegetative cell","type":"exact"},{"name":"inviable small skittle-shaped vegetative cell","type":"exact"},{"name":"inviable small tapered cell during vegetative growth","type":"exact"},{"name":"lethal; small tapered vegetative cell","type":"exact"}],"termid":"FYPO:0002483"}


id: PBO:0049440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GUSB pseudogene 17","termid":"PBO:0049440"}


id: MONDO:0003848
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition in which the thymus gland is abnomally located; this can be secondary to failure of descent during fetal development, or failure of involution.","definition_xrefs":["NCIT:C27804"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thymus gland disorder","termid":"MONDO:0003393"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"ectopic thymus","secondary_identifiers":["DOID:6307","MEDGEN:232148","UMLS:C1333375"],"synonyms":[{"name":"ectopic thymus","type":"exact"}],"termid":"MONDO:0003848","xrefs":{"Monarch":{"xref_id":"0003848"}}}


id: PR:Q9US12
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC607.06c gene.","definition_xrefs":["UniProtKB:Q9US12","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":"zinc metalloproteinase C607.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC607.06c","synonyms":[{"name":"Spom972h-SPAC607.06c","type":"exact"}],"termid":"PR:Q9US12"}


id: PATO:0002280
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a bearer by virtue of the bearer's possessing a broad surface in articulation with another entity.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"articulated with","termid":"PATO:0002278"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"broadly articulated with","termid":"PATO:0002280"}


id: PBO:0043485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cannabinoid receptor interacting protein 1","termid":"PBO:0043485"}


id: PBO:0067194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 258, pseudogene","termid":"PBO:0067194"}


id: MONDO:0001552
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A wide group of related learning disorders characterized by difficulties with mathematics and manipulating numbers; the difficulty with math may be caused or exacerbated by visuo-spatial or language processing difficulties.","definition_xrefs":["NCIT:C97165"],"direct_ancestors":[{"relation_name":"is_a","term_name":"learning disability","termid":"MONDO:0004681"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dyscalculia","secondary_identifiers":["UMLS:C0869474","HP:0002442","MESH:D060705","ICD9:315.1","MEDGEN:452779","DOID:12568","icd11.foundation:308101648","SCTID:47916000"],"synonyms":[{"name":"disorder of arithmetical skills","type":"exact"},{"name":"dyscalculia","type":"exact"},{"name":"dyscalculia (disease)","type":"exact"},{"name":"mathematics disorder","type":"exact"}],"termid":"MONDO:0001552","xrefs":{"Monarch":{"xref_id":"0001552"}}}


id: GO:0009982
data:
  {"annotated_genes":["SJAG_00319","SJAG_04065","SJAG_03572","SJAG_04754","SJAG_02978","SJAG_01172","SJAG_00088"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[90414,113428],"is_not":false,"summary":null,"term":"GO:0009982"},{"annotations":[105393,94553,113430],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106032"},{"annotations":[93860,111624,113431],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106029"},{"annotations":[105394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160150"},{"annotations":[101679],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0160148"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a uridine in RNA = a pseudouridine in RNA. Conversion of uridine in an RNA molecule to pseudouridine by rotation of the C1'-N-1 glycosidic bond of uridine in RNA to a C1'-C5.","definition_xrefs":["GOC:mah","RHEA:48348"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular transferase activity","termid":"GO:0016866"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00088":null,"SJAG_00319":null,"SJAG_01172":null,"SJAG_02978":null,"SJAG_03572":null,"SJAG_04065":null,"SJAG_04754":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016853"],"is_obsolete":false,"name":"pseudouridine synthase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-6786583","Reactome:R-HSA-6787566","Reactome:R-HSA-8870289","Reactome:R-HSA-6790905","GO:0016439","Reactome:R-HSA-6782381"],"termid":"GO:0009982","terms_by_termid":{"GO:0009982":null,"GO:0106029":null,"GO:0106032":null,"GO:0160148":null,"GO:0160150":null}}


id: PBO:0070445
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L3 pseudogene 2","termid":"PBO:0070445"}


id: PBO:0082498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catalytic subunit of a tRNA methyltransferase complex; Trm8p and Trm82p comprise an enzyme that catalyzes a methyl-transfer from S-adenosyl-l-methionine to the N(7) atom of guanine at position 46 in tRNA; Trm8 lacks catalytic activity if not bound to Trm82p","termid":"PBO:0082498"}


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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abnormal chromosome morphology","termid":"FYPO:0005600"}


id: PBO:0068356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 138 pseudogene 1","termid":"PBO:0068356"}


id: GO:0102208
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 3-(all-trans-polyprenyl)benzene-1,2-diol + S-adenosyl-L-methionine = a 2-methoxy-6-(all-trans-polyprenyl)phenol + H+ + S-adenosyl-L-homocysteine.","definition_xrefs":["RHEA:31411","GOC:pz"],"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:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016741"],"is_obsolete":false,"name":"2-polyprenyl-6-hydroxyphenol methylase activity","secondary_identifiers":["MetaCyc:RXN-12160","EC:2.1.1.222"],"termid":"GO:0102208"}


id: PR:P34068
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An M-factor precursor mfm1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:MSY","UniProtKB:P34068"],"direct_ancestors":[{"relation_name":"is_a","term_name":"M-factor precursor mfm1","termid":"PR:000025003"},{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"M-factor precursor mfm1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB8E5.05","synonyms":[{"name":"Spom972h-mfm1","type":"exact"}],"termid":"PR:P34068"}


id: MONDO:0003043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A rare malignant tumor of soft tissue characterized by a bimorphic pattern composed of undifferentiated small round cells and islands of well differentiated hyaline cartilage.","definition_xrefs":["NCIT:P378"],"gene_count":0,"genotype_count":0,"name":"obsolete extraskeletal mesenchymal chondrosarcoma (obsolete MONDO:0003043)","secondary_identifiers":["ICD9:171.9","DOID:4548","SCTID:404080006","NCIT:C27481"],"synonyms":[{"name":"mesenchymal extraosseous chondrosarcoma","type":"exact"},{"name":"mesenchymal extraskeletal chondrosarcoma","type":"exact"}],"termid":"MONDO:0003043","xrefs":{"Monarch":{"xref_id":"0003043"}}}


id: PBO:0047768
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FOSL2 antisense RNA 1","termid":"PBO:0047768"}


id: PBO:0027193
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-astral_microtubules_present_in_decreased_numbers","termid":"PBO:0027193"}


id: GO:0035711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The change in morphology and behavior of a T-helper 1 cell resulting from exposure to a mitogen, cytokine, chemokine, cellular ligand, or an antigen for which it is specific.","definition_xrefs":["GOC:BHF","CL:0000545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CD4-positive, alpha-beta T cell activation","termid":"GO:0035710"}],"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":"T-helper 1 cell activation","synonyms":[{"name":"Th1 cell activation","type":"exact"}],"termid":"GO:0035711"}


id: PBO:0086146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for normal mitochondrial morphology; localized to mitochondrial inner membrane; may be involved in fission of the inner membrane; forms a homo-oligomeric complex","termid":"PBO:0086146"}


id: GO:0044027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An epigenetic gene regulation mechanism that negatively regulates gene expression by methylation of cytosine residues in chromosomal CpG islands. CpG islands are genomic regions that contain a high frequency of the CG dinucleotide associated with the transcription start site of genes.","definition_xrefs":["PMID:11898023","Wikipedia:Cpg_island"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of gene expression, epigenetic","termid":"GO:0045814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0006325","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of gene expression via chromosomal CpG island methylation","synonyms":[{"name":"DNA hypermethylation of CG island","type":"related"},{"name":"DNA hypermethylation of CpG island","type":"exact"},{"name":"epigenetic regulation of gene expression via CpG island hypermethylation","type":"exact"},{"name":"hypermethylation of CpG island","type":"exact"},{"name":"maintenance of DNA methylation","type":"broad"},{"name":"negative regulation of gene expression via CpG island hypermethylation","type":"exact"},{"name":"negative regulation of gene expression via CpG island methylation","type":"related"},{"name":"negative regulation of gene expression via chromosomal CG dinucleotide methylation","type":"related"},{"name":"negative regulation of gene expression via chromosomal CpG dinucleotide methylation","type":"exact"},{"name":"negative regulation of gene expression via chromosomal DNA cytosine methylation","type":"exact"}],"termid":"GO:0044027"}


id: GO:0055068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process involved in the maintenance of an internal steady state of cobalt ions within an organism or cell.","definition_xrefs":["GOC:mah","GOC:ai","GOC:jid"],"gene_count":0,"genotype_count":0,"name":"obsolete cobalt ion homeostasis (obsolete GO:0055068)","synonyms":[{"name":"cobalt homeostasis","type":"broad"}],"termid":"GO:0055068"}


id: PBO:0074947
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 111","termid":"PBO:0074947"}


id: MOD:01436
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to cyclo[(prolylserin)-O-yl] cysteinate.","definition_xrefs":["PubMed:7961166","RESID:AA0489#CYS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclo[(prolylserin)-O-yl] cysteinate","termid":"MOD:01629"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"cyclo[(prolylserin)-O-yl] cysteinate (Cys)","synonyms":[{"name":"(3,6-dioxopyrrolo[4,5-a]piperazin-2-yl)methyl cysteinate","type":"exact"},{"name":"MOD_RES Cyclo[(prolylserin)-O-yl] cysteinate","type":"exact"},{"name":"[(3S,8aS)-1,4-dioxooctahydropyrrolo[1,2-a]pyrazin-3-yl]methyl (2R)-2-amino-3-sulfanylpropanoate","type":"exact"},{"name":"cyclo[(prolylserin)-O-yl] cysteinate","type":"exact"}],"termid":"MOD:01436"}


id: GO:0035968
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of sterol import, by regulation of transcription from an RNA polymerase II promoter.","definition_xrefs":["PMID:12077145","GOC:dgf"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of sterol import by regulation of transcription from RNA polymerase II promoter (obsolete GO:0035968)","synonyms":[{"name":"regulation of sterol import by regulation of transcription from Pol II promoter","type":"exact"},{"name":"regulation of sterol influx by regulation of transcription from Pol II promoter","type":"exact"},{"name":"regulation of sterol influx by regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"regulation of sterol uptake by regulation of transcription from Pol II promoter","type":"exact"},{"name":"regulation of sterol uptake by regulation of transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:0035968"}


id: PBO:0058723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6851","termid":"PBO:0058723"}


id: GO:0050158
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-dihydroorotate + NADP+ = H+ + NADPH + orotate.","definition_xrefs":["RHEA:14861"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dihydroorotate dehydrogenase activity","termid":"GO:0004152"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"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:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"dihydroorotate dehydrogenase (NADP+) activity","secondary_identifiers":["MetaCyc:OROTATE-REDUCTASE-NADPH-RXN","KEGG_REACTION:R01866","EC:1.3.1.15"],"synonyms":[{"name":"(S)-dihydroorotate:NADP+ oxidoreductase activity","type":"related"},{"name":"L-5,6-dihydro-orotate:NAD oxidoreductase activity","type":"related"},{"name":"dihydro-orotic dehydrogenase activity","type":"related"},{"name":"orotate reductase (NADPH) activity","type":"exact"},{"name":"orotate reductase activity","type":"related"}],"termid":"GO:0050158"}


id: MONDO:0006418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An enteropathy-associated T-cell lymphoma arising from the small intestine, most commonly the jejunum or ileum. Patients usually present with abdominal pain, often associated with intestinal perforation. There is often a history of celiac disease. The lymphoma cells are usually medium-sized to large and form an ulcerating mucosal lesion with invasion of the small intestinal wall. Villous atrophy is present in the adjacent small intestinal mucosa. In a minority of cases the lymphoma cells are medium-sized and form a monomorphic infiltrate.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system cancer","termid":"MONDO:0000621"},{"relation_name":"is_a","term_name":"small intestine lymphoma","termid":"MONDO:0001852"},{"relation_name":"is_a","term_name":"leukocyte disorder","termid":"MONDO:0004805"},{"relation_name":"is_a","term_name":"enteropathy-associated T-cell lymphoma","termid":"MONDO:0019473"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005046","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"small intestinal enteropathy-associated T-cell lymphoma","secondary_identifiers":["MEDGEN:275445","NCIT:C39610","UMLS:C1519371","EFO:1000535"],"synonyms":[{"name":"enteropathy-associated T-cell lymphoma of small intestine","type":"exact"},{"name":"small intestinal EATL","type":"exact"},{"name":"small intestinal enteropathy-type T-cell lymphoma","type":"exact"},{"name":"small intestine enteropathy-associated T-cell lymphoma","type":"exact"}],"termid":"MONDO:0006418","xrefs":{"Monarch":{"xref_id":"0006418"}}}


id: GO:0002234
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a stimulus generated by the accumulation of normal or misfolded proteins in the endoplasmic reticulum is received and converted into a molecular signal.","definition_xrefs":["PMID:10390516","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ER overload response","termid":"GO:0006983"},{"relation_name":"is_a","term_name":"detection of biotic stimulus","termid":"GO:0009595"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"detection of endoplasmic reticulum overloading","synonyms":[{"name":"detection of ER overloading","type":"exact"}],"termid":"GO:0002234"}


id: GO:0047491
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: polysaccharides containing a terminal alpha-L-guluronate group = oligosaccharides with 4-deoxy-alpha-L-erythro-hex-4-enuronosyl end. This reaction is the eliminative cleavage of polysaccharides containing a terminal a-L-guluronate group, to give oligopolysaccharides with 4-deoxy-a-L-erythro-hex-4-enuronosyl groups at their nonreducing ends.","definition_xrefs":["EC:4.2.2.11"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on polysaccharides","termid":"GO:0016837"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"poly(alpha-L-guluronate) lyase activity","secondary_identifiers":["MetaCyc:4.2.2.11-RXN"],"synonyms":[{"name":"L-guluronan lyase activity","type":"related"},{"name":"L-guluronate lyase activity","type":"related"},{"name":"alginase II activity","type":"related"},{"name":"guluronate lyase activity","type":"related"},{"name":"poly(alpha-L-1,4-guluronide) exo-lyase activity","type":"related"},{"name":"poly-alpha-L-guluronate lyase activity","type":"related"},{"name":"polyguluronate-specific alginate lyase activity","type":"related"}],"termid":"GO:0047491"}


id: SO:0000702
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of sequence where there may have been an error in the assembly.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_difference","termid":"SO:0000413"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"possible_assembly_error","synonyms":[{"name":"possible assembly error","type":"exact"}],"termid":"SO:0000702"}


id: PBO:0063856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P38 inhibited cutaneous squamous cell carcinoma associated lincRNA","termid":"PBO:0063856"}


id: PATO:0002343
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's lying or growing on the ground but with erect or rising tips.","definition_xrefs":["thefreedictionary:www.thefreedictionary.com"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostrate","termid":"PATO:0000631"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decumbent","termid":"PATO:0002343"}


id: PBO:0061422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropeptide Y receptor Y6 (pseudogene)","termid":"PBO:0061422"}


id: PBO:0013469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosyltransferase Alg6","termid":"PBO:0013469"}


id: GO:0098883
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cellular process that results in the controlled breakdown of synapse. After it starts the process is continuous until the synapse has disappeared.","definition_xrefs":["PMID:18083105","PMID:22632716","PMID:29844190","GOC:dos","PMID:12062020"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synapse organization","termid":"GO:0050808"},{"relation_name":"is_a","term_name":"cell junction disassembly","termid":"GO:0150146"}],"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":"synapse pruning","synonyms":[{"name":"synapse clearance","type":"exact"},{"name":"synapse disassembly","type":"exact"},{"name":"synapse elimination","type":"exact"},{"name":"synapse removal","type":"exact"}],"termid":"GO:0098883"}


id: GO:0072199
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mesenchymal cell proliferation that contributes to the progression of the ureter gland over time. A mesenchymal cell is a cell that normally gives rise to other cells that are organized as three-dimensional masses, rather than sheets.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mesenchymal cell proliferation","termid":"GO:0010464"},{"relation_name":"regulates","term_name":"mesenchymal cell proliferation involved in ureter development","termid":"GO:0072198"}],"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 mesenchymal cell proliferation involved in ureter development","synonyms":[{"name":"regulation of ureter mesenchymal cell proliferation","type":"related"},{"name":"regulation of ureteral mesenchymal cell proliferation","type":"related"}],"termid":"GO:0072199"}


id: GO:0034014
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a triglyceride stimulus.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to lipid","termid":"GO:0033993"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"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 triglyceride","synonyms":[{"name":"response to triacylglyceride","type":"exact"},{"name":"response to triacylglycerol","type":"exact"}],"termid":"GO:0034014"}


id: GO:0007403
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell fate determination process in which a cell becomes capable of differentiating autonomously into a glial cell regardless of its environment; upon determination, the cell fate cannot be reversed.","definition_xrefs":["GOC:go_curators","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate determination","termid":"GO:0001709"},{"relation_name":"part_of","term_name":"glial cell fate commitment","termid":"GO:0021781"}],"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":"glial cell fate determination","secondary_identifiers":["GO:0043361"],"termid":"GO:0007403"}


id: PBO:0050683
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family A (Hsp70) member 8 pseudogene 10","termid":"PBO:0050683"}


id: PBO:0071471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L32 pseudogene 12","termid":"PBO:0071471"}


id: PR:Q09788
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- asl1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09788"],"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":"alkali-sensitive linkage protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13G6.10c","synonyms":[{"name":"Spom972h-asl1","type":"exact"}],"termid":"PR:Q09788"}


id: PBO:0031045
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_diamide","termid":"PBO:0031045"}


id: GO:0004941
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with epinephrine or norepinephrine to initiate a change in cell activity via activation of a G protein, with pharmacological characteristics of beta2-adrenergic receptors.","definition_xrefs":["GOC:mah","IUPHAR_GPCR:1274"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-adrenergic receptor activity","termid":"GO:0004939"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"beta2-adrenergic receptor activity","synonyms":[{"name":"beta2 adrenoceptor","type":"exact"}],"termid":"GO:0004941"}


id: GO:0120182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of disaggregation of a focal adhesion into its constituent components.","definition_xrefs":["PMID:25490267"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell-substrate junction organization","termid":"GO:0150116"},{"relation_name":"regulates","term_name":"focal adhesion disassembly","termid":"GO:0120181"}],"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 focal adhesion disassembly","termid":"GO:0120182"}


id: PBO:0040442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase phospholipid transporting 8B3","termid":"PBO:0040442"}


id: PBO:0000759
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene structure uopdated","termid":"PBO:0000759"}


id: GO:0103040
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + an aldose + an oxidized electron acceptor = H+ + an aldonate + a reduced electron acceptor.","definition_xrefs":["MetaCyc:RXN0-6371","PMID:16864586","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor","termid":"GO:0016901"}],"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:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"aldose sugar dehydrogenase activity","termid":"GO:0103040"}


id: MONDO:0030457
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive immunologic disorder with wide phenotypic variation and severity. Affected individuals usually present in infancy or early childhood with increased susceptibility to infections, often Epstein-Barr virus (EBV), as well as with lymphadenopathy or autoimmune manifestations, predominantly hemolytic anemia. Laboratory studies may show low or normal lymphocyte numbers, often with skewed T-cell subset ratios. The disorder results primarily from defects in T-cell function, which causes both immunodeficiency and overall immune dysregulation.","definition_xrefs":["OMIM:619573"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency 87 and autoimmunity","secondary_identifiers":["MEDGEN:1794280","UMLS:C5562070"],"synonyms":[{"name":"IMD87","type":"exact"},{"name":"immunodeficiency due to DEF6 deficiency","type":"exact"}],"termid":"MONDO:0030457","xrefs":{"Monarch":{"xref_id":"0030457"}}}


id: PBO:0080861
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Yip1 domain family member 2","termid":"PBO:0080861"}


id: PBO:0000234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nicotinamide mononucleotide (NMN) adenylyltransferase (predicted)","termid":"PBO:0000234"}


id: PBO:0034172
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_fasciculating_neuron_projection","termid":"PBO:0034172"}


id: GO:0031644
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of a neurophysiological process, an organ system process carried out by any of the organs or tissues of the nervous system.","definition_xrefs":["GOC:dph","GOC:mah","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of system process","termid":"GO:0044057"},{"relation_name":"regulates","term_name":"nervous system process","termid":"GO:0050877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of nervous system process","synonyms":[{"name":"regulation of neurological process","type":"exact"},{"name":"regulation of neurological system process","type":"exact"},{"name":"regulation of neurophysiological process","type":"exact"}],"termid":"GO:0031644"}


id: PBO:0039288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG3 alpha-1,3- mannosyltransferase","termid":"PBO:0039288"}


id: GO:0140719
data:
  {"annotated_genes":["SJAG_02846","SJAG_04039","SJAG_00961","SJAG_02592","SJAG_01540","SJAG_03680","SJAG_04574","SJAG_03624","SJAG_01579","SJAG_04141","SJAG_02416","SJAG_00160","SJAG_02576","SJAG_03997","SJAG_00414","SJAG_03356","SJAG_00058","SJAG_02778","SJAG_02311","SJAG_03128","SJAG_00266","SJAG_02119","SJAG_02594","SJAG_04030","SJAG_04253","SJAG_02409","SJAG_03193","SJAG_02725","SJAG_02401","SJAG_00302","SJAG_00769","SJAG_01599","SJAG_03689","SJAG_03982","SJAG_04942","SJAG_02621","SJAG_01008","SJAG_04061","SJAG_02342","SJAG_04186","SJAG_00756","SJAG_00142","SJAG_00087","SJAG_00676","SJAG_00335","SJAG_00934","SJAG_01601","SJAG_01075","SJAG_03042","SJAG_01675","SJAG_03543","SJAG_03844","SJAG_03916"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[110411,112735],"is_not":false,"summary":null,"term":"GO:0140719"},{"annotations":[111247,113551,93279,92641,111346,89420,102402,109629,103267,111756,91273,101201,98325,92025,111754,112427,90476,113121,95925,97454,101203,101960,107315,111755,110414,89256,101202],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031508"},{"annotations":[90389],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090053"},{"annotations":[109491,90390,93572],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0090055"},{"annotations":[99489,96384],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0090052"},{"annotations":[117219,90477,103270,107132,110352,117939,111249,98758,103366,94717,115120,113122,98326,107317,112802,93280,109630,91275,111347,112429,116826,95926,91951,102405,110415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030466"},{"annotations":[95927,98327,117221,98760,105709,111348,112803,109632,88044,109797,113438,93292,90478,113704,114557,115121,94533,116827,117940,110353,117107,87989],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140727"},{"annotations":[89259,91276,103271,109633,93281,107318,112430,90479,111251,116828,98328,89421,117941,97455,87639,110416,112804,102406,113124,103368,117222,95928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031509"},{"annotations":[115674],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141005"}]},"cv_name":"biological_process","definition":"The compaction of chromatin into heterochromatin, a conformation that is refractory to transcription. Constitutive heterochromatin cannot be converted back to euchromatin, the transcriptionally-active conformation. In metazoa, this involves the methylation of histone H3K9.","definition_xrefs":["PMID:17936700"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heterochromatin formation","termid":"GO:0031507"}],"gene_count":53,"genes_by_uniquename":{"SJAG_00058":null,"SJAG_00087":null,"SJAG_00142":null,"SJAG_00160":null,"SJAG_00266":null,"SJAG_00302":null,"SJAG_00335":null,"SJAG_00414":null,"SJAG_00676":null,"SJAG_00756":null,"SJAG_00769":null,"SJAG_00934":null,"SJAG_00961":null,"SJAG_01008":null,"SJAG_01075":null,"SJAG_01540":null,"SJAG_01579":null,"SJAG_01599":null,"SJAG_01601":null,"SJAG_01675":null,"SJAG_02119":null,"SJAG_02311":null,"SJAG_02342":null,"SJAG_02401":null,"SJAG_02409":null,"SJAG_02416":null,"SJAG_02576":null,"SJAG_02592":null,"SJAG_02594":null,"SJAG_02621":null,"SJAG_02725":null,"SJAG_02778":null,"SJAG_02846":null,"SJAG_03042":null,"SJAG_03128":null,"SJAG_03193":null,"SJAG_03356":null,"SJAG_03543":null,"SJAG_03624":null,"SJAG_03680":null,"SJAG_03689":null,"SJAG_03844":null,"SJAG_03916":null,"SJAG_03982":null,"SJAG_03997":null,"SJAG_04030":null,"SJAG_04039":null,"SJAG_04061":null,"SJAG_04141":null,"SJAG_04186":null,"SJAG_04253":null,"SJAG_04574":null,"SJAG_04942":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006325","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"constitutive heterochromatin formation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"constitutive heterochromatin assembly","type":"exact"}],"termid":"GO:0140719","terms_by_termid":{"GO:0030466":null,"GO:0031508":null,"GO:0031509":null,"GO:0090052":null,"GO:0090053":null,"GO:0090055":null,"GO:0140719":null,"GO:0140727":null,"GO:0141005":null}}


id: GO:0047018
data:
  {"annotated_genes":["SJAG_01869"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91015],"is_not":false,"summary":null,"term":"GO:0047018"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: indole-3-ethanol + NAD+ = (indol-3-yl)acetaldehyde + H+ + NADH.","definition_xrefs":["EC:1.1.1.190","RHEA:14873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alcohol dehydrogenase (NAD+) activity","termid":"GO:0004022"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01869":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"indole-3-acetaldehyde reductase (NADH) activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["KEGG_REACTION:R02679","MetaCyc:1.1.1.190-RXN"],"synonyms":[{"name":"(indol-3-yl)ethanol:NAD+ oxidoreductase activity","type":"related"},{"name":"indole-3-ethanol:NAD+ oxidoreductase activity","type":"related"},{"name":"indoleacetaldehyde reductase activity","type":"related"}],"termid":"GO:0047018","terms_by_termid":{"GO:0047018":null}}


id: PBO:0061757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-acyl-ADP-ribose deacylase 1","termid":"PBO:0061757"}


id: GO:0043459
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a single or short exposure to a lithium ion stimulus.","definition_xrefs":["PMID:10208444"],"gene_count":0,"genotype_count":0,"name":"obsolete response to short exposure to lithium ion (obsolete GO:0043459)","synonyms":[{"name":"response to short exposure to lithium ion","type":"exact"}],"termid":"GO:0043459"}


id: PR:Q92342
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1F8.04c gene.","definition_xrefs":["UniProtKB:Q92342","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 C1F8.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F8.04c","synonyms":[{"name":"Spom972h-SPAC1F8.04c","type":"exact"}],"termid":"PR:Q92342"}


id: MONDO:0014885
data:
  {"annotated_genes":["SJAG_00108"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85347],"is_not":false,"summary":null,"term":"MONDO:0014885"}]},"cv_name":"mondo","definition":"Any Hermansky-Pudlak syndrome in which the cause of the disease is a mutation in the AP3D1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Hermansky-Pudlak syndrome","termid":"MONDO:0019312"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00108":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005066","MONDO:0005093"],"is_obsolete":false,"name":"Hermansky-Pudlak syndrome 10","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4310746","OMIM:617050","Orphanet:664511","MEDGEN:934713","GARD:16180"],"synonyms":[{"name":"AP3D1 Hermansky-Pudlak syndrome","type":"exact"},{"name":"HPS10","type":"exact"},{"name":"Hermansky-Pudlak syndrome 10","type":"exact"},{"name":"Hermansky-Pudlak syndrome 10; HPS10","type":"exact"},{"name":"Hermansky-Pudlak syndrome caused by mutation in AP3D1","type":"exact"},{"name":"Hermansky-Pudlak syndrome type 10","type":"exact"}],"termid":"MONDO:0014885","terms_by_termid":{"MONDO:0014885":null},"xrefs":{"Monarch":{"xref_id":"0014885"}}}


id: FYPO:0007459
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, or structure of the portion of the nuclear envelope enclosing the mitotic nuclear bridge is abnormal. The nuclear bridge is a narrow constricted region of the nucleus that forms around the mitotic spindle during anaphase.","definition_xrefs":["PMID:32848252","GO:0140510","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear envelope morphology during mitosis","termid":"FYPO:0003779"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0002403"],"is_obsolete":false,"name":"abnormal nuclear envelope morphology at mitotic nuclear bridge","synonyms":[{"name":"abnormal nuclear envelope morphology at mitotic nuclear bridge during mitotic cell cycle","type":"related"},{"name":"abnormal nuclear envelope morphology at mitotic nuclear bridge during vegetative growth","type":"exact"}],"termid":"FYPO:0007459"}


id: PBO:0047908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, distamycin A type, rare, fra(8)(q24.1)","termid":"PBO:0047908"}


id: MONDO:0000906
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Alzheimer disease 5 (obsolete MONDO:0000906)","synonyms":[{"name":"obsolete Alzheimer's disease 5","type":"exact"}],"termid":"MONDO:0000906","xrefs":{"Monarch":{"xref_id":"0000906"}}}


id: PBO:0082798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of transport protein particle (TRAPP) complex II; TRAPPII is a multimeric guanine nucleotide-exchange factor for the GTPase Ypt1p, regulating intra-Golgi and endosome-Golgi traffic","termid":"PBO:0082798"}


id: PBO:0000273
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Lcp5 (predicted)","termid":"PBO:0000273"}


id: PBO:0046388
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E1A binding protein p300","termid":"PBO:0046388"}


id: PBO:0034735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil protein involved in septum formation Rng10","termid":"PBO:0034735"}


id: PBO:0084396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lsm (Like Sm) protein; part of heteroheptameric complexes (Lsm2p-7p and either Lsm1p or 8p): cytoplasmic Lsm1p complex involved in mRNA decay; nuclear Lsm8p complex part of U6 snRNP and possibly involved in processing tRNA, snoRNA, and rRNA; protein abundance increases and forms cytoplasmic foci in response to DNA replication stress","termid":"PBO:0084396"}


id: GO:0071129
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alphaV-beta3 integrin complex bound to lipid phosphate phosphohydrolase-3.","definition_xrefs":["PMID:16099422"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005886","GO:0005575"],"is_obsolete":false,"name":"alphaV-beta3 integrin-LPP3 complex","synonyms":[{"name":"ITGAV-ITGB3-PPAP2B complex","type":"narrow"}],"termid":"GO:0071129"}


id: MONDO:0044626
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"female infertility","termid":"MONDO:0021124"}],"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":"female infertility due to oocyte meiotic arrest","secondary_identifiers":["MEDGEN:1798912","GARD:17887","Orphanet:488191","UMLS:C5567489"],"termid":"MONDO:0044626","xrefs":{"Monarch":{"xref_id":"0044626"}}}


id: MONDO:0011377
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal dominant condition caused by mutation(s) in the SCN5A gene, encoding sodium channel protein type 5 subunit alpha. It is characterized by a prolonged QT interval that may result in torsade de pointes, ventricular fibrillation and/or sudden cardiac death.","definition_xrefs":["NCIT:C137959"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"long QT syndrome","termid":"MONDO:0002442"},{"relation_name":"is_a","term_name":"familial long QT syndrome","termid":"MONDO:0019171"}],"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":"long QT syndrome 3","secondary_identifiers":["MESH:C565840","UMLS:C1859062","GARD:3286","DOID:0110646","MEDGEN:349087","OMIM:603830"],"synonyms":[{"name":"LQT3","type":"exact"},{"name":"SCN5A long QT syndrome","type":"exact"},{"name":"long QT syndrome 2/3, digenic","type":"related"},{"name":"long QT syndrome 3","type":"exact"},{"name":"long QT syndrome 3, acquired, susceptibility to","type":"related"},{"name":"long QT syndrome 3/6, digenic","type":"related"},{"name":"long QT syndrome caused by mutation in SCN5A","type":"exact"},{"name":"long QT syndrome type 3","type":"exact"}],"termid":"MONDO:0011377","xrefs":{"Monarch":{"xref_id":"0011377"}}}


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


id: PBO:0038517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily F member 2","termid":"PBO:0038517"}


id: PBO:0079755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urocortin","termid":"PBO:0079755"}


id: GO:0050613
data:
  {"annotated_genes":["SJAG_04810"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[103635],"is_not":false,"summary":null,"term":"GO:0050613"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: NADP+ + 4,4-dimethyl-5-alpha-cholesta-8,24-dien-3-beta-ol = NADPH + H+ + 4,4-dimethyl-5-alpha-cholesta-8,14,24-trien-3-beta-ol.","definition_xrefs":["EC:1.3.1.70"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04810":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"Delta14-sterol reductase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0000251","MetaCyc:RXN66-14","Reactome:R-HSA-194698","Reactome:R-HSA-194674","RHEA:18561"],"synonyms":[{"name":"4,4-dimethyl-5alpha-cholesta-8,24-dien-3beta-ol:NADP+ delta14-oxidoreductase activity","type":"related"},{"name":"C-14 sterol reductase activity","type":"exact"},{"name":"D14-sterol reductase activity","type":"exact"},{"name":"sterol C-14 reductase activity","type":"exact"},{"name":"sterol C14-reductase activity","type":"related"}],"termid":"GO:0050613","terms_by_termid":{"GO:0050613":null}}


id: GO:0102182
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4alpha-carboxy-stigmasta-7,24(241)-dien-3beta-ol + NAD = avenastenone + NADH + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 4alpha-carboxy-stigmasta-7,24(241)-dien-3beta-ol dehydrogenase/C4-decarboxylase activity (obsolete GO:0102182)","termid":"GO:0102182"}


id: PBO:0071886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 24","termid":"PBO:0071886"}


id: MONDO:0017504
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"apodia","termid":"MONDO:0017446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"apodia, unilateral","secondary_identifiers":["icd11.foundation:1499762342","Orphanet:295105"],"synonyms":[{"name":"congenital absence of foot, unilateral","type":"exact"}],"termid":"MONDO:0017504","xrefs":{"Monarch":{"xref_id":"0017504"}}}


id: MONDO:0033115
data:
  {"annotated_genes":["SJAG_00059"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84650],"is_not":false,"summary":null,"term":"MONDO:0033115"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00059":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"spinocerebellar ataxia, autosomal recessive 25","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4539808","OMIM:617584","MEDGEN:1618081","DOID:0080259"],"synonyms":[{"name":"SCAR25","type":"related"},{"name":"autosomal recessive spinocerebellar ataxia 25","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive 25","type":"exact"}],"termid":"MONDO:0033115","terms_by_termid":{"MONDO:0033115":null},"xrefs":{"Monarch":{"xref_id":"0033115"}}}


id: PBO:0039469
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 17","termid":"PBO:0039469"}


id: PBO:0066244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif single stranded interacting protein 1 pseudogene 1","termid":"PBO:0066244"}


id: PBO:0075791
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine and arginine rich splicing factor 10 pseudogene 2","termid":"PBO:0075791"}


id: PBO:0004563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L38 (predicted)","termid":"PBO:0004563"}


id: MONDO:0018474
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"13q12.3 microdeletion syndrome is a rare chromosomal anomaly characterized by moderate intellectual disability, speech delay, postnatal microcephaly, eczema or atopic dermatitis, characteristic facial features (malar flattening, prominent nose, underdeveloped alae nasi, smooth philtrum, and thin vermillion of the upper lip), and reduced sensitivity to pain.","definition_xrefs":["Orphanet:412035"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 13","termid":"MONDO:0016911"},{"relation_name":"is_a","term_name":"epidermal disease","termid":"MONDO:0019268"}],"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":"13q12.3 microdeletion syndrome","secondary_identifiers":["GARD:21737","UMLS:C4750951","MEDGEN:1657124"],"synonyms":[{"name":"Del(13)(q12.3)","type":"exact"},{"name":"monosomy 13q12.3","type":"exact"}],"termid":"MONDO:0018474","xrefs":{"Monarch":{"xref_id":"0018474"}}}


id: MONDO:1010678
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"AA amyloidosis that occurs in island gray fox.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AA amyloidosis, non-human animal","termid":"MONDO:1010092"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AA amyloidosis, island gray fox","secondary_identifiers":["OMIA:000038-244585"],"termid":"MONDO:1010678","xrefs":{"Monarch":{"xref_id":"1010678"}}}


id: GO:0042406
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The component of the endoplasmic reticulum membrane consisting of gene products and protein complexes that are loosely bound to one of its surfaces, but not integrated into the hydrophobic region.","definition_xrefs":["GOC:curators","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrinsic component of organelle membrane","termid":"GO:0031312"},{"relation_name":"part_of","term_name":"endoplasmic reticulum membrane","termid":"GO:0005789"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0005783","GO:0005789","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"extrinsic component of endoplasmic reticulum membrane","synonyms":[{"name":"extrinsic to ER membrane","type":"exact"},{"name":"extrinsic to endoplasmic reticulum membrane","type":"narrow"}],"termid":"GO:0042406"}


id: PBO:0090842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial membrane protein, human TMEM186 ortholog, implicated in respiratory complex assembly","termid":"PBO:0090842"}


id: PBO:0062026
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 N member 1 pseudogene","termid":"PBO:0062026"}


id: MONDO:0001853
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"blepharoconjunctivitis","termid":"MONDO:0002307"}],"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":"contact blepharoconjunctivitis","secondary_identifiers":["icd11.foundation:1096051270","ICD9:372.22","MEDGEN:509811","DOID:13999","SCTID:10813004","UMLS:C0155150"],"termid":"MONDO:0001853","xrefs":{"Monarch":{"xref_id":"0001853"}}}


id: PATO:0000002
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000002 value (obsolete PATO:0000002)","termid":"PATO:0000002"}


id: PBO:0083032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Delta-1-pyrroline-5-carboxylate dehydrogenase; nuclear-encoded mitochondrial protein involved in utilization of proline as sole nitrogen source; deficiency of human homolog ALDH4A1 causes type II hyperprolinemia (HPII), an autosomal recessive inborn error of metabolism; human homolog ALDH4A1 can complement yeast null mutant","termid":"PBO:0083032"}


id: PBO:0042414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell division cycle 26","termid":"PBO:0042414"}


id: MONDO:0850287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An intrinsic asthma that is characertized by severe and prolonged airway obstruction after the ingestion of aspirin or other non-steroidal anti-inflammatory drugs.","definition_xrefs":["DOID:0080822"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intrinsic asthma","termid":"MONDO:0004765"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspirin-induced respiratory disease","termid":"MONDO:0850287","xrefs":{"Monarch":{"xref_id":"0850287"}}}


id: MONDO:0018546
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Serotoninergic syndrome is characterized by an excess of serotonin in the central nervous system, associated with the use of various agents, including selective serotonin reuptake inhibitors (SSRIs).","definition_xrefs":["Orphanet:43116"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serotonin syndrome","secondary_identifiers":["SCTID:371089000","MedDRA:10040108","MEDGEN:152119","EFO:1001842","ICD9:333.99","GARD:18828","MESH:D020230","icd11.foundation:678764364","UMLS:C0699828"],"synonyms":[{"name":"serotonergic syndrome","type":"exact"},{"name":"serotonin storm","type":"exact"},{"name":"serotonin toxicity","type":"exact"},{"name":"serotonin toxidrome","type":"exact"}],"termid":"MONDO:0018546","xrefs":{"Monarch":{"xref_id":"0018546"}}}


id: PBO:0076689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor A like 6","termid":"PBO:0076689"}


id: GO:0102502
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ADP alpha-D-glucoside + n a 1,4-alpha-D-glucan = ADP + n alpha-amylose.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete ADP-glucose-starch glucosyltransferase activity (obsolete GO:0102502)","termid":"GO:0102502"}


id: PBO:0059212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MRM3 pseudogene 1","termid":"PBO:0059212"}


id: GO:1904826
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of hydrogen sulfide biosynthetic process.","definition_xrefs":["GOC:BHF","GOC:rph","GOC:TermGenie","PMID:22034194","GO_REF:0000058","GOC:BHF_miRNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biosynthetic process","termid":"GO:0009889"},{"relation_name":"is_a","term_name":"regulation of sulfur metabolic process","termid":"GO:0042762"},{"relation_name":"regulates","term_name":"hydrogen sulfide biosynthetic process","termid":"GO:0070814"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0008150","GO:0006790"],"is_obsolete":false,"name":"regulation of hydrogen sulfide biosynthetic process","synonyms":[{"name":"regulation of hydrogen sulfide anabolism","type":"exact"},{"name":"regulation of hydrogen sulfide biosynthesis","type":"exact"},{"name":"regulation of hydrogen sulfide formation","type":"exact"},{"name":"regulation of hydrogen sulfide synthesis","type":"exact"},{"name":"regulation of hydrogen sulphide biosynthesis","type":"exact"},{"name":"regulation of hydrogen sulphide biosynthetic process","type":"exact"}],"termid":"GO:1904826"}


id: PBO:0111344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small subunit processome, U3 snoRNA associated protein Dip2","termid":"PBO:0111344"}


id: MONDO:0032712
data:
  {"annotated_genes":["SJAG_02452"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85340],"is_not":false,"summary":null,"term":"MONDO:0032712"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"combined oxidative phosphorylation deficiency","termid":"MONDO:0000732"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02452":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"combined oxidative phosphorylation deficiency 38","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5193064","MEDGEN:1682102","OMIM:618378","DOID:0111466"],"synonyms":[{"name":"COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 38","type":"related"},{"name":"COXPD38","type":"related"}],"termid":"MONDO:0032712","terms_by_termid":{"MONDO:0032712":null},"xrefs":{"Monarch":{"xref_id":"0032712"}}}


id: GO:0098617
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + adenylylselenate => ADP + 3'-phosphoadenylylselenate.","definition_xrefs":["PMID:2537056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"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:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"adenylylselenate kinase activity","secondary_identifiers":["Reactome:R-HSA-2408540"],"termid":"GO:0098617"}


id: PBO:0115007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper-binding protein involved in respiratory complex assembly Cmc2","termid":"PBO:0115007"}


id: PBO:0068293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho family GTPase 2","termid":"PBO:0068293"}


id: PBO:0055483
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 2916","termid":"PBO:0055483"}


id: GO:0000216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Progression from M phase to G1 phase of the mitotic cell cycle.","definition_xrefs":["GOC:mah","GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete M/G1 transition of mitotic cell cycle (obsolete GO:0000216)","synonyms":[{"name":"M/G1 transition of mitotic cell cycle","type":"exact"}],"termid":"GO:0000216"}


id: PBO:0089482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"arrestin-related substrate adaptor for RhoGEF, Art1","termid":"PBO:0089482"}


id: PBO:0068250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 28S ribosomal N2","termid":"PBO:0068250"}


id: PR:O60148
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC18H10.18c gene.","definition_xrefs":["UniProtKB:O60148","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 membrane protein C18H10.18c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC18H10.18c","synonyms":[{"name":"Spom972h-SPBC18H10.18c","type":"exact"}],"termid":"PR:O60148"}


id: MONDO:1010667
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary thrombopathia associated with a defect in the ADP receptor P2Y12 in dogs due to a variation in the P2Y12 gene.","definition_xrefs":["PMID:36815741"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"thrombopathia, non-human animal","termid":"MONDO:1011695"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bleeding disorder P2RY12-related, dog","secondary_identifiers":["OMIA:001564-9615"],"termid":"MONDO:1010667","xrefs":{"Monarch":{"xref_id":"1010667"}}}


id: GO:0047030
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: trans-4-hydroxycyclohexanecarboxylate + NAD+ = 4-oxocyclohexanecarboxylate + H+ + NADH.","definition_xrefs":["EC:1.1.1.226","RHEA:17429"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"4-hydroxycyclohexanecarboxylate dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R04307","MetaCyc:1.1.1.226-RXN"],"synonyms":[{"name":"trans-4-hydroxycyclohexanecarboxylate dehydrogenase activity","type":"related"},{"name":"trans-4-hydroxycyclohexanecarboxylate:NAD+ 4-oxidoreductase activity","type":"related"}],"termid":"GO:0047030"}


id: PBO:0085274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peroxisomal integral membrane protein; involved in negative regulation of peroxisome size; partially functionally redundant with Pex30p and Pex32p; probably acts at a step downstream of steps mediated by Pex28p and Pex29p; PEX31 has a paralog, PEX30, that arose from the whole genome duplication","termid":"PBO:0085274"}


id: MONDO:0011909
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant intermediate Charcot-Marie-Tooth disease type D is a rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies. It presents with usual Charcot-Marie-Tooth disease clinical features of variable severity (progressive muscle weakness and atrophy of the distal extremities, distal sensory loss, reduced or absent deep tendon reflexes, and feet deformities). Other findings in some of the families include debilitating neuropathic pain and mild postural/kinetic upper limb tremor.","definition_xrefs":["Orphanet:100046"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant intermediate Charcot-Marie-Tooth disease","termid":"MONDO:0019548"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005244"],"is_obsolete":false,"name":"Charcot-Marie-Tooth disease dominant intermediate D","secondary_identifiers":["UMLS:C1843075","SCTID:765747004","MESH:C564333","DOID:0110200","MEDGEN:334318","OMIM:607791","GARD:9207"],"synonyms":[{"name":"CMTDID","type":"exact"},{"name":"Charcot Marie Tooth disease dominant intermediate 3","type":"related"},{"name":"Charcot-Marie-Tooth disease caused by mutation in MPZ","type":"exact"},{"name":"Charcot-Marie-Tooth disease dominant intermediate type D","type":"exact"},{"name":"Charcot-Marie-Tooth disease, dominant Intermediate type D","type":"exact"},{"name":"Charcot-Marie-Tooth disease, dominant intermediate D","type":"related"},{"name":"Charcot-Marie-Tooth neuropathy dominant intermediate D","type":"exact"},{"name":"Charcot-Marie-Tooth neuropathy, dominant Intermediate D","type":"related"},{"name":"DI-CMTD","type":"exact"},{"name":"Di-Cmtd","type":"related"},{"name":"MPZ Charcot-Marie-Tooth disease","type":"exact"},{"name":"MPZ-related intermediate Charcot-Marie-Tooth neuropathy","type":"related"},{"name":"autosomal dominant intermediate Charcot-Marie-Tooth disease type D","type":"exact"}],"termid":"MONDO:0011909","xrefs":{"Monarch":{"xref_id":"0011909"}}}


id: GO:0002812
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an antibacterial peptide with activity against Gram-negative bacteria.","definition_xrefs":["PMID:11807545","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antibacterial peptide biosynthetic process","termid":"GO:0002780"},{"relation_name":"part_of","term_name":"defense response to Gram-negative bacterium","termid":"GO:0050829"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"biosynthetic process of antibacterial peptides active against Gram-negative bacteria","termid":"GO:0002812"}


id: PBO:0033759
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_exit_from_meiosis","termid":"PBO:0033759"}


id: PBO:0090220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Sof1","termid":"PBO:0090220"}


id: PBO:0005007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rad16 homolog Rhp16","termid":"PBO:0005007"}


id: PBO:0083508
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 the verified ORF CDC7/YDL153C, the catalytic subunit of a complex that regulates DNA replication","termid":"PBO:0083508"}


id: FYPO:0001953
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the import of calcium ions into a cell is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation phenotype during vegetative growth","termid":"FYPO:0001334"},{"relation_name":"is_a","term_name":"abnormal transport during vegetative growth","termid":"FYPO:0005973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abnormal calcium import","synonyms":[{"name":"abnormal calcium import during mitotic cell cycle","type":"related"},{"name":"abnormal calcium import during vegetative growth","type":"exact"},{"name":"abnormal calcium import into cell","type":"exact"},{"name":"abnormal calcium ion import","type":"exact"},{"name":"abnormal calcium ion import across plasma membrane","type":"exact"},{"name":"abnormal cellular calcium import","type":"exact"}],"termid":"FYPO:0001953"}


id: PBO:0031503
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_actinomycin_D","termid":"PBO:0031503"}


id: GO:0050763
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of depsipeptides, a linear or cyclic compound composed of both amino acids and hydroxy acids in peptide and ester bonds respectively.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"depsipeptide metabolic process","termid":"GO:0050761"}],"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":"depsipeptide biosynthetic process","synonyms":[{"name":"depsipeptide anabolism","type":"exact"},{"name":"depsipeptide biosynthesis","type":"exact"},{"name":"depsipeptide formation","type":"exact"},{"name":"depsipeptide synthesis","type":"exact"}],"termid":"GO:0050763"}


id: MONDO:0001779
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign papillary neoplasm that arises from the vagina and is characterized by the presence of a fibrovascular stalk lined by normal squamous epithelium. There is no evidence of atypia or relation to human papillomavirus.","definition_xrefs":["NCIT:C6374"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign vaginal neoplasm","termid":"MONDO:0000647"},{"relation_name":"is_a","term_name":"vaginal squamous tumor","termid":"MONDO:0001806"},{"relation_name":"is_a","term_name":"squamous papilloma","termid":"MONDO:0001825"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vaginal squamous papilloma","secondary_identifiers":["UMLS:C1336943","MEDGEN:234983","DOID:137"],"synonyms":[{"name":"squamous papilloma of the vagina","type":"exact"},{"name":"squamous papilloma of vagina","type":"exact"},{"name":"vagina squamous papilloma","type":"exact"},{"name":"vaginal squamous papilloma","type":"exact"}],"termid":"MONDO:0001779","xrefs":{"Monarch":{"xref_id":"0001779"}}}


id: PBO:0087899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcription factor; involved in regulating multidrug resistance and oxidative stress response; forms a heterodimer with Pdr1p; contains a Zn(II)2Cys6 zinc finger domain that interacts with a pleiotropic drug resistance element in vitro","termid":"PBO:0087899"}


id: MONDO:0044214
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete androstenone, ability to smell (obsolete MONDO:0044214)","secondary_identifiers":["OMIM:105570"],"synonyms":[{"name":"ANDROSTENONE, ability to smell","type":"related"}],"termid":"MONDO:0044214","xrefs":{"Monarch":{"xref_id":"0044214"}}}


id: PBO:0035831
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_H4_acetylation_during_vegetative_growth","termid":"PBO:0035831"}


id: PBO:0084324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Karyopherin/importin that interacts with the nuclear pore complex; acts as the nuclear import receptor for specific proteins, including Pdr1p, Yap1p, Ste12p, and Aft1p; required for stability of the Dam1p-Duo1p complex","termid":"PBO:0084324"}


id: GO:1900543
data:
  {"annotated_genes":["SJAG_00685","SJAG_05314"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72412,75326],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of purine nucleotide metabolic process.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of nucleotide metabolic process","termid":"GO:0045980"},{"relation_name":"is_a","term_name":"regulation of purine nucleotide metabolic process","termid":"GO:1900542"},{"relation_name":"negatively_regulates","term_name":"purine nucleotide metabolic process","termid":"GO:0006163"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00685":null,"SJAG_05314":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"negative regulation of purine nucleotide metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"down regulation of purine metabolic process","type":"narrow"},{"name":"down regulation of purine metabolism","type":"narrow"},{"name":"down regulation of purine nucleotide metabolic process","type":"exact"},{"name":"down regulation of purine nucleotide metabolism","type":"exact"},{"name":"down-regulation of purine metabolic process","type":"narrow"},{"name":"down-regulation of purine metabolism","type":"narrow"},{"name":"down-regulation of purine nucleotide metabolic process","type":"exact"},{"name":"down-regulation of purine nucleotide metabolism","type":"exact"},{"name":"downregulation of purine metabolic process","type":"narrow"},{"name":"downregulation of purine metabolism","type":"narrow"},{"name":"downregulation of purine nucleotide metabolic process","type":"exact"},{"name":"downregulation of purine nucleotide metabolism","type":"exact"},{"name":"inhibition of purine metabolic process","type":"narrow"},{"name":"inhibition of purine metabolism","type":"narrow"},{"name":"inhibition of purine nucleotide metabolic process","type":"narrow"},{"name":"inhibition of purine nucleotide metabolism","type":"narrow"},{"name":"negative regulation of purine metabolic process","type":"narrow"},{"name":"negative regulation of purine metabolism","type":"narrow"},{"name":"negative regulation of purine nucleotide metabolism","type":"exact"}],"termid":"GO:1900543","terms_by_termid":{"GO:0045820":null}}


id: GO:1903090
data:
  {"annotated_genes":["SJAG_02962","SJAG_03652","SJAG_02152","SJAG_03808"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89345,89346,116599,117873],"is_not":false,"summary":null,"term":"GO:1903090"}]},"cv_name":"biological_process","definition":"The process in which pyridoxal is transported across a membrane.","definition_xrefs":["GOC:TermGenie","GO_REF:0000069","PMID:15701794"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyridoxal transport","termid":"GO:0031920"},{"relation_name":"is_a","term_name":"vitamin transmembrane transport","termid":"GO:0035461"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02152":null,"SJAG_02962":null,"SJAG_03652":null,"SJAG_03808":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0055085","GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"pyridoxal transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1903090","terms_by_termid":{"GO:1903090":null}}


id: PBO:0052019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"jumonji domain containing 8","termid":"PBO:0052019"}


id: PBO:0040801
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 e23","termid":"PBO:0040801"}


id: PBO:0043144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 12","termid":"PBO:0043144"}


id: GO:0071464
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 hydrostatic pressure stimulus. Hydrostatic pressure is the force acting on an object in a system where the fluid is at rest (as opposed to moving). The weight of the fluid above the object creates pressure on it.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to hydrostatic pressure","termid":"GO:0051599"},{"relation_name":"is_a","term_name":"cellular response to chemical stress","termid":"GO:0062197"},{"relation_name":"is_a","term_name":"cellular response to water stimulus","termid":"GO:0071462"}],"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 hydrostatic pressure","synonyms":[{"name":"cellular response to biomechanical stress","type":"broad"},{"name":"cellular response to static fluid pressure","type":"exact"}],"termid":"GO:0071464"}


id: PBO:0076864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 13B","termid":"PBO:0076864"}


id: MONDO:0008266
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"postaxial polydactyly type A","termid":"MONDO:0019673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polydactyly, postaxial, type A1","secondary_identifiers":["MEDGEN:924305","OMIM:174200","UMLS:C4282400","GARD:4414"],"synonyms":[{"name":"PAPA1","type":"related"},{"name":"polydactyly, postaxial","type":"related"},{"name":"polydactyly, postaxial, type A1","type":"exact"},{"name":"polydactyly, postaxial, types A1 and B","type":"exact"},{"name":"postaxial polydactyly, type A","type":"related"},{"name":"postaxial polydactyly, type B","type":"related"}],"termid":"MONDO:0008266","xrefs":{"Monarch":{"xref_id":"0008266"}}}


id: GO:0098027
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The external contractile envelope of the tail of some viruses. Its contraction ensures ejection of the virus DNA into the host cytoplasm.","definition_xrefs":["GOC:bm","VZ:3959"],"direct_ancestors":[{"relation_name":"is_a","term_name":"virion component","termid":"GO:0044423"},{"relation_name":"part_of","term_name":"virus tail","termid":"GO:0098015"}],"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":"virus tail, sheath","synonyms":[{"name":"bacteriophage tail sheath","type":"narrow"}],"termid":"GO:0098027"}


id: PBO:0041297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C2 calcium dependent domain containing 4A","termid":"PBO:0041297"}


id: PBO:0086163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for ribosomal large subunit maturation; functionally redundant with Ssf1p; member of the Brix family; SSF2 has a paralog, SSF1, that arose from the whole genome duplication","termid":"PBO:0086163"}


id: GO:0030641
data:
  {"annotated_genes":["SJAG_00301","SJAG_03962","SJAG_01913","SJAG_05294","SJAG_02470","SJAG_02716","SJAG_00212","SJAG_04616","SJAG_02023","SJAG_01129","SJAG_00516","SJAG_00136","SJAG_01397","SJAG_04955","SJAG_01669","SJAG_04258","SJAG_01817"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99695],"is_not":false,"summary":null,"term":"GO:0030641"},{"annotations":[86910,98020,112902,86911],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051453"},{"annotations":[101168,95029,89052,98112,87249,99201,94849,117852,89368,103086,100822,88525],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007035"}]},"cv_name":"biological_process","definition":"Any process involved in the maintenance of an internal equilibrium of hydrogen ions (protons) within a cell or between a cell and its external environment.","definition_xrefs":["GOC:mah","GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of pH","termid":"GO:0006885"},{"relation_name":"is_a","term_name":"intracellular monoatomic cation homeostasis","termid":"GO:0030003"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00136":null,"SJAG_00212":null,"SJAG_00301":null,"SJAG_00516":null,"SJAG_01129":null,"SJAG_01397":null,"SJAG_01669":null,"SJAG_01817":null,"SJAG_01913":null,"SJAG_02023":null,"SJAG_02470":null,"SJAG_02716":null,"SJAG_03962":null,"SJAG_04258":null,"SJAG_04616":null,"SJAG_04955":null,"SJAG_05294":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cellular pH","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"cellular hydrogen ion homeostasis","type":"exact"},{"name":"proton homeostasis","type":"exact"}],"termid":"GO:0030641","terms_by_termid":{"GO:0007035":null,"GO:0030641":null,"GO:0051453":null}}


id: PBO:0065870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB27A, member RAS oncogene family","termid":"PBO:0065870"}


id: PBO:0050342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 44","termid":"PBO:0050342"}


id: PBO:0063381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"programmed cell death 1 ligand 2","termid":"PBO:0063381"}


id: GO:0034432
data:
  {"annotated_genes":["SJAG_04870"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[87927],"is_not":false,"summary":null,"term":"GO:0034432"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: P1-P6-bis(5'-adenosyl) pentaphosphate + H2O = AMP + adenosine 5'-tetraphosphate.","definition_xrefs":["PMID:9450008","PMID:10085096"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04870":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"bis(5'-adenosyl)-pentaphosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"AP(5)A hydrolase activity","type":"exact"},{"name":"AP-5-A hydrolase activity","type":"exact"},{"name":"AP5A hydrolase activity","type":"exact"},{"name":"Ap5a pyrophosphohydrolase activity","type":"exact"},{"name":"diadenosine 5',5'''-P1,P6-pentaphosphate hydrolase activity","type":"exact"}],"termid":"GO:0034432","terms_by_termid":{"GO:0034432":null}}


id: PBO:0070450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L3 pseudogene 7","termid":"PBO:0070450"}


id: GO:0034182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the extent to which the association between sister chromatids of a replicated chromosome is maintained during a mitotic cell cycle.","definition_xrefs":["GOC:vw","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of maintenance of sister chromatid cohesion","termid":"GO:0034091"},{"relation_name":"regulates","term_name":"maintenance of mitotic sister chromatid cohesion","termid":"GO:0034088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of maintenance of mitotic sister chromatid cohesion","termid":"GO:0034182"}


id: PBO:0045128
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DMXL1 divergent transcript","termid":"PBO:0045128"}


id: PBO:0027155
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_vacuolar_glutamine_level","termid":"PBO:0027155"}


id: PBO:0064501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit D","termid":"PBO:0064501"}


id: MONDO:0007932
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An age related macular degeneration conferred by variation in the ABCA4 gene on chromosome 1p22.","definition_xrefs":["PMID:10396622","DOID:0110015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"age-related macular degeneration","termid":"MONDO:0005150"}],"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":"age related macular degeneration 2","secondary_identifiers":["MESH:C562479","MEDGEN:501183","OMIM:153800","UMLS:C3495438"],"synonyms":[{"name":"ARMD2","type":"exact"},{"name":"age related macular degeneration type 2","type":"exact"},{"name":"macular Degeneration, Senile","type":"related"},{"name":"macular Degeneration, age-related, type 2","type":"exact"},{"name":"macular degeneration, age-related, 2","type":"related"},{"name":"maculopathy, age-related, 2","type":"related"}],"termid":"MONDO:0007932","xrefs":{"Monarch":{"xref_id":"0007932"}}}


id: PBO:0059194
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAS related GPR family member X1","termid":"PBO:0059194"}


id: PBO:0031263
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_DNA_recombination_at_mitotic_DNA_replication_fork_barriers","termid":"PBO:0031263"}


id: MONDO:0002500
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete gliosarcoma (obsolete MONDO:0002500)","termid":"MONDO:0002500","xrefs":{"Monarch":{"xref_id":"0002500"}}}


id: GO:0043936
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a cellular spore derived from the products of mitosis. A cellular spore is a cell form that can be used for dissemination, for survival of adverse conditions because of its heat and desiccation resistance, and/or for reproduction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sporulation resulting in formation of a cellular spore","termid":"GO:0030435"},{"relation_name":"is_a","term_name":"asexual sporulation","termid":"GO:0030436"}],"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":"asexual sporulation resulting in formation of a cellular spore","synonyms":[{"name":"asexual reproduction resulting in the formation of a cellular spore","type":"exact"},{"name":"asexual sporulation resulting in the formation of a viable spore","type":"broad"}],"termid":"GO:0043936"}


id: PBO:0004307
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"target of chaperonin-containing T-complex","termid":"PBO:0004307"}


id: GO:1905235
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a quercetin stimulus.","definition_xrefs":["GOC:TermGenie","PMID:24914722","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to flavonoid","termid":"GO:1905395"}],"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 quercetin","termid":"GO:1905235"}


id: GO:1990013
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A hexagonal array of electron dense particles attached to the cytoplasmic face of the presynaptic membrane.","definition_xrefs":["NIF_Subcellular:sao1730664005","ISBN:0716723808"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"presynaptic active zone","termid":"GO:0048786"}],"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":"presynaptic grid","synonyms":[{"name":"pre-synaptic grid","type":"exact"}],"termid":"GO:1990013"}


id: PR:O14026
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- set2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14026"],"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":"histone-lysine N-methyltransferase, H3 lysine-36 specific (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29B12.02c","synonyms":[{"name":"SET domain-containing protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-set2","type":"exact"},{"name":"lysine N-methyltransferase 3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14026"}


id: PBO:0063881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol glycan anchor biosynthesis class K","termid":"PBO:0063881"}


id: PBO:0060913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurofibromin 1","termid":"PBO:0060913"}


id: PBO:0078721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Leu (anticodon TAG) 1-1","termid":"PBO:0078721"}


id: GO:0140403
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process mediated by a molecule secreted by a symbiont that results in the suppression of a host innate immune response. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:21467214","PMID:30584105"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host innate immune response","termid":"GO:0052170"},{"relation_name":"is_a","term_name":"effector-mediated perturbation of host innate immune response by symbiont","termid":"GO:0140404"},{"relation_name":"is_a","term_name":"effector-mediated suppression of host defense response","termid":"GO:0140590"}],"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":"effector-mediated suppression of host innate immune response","synonyms":[{"name":"effector dependent suppression of host immune innate response by symbiont","type":"exact"},{"name":"effector triggered suppression of host immune innate response by symbiont","type":"exact"},{"name":"effector-dependent suppression of host immune innate response by symbiont","type":"exact"},{"name":"effector-mediated suppression of host immune innate response by symbiont","type":"exact"},{"name":"effector-mediated suppression of host innate immune response by symbiont","type":"exact"},{"name":"effector-mediated suppression of host innate immunity","type":"exact"},{"name":"effector-triggered suppression of host immune innate response by symbiont","type":"exact"}],"termid":"GO:0140403"}


id: GO:1904855
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a proteasome regulatory particle.","definition_xrefs":["GOC:TermGenie","PMID:16096059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex binding","termid":"GO:0044877"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"proteasome regulatory particle binding","synonyms":[{"name":"19S regulatory particle binding","type":"narrow"},{"name":"PA700 proteasome activator binding","type":"narrow"},{"name":"PA700-dependent proteasome activator binding","type":"exact"},{"name":"modulator complex binding","type":"related"}],"termid":"GO:1904855"}


id: PBO:0065325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 48","termid":"PBO:0065325"}


id: PBO:0038819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 22","termid":"PBO:0038819"}


id: SO:0001358
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"5_carboxyhydroxymethyl_uridine is a modified uridine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_uridine","termid":"SO:0001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_carboxyhydroxymethyl_uridine","secondary_identifiers":["RNAMOD:066"],"synonyms":[{"name":"5-(carboxyhydroxymethyl)uridine","type":"exact"},{"name":"chm5U","type":"exact"},{"name":"five carboxyhydroxymethyl uridine","type":"exact"}],"termid":"SO:0001358"}


id: GO:0050057
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucose + 2-hydroxy-2-methylpropanenitrile = UDP + linamarin.","definition_xrefs":["EC:2.4.1.63","MetaCyc:LINAMARIN-SYNTHASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glycosyltransferase activity","termid":"GO:0008194"},{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"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:0016740"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016757","GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"linamarin synthase activity","secondary_identifiers":["RHEA:20009"],"synonyms":[{"name":"UDP glucose ketone cyanohydrin glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:2-hydroxy-2-methylpropanenitrile beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:2-hydroxy-2-methylpropanenitrile beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:ketone cyanohydrin beta-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphate-glucose-ketone cyanohydrin beta-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-ketone cyanohydrin glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-ketone glucosyltransferase activity","type":"related"}],"termid":"GO:0050057"}


id: MONDO:0006975
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant myomatous neoplasm arising from smooth muscle.","definition_xrefs":["NCIT:C3751"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myomatous neoplasm","termid":"MONDO:0021545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"smooth muscle tumor","secondary_identifiers":["UMLS:C0206658","EFO:1001185","DOID:4310","MESH:D018235","MEDGEN:104911"],"synonyms":[{"name":"neoplasm of smooth muscle","type":"exact"},{"name":"neoplasm of the smooth muscle","type":"exact"},{"name":"smooth muscle neoplasm","type":"exact"},{"name":"smooth muscle tumor","type":"exact"},{"name":"tumor of smooth muscle","type":"exact"},{"name":"tumor of the smooth muscle","type":"exact"},{"name":"tumour of smooth muscle","type":"exact"},{"name":"tumour of the smooth muscle","type":"exact"}],"termid":"MONDO:0006975","xrefs":{"Monarch":{"xref_id":"0006975"}}}


id: MONDO:0019397
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"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":"unknown leukodystrophy","secondary_identifiers":["Orphanet:84096"],"termid":"MONDO:0019397","xrefs":{"Monarch":{"xref_id":"0019397"}}}


id: GO:0008553
data:
  {"annotated_genes":["SJAG_01129","SJAG_01669","SJAG_04258","SJAG_04167"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[86916,86917,112905],"is_not":false,"summary":null,"term":"GO:0008553"},{"annotations":[111486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008900"}]},"cv_name":"molecular_function","definition":"Enables the transfer of protons from one side of a membrane to the other according to the reaction: ATP + H2O + H+(in) = ADP + phosphate + H+(out). These transporters use a phosphorylative mechanism, which have a phosphorylated intermediate state during the ion transport cycle.","definition_xrefs":["RHEA:20852"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton transmembrane transporter activity","termid":"GO:0015078"},{"relation_name":"is_a","term_name":"P-type ion transporter activity","termid":"GO:0015662"},{"relation_name":"is_a","term_name":"ATPase-coupled monoatomic cation transmembrane transporter activity","termid":"GO:0019829"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01129":null,"SJAG_01669":null,"SJAG_04167":null,"SJAG_04258":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:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"P-type proton-exporting transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:3.6.3.6-RXN","GO:0036442","EC:7.1.2.1"],"synonyms":[{"name":"H+-exporting ATPase activity","type":"related"},{"name":"H+-transporting ATPase","type":"broad"},{"name":"H+-transporting ATPase activity","type":"broad"},{"name":"P-type H+-exporting ATPase activity","type":"broad"},{"name":"hydrogen exporting ATPase activity, phosphorylative mechanism","type":"exact"},{"name":"hydrogen-/sodium-translocating ATPase activity","type":"related"},{"name":"hydrogen-exporting ATPase activity","type":"broad"},{"name":"hydrogen-exporting ATPase activity, phosphorylative mechanism","type":"related"},{"name":"proton transport ATPase activity","type":"related"},{"name":"proton-exporting ATPase activity","type":"broad"},{"name":"proton-exporting ATPase activity, phosphorylative mechanism","type":"related"},{"name":"proton-translocating ATPase activity","type":"related"},{"name":"proton-transporting ATPase activity","type":"exact"}],"termid":"GO:0008553","terms_by_termid":{"GO:0008553":null,"GO:0008900":null}}


id: PBO:0081640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 567","termid":"PBO:0081640"}


id: GO:0021803
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The extension of a long process to the pial surface as a cell leaves the ventricular zone.","definition_xrefs":["GOC:cls","GOC:jid","PMID:12626695","GO_REF:0000021","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection assembly","termid":"GO:0120031"},{"relation_name":"part_of","term_name":"somal translocation","termid":"GO:0021802"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"extension of leading cell process to pial surface","termid":"GO:0021803"}


id: PBO:0085183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"One of three alternate beta-subunits of the Snf1p kinase complex; may confer substrate specificity; vacuolar protein containing KIS (Kinase-Interacting Sequence) and ASC (Association with Snf1 kinase Complex) domains involved in protein interactions","termid":"PBO:0085183"}


id: GO:0052881
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (4-hydroxyphenyl)acetate + FADH(2) + O2 = 3,4-dihydroxyphenylacetate + FAD + H+ + H2O.","definition_xrefs":["RHEA:30595"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"4-hydroxyphenylacetate 3-monooxygenase activity","secondary_identifiers":["EC:1.14.14.9","MetaCyc:RXN-8505","UM-BBD_reactionID:r0301"],"synonyms":[{"name":"4 HPA 3-hydroxylase activity","type":"broad"},{"name":"4-hydroxyphenylacetate,FADH:oxygen oxidoreductase (3-hydroxylating) activity","type":"exact"},{"name":"4-hydroxyphenylacetic acid-3-hydroxylase activity","type":"broad"},{"name":"p-hydroxyphenylacetate 3-hydroxylase (FAD) activity","type":"related"},{"name":"p-hydroxyphenylacetate 3-hydroxylase activity","type":"broad"},{"name":"p-hydroxyphenylacetate hydroxylase (FAD) activity","type":"related"},{"name":"p-hydroxyphenylacetate hydroxylase activity","type":"broad"}],"termid":"GO:0052881"}


id: GO:0004983
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with neuropeptide Y to initiate a change in cell activity.","definition_xrefs":["PMID:9315606"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide receptor activity","termid":"GO:0008188"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"neuropeptide Y receptor activity","termid":"GO:0004983"}


id: GO:0050196
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: [phosphorylase a] + 4 H2O = 2 [phosphorylase b] + 4 phosphate.","definition_xrefs":["EC:3.1.3.17","MetaCyc:PHOSPHORYLASE-PHOSPHATASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoprotein phosphatase activity","termid":"GO:0004721"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0004721","GO:0003674","GO:0016788","GO:0016787","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"[phosphorylase] phosphatase activity","synonyms":[{"name":"PR-enzyme","type":"related"},{"name":"glycogen phosphorylase phosphatase activity","type":"related"},{"name":"phosphorylase a phosphatase activity","type":"related"},{"name":"phosphorylase a phosphohydrolase activity","type":"related"},{"name":"phosphorylase phosphatase activity","type":"exact"},{"name":"protein phosphatase C","type":"related"},{"name":"type 1 protein phosphatase activity","type":"related"}],"termid":"GO:0050196"}


id: GO:0060717
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of a chorion from an initial condition to its mature state. This process begins with the formation of the structure and ends with the mature structure. The chorion is an extraembryonic membrane.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extraembryonic membrane development","termid":"GO:1903867"}],"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":"chorion development","termid":"GO:0060717"}


id: PBO:0080662
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 8","termid":"PBO:0080662"}


id: GO:0033492
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving esculetin, 6,7-dihydroxycoumarin.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coumarin metabolic process","termid":"GO:0009804"}],"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:0019748","GO:0008150"],"is_obsolete":false,"name":"esculetin metabolic process","synonyms":[{"name":"esculetin metabolism","type":"exact"}],"termid":"GO:0033492"}


id: GO:0050467
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-trans,6-trans-farnesyl diphosphate = diphosphate + pentalenene.","definition_xrefs":["EC:4.2.3.7","RHEA:18081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpene synthase activity","termid":"GO:0010334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"pentalenene synthase activity","secondary_identifiers":["KEGG_REACTION:R02305","MetaCyc:PENTALENENE-SYNTHASE-RXN"],"synonyms":[{"name":"2-trans,6-trans-farnesyl-diphosphate diphosphate-lyase (cyclizing, pentalenene-forming)","type":"related"},{"name":"2-trans,6-trans-farnesyldiphosphate diphosphate-lyase (cyclizing, pentalenene-forming)","type":"related"},{"name":"pentalenene synthetase activity","type":"related"}],"termid":"GO:0050467"}


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


id: PBO:0069225
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 480, pseudogene","termid":"PBO:0069225"}


id: PBO:0066047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAP1B pseudogene 3","termid":"PBO:0066047"}


id: PR:O14356
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tor1 gene.","definition_xrefs":["UniProtKB:O14356","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":"phosphatidylinositol 3-kinase tor1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC30D10.10c","synonyms":[{"name":"PI3-kinase tor1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PI3K tor1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"PtdIns-3-kinase tor1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-tor1","type":"exact"}],"termid":"PR:O14356"}


id: PBO:0091060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial tRNA(Ile)-lysidine synthetase Til1","termid":"PBO:0091060"}


id: PBO:0030460
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_biotin_import","termid":"PBO:0030460"}


id: PBO:0087281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Shuttling pre-60S factor; involved in the biogenesis of ribosomal large subunit; interacts directly with Arx1p; responsible for Tif6p recycling defects in absence of Rei1p","termid":"PBO:0087281"}


id: MONDO:0010663
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of X-linked syndromes characterized by severe intellectual deficit and facial dysmorphism, with variable other features.","definition_xrefs":["Orphanet:73220"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATR-X-related syndrome","termid":"MONDO:0016980"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual disability-hypotonic facies syndrome, X-linked, 1","secondary_identifiers":["MEDGEN:1676827","Orphanet:93971","Orphanet:93972","GARD:3521","Orphanet:93970","Orphanet:93973","Orphanet:93974","DOID:0080982","UMLS:C4759781","OMIM:309580","SCTID:719212004","SCTID:717763008","MESH:C537445"],"synonyms":[{"name":"Carpenter-Waziri syndrome","type":"exact"},{"name":"Chudley Lowry Hoar syndrome","type":"exact"},{"name":"Chudley intellectual disability syndrome","type":"related"},{"name":"Chudley mental retardation syndrome","type":"related"},{"name":"Chudley syndrome 1","type":"related"},{"name":"Chudley-Lowry syndrome","type":"exact"},{"name":"Chudley-Lowry-Hoar syndrome","type":"exact"},{"name":"Holmes-Gang syndrome","type":"exact"},{"name":"JMS","type":"related"},{"name":"Juberg Marsidi syndrome","type":"narrow"},{"name":"Juberg-Marsidi mental retardation syndrome","type":"narrow"},{"name":"Juberg-Marsidi syndrome","type":"narrow"},{"name":"MRXHF1","type":"exact"},{"name":"SFM1","type":"related"},{"name":"SFMS","type":"exact"},{"name":"Smith Fineman Myers syndrome 1","type":"related"},{"name":"Smith-Fineman-Myers syndrome","type":"exact"},{"name":"X-linked hypogonadism gynecomastia intellectual disability","type":"related"},{"name":"X-linked hypogonadism gynecomastia mental retardation","type":"related"},{"name":"X-linked intellectual disability-hypotonic face syndrome","type":"exact"},{"name":"XLMR-hypotonic facies syndrome","type":"exact"},{"name":"intellectual disability Smith Fineman Myers type","type":"related"},{"name":"intellectual disability, X-linked, with growth retardation, deafness, and microgenitalism","type":"related"},{"name":"intellectual disability-hypotonic facies syndrome X-linked, 1","type":"related"},{"name":"intellectual disability-hypotonic facies syndrome, X-linked, 1","type":"exact"},{"name":"intellectual disability-hypotonic facies syndrome, X-linked, type 1","type":"exact"},{"name":"mental retardation Smith Fineman Myers type","type":"related"},{"name":"mental retardation, X-linked, with growth retardation, deafness, and microgenitalism","type":"related"},{"name":"mental retardation-hypotonic facies syndrome X-linked, 1","type":"related"},{"name":"mental retardation-hypotonic facies syndrome, X-linked, 1","type":"related"},{"name":"mental retardation-hypotonic facies syndrome, X-linked, X-linked recessive","type":"exact"},{"name":"mental retardation-hypotonic facies syndrome, X-linked, type 1","type":"exact"},{"name":"mental retradation, X-linked with Growth delay, deafness, microgenitalism","type":"related"}],"termid":"MONDO:0010663","xrefs":{"Monarch":{"xref_id":"0010663"}}}


id: GO:0006493
data:
  {"annotated_genes":["SJAG_03150","SJAG_04095","SJAG_00598","SJAG_03149","SJAG_01021","SJAG_01264","SJAG_04906","SJAG_00183","SJAG_01491","SJAG_04053","SJAG_04316"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[78763,97961,99951,101899,103258,103686,109849,109855,117174,117501],"is_not":false,"summary":null,"term":"GO:0006493"},{"annotations":[92234,100726,105124],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035269"}]},"cv_name":"biological_process","definition":"A protein glycosylation process in which a carbohydrate or carbohydrate derivative unit is added to a protein via the hydroxyl group of peptidyl-serine, peptidyl-threonine, peptidyl-hydroxylysine, or peptidyl-hydroxyproline, or via the phenol group of peptidyl-tyrosine, forming an O-glycan.","definition_xrefs":["PMID:33775405","ISBN:0879695595","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein glycosylation","termid":"GO:0006486"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00183":null,"SJAG_00598":null,"SJAG_01021":null,"SJAG_01264":null,"SJAG_01491":null,"SJAG_03149":null,"SJAG_03150":null,"SJAG_04053":null,"SJAG_04095":null,"SJAG_04316":null,"SJAG_04906":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006486"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006486","GO:0008150"],"is_obsolete":false,"name":"protein O-linked glycosylation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["RESID:AA0212","RESID:AA0155","RESID:AA0157","RESID:AA0154","RESID:AA0153"],"synonyms":[{"name":"protein amino acid O-linked glycosylation","type":"exact"}],"termid":"GO:0006493","terms_by_termid":{"GO:0006493":null,"GO:0035269":null}}


id: FYPO:0004207
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of mature siRNA measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased ncRNA level during vegetative growth","termid":"FYPO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0006551","FYPO:0001320"],"is_obsolete":false,"name":"increased siRNA level","synonyms":[{"name":"increased mature siRNA level","type":"exact"},{"name":"increased siRNA accumulation","type":"related"},{"name":"increased siRNA level during mitotic cell cycle","type":"related"},{"name":"increased siRNA level during vegetative growth","type":"exact"},{"name":"increased siRNA transcript level","type":"exact"},{"name":"increased small interfering RNA level","type":"exact"}],"termid":"FYPO:0004207"}


id: MONDO:0012230
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 10","secondary_identifiers":["OMIM:609259","UMLS:C1836503","MEDGEN:373104","MESH:C563758"],"synonyms":[{"name":"MYP10","type":"exact"},{"name":"myopia 10","type":"exact"}],"termid":"MONDO:0012230","xrefs":{"Monarch":{"xref_id":"0012230"}}}


id: MONDO:0019511
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autosomal dominant medullary cystic kidney disease with hyperuricemia (obsolete MONDO:0019511)","termid":"MONDO:0019511","xrefs":{"Monarch":{"xref_id":"0019511"}}}


id: GO:0042264
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The hydroxylation of peptidyl-aspartic acid to form peptidyl-hydroxyaspartic acid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein hydroxylation","termid":"GO:0018126"},{"relation_name":"is_a","term_name":"peptidyl-aspartic acid modification","termid":"GO:0018197"}],"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-aspartic acid hydroxylation","synonyms":[{"name":"peptidyl-aspartic acid/asparagine hydroxylation","type":"broad"}],"termid":"GO:0042264"}


id: PBO:0041851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase 1 pseudogene 1","termid":"PBO:0041851"}


id: GO:0010619
data:
  {"annotated_genes":["SJAG_04026","SJAG_00574","SJAG_04312","SJAG_02444","SJAG_01699","SJAG_00472","SJAG_00266","SJAG_01254","SJAG_03081","SJAG_01754","SJAG_02426","SJAG_01245","SJAG_02481","SJAG_02311"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93427,101032,105065,105654,106003,108163,108669,114664,115696],"is_not":false,"summary":null,"term":"GO:0010619"},{"annotations":[91288,99626,115516,107126,91947],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:0110034"}]},"cv_name":"biological_process","definition":"An adenylate cyclase-activating G protein-coupled receptor signaling pathway initiated by glucose binding to its receptor on the surface of the target cell, and ending with the regulation of a downstream cellular process.","definition_xrefs":["GOC:signaling","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenylate cyclase-activating G protein-coupled receptor signaling pathway","termid":"GO:0007189"},{"relation_name":"part_of","term_name":"glucose mediated signaling pathway","termid":"GO:0010255"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00266":null,"SJAG_00472":null,"SJAG_00574":null,"SJAG_01245":null,"SJAG_01254":null,"SJAG_01699":null,"SJAG_01754":null,"SJAG_02311":null,"SJAG_02426":null,"SJAG_02444":null,"SJAG_02481":null,"SJAG_03081":null,"SJAG_04026":null,"SJAG_04312":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"adenylate cyclase-activating glucose-activated G protein-coupled receptor signaling pathway","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of adenylate cyclase activity by glucose involved in G-protein signaling","type":"exact"},{"name":"activation of adenylate cyclase activity by glucose-triggered G-protein signaling pathway","type":"exact"},{"name":"activation of adenylate cyclase activity by glucose-triggered G-protein signalling pathway","type":"exact"},{"name":"glucose-sensing PKA pathway","type":"exact"}],"termid":"GO:0010619","terms_by_termid":{"GO:0010619":null,"GO:0110034":null}}


id: GO:2001005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of pectin catabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of catabolic process","termid":"GO:0009896"},{"relation_name":"is_a","term_name":"positive regulation of macromolecule metabolic process","termid":"GO:0010604"},{"relation_name":"is_a","term_name":"positive regulation of carbohydrate metabolic process","termid":"GO:0045913"},{"relation_name":"is_a","term_name":"regulation of pectin catabolic process","termid":"GO:2001003"},{"relation_name":"positively_regulates","term_name":"pectin catabolic process","termid":"GO:0045490"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"positive regulation of pectin catabolic process","synonyms":[{"name":"positive regulation of pectin breakdown","type":"exact"},{"name":"positive regulation of pectin catabolism","type":"exact"},{"name":"positive regulation of pectin degradation","type":"exact"}],"termid":"GO:2001005"}


id: PBO:0085355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphomannomutase; involved in synthesis of GDP-mannose and dolichol-phosphate-mannose; required for folding and glycosylation of secretory proteins in the ER lumen; human homolog PMM2 complements yeast mutants","termid":"PBO:0085355"}


id: MONDO:0043096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital acardia","termid":"MONDO:0022357"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"holoacardius amorphus","secondary_identifiers":["SCTID:41049003","UMLS:C0266719","Orphanet:2161","MEDGEN:75621","GARD:2720"],"synonyms":[{"name":"Holoacardius amorphus","type":"exact"},{"name":"amorphous globosus","type":"related"},{"name":"amorphus globosus","type":"related"},{"name":"fetus anideus","type":"related"},{"name":"foetus anideus","type":"related"}],"termid":"MONDO:0043096","xrefs":{"Monarch":{"xref_id":"0043096"}}}


id: MONDO:0004321
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenocarcinoma that arises from the endometrium and is characterized by the presence of both type I and type II endometrial adenocarcinoma components. The minor component constitutes at least 5% of the entire tumor.","definition_xrefs":["NCIT:C40153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endometrium adenocarcinoma","termid":"MONDO:0005461"}],"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":"endometrial mixed adenocarcinoma","secondary_identifiers":["DOID:7664","UMLS:C4745252","icd11.foundation:575106861","MEDGEN:1670192"],"synonyms":[{"name":"endometrial mixed adenocarcinoma","type":"exact"}],"termid":"MONDO:0004321","xrefs":{"Monarch":{"xref_id":"0004321"}}}


id: GO:0035100
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to 20-hydroxyecdysone (ecdysone). Ecdysone is an ecdysteroid produced by the prothoracic glands of immature insects and the ovaries of adult females, which stimulates growth and molting.","definition_xrefs":["GOC:bf","ISBN:0582227089","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sterol binding","termid":"GO:0032934"},{"relation_name":"is_a","term_name":"hormone binding","termid":"GO:0042562"},{"relation_name":"is_a","term_name":"alcohol binding","termid":"GO:0043178"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0008289"],"is_obsolete":false,"name":"ecdysone binding","termid":"GO:0035100"}


id: GO:1901213
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of transcription from an RNA polymerase II promoter that contributes to the development of the heart over time.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transcription from RNA polymerase II promoter involved in heart development (obsolete GO:1901213)","synonyms":[{"name":"global transcription regulation from Pol II promoter involved in cardiac development","type":"related"},{"name":"global transcription regulation from Pol II promoter involved in dorsal vessel development","type":"related"},{"name":"global transcription regulation from Pol II promoter involved in heart development","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter involved in cardiac development","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter involved in dorsal vessel development","type":"related"},{"name":"regulation of gene-specific transcription from RNA polymerase II promoter involved in heart development","type":"related"},{"name":"regulation of global transcription from Pol II promoter involved in cardiac development","type":"related"},{"name":"regulation of global transcription from Pol II promoter involved in dorsal vessel development","type":"related"},{"name":"regulation of global transcription from Pol II promoter involved in heart development","type":"related"},{"name":"regulation of transcription from Pol II promoter involved in cardiac development","type":"related"},{"name":"regulation of transcription from Pol II promoter involved in dorsal vessel development","type":"narrow"},{"name":"regulation of transcription from Pol II promoter involved in heart development","type":"exact"},{"name":"regulation of transcription from RNA polymerase II promoter involved in cardiac development","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter involved in dorsal vessel development","type":"narrow"},{"name":"regulation of transcription from RNA polymerase II promoter, global involved in cardiac development","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter, global involved in dorsal vessel development","type":"related"},{"name":"regulation of transcription from RNA polymerase II promoter, global involved in heart development","type":"related"}],"termid":"GO:1901213"}


id: GO:0044432
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. Any constituent part of the endoplasmic reticulum, the irregular network of unit membranes, visible only by electron microscopy, that occurs in the cytoplasm of many eukaryotic cells. The membranes form a complex meshwork of tubular channels, which are often expanded into slitlike cavities called cisternae.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete endoplasmic reticulum part (obsolete GO:0044432)","synonyms":[{"name":"ER component","type":"exact"}],"termid":"GO:0044432"}


id: SO:1000047
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A chromosomal inversion that does not include the centromere.","definition_xrefs":["FB:reference_manual"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"paracentric","termid":"SO:0001519"},{"relation_name":"is_a","term_name":"chromosomal_inversion","termid":"SO:1000030"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paracentric_inversion","synonyms":[{"name":"paracentric inversion","type":"exact"}],"termid":"SO:1000047"}


id: GO:0070127
data:
  {"annotated_genes":["SJAG_02428","SJAG_04840","SJAG_01352","SJAG_02977","SJAG_01797","SJAG_04094","SJAG_00653"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070143"},{"annotations":[106378],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070144"},{"annotations":[117178],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070146"},{"annotations":[96202],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070150"},{"annotations":[93864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070158"},{"annotations":[96488],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070183"},{"annotations":[96862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070185"}]},"cv_name":"biological_process","definition":"The synthesis of aminoacyl tRNA by the formation of an ester bond between the 3'-hydroxyl group of the most 3' adenosine of the tRNA, to be used in ribosome-mediated polypeptide synthesis in a mitochondrion.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial RNA metabolic process","termid":"GO:0000959"},{"relation_name":"is_a","term_name":"tRNA aminoacylation for protein translation","termid":"GO:0006418"},{"relation_name":"part_of","term_name":"mitochondrial translation","termid":"GO:0032543"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00653":null,"SJAG_01352":null,"SJAG_01797":null,"SJAG_02428":null,"SJAG_02977":null,"SJAG_04094":null,"SJAG_04840":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0140053"}],"interesting_parent_ids":["GO:0140053","GO:0006399","GO:0006520","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"tRNA aminoacylation for mitochondrial protein translation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0070127","terms_by_termid":{"GO:0070143":null,"GO:0070144":null,"GO:0070146":null,"GO:0070150":null,"GO:0070158":null,"GO:0070183":null,"GO:0070185":null}}


id: GO:1905805
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of an excitatory synapse into its constituent components.","definition_xrefs":["PMID:27779093","GO_REF:0000079","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synapse pruning","termid":"GO:0098883"}],"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":"excitatory synapse pruning","synonyms":[{"name":"synapse clearance","type":"broad"},{"name":"synapse disassembly","type":"broad"},{"name":"synapse elimination","type":"broad"},{"name":"synapse removal","type":"broad"}],"termid":"GO:1905805"}


id: GO:0014896
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The muscle system process that results in enlargement or overgrowth of all or part of a muscle organ due to an increase in the size of its muscle cells. Physiological hypertrophy is a normal process during development (it stops in cardiac muscle after adolescence) and can also be brought on in response to demand. In athletes cardiac and skeletal muscles undergo hypertrophy stimulated by increasing muscle activity on exercise. Smooth muscle cells in the uterus undergo hypertrophy during pregnancy.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"muscle system process","termid":"GO:0003012"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"muscle hypertrophy","secondary_identifiers":["Wikipedia:Muscle_hypertrophy"],"termid":"GO:0014896"}


id: GO:1905092
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a diosgenin stimulus.","definition_xrefs":["GOC:BHF_miRNA","GOC:BHF","GOC:TermGenie","PMID:25765596","GOC:bc","GO_REF:0000071"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to sterol","termid":"GO:0036314"},{"relation_name":"is_a","term_name":"response to alcohol","termid":"GO:0097305"},{"relation_name":"is_a","term_name":"response to triterpenoid","termid":"GO:1905836"}],"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 diosgenin","termid":"GO:1905092"}


id: MONDO:0016012
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diethylstilbestrol (DES) syndrome is a malformation syndrome reported in offspring (children and grandchildren) of women exposed to DES during pregnancy and is characterized by reproductive tract malformations, decreased fertility and increased risk of developing clear cell carcinoma of the vagina and cervix in young women. Reproductive malformations reported in DES syndrome include small, T-shaped uteri and other uterotubal anomalies that increase the risk of miscarriages in women and epididymal cysts, microphallus, cryptorchidism, or testicular hypoplasia in men. DES, a synthetic nonsteroidal estrogen was widely prescribed from 1940-1970 to prevent miscarriage.","definition_xrefs":["Orphanet:1916"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive system disorder","termid":"MONDO:0005039"},{"relation_name":"is_a","term_name":"toxic or drug-related embryofetopathy","termid":"MONDO:0016677"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diethylstilbestrol syndrome","secondary_identifiers":["NCIT:C113422","GARD:1859","MedDRA:10012780","MEDGEN:799290","icd11.foundation:1134098724","SCTID:716005004","UMLS:C0853695"],"synonyms":[{"name":"DES embryofetopathy","type":"exact"},{"name":"DES syndrome","type":"exact"},{"name":"Distilbene embryofetopathy","type":"exact"},{"name":"antenatal diethylstilbestrol exposure","type":"related"},{"name":"diethylstilbestrol embryofetopathy","type":"exact"},{"name":"fetal diethylstilbestrol syndrome","type":"related"},{"name":"foetal diethylstilbestrol syndrome","type":"related"}],"termid":"MONDO:0016012","xrefs":{"Monarch":{"xref_id":"0016012"}}}


id: FYPO:0003775
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of DNA recombination between cDNAs derived from transposon-encoded genes is decreased.","definition_xrefs":["PMID:10022921","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased DNA recombination","termid":"FYPO:0002712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased transposon-derived cDNA recombination","synonyms":[{"name":"decreased recombination of transposon-derived cDNAs","type":"exact"},{"name":"decreased transposon-derived cDNA recombination frequency","type":"exact"},{"name":"decreased transposon-derived cDNA recombination rate","type":"related"},{"name":"reduced transposon-derived cDNA recombination","type":"exact"}],"termid":"FYPO:0003775"}


id: PBO:0053906
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 1198","termid":"PBO:0053906"}


id: PR:Q9P7C8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA replication complex GINS protein SLD5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR21206:SF0","OMA:SCHPO03471","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":"DNA replication complex GINS protein sld5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP4H10.21c","secondary_identifiers":["UniProtKB:Q9P7C8"],"synonyms":[{"name":"Spom972h-GINS4","type":"exact"}],"termid":"PR:Q9P7C8"}


id: GO:0050212
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: AH2 + O2 + progesterone = 11alpha-hydroxyprogesterone + A + H2O.","definition_xrefs":["RHEA:18205"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progesterone monooxygenase activity","termid":"GO:0050214"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"progesterone 11-alpha-monooxygenase activity","secondary_identifiers":["KEGG_REACTION:R02214","MetaCyc:PROGESTERONE-11-ALPHA-MONOOXYGENASE-RXN","EC:1.14.99.14"],"synonyms":[{"name":"progesterone 11-alpha-hydroxylase activity","type":"related"},{"name":"progesterone 11a-monooxygenase activity","type":"exact"},{"name":"progesterone 11alpha-hydroxylase activity","type":"related"},{"name":"progesterone 11alpha-monooxygenase activity","type":"related"},{"name":"progesterone,hydrogen-donor:oxygen oxidoreductase (11alpha-hydroxylating)","type":"related"}],"termid":"GO:0050212"}


id: PBO:0060458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAIP pseudogene 1","termid":"PBO:0060458"}


id: PBO:0066931
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 233","termid":"PBO:0066931"}


id: FYPO:0008289
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which a guanyl-nucleotide exchange factor activity is abnormal.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000661","FYPO:0001985","FYPO:0000654","FYPO:0000707"],"is_obsolete":false,"name":"abnormal guanyl-nucleotide exchange factor activity","synonyms":[{"name":"abnormal GEF activity","type":"exact"}],"termid":"FYPO:0008289"}


id: PBO:0068056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 361","termid":"PBO:0068056"}


id: MONDO:0031169
data:
  {"annotated_genes":["SJAG_04528"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84430],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100325"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondylometaphyseal dysplasia","termid":"MONDO:0016763"},{"relation_name":"is_a","term_name":"TRIP11-related skeletal dysplasia","termid":"MONDO:1040009"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04528":null},"genotype_count":0,"is_obsolete":false,"name":"odontochondrodysplasia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:411198","OMIMPS:184260","UMLS:C2745953"],"termid":"MONDO:0031169","terms_by_termid":{"MONDO:0100325":null},"xrefs":{"Monarch":{"xref_id":"0031169"}}}


id: GO:2000005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of metanephric S-shaped body morphogenesis.","definition_xrefs":["GOC:obol","GOC:mtg_kidney_jan10","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"regulation of metanephric S-shaped body morphogenesis","termid":"GO:2000004"},{"relation_name":"negatively_regulates","term_name":"metanephric S-shaped body morphogenesis","termid":"GO:0072284"}],"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 metanephric S-shaped body morphogenesis","termid":"GO:2000005"}


id: PBO:0011468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved eukaryotic protein, thioredoxin family","termid":"PBO:0011468"}


id: GO:0031945
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving glucocorticoids.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glucocorticoid metabolic process","termid":"GO:0031943"},{"relation_name":"is_a","term_name":"positive regulation of hormone metabolic process","termid":"GO:0032352"},{"relation_name":"is_a","term_name":"positive regulation of steroid metabolic process","termid":"GO:0045940"},{"relation_name":"positively_regulates","term_name":"glucocorticoid metabolic process","termid":"GO:0008211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"positive regulation of glucocorticoid metabolic process","synonyms":[{"name":"activation of glucocorticoid metabolic process","type":"narrow"},{"name":"positive regulation of glucocorticoid metabolism","type":"exact"},{"name":"stimulation of glucocorticoid metabolic process","type":"narrow"},{"name":"up regulation of glucocorticoid metabolic process","type":"exact"},{"name":"up-regulation of glucocorticoid metabolic process","type":"exact"},{"name":"upregulation of glucocorticoid metabolic process","type":"exact"}],"termid":"GO:0031945"}


id: MONDO:0018757
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Supratip dysplasia is a rare, congenital, non-syndromic, nose and cavum malformation characterized by the presence of a bulbous, soft tissue hypertrophy located in the middle-to-distal third of the nasal dorsum, in association with deformed, slightly laterally- and caudally-placed nasal alae and a scar-like atrophic skin lesion located at the nasal tip. Respiratory function is not affected.","definition_xrefs":["Orphanet:466695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"otorhinolaryngologic disease","termid":"MONDO:0024623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"supratip dysplasia","secondary_identifiers":["UMLS:C5681127","GARD:21941","MEDGEN:1807664"],"termid":"MONDO:0018757","xrefs":{"Monarch":{"xref_id":"0018757"}}}


id: GO:2000100
data:
  {"annotated_genes":["SJAG_00333","SJAG_04461","SJAG_00661","SJAG_00596","SJAG_03637","SJAG_02022","SJAG_00236","SJAG_03581","SJAG_01799","SJAG_00845"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90344,93782,94858,99364,103710,104521,112184,117910],"is_not":false,"summary":null,"term":"GO:2000100"},{"annotations":[99361,92937,104518,102879],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000247"},{"annotations":[102880],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061361"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of establishment or maintenance of bipolar cell polarity regulating cell shape.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of establishment or maintenance of bipolar cell polarity","termid":"GO:2000099"},{"relation_name":"is_a","term_name":"regulation of establishment or maintenance of cell polarity regulating cell shape","termid":"GO:2000769"},{"relation_name":"regulates","term_name":"establishment or maintenance of bipolar cell polarity regulating cell shape","termid":"GO:0061246"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00236":null,"SJAG_00333":null,"SJAG_00596":null,"SJAG_00661":null,"SJAG_00845":null,"SJAG_01799":null,"SJAG_02022":null,"SJAG_03581":null,"SJAG_03637":null,"SJAG_04461":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007163"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007163","GO:0008150"],"is_obsolete":false,"name":"regulation of establishment or maintenance of bipolar cell polarity regulating cell shape","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:2000100","terms_by_termid":{"GO:0061361":null,"GO:2000100":null,"GO:2000247":null}}


id: MONDO:1012007
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"alloimmune hemolytic anemia of the newborn, non-human animal","termid":"MONDO:1011684"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alloimmune hemolytic anemia of the newborn, horse","secondary_identifiers":["OMIA:000028-9796"],"termid":"MONDO:1012007","xrefs":{"Monarch":{"xref_id":"1012007"}}}


id: PBO:0056354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP7 domain containing 3","termid":"PBO:0056354"}


id: MONDO:0004703
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Also known as carcinoma in situ of the urinary bladder or high grade intraurothelial neoplasia, this is a flat lesion of the transitional cell epithelium characterized by severe cytologic atypia. This lesion is confined to the urothelium, and is a precursor of invasive transitional cell carcinoma of the bladder. Stage 0is includes: Tis, N0, M0. Tis: Carcinoma in situ: \\\"flat tumor\\\". N0: No regional lymph node metastasis. M0: No distant metastasis. (AJCC 6th and 7th eds.)","definition_xrefs":["NCIT:C3644"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-invasive bladder urothelial carcinoma","termid":"MONDO:0003930"},{"relation_name":"is_a","term_name":"in situ carcinoma","termid":"MONDO:0004647"},{"relation_name":"is_a","term_name":"bladder flat intraepithelial lesion","termid":"MONDO:0006111"}],"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 carcinoma in situ","secondary_identifiers":["ICD9:233.7","MEDGEN:57584","UMLS:C0154091","SCTID:92546004","ICD10CM:D09.0","DOID:9053"],"synonyms":[{"name":"bladder Ca in situ","type":"exact"},{"name":"bladder flat CIS","type":"exact"},{"name":"bladder flat carcinoma in situ","type":"exact"},{"name":"cancer in situ of urinary bladder","type":"broad"},{"name":"carcinoma in situ of bladder","type":"exact"},{"name":"carcinoma in situ of the urinary bladder","type":"exact"},{"name":"carcinoma in situ of urinary bladder","type":"exact"},{"name":"flat CIS of the bladder","type":"exact"},{"name":"flat CIS of the urinary bladder","type":"exact"},{"name":"flat carcinoma in situ of the bladder","type":"exact"},{"name":"flat carcinoma in situ of the urinary bladder","type":"exact"},{"name":"high grade bladder Intraurothelial neoplasia","type":"exact"},{"name":"stage 0 urinary bladder carcinoma","type":"exact"},{"name":"stage 0is bladder cancer","type":"exact"},{"name":"stage 0is bladder carcinoma","type":"exact"},{"name":"stage 0is bladder urothelial cancer","type":"exact"},{"name":"stage 0is bladder urothelial carcinoma","type":"exact"},{"name":"stage 0is bladder urothelial carcinoma aJCC v6","type":"exact"},{"name":"stage 0is bladder urothelial carcinoma aJCC v6 and v7","type":"exact"},{"name":"stage 0is bladder urothelial carcinoma aJCC v7","type":"exact"},{"name":"stage 0is carcinoma of bladder","type":"exact"},{"name":"stage 0is carcinoma of the bladder","type":"exact"},{"name":"stage 0is carcinoma of the urinary bladder","type":"exact"},{"name":"stage 0is carcinoma of urinary bladder","type":"exact"},{"name":"stage 0is urinary bladder carcinoma","type":"exact"},{"name":"urinary bladder carcinoma in situ","type":"exact"},{"name":"urinary bladder flat CIS","type":"exact"},{"name":"urinary bladder flat carcinoma in situ","type":"exact"},{"name":"urinary bladder in situ carcinoma","type":"exact"}],"termid":"MONDO:0004703","xrefs":{"Monarch":{"xref_id":"0004703"}}}


id: GO:0031509
data:
  {"annotated_genes":["SJAG_00934","SJAG_04039","SJAG_03680","SJAG_01540","SJAG_01675","SJAG_03916","SJAG_03982","SJAG_04574","SJAG_02621","SJAG_02119","SJAG_02401","SJAG_03997","SJAG_01579","SJAG_04186","SJAG_00756","SJAG_02409","SJAG_01601","SJAG_03844","SJAG_02778","SJAG_03128","SJAG_00676","SJAG_02576"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87639,89259,89421,90479,91276,93281,95928,97455,98328,102406,103271,103368,107318,109633,110416,111251,112430,112804,113124,116828,117222,117941],"is_not":false,"summary":null,"term":"GO:0031509"}]},"cv_name":"biological_process","definition":"The compaction of chromatin into heterochromatin at the subtelomeric region.","definition_xrefs":["PMID:26205977","GOC:mah","PMID:10219245"],"direct_ancestors":[{"relation_name":"is_a","term_name":"constitutive heterochromatin formation","termid":"GO:0140719"},{"relation_name":"part_of","term_name":"telomere organization","termid":"GO:0032200"}],"gene_count":22,"genes_by_uniquename":{"SJAG_00676":null,"SJAG_00756":null,"SJAG_00934":null,"SJAG_01540":null,"SJAG_01579":null,"SJAG_01601":null,"SJAG_01675":null,"SJAG_02119":null,"SJAG_02401":null,"SJAG_02409":null,"SJAG_02576":null,"SJAG_02621":null,"SJAG_02778":null,"SJAG_03128":null,"SJAG_03680":null,"SJAG_03844":null,"SJAG_03916":null,"SJAG_03982":null,"SJAG_03997":null,"SJAG_04039":null,"SJAG_04186":null,"SJAG_04574":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032200"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006325"}],"interesting_parent_ids":["GO:0010467","GO:0032200","GO:0006325","GO:0008150"],"is_obsolete":false,"name":"subtelomeric heterochromatin formation","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0099114","GO:0006348","GO:0035390"],"synonyms":[{"name":"Telomere Position Effect","type":"exact"},{"name":"chromatin silencing at subtelomere","type":"related"},{"name":"chromatin silencing at telomere","type":"exact"},{"name":"establishment of chromatin silencing at telomere","type":"related"},{"name":"heterochromatic silencing at subtelomere","type":"related"},{"name":"heterochromatic silencing at telomere","type":"exact"},{"name":"regulation of chromatin silencing at telomere","type":"related"},{"name":"regulation of subtelomeric heterochromatin assembly","type":"related"},{"name":"subtelomere chromatin silencing","type":"related"},{"name":"subtelomeric heterochromatin assembly","type":"exact"},{"name":"subtelomeric silencing","type":"exact"},{"name":"telomere chromatin silencing","type":"exact"},{"name":"telomeric heterochromatin assembly","type":"related"},{"name":"telomeric heterochromatin formation","type":"related"},{"name":"telomeric silencing","type":"exact"}],"termid":"GO:0031509","terms_by_termid":{"GO:0031509":null}}


id: MONDO:0009016
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The deposition of calcium on the cornea, resulting in pain and decreased visual acuity.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"corneal degeneration","termid":"MONDO:0001515"},{"relation_name":"is_a","term_name":"keratopathy","termid":"MONDO:0002261"},{"relation_name":"is_a","term_name":"corneal dystrophy","termid":"MONDO:0018102"}],"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":"band keratopathy","secondary_identifiers":["MESH:C562399","OMIM:217500","SCTID:35055000","NCIT:C118765","ICD9:371.43","MEDGEN:56354","UMLS:C0155120","DOID:11164","icd11.foundation:184627034"],"synonyms":[{"name":"band keratopathy","type":"exact"},{"name":"band-shaped keratopathy","type":"exact"},{"name":"corneal dystrophy, band-SHAPED","type":"related"}],"termid":"MONDO:0009016","xrefs":{"Monarch":{"xref_id":"0009016"}}}


id: PBO:0087251
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Serine/threonine protein kinase; associates with TORC1 and likely involved in TOR signaling cascades; negative regulator of autophagy; nuclear translocation required for haploid filamentous growth; regulates filamentous growth induced nuclear translocation of Bcy1p, Fus3p, and Sks1p; overproduction causes allele-specific suppression of prp20-10; protein abundance increases in response to DNA replication stress","termid":"PBO:0087251"}


id: GO:0043580
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the periplasmic space, the region between the inner (cytoplasmic) and outer membrane in Gram-negative bacteria, or the inner membrane and cell wall in fungi.","definition_xrefs":["GOC:dph","GOC:jl","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component organization","termid":"GO:0016043"}],"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":"periplasmic space organization","synonyms":[{"name":"periplasmic space organisation","type":"exact"},{"name":"periplasmic space organization and biogenesis","type":"exact"}],"termid":"GO:0043580"}


id: PBO:0076866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TEX13 family member D","termid":"PBO:0076866"}


id: PR:Q9P6I5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A guanylate kinase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR23117:SF1","OMA:SCHPO02351","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":"guanylate kinase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1198.05","secondary_identifiers":["UniProtKB:Q9P6I5"],"synonyms":[{"name":"GMP kinase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-GUK1","type":"exact"}],"termid":"PR:Q9P6I5"}


id: GO:0030029
data:
  {"annotated_genes":["SJAG_02392","SJAG_02228","SJAG_04597","SJAG_03625","SJAG_03655","SJAG_00907","SJAG_00424","SJAG_04052","SJAG_02366","SJAG_05000","SJAG_00938","SJAG_03455","SJAG_03011","SJAG_00551","SJAG_03229","SJAG_04703","SJAG_01964","SJAG_03146","SJAG_03748","SJAG_04781","SJAG_04001","SJAG_01821","SJAG_04887","SJAG_04461","SJAG_03705","SJAG_00268","SJAG_00521","SJAG_02177","SJAG_00858","SJAG_00152","SJAG_04554","SJAG_00677","SJAG_03465","SJAG_03380","SJAG_00082","SJAG_01826","SJAG_02989","SJAG_02431","SJAG_02795","SJAG_02700","SJAG_02831","SJAG_01384","SJAG_02075","SJAG_04982","SJAG_02511","SJAG_04465","SJAG_03088","SJAG_00970","SJAG_01993","SJAG_01048","SJAG_02245","SJAG_01143","SJAG_00030","SJAG_04172","SJAG_02838","SJAG_01114","SJAG_03086","SJAG_01268","SJAG_00228","SJAG_01665","SJAG_04666","SJAG_04498","SJAG_03379","SJAG_03703","SJAG_03025","SJAG_04621","SJAG_04624","SJAG_02684","SJAG_00750","SJAG_03044","SJAG_03045","SJAG_03361","SJAG_04522","SJAG_02566","SJAG_01774","SJAG_03048","SJAG_04930","SJAG_01894","SJAG_02202","SJAG_01320","SJAG_01388","SJAG_03486","SJAG_01943","SJAG_04644","SJAG_01732","SJAG_00279","SJAG_02864","SJAG_04479","SJAG_04100","SJAG_04886","SJAG_00700","SJAG_00649","SJAG_00661","SJAG_04077","SJAG_02592","SJAG_03596","SJAG_03119","SJAG_01805","SJAG_00610"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87361,110161,102241,114014,98875,99053,106319,111327,110810,102431,104323,109829,102487,111304,89032,117620,93994,117979,89882,97110],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0000147"},{"annotations":[87466,96914,104306,94481,98092,98031,104324],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0044396"},{"annotations":[88533],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051764"},{"annotations":[94564,76213,101694,92849,105571,111009,96397,114015,117761,116267,98728,87467,98515,93038,106201,103894,101302,107892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030036"},{"annotations":[98876,99054,104325,98032,89883,102488,97111,87362],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090135"},{"annotations":[93018,104307,88534,100901,117762],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051017"},{"annotations":[115311,117763,98841,107288],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061572"},{"annotations":[115312],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061573"},{"annotations":[90081],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071846"},{"annotations":[91738,100108],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030042"},{"annotations":[104308],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051639"},{"annotations":[104728],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007015"},{"annotations":[96915,98033,91526,93019,64236],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030041"},{"annotations":[100109,91739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051014"},{"annotations":[88575],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0045010"},{"annotations":[116769],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033275"},{"annotations":[109941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000915"},{"annotations":[97223,107289,97488,88535],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071520"},{"annotations":[109942,104309],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044837"},{"annotations":[79102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031032"},{"annotations":[98877,87363,98034,99055,102489,106321,97112,104326,89884,101922],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034314"},{"annotations":[87468,98093,91527,113451],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0051016"},{"annotations":[102490,117032,99358],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030866"},{"annotations":[87678,95045,104516,109904,88643,99359,103819,98518],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030950"},{"annotations":[115314,107291],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070649"},{"annotations":[104311],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0110009"},{"annotations":[87469,91712,97490,98175,98094,113453],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904600"},{"annotations":[91788,87470,94482,117006,97224,96842,101746,91740,91528,118553,98095,111011,111441,100449,96917,116165,117586,117765,97115,101606],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903475"},{"annotations":[97225],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1903479"},{"annotations":[96843,97226,99886,87471,100118,98096,94483,101607,111442,117007],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1902404"},{"annotations":[90082],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0034316"},{"annotations":[97477],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:2000432"},{"annotations":[101550],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1903500"},{"annotations":[93610,89203],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903501"},{"annotations":[114481,105842,88941,98639,115622,102025,88646,91623,91906,93615,109254,95053,114453,93041],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032956"},{"annotations":[106772],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032231"},{"annotations":[101924,89886,104329,100934,89034],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0030833"},{"annotations":[118658,93005,93576],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1903499"},{"annotations":[69324,115319],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030050"}]},"cv_name":"biological_process","definition":"Any cellular process that depends upon or alters the actin cytoskeleton, that part of the cytoskeleton comprising actin filaments and their associated proteins.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process","termid":"GO:0009987"}],"gene_count":99,"genes_by_uniquename":{"SJAG_00030":null,"SJAG_00082":null,"SJAG_00152":null,"SJAG_00228":null,"SJAG_00268":null,"SJAG_00279":null,"SJAG_00424":null,"SJAG_00521":null,"SJAG_00551":null,"SJAG_00610":null,"SJAG_00649":null,"SJAG_00661":null,"SJAG_00677":null,"SJAG_00700":null,"SJAG_00750":null,"SJAG_00858":null,"SJAG_00907":null,"SJAG_00938":null,"SJAG_00970":null,"SJAG_01048":null,"SJAG_01114":null,"SJAG_01143":null,"SJAG_01268":null,"SJAG_01320":null,"SJAG_01384":null,"SJAG_01388":null,"SJAG_01665":null,"SJAG_01732":null,"SJAG_01774":null,"SJAG_01805":null,"SJAG_01821":null,"SJAG_01826":null,"SJAG_01894":null,"SJAG_01943":null,"SJAG_01964":null,"SJAG_01993":null,"SJAG_02075":null,"SJAG_02177":null,"SJAG_02202":null,"SJAG_02228":null,"SJAG_02245":null,"SJAG_02366":null,"SJAG_02392":null,"SJAG_02431":null,"SJAG_02511":null,"SJAG_02566":null,"SJAG_02592":null,"SJAG_02684":null,"SJAG_02700":null,"SJAG_02795":null,"SJAG_02831":null,"SJAG_02838":null,"SJAG_02864":null,"SJAG_02989":null,"SJAG_03011":null,"SJAG_03025":null,"SJAG_03044":null,"SJAG_03045":null,"SJAG_03048":null,"SJAG_03086":null,"SJAG_03088":null,"SJAG_03119":null,"SJAG_03146":null,"SJAG_03229":null,"SJAG_03361":null,"SJAG_03379":null,"SJAG_03380":null,"SJAG_03455":null,"SJAG_03465":null,"SJAG_03486":null,"SJAG_03596":null,"SJAG_03625":null,"SJAG_03655":null,"SJAG_03703":null,"SJAG_03705":null,"SJAG_03748":null,"SJAG_04001":null,"SJAG_04052":null,"SJAG_04077":null,"SJAG_04100":null,"SJAG_04172":null,"SJAG_04461":null,"SJAG_04465":null,"SJAG_04479":null,"SJAG_04498":null,"SJAG_04522":null,"SJAG_04554":null,"SJAG_04597":null,"SJAG_04621":null,"SJAG_04624":null,"SJAG_04644":null,"SJAG_04666":null,"SJAG_04703":null,"SJAG_04781":null,"SJAG_04886":null,"SJAG_04887":null,"SJAG_04930":null,"SJAG_04982":null,"SJAG_05000":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"actin filament-based process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null,"PMID:27059155":null,"PMID:32915139":null},"synonyms":[{"name":"microfilament-based process","type":"related"}],"termid":"GO:0030029","terms_by_termid":{"GO:0000147":null,"GO:0000915":null,"GO:0007015":null,"GO:0030036":null,"GO:0030041":null,"GO:0030042":null,"GO:0030050":null,"GO:0030833":null,"GO:0030866":null,"GO:0030950":null,"GO:0031032":null,"GO:0032231":null,"GO:0032956":null,"GO:0033275":null,"GO:0034314":null,"GO:0034316":null,"GO:0044396":null,"GO:0044837":null,"GO:0045010":null,"GO:0051014":null,"GO:0051016":null,"GO:0051017":null,"GO:0051639":null,"GO:0051764":null,"GO:0061572":null,"GO:0061573":null,"GO:0070649":null,"GO:0071520":null,"GO:0071846":null,"GO:0090135":null,"GO:0110009":null,"GO:0120306":null,"GO:1902404":null,"GO:1903475":null,"GO:1903479":null,"GO:1903499":null,"GO:1903500":null,"GO:1903501":null,"GO:1904600":null,"GO:2000432":null}}


id: FYPO:0007508
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 trimethylation of lysine at position 9 of histone H3 at subtelomeric regions occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah","PMID:17434129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H3-K9 trimethylation during vegetative growth","termid":"FYPO:0000879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0002274","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased histone H3-K9 trimethylation at subtelomeric heterochromatin during vegetative growth","synonyms":[{"name":"increased histone H3 K9 trimethylation at subtelomeric heterochromatin during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 trimethylation at subtelomere during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 trimethylation at subtelomeric heterochromatin during mitotic cell cycle","type":"related"},{"name":"increased histone H3K9 trimethylation at subtelomeric heterochromatin during vegetative growth","type":"exact"},{"name":"increased histone H3K9me3 at subtelomeric heterochromatin during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K9 trimethylation at subtelomeric heterochromatin during vegetative growth","type":"exact"}],"termid":"FYPO:0007508"}


id: FYPO:0006591
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of DNA damage measured in a cell during S phase of the mitotic cell cycle is greater than normal. The number, extent, or both of damage sites may be increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased DNA damage during vegetative growth","termid":"FYPO:0003547"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"name":"increased DNA damage during mitotic S phase","synonyms":[{"name":"increased DNA damage during S phase during vegetative growth","type":"exact"},{"name":"increased DNA damage during S phase of mitotic cell cycle","type":"exact"},{"name":"increased number of DNA lesions during mitotic S phase","type":"related"}],"termid":"FYPO:0006591"}


id: PBO:0064913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPP4R2 pseudogene 2","termid":"PBO:0064913"}


id: PBO:0047891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(6)(q26)","termid":"PBO:0047891"}


id: PBO:0059563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"metallothionein 1G","termid":"PBO:0059563"}


id: PBO:0080048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 21","termid":"PBO:0080048"}


id: GO:0032697
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate, or extent of interleukin-14 production.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of interleukin-14 production (obsolete GO:0032697)","synonyms":[{"name":"down regulation of interleukin-14 production","type":"exact"},{"name":"down-regulation of interleukin-14 production","type":"exact"},{"name":"downregulation of interleukin-14 production","type":"exact"},{"name":"inhibition of interleukin-14 production","type":"narrow"},{"name":"negative regulation of IL-14 production","type":"exact"},{"name":"negative regulation of interleukin-14 biosynthetic process","type":"narrow"}],"termid":"GO:0032697"}


id: GO:0004230
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the release of a N-terminal glutamate (and to a lesser extent aspartate) from a peptide.","definition_xrefs":["EC:3.4.11.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminopeptidase activity","termid":"GO:0004177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0008233","GO:0016787","GO:0003824","GO:0140096","GO:0003674"],"is_obsolete":false,"name":"glutamyl aminopeptidase activity","secondary_identifiers":["MetaCyc:3.4.11.7-RXN"],"synonyms":[{"name":"Ca2+-activated glutamate aminopeptidase activity","type":"related"},{"name":"L-aspartate aminopeptidase activity","type":"related"},{"name":"aminopeptidase A","type":"related"},{"name":"angiotensinase A","type":"related"},{"name":"angiotensinase A2","type":"related"},{"name":"antigen BP-1/6C3 of mouse B lymphocytes","type":"related"},{"name":"aspartate aminopeptidase activity","type":"related"},{"name":"glutamyl peptidase activity","type":"related"},{"name":"membrane aminopeptidase II","type":"related"}],"termid":"GO:0004230"}


id: GO:0045936
data:
  {"annotated_genes":["SJAG_05314","SJAG_00053","SJAG_02380","SJAG_03170","SJAG_01187","SJAG_03940","SJAG_01906","SJAG_00685"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103552,89618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902647"},{"annotations":[75326,72412],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"},{"annotations":[110515,114613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001211"},{"annotations":[108882,111878],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071072"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the chemical reactions and pathways involving phosphates.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of phosphorus metabolic process","termid":"GO:0010563"},{"relation_name":"is_a","term_name":"regulation of phosphate metabolic process","termid":"GO:0019220"},{"relation_name":"negatively_regulates","term_name":"phosphate-containing compound metabolic process","termid":"GO:0006796"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00685":null,"SJAG_01187":null,"SJAG_01906":null,"SJAG_02380":null,"SJAG_03170":null,"SJAG_03940":null,"SJAG_05314":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of phosphate metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of phosphate metabolic process","type":"exact"},{"name":"down-regulation of phosphate metabolic process","type":"exact"},{"name":"downregulation of phosphate metabolic process","type":"exact"},{"name":"inhibition of phosphate metabolic process","type":"narrow"},{"name":"negative regulation of phosphate metabolism","type":"exact"}],"termid":"GO:0045936","terms_by_termid":{"GO:0045820":null,"GO:0071072":null,"GO:1902647":null,"GO:2001211":null}}


id: PR:O14018
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A serine--tRNA ligase, cytoplasmic that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11778:SF0","PRO:DNx","OMA:SCHPO02129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine--tRNA ligase, cytoplasmic (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC29A4.15","secondary_identifiers":["UniProtKB:O14018"],"synonyms":[{"name":"SerRS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SARS","type":"exact"},{"name":"seryl-tRNA synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"seryl-tRNA(Ser/Sec) synthetase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14018"}


id: PBO:0057309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 516b-2","termid":"PBO:0057309"}


id: GO:0070997
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of cell death in a neuron.","definition_xrefs":["GOC:BHF","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete neuron death (obsolete GO:0070997)","synonyms":[{"name":"neuron cell death","type":"exact"},{"name":"neuronal cell death","type":"exact"}],"termid":"GO:0070997"}


id: GO:0019185
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that recognizes the proximal sequence element of RNA polymerase II and III snRNA promoters.","definition_xrefs":["PMID:7715707","PMID:9003788"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription regulator complex","termid":"GO:0005667"}],"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":"snRNA-activating protein complex","synonyms":[{"name":"SNAPc","type":"exact"}],"termid":"GO:0019185"}


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


id: SO:1001244
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1001244 alternatively_spliced_transcript_encoding_greater_than_1_polypeptide_different_start_codon_different_stop_codon_coding_regions_non_overlapping (obsolete SO:1001244)","synonyms":[{"name":"alternatively_spliced_transcript_encoding_greater_than_1_polypeptide_different_start_codon_different_stop_codon_coding_regions_non-overlapping","type":"related"}],"termid":"SO:1001244"}


id: PBO:0001155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat protein, implicated in meiosis","termid":"PBO:0001155"}


id: PBO:0090385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KH domain RNA-binding protein Pno1","termid":"PBO:0090385"}


id: GO:0106135
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of cardiac muscle cell contraction.","definition_xrefs":["PMID:19525381"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"negative regulation of cardiac muscle contraction","termid":"GO:0055118"},{"relation_name":"is_a","term_name":"regulation of cardiac muscle cell contraction","termid":"GO:0086004"},{"relation_name":"negatively_regulates","term_name":"cardiac muscle cell contraction","termid":"GO:0086003"}],"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 cardiac muscle cell contraction","termid":"GO:0106135"}


id: PBO:0052080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"katanin regulatory subunit B1 like 1 pseudogene 5","termid":"PBO:0052080"}


id: PBO:0046743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocyst complex component 2","termid":"PBO:0046743"}


id: GO:0043578
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of the nuclear matrix, the dense fibrillar network lying on the inner side of the nuclear membrane.","definition_xrefs":["GOC:jl","GOC:dph","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus organization","termid":"GO:0006997"}],"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":"nuclear matrix organization","synonyms":[{"name":"nuclear matrix organisation","type":"exact"},{"name":"nuclear matrix organization and biogenesis","type":"related"},{"name":"nucleoskeleton organization","type":"exact"}],"termid":"GO:0043578"}


id: PBO:0046779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EXTL3 antisense RNA 1","termid":"PBO:0046779"}


id: FYPO:0002182
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, germinated spores and spheroid vegetative cells. The spheroid cells arise from division of some of the germinated spores, and may form a microcolony of up to 64 cells.","definition_xrefs":["PomBase:mah","PomBase:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable mixed population including spores, germinated spores and spheroid cells (obsolete FYPO:0002182)","synonyms":[{"name":"inviable mixed population including spores, germinated spores and rounded cells","type":"exact"}],"termid":"FYPO:0002182"}


id: PR:Q9UUH4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- erg25 gene.","definition_xrefs":["UniProtKB:Q9UUH4","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":"methylsterol monooxygenase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC630.08c","synonyms":[{"name":"C-4 methylsterol oxidase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-erg25","type":"exact"}],"termid":"PR:Q9UUH4"}


id: GO:0001785
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with prostaglandin J (PGJ(2)), a metabolite of prostaglandin D (PGD(2)) to initiate a change in cell activity.","definition_xrefs":["PMID:12878180"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostaglandin receptor activity","termid":"GO:0004955"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"prostaglandin J receptor activity","synonyms":[{"name":"PGJ receptor activity","type":"related"},{"name":"PGJ(2) receptor activity","type":"exact"}],"termid":"GO:0001785"}


id: PBO:0041639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel subunit alpha1 F","termid":"PBO:0041639"}


id: PBO:0001248
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.4.24.-","termid":"PBO:0001248"}


id: MONDO:0002161
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete fallopian tube carcinosarcoma (obsolete MONDO:0002161)","termid":"MONDO:0002161","xrefs":{"Monarch":{"xref_id":"0002161"}}}


id: GO:0030626
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a U12 small nuclear RNA (U12 snRNA).","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA binding","termid":"GO:0017069"}],"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:0003723"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0003723"],"is_obsolete":false,"name":"U12 snRNA binding","termid":"GO:0030626"}


id: MONDO:0044917
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The most frequent type of lymphoblastic lymphoma. It comprises approximately 85-90% of cases. It is more frequently seen in adolescent males. It frequently presents with a mass lesion in the mediastinum. Pleural effusions are common. (WHO, 2001)","definition_xrefs":["NCIT:C6919"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoblastic lymphoma","termid":"MONDO:0000873"},{"relation_name":"is_a","term_name":"precursor T-lymphoblastic lymphoma/leukemia","termid":"MONDO:0003537"},{"relation_name":"is_a","term_name":"T-cell non-Hodgkin lymphoma","termid":"MONDO:0015760"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"T-lymphoblastic lymphoma","secondary_identifiers":["UMLS:C1292758","MEDGEN:266232","NANDO:2200023","SCTID:421246008"],"synonyms":[{"name":"Precur. T-lymphoblastic lymphoma","type":"exact"},{"name":"T Lymphoblastic lymphoma","type":"exact"},{"name":"T-Lymphoblastic lymphoma","type":"exact"},{"name":"T-lymphoblastic lymphoma","type":"exact"},{"name":"precursor T Lymphoblastic lymphoma","type":"exact"},{"name":"precursor T-Lymphoblastic lymphoma","type":"exact"},{"name":"precursor T-cell Lymphoblastic lymphoma","type":"exact"},{"name":"precursor T-lymphoblastic lymphoma","type":"exact"}],"termid":"MONDO:0044917","xrefs":{"Monarch":{"xref_id":"0044917"}}}


id: GO:0030279
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of ossification, the formation of bone or of a bony substance or the conversion of fibrous tissue or of cartilage into bone or a bony substance.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ossification","termid":"GO:0030278"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"ossification","termid":"GO:0001503"}],"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 ossification","synonyms":[{"name":"down regulation of ossification","type":"exact"},{"name":"down-regulation of ossification","type":"exact"},{"name":"downregulation of ossification","type":"exact"},{"name":"inhibition of ossification","type":"narrow"},{"name":"negative regulation of bone biosynthesis","type":"exact"},{"name":"negative regulation of bone formation","type":"exact"}],"termid":"GO:0030279"}


id: PBO:0083436
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 the uncharacterized ORF YNL108C","termid":"PBO:0083436"}


id: PBO:0044886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"density regulated re-initiation and release factor","termid":"PBO:0044886"}


id: MONDO:0001257
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinal vascular disorder","termid":"MONDO:0002311"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"retinal microaneurysm","secondary_identifiers":["ICD9:362.14","SCTID:34037000","DOID:11295","MEDGEN:472899","UMLS:C0154834"],"termid":"MONDO:0001257","xrefs":{"Monarch":{"xref_id":"0001257"}}}


id: GO:0034360
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A lipoprotein particle that is derived from a mature chylomicron particle by the removal of triglycerides from the chylomicron core by lipoprotein lipase and the subsequent loss of surface components. It characteristically contains apolipoprotein E (APOE) and is cleared from the blood by the liver.","definition_xrefs":["GOC:mah","GOC:rl","GOC:expert_pt","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chylomicron","termid":"GO:0042627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005576","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"chylomicron remnant","termid":"GO:0034360"}


id: GO:2001090
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a maltotriuloseacetate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trisaccharide transport","termid":"GO:2001088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"maltotriulose transport","termid":"GO:2001090"}


id: GO:0050793
data:
  {"annotated_genes":["SJAG_02838","SJAG_00244","SJAG_02392","SJAG_04509","SJAG_03501","SJAG_02536","SJAG_00028","SJAG_03705","SJAG_00855","SJAG_04724","SJAG_04666","SJAG_00661","SJAG_04853","SJAG_00514","SJAG_04140","SJAG_04461","SJAG_03453","SJAG_00236","SJAG_01799","SJAG_02022","SJAG_00845","SJAG_04522","SJAG_04322","SJAG_00216","SJAG_03637","SJAG_00610","SJAG_01456","SJAG_04203","SJAG_00333","SJAG_00596","SJAG_01794","SJAG_00304","SJAG_00993","SJAG_02379","SJAG_01212","SJAG_02736","SJAG_03581","SJAG_02169","SJAG_03486"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95044,89070,93776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051519"},{"annotations":[117031,102667,109903,115616,98933,106011,87267],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051523"},{"annotations":[103706],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061246"},{"annotations":[110342],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075297"},{"annotations":[89935],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051517"},{"annotations":[115440],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090258"},{"annotations":[105613,101229],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010637"},{"annotations":[101473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075296"},{"annotations":[89937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"},{"annotations":[117354],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075319"},{"annotations":[106771,115719],"is_not":false,"rel_names":["positively_regulates","regulates","is_a"],"summary":null,"term":"GO:2000784"},{"annotations":[99361,92937,104518,102879],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:2000247"},{"annotations":[102880],"is_not":false,"rel_names":["positively_regulates","regulates","is_a"],"summary":null,"term":"GO:0061361"},{"annotations":[90054,110508,87107,89074,92674],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902917"},{"annotations":[108029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090141"},{"annotations":[89938],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043938"},{"annotations":[91389],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034307"},{"annotations":[116063],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903023"},{"annotations":[114182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051516"},{"annotations":[118504,118503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008360"},{"annotations":[90344,103710,99364,112184,117910,93782,104521,94858],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:2000100"},{"annotations":[91627,87112,102027],"is_not":false,"rel_names":["regulates","is_a"],"summary":null,"term":"GO:2000769"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of development, the biological process whose specific outcome is the progression of a multicellular organism over time from an initial condition (e.g. a zygote, or a young adult) to a later condition (e.g. a multicellular animal or an aged adult).","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological process","termid":"GO:0050789"},{"relation_name":"regulates","term_name":"developmental process","termid":"GO:0032502"}],"gene_count":39,"genes_by_uniquename":{"SJAG_00028":null,"SJAG_00216":null,"SJAG_00236":null,"SJAG_00244":null,"SJAG_00304":null,"SJAG_00333":null,"SJAG_00514":null,"SJAG_00596":null,"SJAG_00610":null,"SJAG_00661":null,"SJAG_00845":null,"SJAG_00855":null,"SJAG_00993":null,"SJAG_01212":null,"SJAG_01456":null,"SJAG_01794":null,"SJAG_01799":null,"SJAG_02022":null,"SJAG_02169":null,"SJAG_02379":null,"SJAG_02392":null,"SJAG_02536":null,"SJAG_02736":null,"SJAG_02838":null,"SJAG_03453":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03581":null,"SJAG_03637":null,"SJAG_03705":null,"SJAG_04140":null,"SJAG_04203":null,"SJAG_04322":null,"SJAG_04461":null,"SJAG_04509":null,"SJAG_04522":null,"SJAG_04666":null,"SJAG_04724":null,"SJAG_04853":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of developmental process","references_by_uniquename":{"GO_REF:0000107":null,"PMID:30664646":null},"termid":"GO:0050793","terms_by_termid":{"GO:0008360":null,"GO:0010637":null,"GO:0034307":null,"GO:0043938":null,"GO:0051516":null,"GO:0051517":null,"GO:0051519":null,"GO:0051523":null,"GO:0061246":null,"GO:0061361":null,"GO:0075296":null,"GO:0075297":null,"GO:0075319":null,"GO:0090141":null,"GO:0090258":null,"GO:1902917":null,"GO:1903023":null,"GO:1903024":null,"GO:2000100":null,"GO:2000247":null,"GO:2000769":null,"GO:2000784":null}}


id: FYPO:0000933
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 microtubule cytoskeleton is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule cytoskeleton during vegetative growth","termid":"FYPO:0000931"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to microtubule cytoskeleton during vegetative growth","synonyms":[{"name":"decreased protein localisation to microtubule cytoskeleton during vegetative growth","type":"exact"},{"name":"decreased protein localization to microtubule cytoskeleton during mitotic cell cycle","type":"related"},{"name":"reduced protein localization to microtubule cytoskeleton during vegetative growth","type":"exact"}],"termid":"FYPO:0000933"}


id: GO:0019798
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: procollagen L-proline + 2-oxoglutarate + O2 = procollagen trans-hydroxy-L-proline + succinate + CO2.","definition_xrefs":["PMID:4371784","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-proline dioxygenase activity","termid":"GO:0031543"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0140096","GO:0016491"],"is_obsolete":false,"name":"procollagen-proline dioxygenase activity","termid":"GO:0019798"}


id: MONDO:0019708
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete primary bone dysplasia with disorganized development of skeletal components (obsolete MONDO:0019708)","synonyms":[{"name":"primary osteodysplasia with disorganized development of skeletal components","type":"related"},{"name":"primary skeletal dysplasia with disorganized development of skeletal components","type":"related"}],"termid":"MONDO:0019708","xrefs":{"Monarch":{"xref_id":"0019708"}}}


id: GO:0043243
data:
  {"annotated_genes":["SJAG_02189","SJAG_04312","SJAG_02812","SJAG_02433","SJAG_03126","SJAG_05265"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96815],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901098"},{"annotations":[101035],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031117"},{"annotations":[111104],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904595"},{"annotations":[108317,94003,108316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045905"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein complex disassembly, the disaggregation of a protein complex into its constituent components.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein-containing complex disassembly","termid":"GO:0043244"},{"relation_name":"is_a","term_name":"positive regulation of cellular component organization","termid":"GO:0051130"},{"relation_name":"positively_regulates","term_name":"protein-containing complex disassembly","termid":"GO:0032984"}],"gene_count":6,"genes_by_uniquename":{"SJAG_02189":null,"SJAG_02433":null,"SJAG_02812":null,"SJAG_03126":null,"SJAG_04312":null,"SJAG_05265":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of protein-containing complex disassembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of protein complex disassembly","type":"narrow"},{"name":"positive regulation of protein complex disassembly","type":"related"},{"name":"stimulation of protein complex disassembly","type":"narrow"},{"name":"up regulation of protein complex disassembly","type":"exact"},{"name":"up-regulation of protein complex disassembly","type":"exact"},{"name":"upregulation of protein complex disassembly","type":"exact"}],"termid":"GO:0043243","terms_by_termid":{"GO:0031117":null,"GO:0045905":null,"GO:1901098":null,"GO:1904595":null}}


id: PBO:0050877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isopentenyl-diphosphate delta isomerase 1","termid":"PBO:0050877"}


id: GO:1901833
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of trans-neoxanthin and 9'-cis-neoxanthin.","definition_xrefs":["MetaCyc:PWY-6809","GOC:yaf","PMID:11029576","GOC:TermGenie","UniPathway:UPA00388"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xanthophyll biosynthetic process","termid":"GO:0016123"},{"relation_name":"is_a","term_name":"olefinic compound biosynthetic process","termid":"GO:0120255"},{"relation_name":"is_a","term_name":"ether biosynthetic process","termid":"GO:1901503"},{"relation_name":"is_a","term_name":"all-trans-neoxanthin metabolic process","termid":"GO:1901831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"neoxanthin biosynthetic process","synonyms":[{"name":"all-trans-neoxanthin anabolism","type":"exact"},{"name":"all-trans-neoxanthin biosynthesis","type":"exact"},{"name":"all-trans-neoxanthin biosynthetic process","type":"narrow"},{"name":"all-trans-neoxanthin formation","type":"exact"},{"name":"all-trans-neoxanthin synthesis","type":"exact"},{"name":"neoxanthin anabolism","type":"exact"},{"name":"neoxanthin biosynthesis","type":"exact"},{"name":"neoxanthin formation","type":"exact"},{"name":"neoxanthin synthesis","type":"exact"}],"termid":"GO:1901833"}


id: PBO:0033747
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_DNA_recombination_during_cellular_response_to_ionizing_radiation","termid":"PBO:0033747"}


id: MONDO:0005401
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the colon. Representative examples of benign neoplasms include lipoma and leiomyoma. Representative examples of malignant neoplasms include carcinoma, lymphoma, and sarcoma. Colonic adenomas always exhibit epithelial dysplasia and are considered premalignant neoplasms.","definition_xrefs":["NCIT:C2953"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colonic disorder","termid":"MONDO:0003409"},{"relation_name":"is_a","term_name":"colorectal neoplasm","termid":"MONDO:0005335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"colonic neoplasm","secondary_identifiers":["UMLS:C0009375","EFO:0004288","MEDGEN:3165","MESH:D003110"],"synonyms":[{"name":"colon neoplasm","type":"exact"},{"name":"colon neoplasm (disease)","type":"exact"},{"name":"colon tumor","type":"exact"},{"name":"colon tumour","type":"exact"},{"name":"colonic neoplasm","type":"exact"},{"name":"colonic tumor","type":"exact"},{"name":"colonic tumour","type":"exact"},{"name":"neoplasm of colon","type":"exact"},{"name":"neoplasm of the colon","type":"exact"},{"name":"tumor of colon","type":"exact"},{"name":"tumor of the colon","type":"exact"},{"name":"tumour of colon","type":"exact"},{"name":"tumour of the colon","type":"exact"}],"termid":"MONDO:0005401","xrefs":{"Monarch":{"xref_id":"0005401"}}}


id: GO:0044374
data:
  {"annotated_genes":["SJAG_05153","SJAG_04855","SJAG_04009"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[106217],"is_not":false,"summary":null,"term":"GO:0044374"},{"annotations":[101466],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110035"},{"annotations":[106216,107962],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044377"}]},"cv_name":"molecular_function","definition":"The activity of binding selectively and non-covalently to DNA in a sequence-specific manner and distorting the original structure of DNA, typically a straight helix, into a bend, or increasing the bend if the original structure was intrinsically bent due to its sequence.","definition_xrefs":["GOC:jl","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA binding, bending","termid":"GO:0008301"},{"relation_name":"is_a","term_name":"sequence-specific double-stranded DNA binding","termid":"GO:1990837"}],"gene_count":3,"genes_by_uniquename":{"SJAG_04009":null,"SJAG_04855":null,"SJAG_05153":null},"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:0003677"}],"interesting_parent_ids":["GO:0005488","GO:0003677","GO:0003674"],"is_obsolete":false,"name":"sequence-specific DNA binding, bending","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"DNA bending involving sequence-specific DNA binding","type":"exact"}],"termid":"GO:0044374","terms_by_termid":{"GO:0044374":null,"GO:0044377":null,"GO:0110035":null}}


id: GO:0043158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cellular developmental process by which a cell becomes a heterocyst, a cell that carries out nitrogen fixation. This process involves changes to the cell wall, expression of nitrogenase and other proteins involved in nitrogen fixation, and degradation of photosystem II, which produces oxygen. This process is known to occur in some cyanobacteria.","definition_xrefs":["PMID:35744626","PMID:11121783"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular developmental process","termid":"GO:0048869"}],"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":"heterocyst development","synonyms":[{"name":"heterocyst cell differentiation","type":"related"},{"name":"heterocyst differentiation","type":"related"},{"name":"heterocyst formation","type":"exact"}],"termid":"GO:0043158"}


id: MONDO:0024540
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Jervell and Lange-Nielsen syndrome in which the cause of the disease is a mutation in the KCNQ1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Jervell and Lange-Nielsen syndrome","termid":"MONDO:0002441"}],"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":"Jervell and Lange-Nielsen syndrome 1","secondary_identifiers":["UMLS:C4551509","OMIM:220400","MEDGEN:1646925"],"synonyms":[{"name":"Cardioauditory syndrome of Jervell and Lange-Nielsen","type":"related"},{"name":"JLNS1","type":"related"},{"name":"Jervell and Lange-Nielsen syndrome","type":"broad"},{"name":"Jervell and Lange-Nielsen syndrome 1","type":"exact"},{"name":"Jervell and Lange-Nielsen syndrome caused by mutation in KCNQ1","type":"exact"},{"name":"KCNQ1 Jervell and Lange-Nielsen syndrome","type":"exact"},{"name":"Surdo-Cardiac syndrome","type":"related"},{"name":"deafness, congenital, and functional heart disease","type":"related"},{"name":"prolonged QT interval in Ekg and sudden death","type":"related"}],"termid":"MONDO:0024540","xrefs":{"Monarch":{"xref_id":"0024540"}}}


id: FYPO:0005192
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A stress response phenotype in which the response to nitrogen starvation is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular response to stress","termid":"FYPO:0005191"}],"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:0000298"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0000298"],"is_obsolete":false,"name":"normal cellular response to nitrogen starvation","synonyms":[{"name":"normal cellular response to nitrogen depletion","type":"exact"},{"name":"normal cellular response to nitrogen deprivation","type":"exact"}],"termid":"FYPO:0005192"}


id: PBO:0088489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal export complex protein Arx1, peptidase family","termid":"PBO:0088489"}


id: PBO:0053267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukocyte immunoglobulin like receptor A1","termid":"PBO:0053267"}


id: GO:0018894
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving dibenzo-p-dioxin, a substance composed of two benzene rings linked by two ether bonds. Dibenzo-p-dioxins are generated as by-products in the manufacturing of herbicides, insecticides, fungicides, paper pulp bleaching, and in incineration, and can accumulate in milk and throughout the food chain, creating significant health concern.","definition_xrefs":["UM-BBD_pathwayID:dpd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small molecule metabolic process","termid":"GO:0044281"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"dibenzo-p-dioxin metabolic process","synonyms":[{"name":"dibenzo-p-dioxin metabolism","type":"exact"},{"name":"oxanthrene metabolic process","type":"exact"},{"name":"oxanthrene metabolism","type":"exact"},{"name":"phenodioxin metabolic process","type":"exact"},{"name":"phenodioxin metabolism","type":"exact"}],"termid":"GO:0018894"}


id: PBO:0018188
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial magnesium ion transmembrane transporter Mme1 (predicted)","termid":"PBO:0018188"}


id: PBO:0030252
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-altered_cellular_trehalose_level","termid":"PBO:0030252"}


id: MONDO:0008126
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete oncogene Yuasa (obsolete MONDO:0008126)","secondary_identifiers":["OMIM:164891"],"synonyms":[{"name":"oncogene Yuasa","type":"exact"}],"termid":"MONDO:0008126","xrefs":{"Monarch":{"xref_id":"0008126"}}}


id: PBO:0027433
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_replication_fork_arrest_at_rDNA_repeats","termid":"PBO:0027433"}


id: PBO:0113067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the TOM (translocase of outer membrane) complex; involved in the recognition and initial import steps for all mitochondrially-directed proteins, acting as a receptor for incoming precursor proteins; moonlighting role as a transcriptional regulator of mitochondrial proteins; age-dependent reduction in Tom70p results in mitochondrial dysfunction, a hallmark of aging; localizes to mitochondria–ER contact sites; TOM70 has a paralog, TOM71, that arose from the whole genome duplication","termid":"PBO:0113067"}


id: GO:0005819
data:
  {"annotated_genes":["SJAG_02761","SJAG_05205","SJAG_02045","SJAG_04140","SJAG_01224","SJAG_05313","SJAG_02248","SJAG_02807","SJAG_07018","SJAG_00526","SJAG_00800","SJAG_02608","SJAG_03387","SJAG_00879","SJAG_00666","SJAG_00918","SJAG_00460","SJAG_02311","SJAG_02336","SJAG_04607","SJAG_03116","SJAG_01215","SJAG_03592","SJAG_04940","SJAG_02695","SJAG_01371","SJAG_04074","SJAG_01429","SJAG_02368","SJAG_00723","SJAG_03540","SJAG_04257","SJAG_03959","SJAG_04464","SJAG_00697","SJAG_01391","SJAG_03073","SJAG_03906","SJAG_01837","SJAG_05266","SJAG_01634","SJAG_00943","SJAG_03437","SJAG_00930","SJAG_02286","SJAG_01546","SJAG_00207","SJAG_02624","SJAG_05315","SJAG_01805","SJAG_02460","SJAG_05196","SJAG_02209","SJAG_02098","SJAG_03989","SJAG_00883","SJAG_02320","SJAG_03062","SJAG_00655","SJAG_01775","SJAG_04412","SJAG_01370","SJAG_02542","SJAG_02821","SJAG_01211","SJAG_02266","SJAG_04003","SJAG_01557","SJAG_01887","SJAG_03901","SJAG_04010","SJAG_03846","SJAG_01849","SJAG_03569","SJAG_04623","SJAG_01110","SJAG_03911","SJAG_00646","SJAG_03731","SJAG_01330","SJAG_01909","SJAG_02025","SJAG_00724","SJAG_03926","SJAG_01832","SJAG_03681","SJAG_01464","SJAG_00163","SJAG_00514","SJAG_00840","SJAG_03345","SJAG_05220","SJAG_05319","SJAG_04387","SJAG_02509","SJAG_00082","SJAG_04931","SJAG_01613","SJAG_02241","SJAG_00762","SJAG_00692","SJAG_01232","SJAG_00140","SJAG_00773","SJAG_00245","SJAG_04841","SJAG_00845","SJAG_04884","SJAG_01297","SJAG_03915","SJAG_03048","SJAG_04745"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[100172,108000],"is_not":false,"summary":null,"term":"GO:0005819"},{"annotations":[106578,111262,98399,106370,103185,90577],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0000235"},{"annotations":[90193],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032117"},{"annotations":[112355,92981,88564,106974,115795,101530,110329,102450,115030,93959,117775],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072687"},{"annotations":[86964],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990574"},{"annotations":[100605,115796,102715,117811],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990385"},{"annotations":[92982,93960,99090,95957,90490,101989,106252,117955,93055,98403],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0090619"},{"annotations":[88817,97814,88348,98409,117812,107398,92984,99017,106903,109043,117777,86804,89191,108243,109055,102073,105321,90516,99701,95464,87211,105374,110581,116698,108173,94739,96576,99018,114136,88565,114196,87495,95079,110646,111031,88495,95960,99557,102892,111069,113818,95231,88948,89066,112536,108033,91945,101532,96473,93132,94399,101627,105136,108361,102222,110330,117262,95662,74946,99716,103432,106391,108898,113674,107851,92121,110821,98829,107243,109707,97575,99319,110639,103062,90926],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0072686"},{"annotations":[107399,90583,73141,103063],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061673"},{"annotations":[96168],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905721"},{"annotations":[106657],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990941"},{"annotations":[117778,100607,99558,105474],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990498"},{"annotations":[89192,90584,92985,102835,94953,93963,90184,100234,107400,103064,99717,101533,110150,116699,91122,117813,88463,110331,114286,115797,88827,111032,102717,100608,96474],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990023"},{"annotations":[117263,106658,97815,98410],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990537"},{"annotations":[99559,117264],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0097431"},{"annotations":[98412,93966,100610],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005827"},{"annotations":[74948,88952,96478,102874,115799,106582,111266,99704,113228],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0005876"}]},"cv_name":"cellular_component","definition":"The array of microtubules and associated molecules that forms between opposite poles of a eukaryotic cell during mitosis or meiosis and serves to move the duplicated chromosomes apart.","definition_xrefs":["ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membraneless organelle","termid":"GO:0043232"},{"relation_name":"part_of","term_name":"microtubule cytoskeleton","termid":"GO:0015630"}],"gene_count":112,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00140":null,"SJAG_00163":null,"SJAG_00207":null,"SJAG_00245":null,"SJAG_00460":null,"SJAG_00514":null,"SJAG_00526":null,"SJAG_00646":null,"SJAG_00655":null,"SJAG_00666":null,"SJAG_00692":null,"SJAG_00697":null,"SJAG_00723":null,"SJAG_00724":null,"SJAG_00762":null,"SJAG_00773":null,"SJAG_00800":null,"SJAG_00840":null,"SJAG_00845":null,"SJAG_00879":null,"SJAG_00883":null,"SJAG_00918":null,"SJAG_00930":null,"SJAG_00943":null,"SJAG_01110":null,"SJAG_01211":null,"SJAG_01215":null,"SJAG_01224":null,"SJAG_01232":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01391":null,"SJAG_01429":null,"SJAG_01464":null,"SJAG_01546":null,"SJAG_01557":null,"SJAG_01613":null,"SJAG_01634":null,"SJAG_01775":null,"SJAG_01805":null,"SJAG_01832":null,"SJAG_01837":null,"SJAG_01849":null,"SJAG_01887":null,"SJAG_01909":null,"SJAG_02025":null,"SJAG_02045":null,"SJAG_02098":null,"SJAG_02209":null,"SJAG_02241":null,"SJAG_02248":null,"SJAG_02266":null,"SJAG_02286":null,"SJAG_02311":null,"SJAG_02320":null,"SJAG_02336":null,"SJAG_02368":null,"SJAG_02460":null,"SJAG_02509":null,"SJAG_02542":null,"SJAG_02608":null,"SJAG_02624":null,"SJAG_02695":null,"SJAG_02761":null,"SJAG_02807":null,"SJAG_02821":null,"SJAG_03048":null,"SJAG_03062":null,"SJAG_03073":null,"SJAG_03116":null,"SJAG_03345":null,"SJAG_03387":null,"SJAG_03437":null,"SJAG_03540":null,"SJAG_03569":null,"SJAG_03592":null,"SJAG_03681":null,"SJAG_03731":null,"SJAG_03846":null,"SJAG_03901":null,"SJAG_03906":null,"SJAG_03911":null,"SJAG_03915":null,"SJAG_03926":null,"SJAG_03959":null,"SJAG_03989":null,"SJAG_04003":null,"SJAG_04010":null,"SJAG_04074":null,"SJAG_04140":null,"SJAG_04257":null,"SJAG_04387":null,"SJAG_04412":null,"SJAG_04464":null,"SJAG_04607":null,"SJAG_04623":null,"SJAG_04745":null,"SJAG_04841":null,"SJAG_04884":null,"SJAG_04931":null,"SJAG_04940":null,"SJAG_05196":null,"SJAG_05205":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05313":null,"SJAG_05315":null,"SJAG_05319":null,"SJAG_07018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0015630","GO:0005575"],"is_obsolete":false,"name":"spindle","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Wikipedia:Spindle_apparatus"],"termid":"GO:0005819","terms_by_termid":{"GO:0000235":null,"GO:0005819":null,"GO:0005827":null,"GO:0005876":null,"GO:0032117":null,"GO:0061673":null,"GO:0072686":null,"GO:0072687":null,"GO:0090619":null,"GO:0097431":null,"GO:1905721":null,"GO:1990023":null,"GO:1990385":null,"GO:1990498":null,"GO:1990537":null,"GO:1990574":null,"GO:1990941":null}}


id: PBO:0054284
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 1675","termid":"PBO:0054284"}


id: GO:1900352
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of methanofuran biosynthetic process.","definition_xrefs":["GOC:mengo_curators","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 pteridine metabolic process","termid":"GO:0045863"},{"relation_name":"is_a","term_name":"regulation of methanofuran biosynthetic process","termid":"GO:1900351"},{"relation_name":"is_a","term_name":"negative regulation of methanofuran metabolic process","termid":"GO:1900355"},{"relation_name":"negatively_regulates","term_name":"methanofuran biosynthetic process","termid":"GO:2001120"}],"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 methanofuran biosynthetic process","synonyms":[{"name":"down regulation of methanofuran biosynthesis","type":"exact"},{"name":"down regulation of methanofuran biosynthetic process","type":"exact"},{"name":"down-regulation of methanofuran biosynthesis","type":"exact"},{"name":"down-regulation of methanofuran biosynthetic process","type":"exact"},{"name":"downregulation of methanofuran biosynthesis","type":"exact"},{"name":"downregulation of methanofuran biosynthetic process","type":"exact"},{"name":"inhibition of methanofuran biosynthesis","type":"exact"},{"name":"inhibition of methanofuran biosynthetic process","type":"narrow"},{"name":"negative regulation of methanofuran biosynthesis","type":"exact"}],"termid":"GO:1900352"}


id: PBO:0082280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Anti-silencing protein; causes derepression of silent loci when overexpressed","termid":"PBO:0082280"}


id: PBO:0077856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPM1 antisense RNA","termid":"PBO:0077856"}


id: GO:0008391
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the incorporation of one atom from molecular oxygen into arachidonic acid and the reduction of the other atom of oxygen to water.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"arachidonate monooxygenase activity","synonyms":[{"name":"arachidonic acid monooxygenase activity","type":"exact"},{"name":"cytochrome P450 CYP2B19","type":"narrow"}],"termid":"GO:0008391"}


id: PBO:0070837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L13a pseudogene 16","termid":"PBO:0070837"}


id: PBO:0014605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sm snRNP core protein Smg1","termid":"PBO:0014605"}


id: PBO:0085625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in establishment of cell polarity and bud emergence; interacts with the Rho1p small GTP-binding protein and with the Rho-type GTPase Cdc42p; involved in maintenance of proper telomere length","termid":"PBO:0085625"}


id: MONDO:0011109
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple epiphyseal dysplasia, Lowry type is a rare primary bone dysplasia characterized by small, flat epiphyses (esp. the capital femoral epiphyses), rhizomelic shortening of limbs, cleft of secondary palate, micrognathia, mild joint contractures and facial dysmorphism (incl. mildly upward-slanting palpebral fissures, hypertelorism, broad nasal tip). Additionally reported features include scoliosis, genu valgum, mild pectus excavatum, platyspondyly, dislocated radial heads, brachydactyly, hypoplastic fibulae and talipes equinovarus.","definition_xrefs":["Orphanet:166016"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple epiphyseal dysplasia","termid":"MONDO:0016648"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"multiple epiphyseal dysplasia, Lowry type","secondary_identifiers":["MESH:C563291","OMIM:601560","GARD:17013","SCTID:768935003","UMLS:C1832112","MEDGEN:321890"],"synonyms":[{"name":"epiphyseal dysplasia, multiple, with Robin phenotype","type":"related"},{"name":"multiple epiphyseal dysplasia with ROBIN phenotype","type":"related"},{"name":"multiple epiphyseal dysplasia with Robin phenotype","type":"exact"}],"termid":"MONDO:0011109","xrefs":{"Monarch":{"xref_id":"0011109"}}}


id: MONDO:0030883
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"carpal tunnel syndrome","termid":"MONDO:0007275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"carpal tunnel syndrome 2","secondary_identifiers":["DOID:0070467","OMIM:619161","MEDGEN:1725962","UMLS:C5436916"],"synonyms":[{"name":"CTS2","type":"exact"},{"name":"carpal tunnel syndrome 2","type":"exact"}],"termid":"MONDO:0030883","xrefs":{"Monarch":{"xref_id":"0030883"}}}


id: MONDO:0005219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fibrosis associated with cyst formation in the breast parenchyma.","definition_xrefs":["NCIT:C3039"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"breast benign neoplasm","termid":"MONDO:0000620"},{"relation_name":"is_a","term_name":"breast disorder","termid":"MONDO:0002657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast fibrocystic disease","secondary_identifiers":["MEDGEN:42015","DOID:10354","ICD9:610.1","EFO:0003014","MESH:D005348","UMLS:C0016034"],"synonyms":[{"name":"benign breast disease","type":"exact"},{"name":"breast fibrocystic change","type":"exact"},{"name":"cystic disease of breast","type":"exact"},{"name":"cystic disease of the breast","type":"exact"},{"name":"diffuse cystic mastopathy","type":"exact"},{"name":"fibrocystic breast","type":"exact"},{"name":"fibrocystic breast changes","type":"exact"},{"name":"fibrocystic breast disease","type":"exact"},{"name":"fibrocystic change of breast","type":"exact"},{"name":"fibrocystic change of the breast","type":"exact"},{"name":"fibrocystic disease","type":"exact"},{"name":"fibrocystic disease of breast","type":"exact"},{"name":"fibrocystic disease of the breast","type":"exact"},{"name":"fibrocystic mastopathy","type":"exact"},{"name":"mammary dysplasia","type":"exact"}],"termid":"MONDO:0005219","xrefs":{"Monarch":{"xref_id":"0005219"}}}


id: PBO:0078851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRPC5 opposite strand","termid":"PBO:0078851"}


id: GO:0007319
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate that oskar mRNAs are effectively translated into protein.","definition_xrefs":["GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of translation","termid":"GO:0017148"},{"relation_name":"is_a","term_name":"regulation of oskar mRNA translation","termid":"GO:0046011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of oskar mRNA translation","synonyms":[{"name":"down regulation of oskar mRNA translation","type":"exact"},{"name":"down-regulation of oskar mRNA translation","type":"exact"},{"name":"downregulation of oskar mRNA translation","type":"exact"},{"name":"inhibition of oskar mRNA translation","type":"narrow"}],"termid":"GO:0007319"}


id: GO:0099155
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The vesicular release of noradrenaline (norepinephrine) a presynapse, across a chemical synapse, the subsequent activation of noradrenaline receptors at the postsynapse of a target cell (neuron, muscle, or secretory cell) and the effects of this activation on the postsynaptic membrane potential and ionic composition of the postsynaptic cytosol. This process encompasses both spontaneous and evoked release of neurotransmitter and all parts of synaptic vesicle exocytosis. Evoked transmission starts with the arrival of an action potential at the presynapse.","definition_xrefs":["GOC:dos","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemical synaptic transmission","termid":"GO:0007268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"synaptic transmission, noradrenergic","synonyms":[{"name":"noradrenergic synaptic transmission","type":"exact"}],"termid":"GO:0099155"}


id: MONDO:0009521
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leukemia, acute myelocytic, with polyposis coli and colon cancer","secondary_identifiers":["UMLS:C1855505","MEDGEN:383699","MESH:C565441","OMIM:246470"],"synonyms":[{"name":"leukemia, acute myelocytic, with polyposis coli and colon cancer","type":"exact"}],"termid":"MONDO:0009521","xrefs":{"Monarch":{"xref_id":"0009521"}}}


id: FYPO:0005992
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 P-bodies is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000138","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein localization to P-bodies","synonyms":[{"name":"decreased protein localisation to P-bodies","type":"exact"},{"name":"decreased protein localization to P-bodies during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to P-bodies during vegetative growth","type":"exact"},{"name":"decreased protein localization to P-body","type":"exact"},{"name":"decreased protein localization to cytoplasmic P-bodies","type":"exact"},{"name":"reduced protein localization to P-bodies","type":"exact"}],"termid":"FYPO:0005992"}


id: PBO:0000618
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bloom's syndrome","termid":"PBO:0000618"}


id: PBO:0057284
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 504","termid":"PBO:0057284"}


id: GO:0050344
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: trans-cinnamate + H+ + NADPH + O2 = 2-coumarate + H2O + NADP+.","definition_xrefs":["EC:1.14.13.14","RHEA:10956"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"trans-cinnamate 2-monooxygenase activity","secondary_identifiers":["KEGG_REACTION:R02254","MetaCyc:TRANS-CINNAMATE-2-MONOOXYGENASE-RXN"],"synonyms":[{"name":"cinnamate 2-hydroxylase activity","type":"related"},{"name":"cinnamate 2-monooxygenase activity","type":"related"},{"name":"cinnamic 2-hydroxylase activity","type":"related"},{"name":"cinnamic acid 2-hydroxylase activity","type":"related"},{"name":"trans-cinnamate,NADPH:oxygen oxidoreductase (2-hydroxylating)","type":"related"},{"name":"trans-cinnamic acid 2-hydroxylase activity","type":"exact"}],"termid":"GO:0050344"}


id: PBO:0076495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"threonyl-tRNA synthetase 2, mitochondrial","termid":"PBO:0076495"}


id: PBO:0051685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inka box actin regulator 1","termid":"PBO:0051685"}


id: GO:0005503
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to all-trans retinal, a compound that plays an important role in the visual process in most vertebrates. All-trans retinal (trans r., visual yellow) results from the bleaching of rhodopsin by light, in which the 11-cis form is converted to the all-trans form. Retinal is one of the forms of vitamin A.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal binding","termid":"GO:0016918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0008289","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"all-trans retinal binding","synonyms":[{"name":"all-trans retinaldehyde binding","type":"exact"},{"name":"trans retinal binding","type":"exact"},{"name":"visual yellow binding","type":"exact"},{"name":"vitamin A binding","type":"broad"},{"name":"xanthopsin","type":"related"}],"termid":"GO:0005503"}


id: GO:0008407
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the chaeta are generated and organized. A chaeta is a sensory multicellular cuticular outgrowth of a specifically differentiated cell.","definition_xrefs":["FBbt:00005177","GOC:dos","GOC:go_curators","GOC:cjm","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ morphogenesis","termid":"GO:0009887"},{"relation_name":"part_of","term_name":"chaeta development","termid":"GO:0022416"}],"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":"chaeta morphogenesis","synonyms":[{"name":"bristle morphogenesis","type":"narrow"}],"termid":"GO:0008407"}


id: PBO:0027312
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_5'_deoxyribonuclease_(pyrimidine_dimer)_activity","termid":"PBO:0027312"}


id: PBO:0113428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Serine palmitoyltransferase component; responsible along with Lcb1p for the first committed step in sphingolipid synthesis, which is the condensation of serine with palmitoyl-CoA to form 3-ketosphinganine","termid":"PBO:0113428"}


id: GO:2000936
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellotriose catabolic process.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of carbohydrate catabolic process","termid":"GO:0043470"},{"relation_name":"is_a","term_name":"regulation of cellotriose metabolic process","termid":"GO:2000933"},{"relation_name":"regulates","term_name":"cellotriose catabolic process","termid":"GO:2000894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"regulation of cellotriose catabolic process","synonyms":[{"name":"regulation of cellotriose catabolism","type":"exact"}],"termid":"GO:2000936"}


id: MONDO:0015415
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete oblique facial cleft (obsolete MONDO:0015415)","secondary_identifiers":["Orphanet:141253"],"synonyms":[{"name":"Orbitofacial cleft","type":"exact"}],"termid":"MONDO:0015415","xrefs":{"Monarch":{"xref_id":"0015415"}}}


id: PBO:0081327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 121","termid":"PBO:0081327"}


id: PBO:0078055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 45","termid":"PBO:0078055"}


id: PBO:0043143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 11","termid":"PBO:0043143"}


id: PBO:0052047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KN motif and ankyrin repeat domains 3","termid":"PBO:0052047"}


id: GO:0006679
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of glucosylceramides, any compound formed by the replacement of the glycosidic hydroxyl group of a cyclic form of glucose by a ceramide group.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucosylceramide metabolic process","termid":"GO:0006678"},{"relation_name":"is_a","term_name":"glycosylceramide biosynthetic process","termid":"GO:0046476"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"glucosylceramide biosynthetic process","synonyms":[{"name":"glucosylceramide anabolism","type":"exact"},{"name":"glucosylceramide biosynthesis","type":"exact"},{"name":"glucosylceramide formation","type":"exact"},{"name":"glucosylceramide synthesis","type":"exact"}],"termid":"GO:0006679"}


id: GO:0036234
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of glucuronic acid from a conjugated substrate.","definition_xrefs":["PMID:22294686","PMID:8560473","GOC:vk","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucuronate metabolic process","termid":"GO:0019585"}],"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:0044281","GO:0008150"],"is_obsolete":false,"name":"deglucuronidation","termid":"GO:0036234"}


id: MONDO:0800114
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polyclonal hyperplasia of bronchiolar associated lymphoid tissue characterized by the development of lymphoid follicles with germinal centers in walls of the small airways.","definition_xrefs":["PMID:32040879"],"direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic interstitial pneumonia","termid":"MONDO:0002429"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"follicular bronchiolits","termid":"MONDO:0800114","xrefs":{"Monarch":{"xref_id":"0800114"}}}


id: PBO:0047506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FER1L6 antisense RNA 1","termid":"PBO:0047506"}


id: GO:0036024
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A heterodimeric protein complex that contains protein C inhibitor (SERPINA5) and transmembrane protease serine 7 (TMPRSS7); formation of the complex inhibits the serine protease activity of transmembrane protease serine 7.","definition_xrefs":["PMID:15853774","GOC:ans"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine protease inhibitor complex","termid":"GO:0097180"}],"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":"protein C inhibitor-TMPRSS7 complex","synonyms":[{"name":"PCI-TMPRSS7 complex","type":"exact"},{"name":"SERPINA5-TMPRSS7 complex","type":"exact"},{"name":"plasma serine protease inhibitor-TMPRSS7 complex","type":"exact"},{"name":"protein C inhibitor-matriptase-3 complex","type":"exact"},{"name":"protein C inhibitor-transmembrane protease serine 7 complex","type":"exact"},{"name":"serpin A5-TMPRSS7 complex","type":"exact"}],"termid":"GO:0036024"}


id: GO:1902636
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A ciliary basal body that is part of a kinocilium.","definition_xrefs":["GOC:cilia","GO_REF:0000064","GOC:TermGenie","GOC:krc","PMID:15882574","PMID:15855039"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ciliary basal body","termid":"GO:0036064"},{"relation_name":"part_of","term_name":"kinocilium","termid":"GO:0060091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0015630"],"is_obsolete":false,"name":"kinociliary basal body","synonyms":[{"name":"cilial basal body of kinocilium","type":"exact"},{"name":"ciliary basal body of kinocilium","type":"exact"},{"name":"cilium basal body of kinocilium","type":"exact"},{"name":"kinocilial basal body","type":"exact"},{"name":"kinocilium basal body","type":"exact"},{"name":"kinocilium ciliary basal body","type":"exact"},{"name":"microtubule basal body of kinocilium","type":"exact"}],"termid":"GO:1902636"}


id: GO:0006256
data:
  {"annotated_genes":["SJAG_03676"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113089],"is_not":false,"summary":null,"term":"GO:0006256"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of UDP, uridine (5'-)diphosphate.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine ribonucleoside diphosphate catabolic process","termid":"GO:0009195"},{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide catabolic process","termid":"GO:0009222"},{"relation_name":"is_a","term_name":"UDP metabolic process","termid":"GO:0046048"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03676":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"UDP catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"UDP breakdown","type":"exact"},{"name":"UDP catabolism","type":"exact"},{"name":"UDP degradation","type":"exact"}],"termid":"GO:0006256","terms_by_termid":{"GO:0006256":null}}


id: MONDO:0009981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete retinitis pigmentosa type 1 (obsolete MONDO:0009981)","termid":"MONDO:0009981","xrefs":{"Monarch":{"xref_id":"0009981"}}}


id: GO:0016738
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which reduced flavodoxin acts as a hydrogen or electron donor and reduces dinitrogen.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on reduced flavodoxin as donor","termid":"GO:0016737"}],"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:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"oxidoreductase activity, acting on reduced flavodoxin as donor, dinitrogen as acceptor","secondary_identifiers":["EC:1.19.6.-"],"termid":"GO:0016738"}


id: GO:1905393
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the plant organ. This process pertains to the initial formation of a structure from unspecified parts.","definition_xrefs":["GOC:TermGenie","GOC:tb","GO_REF:0000081"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"plant organ formation","termid":"GO:1905393"}


id: PBO:0111860
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calponin homology (CH) domain","termid":"PBO:0111860"}


id: PBO:0046333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ecto-NOX disulfide-thiol exchanger 2","termid":"PBO:0046333"}


id: PBO:0085557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein containing an N-terminal epsin-like domain; involved in clathrin recruitment and traffic between the Golgi and endosomes; associates with the clathrin adaptor Gga2p, clathrin adaptor complex AP-1, and clathrin","termid":"PBO:0085557"}


id: PBO:0085136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar protein required for export of tRNAs from the nucleus; also copurifies with the small subunit (SSU) processome containing the U3 snoRNA that is involved in processing of pre-18S rRNA","termid":"PBO:0085136"}


id: PBO:0081296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 76","termid":"PBO:0081296"}


id: FYPO:0000895
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An abnormal intracellular mitochondrion distribution phenotype observed in the vegetative growth phase of the life cycle in which mitochondria cluster together more than normal with a cluster distal to one or both sides of the nucleus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitochondrial morphology","termid":"FYPO:0000359"},{"relation_name":"is_a","term_name":"abnormal intracellular mitochondrion distribution","termid":"FYPO:0000894"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0001985","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"mitochondrial aggregation","secondary_identifiers":["FYPO:0000896"],"synonyms":[{"name":"aggregated mitochondria","type":"exact"},{"name":"mitochondrial aggregation at cell end","type":"related"},{"name":"mitochondrial aggregation at cell tip","type":"related"},{"name":"mitochondrial aggregation during mitotic cell cycle","type":"related"},{"name":"mitochondrial aggregation during vegetative growth","type":"exact"}],"termid":"FYPO:0000895"}


id: PBO:0002847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Clr6 histone deacetylase complex subunit Prw1","termid":"PBO:0002847"}


id: GO:0052624
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: demethylphylloquinol + S-adenosyl-L-methionine = H+ + phylloquinol + S-adenosyl-L-homocysteine.","definition_xrefs":["RHEA:40551","PMID:14617060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-methyltransferase activity","termid":"GO:0008169"},{"relation_name":"is_a","term_name":"O-methyltransferase activity","termid":"GO:0008171"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016741","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2-phytyl-1,4-naphthoquinone methyltransferase activity","secondary_identifiers":["KEGG_REACTION:R06859","MetaCyc:RXN-7569","EC:2.1.1.329"],"synonyms":[{"name":"S-adenosyl-L-methionine:2-phytyl-1,4-naphthoquinone methyltransferase activity","type":"exact"},{"name":"S-adenosyl-L-methionine:demethylphylloquinone methyltransferase activity","type":"exact"},{"name":"S-adenosyl-L-methionine:salicylate carboxyl methyltransferase activity","type":"exact"},{"name":"SA methyltransferase activity","type":"broad"},{"name":"demethylphylloquinone methyltransferase activity","type":"exact"},{"name":"salicylate methyltransferase activity","type":"broad"},{"name":"salicylic acid methyltransferase activity","type":"broad"}],"termid":"GO:0052624"}


id: MONDO:0859223
data:
  {"annotated_genes":["SJAG_04127"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86316],"is_not":false,"summary":null,"term":"MONDO:0859223"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04127":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0024322","MONDO:0005066"],"is_obsolete":false,"name":"congenital disorder of glycosylation, type Iw, autosomal dominant","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5562068","MEDGEN:1794278","OMIM:619714"],"termid":"MONDO:0859223","terms_by_termid":{"MONDO:0859223":null},"xrefs":{"Monarch":{"xref_id":"0859223"}}}


id: MONDO:0003128
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pulmonary blastoma composed of a mixture of irregular tubular structures and mesenchymal elements.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pulmonary blastoma","termid":"MONDO:0005933"}],"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":"classic pulmonary blastoma","secondary_identifiers":["DOID:4767","NCIT:C36054","UMLS:C1332556","MEDGEN:231445"],"synonyms":[{"name":"biphasic pulmonary blastoma","type":"exact"},{"name":"classic pulmonary blastoma","type":"exact"}],"termid":"MONDO:0003128","xrefs":{"Monarch":{"xref_id":"0003128"}}}


id: PBO:0076234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"surfeit 2","termid":"PBO:0076234"}


id: GO:0034760
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of iron ions from one side of a membrane to the other by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of iron ion transport","termid":"GO:0034757"},{"relation_name":"is_a","term_name":"regulation of iron ion transmembrane transport","termid":"GO:0034759"},{"relation_name":"is_a","term_name":"negative regulation of cation transmembrane transport","termid":"GO:1904063"},{"relation_name":"negatively_regulates","term_name":"iron ion transmembrane transport","termid":"GO:0034755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"negative regulation of iron ion transmembrane transport","synonyms":[{"name":"down regulation of transmembrane iron ion transport","type":"exact"},{"name":"down-regulation of transmembrane iron ion transport","type":"exact"},{"name":"downregulation of transmembrane iron ion transport","type":"exact"},{"name":"inhibition of transmembrane iron ion transport","type":"narrow"},{"name":"negative regulation of iron ion membrane transport","type":"exact"},{"name":"negative regulation of transmembrane iron ion transport","type":"exact"},{"name":"negative regulation of transmembrane iron transport","type":"exact"}],"termid":"GO:0034760"}


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


id: GO:1904372
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein localization to actin cortical patch.","definition_xrefs":["GOC:TermGenie","PMID:18216290","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to actin cortical patch","termid":"GO:1904370"},{"relation_name":"is_a","term_name":"positive regulation of protein localization to cell cortex","termid":"GO:1904778"},{"relation_name":"positively_regulates","term_name":"protein localization to actin cortical patch","termid":"GO:0044379"}],"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 protein localization to actin cortical patch","synonyms":[{"name":"activation of protein localisation to actin cortical patch","type":"narrow"},{"name":"activation of protein localization to actin cortical patch","type":"narrow"},{"name":"positive regulation of protein localisation to actin cortical patch","type":"exact"},{"name":"up regulation of protein localisation to actin cortical patch","type":"exact"},{"name":"up regulation of protein localization to actin cortical patch","type":"exact"},{"name":"up-regulation of protein localisation to actin cortical patch","type":"exact"},{"name":"up-regulation of protein localization to actin cortical patch","type":"exact"},{"name":"upregulation of protein localisation to actin cortical patch","type":"exact"},{"name":"upregulation of protein localization to actin cortical patch","type":"exact"}],"termid":"GO:1904372"}


id: GO:0140985
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a chemorepellent and transmitting the signal across the membrane by activating an associated G-protein; promotes the exchange of GDP for GTP on the alpha subunit of a heterotrimeric G-protein complex.","definition_xrefs":["PMID:30462573"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"G protein-coupled chemorepellent receptor activity","synonyms":[{"name":"G protein chemorepellent receptor activity","type":"exact"},{"name":"G-protein chemorepellent receptor activity","type":"exact"},{"name":"G-protein coupled chemorepellent receptor activity","type":"exact"}],"termid":"GO:0140985"}


id: GO:0006774
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete vitamin B12 reduction (obsolete GO:0006774)","synonyms":[{"name":"vitamin B12 reduction","type":"exact"}],"termid":"GO:0006774"}


id: GO:1903483
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of maintenance of mitotic actomyosin contractile ring localization.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:mtg_cell_cycle"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of maintenance of mitotic actomyosin contractile ring localization (obsolete GO:1903483)","synonyms":[{"name":"regulation of cytokinetic ring anchoring involved in mitotic cell cycle","type":"related"},{"name":"regulation of maintenance of contractile ring localisation involved in cell cycle cytokinesis involved in mitotic cell cycle","type":"exact"},{"name":"regulation of maintenance of contractile ring localization involved in cell cycle cytokinesis involved in mitotic cell cycle","type":"exact"},{"name":"regulation of maintenance of contractile ring localization involved in cytokinesis during cell cycle involved in mitotic cell cycle","type":"related"}],"termid":"GO:1903483"}


id: PBO:0053416
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 354","termid":"PBO:0053416"}


id: PBO:0071811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S2 pseudogene 6","termid":"PBO:0071811"}


id: GO:0072127
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the renal capsule over time, from its formation to the mature structure. The renal capsule is the tough fibrous layer surrounding the kidney, covered in a thick layer of perinephric adipose tissue. It provides some protection from trauma and damage. During development, it comprises a single layer of flattened cells that lie just above the cortical stroma and the condensed mesenchyme of the nephrogenic zone. It is in this region that the early stages of nephron induction and formation of new generations ureteric bud branches occur, as the kidney expands.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"connective tissue development","termid":"GO:0061448"},{"relation_name":"part_of","term_name":"kidney development","termid":"GO:0001822"}],"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":"renal capsule development","termid":"GO:0072127"}


id: PBO:0082952
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic phosphorelay intermediate osmosensor and regulator; part of a two-component signal transducer that mediates osmosensing via a phosphorelay mechanism; required for mitophagy; dephosphorylated form is degraded by the ubiquitin-proteasome system; potential Cdc28p substrate","termid":"PBO:0082952"}


id: PBO:0005352
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.4.-","termid":"PBO:0005352"}


id: PBO:0078272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 8-1","termid":"PBO:0078272"}


id: GO:1901223
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of non-canonical NF-kappaB signaling cascade.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of non-canonical NF-kappaB signal transduction","termid":"GO:1901222"},{"relation_name":"is_a","term_name":"negative regulation of intracellular signal transduction","termid":"GO:1902532"},{"relation_name":"negatively_regulates","term_name":"non-canonical NF-kappaB signal transduction","termid":"GO:0038061"}],"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:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of non-canonical NF-kappaB signal transduction","secondary_identifiers":["GO:0042347"],"synonyms":[{"name":"down regulation of NIK/NF-kappaB cascade","type":"exact"},{"name":"down regulation of non-canonical NF-KB signaling","type":"exact"},{"name":"down regulation of noncanonical NF-kappaB signaling","type":"exact"},{"name":"down regulation of noncanonical nuclear factor kappaB (NF-kappaB) pathway","type":"exact"},{"name":"down regulation of p52-dependent NF-kappaB signaling","type":"narrow"},{"name":"down-regulation of NIK/NF-kappaB cascade","type":"exact"},{"name":"down-regulation of non-canonical NF-KB signaling","type":"exact"},{"name":"down-regulation of noncanonical NF-kappaB signaling","type":"exact"},{"name":"down-regulation of noncanonical nuclear factor kappaB (NF-kappaB) pathway","type":"exact"},{"name":"down-regulation of p52-dependent NF-kappaB signaling","type":"narrow"},{"name":"downregulation of NIK/NF-kappaB cascade","type":"exact"},{"name":"downregulation of non-canonical NF-KB signaling","type":"exact"},{"name":"downregulation of noncanonical NF-kappaB signaling","type":"exact"},{"name":"downregulation of noncanonical nuclear factor kappaB (NF-kappaB) pathway","type":"exact"},{"name":"downregulation of p52-dependent NF-kappaB signaling","type":"narrow"},{"name":"inhibition of NIK/NF-kappaB cascade","type":"narrow"},{"name":"inhibition of non-canonical NF-KB signaling","type":"exact"},{"name":"inhibition of noncanonical NF-kappaB signaling","type":"exact"},{"name":"inhibition of noncanonical nuclear factor kappaB (NF-kappaB) pathway","type":"exact"},{"name":"inhibition of p52-dependent NF-kappaB signaling","type":"narrow"},{"name":"negative regulation of NF-kappaB import into nucleus","type":"narrow"},{"name":"negative regulation of NIK/NF-kappaB cascade","type":"exact"},{"name":"negative regulation of NIK/NF-kappaB signaling","type":"exact"},{"name":"negative regulation of non-canonical NF-KB signaling","type":"exact"},{"name":"negative regulation of noncanonical NF-kappaB signaling","type":"exact"},{"name":"negative regulation of noncanonical nuclear factor kappaB (NF-kappaB) pathway","type":"exact"},{"name":"negative regulation of p52-dependent NF-kappaB signaling","type":"narrow"}],"termid":"GO:1901223"}


id: PBO:0048702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucagon like peptide 1 receptor","termid":"PBO:0048702"}


id: MONDO:0012092
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary sensory and autonomic neuropathy, type 5 (HSAN5) is characterized by loss of pain perception and impaired temperature sensitivity, in the absence of any other major neurological anomalies.","definition_xrefs":["Orphanet:64752"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary sensory and autonomic neuropathy","termid":"MONDO:0015364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"hereditary sensory and autonomic neuropathy type 5","secondary_identifiers":["PMID:14976160","OMIM:608654","UMLS:C0020075","DOID:0070145","GARD:12328","icd11.foundation:1411011731","SCTID:128206006","PMID:77656","MEDGEN:6916"],"synonyms":[{"name":"HSAN 5","type":"related"},{"name":"HSAN V","type":"related"},{"name":"HSAN5","type":"exact"},{"name":"NGF autosomal recessive hereditary sensory and autonomic neuropathy","type":"exact"},{"name":"autosomal recessive hereditary sensory and autonomic neuropathy caused by mutation in NGF","type":"exact"},{"name":"congenital insensitivity to pain and thermal analgesia","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy type V","type":"exact"},{"name":"insensitivity to pain, congenital","type":"related"},{"name":"neuropathy, hereditary sensory and autonomic, type 5","type":"related"},{"name":"neuropathy, hereditary sensory and autonomic, type V","type":"related"}],"termid":"MONDO:0012092","xrefs":{"Monarch":{"xref_id":"0012092"}}}


id: PBO:0077189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell leukemia homeobox 1","termid":"PBO:0077189"}


id: MONDO:0015904
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare hypolipidemia (obsolete MONDO:0015904)","secondary_identifiers":["Orphanet:181431"],"termid":"MONDO:0015904","xrefs":{"Monarch":{"xref_id":"0015904"}}}


id: MONDO:0003881
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An apocrine adenocarcinoma that arises from the sweat glands in the vulva.","definition_xrefs":["NCIT:C40308"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apocrine adenocarcinoma","termid":"MONDO:0003214"},{"relation_name":"is_a","term_name":"vulvar adenocarcinoma","termid":"MONDO:0024336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"vulvar apocrine adenocarcinoma","secondary_identifiers":["DOID:6448","UMLS:C2202741","MEDGEN:384494"],"synonyms":[{"name":"apocrine adenocarcinoma of mammalian vulva","type":"exact"},{"name":"mammalian vulva apocrine adenocarcinoma","type":"exact"},{"name":"vulvar apocrine adenocarcinoma","type":"exact"}],"termid":"MONDO:0003881","xrefs":{"Monarch":{"xref_id":"0003881"}}}


id: FYPO:0007553
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the G1 to G0 transition is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation phenotype","termid":"FYPO:0000145"},{"relation_name":"is_a","term_name":"normal cell cycle process","termid":"FYPO:0006915"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal G1 to G0 transition","synonyms":[{"name":"normal G1/G0 transition","type":"exact"},{"name":"normal cell cycle quiescence","type":"related"},{"name":"normal establishment of cell quiescence","type":"exact"}],"termid":"FYPO:0007553"}


id: PBO:0077472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 191C","termid":"PBO:0077472"}


id: MONDO:0018118
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement (obsolete MONDO:0018118)","secondary_identifiers":["Orphanet:352306"],"termid":"MONDO:0018118","xrefs":{"Monarch":{"xref_id":"0018118"}}}


id: PBO:0067274
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 352, pseudogene","termid":"PBO:0067274"}


id: GO:0015757
data:
  {"annotated_genes":["SJAG_00057"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109789],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140425"}]},"cv_name":"biological_process","definition":"The process in which galactose is transported across a lipid bilayer, from one side of a membrane to the other. D-galactose is widely distributed in combined form in plants, animals and microorganisms as a constituent of oligo- and polysaccharides; it also occurs in galactolipids and as its glucoside in lactose and melibiose.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexose transmembrane transport","termid":"GO:0008645"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00057":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"galactose transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"galactose transport","type":"related"}],"termid":"GO:0015757","terms_by_termid":{"GO:0140425":null}}


id: MONDO:0007804
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pallister-Hall syndrome (PHS), a pleiotropic autosomal dominant malformative disorder, is characterized by hypothalamic hamartoma, pituitary dysfunction, bifid epiglottis, polydactyly, and, more rarely, renal abnormalities and genitourinary malformations.","definition_xrefs":["Orphanet:672"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"is_a","term_name":"non-acquired combined pituitary hormone deficiency","termid":"MONDO:0018762"},{"relation_name":"is_a","term_name":"polydactyly-syndactyly-triphalangism","termid":"MONDO:0800066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pallister-Hall syndrome","secondary_identifiers":["SCTID:56677004","OMIM:146510","MEDGEN:120514","NCIT:C84987","GARD:7305","UMLS:C0265220","DOID:9248","icd11.foundation:1845613381","MESH:D054975","NORD:1545","ICD9:759.89"],"synonyms":[{"name":"PHS","type":"exact"},{"name":"Pallister Hall syndrome","type":"exact"},{"name":"Pallister-Hall syndrome","type":"exact"},{"name":"ano-cerebro-digital syndrome","type":"exact"},{"name":"hypothalamic hamartoblastoma syndrome","type":"exact"},{"name":"hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly","type":"exact"}],"termid":"MONDO:0007804","xrefs":{"Monarch":{"xref_id":"0007804"}}}


id: RO:0002336
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of positively regulates","direct_ancestors":[{"relation_name":"is_a","term_name":"regulated_by","termid":"RO:0002334"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"positively_regulated_by","termid":"RO:0002336"}


id: MONDO:0017753
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete disorder of peroxisomal alpha-, beta- and omega-oxidation (obsolete MONDO:0017753)","secondary_identifiers":["Orphanet:309810","icd11.foundation:1092479335"],"synonyms":[{"name":"disorder of peroxisomal alpha-, beta- and omega-oxidation","type":"exact"}],"termid":"MONDO:0017753","xrefs":{"Monarch":{"xref_id":"0017753"}}}


id: MONDO:0007183
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"azotemia, familial","secondary_identifiers":["MESH:C566233","UMLS:C1862358","OMIM:109160","MEDGEN:400033"],"synonyms":[{"name":"azotemia, familial","type":"exact"}],"termid":"MONDO:0007183","xrefs":{"Monarch":{"xref_id":"0007183"}}}


id: PBO:0052160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium inwardly rectifying channel subfamily J member 8","termid":"PBO:0052160"}


id: MONDO:0100490
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"isolated congenital breast hypoplasia/aplasia","termid":"MONDO:0015855"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breasts and/or nipples, aplasia or hypoplasia of, 1","secondary_identifiers":["GARD:15045","OMIM:113700"],"synonyms":[{"name":"BNAH1","type":"exact"},{"name":"amastia","type":"related"},{"name":"amazia","type":"related"},{"name":"athelia","type":"related"},{"name":"breasts and/or nipples, aplasia or hypoplasia of, 1","type":"exact"}],"termid":"MONDO:0100490","xrefs":{"Monarch":{"xref_id":"0100490"}}}


id: MONDO:0031037
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare evolutive vascular malformation disorder characterized by closely clustered irregular dilated capillaries that can be asymptomatic or that can cause variable neurological manifestations such as seizures, non-specific headaches, progressive or transient focal neurologic deficits, and/or cerebral hemorrhages.","definition_xrefs":["Orphanet:221061"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral cavernous malformation","termid":"MONDO:0000820"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"famililal cerebral cavernous malformations","secondary_identifiers":["GARD:13641","MEDGEN:419031","SCTID:717003001","OMIMPS:116860","UMLS:C2931263"],"synonyms":[{"name":"CCM","type":"related"},{"name":"cavernous angioma, familial","type":"related"},{"name":"cavernous angiomatous malformations","type":"related"},{"name":"cavernous malformations of CNS and retina","type":"related"},{"name":"cerebral capillary malformations","type":"related"},{"name":"cerebral cavernous malformations","type":"related"},{"name":"familial brain cavernous angioma","type":"exact"},{"name":"familial brain cavernous hemangioma","type":"exact"},{"name":"familial cerebral cavernoma","type":"exact"},{"name":"familial cerebral cavernous malformation","type":"exact"},{"name":"famililal cerebral cavernous malformations","type":"exact"},{"name":"hereditary brain cavernous angioma","type":"exact"},{"name":"hereditary brain cavernous hemangioma","type":"exact"},{"name":"hereditary cerebral cavernoma","type":"exact"},{"name":"hereditary cerebral cavernous malformation","type":"exact"},{"name":"hyperkeratotic cutaneous capillary-Venous malformations associated with cerebral capillary malformations","type":"related"}],"termid":"MONDO:0031037","xrefs":{"Monarch":{"xref_id":"0031037"}}}


id: PBO:0030932
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_glutamate-ammonia_ligase_activity","termid":"PBO:0030932"}


id: MONDO:0850009
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":"syndromic microspherophakia","secondary_identifiers":["UMLS:C5681371","Orphanet:519294","GARD:22093","MEDGEN:1842434"],"termid":"MONDO:0850009","xrefs":{"Monarch":{"xref_id":"0850009"}}}


id: PBO:0063514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decaprenyl diphosphate synthase subunit 2","termid":"PBO:0063514"}


id: FYPO:0003247
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of histone H3 binding by a gene product (usually a protein) in a mutant does not occur. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone binding","termid":"FYPO:0007157"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0001985","FYPO:0000702"],"is_obsolete":false,"name":"abolished histone H3 binding","synonyms":[{"name":"abolished protein-histone H3 interaction","type":"exact"},{"name":"histone H3 binding abolished","type":"exact"}],"termid":"FYPO:0003247"}


id: GO:1990074
data:
  {"annotated_genes":["SJAG_04118","SJAG_02370","SJAG_03876","SJAG_02383"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89991,94821,116359],"is_not":false,"summary":null,"term":"GO:1990074"},{"annotations":[90870],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0036450"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of a messenger RNA (mRNA) molecule, initiated by the enzymatic addition of a sequence of uridylyl residues (polyuridylation) at the 3' end of the target mRNA.","definition_xrefs":["PMID:23503588","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA catabolic process","termid":"GO:0006402"},{"relation_name":"is_a","term_name":"modification-dependent macromolecule catabolic process","termid":"GO:0043632"},{"relation_name":"is_a","term_name":"mRNA destabilization","termid":"GO:0061157"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02370":null,"SJAG_02383":null,"SJAG_03876":null,"SJAG_04118":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0016071"],"is_obsolete":false,"name":"polyuridylation-dependent mRNA catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990074","terms_by_termid":{"GO:0036450":null,"GO:1990074":null}}


id: PBO:0065613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PTP4A1 pseudogene 7","termid":"PBO:0065613"}


id: GO:0051981
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a copper chelate from one side of a membrane to the other. A copper chelate is a heterocyclic compound having a metal ion attached by coordinate bonds to at least two nonmetal ions.","definition_xrefs":["PMID:26512647"],"direct_ancestors":[{"relation_name":"is_a","term_name":"copper ion transmembrane transporter activity","termid":"GO:0005375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"copper chelate transmembrane transporter activity","termid":"GO:0051981"}


id: PBO:0084330
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Killer toxin; encoded on the left arm of chromosome IX in some strains, including YJM789","termid":"PBO:0084330"}


id: PBO:0000347
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Binding Upb Nine of 107 kDa","termid":"PBO:0000347"}


id: MONDO:0850473
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diffuse large B-cell lymphoma that is characterized by aneuploidy with TP53 inactivation.","definition_xrefs":["DOID:0081069"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"A53 diffuse large B-cell lymphoma","secondary_identifiers":["UMLS:C5707085","MEDGEN:1815990"],"termid":"MONDO:0850473","xrefs":{"Monarch":{"xref_id":"0850473"}}}


id: PATO:0000110
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000110 drought sensitivity (obsolete PATO:0000110)","termid":"PATO:0000110"}


id: PBO:0042842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 46","termid":"PBO:0042842"}


id: PBO:0028100
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_alcohol_dehydrogenase_activity","termid":"PBO:0028100"}


id: GO:0009806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving lignans, any member of a class of plant metabolites related to lignins. Lignans are usually found as phenylpropanoid dimers in which the phenylpropanoid units are linked tail to tail and thus having a 2,3 dibenzylbutane skeleton, but higher oligomers can also exist.","definition_xrefs":["PMID:10074466","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenylpropanoid metabolic process","termid":"GO:0009698"}],"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":"lignan metabolic process","synonyms":[{"name":"lignan metabolism","type":"exact"}],"termid":"GO:0009806"}


id: MONDO:0020088
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial partial lipodystrophy (FPLD) is a group of rare genetic lipodystrophic syndromes characterized, in most cases, by fat loss from the limbs and buttocks, from childhood or early adulthood, and often associated with acanthosis nigricans, insulin resistance, diabetes, hypertriglyceridemia and liver steatosis.","definition_xrefs":["Orphanet:98306"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary lipodystrophy","termid":"MONDO:0020087"},{"relation_name":"is_a","term_name":"laminopathy","termid":"MONDO:0021106"},{"relation_name":"is_a","term_name":"partial lipodystrophy","termid":"MONDO:0027767"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005066"],"is_obsolete":false,"name":"familial partial lipodystrophy","secondary_identifiers":["DOID:0050440","GARD:11962","icd11.foundation:1661968243","OMIMPS:151660","MEDGEN:124408","NANDO:1200861","SCTID:49292002","NCIT:C84708","NORD:1131","UMLS:C0271694","MESH:D052496"],"synonyms":[{"name":"FPLD","type":"exact"},{"name":"Koberling-Dunnigan syndrome","type":"exact"},{"name":"congenital partial lipodystrophy","type":"exact"},{"name":"genetic partial lipodystrophy","type":"exact"},{"name":"lipodystrophy, familial partial","type":"exact"}],"termid":"MONDO:0020088","xrefs":{"Monarch":{"xref_id":"0020088"}}}


id: MONDO:1011849
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myasthenia, non-human animal","secondary_identifiers":["OMIA:000684"],"termid":"MONDO:1011849","xrefs":{"Monarch":{"xref_id":"1011849"}}}


id: PBO:0045441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPY19L4 pseudogene 1","termid":"PBO:0045441"}


id: MONDO:0003841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign adipose tissue neoplasm of the heart usually originating in the epicardial or pericardial fatty tissue.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoma","termid":"MONDO:0005106"},{"relation_name":"is_a","term_name":"benign neoplasm of heart","termid":"MONDO:0021450"}],"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":"heart lipoma","secondary_identifiers":["NCIT:C6741","UMLS:C1332849","DOID:6285","MEDGEN:272436"],"synonyms":[{"name":"Cardiac lipoma","type":"exact"},{"name":"heart lipoma","type":"exact"},{"name":"lipoma of heart","type":"exact"},{"name":"lipoma of the heart","type":"exact"}],"termid":"MONDO:0003841","xrefs":{"Monarch":{"xref_id":"0003841"}}}


id: PBO:0042744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromere protein S","termid":"PBO:0042744"}


id: GO:0050407
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: [glycogen-synthase D] + H2O = [glycogen-synthase I] + phosphate.","definition_xrefs":["EC:3.1.3.42","MetaCyc:GLYCOGEN-SYNTHASE-D-PHOSPHATASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoprotein phosphatase activity","termid":"GO:0004721"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0004721"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0003824","GO:0004721","GO:0016787","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"[glycogen-synthase-D] phosphatase activity","synonyms":[{"name":"Mg2+ dependent glycogen synthase phosphatase activity","type":"related"},{"name":"UDP-glucose:glycogen 4-alpha-D-glucosyltransferase-D phosphohydrolase activity","type":"related"},{"name":"UDP-glycogen glucosyltransferase phosphatase activity","type":"related"},{"name":"UDPglucose-glycogen glucosyltransferase phosphatase activity","type":"related"},{"name":"UDPglucose:glycogen 4-alpha-D-glucosyltransferase-D phosphohydrolase activity","type":"related"},{"name":"glycogen glucosyltransferase phosphatase activity","type":"related"},{"name":"glycogen synthase D phosphatase activity","type":"related"},{"name":"glycogen synthase phosphatase activity","type":"related"},{"name":"glycogen synthetase phosphatase activity","type":"related"},{"name":"glycogen-synthase-D phosphatase activity","type":"related"},{"name":"phosphatase type 2oC","type":"related"},{"name":"uridine diphosphoglucose-glycogen glucosyltransferase phosphatase activity","type":"related"}],"termid":"GO:0050407"}


id: FYPO:0001217
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which nuclear import is abnormal. Nuclear import is the directed movement of any substance out of the nucleus; import of all substances or a specific substance may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nuclear transport during vegetative growth","termid":"FYPO:0000518"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"abnormal nuclear import","synonyms":[{"name":"abnormal nuclear import during mitotic cell cycle","type":"related"},{"name":"abnormal nuclear import during vegetative growth","type":"exact"}],"termid":"FYPO:0001217"}


id: PBO:0072638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retbindin","termid":"PBO:0072638"}


id: PBO:0050642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock transcription factor Y-linked 7, pseudogene","termid":"PBO:0050642"}


id: GO:0042826
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to histone deacetylase.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme binding","termid":"GO:0019899"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"histone deacetylase binding","termid":"GO:0042826"}


id: PBO:0002457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotic recombination protein Rec10","termid":"PBO:0002457"}


id: GO:0019031
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer of a virion that surrounds the protein capsid. May also contain glycoproteins.","definition_xrefs":["Wikipedia:Viral_envelope","GOC:bm","GOC:bf","GOC:jl","ISBN:0781718325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral membrane","termid":"GO:0036338"}],"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":"viral envelope","synonyms":[{"name":"viral glycoprotein","type":"related"},{"name":"viral outside membrane","type":"exact"}],"termid":"GO:0019031"}


id: PBO:0090754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERCC8 DNA repair homolog","termid":"PBO:0090754"}


id: GO:0000474
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process involved in the maturation of a precursor Small SubUnit (SSU) ribosomal RNA (rRNA) molecule into a mature SSU-rRNA molecule from the pre-rRNA molecule originally produced as a tetracistronic rRNA transcript that contains the Small Subunit (SSU) rRNA, 5.8 S rRNA, 2S rRNA, and Large Subunit (LSU) in that order from 5' to 3' along the primary transcript.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maturation of SSU-rRNA","termid":"GO:0030490"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0042254"}],"interesting_parent_ids":["GO:0010467","GO:0044085","GO:0008150","GO:0042254"],"is_obsolete":false,"name":"maturation of SSU-rRNA from tetracistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, 2S rRNA, LSU-rRNA)","termid":"GO:0000474"}


id: MONDO:0019858
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown.","definition_xrefs":["Orphanet:95717"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital hypothyroidism","termid":"MONDO:0018612"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"idiopathic congenital hypothyroidism","secondary_identifiers":["MEDGEN:901252","UMLS:C4273913","GARD:19298","SCTID:717334008"],"termid":"MONDO:0019858","xrefs":{"Monarch":{"xref_id":"0019858"}}}


id: PBO:0087266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ser/Thr kinase involved in transcription and stress response; functions as part of a network of genes in exit from mitosis; localization is cell cycle regulated; activated by Cdc15p during the exit from mitosis; also plays a role in regulating the stability of SWI5 and CLB2 mRNAs; phosphorylates Chs2p to regulate primary septum formation and Hof1p to regulate cytokinesis; DBF2 has a paralog, DBF20, that arose from the whole genome duplication","termid":"PBO:0087266"}


id: MONDO:0001543
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A peripheral nerve lesion that involves the sciatic nerve.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"mononeuritis of lower limb","termid":"MONDO:0004797"},{"relation_name":"is_a","term_name":"lumbosacral plexus lesion","termid":"MONDO:0001829"},{"relation_name":"is_a","term_name":"sciatic neuropathy","termid":"MONDO:0006960"},{"relation_name":"is_a","term_name":"peripheral nerve lesion","termid":"MONDO:0024334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"lesion of sciatic nerve","secondary_identifiers":["icd11.foundation:1358497313","DOID:12528","MEDGEN:56346","SCTID:367137004","ICD9:355.0","ICD10CM:G57.0","UMLS:C0154748"],"synonyms":[{"name":"peripheral nerve lesion of sciatic nerve","type":"exact"},{"name":"sciatic nerve peripheral nerve lesion","type":"exact"}],"termid":"MONDO:0001543","xrefs":{"Monarch":{"xref_id":"0001543"}}}


id: PBO:0065900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB42, member RAS oncogene family, pseudogene 1","termid":"PBO:0065900"}


id: PBO:0046206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongin B pseudogene 3","termid":"PBO:0046206"}


id: PBO:0085475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Probable Hsp40p co-chaperone; has a DnaJ-like domain and appears to be involved in ER-associated degradation of misfolded proteins containing a tightly folded cytoplasmic domain; inhibits replication of Brome mosaic virus in S. cerevisiae","termid":"PBO:0085475"}


id: GO:0031243
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the cell outer membrane consisting of the gene products and protein complexes that penetrate the external side of the cell outer membrane only, either directly or via some covalently attached hydrophobic anchor.","definition_xrefs":["GOC:mtg_sensu","GOC:mah","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete intrinsic component of external side of cell outer membrane (obsolete GO:0031243)","synonyms":[{"name":"intrinsic to external leaflet of cell outer membrane","type":"exact"},{"name":"intrinsic to external side of cell outer membrane","type":"narrow"},{"name":"intrinsic to external side of outer membrane","type":"exact"}],"termid":"GO:0031243"}


id: PBO:0012287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pre-60S shuttling factor (predicted)","termid":"PBO:0012287"}


id: PBO:0002893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LEM domain protein Man1, Sad1 interacting factor (predicted)","termid":"PBO:0002893"}


id: PBO:0070254
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 197 pseudogene","termid":"PBO:0070254"}


id: GO:0004932
data:
  {"annotated_genes":["SJAG_01345","SJAG_01978"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96242],"is_not":false,"summary":null,"term":"GO:0004932"},{"annotations":[87356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036320"}]},"cv_name":"molecular_function","definition":"Combining with a mating-type factor pheromone to initiate a change in cell activity.","definition_xrefs":["GOC:dph","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled peptide receptor activity","termid":"GO:0008528"},{"relation_name":"is_a","term_name":"pheromone receptor activity","termid":"GO:0016503"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01345":null,"SJAG_01978":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"mating-type factor pheromone receptor activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0004932","terms_by_termid":{"GO:0004932":null,"GO:0036320":null}}


id: MONDO:0002350
data:
  {"annotated_genes":["SJAG_03986","SJAG_04000","SJAG_03361","SJAG_04148","SJAG_03182","SJAG_00933","SJAG_01374","SJAG_04017","SJAG_01185","SJAG_00093","SJAG_04621","SJAG_04013","SJAG_00864","SJAG_00471"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85522],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013836"},{"annotations":[84323],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011303"},{"annotations":[85129],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014752"},{"annotations":[85053,85054],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014817"},{"annotations":[85052],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014818"},{"annotations":[85613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032580"},{"annotations":[85614,85615],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032581"},{"annotations":[85611],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032582"},{"annotations":[85138,85139],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0026726"},{"annotations":[84240],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014099"},{"annotations":[85058],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014257"}]},"cv_name":"mondo","definition":"An instance of nephrotic syndrome that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephrotic syndrome","termid":"MONDO:0005377"},{"relation_name":"is_a","term_name":"inherited kidney disorder","termid":"MONDO:0100191"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00093":null,"SJAG_00471":null,"SJAG_00864":null,"SJAG_00933":null,"SJAG_01185":null,"SJAG_01374":null,"SJAG_03182":null,"SJAG_03361":null,"SJAG_03986":null,"SJAG_04000":null,"SJAG_04013":null,"SJAG_04017":null,"SJAG_04148":null,"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"familial nephrotic syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:256300","icd11.foundation:1524476844","DOID:2590","SCTID:48796009","UMLS:C3501848","MEDGEN:502251","NCIT:C35337"],"synonyms":[{"name":"congenital nephrotic syndrome","type":"exact"},{"name":"hereditary nephrotic syndrome","type":"exact"}],"termid":"MONDO:0002350","terms_by_termid":{"MONDO:0011303":null,"MONDO:0013836":null,"MONDO:0014099":null,"MONDO:0014257":null,"MONDO:0014752":null,"MONDO:0014817":null,"MONDO:0014818":null,"MONDO:0026726":null,"MONDO:0032580":null,"MONDO:0032581":null,"MONDO:0032582":null},"xrefs":{"Monarch":{"xref_id":"0002350"}}}


id: PBO:0011114
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin-tyrosine ligase Pby1 (predicted)","termid":"PBO:0011114"}


id: MONDO:1011400
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pituitary-dependent hyperadrenocorticism that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenoma, non-human","termid":"MONDO:0700133"},{"relation_name":"is_a","term_name":"connective tissue disorder, non-human animal","termid":"MONDO:1011309"},{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"},{"relation_name":"is_a","term_name":"reproductive system disorder, non-human animal","termid":"MONDO:1011354"},{"relation_name":"is_a","term_name":"hyperadrenocorticism, non-human animal","termid":"MONDO:1011403"},{"relation_name":"is_a","term_name":"hereditary neurological disease, non-human animal","termid":"MONDO:1012972"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pituitary-dependent hyperadrenocorticism, non-human animal","secondary_identifiers":["OMIA:000247"],"termid":"MONDO:1011400","xrefs":{"Monarch":{"xref_id":"1011400"}}}


id: PBO:0040748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain cytoplasmic RNA 1, pseudogene 3","termid":"PBO:0040748"}


id: GO:1901337
data:
  {"annotated_genes":["SJAG_04325"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035348"}]},"cv_name":"biological_process","definition":"The directed movement of a thioester into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound transport","termid":"GO:0072348"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04325":null},"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":"thioester transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1901337","terms_by_termid":{"GO:0035348":null}}


id: PR:Q9Y7P8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC191.04c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7P8"],"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 membrane protein C191.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC191.04c","synonyms":[{"name":"Spom972h-SPCC191.04c","type":"exact"}],"termid":"PR:Q9Y7P8"}


id: PBO:0027162
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_kinetochore_during_meiosis_I","termid":"PBO:0027162"}


id: PBO:0005680
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expressed during stationary phase","termid":"PBO:0005680"}


id: MONDO:0004640
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the stomach resulting from alcohol ingestion.","definition_xrefs":["NCIT:C26977"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gastritis","termid":"MONDO:0004966"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"alcoholic gastritis","secondary_identifiers":["ICD9:535.3","SCTID:2043009","ICD9:535.30","UMLS:C0156076","ICD10CM:K29.2","MEDGEN:102345","DOID:8680","icd11.foundation:1081291109"],"synonyms":[{"name":"alcoholic gastritis","type":"exact"},{"name":"alcoholic gastritis, with haemorrhage","type":"exact"},{"name":"alcoholic gastritis, with hemorrhage","type":"exact"},{"name":"alcoholic gastritis, without mention of haemorrhage","type":"exact"},{"name":"alcoholic gastritis, without mention of hemorrhage","type":"exact"}],"termid":"MONDO:0004640","xrefs":{"Monarch":{"xref_id":"0004640"}}}


id: GO:0052432
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism modulates the frequency, rate or extent of programmed cell death in the symbiont, where programmed cell death proceeds by apoptosis. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation by organism of symbiont apoptosis (obsolete GO:0052432)","synonyms":[{"name":"modulation by organism of symbiont apoptosis","type":"exact"},{"name":"modulation by organism of symbiont apoptotic programmed cell death","type":"exact"}],"termid":"GO:0052432"}


id: PBO:0068959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 203, pseudogene","termid":"PBO:0068959"}


id: PBO:0012579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diphthamide synthetase (predicted)","termid":"PBO:0012579"}


id: PR:O42853
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rtr1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42853"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit B1 CTD phosphatase rtr1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23A1.16c","synonyms":[{"name":"RNA polymerase II-associated protein 2 homolog rtr1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-rtr1","type":"exact"}],"termid":"PR:O42853"}


id: GO:0043409
data:
  {"annotated_genes":["SJAG_02392","SJAG_00975","SJAG_03185","SJAG_05000","SJAG_03263","SJAG_04825","SJAG_01114","SJAG_03893","SJAG_02000","SJAG_02013","SJAG_04522","SJAG_02233"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87418,106295],"is_not":false,"summary":null,"term":"GO:0043409"},{"annotations":[106204,102980,117439,95048,106769,98633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903138"},{"annotations":[90862,98635,94230,95168,116210,117440],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903753"},{"annotations":[106296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180040"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of signal transduction mediated by the MAPKKK cascade.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of MAPK cascade","termid":"GO:0043408"},{"relation_name":"is_a","term_name":"negative regulation of intracellular signal transduction","termid":"GO:1902532"},{"relation_name":"negatively_regulates","term_name":"MAPK cascade","termid":"GO:0000165"}],"gene_count":12,"genes_by_uniquename":{"SJAG_00975":null,"SJAG_01114":null,"SJAG_02000":null,"SJAG_02013":null,"SJAG_02233":null,"SJAG_02392":null,"SJAG_03185":null,"SJAG_03263":null,"SJAG_03893":null,"SJAG_04522":null,"SJAG_04825":null,"SJAG_05000":null},"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:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of MAPK cascade","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of MAPK cascade","type":"exact"},{"name":"down regulation of MAPKKK cascade","type":"exact"},{"name":"down-regulation of MAPK cascade","type":"exact"},{"name":"down-regulation of MAPKKK cascade","type":"exact"},{"name":"downregulation of MAPK cascade","type":"exact"},{"name":"downregulation of MAPKKK cascade","type":"exact"},{"name":"inhibition of MAPK cascade","type":"narrow"},{"name":"inhibition of MAPKKK cascade","type":"narrow"},{"name":"negative regulation of MAP kinase cascade","type":"exact"},{"name":"negative regulation of MAP kinase kinase kinase cascade","type":"exact"},{"name":"negative regulation of MAPKKK cascade","type":"exact"},{"name":"negative regulation of mitogen activated protein kinase cascade","type":"exact"},{"name":"negative regulation of mitogen activated protein kinase kinase kinase cascade","type":"exact"},{"name":"negative regulation of mitogen-activated protein kinase cascade","type":"exact"},{"name":"negative regulation of mitogen-activated protein kinase kinase kinase cascade","type":"exact"}],"termid":"GO:0043409","terms_by_termid":{"GO:0043409":null,"GO:0180040":null,"GO:1903138":null,"GO:1903753":null}}


id: MOD:00416
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A change resulting in an alteration of the measured molecular mass of a peptide or protein hydroxyl amino acid phosphorylated promptly followed by secondary loss of a neutral trihydrogen phosphate molecular fragment.","definition_xrefs":["Unimod:23"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified residue with neutral loss of phosphate","termid":"MOD:00432"},{"relation_name":"is_a","term_name":"dehydrated residue","termid":"MOD:00704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphorylation of an hydroxyl amino acid with prompt loss of phosphate","synonyms":[{"name":"Dehydrated","type":"related"},{"name":"Dehydration","type":"related"}],"termid":"MOD:00416"}


id: PBO:0082552
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Central kinetochore protein and subunit of the Ctf19 complex; mutants have elevated rates of chromosome loss; orthologous to fission yeast kinetochore protein cnl2","termid":"PBO:0082552"}


id: PBO:0076838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TERF1 pseudogene 5","termid":"PBO:0076838"}


id: PBO:0040727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCL2 associated transcription factor 1 pseudogene 2","termid":"PBO:0040727"}


id: FYPO:0005174
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 uracil into the cell does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal uracil import","termid":"FYPO:0005170"},{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"}],"gene_count":0,"genotype_count":0,"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"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abolished uracil import","synonyms":[{"name":"abolished uracil import across plasma membrane","type":"exact"},{"name":"abolished uracil import during mitotic cell cycle","type":"related"},{"name":"abolished uracil import during vegetative growth","type":"exact"},{"name":"abolished uracil import into cell","type":"exact"},{"name":"abolished uracil uptake","type":"exact"},{"name":"uracil import abolished","type":"exact"}],"termid":"FYPO:0005174"}


id: PBO:0113395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative pyridoxal kinase; a key enzyme involved in pyridoxal 5'-phosphate synthesis, the active form of vitamin B6; required for genome integrity; involved in bud-site selection; localizes to cytosol and peroxisomes; similarity to yeast BUD17 and human pyridoxal kinase (PDXK)","termid":"PBO:0113395"}


id: GO:0045642
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of basophil differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of granulocyte differentiation","termid":"GO:0030854"},{"relation_name":"is_a","term_name":"regulation of basophil differentiation","termid":"GO:0045640"},{"relation_name":"positively_regulates","term_name":"basophil differentiation","termid":"GO:0030221"}],"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 basophil differentiation","synonyms":[{"name":"activation of basophil differentiation","type":"narrow"},{"name":"stimulation of basophil differentiation","type":"narrow"},{"name":"up regulation of basophil differentiation","type":"exact"},{"name":"up-regulation of basophil differentiation","type":"exact"},{"name":"upregulation of basophil differentiation","type":"exact"}],"termid":"GO:0045642"}


id: PBO:0003178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocyst complex subunit Exo70 (predicted)","termid":"PBO:0003178"}


id: PBO:0074643
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 35B","termid":"PBO:0074643"}


id: MONDO:0019502
data:
  {"annotated_genes":["SJAG_00898","SJAG_01536","SJAG_04640","SJAG_04119","SJAG_01826","SJAG_00325","SJAG_00886","SJAG_03147","SJAG_01570","SJAG_04704","SJAG_01702","SJAG_02099","SJAG_03635","SJAG_01625","SJAG_03286","SJAG_02717","SJAG_01465","SJAG_01070","SJAG_03333","SJAG_01991","SJAG_04084","SJAG_03448","SJAG_03032","SJAG_04321","SJAG_04645","SJAG_04358","SJAG_04654","SJAG_02042"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84860],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0100255"},{"annotations":[84347],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014648"},{"annotations":[84311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0040500"},{"annotations":[85494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032662"},{"annotations":[85272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032665"},{"annotations":[86179],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032789"},{"annotations":[86314],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030533"},{"annotations":[85629],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957288"},{"annotations":[86315],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958204"},{"annotations":[85714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013173"},{"annotations":[85172],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013528"},{"annotations":[85624],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014348"},{"annotations":[85513],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014409"},{"annotations":[86307,86308],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012613"},{"annotations":[84348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014649"},{"annotations":[85044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014815"},{"annotations":[86370],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014930"},{"annotations":[86236],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014996"},{"annotations":[86080],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015020"},{"annotations":[85918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044313"},{"annotations":[85567,85568,85566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020850"},{"annotations":[86309],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012615"},{"annotations":[85536],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013853"},{"annotations":[86126],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014485"},{"annotations":[85031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013624"}]},"cv_name":"mondo","definition":"Autosomal recessive form of non-syndromic intellectual disability.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic intellectual disability","termid":"MONDO:0000509"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"disorder of carbohydrate transmembrane transport and absorption","termid":"MONDO:0017706"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":28,"genes_by_uniquename":{"SJAG_00325":null,"SJAG_00886":null,"SJAG_00898":null,"SJAG_01070":null,"SJAG_01465":null,"SJAG_01536":null,"SJAG_01570":null,"SJAG_01625":null,"SJAG_01702":null,"SJAG_01826":null,"SJAG_01991":null,"SJAG_02042":null,"SJAG_02099":null,"SJAG_02717":null,"SJAG_03032":null,"SJAG_03147":null,"SJAG_03286":null,"SJAG_03333":null,"SJAG_03448":null,"SJAG_03635":null,"SJAG_04084":null,"SJAG_04119":null,"SJAG_04321":null,"SJAG_04358":null,"SJAG_04640":null,"SJAG_04645":null,"SJAG_04654":null,"SJAG_04704":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive non-syndromic intellectual disability","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:249500","MEDGEN:1826073","GARD:18643","Orphanet:88616","UMLS:C5680181","DOID:0060308"],"synonyms":[{"name":"AR-NSID","type":"exact"},{"name":"NS-ARID","type":"exact"},{"name":"autosomal recessive intellectual disability","type":"exact"},{"name":"autosomal recessive mental retardation","type":"exact"},{"name":"autosomal recessive non-syndromic intellectual disability","type":"exact"},{"name":"autosomal recessive non-syndromic mental retardation","type":"exact"},{"name":"intellectual disability, autosomal recessive","type":"exact"},{"name":"mental retardation, autosomal recessive","type":"exact"},{"name":"non-syndromic intellectual disability, autosomal recessive","type":"exact"}],"termid":"MONDO:0019502","terms_by_termid":{"MONDO:0012613":null,"MONDO:0012615":null,"MONDO:0013173":null,"MONDO:0013528":null,"MONDO:0013624":null,"MONDO:0013853":null,"MONDO:0014348":null,"MONDO:0014409":null,"MONDO:0014485":null,"MONDO:0014648":null,"MONDO:0014649":null,"MONDO:0014815":null,"MONDO:0014930":null,"MONDO:0014996":null,"MONDO:0015020":null,"MONDO:0020850":null,"MONDO:0030533":null,"MONDO:0032662":null,"MONDO:0032665":null,"MONDO:0032789":null,"MONDO:0040500":null,"MONDO:0044313":null,"MONDO:0100255":null,"MONDO:0957288":null,"MONDO:0958204":null},"xrefs":{"Monarch":{"xref_id":"0019502"}}}


id: GO:0050820
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of coagulation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of coagulation","termid":"GO:0050818"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"coagulation","termid":"GO:0050817"}],"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 coagulation","synonyms":[{"name":"activation of coagulation","type":"narrow"},{"name":"positive regulation of clotting","type":"exact"},{"name":"stimulation of coagulation","type":"narrow"},{"name":"up regulation of coagulation","type":"exact"},{"name":"up-regulation of coagulation","type":"exact"},{"name":"upregulation of coagulation","type":"exact"}],"termid":"GO:0050820"}


id: PBO:0049892
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HERC2 pseudogene 11","termid":"PBO:0049892"}


id: MONDO:1012424
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"llama syndrome chondrodysplasia, sheep","secondary_identifiers":["OMIA:001616-9940"],"termid":"MONDO:1012424","xrefs":{"Monarch":{"xref_id":"1012424"}}}


id: GO:0002090
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of receptor internalization.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of receptor-mediated endocytosis","termid":"GO:0048259"},{"relation_name":"regulates","term_name":"receptor internalization","termid":"GO:0031623"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of receptor internalization","termid":"GO:0002090"}


id: GO:2000689
data:
  {"annotated_genes":["SJAG_02864","SJAG_04498","SJAG_04621","SJAG_00938"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[107289,97223,97488,88535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071520"},{"annotations":[97225],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903479"}]},"cv_name":"biological_process","definition":"An actin filament organization process that contributes to actomyosin contractile ring assembly during cytokinesis.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"actin filament organization","termid":"GO:0007015"},{"relation_name":"is_a","term_name":"cell cycle process","termid":"GO:0022402"},{"relation_name":"part_of","term_name":"actomyosin contractile ring assembly","termid":"GO:0000915"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_02864":null,"SJAG_04498":null,"SJAG_04621":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0007010","GO:0030036","GO:0044085"],"is_obsolete":false,"name":"actomyosin contractile ring assembly actin filament organization","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"actin filament organisation of constriction ring assembly","type":"related"},{"name":"actin filament organisation of contractile ring assembly","type":"exact"},{"name":"actin filament organisation of cytokinesis, actomyosin contractile ring assembly","type":"exact"},{"name":"actin filament organisation of cytokinesis, actomyosin contractile ring formation","type":"related"},{"name":"actin filament organisation of cytokinesis, actomyosin ring biosynthesis","type":"related"},{"name":"actin filament organisation of cytokinesis, actomyosin ring formation","type":"related"},{"name":"actin filament organisation of cytokinesis, contractile ring assembly","type":"related"},{"name":"actin filament organization involved in cytokinetic actomyosin contractile ring assembly","type":"exact"},{"name":"actin filament organization of constriction ring assembly","type":"related"},{"name":"actin filament organization of contractile ring assembly","type":"exact"},{"name":"actin filament organization of cytokinesis, actomyosin contractile ring assembly","type":"exact"},{"name":"actin filament organization of cytokinesis, actomyosin contractile ring formation","type":"related"},{"name":"actin filament organization of cytokinesis, actomyosin ring biosynthesis","type":"related"},{"name":"actin filament organization of cytokinesis, actomyosin ring formation","type":"related"},{"name":"actin filament organization of cytokinesis, contractile ring assembly","type":"related"},{"name":"regulation of actin filament localization of constriction ring assembly","type":"related"},{"name":"regulation of actin filament localization of contractile ring assembly","type":"related"},{"name":"regulation of actin filament localization of cytokinesis, actomyosin contractile ring assembly","type":"related"},{"name":"regulation of actin filament localization of cytokinesis, actomyosin contractile ring formation","type":"related"},{"name":"regulation of actin filament localization of cytokinesis, actomyosin ring biosynthesis","type":"related"},{"name":"regulation of actin filament localization of cytokinesis, actomyosin ring formation","type":"related"},{"name":"regulation of actin filament localization of cytokinesis, contractile ring assembly","type":"related"}],"termid":"GO:2000689","terms_by_termid":{"GO:0071520":null,"GO:1903479":null}}


id: MONDO:0008409
data:
  {"annotated_genes":["SJAG_02431","SJAG_03703"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85108,85109],"is_not":false,"summary":null,"term":"MONDO:0008409"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"scapuloperoneal myopathy","termid":"MONDO:0000727"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of beta-myosin heavy chain (MYH7)","termid":"MONDO:0016195"},{"relation_name":"is_a","term_name":"congenital myopathy","termid":"MONDO:0019952"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02431":null,"SJAG_03703":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320","MONDO:0005267"],"is_obsolete":false,"name":"congenital myopathy 7A, myosin storage, autosomal dominant","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:437572","OMIM:608358","MEDGEN:374868","OMIM:181430","DOID:0111269","ICD9:359.89","Orphanet:636965","GARD:15429","MESH:C564253","UMLS:C1842160"],"synonyms":[{"name":"MSMA","type":"exact"},{"name":"MYH7-related late-onset SPMD","type":"exact"},{"name":"MYH7-related late-onset scapuloperoneal muscular dystrophy","type":"exact"},{"name":"MYH7-related late-onset scapuloperoneal syndrome","type":"exact"},{"name":"MYH7-related scapuloperoneal myopathy","type":"exact"},{"name":"SPMD","type":"exact"},{"name":"SPMM","type":"exact"},{"name":"autosomal dominant myosin storage myopathy","type":"exact"},{"name":"myopathy with lysis of type 1 myofibrils","type":"exact"},{"name":"myopathy, hyaline body, autosomal dominant","type":"exact"},{"name":"myopathy, myosin storage, autosomal dominant","type":"exact"},{"name":"scapuloperoneal muscular dystrophy","type":"exact"},{"name":"scapuloperoneal myopathy, MYH7-related","type":"exact"},{"name":"scapuloperoneal syndrome, myopathic type","type":"exact"}],"termid":"MONDO:0008409","terms_by_termid":{"MONDO:0008409":null},"xrefs":{"Monarch":{"xref_id":"0008409"}}}


id: PBO:0016918
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"does not functionally complement A. nidulans nimA","termid":"PBO:0016918"}


id: PBO:0050938
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon alpha 8","termid":"PBO:0050938"}


id: PR:Q9UTE0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sey1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UTE0"],"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":"protein sey1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC222.14c","synonyms":[{"name":"Spom972h-sey1","type":"exact"}],"termid":"PR:Q9UTE0"}


id: MONDO:0032672
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, neurodevelopmental disorder characterized by global developmental delay, congenital heart defects, generalized hypertrichosis and dysmorphic facial features, most commonly triangular face, thick arched eyebrows, widely spaced eyes, posteriorly rotated low set ears, depressed nasal bridge, broad nasal root and tip, and pointed chin.","definition_xrefs":["Orphanet:562569"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"intellectual developmental disorder with cardiac defects and dysmorphic facies","secondary_identifiers":["GARD:17998","MEDGEN:1675627","UMLS:C5193024","OMIM:618316"],"synonyms":[{"name":"IDDCDF","type":"related"},{"name":"TMEM94-associated congenital heart defect-facial dysmorphism-developmental delay syndrome","type":"exact"},{"name":"intellectual developmental disorder with cardiac defects and dysmorphic facies","type":"exact"}],"termid":"MONDO:0032672","xrefs":{"Monarch":{"xref_id":"0032672"}}}


id: PBO:0077532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 245","termid":"PBO:0077532"}


id: GO:0050047
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-leucine = (3R)-beta-leucine.","definition_xrefs":["RHEA:10284"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular aminotransferase activity","termid":"GO:0016869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0016853","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"L-leucine 2,3-aminomutase activity","secondary_identifiers":["EC:5.4.3.7","MetaCyc:LEUCINE-23-AMINOMUTASE-RXN","KEGG_REACTION:R01091"],"synonyms":[{"name":"(2S)-alpha-leucine 2,3-aminomutase activity","type":"related"},{"name":"leucine 2,3-aminomutase activity","type":"related"}],"termid":"GO:0050047"}


id: PBO:0042081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCDC148 antisense RNA 1","termid":"PBO:0042081"}


id: PBO:0083550
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 YJL181W","termid":"PBO:0083550"}


id: PBO:0110040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAA40 pseudogene 1","termid":"PBO:0110040"}


id: PBO:0027205
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_viability_following_cellular_response_to_heat_shock","termid":"PBO:0027205"}


id: MONDO:0044305
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"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":"ectodermal dysplasia 13, hair/tooth type","secondary_identifiers":["DOID:0111650","MEDGEN:1387448","UMLS:C4479322","OMIM:617392"],"synonyms":[{"name":"ECTD13","type":"related"},{"name":"ectodermal dysplasia 13, hair/tooth type","type":"exact"}],"termid":"MONDO:0044305","xrefs":{"Monarch":{"xref_id":"0044305"}}}


id: MONDO:0005570
data:
  {"annotated_genes":["SJAG_05283","SJAG_05180","SJAG_04003","SJAG_03081","SJAG_00222","SJAG_00980","SJAG_01621","SJAG_01798","SJAG_02457","SJAG_00749","SJAG_03818","SJAG_04887","SJAG_04204","SJAG_00487","SJAG_03153","SJAG_01077","SJAG_01466","SJAG_02509","SJAG_01732","SJAG_05979","SJAG_01183","SJAG_02527","SJAG_04387","SJAG_04478","SJAG_02597","SJAG_02460","SJAG_01008","SJAG_02585","SJAG_04991","SJAG_02453","SJAG_03447","SJAG_04495","SJAG_02763","SJAG_01852","SJAG_02335","SJAG_04491","SJAG_04312","SJAG_04881","SJAG_02690","SJAG_01296","SJAG_00088","SJAG_03898","SJAG_04746","SJAG_04042","SJAG_01349","SJAG_03762","SJAG_02796","SJAG_01013","SJAG_00066","SJAG_04984","SJAG_00328","SJAG_02904","SJAG_04168","SJAG_00739","SJAG_03703","SJAG_00319","SJAG_03497","SJAG_01378","SJAG_04414","SJAG_01199","SJAG_03712","SJAG_04459","SJAG_02294","SJAG_01512","SJAG_01568","SJAG_01960","SJAG_01704","SJAG_02093","SJAG_02339","SJAG_03453","SJAG_02556","SJAG_04425","SJAG_03929","SJAG_03889","SJAG_02708","SJAG_02280","SJAG_02046","SJAG_01162","SJAG_03115","SJAG_04731","SJAG_01840","SJAG_02208","SJAG_04217","SJAG_04473","SJAG_02431","SJAG_04334","SJAG_00846","SJAG_02951","SJAG_00605","SJAG_02528","SJAG_04509","SJAG_03204","SJAG_04810","SJAG_00166","SJAG_00930","SJAG_02894","SJAG_03089","SJAG_02749","SJAG_02340","SJAG_03684","SJAG_03905","SJAG_00108","SJAG_04066","SJAG_01615","SJAG_02802","SJAG_00640","SJAG_02009","SJAG_01588","SJAG_02288","SJAG_03424","SJAG_01748","SJAG_01457","SJAG_00921","SJAG_04695","SJAG_01548","SJAG_04621","SJAG_02330","SJAG_01417","SJAG_01366","SJAG_02539","SJAG_00468","SJAG_00465","SJAG_02839","SJAG_01410","SJAG_02091","SJAG_01759","SJAG_00611","SJAG_04192","SJAG_01784","SJAG_03961","SJAG_03919","SJAG_04743","SJAG_00839","SJAG_02297","SJAG_03254","SJAG_01007","SJAG_03335","SJAG_00235","SJAG_02744","SJAG_02358"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86432,86430,86586,86433,86431,86585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018874"},{"annotations":[85332],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030519"},{"annotations":[84807],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030894"},{"annotations":[84470],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010480"},{"annotations":[85447],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030436"},{"annotations":[85533],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013851"},{"annotations":[84849],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008422"},{"annotations":[85607],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957580"},{"annotations":[86214],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008876"},{"annotations":[85349],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014887"},{"annotations":[84682,84683],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009134"},{"annotations":[84726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007109"},{"annotations":[84262],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014118"},{"annotations":[86129,86128],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014487"},{"annotations":[85619],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008494"},{"annotations":[84687],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009902"},{"annotations":[85342,85343,85344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018794"},{"annotations":[84746,84745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007110"},{"annotations":[85518,85519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013217"},{"annotations":[86408],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013964"},{"annotations":[85042,85043],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014245"},{"annotations":[85618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014394"},{"annotations":[84554],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010493"},{"annotations":[85647,85648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011639"},{"annotations":[86042,86043],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044309"},{"annotations":[86046],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044310"},{"annotations":[85277,85276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032668"},{"annotations":[85278],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032669"},{"annotations":[85281,85280],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032670"},{"annotations":[84997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031071"},{"annotations":[85077,85076],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012529"},{"annotations":[85981,85980],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012924"},{"annotations":[85978,85979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012925"},{"annotations":[85996,85997],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012937"},{"annotations":[85995,85994],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012938"},{"annotations":[85998],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012939"},{"annotations":[85521,85520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013216"},{"annotations":[84333],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014690"},{"annotations":[85549],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009206"},{"annotations":[84528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012204"},{"annotations":[85544],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013248"},{"annotations":[85968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013499"},{"annotations":[84250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014108"},{"annotations":[86223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014986"},{"annotations":[86227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014987"},{"annotations":[86224],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014985"},{"annotations":[84906],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009295"},{"annotations":[85291],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010600"},{"annotations":[86294],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009113"},{"annotations":[85410],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013275"},{"annotations":[86086],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019531"},{"annotations":[86555],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859172"},{"annotations":[84567],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009238"},{"annotations":[84697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012981"},{"annotations":[85347],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014885"},{"annotations":[85207],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011997"},{"annotations":[84298],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011971"},{"annotations":[84436],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012465"},{"annotations":[84544,86508,84545,86507],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012197"},{"annotations":[85324,85325],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958013"},{"annotations":[84842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009953"},{"annotations":[85406,85407],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011508"},{"annotations":[85582,85583],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015912"},{"annotations":[85862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0800047"},{"annotations":[86180,86181],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030827"},{"annotations":[85130],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014757"},{"annotations":[85118],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012316"},{"annotations":[85217],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009606"},{"annotations":[84764,84765],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009605"},{"annotations":[84473,84474],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009354"},{"annotations":[85085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009609"},{"annotations":[85905],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010184"},{"annotations":[84320],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008787"},{"annotations":[84897,84896],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018881"},{"annotations":[84948,84947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007925"},{"annotations":[86116,86117],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024553"},{"annotations":[86468],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013307"},{"annotations":[85462],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957809"},{"annotations":[85322,85321],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958017"},{"annotations":[85915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032899"},{"annotations":[85693,85692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009340"},{"annotations":[85631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008493"},{"annotations":[84676],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012992"},{"annotations":[86134],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010438"},{"annotations":[85188],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014166"},{"annotations":[85456],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008214"},{"annotations":[86552],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009693"},{"annotations":[84380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014078"},{"annotations":[85950],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014518"},{"annotations":[86009],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011405"},{"annotations":[85641,85640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054862"},{"annotations":[84932],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012559"},{"annotations":[84827],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009950"},{"annotations":[84428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012700"},{"annotations":[86423],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0019107"},{"annotations":[85603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008785"},{"annotations":[85028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014804"},{"annotations":[84868],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008165"},{"annotations":[85939],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044208"},{"annotations":[86414],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010743"},{"annotations":[86375,86377,86376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958333"},{"annotations":[85531],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012775"},{"annotations":[86310],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010121"},{"annotations":[86502,86503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008559"},{"annotations":[85019],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014221"},{"annotations":[85146],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010518"},{"annotations":[85854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010294"},{"annotations":[85944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020721"},{"annotations":[84975],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010524"},{"annotations":[85445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957595"}]},"cv_name":"mondo","definition":"A disease involving the hematopoietic system.","direct_ancestors":[{"relation_name":"is_a","term_name":"human disease","termid":"MONDO:0700096"}],"gene_count":140,"genes_by_uniquename":{"SJAG_00066":null,"SJAG_00088":null,"SJAG_00108":null,"SJAG_00166":null,"SJAG_00222":null,"SJAG_00235":null,"SJAG_00319":null,"SJAG_00328":null,"SJAG_00465":null,"SJAG_00468":null,"SJAG_00487":null,"SJAG_00605":null,"SJAG_00611":null,"SJAG_00640":null,"SJAG_00739":null,"SJAG_00749":null,"SJAG_00839":null,"SJAG_00846":null,"SJAG_00921":null,"SJAG_00930":null,"SJAG_00980":null,"SJAG_01007":null,"SJAG_01008":null,"SJAG_01013":null,"SJAG_01077":null,"SJAG_01162":null,"SJAG_01183":null,"SJAG_01199":null,"SJAG_01296":null,"SJAG_01349":null,"SJAG_01366":null,"SJAG_01378":null,"SJAG_01410":null,"SJAG_01417":null,"SJAG_01457":null,"SJAG_01466":null,"SJAG_01512":null,"SJAG_01548":null,"SJAG_01568":null,"SJAG_01588":null,"SJAG_01615":null,"SJAG_01621":null,"SJAG_01704":null,"SJAG_01732":null,"SJAG_01748":null,"SJAG_01759":null,"SJAG_01784":null,"SJAG_01798":null,"SJAG_01840":null,"SJAG_01852":null,"SJAG_01960":null,"SJAG_02009":null,"SJAG_02046":null,"SJAG_02091":null,"SJAG_02093":null,"SJAG_02208":null,"SJAG_02280":null,"SJAG_02288":null,"SJAG_02294":null,"SJAG_02297":null,"SJAG_02330":null,"SJAG_02335":null,"SJAG_02339":null,"SJAG_02340":null,"SJAG_02358":null,"SJAG_02431":null,"SJAG_02453":null,"SJAG_02457":null,"SJAG_02460":null,"SJAG_02509":null,"SJAG_02527":null,"SJAG_02528":null,"SJAG_02539":null,"SJAG_02556":null,"SJAG_02585":null,"SJAG_02597":null,"SJAG_02690":null,"SJAG_02708":null,"SJAG_02744":null,"SJAG_02749":null,"SJAG_02763":null,"SJAG_02796":null,"SJAG_02802":null,"SJAG_02839":null,"SJAG_02894":null,"SJAG_02904":null,"SJAG_02951":null,"SJAG_03081":null,"SJAG_03089":null,"SJAG_03115":null,"SJAG_03153":null,"SJAG_03204":null,"SJAG_03254":null,"SJAG_03335":null,"SJAG_03424":null,"SJAG_03447":null,"SJAG_03453":null,"SJAG_03497":null,"SJAG_03684":null,"SJAG_03703":null,"SJAG_03712":null,"SJAG_03762":null,"SJAG_03818":null,"SJAG_03889":null,"SJAG_03898":null,"SJAG_03905":null,"SJAG_03919":null,"SJAG_03929":null,"SJAG_03961":null,"SJAG_04003":null,"SJAG_04042":null,"SJAG_04066":null,"SJAG_04168":null,"SJAG_04192":null,"SJAG_04204":null,"SJAG_04217":null,"SJAG_04312":null,"SJAG_04334":null,"SJAG_04387":null,"SJAG_04414":null,"SJAG_04425":null,"SJAG_04459":null,"SJAG_04473":null,"SJAG_04478":null,"SJAG_04491":null,"SJAG_04495":null,"SJAG_04509":null,"SJAG_04621":null,"SJAG_04695":null,"SJAG_04731":null,"SJAG_04743":null,"SJAG_04746":null,"SJAG_04810":null,"SJAG_04881":null,"SJAG_04887":null,"SJAG_04984":null,"SJAG_04991":null,"SJAG_05180":null,"SJAG_05283":null,"SJAG_05979":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"is_obsolete":false,"name":"hematologic disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:414022008","GTR:AN1320635","Orphanet:97992","DOID:74","ICD9:289.8","ICD10CM:D50-D89","NANDO:1100006","MESH:D006402","MEDGEN:5483","ICD9:289.9","NANDO:2100175","NCIT:C26323","ICD9:280-289.99","EFO:0005803","UMLS:C0018939"],"synonyms":[{"name":"blood disease","type":"exact"},{"name":"blood disorder","type":"exact"},{"name":"blood dyscrasia","type":"exact"},{"name":"disease of haematopoietic system","type":"exact"},{"name":"disease of hematopoietic system","type":"exact"},{"name":"disease of the blood and blood-forming organs","type":"exact"},{"name":"disease or disorder of haematopoietic system","type":"exact"},{"name":"disease or disorder of hematopoietic system","type":"exact"},{"name":"disorder of haematopoietic system","type":"exact"},{"name":"disorder of hematopoietic system","type":"exact"},{"name":"haematological disease","type":"exact"},{"name":"haematological disorder","type":"exact"},{"name":"haematological disorders and malignancies","type":"related"},{"name":"haematological system disease","type":"exact"},{"name":"haematopoietic disease","type":"exact"},{"name":"haematopoietic system disease","type":"exact"},{"name":"haematopoietic system disease or disorder","type":"exact"},{"name":"hematologic and lymphocytic disorder","type":"exact"},{"name":"hematologic disorder","type":"exact"},{"name":"hematological disease","type":"exact"},{"name":"hematological disorder","type":"exact"},{"name":"hematological disorders and malignancies","type":"related"},{"name":"hematological system disease","type":"exact"},{"name":"hematopoietic disease","type":"exact"},{"name":"hematopoietic system disease","type":"exact"},{"name":"hematopoietic system disease or disorder","type":"exact"},{"name":"rare hematologic disease","type":"exact"}],"termid":"MONDO:0005570","terms_by_termid":{"MONDO:0007109":null,"MONDO:0007110":null,"MONDO:0007925":null,"MONDO:0008165":null,"MONDO:0008214":null,"MONDO:0008422":null,"MONDO:0008493":null,"MONDO:0008494":null,"MONDO:0008559":null,"MONDO:0008785":null,"MONDO:0008787":null,"MONDO:0008876":null,"MONDO:0009113":null,"MONDO:0009134":null,"MONDO:0009206":null,"MONDO:0009238":null,"MONDO:0009295":null,"MONDO:0009340":null,"MONDO:0009354":null,"MONDO:0009605":null,"MONDO:0009606":null,"MONDO:0009609":null,"MONDO:0009693":null,"MONDO:0009902":null,"MONDO:0009950":null,"MONDO:0009953":null,"MONDO:0010121":null,"MONDO:0010184":null,"MONDO:0010294":null,"MONDO:0010438":null,"MONDO:0010480":null,"MONDO:0010493":null,"MONDO:0010518":null,"MONDO:0010524":null,"MONDO:0010600":null,"MONDO:0010743":null,"MONDO:0011405":null,"MONDO:0011508":null,"MONDO:0011639":null,"MONDO:0011971":null,"MONDO:0011997":null,"MONDO:0012197":null,"MONDO:0012204":null,"MONDO:0012316":null,"MONDO:0012465":null,"MONDO:0012529":null,"MONDO:0012559":null,"MONDO:0012700":null,"MONDO:0012775":null,"MONDO:0012924":null,"MONDO:0012925":null,"MONDO:0012937":null,"MONDO:0012938":null,"MONDO:0012939":null,"MONDO:0012981":null,"MONDO:0012992":null,"MONDO:0013216":null,"MONDO:0013217":null,"MONDO:0013248":null,"MONDO:0013275":null,"MONDO:0013307":null,"MONDO:0013499":null,"MONDO:0013851":null,"MONDO:0013964":null,"MONDO:0014078":null,"MONDO:0014108":null,"MONDO:0014118":null,"MONDO:0014166":null,"MONDO:0014221":null,"MONDO:0014245":null,"MONDO:0014394":null,"MONDO:0014487":null,"MONDO:0014518":null,"MONDO:0014690":null,"MONDO:0014757":null,"MONDO:0014804":null,"MONDO:0014885":null,"MONDO:0014887":null,"MONDO:0014985":null,"MONDO:0014986":null,"MONDO:0014987":null,"MONDO:0015912":null,"MONDO:0018794":null,"MONDO:0018874":null,"MONDO:0018881":null,"MONDO:0019107":null,"MONDO:0019531":null,"MONDO:0020721":null,"MONDO:0024553":null,"MONDO:0030436":null,"MONDO:0030519":null,"MONDO:0030827":null,"MONDO:0030894":null,"MONDO:0031071":null,"MONDO:0032668":null,"MONDO:0032669":null,"MONDO:0032670":null,"MONDO:0032899":null,"MONDO:0044208":null,"MONDO:0044309":null,"MONDO:0044310":null,"MONDO:0054862":null,"MONDO:0800047":null,"MONDO:0859172":null,"MONDO:0957580":null,"MONDO:0957595":null,"MONDO:0957809":null,"MONDO:0958013":null,"MONDO:0958017":null,"MONDO:0958333":null},"xrefs":{"Monarch":{"xref_id":"0005570"}}}


