# terms

id: GO:0018744
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: limonene-1,2-epoxide + H2O = limonene-1,2-diol. Other substrates include alicyclic and 1-methyl-substituted epoxides, such as 1-methylcyclohexene oxide, indene oxide and cyclohexene oxide.","definition_xrefs":["EC:3.3.2.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epoxide hydrolase activity","termid":"GO:0004301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"limonene-1,2-epoxide hydrolase activity","secondary_identifiers":["RHEA:10700","UM-BBD_reactionID:r0734","MetaCyc:3.3.2.8-RXN"],"synonyms":[{"name":"limonene oxide hydrolase activity","type":"related"}],"termid":"GO:0018744"}


id: MOD:00005
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to O3-glycosylthreonine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-glycosylated residue","termid":"MOD:00396"},{"relation_name":"is_a","term_name":"modified L-threonine residue","termid":"MOD:00917"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00764"}],"interesting_parent_ids":["MOD:00764"],"is_obsolete":false,"name":"O-glycosyl-L-threonine","synonyms":[{"name":"OGlycoThr","type":"exact"}],"termid":"MOD:00005"}


id: PBO:0069569
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 841, pseudogene","termid":"PBO:0069569"}


id: PBO:0079548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin A-52 residue ribosomal protein fusion product 1 pseudogene 1","termid":"PBO:0079548"}


id: PBO:0043139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 7","termid":"PBO:0043139"}


id: MONDO:0004008
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A breast lesion characterized by the presence of dilated terminal ductal lobular units in which the epithelial lining has been replaced by a single layer of mildly atypical cells, or there is atypical, monotonous epithelial hyperplasia of three to five layers. This lesion relates to columnar cell change with atypia and columnar cell hyperplasia with atypia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast intraductal proliferative lesion","termid":"MONDO:0004007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"flat ductal epithelial atypia","secondary_identifiers":["DOID:6841","UMLS:C1333620","NCIT:C36086","MEDGEN:232508"],"synonyms":[{"name":"DIN 1A","type":"exact"},{"name":"FEA","type":"exact"},{"name":"clinging carcinoma","type":"exact"},{"name":"ductal intraepithelial neoplasia, grade 1A","type":"exact"},{"name":"flat ductal epithelial atypia","type":"exact"},{"name":"flat ductal epithelial atypia of the breast","type":"exact"},{"name":"flat epithelial atypia","type":"exact"},{"name":"flat epithelial atypia of the breast","type":"exact"}],"termid":"MONDO:0004008","xrefs":{"Monarch":{"xref_id":"0004008"}}}


id: GO:0072749
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 cytochalasin B stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cytochalasin B","termid":"GO:1901328"},{"relation_name":"is_a","term_name":"cellular response to nitrogen compound","termid":"GO:1901699"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"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 cytochalasin B","termid":"GO:0072749"}


id: PBO:0114750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic and meiotic cohesin unloading complex subunit Pds5","termid":"PBO:0114750"}


id: GO:0008737
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-fuculose + ATP = L-fuculose 1-phosphate + ADP + 2 H+.","definition_xrefs":["EC:2.7.1.51","RHEA:12376"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"},{"relation_name":"is_a","term_name":"carbohydrate kinase activity","termid":"GO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016301"],"is_obsolete":false,"name":"L-fuculokinase activity","secondary_identifiers":["MetaCyc:FUCULOKIN-RXN","KEGG_REACTION:R03241"],"synonyms":[{"name":"ATP:L-fuculose 1-phosphotransferase activity","type":"related"},{"name":"L-fuculokinase (phosphorylating)","type":"related"},{"name":"L-fuculose kinase activity","type":"related"}],"termid":"GO:0008737"}


id: PBO:0084020
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glycosylphosphatidylinositol-alpha 1,4 mannosyltransferase I; involved in GPI anchor biosynthesis, requires Pbn1p for function; homolog of mammalian PIG-M","termid":"PBO:0084020"}


id: FYPO:0005175
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of catalase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal catalase activity","termid":"FYPO:0001104"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0005447","FYPO:0000002","FYPO:0000654","FYPO:0000652","FYPO:0001985","FYPO:0000661"],"is_obsolete":false,"name":"increased catalase activity","termid":"FYPO:0005175"}


id: PBO:0003891
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c1 Cyt1 (predicted)","termid":"PBO:0003891"}


id: PBO:0049532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A.Z histone pseudogene 3","termid":"PBO:0049532"}


id: GO:0072257
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and/or functional features that characterize the cells of the metanephric nephron tubule as it progresses from its formation to the mature state.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephron tubule epithelial cell differentiation","termid":"GO:0072160"},{"relation_name":"is_a","term_name":"cell differentiation involved in metanephros development","termid":"GO:0072202"},{"relation_name":"part_of","term_name":"metanephric nephron tubule development","termid":"GO:0072234"}],"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":"metanephric nephron tubule epithelial cell differentiation","termid":"GO:0072257"}


id: PBO:0083755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential DNA-binding transcription regulator that binds many loci; involved in transcription activation, repression, chromatin silencing, telomere length maintenance; represses divergent noncoding transcription at highly expressed genes, prevents transcription initiation at cryptic promoters near its binding sites; relocalizes to cytosol under hypoxia; recruits Sir complex to telomeric DNA; present in quiescent cell telomere hyperclusters","termid":"PBO:0083755"}


id: GO:0062126
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways, including anabolism and catabolism, by which living organisms transform primary fatty amides.","definition_xrefs":["PMID:11128635"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"},{"relation_name":"is_a","term_name":"fatty acid derivative metabolic process","termid":"GO:1901568"}],"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":"fatty acid primary amide metabolic process","synonyms":[{"name":"primary fatty amide metabolic process","type":"exact"}],"termid":"GO:0062126"}


id: PATO:0001057
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001057 relative acceleration (obsolete PATO:0001057)","termid":"PATO:0001057"}


id: GO:0052447
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism modulates the frequency, rate or extent of the ethylene-mediated defense response of 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 symbiont ethylene-mediated defense response (obsolete GO:0052447)","synonyms":[{"name":"modulation by organism of symbiont ethylene-mediated defense response","type":"exact"}],"termid":"GO:0052447"}


id: MONDO:0020021
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete diaphragmatic or abdominal wall malformation (obsolete MONDO:0020021)","secondary_identifiers":["Orphanet:98043"],"termid":"MONDO:0020021","xrefs":{"Monarch":{"xref_id":"0020021"}}}


id: MONDO:0017438
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-syndromic amelia that involves the hindlimb.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-syndromic amelia","termid":"MONDO:0017419"}],"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":"amelia of lower limb","secondary_identifiers":["GARD:21191","HP:0009818","MEDGEN:539370","icd11.foundation:540310468","Orphanet:294969","SCTID:265798000","UMLS:C0265621"],"synonyms":[{"name":"hindlimb non-syndromic amelia","type":"exact"},{"name":"non-syndromic amelia of hindlimb","type":"exact"}],"termid":"MONDO:0017438","xrefs":{"Monarch":{"xref_id":"0017438"}}}


id: MONDO:0000173
data:
  {"annotated_genes":["SJAG_04053","SJAG_03188","SJAG_01491","SJAG_04316"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012248"},{"annotations":[86153,86154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013162"},{"annotations":[85435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014142"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy","termid":"MONDO:0018276"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01491":null,"SJAG_03188":null,"SJAG_04053":null,"SJAG_04316":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy, type C","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIMPS:609308"],"termid":"MONDO:0000173","terms_by_termid":{"MONDO:0012248":null,"MONDO:0013162":null,"MONDO:0014142":null},"xrefs":{"Monarch":{"xref_id":"0000173"}}}


id: PBO:0044478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 21 subfamily A member 1, pseudogene","termid":"PBO:0044478"}


id: FYPO:0001632
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 L-tyrosine measured in the vacuole is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in vacuole","termid":"FYPO:0001603"},{"relation_name":"is_a","term_name":"normal cellular tyrosine level","termid":"FYPO:0001641"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal vacuolar tyrosine level","synonyms":[{"name":"normal level of tyrosine in vacuole","type":"exact"},{"name":"normal vacuolar L-tyrosine level","type":"exact"},{"name":"normal vacuolar tyrosine level during mitotic cell cycle","type":"related"},{"name":"normal vacuolar tyrosine level during vegetative growth","type":"exact"}],"termid":"FYPO:0001632"}


id: PBO:0076186
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO1 pseudogene 1","termid":"PBO:0076186"}


id: PBO:0027338
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_glutathione_level","termid":"PBO:0027338"}


id: PBO:0085992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; required for survival upon exposure to K1 killer toxin","termid":"PBO:0085992"}


id: MONDO:1012449
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma of the digit, non-human animal","termid":"MONDO:1011822"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"squamous cell carcinoma of the digit, dog","secondary_identifiers":["OMIA:001787-9615"],"termid":"MONDO:1012449","xrefs":{"Monarch":{"xref_id":"1012449"}}}


id: GO:0035478
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a chylomicron, a large lipoprotein particle (diameter 75-1200 nm) composed of a central core of triglycerides and cholesterol surrounded by a protein-phospholipid coating. The proteins include one molecule of apolipoprotein B-48 and may include a variety of apolipoproteins, including APOAs, APOCs and APOE.","definition_xrefs":["GOC:BHF","PMID:17403372"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein particle binding","termid":"GO:0071813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"chylomicron binding","termid":"GO:0035478"}


id: PBO:0064071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 105","termid":"PBO:0064071"}


id: PBO:0065159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein arginine methyltransferase 9","termid":"PBO:0065159"}


id: SO:0000282
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An mRNA with a minus 1 frameshift.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"minus_1_frameshift","termid":"SO:0000866"},{"relation_name":"is_a","term_name":"mRNA_with_frameshift","termid":"SO:0000108"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA_with_minus_1_frameshift","synonyms":[{"name":"mRNA with minus 1 frameshift","type":"exact"}],"termid":"SO:0000282"}


id: MONDO:0004131
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A large, well differentiated squamous cell carcinoma with a cauliflower-like appearance, characterized by the presence of an exophytic and endophytic growth pattern. Morphologically, there is papillomatosis and acanthosis present, however cytologically the neoplastic squamous cells have a benign appearance. Dysplastic changes are minimal. It does not respond to conservative treatment and it is regarded by many authors as an intermediate lesion between condyloma acuminatum and squamous cell carcinoma.","definition_xrefs":["NCIT:C7470"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anal squamous cell carcinoma","termid":"MONDO:0006082"},{"relation_name":"is_a","term_name":"Buschke Lowenstein tumor","termid":"MONDO:0027026"},{"relation_name":"is_a","term_name":"digestive system infectious disorder","termid":"MONDO:0043424"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"anal verrucous carcinoma","secondary_identifiers":["MEDGEN:231066","UMLS:C1332278","DOID:7175"],"synonyms":[{"name":"anal Buschke-Lowenstein tumor","type":"exact"},{"name":"anal Buschke-Lowenstein tumour","type":"exact"},{"name":"anal giant (malignant) condyloma","type":"exact"},{"name":"anal verrucous carcinoma","type":"exact"}],"termid":"MONDO:0004131","xrefs":{"Monarch":{"xref_id":"0004131"}}}


id: MONDO:0005472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital heart malformation (obsolete MONDO:0005472)","termid":"MONDO:0005472","xrefs":{"Monarch":{"xref_id":"0005472"}}}


id: SO:0000157
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A plasmid which carries within its sequence a bacteriophage replication origin. When the host bacterium is infected with \\\"helper\\\" phage, a phagemid is replicated along with the phage DNA and packaged into phage capsids.","definition_xrefs":["SO:ma"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vector_replicon","termid":"SO:0000440"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phagemid","secondary_identifiers":["http://en.wikipedia.org/wiki/Phagemid"],"synonyms":[{"name":"phagemid vector","type":"related"}],"termid":"SO:0000157"}


id: PR:O74381
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pof9 gene.","definition_xrefs":["UniProtKB:O74381","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein pof9 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3H7.06c","synonyms":[{"name":"Spom972h-pof9","type":"exact"}],"termid":"PR:O74381"}


id: GO:0031389
data:
  {"annotated_genes":["SJAG_02563","SJAG_02182","SJAG_01010","SJAG_00729","SJAG_00272"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88594,89050,93443,94751,111765],"is_not":false,"summary":null,"term":"GO:0031389"}]},"cv_name":"cellular_component","definition":"A pentameric protein complex related to replication factor C, which loads a trimeric complex of checkpoint proteins (known as the checkpoint clamp or 9-1-1 complex) onto DNA at damage sites; functions in DNA damage cell cycle checkpoints. In Schizosaccharomyces pombe the subunits are known as Rad17, Rfc2, Rfc3, Rfc4, and Rfc5, while in Saccharomyces cerevisiae the subunits are known as Rad24p, Rfc2p, Rfc3p, Rfc4p, and Rfc5p.","definition_xrefs":["PMID:14614842"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"chromosome","termid":"GO:0005694"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00272":null,"SJAG_00729":null,"SJAG_01010":null,"SJAG_02182":null,"SJAG_02563":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005694","GO:0032991"],"is_obsolete":false,"name":"Rad17 RFC-like complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"RFC (Rad17)","type":"exact"},{"name":"Rad17-RFC","type":"exact"},{"name":"Rad17-RLC","type":"exact"},{"name":"Rad24p RFC-like complex","type":"exact"}],"termid":"GO:0031389","terms_by_termid":{"GO:0031389":null}}


id: PBO:0049463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycophorin A (MNS blood group)","termid":"PBO:0049463"}


id: PBO:0088040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-conjugating enzyme; most similar in sequence to Xenopus ubiquitin-conjugating enzyme E2-C, but not a true functional homolog of this E2; unlike E2-C, not required for the degradation of mitotic cyclin Clb2","termid":"PBO:0088040"}


id: SO:0000855
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A homologous_region that is orthologous to another region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"orthologous","termid":"SO:0000858"},{"relation_name":"is_a","term_name":"homologous_region","termid":"SO:0000853"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"orthologous_region","secondary_identifiers":["http://en.wikipedia.org/wiki/Ortholog#Orthology"],"synonyms":[{"name":"ortholog","type":"exact"},{"name":"orthologous region","type":"exact"},{"name":"orthologue","type":"exact"}],"termid":"SO:0000855"}


id: PBO:0055609
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 3048","termid":"PBO:0055609"}


id: GO:1904780
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein localization to centrosome.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:17115027"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein localization","termid":"GO:1903828"},{"relation_name":"is_a","term_name":"regulation of protein localization to centrosome","termid":"GO:1904779"},{"relation_name":"negatively_regulates","term_name":"protein localization to centrosome","termid":"GO:0071539"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein localization to centrosome","synonyms":[{"name":"down regulation of protein localisation to centrosome","type":"exact"},{"name":"down regulation of protein localization to centrosome","type":"exact"},{"name":"down-regulation of protein localisation to centrosome","type":"exact"},{"name":"down-regulation of protein localization to centrosome","type":"exact"},{"name":"downregulation of protein localisation to centrosome","type":"exact"},{"name":"downregulation of protein localization to centrosome","type":"exact"},{"name":"inhibition of protein localisation to centrosome","type":"narrow"},{"name":"inhibition of protein localization to centrosome","type":"narrow"},{"name":"negative regulation of protein localisation to centrosome","type":"exact"}],"termid":"GO:1904780"}


id: MONDO:1011754
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder, non-human animal","termid":"MONDO:1011328"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"reactive perforating collagenosis, non-human animal","secondary_identifiers":["OMIA:001476"],"termid":"MONDO:1011754","xrefs":{"Monarch":{"xref_id":"1011754"}}}


id: GO:0015349
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of thyroid hormones from one side of a membrane to the other. Thyroid hormone are any of the compounds secreted by the thyroid gland, largely thyroxine and triiodothyronine.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary active transmembrane transporter activity","termid":"GO:0015291"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"thyroid hormone transmembrane transporter activity","secondary_identifiers":["Reactome:R-HSA-9631987","Reactome:R-HSA-879575"],"termid":"GO:0015349"}


id: PBO:0050138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 48","termid":"PBO:0050138"}


id: PBO:0050287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HNF1 homeobox A","termid":"PBO:0050287"}


id: GO:0030848
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (3S)-3-hydroxy-L-aspartate = NH4 + oxaloacetate.","definition_xrefs":["EC:4.3.1.16","RHEA:12424"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ammonia-lyase activity","termid":"GO:0016841"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"threo-3-hydroxyaspartate ammonia-lyase activity","secondary_identifiers":["KEGG_REACTION:R05758","MetaCyc:4.3.1.16-RXN"],"synonyms":[{"name":"3-hydroxyaspartate dehydratase activity","type":"broad"},{"name":"L-threo-3-hydroxyaspartate dehydratase activity","type":"related"},{"name":"threo-3-hydroxy-L-aspartate ammonia-lyase (oxaloacetate-forming)","type":"related"},{"name":"threo-3-hydroxy-L-aspartate ammonia-lyase activity","type":"related"},{"name":"threo-3-hydroxyaspartate dehydratase activity","type":"related"}],"termid":"GO:0030848"}


id: GO:0071343
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of the process in which a contractile ring is assembled in a specific location.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of establishment of actomyosin contractile ring localization (obsolete GO:0071343)","synonyms":[{"name":"negative regulation of establishment of actomyosin contractile ring localization","type":"exact"},{"name":"negative regulation of establishment of contractile ring localisation involved in cell cycle cytokinesis","type":"exact"},{"name":"negative regulation of establishment of contractile ring localization involved in cell cycle cytokinesis","type":"exact"},{"name":"negative regulation of establishment of contractile ring localization involved in cytokinesis during cell cycle","type":"related"}],"termid":"GO:0071343"}


id: GO:1990182
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whereby a membrane-bounded vesicle is released into the extracellular region by fusion of the limiting endosomal membrane of a multivesicular body with the plasma membrane.","definition_xrefs":["PMID:18617898","PMID:10572093","PMID:16773132","GOC:hjd","PMID:12154376"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exocytosis","termid":"GO:0006887"},{"relation_name":"is_a","term_name":"establishment of vesicle localization","termid":"GO:0051650"},{"relation_name":"part_of","term_name":"extracellular exosome biogenesis","termid":"GO:0097734"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0006810","GO:0044085","GO:0051179"],"is_obsolete":false,"name":"exosomal secretion","synonyms":[{"name":"exosomal protein secretion","type":"narrow"},{"name":"exosomal secretory pathway","type":"exact"},{"name":"extracellular vesicular exosome secretion","type":"exact"},{"name":"multi-vesicular body fusion with plasma membrane","type":"exact"},{"name":"secretion of exosome","type":"exact"}],"termid":"GO:1990182"}


id: GO:0019066
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The translocation of an entire virus particle across the host cell plasma membrane.","definition_xrefs":["ISBN:0781702534"],"gene_count":0,"genotype_count":0,"name":"obsolete translocation of virus into host cell (obsolete GO:0019066)","synonyms":[{"name":"translocation of virus into host cell","type":"exact"},{"name":"viral translocation","type":"exact"}],"termid":"GO:0019066"}


id: GO:2001250
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ammonia assimilation cycle.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of nitrogen utilization","termid":"GO:0045848"},{"relation_name":"is_a","term_name":"positive regulation of glutamate metabolic process","termid":"GO:2000213"},{"relation_name":"is_a","term_name":"regulation of ammonia assimilation cycle","termid":"GO:2001248"},{"relation_name":"positively_regulates","term_name":"ammonia assimilation cycle","termid":"GO:0019676"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"positively_regulates","termid":"GO:0006520"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006520"],"is_obsolete":false,"name":"positive regulation of ammonia assimilation cycle","synonyms":[{"name":"positive regulation of glutamate metabolic process via glutamine and ammonia","type":"exact"},{"name":"positive regulation of glutamate metabolism via glutamine and ammonia","type":"exact"}],"termid":"GO:2001250"}


id: PBO:0071717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 15","termid":"PBO:0071717"}


id: PBO:0004812
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.4.1.117","termid":"PBO:0004812"}


id: FYPO:0002915
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which RNA splicing is abnormal. All RNA splicing may be abnormal, or one splicing of or more specific RNA molecules may be selectively affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal RNA metabolic process","termid":"FYPO:0004851"},{"relation_name":"is_a","term_name":"abnormal gene expression","termid":"FYPO:0006551"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0006551","FYPO:0000294","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abnormal RNA splicing","synonyms":[{"name":"abnormal RNA splicing during mitotic cell cycle","type":"related"},{"name":"abnormal RNA splicing during vegetative growth","type":"exact"},{"name":"abnormal RNA splicing, via transesterification reactions with bulged adenosine as nucleophile","type":"exact"}],"termid":"FYPO:0002915"}


id: GO:0004518
data:
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id: PBO:0066358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"REST corepressor 2","termid":"PBO:0066358"}


id: PBO:0111873
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nedd4/Rsp5 family","termid":"PBO:0111873"}


id: PBO:0054329
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 1722","termid":"PBO:0054329"}


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


id: PBO:0047930
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(11)(q13)","termid":"PBO:0047930"}


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


id: FYECO:0000185
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which sodium was added to the medium or assay buffers in a limiting quantity compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping limited","termid":"FYECO:0000011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ limited sodium","termid":"FYECO:0000185"}


id: GO:0075153
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont organism modulates the frequency, rate or extent of its transmembrane receptor-mediated signal transduction as a result of detecting molecules of its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of transmembrane receptor-mediated signal transduction in response to host (obsolete GO:0075153)","synonyms":[{"name":"regulation of symbiont transmembrane receptor-mediated signal transduction in response to host","type":"exact"}],"termid":"GO:0075153"}


id: PBO:0087875
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional regulator; facilitates elongation through factors that modify RNAP II; role in peroxide resistance involving Rad2p; role in nonhomologous end-joining (NHEJ) of ds breaks in plasmid DNA, but not chromosomal DNA; role in the hyperosmotic stress response through polymerase recruitment at RNAP II and RNAP III genes; negatively regulates sporulation; protein abundance increases in response to DNA replication stress; functionally complemented by human SUB1 (PC4)","termid":"PBO:0087875"}


id: PBO:0027648
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_swollen_spheroid_vegetative_cell","termid":"PBO:0027648"}


id: MONDO:1010237
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polymicrogyria that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder, non-human animal","termid":"MONDO:1011308"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polymicrogyria, non-human animal","secondary_identifiers":["OMIA:001100"],"termid":"MONDO:1010237","xrefs":{"Monarch":{"xref_id":"1010237"}}}


id: MONDO:1040010
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Van der Woude syndrome, popliteal pterygium syndrome, cleft lip with or without palate, or a spectrum of one or two of those conditions in which the cause of the disease is a mutation in the IRF6 gene.","definition_xrefs":["PMID:12219090","PMID:20301581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IRF6-related condition","termid":"MONDO:1040010","xrefs":{"Monarch":{"xref_id":"1040010"}}}


id: PBO:0090146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar transporter chaperone (VTC) complex polyphosphate synthetase subunit Vtc2/3","termid":"PBO:0090146"}


id: GO:1902365
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 spindle pole body.","definition_xrefs":["PMID:21131906","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein localization to spindle pole body","termid":"GO:1902363"},{"relation_name":"is_a","term_name":"positive regulation of protein localization","termid":"GO:1903829"},{"relation_name":"positively_regulates","term_name":"protein localization to spindle pole body","termid":"GO:0071988"}],"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 spindle pole body","synonyms":[{"name":"activation of protein localisation to spindle pole body","type":"narrow"},{"name":"activation of protein localization to spindle pole body","type":"narrow"},{"name":"positive regulation of protein localisation to spindle pole body","type":"exact"},{"name":"up regulation of protein localisation to spindle pole body","type":"exact"},{"name":"up regulation of protein localization to spindle pole body","type":"exact"},{"name":"up-regulation of protein localisation to spindle pole body","type":"exact"},{"name":"up-regulation of protein localization to spindle pole body","type":"exact"},{"name":"upregulation of protein localisation to spindle pole body","type":"exact"},{"name":"upregulation of protein localization to spindle pole body","type":"exact"}],"termid":"GO:1902365"}


id: GO:0015611
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + D-ribose(out) = ADP + phosphate + D-ribose(in).","definition_xrefs":["RHEA:29903"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ABC-type monosaccharide transporter activity","termid":"GO:0015407"},{"relation_name":"is_a","term_name":"D-ribose transmembrane transporter activity","termid":"GO:0015591"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"ABC-type D-ribose transporter activity","secondary_identifiers":["EC:7.5.2.7","MetaCyc:ABC-28-RXN"],"synonyms":[{"name":"D-ribose porter activity","type":"broad"},{"name":"D-ribose-importing ATPase activity","type":"related"}],"termid":"GO:0015611"}


id: FYPO:0002398
data:
  {"alleles_by_uniquename":{"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_04280:allele-1":{"allele_type":"amino_acid_mutation","description":"T582G","gene_uniquename":"SJAG_04280","name":"wee1-as8","uniquename":"SJAG_04280:allele-1"},"SJAG_04522:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04522","name":"rga4delta","uniquename":"SJAG_04522:allele-1"},"SJAG_04703:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04703","name":"for3delta","uniquename":"SJAG_04703:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[118799],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001369"}],"single_locus_phenotype":[{"annotations":[118881],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0003315"},{"annotations":[118777],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0002026"},{"annotations":[118800],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001369"}]},"cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the amount, distribution, or morphology of all or part of the actin cytoskeleton is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"is_a","term_name":"abnormal actin cytoskeleton","termid":"FYPO:0005665"},{"relation_name":"output_of","term_name":"abnormal actin cytoskeleton organization during vegetative growth","termid":"FYPO:0000801"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02392":null,"SJAG_04280":null,"SJAG_04522":null,"SJAG_04703":null},"genotype_count":4,"genotypes_by_uniquename":{"for3delta":{"display_name":"for3delta","display_uniquename":"for3delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04703:allele-1","expression":"Null"}]}]},"pom1delta":{"display_name":"pom1delta","display_uniquename":"pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"rga4delta":{"display_name":"rga4delta","display_uniquename":"rga4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]}]},"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"rga4delta wee1-as8(T582G aa)","display_uniquename":"rga4delta__wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04522:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_04280:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0004803"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_04522","SJAG_04280"],"name":"abnormal actin cytoskeleton during vegetative growth","references_by_uniquename":{"PMID:25866389":null,"PMID:30664646":null,"PMID:30726171":null},"single_locus_annotated_genes":["SJAG_04703","SJAG_04522","SJAG_02392"],"single_locus_genotype_uniquenames":["pom1delta","rga4delta","for3delta"],"synonyms":[{"name":"abnormal actin cytoskeleton during mitotic cell cycle","type":"related"},{"name":"abnormal actin cytoskeleton physical object quality during vegetative growth","type":"exact"}],"termid":"FYPO:0002398","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000338":null,"FYPO:0001369":null,"FYPO:0002026":null,"FYPO:0003315":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: PBO:0076208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO2 pseudogene 18","termid":"PBO:0076208"}


id: FYPO:0007372
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of chlorpromazine than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0002682","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"resistance to chlorpromazine","synonyms":[{"name":"resistance to chlorpromazine during mitotic cell cycle","type":"related"},{"name":"resistance to chlorpromazine during vegetative growth","type":"exact"},{"name":"resistant to chlorpromazine","type":"exact"}],"termid":"FYPO:0007372"}


id: PBO:0002129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein farnesyltransferase beta subunit Cpp1","termid":"PBO:0002129"}


id: PBO:0028680
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K9_methylation_at_mating-type_region_heterochromatin","termid":"PBO:0028680"}


id: GO:0140233
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a cation by a channel that opens when intracellular cAMP has been bound by the channel complex or one of its constituent parts, to regulate the postsynaptic membrane potential.","definition_xrefs":["GOC:pvn"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellularly cAMP-activated cation channel activity","termid":"GO:0005222"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"intracellular cAMP-activated cation channel activity involved in regulation of postsynaptic membrane potential","synonyms":[{"name":"intracellular cAMP activated cation channel activity involved in regulation of postsynaptic membrane potential","type":"exact"}],"termid":"GO:0140233"}


id: MOD:01161
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively removes oxygen atoms from a residue without the removal of hydrogen atoms.","definition_xrefs":["PubMed:14235557","Unimod:447"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reduced residue","termid":"MOD:01472"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deoxygenated residue","synonyms":[{"name":"Deoxy","type":"related"},{"name":"dOxyRes","type":"exact"},{"name":"reduction","type":"related"}],"termid":"MOD:01161"}


id: FYPO:0002953
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of S-adenosyl-L-methionine measured in a cell is higher than normal when the cell is in G0 phase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during G0","termid":"FYPO:0002949"}],"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:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased S-adenosyl-L-methionine level during G0","synonyms":[{"name":"increased S-adenosyl-L-methionine accumulation during G0","type":"related"},{"name":"increased S-adenosyl-L-methionine level during cell quiescence","type":"exact"},{"name":"increased S-adenosyl-L-methionine level during quiescence","type":"exact"},{"name":"increased S-adenosylmethionine level during G0","type":"exact"},{"name":"increased SAM level during G0","type":"exact"}],"termid":"FYPO:0002953"}


id: GO:0061276
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a mesonephric proximal tubule are generated and organized. The mesonephric proximal tubule extends from the capsule to the distal tubule.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesonephric nephron tubule morphogenesis","termid":"GO:0061240"},{"relation_name":"is_a","term_name":"proximal tubule morphogenesis","termid":"GO:0072158"},{"relation_name":"part_of","term_name":"mesonephric proximal tubule development","termid":"GO:0061275"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mesonephric proximal tubule morphogenesis","termid":"GO:0061276"}


id: MONDO:0020352
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple system atrophy, parkinsonian type (MSA-p) is a form of multiple system atrophy (MSA) with predominant parkinsonian features (bradykinesia, rigidity, irregular jerky postural tremor, and postural instability).","definition_xrefs":["Orphanet:98933"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple system atrophy","termid":"MONDO:0007803"},{"relation_name":"is_a","term_name":"parkinsonian disorder","termid":"MONDO:0021095"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0021179"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0021179","MONDO:0005066"],"is_obsolete":false,"name":"multiple system atrophy, parkinsonian type","secondary_identifiers":["GARD:19604","icd11.foundation:296753000","NANDO:1200036","ICD10CM:G23.2","MEDGEN:1842393","UMLS:C5554235"],"synonyms":[{"name":"MSA, parkinsonian type","type":"exact"},{"name":"MSA-p","type":"exact"}],"termid":"MONDO:0020352","xrefs":{"Monarch":{"xref_id":"0020352"}}}


id: MONDO:0044965
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A disease or disorder that involves the abdominal segment of trunk.","definition_xrefs":["MONDO:design_pattern"],"gene_count":0,"genotype_count":0,"name":"obsolete abdominal and pelvic region disorder (obsolete MONDO:0044965)","secondary_identifiers":["SCTID:609618002"],"synonyms":[{"name":"abdominal segment of trunk disease","type":"exact"},{"name":"abdominal segment of trunk disease or disorder","type":"exact"},{"name":"disease of abdominal segment of trunk","type":"exact"},{"name":"disease or disorder of abdominal segment of trunk","type":"exact"},{"name":"disorder of abdominal segment of trunk","type":"exact"}],"termid":"MONDO:0044965","xrefs":{"Monarch":{"xref_id":"0044965"}}}


id: MONDO:0957481
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"pregnancy associated osteoporosis","termid":"MONDO:0100194"}],"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":"idiopathic pregnancy-associated osteoporosis","secondary_identifiers":["MEDGEN:1843391","Orphanet:647823","UMLS:C5782297"],"termid":"MONDO:0957481","xrefs":{"Monarch":{"xref_id":"0957481"}}}


id: PBO:0027415
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_m7G(5')pppN_diphosphatase_activity","termid":"PBO:0027415"}


id: PBO:0070421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoid isomerohydrolase RPE65","termid":"PBO:0070421"}


id: PBO:0073179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenoprotein K pseudogene 1","termid":"PBO:0073179"}


id: PBO:0065901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB43, member RAS oncogene family","termid":"PBO:0065901"}


id: PBO:0070145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 59 pseudogene","termid":"PBO:0070145"}


id: SO:0001731
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 8th residue (a lysine), from the start of the H4 histone protein is acetylated.","definition_xrefs":["SO:KE"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_4_acetylation_site","termid":"SO:0001972"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"H4K8_acetylation_site","synonyms":[{"name":"H4K8 acetylation site","type":"exact"},{"name":"H4K8ac","type":"exact"}],"termid":"SO:0001731"}


id: PBO:0074447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small lysine rich protein 1","termid":"PBO:0074447"}


id: GO:0044232
data:
  {"annotated_genes":["SJAG_04413","SJAG_04221","SJAG_04370","SJAG_02028","SJAG_03710","SJAG_01305","SJAG_02002","SJAG_02501","SJAG_01564","SJAG_02613","SJAG_02578","SJAG_03416","SJAG_01929","SJAG_04552","SJAG_03247","SJAG_01329","SJAG_01168","SJAG_05241","SJAG_03170","SJAG_01116","SJAG_03282","SJAG_05184"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[118173,103873,90966,105814,111153,117028,96946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140268"},{"annotations":[114697],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0098853"},{"annotations":[105336,107135,90380,116108,107008],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032865"},{"annotations":[106809,88969,101200,109512,114133],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044284"},{"annotations":[101628,114698,105816,106513],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071561"},{"annotations":[93801,89696],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990816"}]},"cv_name":"cellular_component","definition":"A zone of apposition between the membranes of an organelle with another membrane, either another membrane of the same organelle, a membrane of another organelle, or the plasma membrane. Membrane contact sites (MCSs) are structured by bridging complexes. They are specialized for communication, including the efficient traffic of small molecules such as Ca2+ ions and lipids, as well as enzyme-substrate interactions.","definition_xrefs":["GOC:jl","PMID:16806880"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"organelle","termid":"GO:0043226"}],"gene_count":22,"genes_by_uniquename":{"SJAG_01116":null,"SJAG_01168":null,"SJAG_01305":null,"SJAG_01329":null,"SJAG_01564":null,"SJAG_01929":null,"SJAG_02002":null,"SJAG_02028":null,"SJAG_02501":null,"SJAG_02578":null,"SJAG_02613":null,"SJAG_03170":null,"SJAG_03247":null,"SJAG_03282":null,"SJAG_03416":null,"SJAG_03710":null,"SJAG_04221":null,"SJAG_04370":null,"SJAG_04413":null,"SJAG_04552":null,"SJAG_05184":null,"SJAG_05241":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"organelle membrane contact site","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"MCS","type":"exact"},{"name":"inter-organelle junction","type":"narrow"},{"name":"interorganelle junction","type":"narrow"}],"termid":"GO:0044232","terms_by_termid":{"GO:0032865":null,"GO:0044284":null,"GO:0071561":null,"GO:0098853":null,"GO:0140268":null,"GO:1990816":null}}


id: _global:gained
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"X gained Y if X is a variant_of X' and Y part of X but not X'.","definition_xrefs":["SO:ke"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gained","termid":"_global:gained"}


id: GO:0035473
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a lipase.","definition_xrefs":["GOC:BHF"],"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:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"lipase binding","termid":"GO:0035473"}


id: MONDO:0005691
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections caused by viruses of the genus cardiovirus, family picornaviridae.","definition_xrefs":["MESH:D018188"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Picornaviridae infectious disease","termid":"MONDO:0005914"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardiovirus infectious disease","secondary_identifiers":["EFO:0007194","MEDGEN:60193","UMLS:C0206617"],"synonyms":[{"name":"Cardiovirus infection","type":"related"},{"name":"infection, Cardiovirus","type":"related"},{"name":"infections, Cardiovirus","type":"related"}],"termid":"MONDO:0005691","xrefs":{"Monarch":{"xref_id":"0005691"}}}


id: PBO:0073647
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"salt inducible kinase 1","termid":"PBO:0073647"}


id: MONDO:0019137
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Non-24-hour sleep-wake disorder (non-24 disorder), also known as hypernychthemeral syndrome, is a circadian rhythm sleep disorder characterized by non-synchronization to a 24-hour day leading to insomnia and daytime sleepiness with sometimes severe associated manifestations.","definition_xrefs":["Orphanet:73267"],"direct_ancestors":[{"relation_name":"is_a","term_name":"circadian rhythm sleep disorder","termid":"MONDO:0024361"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-24-hour sleep-wake syndrome","secondary_identifiers":["GARD:10949","ICD10CM:G47.24","UMLS:C0751759","MEDGEN:148383","NORD:1511","SCTID:230496009"],"synonyms":[{"name":"Non-24-Hour Sleep-Wake Disorder","type":"exact"},{"name":"circadian rhythm sleep disorder, free running type","type":"exact"},{"name":"circadian rhythm sleep disorder, free-running type","type":"exact"},{"name":"hypernychthemeral syndrome","type":"exact"},{"name":"non 24 hour sleep wake disorder","type":"related"},{"name":"non-24","type":"exact"}],"termid":"MONDO:0019137","xrefs":{"Monarch":{"xref_id":"0019137"}}}


id: FYECO:0000335
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which AP20187 was added to the medium or assay buffer.","definition_xrefs":["CHEBI:136847"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ AP20187","termid":"FYECO:0000335"}


id: PBO:0047096
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 149 member B1","termid":"PBO:0047096"}


id: GO:0035981
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a tongue muscle cell.","definition_xrefs":["PMID:3393851","CL:0002673","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal muscle fiber differentiation","termid":"GO:0098528"}],"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":"tongue muscle cell differentiation","termid":"GO:0035981"}


id: GO:0141201
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A inflammatory cell death process associated with the generation of pyrogenic mediators that result from the activation of gasdermins.","definition_xrefs":["PMID:18846107","PMID:33883744","PMID:21760595"],"direct_ancestors":[{"relation_name":"is_a","term_name":"programmed cell death","termid":"GO:0012501"},{"relation_name":"is_a","term_name":"pyroptotic inflammatory response","termid":"GO:0070269"}],"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":"pyroptotic cell death","synonyms":[{"name":"pyroptosis","type":"broad"}],"termid":"GO:0141201"}


id: PBO:0112594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial oxidoreductase for ubiquinone biosynthesis","termid":"PBO:0112594"}


id: PBO:0068357
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 2","termid":"PBO:0068357"}


id: MONDO:0006219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An aggressive, high-grade and poorly differentiated carcinoma with neuroendocrine differentiation that arises from the gallbladder. It is characterized by the presence of malignant small cells.","definition_xrefs":["NCIT:C6763"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small cell carcinoma","termid":"MONDO:0000402"},{"relation_name":"is_a","term_name":"gallbladder carcinoma","termid":"MONDO:0003220"},{"relation_name":"is_a","term_name":"gallbladder neuroendocrine neoplasm","termid":"MONDO:0024502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"gallbladder small cell neuroendocrine carcinoma","secondary_identifiers":["EFO:1000266","UMLS:C1333759","DOID:7133","MEDGEN:232229"],"synonyms":[{"name":"Oat cell carcinoma of gallbladder","type":"exact"},{"name":"Oat cell carcinoma of the gallbladder","type":"exact"},{"name":"gall bladder small cell carcinoma","type":"exact"},{"name":"gallbladder Oat cell carcinoma","type":"exact"},{"name":"gallbladder small cell NEC","type":"exact"},{"name":"gallbladder small cell carcinoma","type":"exact"},{"name":"gallbladder small cell neuroendocrine carcinoma","type":"exact"},{"name":"small cell carcinoma of gall bladder","type":"exact"},{"name":"small cell carcinoma of gallbladder","type":"exact"},{"name":"small cell carcinoma of the gallbladder","type":"exact"}],"termid":"MONDO:0006219","xrefs":{"Monarch":{"xref_id":"0006219"}}}


id: SO:0002149
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 15th residue (a lysine), from the start of the H2AZ histone protein is acetylated.","definition_xrefs":["PMID:24316985","PMID:19385636","PMID:27087541"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_2AZ_acetylation_site","termid":"SO:0002144"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"H2AZK15_acetylation_site","synonyms":[{"name":"H2A.ZK15ac","type":"exact"},{"name":"H2AZK15 acetylation site","type":"exact"},{"name":"H2AZK15ac","type":"exact"}],"termid":"SO:0002149"}


id: PBO:0083688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Enolase II, a phosphopyruvate hydratase; catalyzes conversion of 2-phosphoglycerate to phosphoenolpyruvate during glycolysis and the reverse reaction during gluconeogenesis; expression induced in response to glucose; ENO2 has a paralog, ENO1, that arose from the whole genome duplication","termid":"PBO:0083688"}


id: MONDO:0010095
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary ataxia","termid":"MONDO:0100309"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ataxia-tapetoretinal degeneration syndrome","secondary_identifiers":["MEDGEN:336461","OMIM:272600","UMLS:C1848932","MESH:C564788","Orphanet:1178","GARD:16559"],"synonyms":[{"name":"tapetoretinal degeneration with ataxia","type":"related"}],"termid":"MONDO:0010095","xrefs":{"Monarch":{"xref_id":"0010095"}}}


id: GO:0035909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of an aorta are generated and organized. An aorta is an artery that carries blood from the heart to other parts of the body.","definition_xrefs":["Wikipedia:Aorta","GOC:dgh","UBERON:0000947","GOC:bf","MA:0000062"],"direct_ancestors":[{"relation_name":"is_a","term_name":"artery morphogenesis","termid":"GO:0048844"},{"relation_name":"part_of","term_name":"aorta development","termid":"GO:0035904"}],"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":"aorta morphogenesis","termid":"GO:0035909"}


id: GO:0047451
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (3R)-3-hydroxyoctanoyl-[acyl-carrier protein] = H2O + (2E)-octenoyl-[acyl-carrier protein].","definition_xrefs":["PMID:8910376"],"gene_count":0,"genotype_count":0,"name":"obsolete (3R)-3-hydroxyoctanoyl-[acyl-carrier-protein] dehydratase activity (obsolete GO:0047451)","synonyms":[{"name":"(3R)-3-hydroxyoctanoyl-[acyl-carrier-protein] hydro-lyase activity","type":"related"},{"name":"3-hydroxyoctanoyl-ACP dehydratase activity","type":"exact"},{"name":"3-hydroxyoctanoyl-[acyl-carrier protein] dehydratase activity","type":"exact"},{"name":"3-hydroxyoctanoyl-[acyl-carrier-protein] dehydratase activity","type":"broad"}],"termid":"GO:0047451"}


id: PBO:0002153
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GET complex ATPase subunit Get3 (predicted)","termid":"PBO:0002153"}


id: FYPO:0009000
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A microtubule cytoskeleton organization phenotype observed during mitotic interphase in which cytoplasmic microtubule polymerization, i.e. the addition of tubulin dimers to the plus end of a microtubule occurs at a lower rate, or speed, than normal.","definition_xrefs":["PomBase:mlr","PMID:36633091"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased rate of microtubule polymerization during vegetative growth","termid":"FYPO:0005703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000054","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"decreased rate of cytoplasmic microtubule polymerization during mitotic interphase","synonyms":[{"name":"decreased cytoplasmic microtubule growth rate during mitotic interphase","type":"exact"},{"name":"decreased cytoplasmic microtubule growth speed during mitotic interphase","type":"exact"},{"name":"decreased cytoplasmic microtubule polymerisation speed during mitotic interphase","type":"exact"},{"name":"decreased cytoplasmic microtubule polymerization speed during mitotic interphase","type":"exact"},{"name":"decreased rate of cytoplasmic microtubule polymerisation during mitotic interphase","type":"exact"}],"termid":"FYPO:0009000"}


id: MONDO:0054781
data:
  {"annotated_genes":["SJAG_03584"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85488],"is_not":false,"summary":null,"term":"MONDO:0054781"}]},"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_03584":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 36","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1644927","UMLS:C4693722","DOID:0111482","OMIM:617950"],"synonyms":[{"name":"COXPD36","type":"related"},{"name":"combined oxidative phosphorylation deficiency 36","type":"exact"}],"termid":"MONDO:0054781","terms_by_termid":{"MONDO:0054781":null},"xrefs":{"Monarch":{"xref_id":"0054781"}}}


id: PBO:0029542
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-viable_mixed_vegetative_cell_population_including_cell_with_normal_morphology_and_long_cells_(obsolete_FYPO:0002180)","termid":"PBO:0029542"}


id: PBO:0062873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OTU deubiquitinase 7B","termid":"PBO:0062873"}


id: MONDO:0800304
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"neuropathy, hereditary sensory and autonomic, type IId","secondary_identifiers":["UMLS:C4012054","MEDGEN:860491"],"synonyms":[{"name":"HSAN2D","type":"exact"}],"termid":"MONDO:0800304","xrefs":{"Monarch":{"xref_id":"0800304"}}}


id: MONDO:0000912
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 14q12.","definition_xrefs":["DOID:0110507","PMID:8944017"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 5","secondary_identifiers":["OMIM:600792","GARD:22585","MESH:C563444","MEDGEN:331485","UMLS:C1833319"],"synonyms":[{"name":"DFNB5","type":"narrow"},{"name":"autosomal recessive deafness 5","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 5","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 5","type":"narrow"},{"name":"deafness, autosomal recessive 5","type":"narrow"},{"name":"neurosensory nonsyndromic recessive deafness 5","type":"narrow"}],"termid":"MONDO:0000912","xrefs":{"Monarch":{"xref_id":"0000912"}}}


id: GO:0002596
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of antigen processing and presentation of peptide antigen via MHC class Ib.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of antigen processing and presentation of peptide antigen","termid":"GO:0002584"},{"relation_name":"is_a","term_name":"negative regulation of antigen processing and presentation via MHC class Ib","termid":"GO:0002593"},{"relation_name":"is_a","term_name":"regulation of antigen processing and presentation of peptide antigen via MHC class Ib","termid":"GO:0002595"},{"relation_name":"negatively_regulates","term_name":"antigen processing and presentation of peptide antigen via MHC class Ib","termid":"GO:0002428"}],"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 antigen processing and presentation of peptide antigen via MHC class Ib","synonyms":[{"name":"down regulation of antigen processing and presentation of peptide antigen via MHC class Ib","type":"exact"},{"name":"down-regulation of antigen processing and presentation of peptide antigen via MHC class Ib","type":"exact"},{"name":"downregulation of antigen processing and presentation of peptide antigen via MHC class Ib","type":"exact"},{"name":"inhibition of antigen processing and presentation of peptide antigen via MHC class Ib","type":"narrow"},{"name":"negative regulation of peptide antigen processing and presentation via MHC class Ib","type":"exact"}],"termid":"GO:0002596"}


id: PBO:0029438
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_degradation_during_nitrogen_starvation","termid":"PBO:0029438"}


id: PR:Q9US22
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rpl1502 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9US22"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L15-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1783.08c","synonyms":[{"name":"Spom972h-rpl1502","type":"exact"}],"termid":"PR:Q9US22"}


id: MONDO:1010969
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dysautonomia that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dysautonomia, non-human animal","termid":"MONDO:1010229"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dysautonomia, domestic cat","secondary_identifiers":["OMIA:000312-9685"],"termid":"MONDO:1010969","xrefs":{"Monarch":{"xref_id":"1010969"}}}


id: PBO:0074300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLX1 homolog A, structure-specific endonuclease subunit","termid":"PBO:0074300"}


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


id: PBO:0063542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylethanolamine binding protein 1 pseudogene 1","termid":"PBO:0063542"}


id: GO:0021587
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the cerebellum is generated and organized. The cerebellum is the portion of the brain in the back of the head between the cerebrum and the pons. The cerebellum controls balance for walking and standing, modulates the force and range of movement and is involved in the learning of motor skills.","definition_xrefs":["GOC:jid","ISBN:0838580343","GO_REF:0000021","GOC:dph","GOC:cls","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"cerebellum development","termid":"GO:0021549"},{"relation_name":"part_of","term_name":"hindbrain morphogenesis","termid":"GO:0021575"}],"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":"cerebellum morphogenesis","termid":"GO:0021587"}


id: PBO:0060275
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin heavy chain 9","termid":"PBO:0060275"}


id: PBO:0088836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin, WD repeat Nup82","termid":"PBO:0088836"}


id: MONDO:0013650
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hypotrichosis that has material basis in an autosomal recessive mutation on chromosome 7p22.3-p21.3.","definition_xrefs":["PMID:20544222","DOID:0110707"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypotrichosis","termid":"MONDO:0003037"},{"relation_name":"is_a","term_name":"hypotrichosis simplex","termid":"MONDO:0018914"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypotrichosis 10","secondary_identifiers":["MEDGEN:481883","UMLS:C3280253","OMIM:614238","GARD:15782"],"synonyms":[{"name":"HYPT10","type":"exact"},{"name":"hypotrichosis 10","type":"exact"},{"name":"hypotrichosis type 10","type":"exact"},{"name":"hypt10","type":"exact"}],"termid":"MONDO:0013650","xrefs":{"Monarch":{"xref_id":"0013650"}}}


id: _global:produces
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"a produces b if some process that occurs_in a has_output b, where a and b are material entities. Examples: hybridoma cell line produces monoclonal antibody reagent; chondroblast produces avascular GAG-rich matrix.","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"produces","secondary_identifiers":["RO:0003000"],"termid":"_global:produces"}


id: PBO:0030339
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level_during_cellular_response_to_oxidative_stress","termid":"PBO:0030339"}


id: PBO:0088841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prohibitin Phb2","termid":"PBO:0088841"}


id: PBO:0063885
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 O","termid":"PBO:0063885"}


id: GO:0033604
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the regulated release of a catecholamine.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catecholamine secretion","termid":"GO:0050433"},{"relation_name":"is_a","term_name":"negative regulation of amine transport","termid":"GO:0051953"},{"relation_name":"is_a","term_name":"negative regulation of secretion by cell","termid":"GO:1903531"},{"relation_name":"negatively_regulates","term_name":"catecholamine secretion","termid":"GO:0050432"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of catecholamine secretion","synonyms":[{"name":"down regulation of catecholamine secretion","type":"exact"},{"name":"down-regulation of catecholamine secretion","type":"exact"},{"name":"downregulation of catecholamine secretion","type":"exact"},{"name":"inhibition of catecholamine secretion","type":"narrow"}],"termid":"GO:0033604"}


id: PR:Q9UTK5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- alm1 gene.","definition_xrefs":["UniProtKB:Q9UTK5","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":"abnormal long morphology protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1486.04c","synonyms":[{"name":"Sp8 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-alm1","type":"exact"}],"termid":"PR:Q9UTK5"}


id: MONDO:0007053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"restless legs syndrome, susceptibility to","termid":"MONDO:0100170"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restless legs syndrome, susceptibility to, 1","secondary_identifiers":["UMLS:C1876177","MEDGEN:360293","MESH:C538443","OMIM:102300"],"synonyms":[{"name":"Ekbom syndrome","type":"related"},{"name":"RLS1","type":"related"},{"name":"acromelalgia, hereditary","type":"related"},{"name":"restless legs syndrome, susceptibility to, 1","type":"exact"}],"termid":"MONDO:0007053","xrefs":{"Monarch":{"xref_id":"0007053"}}}


id: GO:0001080
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A transcription regulation process in which the presence of one nitrogen source leads to an increase in the frequency, rate, or extent of transcription, from an RNA polymerase II promoter, of specific genes involved in the metabolism of other nitrogen sources.","definition_xrefs":["PMID:19104072","GOC:mah","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrogen catabolite regulation of transcription from RNA polymerase II promoter","termid":"GO:0001079"},{"relation_name":"is_a","term_name":"nitrogen catabolite activation of transcription","termid":"GO:0090294"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0006351","GO:0008150","GO:0010467","GO:0006355"],"is_obsolete":false,"name":"nitrogen catabolite activation of transcription from RNA polymerase II promoter","synonyms":[{"name":"positive regulation of transcription from RNA polymerase II promoter by nitrogen catabolites","type":"exact"}],"termid":"GO:0001080"}


id: MONDO:0968944
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0037792","MONDO:0005066","MONDO:0006025"],"is_obsolete":false,"name":"intellectual developmental disorder, autosomal recessive 82","secondary_identifiers":["DOID:0060947","OMIM:620779"],"termid":"MONDO:0968944","xrefs":{"Monarch":{"xref_id":"0968944"}}}


id: PBO:0078823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Pro (anticodon AGG) 2-6","termid":"PBO:0078823"}


id: PR:Q9URX0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC922.06 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9URX0"],"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 oxidoreductase C922.06 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC922.06","synonyms":[{"name":"Spom972h-SPAC922.06","type":"exact"}],"termid":"PR:Q9URX0"}


id: PBO:0050521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homeobox D9","termid":"PBO:0050521"}


id: GO:0007342
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The binding and fusion of a sperm, with the plasma membrane of the oocyte as part of the process of single fertilization. In sperm with flagella, binding occurs at the posterior (post-acrosomal) region of the sperm head.","definition_xrefs":["GOC:jl","GOC:dph","PMID:17644969"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"is_a","term_name":"plasma membrane fusion","termid":"GO:0045026"},{"relation_name":"part_of","term_name":"single fertilization","termid":"GO:0007338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"fusion of sperm to egg plasma membrane involved in single fertilization","synonyms":[{"name":"sperm-oocyte fusion","type":"narrow"}],"termid":"GO:0007342"}


id: MONDO:0008701
data:
  {"annotated_genes":["SJAG_04528"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85421],"is_not":false,"summary":null,"term":"MONDO:0008701"}]},"cv_name":"mondo","definition":"Achondrogenesis type 1A (ACG1A), a form of achondrogenesis, is a very rare, lethal skeletal dysplasia characterized by dwarfism with extremely short limbs, narrow chest, short ribs that are easily fractured, soft skull bones and distinctive histological features of the cartilage.","definition_xrefs":["Orphanet:93299"],"direct_ancestors":[{"relation_name":"is_a","term_name":"achondrogenesis","termid":"MONDO:0019648"},{"relation_name":"is_a","term_name":"severe spondylodysplastic dysplasia","termid":"MONDO:0800080"},{"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,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"achondrogenesis type IA","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:78546","OMIM:200600","MESH:C536015","ICD9:756.9","GARD:459","DOID:0080054","SCTID:42725006","UMLS:C0265273"],"synonyms":[{"name":"ACG1A","type":"related"},{"name":"Houston-Harris achondrogenesis","type":"related"},{"name":"achondrogenesis Houston-Harris type","type":"exact"},{"name":"achondrogenesis type 1A","type":"related"},{"name":"achondrogenesis, Houston-Harris type","type":"exact"},{"name":"achondrogenesis, type 1A","type":"related"},{"name":"achondrogenesis, type IA","type":"related"}],"termid":"MONDO:0008701","terms_by_termid":{"MONDO:0008701":null},"xrefs":{"Monarch":{"xref_id":"0008701"}}}


id: PBO:0075240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNX10 antisense RNA 1","termid":"PBO:0075240"}


id: PBO:0024475
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human USB1","termid":"PBO:0024475"}


id: PBO:0067823
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 125","termid":"PBO:0067823"}


id: PBO:0004003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial proline-tRNA ligase (predicted)","termid":"PBO:0004003"}


id: PBO:0072125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 2","termid":"PBO:0072125"}


id: GO:0050802
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The part of the circadian sleep/wake cycle where the organism is asleep.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"circadian sleep/wake cycle process","termid":"GO:0022410"},{"relation_name":"is_a","term_name":"sleep","termid":"GO:0030431"}],"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":"circadian sleep/wake cycle, sleep","termid":"GO:0050802"}


id: PBO:0059325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L57 pseudogene 10","termid":"PBO:0059325"}


id: PBO:0047845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"formyl peptide receptor 1","termid":"PBO:0047845"}


id: PBO:0030261
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_antimycin_A","termid":"PBO:0030261"}


id: GO:0150071
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of arginase activity.","definition_xrefs":["GOC:aruk","GOC:bc"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of arginase activity (obsolete GO:0150071)","termid":"GO:0150071"}


id: GO:0016279
data:
  {"annotated_genes":["SJAG_04574","SJAG_04159","SJAG_03487","SJAG_01425","SJAG_01079","SJAG_00769","SJAG_03869","SJAG_03228","SJAG_03630","SJAG_01146","SJAG_02873","SJAG_02692","SJAG_01536","SJAG_01482","SJAG_01193"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96195,96442,98836,100115,103543,104226,109990,111885,113511,114929,116318],"is_not":false,"summary":null,"term":"GO:0016279"},{"annotations":[94968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140954"},{"annotations":[113509],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046975"},{"annotations":[94969],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140955"},{"annotations":[115993],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0062122"},{"annotations":[116037,113510],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042800"},{"annotations":[116038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140999"},{"annotations":[109983,109984],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046974"},{"annotations":[109985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140948"},{"annotations":[109986],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140949"},{"annotations":[109987],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140947"},{"annotations":[116514],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140943"}]},"cv_name":"molecular_function","definition":"Catalysis of the transfer of a methyl group from S-adenosyl-L-methionine to the epsilon-amino group of a lysine residue in a protein substrate.","definition_xrefs":["PMID:12054878"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein methyltransferase activity","termid":"GO:0008276"},{"relation_name":"is_a","term_name":"lysine N-methyltransferase activity","termid":"GO:0016278"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00769":null,"SJAG_01079":null,"SJAG_01146":null,"SJAG_01193":null,"SJAG_01425":null,"SJAG_01482":null,"SJAG_01536":null,"SJAG_02692":null,"SJAG_02873":null,"SJAG_03228":null,"SJAG_03487":null,"SJAG_03630":null,"SJAG_03869":null,"SJAG_04159":null,"SJAG_04574":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008276"},{"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"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0016740","GO:0008276","GO:0003674","GO:0016741","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"protein-lysine N-methyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-8932413","Reactome:R-HSA-212263","Reactome:R-HSA-9854315","Reactome:R-HSA-8932243","Reactome:R-HSA-8932276","Reactome:R-HSA-8865237","Reactome:R-HSA-8932221","Reactome:R-HSA-8931858","Reactome:R-HSA-8932275","Reactome:R-HSA-8931974","Reactome:R-HSA-9844111"],"synonyms":[{"name":"protein (lysine) methyltransferase activity","type":"exact"},{"name":"protein lysine methylase activity","type":"exact"}],"termid":"GO:0016279","terms_by_termid":{"GO:0016279":null,"GO:0042800":null,"GO:0046974":null,"GO:0046975":null,"GO:0062122":null,"GO:0140943":null,"GO:0140947":null,"GO:0140948":null,"GO:0140949":null,"GO:0140954":null,"GO:0140955":null,"GO:0140999":null}}


id: MONDO:0015686
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare carcinoma that arises from the peritoneum and resembles the malignant surface epithelial-stromal tumors that arise from the ovary. Serous adenocarcinoma is the most common histologic variant. It affects women almost exclusively. The diagnosis of primary peritoneal carcinoma can be made only if both ovaries are not involved by tumor, or, if the ovaries are involved, the tumor is confined to the ovarian surface without invasion of the ovarian stroma and the peritoneal involvement is greater than the ovarian surface involvement.","definition_xrefs":["NCIT:C40022"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peritoneal carcinoma","termid":"MONDO:0002113"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"primary peritoneal carcinoma","secondary_identifiers":["MEDGEN:269516","HP:0030406","Orphanet:168829","GARD:20103","UMLS:C1514428"],"synonyms":[{"name":"EOPPC","type":"exact"},{"name":"Extra-ovarian primary peritoneal carcinoma","type":"exact"},{"name":"PPC","type":"exact"},{"name":"primary peritoneal cancer","type":"exact"},{"name":"primary peritoneal carcinoma","type":"exact"},{"name":"primary peritoneal carcinoma (disease)","type":"exact"},{"name":"primary peritoneal serous carcinoma","type":"exact"},{"name":"serous surface papillary carcinoma","type":"exact"}],"termid":"MONDO:0015686","xrefs":{"Monarch":{"xref_id":"0015686"}}}


id: SO:0002190
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcriptional cis regulatory region that when located between an enhancer and a gene's promoter prevents the enhancer from modulating the expression of the gene. Sometimes referred to as an insulator but may not include the barrier function of an insulator.","definition_xrefs":["NCBI:cf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"insulator","termid":"SO:0000627"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enhancer_blocking_element","synonyms":[{"name":"INSDC_feature:regulatory","type":"broad"},{"name":"INSDC_qualifier:enhancer_blocking_element","type":"exact"},{"name":"enhancer blocking element","type":"exact"},{"name":"insulator","type":"related"}],"termid":"SO:0002190"}


id: PBO:0061679
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NUP93 divergent transcript","termid":"PBO:0061679"}


id: PBO:0034676
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_frequency_of_meiotic_crossover_associated_with_gene_conversion","termid":"PBO:0034676"}


id: GO:1901672
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of systemic acquired resistance.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to biotic stimulus","termid":"GO:0002833"},{"relation_name":"is_a","term_name":"regulation of systemic acquired resistance","termid":"GO:0010112"},{"relation_name":"is_a","term_name":"positive regulation of defense response","termid":"GO:0031349"},{"relation_name":"is_a","term_name":"positive regulation of response to external stimulus","termid":"GO:0032103"},{"relation_name":"positively_regulates","term_name":"systemic acquired resistance","termid":"GO:0009627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of systemic acquired resistance","synonyms":[{"name":"activation of salicylic acid-dependent systemic resistance","type":"exact"},{"name":"activation of systemic acquired resistance","type":"narrow"},{"name":"positive regulation of salicylic acid-dependent systemic resistance","type":"exact"},{"name":"up regulation of salicylic acid-dependent systemic resistance","type":"exact"},{"name":"up regulation of systemic acquired resistance","type":"exact"},{"name":"up-regulation of salicylic acid-dependent systemic resistance","type":"exact"},{"name":"up-regulation of systemic acquired resistance","type":"exact"},{"name":"upregulation of salicylic acid-dependent systemic resistance","type":"exact"},{"name":"upregulation of systemic acquired resistance","type":"exact"}],"termid":"GO:1901672"}


id: MONDO:0043606
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A traumatic break in an area of bone that has been weakened by another disease process.","definition_xrefs":["NCIT:C3047"],"gene_count":0,"genotype_count":0,"name":"obsolete pathologic fracture (obsolete MONDO:0043606)","secondary_identifiers":["SCTID:268029009","MESH:D005598"],"synonyms":[{"name":"fracture, pathologic","type":"related"},{"name":"fracture, pathological","type":"related"},{"name":"fracture, spontaneous","type":"related"},{"name":"fractures, pathologic","type":"related"},{"name":"fractures, pathological","type":"related"},{"name":"pathologic fracture","type":"exact"},{"name":"pathologic fractures","type":"related"},{"name":"pathological fracture","type":"exact"},{"name":"pathological fractures","type":"related"},{"name":"spontaneous fracture","type":"related"},{"name":"spontaneous fractures","type":"related"}],"termid":"MONDO:0043606","xrefs":{"Monarch":{"xref_id":"0043606"}}}


id: MONDO:0003040
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The loss of access to memories that were previously encoded; this disorder is most commonly preceded by trauma, including physical brain injury, stroke, or seizure, but may also be psychogenic in origin. Memory loss may be temporary or permanent, but the ability to encode new memories or skills is not generally affected.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amnestic disorder","termid":"MONDO:0001152"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"}],"interesting_parent_ids":["MONDO:0002039"],"is_obsolete":false,"name":"retrograde amnesia","secondary_identifiers":["MESH:D000648","ICD10CM:R41.2","icd11.foundation:1405777748","DOID:4543","MEDGEN:264","UMLS:C0002624"],"termid":"MONDO:0003040","xrefs":{"Monarch":{"xref_id":"0003040"}}}


id: PBO:0041170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTG anti-proliferation factor 4","termid":"PBO:0041170"}


id: MONDO:0011178
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurological condition characterized by the occurrence of seizures during the first year of life (Benign familial infantile epilepsy) and choreoathetotic dyskinetic attacks during childhood or adolescence.","definition_xrefs":["Orphanet:31709"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"paroxysmal dyskinesia","termid":"MONDO:0015427"},{"relation_name":"is_a","term_name":"benign partial infantile seizures","termid":"MONDO:0015642"},{"relation_name":"is_a","term_name":"PRRT2-associated paroxysmal movement disorder","termid":"MONDO:0100556"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0003441"],"is_obsolete":false,"name":"infantile convulsions and choreoathetosis","secondary_identifiers":["NCIT:C126650","MESH:C535522","GARD:8553","UMLS:C1865926","OMIM:602066","MEDGEN:356123","SCTID:715534008"],"synonyms":[{"name":"ICCA","type":"related"},{"name":"ICCA syndrome","type":"exact"},{"name":"Icca syndrome","type":"related"},{"name":"PKD/IC","type":"exact"},{"name":"convulsions, familial infantile, with paroxysmal choreoathetosis","type":"related"},{"name":"convulsions, infantile, with paroxysmal choreoathetosis, familial","type":"related"},{"name":"infantile convulsions and choreoathetosis","type":"exact"},{"name":"infantile convulsions and paroxysmal choreoathetosis, familial","type":"related"},{"name":"paroxysmal kinesigenic dyskinesia and infantile convulsions","type":"exact"},{"name":"paroxysmal kinesigenic dyskinesia with infantile convulsions","type":"related"}],"termid":"MONDO:0011178","xrefs":{"Monarch":{"xref_id":"0011178"}}}


id: GO:0000235
data:
  {"annotated_genes":["SJAG_02286","SJAG_02509","SJAG_00655","SJAG_02336","SJAG_02695","SJAG_04003","SJAG_01297","SJAG_01613","SJAG_02045","SJAG_04387"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[90856,98705,103511,106700,106909,111615],"is_not":false,"summary":null,"term":"GO:0000235"},{"annotations":[87227],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990574"},{"annotations":[107733,90862,103388],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061673"},{"annotations":[96462],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1905721"}]},"cv_name":"cellular_component","definition":"Any of the spindle microtubules that radiate in all directions from the spindle poles and are thought to contribute to the forces that separate the poles and position them in relation to the rest of the cell.","definition_xrefs":["ISBN:0815316194"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle microtubule","termid":"GO:0005876"},{"relation_name":"is_a","term_name":"cytoplasmic microtubule","termid":"GO:0005881"},{"relation_name":"part_of","term_name":"aster","termid":"GO:0005818"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00655":null,"SJAG_01297":null,"SJAG_01613":null,"SJAG_02045":null,"SJAG_02286":null,"SJAG_02336":null,"SJAG_02509":null,"SJAG_02695":null,"SJAG_04003":null,"SJAG_04387":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005575","GO:0015630","GO:0005737"],"is_obsolete":false,"name":"astral microtubule","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0000235","terms_by_termid":{"GO:0000235":null,"GO:0061673":null,"GO:1905721":null,"GO:1990574":null}}


id: MONDO:1010536
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Megacolon that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"megacolon, non-human animal","termid":"MONDO:1010039"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"megacolon, horse","secondary_identifiers":["OMIA:000629-9796"],"termid":"MONDO:1010536","xrefs":{"Monarch":{"xref_id":"1010536"}}}


id: MONDO:0859266
data:
  {"annotated_genes":["SJAG_00872"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86332],"is_not":false,"summary":null,"term":"MONDO:0859266"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodevelopmental disorder","termid":"MONDO:0700092"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00872":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1823958","OMIM:619972","UMLS:C5774185"],"termid":"MONDO:0859266","terms_by_termid":{"MONDO:0859266":null},"xrefs":{"Monarch":{"xref_id":"0859266"}}}


id: GO:1990267
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 transition metal nanoparticle.","definition_xrefs":["PMID:23150627"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"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 transition metal nanoparticle","synonyms":[{"name":"response to colloidal metal","type":"related"},{"name":"response to neutral metal atoms","type":"related"}],"termid":"GO:1990267"}


id: GO:0044446
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A constituent part of an intracellular organelle, an organized structure of distinctive morphology and function, occurring within the cell. Includes constituent parts of the nucleus, mitochondria, plastids, vacuoles, vesicles, ribosomes and the cytoskeleton but excludes the plasma membrane.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete intracellular organelle part (obsolete GO:0044446)","termid":"GO:0044446"}


id: PBO:0088851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved fungal cell surface protein, Kre9/Knh1 family","termid":"PBO:0088851"}


id: GO:0010460
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency or rate of heart contraction.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heart rate","termid":"GO:0002027"},{"relation_name":"is_a","term_name":"positive regulation of heart contraction","termid":"GO:0045823"}],"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 heart rate","termid":"GO:0010460"}


id: PBO:0005720
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"renal cell cancer","termid":"PBO:0005720"}


id: MONDO:0004523
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma of the skin with a prominent clear cell component.","definition_xrefs":["NCIT:C4459"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin squamous cell carcinoma","termid":"MONDO:0002529"},{"relation_name":"is_a","term_name":"keratinizing squamous cell carcinoma","termid":"MONDO:0005056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"clear cell squamous cell skin carcinoma","secondary_identifiers":["UMLS:C0345978","DOID:8288","MEDGEN:91064","SCTID:254652000"],"synonyms":[{"name":"clear cell squamous cell carcinoma of skin","type":"exact"},{"name":"clear cell squamous cell carcinoma of the skin","type":"exact"},{"name":"clear cell squamous cell skin carcinoma","type":"exact"}],"termid":"MONDO:0004523","xrefs":{"Monarch":{"xref_id":"0004523"}}}


id: PBO:0002870
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.1.1.21","termid":"PBO:0002870"}


id: GO:1904811
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of dense core granule transport.","definition_xrefs":["GO_REF:0000058","PMID:22699897","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of intracellular transport","termid":"GO:0032388"},{"relation_name":"is_a","term_name":"regulation of dense core granule transport","termid":"GO:1904809"},{"relation_name":"positively_regulates","term_name":"dense core granule transport","termid":"GO:1901950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of dense core granule transport","synonyms":[{"name":"activation of dense core granule transport","type":"narrow"},{"name":"activation of dense core vesicle transport","type":"narrow"},{"name":"positive regulation of dense core vesicle transport","type":"exact"},{"name":"up regulation of dense core granule transport","type":"exact"},{"name":"up regulation of dense core vesicle transport","type":"exact"},{"name":"up-regulation of dense core granule transport","type":"exact"},{"name":"up-regulation of dense core vesicle transport","type":"exact"},{"name":"upregulation of dense core granule transport","type":"exact"},{"name":"upregulation of dense core vesicle transport","type":"exact"}],"termid":"GO:1904811"}


id: PBO:0042732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromere protein J","termid":"PBO:0042732"}


id: MOD:01490
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an O3-hydrogen atom of a serine residue with the Applied Biosystems iTRAQ4plex-114 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ4plex-114 reporter+balance reagent acylated residue","termid":"MOD:01485"},{"relation_name":"is_a","term_name":"iTRAQ4plex reporter+balance reagent O-acylated residue","termid":"MOD:01713"},{"relation_name":"is_a","term_name":"O3-acylated L-serine","termid":"MOD:02003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ4plex-114 reporter+balance reagent O3-acylated serine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"iTRAQ4plex114","type":"related"}],"termid":"MOD:01490"}


id: GO:0005532
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete mannose binding lectin (obsolete GO:0005532)","synonyms":[{"name":"mannose binding lectin","type":"exact"},{"name":"mannose receptor","type":"related"}],"termid":"GO:0005532"}


id: MONDO:1011827
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cancer or benign tumor, non-human animal","termid":"MONDO:1011305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital mast cell tumor, non-human animal","secondary_identifiers":["OMIA:002578"],"termid":"MONDO:1011827","xrefs":{"Monarch":{"xref_id":"1011827"}}}


id: FYPO:0006693
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 dimethylation of lysine at position 4 of histone H3 occurs to a lower extent than normal during G0 phase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal chromatin organization during G0","termid":"FYPO:0003871"},{"relation_name":"is_a","term_name":"abnormal histone methylation","termid":"FYPO:0006870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0000002","FYPO:0002274","FYPO:0005447","FYPO:0002494","FYPO:0001985"],"is_obsolete":false,"name":"decreased histone H3-K4 dimethylation during G0","synonyms":[{"name":"decreased histone H3 K4 dimethylation during G0","type":"exact"},{"name":"decreased histone H3-K4 dimethylation during cell quiescence","type":"exact"},{"name":"decreased histone H3-K4 dimethylation during quiescence","type":"exact"},{"name":"decreased histone H3K4 dimethylation during G0","type":"exact"},{"name":"decreased histone H3K4me2 during G0","type":"exact"},{"name":"decreased histone lysine H3 K4 dimethylation during G0","type":"exact"},{"name":"reduced histone H3-K4 dimethylation during G0","type":"exact"}],"termid":"FYPO:0006693"}


id: PBO:0061990
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 BH member 1 pseudogene","termid":"PBO:0061990"}


id: PBO:0064788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase, Mg2+/Mn2+ dependent 1H","termid":"PBO:0064788"}


id: PBO:0048574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gametogenetin binding protein 1 (pseudogene)","termid":"PBO:0048574"}


id: GO:0045570
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the growth of the imaginal disc.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental growth","termid":"GO:0048638"},{"relation_name":"regulates","term_name":"imaginal disc growth","termid":"GO:0007446"}],"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 imaginal disc growth","termid":"GO:0045570"}


id: PBO:0000697
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.7.1.105","termid":"PBO:0000697"}


id: PR:Q9Y7V2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC645.13 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9Y7V2"],"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":"transcription factor bye1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC645.13","synonyms":[{"name":"Spom972h-SPCC645.13","type":"exact"}],"termid":"PR:Q9Y7V2"}


id: PBO:0054313
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 1705","termid":"PBO:0054313"}


id: GO:0032532
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that modulates the length of a microvillus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of microvillus organization","termid":"GO:0032530"},{"relation_name":"is_a","term_name":"regulation of cell projection size","termid":"GO:0032536"}],"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 microvillus length","termid":"GO:0032532"}


id: PBO:0085519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein component of the small (40S) ribosomal subunit; homologous to mammalian ribosomal protein S21, no bacterial homolog; RPS21A has a paralog, RPS21B, that arose from the whole genome duplication","termid":"PBO:0085519"}


id: FYECO:0000055
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Both M-factor and P-factor, endogenously produced by cells, were present in the experiment.","definition_xrefs":["PomBase:al"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE FYECO:0000055 M and P factor produced (obsolete FYECO:0000055)","synonyms":[{"name":"presence of M-factor and P-factor","type":"exact"},{"name":"presence of mating pheromones","type":"exact"}],"termid":"FYECO:0000055"}


id: GO:0103008
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4-chloro-2-methylphenoxyacetate + 2-oxoglutarate + O2 = 4-chloro-2-methylphenol + 2-oxo monocarboxylic acid anion + succinate + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 4-chloro-2-methylphenoxyacetate oxygenase activity (obsolete GO:0103008)","termid":"GO:0103008"}


id: MONDO:0002218
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the temporal lobe.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral hemisphere cancer","termid":"MONDO:0002731"},{"relation_name":"is_a","term_name":"neoplasm of temporal lobe","termid":"MONDO:0021372"}],"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":"temporal lobe cancer","secondary_identifiers":["SCTID:363468009","ICD9:191.2","DOID:2135","ICD10CM:C71.2","UMLS:C0153636","MEDGEN:509347"],"synonyms":[{"name":"cancer of temporal lobe","type":"exact"},{"name":"malignant neoplasm of temporal lobe","type":"exact"},{"name":"malignant temporal lobe neoplasm","type":"exact"},{"name":"temporal lobe cancer","type":"exact"},{"name":"temporal lobe neoplasm","type":"related"},{"name":"tumour of temporal lobe","type":"related"}],"termid":"MONDO:0002218","xrefs":{"Monarch":{"xref_id":"0002218"}}}


id: PBO:0068304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 8","termid":"PBO:0068304"}


id: GO:0045989
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of striated muscle contraction.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of striated muscle contraction","termid":"GO:0006942"},{"relation_name":"is_a","term_name":"positive regulation of muscle contraction","termid":"GO:0045933"},{"relation_name":"positively_regulates","term_name":"striated muscle contraction","termid":"GO:0006941"}],"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 striated muscle contraction","synonyms":[{"name":"activation of striated muscle contraction","type":"narrow"},{"name":"stimulation of striated muscle contraction","type":"narrow"},{"name":"up regulation of striated muscle contraction","type":"exact"},{"name":"up-regulation of striated muscle contraction","type":"exact"},{"name":"upregulation of striated muscle contraction","type":"exact"}],"termid":"GO:0045989"}


id: PBO:0000644
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIIF complex subunit Tfg3","termid":"PBO:0000644"}


id: FYPO:0003349
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 mitotic spindle midzone during anaphase B is normal (i.e. indistinguishable from wild type). The mitotic spindle midzone is the area in the center of the mitotic spindle where the spindle microtubules from opposite poles overlap. Anaphase B is the stage of mitosis in which the polar microtubules elongate and the two poles of the spindle move farther apart.","definition_xrefs":["GO:1990023","PomBase:mah","GO:0000092"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to mitotic spindle midzone","termid":"FYPO:0004692"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002","FYPO:0001320","FYPO:0001312","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to mitotic spindle midzone during anaphase B","synonyms":[{"name":"normal protein localisation to mitotic spindle midzone during anaphase B","type":"exact"},{"name":"normal protein localization to mitotic spindle midzone during anaphase B during vegetative growth","type":"exact"},{"name":"normal protein localization to spindle midzone during anaphase B during mitotic cell cycle","type":"exact"}],"termid":"FYPO:0003349"}


id: PBO:0039525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ANKRD33B pseudogene 6","termid":"PBO:0039525"}


id: PBO:0069702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 982, pseudogene","termid":"PBO:0069702"}


id: GO:0006603
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving phosphocreatine, a phosphagen of creatine present in high concentration in striated muscle which is synthesized and broken down by creatine phosphokinase to buffer ATP concentration. It acts as an immediate energy reserve for muscle.","definition_xrefs":["PMID:16371597"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphagen metabolic process","termid":"GO:0006599"}],"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":"phosphocreatine metabolic process","synonyms":[{"name":"phosphocreatine metabolism","type":"exact"}],"termid":"GO:0006603"}


id: MONDO:0700036
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A sex cord-stromal tumor characterized by mixed features of both fibroma and thecoma.","direct_ancestors":[{"relation_name":"is_a","term_name":"sex cord-stromal tumor","termid":"MONDO:0006055"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrothecoma","secondary_identifiers":["MEDGEN:1668953","UMLS:C4721918"],"termid":"MONDO:0700036","xrefs":{"Monarch":{"xref_id":"0700036"}}}


id: PBO:0068651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 32, pseudogene","termid":"PBO:0068651"}


id: GO:0033556
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the addition of a glucose residue to the lipid-linked oligosaccharide precursor for N-linked glycosylation; the transfer of glucose from dolichyl phosphate glucose (Dol-P-Glc) on to the lipid-linked oligosaccharide Man(7)GlcNAc(2)-PP-Dol.","definition_xrefs":["GOC:mah","PMID:10336995"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucosyltransferase activity","termid":"GO:0046527"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016757","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"dolichyl pyrophosphate Man7GlcNAc2 alpha-1,3-glucosyltransferase activity","synonyms":[{"name":"dolichyl-P-Glc:Man7GlcNAc2-PP-dolichyl glucosyltransferase activity","type":"exact"}],"termid":"GO:0033556"}


id: GO:1900962
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of methanophenazine biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biosynthetic process","termid":"GO:0009889"},{"relation_name":"is_a","term_name":"regulation of methanophenazine metabolic process","termid":"GO:1900965"},{"relation_name":"regulates","term_name":"methanophenazine biosynthetic process","termid":"GO:1900630"}],"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 methanophenazine biosynthetic process","synonyms":[{"name":"regulation of methanophenazine anabolism","type":"exact"},{"name":"regulation of methanophenazine biosynthesis","type":"exact"},{"name":"regulation of methanophenazine formation","type":"exact"},{"name":"regulation of methanophenazine synthesis","type":"exact"}],"termid":"GO:1900962"}


id: GO:0075220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of zoospore encystment on host. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of spore encystment on host","termid":"GO:0075216"},{"relation_name":"is_a","term_name":"modulation of zoospore encystment on host","termid":"GO:0075219"},{"relation_name":"positively_regulates","term_name":"zoospore encystment on host","termid":"GO:0075218"}],"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 zoospore encystment on host","termid":"GO:0075220"}


id: GO:0004177
data:
  {"annotated_genes":["SJAG_03022","SJAG_00969","SJAG_02033","SJAG_03744","SJAG_01896","SJAG_00181","SJAG_01088","SJAG_06636"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[87975],"is_not":false,"summary":null,"term":"GO:0004177"},{"annotations":[102789,109535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004239"},{"annotations":[113949,87977,105251,109536,102791,97335,92876,87722],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070006"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of a single N-terminal amino acid residue from a polypeptide chain.","definition_xrefs":["EC:3.4.11.-","PMID:24157837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exopeptidase activity","termid":"GO:0008238"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00181":null,"SJAG_00969":null,"SJAG_01088":null,"SJAG_01896":null,"SJAG_02033":null,"SJAG_03022":null,"SJAG_03744":null,"SJAG_06636":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0008233","GO:0003674","GO:0140096","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"aminopeptidase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["https://www.ebi.ac.uk/merops/about/glossary.shtml#AMINOPEPTIDASE","MetaCyc:RXN0-5052","Reactome:R-HSA-2534096","Reactome:R-HSA-983162","Reactome:R-HSA-1236954"],"termid":"GO:0004177","terms_by_termid":{"GO:0004177":null,"GO:0004239":null,"GO:0070006":null}}


id: MONDO:0019817
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital mitral malformation","termid":"MONDO:0016582"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital mitral valve insufficiency and/or stenosis","secondary_identifiers":["Orphanet:95464","MEDGEN:1842574","UMLS:C5681577","ICD10CM:Q23","GARD:19266"],"termid":"MONDO:0019817","xrefs":{"Monarch":{"xref_id":"0019817"}}}


id: PBO:0051182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 3-73","termid":"PBO:0051182"}


id: GO:0140641
data:
  {"annotated_genes":["SJAG_03073","SJAG_01613"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98731,100937],"is_not":false,"summary":null,"term":"GO:0140641"}]},"cv_name":"biological_process","definition":"The spindle organization process in which the spindle is maintained at a constant length during mitotic metaphase.","definition_xrefs":["PMID:32723864"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic spindle assembly","termid":"GO:0090307"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01613":null,"SJAG_03073":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0000226"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0000070"},{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0000070","GO:0007010","GO:0000226","GO:0044085","GO:0007049"],"is_obsolete":false,"name":"mitotic spindle formation (spindle phase two)","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"metaphase spindle stability","type":"exact"},{"name":"metaphase spindle stabilization","type":"exact"}],"termid":"GO:0140641","terms_by_termid":{"GO:0140641":null}}


id: GO:0031175
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a neuron projection over time, from its formation to the mature structure. A neuron projection is any process extending from a neural cell, such as axons or dendrites (collectively called neurites).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection organization","termid":"GO:0120036"},{"relation_name":"part_of","term_name":"neuron development","termid":"GO:0048666"}],"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":"neuron projection development","synonyms":[{"name":"neurite biosynthesis","type":"narrow"},{"name":"neurite development","type":"narrow"},{"name":"neurite formation","type":"narrow"},{"name":"neurite growth","type":"narrow"},{"name":"neurite outgrowth","type":"narrow"}],"termid":"GO:0031175"}


id: GO:0047434
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: indolepyruvate = CO2 + indole acetaldehyde.","definition_xrefs":["EC:4.1.1.74","MetaCyc:4.1.1.74-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"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:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"indolepyruvate decarboxylase activity","secondary_identifiers":["RHEA:18017"],"synonyms":[{"name":"3-(indol-3-yl)pyruvate carboxy-lyase [(2-indol-3-yl)acetaldehyde-forming]","type":"related"},{"name":"3-(indol-3-yl)pyruvate carboxy-lyase activity","type":"related"},{"name":"indol-3-yl-pyruvate carboxy-lyase activity","type":"related"},{"name":"indole-3-pyruvate decarboxylase activity","type":"related"}],"termid":"GO:0047434"}


id: GO:0075224
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of sporangium germination.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sporangium germination","termid":"GO:0075223"},{"relation_name":"is_a","term_name":"positive regulation of sporangium development","termid":"GO:0075311"},{"relation_name":"positively_regulates","term_name":"sporangium germination","termid":"GO:0075222"}],"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 sporangium germination","synonyms":[{"name":"positive regulation of sporangium germination on or near host","type":"narrow"}],"termid":"GO:0075224"}


id: PBO:0080181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VDAC2 pseudogene 2","termid":"PBO:0080181"}


id: MONDO:0017755
data:
  {"annotated_genes":["SJAG_05213","SJAG_03363","SJAG_03011","SJAG_01344","SJAG_00938","SJAG_05194","SJAG_03785"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86021],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008822"},{"annotations":[86276],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011559"},{"annotations":[86460,86461],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030810"},{"annotations":[85365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031040"},{"annotations":[84792,84791,84793],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009380"},{"annotations":[86399],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011156"},{"annotations":[85031],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011214"}]},"cv_name":"mondo","definition":"An instance of bilirubin metabolism disease 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":"inborn disorder of porphyrin metabolism","termid":"MONDO:0017754"},{"relation_name":"is_a","term_name":"bilirubin metabolism disease","termid":"MONDO:0024431"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_01344":null,"SJAG_03011":null,"SJAG_03363":null,"SJAG_03785":null,"SJAG_05194":null,"SJAG_05213":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"inborn disorder of bilirubin metabolism","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1671515","icd11.foundation:1297666279","GARD:21347","Orphanet:309816","UMLS:C0349427"],"synonyms":[{"name":"bilirubin metabolism disorder","type":"related"},{"name":"disorder of bilirubin metabolism","type":"broad"},{"name":"disorder of bilirubin metabolism and excretion","type":"exact"},{"name":"hereditary bilirubin metabolism disease","type":"exact"},{"name":"inborn disorder of bilirubin metabolism and excretion","type":"exact"}],"termid":"MONDO:0017755","terms_by_termid":{"MONDO:0008822":null,"MONDO:0009380":null,"MONDO:0011156":null,"MONDO:0011214":null,"MONDO:0011559":null,"MONDO:0030810":null,"MONDO:0031040":null},"xrefs":{"Monarch":{"xref_id":"0017755"}}}


id: PBO:0038562
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ABI family member 3 binding protein","termid":"PBO:0038562"}


id: PBO:0028375
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_oxanine_DNA_N-glycosylase_activity","termid":"PBO:0028375"}


id: PBO:0036428
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 Put2 (predicted)","termid":"PBO:0036428"}


id: MONDO:0009258
data:
  {"annotated_genes":["SJAG_02954"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85451],"is_not":false,"summary":null,"term":"MONDO:0009258"}]},"cv_name":"mondo","definition":"Classic galactosemia is a life-threatening metabolic disease with onset in the neonatal period. Infants usually develop feeding difficulties, lethargy, and severe liver disease.","definition_xrefs":["Orphanet:79239"],"direct_ancestors":[{"relation_name":"is_a","term_name":"galactosemia","termid":"MONDO:0018116"},{"relation_name":"is_a","term_name":"inherited primary ovarian failure","termid":"MONDO:0019852"},{"relation_name":"is_a","term_name":"disorder of galactose and fructose metabolism","termid":"MONDO:0800152"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02954":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047","MONDO:0005328","MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"classic galactosemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:2011000259","MEDGEN:82777","NANDO:2200532","DOID:0111459","GARD:13639","OMIM:230400","SCTID:10899004","UMLS:C0268151","NANDO:1200851"],"synonyms":[{"name":"GALT deficiency","type":"exact"},{"name":"Galt deficiency","type":"related"},{"name":"classic galactosemia","type":"exact"},{"name":"classical galactosemia, homozygous duarte-type","type":"narrow"},{"name":"galactose-1-phosphate uridyltransferase deficiency","type":"exact"},{"name":"galactose-1-phosphate uridylyltransferase deficiency","type":"related"},{"name":"galactosemia","type":"related"},{"name":"galactosemia type 1","type":"exact"},{"name":"galactosemia, Duarte variant","type":"related"},{"name":"galactosemia, classic","type":"related"},{"name":"transferase deficiency","type":"related"}],"termid":"MONDO:0009258","terms_by_termid":{"MONDO:0009258":null},"xrefs":{"Monarch":{"xref_id":"0009258"}}}


id: GO:0120515
data:
  {"annotated_genes":["SJAG_00947","SJAG_03909","SJAG_03471"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[115262],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031956"},{"annotations":[112918,105091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090432"},{"annotations":[105092],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090434"},{"annotations":[105093],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090433"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a fatty acid + ATP + CoA = a fatty acyl-CoA + AMP + diphosphate.","definition_xrefs":["RHEA:38883"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid ligase activity","termid":"GO:0015645"},{"relation_name":"is_a","term_name":"CoA-ligase activity","termid":"GO:0016405"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00947":null,"SJAG_03471":null,"SJAG_03909":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"fatty acid-CoA ligase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:BUTYRATE--COA-LIGASE-RXN"],"termid":"GO:0120515","terms_by_termid":{"GO:0031956":null,"GO:0090432":null,"GO:0090433":null,"GO:0090434":null}}


id: GO:0060075
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the establishment or extent of a resting potential, the electrical charge across the plasma membrane, with the interior of the cell negative with respect to the exterior. The resting potential is the membrane potential of a cell that is not stimulated to be depolarized or hyperpolarized.","definition_xrefs":["GOC:ef","GOC:dph","ISBN:0195088433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of membrane potential","termid":"GO:0042391"}],"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 resting membrane potential","synonyms":[{"name":"regulation of resting potential","type":"exact"}],"termid":"GO:0060075"}


id: PBO:0087161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase III largest subunit C160; part of core enzyme; similar to bacterial beta-prime subunit and to RPA190 and RPO21","termid":"PBO:0087161"}


id: GO:0030354
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action characteristic of melanin-concentrating hormone, a cyclic peptide hormone that, upon receptor binding, induces melanin aggregation in melanocytes, and is also involved in regulating food intake and energy balance in mammals.","definition_xrefs":["GOC:mah","PMID:11416225","PMID:9792536"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone activity","termid":"GO:0005179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0098772","GO:0003674","GO:0140677","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"melanin-concentrating hormone activity","termid":"GO:0030354"}


id: PBO:0050654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein 90 alpha family class B member 4, pseudogene","termid":"PBO:0050654"}


id: PBO:0027316
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_duration_of_protein_localization_to_mitotic_spindle","termid":"PBO:0027316"}


id: PBO:0063192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prostate cancer associated transcript 5","termid":"PBO:0063192"}


id: GO:0090420
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving naphthalene-containing compounds.","definition_xrefs":["GOC:tb","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete naphthalene-containing compound metabolic process (obsolete GO:0090420)","termid":"GO:0090420"}


id: GO:0010177
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acetyl-CoA + an omega-(methylsulfanyl)-2-oxoalkanoate + H2O = a 2-(omega-methylsulfanyl)alkylmalate + CoA + H+.","definition_xrefs":["RHEA:50624"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, acyl groups converted into alkyl on transfer","termid":"GO:0046912"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"methylthioalkylmalate synthase activity","secondary_identifiers":["EC:2.3.3.17","MetaCyc:RXN-18197"],"synonyms":[{"name":"2-(2'-methylthio)ethylmalate synthase activity","type":"narrow"}],"termid":"GO:0010177"}


id: GO:1901748
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving leukotriene D4.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukotriene metabolic process","termid":"GO:0006691"},{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"amide metabolic process","termid":"GO:0043603"},{"relation_name":"is_a","term_name":"fatty acid derivative metabolic process","termid":"GO:1901568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0006790","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"leukotriene D4 metabolic process","synonyms":[{"name":"leukotriene D4 metabolism","type":"exact"}],"termid":"GO:1901748"}


id: GO:0098593
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cup shaped specialization of the cytoskeleton that forms a thin layer located just below the apical mass of mature mucin secretory granules in the cytoplasm of goblet cells of the intestinal epithelium. It consists of an orderly network of intermediate filaments and microtubules. Microtubules are arranged vertically, like barrel staves, along the inner aspect of the theta. Intermediate filaments form two networks: an inner, basketlike network and an outer series of circumferential bundles resembling the hoops of a barrel.","definition_xrefs":["PMID:6541604"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membraneless organelle","termid":"GO:0043232"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"},{"relation_name":"part_of","term_name":"cytoskeleton","termid":"GO:0005856"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"goblet cell theca","termid":"GO:0098593"}


id: MONDO:0060720
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"congenital disorder of glycosylation with defective fucosylation","secondary_identifiers":["UMLS:C4693905","MEDGEN:1647704","OMIMPS:618005"],"synonyms":[{"name":"CDGF","type":"related"},{"name":"congenital disorder of glycosylation with defective fucosylation","type":"exact"}],"termid":"MONDO:0060720","xrefs":{"Monarch":{"xref_id":"0060720"}}}


id: PBO:0055168
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 2591","termid":"PBO:0055168"}


id: PR:Q10438
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pby1 gene.","definition_xrefs":["UniProtKB:Q10438","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":"tubulin--tyrosine ligase C12B10.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC12B10.04","synonyms":[{"name":"Spom972h-pby1","type":"exact"}],"termid":"PR:Q10438"}


id: PBO:0038953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adiponectin receptor 1","termid":"PBO:0038953"}


id: PR:P87168
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- trz2 gene.","definition_xrefs":["UniProtKB:P87168","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":"ribonuclease Z 2, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3D6.03c","synonyms":[{"name":"RNase Z 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-trz2","type":"exact"},{"name":"tRNA 3 endonuclease 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tRNase Z 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87168"}


id: GO:1902069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of sphingolipid signaling.","definition_xrefs":["GOC:TermGenie","PMID:20870412"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"regulation of sphingolipid mediated signaling pathway","termid":"GO:1902068"},{"relation_name":"negatively_regulates","term_name":"sphingolipid mediated signaling pathway","termid":"GO:0090520"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of sphingolipid mediated signaling pathway","synonyms":[{"name":"down regulation of sphingolipid mediated signaling pathway","type":"exact"},{"name":"down regulation of sphingolipid signaling pathway","type":"related"},{"name":"down-regulation of sphingolipid mediated signaling pathway","type":"exact"},{"name":"down-regulation of sphingolipid signaling pathway","type":"related"},{"name":"downregulation of sphingolipid mediated signaling pathway","type":"exact"},{"name":"downregulation of sphingolipid signaling pathway","type":"related"},{"name":"inhibition of sphingolipid mediated signaling pathway","type":"narrow"},{"name":"inhibition of sphingolipid signaling pathway","type":"related"},{"name":"negative regulation of sphingolipid signaling pathway","type":"related"}],"termid":"GO:1902069"}


id: PR:P30655
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A proteasome subunit beta type-5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome subunit beta type-5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4A8.13c","secondary_identifiers":["UniProtKB:P30655"],"synonyms":[{"name":"SPAC4A8.13c","type":"related"},{"name":"Spom972h-PSMB5","type":"exact"},{"name":"macropain subunit pts1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"multicatalytic endopeptidase complex subunit pts1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"proteasome component pts1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P30655"}


id: PBO:0052125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium voltage-gated channel subfamily E regulatory subunit 3","termid":"PBO:0052125"}


id: PBO:0060099
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 46","termid":"PBO:0060099"}


id: PBO:0039992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP ribosylation factor like GTPase 6 interacting protein 6","termid":"PBO:0039992"}


id: PBO:0078777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 3-1","termid":"PBO:0078777"}


id: FYPO:0000228
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 sister chromatids do not move towards the spindle poles at the same time during mitosis, but instead one or more chromosomes remain distant from the spindle pole after the bulk of the DNA has separated. Mitotic sister chromatid segregation may stop before completing separation of chromosomes, or may eventually be completed.","definition_xrefs":["PomBase:mah","PMID:11809834","PMID:20211136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"},{"relation_name":"is_a","term_name":"lagging chromosomes","termid":"FYPO:0002090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0000631","FYPO:0005447","FYPO:0000641","FYPO:0001320","FYPO:0000337"],"is_obsolete":false,"name":"lagging mitotic chromosomes","synonyms":[{"name":"chromosome segregation defects, lagging mitotic chromosomes","type":"exact"},{"name":"lagging chromosomes during mitotic cell cycle","type":"related"},{"name":"lagging chromosomes during vegetative growth","type":"exact"},{"name":"lagging mitotic sister chromatids","type":"exact"}],"termid":"FYPO:0000228"}


id: PBO:0028202
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-elongated_cell_during_cellular_response_to_ionizing_radiation","termid":"PBO:0028202"}


id: PBO:0004970
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactokinase Gal1","termid":"PBO:0004970"}


id: PBO:0071371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 30","termid":"PBO:0071371"}


id: PBO:0004409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinetochore protein Mis17","termid":"PBO:0004409"}


id: MONDO:0043300
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cheilitis","termid":"MONDO:0002102"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actinic cheilitis","secondary_identifiers":["icd11.foundation:436658980","MESH:C535669","SCTID:46795000","UMLS:C0267026","MEDGEN:75625","NCIT:C183562"],"synonyms":[{"name":"actinic cheilitis","type":"exact"},{"name":"actinic cheilosis","type":"related"},{"name":"solar keratosis of lip","type":"related"}],"termid":"MONDO:0043300","xrefs":{"Monarch":{"xref_id":"0043300"}}}


id: PBO:0028461
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_protein_localization_to_septin_ring","termid":"PBO:0028461"}


id: GO:0043774
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: coenzyme F420-2 + L-glutamate + GTP = coenzyme F420-3 + GDP + orthophosphate.","definition_xrefs":["PMID:12909715"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-amino acid ligase activity","termid":"GO:0016881"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0003824","GO:0016874","GO:0003674"],"is_obsolete":false,"name":"coenzyme F420-2 alpha-glutamyl ligase activity","secondary_identifiers":["EC:6.3.2.32","RHEA:42332"],"synonyms":[{"name":"F420-2 alpha-glutamyl ligase activity","type":"exact"}],"termid":"GO:0043774"}


id: PBO:0051407
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 1-36","termid":"PBO:0051407"}


id: MONDO:0006619
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A virus-induced exanthem","definition_xrefs":["EFO:1000776"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exanthem","termid":"MONDO:0006547"}],"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":"viral exanthem","secondary_identifiers":["MEDGEN:509133","DOID:8672","ICD9:057.8","ICD9:057.9","SCTID:49882001","UMLS:C0153062"],"termid":"MONDO:0006619","xrefs":{"Monarch":{"xref_id":"0006619"}}}


id: MONDO:0004957
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive adenocarcinoma composed of malignant glandular cells which contain intracytoplasmic mucin. Often, the infiltrating glandular structures are associated with mucoid stromal formation. It may arise from the large and small intestine, appendix, stomach, lung, ovary, breast, corpus uteri, cervix, vagina, and salivary gland.","definition_xrefs":["NCIT:C26712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"},{"relation_name":"is_a","term_name":"mucin-producing carcinoma","termid":"MONDO:0020596"}],"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":"mucinous adenocarcinoma","secondary_identifiers":["DOID:3030","icd11.foundation:529352875","MESH:D002288","ONCOTREE:CEMU","ICDO:8480/3","MEDGEN:2844","EFO:0000197","UMLS:C0007130"],"synonyms":[{"name":"CEMU","type":"related"},{"name":"adenocarcinoma, mucinous, malignant","type":"exact"},{"name":"colloid adenocarcinoma","type":"exact"},{"name":"colloid carcinoma","type":"exact"},{"name":"gelatinous adenocarcinoma","type":"exact"},{"name":"gelatinous carcinoma","type":"exact"},{"name":"mucin-producing adenocarcinoma","type":"exact"},{"name":"mucin-producing adenocarcinoma (morphologic abnormality)","type":"exact"},{"name":"mucin-secreting adenocarcinoma","type":"exact"},{"name":"mucin-secreting carcinoma","type":"exact"},{"name":"mucinous adenocarcinoma","type":"exact"},{"name":"mucinous carcinoma","type":"exact"},{"name":"mucinuos carcinoma","type":"exact"},{"name":"mucoid adenocarcinoma","type":"exact"},{"name":"mucoid carcinoma","type":"exact"},{"name":"mucous adenocarcinoma","type":"exact"},{"name":"mucous carcinoma","type":"exact"},{"name":"pseudomyxoma peritonei with unknown primary site","type":"exact"}],"termid":"MONDO:0004957","xrefs":{"Monarch":{"xref_id":"0004957"}}}


id: PBO:0088666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ndc80 complex subunit Nuf2","termid":"PBO:0088666"}


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


id: PBO:0049333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIH subunit 1","termid":"PBO:0049333"}


id: GO:2001064
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to cellooligosaccharide.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligosaccharide binding","termid":"GO:0070492"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"cellooligosaccharide binding","termid":"GO:2001064"}


id: PBO:0077257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMED7-TICAM2 readthrough","termid":"PBO:0077257"}


id: GO:0047432
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,2-dialkylglycine + H+ + pyruvate = L-alanine + CO2 + dialkyl ketone.","definition_xrefs":["RHEA:16073","EC:4.1.1.64"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2,2-dialkylglycine decarboxylase (pyruvate) activity","secondary_identifiers":["MetaCyc:4.1.1.64-RXN","KEGG_REACTION:R03854"],"synonyms":[{"name":"2,2-dialkyl-2-amino acid-pyruvate aminotransferase activity","type":"related"},{"name":"2,2-dialkylglycine carboxy-lyase (amino-transferring)","type":"related"},{"name":"2,2-dialkylglycine carboxy-lyase (amino-transferring; L-alanine-forming)","type":"related"},{"name":"L-alanine-alpha-ketobutyrate aminotransferase activity","type":"related"},{"name":"alpha-dialkyl amino acid transaminase activity","type":"related"},{"name":"dialkyl amino acid (pyruvate) decarboxylase activity","type":"related"},{"name":"dialkylamino-acid decarboxylase (pyruvate)","type":"related"}],"termid":"GO:0047432"}


id: PR:Q9P7J0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC24B10.16c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7J0"],"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 C24B10.16c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC24B10.16c","synonyms":[{"name":"Spom972h-SPCC24B10.16c","type":"exact"}],"termid":"PR:Q9P7J0"}


id: PBO:0029129
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-protein_mislocalized_to_Golgi_apparatus","termid":"PBO:0029129"}


id: PBO:0088413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"extracellular leucine-rich repeat domain, receptor L domain-like Ecm33","termid":"PBO:0088413"}


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


id: MONDO:0001765
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"polyneuropathy","termid":"MONDO:0001824"}],"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":"polyneuropathy in collagen vascular disease","secondary_identifiers":["ICD9:357.1","SCTID:193177003","MEDGEN:509648","UMLS:C0154759","DOID:13649","ICD9:357.4"],"termid":"MONDO:0001765","xrefs":{"Monarch":{"xref_id":"0001765"}}}


id: GO:0006429
data:
  {"annotated_genes":["SJAG_02015","SJAG_04738"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[94528,97578],"is_not":false,"summary":null,"term":"GO:0006429"}]},"cv_name":"biological_process","definition":"The process of coupling leucine to leucyl-tRNA, catalyzed by leucyl-tRNA synthetase. The leucyl-tRNA synthetase is a class-I synthetase. The activated amino acid is transferred to the 2'-OH group of a leucine-accetping tRNA. The 2'-O-aminoacyl-tRNA will ultimately migrate to the 3' position via transesterification.","definition_xrefs":["ISBN:0716730510","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA aminoacylation for protein translation","termid":"GO:0006418"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02015":null,"SJAG_04738":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0006399","GO:0006520","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"leucyl-tRNA aminoacylation","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0006429","terms_by_termid":{"GO:0006429":null}}


id: MONDO:0859256
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurodevelopmental disorder","termid":"MONDO:0700092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with language delay and seizures","secondary_identifiers":["UMLS:C5676998","MEDGEN:1805816","DOID:0070444","OMIM:619908"],"termid":"MONDO:0859256","xrefs":{"Monarch":{"xref_id":"0859256"}}}


id: GO:0018049
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of a C-terminal peptidyl-serine amide by hydrolysis and oxidation of an interior Ser-Gly peptide in a secreted protein.","definition_xrefs":["RESID:AA0096"],"gene_count":0,"genotype_count":0,"name":"obsolete C-terminal peptidyl-serine amidation (obsolete GO:0018049)","termid":"GO:0018049"}


id: MONDO:0009960
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any inflammatory bowel disease in which the cause of the disease is a mutation in the NOD2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory bowel disease","termid":"MONDO:0005265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"inflammatory bowel disease 1","secondary_identifiers":["OMIM:266600","SCTID:34000006","DOID:0110892","ICD9:555.9"],"synonyms":[{"name":"Crohn disease","type":"related"},{"name":"Crohn disease-associated Growth failure, susceptibility to","type":"related"},{"name":"IBD1","type":"exact"},{"name":"NOD2 inflammatory bowel disease","type":"exact"},{"name":"crohn disease-associated growth failure","type":"exact"},{"name":"inflammatory bowel disease (Crohn disease) 1","type":"related"},{"name":"inflammatory bowel disease 1","type":"exact"},{"name":"inflammatory bowel disease 1, Crohn disease","type":"exact"},{"name":"inflammatory bowel disease caused by mutation in NOD2","type":"exact"},{"name":"inflammatory bowel disease type 1","type":"exact"},{"name":"paediatric ulcerative colitis","type":"related"},{"name":"pediatric ulcerative colitis","type":"related"},{"name":"regional enteritis","type":"related"},{"name":"ulcerative colitis","type":"related"},{"name":"ulcerative colitis, paediatric","type":"related"},{"name":"ulcerative colitis, pediatric","type":"related"}],"termid":"MONDO:0009960","xrefs":{"Monarch":{"xref_id":"0009960"}}}


id: MONDO:0020053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete total autosomal monosomy (obsolete MONDO:0020053)","secondary_identifiers":["Orphanet:98141","icd11.foundation:599695253"],"termid":"MONDO:0020053","xrefs":{"Monarch":{"xref_id":"0020053"}}}


id: FYPO:0007821
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which vacuoles are larger than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vacuolar morphology","termid":"FYPO:0002257"}],"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:0001985","FYPO:0000002"],"is_obsolete":false,"name":"large vacuoles","synonyms":[{"name":"enlarged vacuoles","type":"exact"}],"termid":"FYPO:0007821"}


id: MONDO:0011627
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autism, susceptiblity to","termid":"MONDO:0020836"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autism, susceptibility to, 5","secondary_identifiers":["UMLS:C1853755","MEDGEN:340048","OMIM:606053"],"synonyms":[{"name":"AUTS5","type":"exact"},{"name":"autism, susceptibility to, 5","type":"exact"},{"name":"autism-related speech delay","type":"related"},{"name":"intellectual developmental disorder with autism and speech delay","type":"exact"},{"name":"phrase speech delay, autism-related","type":"related"}],"termid":"MONDO:0011627","xrefs":{"Monarch":{"xref_id":"0011627"}}}


id: MONDO:0037735
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the sebaceous gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin cancer","termid":"MONDO:0002898"},{"relation_name":"is_a","term_name":"sebaceous gland neoplasm","termid":"MONDO:0006963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"sebaceous gland cancer","secondary_identifiers":["UMLS:C1382026","MEDGEN:235134","NCIT:C8409"],"synonyms":[{"name":"cancer of sebaceous gland","type":"exact"},{"name":"malignant neoplasm of sebaceous gland","type":"exact"},{"name":"malignant neoplasm of the sebaceous gland","type":"exact"},{"name":"malignant sebaceous gland neoplasm","type":"exact"},{"name":"malignant sebaceous gland tumor","type":"exact"},{"name":"malignant sebaceous gland tumour","type":"exact"},{"name":"malignant sebaceous neoplasm","type":"exact"},{"name":"malignant sebaceous tumor","type":"exact"},{"name":"malignant sebaceous tumour","type":"exact"},{"name":"malignant tumor of sebaceous gland","type":"exact"},{"name":"malignant tumor of the sebaceous gland","type":"exact"},{"name":"malignant tumour of sebaceous gland","type":"exact"},{"name":"malignant tumour of the sebaceous gland","type":"exact"}],"termid":"MONDO:0037735","xrefs":{"Monarch":{"xref_id":"0037735"}}}


id: PBO:0046905
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 25 member E, pseudogene","termid":"PBO:0046905"}


id: GO:0000389
data:
  {"annotated_genes":["SJAG_00225","SJAG_01214"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[100746,108355],"is_not":false,"summary":null,"term":"GO:0000389"}]},"cv_name":"biological_process","definition":"Recognition of the intron 3'-splice site by components of the assembling U2- or U12-type spliceosome.","definition_xrefs":["GOC:krc","ISBN:0879695897"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mRNA splice site recognition","termid":"GO:0006376"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00225":null,"SJAG_01214":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0016071"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0016071","GO:0044085","GO:0065003","GO:0010467"],"is_obsolete":false,"name":"mRNA 3'-splice site recognition","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0000383","GO:0000382"],"synonyms":[{"name":"U12-type nuclear mRNA 3'-splice site recognition","type":"narrow"},{"name":"U2-type nuclear mRNA 3'-splice site recognition","type":"narrow"},{"name":"nuclear mRNA 3'-splice site recognition","type":"exact"}],"termid":"GO:0000389","terms_by_termid":{"GO:0000389":null}}


id: MONDO:0043230
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Poisoning caused by ingestion of seafood containing microgram levels of ciguatoxins. The poisoning is characterized by gastrointestinal, neurological and cardiovascular disturbances.","definition_xrefs":["MESH:D036841"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ciguatera fish poisoning","secondary_identifiers":["EFO:1001291","SCTID:241774007"],"synonyms":[{"name":"Poisonings, ciguatera","type":"related"},{"name":"Poisonings, ciguatera fish","type":"related"},{"name":"ciguatera","type":"related"},{"name":"ciguatera Poisonings","type":"related"},{"name":"ciguatera fish Poisonings","type":"related"},{"name":"ciguatera fish poisoning","type":"exact"},{"name":"ciguatera poisoning","type":"related"},{"name":"ciguatoxin causing toxic effect","type":"exact"},{"name":"poisoning, ciguatera","type":"related"},{"name":"poisoning, ciguatera fish","type":"related"},{"name":"toxic effect of ciguatera fish poisoning","type":"related"}],"termid":"MONDO:0043230","xrefs":{"Monarch":{"xref_id":"0043230"}}}


id: PBO:0091268
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homomeric(1)","termid":"PBO:0091268"}


id: GO:0002518
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of a lymphocyte to cross a high endothelial venule in response to an external stimulus.","definition_xrefs":["GOC:add","ISBN:0781735149","PMID:15122201"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphocyte chemotaxis","termid":"GO:0048247"}],"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":"lymphocyte chemotaxis across high endothelial venule","termid":"GO:0002518"}


id: PBO:0061048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NIPA like domain containing 3","termid":"PBO:0061048"}


id: PR:Q9C0X4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC12C2.14c gene.","definition_xrefs":["UniProtKB:Q9C0X4","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 C12C2.14c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC12C2.14c","synonyms":[{"name":"Spom972h-SPBC12C2.14c","type":"exact"}],"termid":"PR:Q9C0X4"}


id: MONDO:0012870
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 2","termid":"MONDO:0016901"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 2q31.2 deletion syndrome","secondary_identifiers":["DOID:0060416","MESH:C567344","UMLS:C2676724","OMIM:612345","MEDGEN:394109"],"synonyms":[{"name":"chromosome 2q31.2 deletion syndrome","type":"exact"}],"termid":"MONDO:0012870","xrefs":{"Monarch":{"xref_id":"0012870"}}}


id: SO:1000104
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:1000104 sequence_variant_increasing_level_of_translation_product (obsolete SO:1000104)","synonyms":[{"name":"mutationt increasing level of translation product","type":"related"},{"name":"sequence variant increasing level of translation product","type":"exact"}],"termid":"SO:1000104"}


id: GO:1905925
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of invadopodium assembly.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:15684033"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of invadopodium assembly (obsolete GO:1905925)","synonyms":[{"name":"down regulation of invadopodium assembly","type":"exact"},{"name":"down regulation of invadopodium formation","type":"exact"},{"name":"down-regulation of invadopodium assembly","type":"exact"},{"name":"down-regulation of invadopodium formation","type":"exact"},{"name":"downregulation of invadopodium assembly","type":"exact"},{"name":"downregulation of invadopodium formation","type":"exact"},{"name":"inhibition of invadopodium assembly","type":"narrow"},{"name":"inhibition of invadopodium formation","type":"narrow"},{"name":"negative regulation of invadopodium formation","type":"exact"}],"termid":"GO:1905925"}


id: MONDO:0025066
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute generalized dermatitis of pigs which occurs from 5 to 35 days of age, characterized by sudden onset, with morbidity of 10 to 90% and mortality of 5 to 90%. The lesions are caused by Staphylococcus hyos but the bacterial agent is unable to penetrate the intact skin. Abrasions on the feet and legs or lacerations on the body frequently precede infection. In acute cases, a vesicular-type virus may be the predisposing factor. The causative organism is inhibited by most antibiotics. (Merck Veterinary Manual, 5th ed)","definition_xrefs":["MESH:D004818"],"direct_ancestors":[{"relation_name":"is_a","term_name":"swine disease","termid":"MONDO:0024990"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epidermitis, exudative, of swine","synonyms":[{"name":"Epidermitis, exudative of swine","type":"related"},{"name":"disease, greasy pig","type":"related"},{"name":"exudative dermatitis of swine","type":"related"},{"name":"greasy pig disease","type":"related"},{"name":"swine exudative Dermatitides","type":"related"},{"name":"swine exudative dermatitis","type":"related"}],"termid":"MONDO:0025066","xrefs":{"Monarch":{"xref_id":"0025066"}}}


id: GO:0035507
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of myosin-light-chain-phosphatase activity.","definition_xrefs":["GOC:go_curators","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of myosin-light-chain-phosphatase activity (obsolete GO:0035507)","termid":"GO:0035507"}


id: MONDO:0006295
data:
  {"annotated_genes":["SJAG_00260","SJAG_03677","SJAG_00440","SJAG_03453","SJAG_03787","SJAG_01671","SJAG_01144","SJAG_01895","SJAG_02231"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014937"},{"annotations":[85647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0003789"},{"annotations":[86265,86267,86266],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007763"},{"annotations":[86508],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011121"},{"annotations":[85121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007273"},{"annotations":[85330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013602"},{"annotations":[85776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0001187"}]},"cv_name":"mondo","definition":"A primary or metastatic malignant tumor involving the urinary system. Common tumor types include carcinomas, lymphomas, and sarcomas.","definition_xrefs":["NCIT:C9297"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cancer","termid":"MONDO:0004992"},{"relation_name":"is_a","term_name":"urinary system neoplasm","termid":"MONDO:0021066"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_00440":null,"SJAG_01144":null,"SJAG_01671":null,"SJAG_01895":null,"SJAG_02231":null,"SJAG_03453":null,"SJAG_03677":null,"SJAG_03787":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant urinary system neoplasm","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:189.9","EFO:1000363","UMLS:C1644719","MEDGEN:738719","ICD10CM:C64-C68","DOID:3996","SCTID:448233000"],"synonyms":[{"name":"cancer of renal system","type":"exact"},{"name":"malignant neoplasm of renal system","type":"exact"},{"name":"malignant renal system neoplasm","type":"exact"},{"name":"malignant urinary system neoplasm","type":"exact"},{"name":"malignant urinary tract neoplasm","type":"exact"},{"name":"renal system cancer","type":"exact"},{"name":"urinary system cancer","type":"exact"}],"termid":"MONDO:0006295","terms_by_termid":{"MONDO:0001187":null,"MONDO:0003789":null,"MONDO:0007273":null,"MONDO:0007763":null,"MONDO:0011121":null,"MONDO:0013602":null,"MONDO:0014937":null},"xrefs":{"Monarch":{"xref_id":"0006295"}}}


id: MONDO:0859591
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low-grade glioma that occurs in children and encompasses tumors of astrocytic, oligodendroglial, and mixed glial-neuronal histology.","definition_xrefs":["DOID:0080830"],"direct_ancestors":[{"relation_name":"is_a","term_name":"low grade glioma","termid":"MONDO:0021637"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood low-grade glioma","termid":"MONDO:0859591","xrefs":{"Monarch":{"xref_id":"0859591"}}}


id: GO:0032841
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to calcitonin, a peptide hormone responsible for reducing serum calcium levels by inhibiting osteoclastic bone reabsorption and promoting renal calcium excretion. It is synthesized and released by the C cells of the thyroid.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcitonin family binding","termid":"GO:0097644"}],"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":"calcitonin binding","termid":"GO:0032841"}


id: PBO:0070523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L6 pseudogene 22","termid":"PBO:0070523"}


id: GO:0004588
data:
  {"annotated_genes":["SJAG_00694"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111406],"is_not":false,"summary":null,"term":"GO:0004588"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: orotidine 5'-phosphate + diphosphate = orotate + 5-phospho-alpha-D-ribose 1-diphosphate.","definition_xrefs":["EC:2.4.2.10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentosyltransferase activity","termid":"GO:0016763"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00694":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0016757","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"orotate phosphoribosyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:10380","MetaCyc:OROPRIBTRANS-RXN","Reactome:R-HSA-73567"],"synonyms":[{"name":"OPRT activity","type":"related"},{"name":"OPRTase activity","type":"related"},{"name":"orotate phosphoribosyl pyrophosphate transferase activity","type":"related"},{"name":"orotic acid phosphoribosyltransferase activity","type":"related"},{"name":"orotidine 5'-monophosphate pyrophosphorylase activity","type":"related"},{"name":"orotidine monophosphate pyrophosphorylase activity","type":"related"},{"name":"orotidine phosphoribosyltransferase activity","type":"related"},{"name":"orotidine-5'-phosphate diphosphorylase activity","type":"related"},{"name":"orotidine-5'-phosphate pyrophosphorylase activity","type":"related"},{"name":"orotidine-5'-phosphate:diphosphate phospho-alpha-D-ribosyl-transferase activity","type":"related"},{"name":"orotidylate phosphoribosyltransferase activity","type":"related"},{"name":"orotidylate pyrophosphorylase activity","type":"related"},{"name":"orotidylic acid phosphorylase activity","type":"related"},{"name":"orotidylic acid pyrophosphorylase activity","type":"related"},{"name":"orotidylic phosphorylase activity","type":"related"},{"name":"orotidylic pyrophosphorylase activity","type":"related"}],"termid":"GO:0004588","terms_by_termid":{"GO:0004588":null}}


id: FYPO:0007638
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 anisotropic movement of chromatin occurs to a lower extent than normal during mitosis. Normally, chromatin moves to a lesser extent, and with less freedom of movement direction (i.e. more anisotropically), during mitosis than during interphase.","definition_xrefs":["PomBase:mah","PMID:33434270"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased chromatin mobility","termid":"FYPO:0007637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000641"],"is_obsolete":false,"name":"decreased anisotropic motion of mitotic chromatin","synonyms":[{"name":"decreased anisotropic chromatin motion during mitosis","type":"exact"},{"name":"decreased anisotropic chromatin motion during mitotic M phase","type":"related"},{"name":"decreased anisotropic chromatin movement during mitosis","type":"exact"},{"name":"decreased anisotropic mitotic chromatin mobility","type":"exact"},{"name":"decreased anisotropic mitotic chromatin motion","type":"exact"},{"name":"decreased anisotropic motion of mitotic chromatin during vegetative growth","type":"exact"},{"name":"decreased anisotropic movement of mitotic chromatin","type":"exact"},{"name":"reduced anisotropic motion of mitotic chromatin","type":"exact"}],"termid":"FYPO:0007638"}


id: PBO:0090480
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA-binding transcription factor, oxidative stress-responsive Pap1/Caf3","termid":"PBO:0090480"}


id: GO:0035423
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that terminates the activity of the active enzyme MAP kinase in the context of an innate immune response, a defense response mediated by germline encoded components that directly recognize components of potential pathogens.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete inactivation of MAPK activity involved in innate immune response (obsolete GO:0035423)","termid":"GO:0035423"}


id: PBO:0025508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase assembly protein Coa6 (predicted)","termid":"PBO:0025508"}


id: MONDO:0018629
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"stiff-person syndrome","termid":"MONDO:0008491"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"focal stiff limb syndrome","secondary_identifiers":["MEDGEN:1672496","GARD:17756","Orphanet:443804","UMLS:C4324606"],"synonyms":[{"name":"Stiff leg syndrome","type":"exact"},{"name":"focal stiff-person syndrome","type":"exact"}],"termid":"MONDO:0018629","xrefs":{"Monarch":{"xref_id":"0018629"}}}


id: GO:0055097
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals mediated by the detection of high density lipoprotein particle.","definition_xrefs":["GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein particle mediated signaling","termid":"GO:0055095"},{"relation_name":"part_of","term_name":"cellular response to high density lipoprotein particle stimulus","termid":"GO:0071403"}],"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":"high density lipoprotein particle mediated signaling","synonyms":[{"name":"high density lipoprotein mediated signalling","type":"exact"},{"name":"high density lipoprotein particle mediated signal transduction","type":"exact"},{"name":"high density lipoprotein particle-mediated signaling","type":"exact"}],"termid":"GO:0055097"}


id: PBO:0073218
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"semaphorin 6A","termid":"PBO:0073218"}


id: GO:0102743
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + eriodictyol + NADPH + O2 = 2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-) + NADP + 2 H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete eriodictyol,NADPH:oxygen oxidoreductase activity (obsolete GO:0102743)","termid":"GO:0102743"}


id: GO:2000669
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of dendritic cell apoptotic process.","definition_xrefs":["GOC:mtg_apoptosis","GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte apoptotic process","termid":"GO:2000107"},{"relation_name":"is_a","term_name":"regulation of dendritic cell apoptotic process","termid":"GO:2000668"},{"relation_name":"negatively_regulates","term_name":"dendritic cell apoptotic process","termid":"GO:0097048"}],"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 dendritic cell apoptotic process","synonyms":[{"name":"negative regulation of dendritic cell apoptosis","type":"narrow"}],"termid":"GO:2000669"}


id: MONDO:1010671
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any methemoglobinemia in cats in which the cause of the disease is a mutation in the CYB5R3 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"methemoglobinemia, domestic cat","termid":"MONDO:1011559"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methemoglobinemia, CYB5R3-related, domestic cat","secondary_identifiers":["OMIA:002131-9685"],"termid":"MONDO:1010671","xrefs":{"Monarch":{"xref_id":"1010671"}}}


id: PBO:0056702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meis homeobox 3","termid":"PBO:0056702"}


id: PBO:0049500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A clustered histone 7","termid":"PBO:0049500"}


id: PBO:0000523
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP kinase kinase Byr1","termid":"PBO:0000523"}


id: PBO:0077515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 231","termid":"PBO:0077515"}


id: MONDO:0958095
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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":"Nodal T-follicular helper cell lymphoma, follicular type","secondary_identifiers":["Orphanet:652650"],"termid":"MONDO:0958095","xrefs":{"Monarch":{"xref_id":"0958095"}}}


id: PBO:0088232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CIA machinery protein Cia2","termid":"PBO:0088232"}


id: GO:0039686
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A viral DNA replication process where replication occurs in both directions from the starting point. This creates two replication forks, moving in opposite directions.","definition_xrefs":["GOC:jl","VZ:1939","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral DNA genome replication","termid":"GO:0039693"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"bidirectional double-stranded viral DNA replication","synonyms":[{"name":"viral bidirectional dsDNA replication","type":"exact"}],"termid":"GO:0039686"}


id: PR:Q9C118
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1687.23c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C118"],"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 C1687.23c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1687.23c","synonyms":[{"name":"Spom972h-SPAC1687.23c","type":"exact"}],"termid":"PR:Q9C118"}


id: PBO:0076445
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TAFA chemokine like family member 1","termid":"PBO:0076445"}


id: PBO:0088603
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"succinate-semialdehyde dehydrogenase","termid":"PBO:0088603"}


id: PBO:0046073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 subunit M","termid":"PBO:0046073"}


id: MONDO:0012848
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Meckel syndrome in which the cause of the disease is a mutation in the CC2D2A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Meckel syndrome","termid":"MONDO:0018921"},{"relation_name":"is_a","term_name":"polydactyly-syndactyly-triphalangism","termid":"MONDO:0800066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Meckel syndrome, type 6","secondary_identifiers":["MESH:C567365","UMLS:C2676790","MEDGEN:382942","OMIM:612284","GARD:15548","DOID:0070120"],"synonyms":[{"name":"CC2D2A Meckel syndrome","type":"exact"},{"name":"MKS6","type":"exact"},{"name":"Meckel syndrome 6","type":"related"},{"name":"Meckel syndrome caused by mutation in CC2D2A","type":"exact"},{"name":"Meckel syndrome, type 6","type":"exact"},{"name":"Meckel-Gruber syndrome, type 6","type":"exact"}],"termid":"MONDO:0012848","xrefs":{"Monarch":{"xref_id":"0012848"}}}


id: GO:0042318
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of any antibiotic that contains the condensed beta-lactamthiazolidine ring system.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-lactam antibiotic biosynthetic process","termid":"GO:0030654"},{"relation_name":"is_a","term_name":"penicillin metabolic process","termid":"GO:0042316"},{"relation_name":"is_a","term_name":"sulfur compound biosynthetic process","termid":"GO:0044272"},{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"},{"relation_name":"is_a","term_name":"monocarboxylic acid biosynthetic process","termid":"GO:0072330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0006790","GO:0019748","GO:0008150"],"is_obsolete":false,"name":"penicillin biosynthetic process","synonyms":[{"name":"penicillin anabolism","type":"exact"},{"name":"penicillin biosynthesis","type":"exact"},{"name":"penicillin formation","type":"exact"},{"name":"penicillin synthesis","type":"exact"}],"termid":"GO:0042318"}


id: PBO:0004801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hexaprenyldihydroxybenzoate methyltransferase (predicted)","termid":"PBO:0004801"}


id: MONDO:0011166
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lymphedema-atrial septal defects-facial changes syndrome is characterized by congenital lymphoedema of the lower limbs, atrial septal defect and a characteristic facies (a round face with a prominent forehead, a flat nasal bridge with a broad nasal tip, epicanthal folds, a thin upper lip and a cleft chin). It has been described in two brothers and a sister. Transmission appears to be autosomal recessive.","definition_xrefs":["Orphanet:86915"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"primary lymphedema","termid":"MONDO:0019175"}],"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":"lymphedema-atrial septal defects-facial changes syndrome","secondary_identifiers":["MESH:C535539","SCTID:721978002","MESH:C567398","GARD:284","MEDGEN:383042","UMLS:C2677167","OMIM:601927"],"synonyms":[{"name":"Irons Bhan syndrome","type":"related"},{"name":"Irons-Bhan syndrome","type":"exact"},{"name":"Irons-Bianchi syndrome","type":"exact"},{"name":"autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes","type":"related"},{"name":"lymphedema, CARDIAC septal defects, and characteristic facies","type":"related"},{"name":"lymphedema, atrial septal defect, and characteristic facial changes","type":"related"},{"name":"lymphedema, atrial septal defect, and characteristic facies","type":"related"}],"termid":"MONDO:0011166","xrefs":{"Monarch":{"xref_id":"0011166"}}}


id: GO:0021574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of rhombomere 8 over time, from its formation to the mature structure. Rhombomeres are transverse segments of the developing rhombencephalon. Rhombomeres are lineage restricted, express different genes from one another, and adopt different developmental fates. Rhombomeres are numbered in anterior to posterior order.","definition_xrefs":["GO_REF:0000021","GOC:curators","GOC:cls","GOC:dph","GOC:jid","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhombomere development","termid":"GO:0021546"}],"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":"rhombomere 8 development","termid":"GO:0021574"}


id: GO:0015870
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of acetylcholine into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Acetylcholine is an acetic acid ester of the organic base choline and functions as a neurotransmitter, released at the synapses of parasympathetic nerves and at neuromuscular junctions.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"},{"relation_name":"is_a","term_name":"acetate ester transport","termid":"GO:1901374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"acetylcholine transport","termid":"GO:0015870"}


id: PR:Q9UT38
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A vacuolar protein sorting-associated protein 16 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00690","PANTHER:PTHR12811:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar protein sorting-associated protein 16 homolog (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC824.05","secondary_identifiers":["UniProtKB:Q9UT38"],"synonyms":[{"name":"Spom972h-VPS16","type":"exact"}],"termid":"PR:Q9UT38"}


id: PBO:0065057
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRELI domain containing 3B pseudogene 11","termid":"PBO:0065057"}


id: GO:0051171
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving nitrogen or nitrogenous compounds.","definition_xrefs":["GOC:tb","GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of nitrogen compound metabolic process (obsolete GO:0051171)","termid":"GO:0051171"}


id: PBO:0083837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Evolutionarily conserved 19S regulatory particle assembly-chaperone; proteasome-interacting protein involved in the assembly of the base subcomplex of the 19S proteasome regulatory particle (RP); null mutants accumulate ubiquitinated Gcn4p and display decreased 26S proteasome stability; interacts with Rpt5p","termid":"PBO:0083837"}


id: PBO:0048288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galanin like peptide","termid":"PBO:0048288"}


id: PBO:0090433
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ATPase","termid":"PBO:0090433"}


id: MONDO:0002012
data:
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id: PBO:0089015
data:
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id: PBO:0003572
data:
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id: MOD:00603
data:
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id: GO:0097064
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id: FYPO:0000335
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organization","references_by_uniquename":{"PMID:21802294":null,"PMID:24184107":null,"PMID:25318672":null,"PMID:25866389":null,"PMID:26774782":null,"PMID:27059155":null,"PMID:28954740":null,"PMID:30664646":null,"PMID:30726171":null,"PMID:32109380":null,"PMID:32243490":null,"PMID:32915139":null,"PMID:33495454":null,"PMID:33791858":null},"single_locus_annotated_genes":["SJAG_00426","SJAG_02592","SJAG_04284","SJAG_04280","SJAG_02392","SJAG_03596","SJAG_04703","SJAG_02763","SJAG_01242","SJAG_03891","SJAG_03449","SJAG_01143","SJAG_04522","SJAG_03892","SJAG_01906","SJAG_05207","SJAG_01374","SJAG_03940","SJAG_04464","SJAG_01745"],"single_locus_genotype_uniquenames":["wee1-as8-T582G-amino_acid_mutation-expression-not_assayed_or_wild_type","man1-1-488-man1-1-488-amino_acid_insertion_and_deletion-expression-not_assayed_or_wild_type","cdc15-A-L264P,P442T-amino_acid_mutation-expression-not_assayed_or_wild_type","nup61delta","ned1-5E-S499E__S538E__T620E__T638E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","mid1delta","vps32delta","ned1S235A_S651-S235A__S651-amino_acid_mutation-expression-not_assayed_or_wild_type","nup132delta","bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type","alx1delta","lem2delta","nem1delta","Man1DHEH-man1DHEH-partial_amino_acid_deletion-expression-not_assayed_or_wild_type","sty1delta","ned1-5A-S499A__S538A__T620A__T638A__S651A-amino_acid_mutation-expression-not_assayed_or_wild_type","man1delta","ned1delta","pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","for3delta","vps4delta","rga4delta","nem2delta","cmp7delta","pom1delta","ned1S235E_S651E-S235E__S651E-amino_acid_mutation-expression-not_assayed_or_wild_type","ned1cat-D422E,D424E-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"abnormal cellular component organisation","type":"exact"},{"name":"abnormal cellular component organization at cellular level","type":"exact"}],"termid":"FYPO:0000335","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000005":null,"FYECO:0000126":null,"FYECO:0000137":null,"FYECO:0000162":null,"FYECO:0000248":null,"FYECO:0000338":null,"FYPO:0000198":null,"FYPO:0000231":null,"FYPO:0000356":null,"FYPO:0000671":null,"FYPO:0000729":null,"FYPO:0000815":null,"FYPO:0001369":null,"FYPO:0001556":null,"FYPO:0001784":null,"FYPO:0002026":null,"FYPO:0002998":null,"FYPO:0003315":null,"FYPO:0003779":null,"FYPO:0003973":null,"FYPO:0003976":null,"FYPO:0006054":null,"FYPO:0006433":null,"FYPO:0006945":null,"FYPO:0007772":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null,"FYPO_EXT:0000003":null}}


id: PBO:0060457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family apoptosis inhibitory protein","termid":"PBO:0060457"}


id: GO:0120072
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of any pyloric antrum smooth muscle contraction.","definition_xrefs":["GOC:sl","PMID:15890336"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of pyloric antrum smooth muscle contraction","termid":"GO:0120071"},{"relation_name":"is_a","term_name":"positive regulation of gastro-intestinal system smooth muscle contraction","termid":"GO:1904306"},{"relation_name":"positively_regulates","term_name":"pyloric antrum smooth muscle contraction","termid":"GO:0120065"}],"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 pyloric antrum smooth muscle contraction","termid":"GO:0120072"}


id: PR:O14239
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rax2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O14239"],"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":"polarized growth protein rax2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F6.06c","synonyms":[{"name":"Spom972h-rax2","type":"exact"},{"name":"revert to axial protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14239"}


id: MONDO:0016703
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An oligoastrocytoma characterized by the presence of increased cellularity, nuclear atypia, pleomorphism, and high mitotic activity.","definition_xrefs":["NCIT:C6959"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant mixed neoplasm","termid":"MONDO:0005853"},{"relation_name":"is_a","term_name":"oligoastrocytoma","termid":"MONDO:0016702"},{"relation_name":"is_a","term_name":"anaplastic cancer","termid":"MONDO:0020633"},{"relation_name":"is_a","term_name":"grade III glioma","termid":"MONDO:0021640"}],"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":"anaplastic oligoastrocytoma","secondary_identifiers":["UMLS:C0431108","GARD:10637","EFO:0002500","MEDGEN:96556","ONCOTREE:AOAST","Orphanet:251663"],"synonyms":[{"name":"AOAST","type":"related"},{"name":"WHO grade III mixed glioma","type":"exact"},{"name":"aMOA","type":"exact"},{"name":"anaplastic mixed glioma","type":"exact"},{"name":"anaplastic oligoastrocytoma","type":"exact"}],"termid":"MONDO:0016703","xrefs":{"Monarch":{"xref_id":"0016703"}}}


id: PBO:0067659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 836, pseudogene","termid":"PBO:0067659"}


id: PBO:0067132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 180, pseudogene","termid":"PBO:0067132"}


id: GO:0010774
data:
  {"annotated_genes":["SJAG_02267","SJAG_03751","SJAG_04950"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87958,92360,100045],"is_not":false,"summary":null,"term":"GO:0010774"}]},"cv_name":"biological_process","definition":"The cell cycle process in which double strand breaks are formed and repaired through a double Holliday junction intermediate resulting in meiotic recombination. Meiotic recombination is the cell cycle process in which double strand breaks are formed and repaired through a double Holliday junction intermediate.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic strand invasion","termid":"GO:0000708"},{"relation_name":"part_of","term_name":"reciprocal meiotic recombination","termid":"GO:0007131"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02267":null,"SJAG_03751":null,"SJAG_04950":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006310"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0140013","GO:0006310","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"meiotic strand invasion involved in reciprocal meiotic recombination","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0010774","terms_by_termid":{"GO:0010774":null}}


id: GO:0035742
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of an activated CD8-positive, alpha-beta T cell population by cell division.","definition_xrefs":["GOC:BHF","CL:0000906"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CD8-positive, alpha-beta T cell proliferation","termid":"GO:0035740"}],"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":"activated CD8-positive, alpha-beta T cell proliferation","termid":"GO:0035742"}


id: MONDO:1011236
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microphthalmia that occurs in water buffalo.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microphthalmia, non-human animal","termid":"MONDO:1010324"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microphthalmia, water buffalo","secondary_identifiers":["OMIA:000649-89462"],"termid":"MONDO:1011236","xrefs":{"Monarch":{"xref_id":"1011236"}}}


id: MONDO:0032616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex I deficiency, nuclear type","termid":"MONDO:0100223"}],"gene_count":0,"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":"mitochondrial complex 1 deficiency, nuclear type 10","secondary_identifiers":["UMLS:C4748768","GARD:16320","MEDGEN:1648426","DOID:0112075","OMIM:618233"],"synonyms":[{"name":"MC1DN10","type":"related"},{"name":"MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10","type":"related"}],"termid":"MONDO:0032616","xrefs":{"Monarch":{"xref_id":"0032616"}}}


id: PBO:0030022
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_asymmetric_protein_localization_to_old_or_new_mitotic_spindle_pole_body","termid":"PBO:0030022"}


id: PBO:0069217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 472, pseudogene","termid":"PBO:0069217"}


id: MONDO:0021445
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the oral cavity.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign neoplasm","termid":"MONDO:0005165"},{"relation_name":"is_a","term_name":"oral cavity neoplasm","termid":"MONDO:0021245"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of oral cavity","secondary_identifiers":["SCTID:419645003","UMLS:C0347197","MEDGEN:91119","ICD9:210.4","NCIT:C7607"],"synonyms":[{"name":"benign mouth neoplasm","type":"exact"},{"name":"benign mouth tumor","type":"exact"},{"name":"benign mouth tumour","type":"exact"},{"name":"benign neoplasm of mouth","type":"exact"},{"name":"benign neoplasm of the mouth","type":"exact"},{"name":"benign neoplasm of the oral cavity","type":"exact"},{"name":"benign oral cavity neoplasm","type":"exact"},{"name":"benign oral cavity tumor","type":"exact"},{"name":"benign oral cavity tumour","type":"exact"},{"name":"benign tumor of mouth","type":"exact"},{"name":"benign tumor of oral cavity","type":"exact"},{"name":"benign tumor of the mouth","type":"exact"},{"name":"benign tumor of the oral cavity","type":"exact"},{"name":"benign tumour of mouth","type":"exact"},{"name":"benign tumour of oral cavity","type":"exact"},{"name":"benign tumour of the mouth","type":"exact"},{"name":"benign tumour of the oral cavity","type":"exact"},{"name":"oral cavity benign neoplasm","type":"exact"}],"termid":"MONDO:0021445","xrefs":{"Monarch":{"xref_id":"0021445"}}}


id: PBO:0080143
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vesicle amine transport 1","termid":"PBO:0080143"}


id: PBO:0056276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mannosidase alpha class 2A member 1","termid":"PBO:0056276"}


id: PBO:0063467
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate dehydrogenase E1 subunit alpha 1","termid":"PBO:0063467"}


id: GO:0047684
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-glucose + an arylamine = UDP + an N-D-glucosylarylamine.","definition_xrefs":["MetaCyc:ARYLAMINE-GLUCOSYLTRANSFERASE-RXN","EC:2.4.1.71"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016757"],"is_obsolete":false,"name":"arylamine glucosyltransferase activity","synonyms":[{"name":"UDP glucose-arylamine glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:arylamine N-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:arylamine N-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-arylamine glucosyltransferase activity","type":"related"}],"termid":"GO:0047684"}


id: PBO:0001235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CUE domain protein","termid":"PBO:0001235"}


id: GO:0060977
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of blood vessels of the heart are generated and organized. The blood vessel is the vasculature carrying blood.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel morphogenesis","termid":"GO:0048514"},{"relation_name":"part_of","term_name":"coronary vasculature development","termid":"GO:0060976"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"coronary vasculature morphogenesis","synonyms":[{"name":"cardiac blood vessel morphogenesis","type":"exact"},{"name":"cardiac vasculature morphogenesis","type":"exact"},{"name":"coronary blood vessel morphogenesis","type":"exact"},{"name":"heart blood vessel morphogenesis","type":"exact"},{"name":"heart vasculature morphogenesis","type":"exact"}],"termid":"GO:0060977"}


id: PBO:0072318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 4","termid":"PBO:0072318"}


id: MONDO:0002421
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete chorioangioma (obsolete MONDO:0002421)","termid":"MONDO:0002421","xrefs":{"Monarch":{"xref_id":"0002421"}}}


id: PBO:0054406
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 1802","termid":"PBO:0054406"}


id: FYPO:0004877
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of chromatin binding by a gene product (usually a protein) is decreased at specific genes that are transcriptionally up-regulated during mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased chromatin binding","termid":"FYPO:0002577"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000702"},{"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:0001985","FYPO:0000707","FYPO:0000702"],"is_obsolete":false,"name":"decreased chromatin binding at mitotically up-regulated genes","synonyms":[{"name":"decreased chromatin binding at mitotically upregulated gene","type":"exact"},{"name":"reduced chromatin binding at mitotically up-regulated genes","type":"exact"}],"termid":"FYPO:0004877"}


id: PBO:0002285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ATPase (predicted)","termid":"PBO:0002285"}


id: PATO:0000573
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A length quality which is relatively large.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"length","termid":"PATO:0000122"},{"relation_name":"is_a","term_name":"increased size","termid":"PATO:0000586"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased length","synonyms":[{"name":"long","type":"exact"}],"termid":"PATO:0000573"}


id: FYPO:0001145
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 Man9GlcNAc2 measured in a cell is higher than normal. Man9GlcNAc2 is any N-glycan that consists of a branched undecasaccharide consisting of nine D-mannosyl residues and two N-acetylglucosamine residues.","definition_xrefs":["CHEBI:59579","PomBase:mah","PMID:12686557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased polysaccharide level during vegetative growth","termid":"FYPO:0001083"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"increased Man9GlcNAc level","synonyms":[{"name":"increased Man9GlcNAc accumulation","type":"related"},{"name":"increased Man9GlcNAc level during mitotic cell cycle","type":"related"},{"name":"increased Man9GlcNAc level during vegetative growth","type":"exact"},{"name":"increased Man9GlcNAc2 level","type":"exact"},{"name":"increased cellular Man9GlcNAc level","type":"exact"}],"termid":"FYPO:0001145"}


id: PBO:0064589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"POTEH antisense RNA 1","termid":"PBO:0064589"}


id: PATO:0000542
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000542 absolute photosensitivity value (obsolete PATO:0000542)","termid":"PATO:0000542"}


id: GO:1905204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of connective tissue replacement.","definition_xrefs":["PMID:25590961","GO_REF:0000058","GOC:bc","GOC:BHF","GOC:BHF_miRNA","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of tissue remodeling","termid":"GO:0034104"},{"relation_name":"is_a","term_name":"regulation of connective tissue replacement","termid":"GO:1905203"},{"relation_name":"negatively_regulates","term_name":"connective tissue replacement","termid":"GO:0097709"}],"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 connective tissue replacement","synonyms":[{"name":"down regulation of connective tissue replacement","type":"exact"},{"name":"down-regulation of connective tissue replacement","type":"exact"},{"name":"downregulation of connective tissue replacement","type":"exact"},{"name":"inhibition of connective tissue replacement","type":"narrow"}],"termid":"GO:1905204"}


id: GO:1900025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of substrate adhesion-dependent cell spreading.","definition_xrefs":["GOC:yaf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell-substrate adhesion","termid":"GO:0010812"},{"relation_name":"is_a","term_name":"regulation of substrate adhesion-dependent cell spreading","termid":"GO:1900024"},{"relation_name":"negatively_regulates","term_name":"substrate adhesion-dependent cell spreading","termid":"GO:0034446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of substrate adhesion-dependent cell spreading","synonyms":[{"name":"down regulation of cell spreading during cell substrate adhesion","type":"exact"},{"name":"down regulation of substrate adhesion dependent cell spreading","type":"exact"},{"name":"down regulation of substrate adhesion-dependent cell spreading","type":"related"},{"name":"negative regulation of cell spreading during cell substrate adhesion","type":"exact"},{"name":"negative regulation of substrate adhesion dependent cell spreading","type":"exact"}],"termid":"GO:1900025"}


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


id: GO:0019912
data:
  {"annotated_genes":["SJAG_01000"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91626],"is_not":false,"summary":null,"term":"GO:0019912"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + a protein = ADP + a phosphoprotein; increases the activity of a cyclin-dependent protein kinase (CDK).","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase activity","termid":"GO:0004672"},{"relation_name":"is_a","term_name":"protein kinase activator activity","termid":"GO:0030295"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01000":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0140677","GO:0016740","GO:0003824","GO:0004672","GO:0016301","GO:0030234","GO:0003674","GO:0140096","GO:0098772"],"is_obsolete":false,"name":"cyclin-dependent protein kinase activating kinase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0019913"],"synonyms":[{"name":"CAK","type":"exact"},{"name":"cdk-activating kinase activity","type":"exact"},{"name":"cyclin-dependent protein kinase activating kinase, intrinsic catalyst activity","type":"exact"}],"termid":"GO:0019912","terms_by_termid":{"GO:0019912":null}}


id: MONDO:0002889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary or metastatic malignant neoplasm involving the orbit.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skull cancer","termid":"MONDO:0002132"},{"relation_name":"is_a","term_name":"orbit neoplasm","termid":"MONDO:0024611"}],"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":"orbital cancer","secondary_identifiers":["EFO:0007408","ICD9:190.1","DOID:4143","MEDGEN:56314","UMLS:C0153626","ICD9:239.89","NCIT:C3290","NCIT:C3562","SCTID:127003006"],"synonyms":[{"name":"cancer of orbit of skull","type":"exact"},{"name":"malignant neoplasm of orbit","type":"exact"},{"name":"malignant neoplasm of orbit of skull","type":"exact"},{"name":"malignant neoplasm of the orbit","type":"exact"},{"name":"malignant orbit neoplasm","type":"exact"},{"name":"malignant orbit of skull neoplasm","type":"exact"},{"name":"malignant orbit tumor","type":"exact"},{"name":"malignant orbit tumour","type":"exact"},{"name":"malignant orbital neoplasm","type":"exact"},{"name":"malignant orbital tumor","type":"exact"},{"name":"malignant orbital tumour","type":"exact"},{"name":"malignant tumor of orbit","type":"exact"},{"name":"malignant tumor of the orbit","type":"exact"},{"name":"malignant tumour of orbit","type":"exact"},{"name":"malignant tumour of the orbit","type":"exact"},{"name":"neoplasm of orbit proper","type":"broad"},{"name":"orbit cancer","type":"exact"},{"name":"orbit of skull cancer","type":"exact"},{"name":"orbital tumor","type":"broad"},{"name":"orbital tumour","type":"broad"}],"termid":"MONDO:0002889","xrefs":{"Monarch":{"xref_id":"0002889"}}}


id: GO:0050731
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the phosphorylation of peptidyl-tyrosine.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein phosphorylation","termid":"GO:0001934"},{"relation_name":"is_a","term_name":"regulation of peptidyl-tyrosine phosphorylation","termid":"GO:0050730"},{"relation_name":"positively_regulates","term_name":"peptidyl-tyrosine phosphorylation","termid":"GO:0018108"}],"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 peptidyl-tyrosine phosphorylation","synonyms":[{"name":"activation of peptidyl-tyrosine phosphorylation","type":"narrow"},{"name":"stimulation of peptidyl-tyrosine phosphorylation","type":"narrow"},{"name":"up regulation of peptidyl-tyrosine phosphorylation","type":"exact"},{"name":"up-regulation of peptidyl-tyrosine phosphorylation","type":"exact"},{"name":"upregulation of peptidyl-tyrosine phosphorylation","type":"exact"}],"termid":"GO:0050731"}


id: PBO:0028989
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_small_RNA_level_(obsolete_FYPO:0003261)","termid":"PBO:0028989"}


id: PBO:0079644
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 Q family like 1","termid":"PBO:0079644"}


id: GO:0050124
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-acylneuraminate 9-phosphate + H2O = N-acylneuraminate + phosphate.","definition_xrefs":["EC:3.1.3.29","MetaCyc:N-ACYLNEURAMINATE-9-PHOSPHATASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"N-acylneuraminate-9-phosphatase activity","secondary_identifiers":["RHEA:13057","Reactome:R-HSA-4084989"],"synonyms":[{"name":"N-acylneuraminate-9-phosphate phosphohydrolase activity","type":"related"},{"name":"N-acylneuraminic (sialic) acid 9-phosphatase activity","type":"related"},{"name":"N-acylneuraminic acid 9-phosphate phosphatase activity","type":"related"},{"name":"acylneuraminate 9-phosphatase activity","type":"related"}],"termid":"GO:0050124"}


id: MONDO:0002286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the renal artery.","direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"},{"relation_name":"is_a","term_name":"aortic disorder","termid":"MONDO:0005561"}],"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":"renal artery disease","secondary_identifiers":["ICD9:593.81","MEDGEN:768693","NCIT:C101254","SCTID:16934004","UMLS:C3640053","DOID:2388"],"synonyms":[{"name":"renal vascular disease","type":"exact"},{"name":"vascular disorder of kidney","type":"exact"}],"termid":"MONDO:0002286","xrefs":{"Monarch":{"xref_id":"0002286"}}}


id: FYPO:0009005
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in mitotic interphase in which microtubule-based movement oscillations occur at a faster speed than normal in a daughter cell that inherits no mitochondria.","definition_xrefs":["PomBase:mlr","PMID:36633091"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule-based movement during vegetative growth","termid":"FYPO:0005461"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased interphase nuclear movement velocity in daughter cell without mitochondria","synonyms":[{"name":"increased interphase nuclear oscillation velocity in daughter cell without mitochondria","type":"exact"}],"termid":"FYPO:0009005"}


id: PBO:0068949
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 193, pseudogene","termid":"PBO:0068949"}


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


id: PBO:0074488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMYD family member 5","termid":"PBO:0074488"}


id: GO:0004409
data:
  {"annotated_genes":["SJAG_01574"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[96167],"is_not":false,"summary":null,"term":"GO:0004409"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: (-)-homoisocitrate = cis-homoaconitate + H2O.","definition_xrefs":["RHEA:15485","EC:4.2.1.36"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01574":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:0016829"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"homoaconitate hydratase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:HOMOACONITATE-HYDRATASE-RXN","KEGG_REACTION:R04371"],"synonyms":[{"name":"(1R,2S)-1-hydroxybutane-1,2,4-tricarboxylate hydro-lyase [(Z)-but-1-ene-1,2,4-tricarboxylate-forming]","type":"related"},{"name":"2-hydroxybutane-1,2,4-tricarboxylate hydro-lyase activity","type":"related"},{"name":"HACN activity","type":"related"},{"name":"Lys4","type":"related"},{"name":"LysF","type":"related"},{"name":"cis-homoaconitase activity","type":"related"},{"name":"homoaconitase activity","type":"related"}],"termid":"GO:0004409","terms_by_termid":{"GO:0004409":null}}


id: GO:0061141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a lung ciliated cell. A lung ciliated cell is a specialized lung epithelial cell that contains cilia for moving substances released from lung secretory cells.","definition_xrefs":["GOC:cilia","GOC:krc","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung epithelial cell differentiation","termid":"GO:0060487"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lung ciliated cell differentiation","termid":"GO:0061141"}


id: PBO:0067582
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 740, pseudogene","termid":"PBO:0067582"}


id: MOD:01239
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification produced by formation of an adduct of an L-histidine residue with 4-hydroxynonenal.","definition_xrefs":["PubMed:11327326","PubMed:10717661","Unimod:53#H","PubMed:15133838"],"direct_ancestors":[{"relation_name":"is_a","term_name":"4-hydroxynonenal adduct","termid":"MOD:00446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"histidine 4-hydroxynonenal adduct","synonyms":[{"name":"4-hydroxynonenal (HNE)","type":"related"},{"name":"HNE","type":"related"}],"termid":"MOD:01239"}


id: PR:G2TRR6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC2A9.14 gene.","definition_xrefs":["UniProtKB:G2TRR6","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 C2A9.14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2A9.14","synonyms":[{"name":"Spom972h-SPBC2A9.14","type":"exact"}],"termid":"PR:G2TRR6"}


id: GO:0072575
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of epithelial cells, resulting in the expansion of a cell population that contributes to the shaping of the liver.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell proliferation","termid":"GO:0050673"},{"relation_name":"part_of","term_name":"liver morphogenesis","termid":"GO:0072576"}],"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":"epithelial cell proliferation involved in liver morphogenesis","termid":"GO:0072575"}


id: FYECO:0000110
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Cells are first grown in minimal medium lacking nitrogen and are then allowed to recover in rich medium.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping sequential growth conditions","termid":"FYECO:0000094"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nitrogen starvation and recovery","synonyms":[{"name":"recovery from nitrogen depletion","type":"exact"},{"name":"recovery from nitrogen starvation","type":"exact"}],"termid":"FYECO:0000110"}


id: MONDO:0002368
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant cystic serous epithelial neoplasm characterized by the presence of malignant glandular epithelial cells forming papillary structures. Stromal invasion is present.","definition_xrefs":["NCIT:C8377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary cystadenocarcinoma","termid":"MONDO:0005074"},{"relation_name":"is_a","term_name":"serous cystadenocarcinoma","termid":"MONDO:0024621"}],"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":"papillary serous cystadenocarcinoma","secondary_identifiers":["MEDGEN:825029","ICDO:8460/3","SCTID:716649003","UMLS:C3839184","DOID:2632"],"synonyms":[{"name":"micropapillary serous carcinoma","type":"narrow"},{"name":"papillary serous adenocarcinoma","type":"exact"},{"name":"papillary serous carcinoma","type":"broad"},{"name":"papillary serous cystadenocarcinoma","type":"exact"},{"name":"serous surface papillary carcinoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0002368","xrefs":{"Monarch":{"xref_id":"0002368"}}}


id: PBO:0030500
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_DNA_damage_checkpoint","termid":"PBO:0030500"}


id: PBO:0044731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 17","termid":"PBO:0044731"}


id: GO:0045497
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the analia of the female over time, from formation to the mature structure. The analia is the posterior-most vertral appendage that develops from the genital disc. An example of this process is found in Drosophila melanogaster.","definition_xrefs":["PMID:11494318","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"analia development","termid":"GO:0007487"}],"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":"female analia development","termid":"GO:0045497"}


id: PBO:0089041
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPP I, II and III complex Rab GEF subunit Bet3","termid":"PBO:0089041"}


id: MONDO:0004238
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that affects the petrous apex.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"petrous apex meningioma","secondary_identifiers":["DOID:7482","MEDGEN:277512","UMLS:C1335396","NCIT:C5271"],"synonyms":[{"name":"meningioma of petrous apex","type":"exact"},{"name":"meningioma of petrous ridge","type":"exact"},{"name":"meningioma of the petrous apex","type":"exact"},{"name":"meningioma of the petrous ridge","type":"exact"},{"name":"petrous ridge meningioma","type":"exact"}],"termid":"MONDO:0004238","xrefs":{"Monarch":{"xref_id":"0004238"}}}


id: PBO:0056260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MALT1 paracaspase","termid":"PBO:0056260"}


id: PBO:0017722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial 2-oxoadipate and 2-oxoglutarate transmembrane transporter (predicted)","termid":"PBO:0017722"}


id: FYPO:0004082
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins is normal (i.e. indistinguishable from wild type) during mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein phosphorylation during vegetative growth","termid":"FYPO:0000776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal protein phosphorylation during mitosis","synonyms":[{"name":"normal protein phosphorylation during mitosis during vegetative growth","type":"exact"},{"name":"normal protein phosphorylation during mitotic M phase","type":"related"},{"name":"normal protein phosphorylation during mitotic nuclear division","type":"exact"}],"termid":"FYPO:0004082"}


id: GO:0018631
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-phenylacetate + O2 + reduced [NADPH--hemoprotein reductase] = (2-hydroxyphenyl)acetate + H+ + H2O + oxidized [NADPH--hemoprotein reductase].","definition_xrefs":["RHEA:53392"],"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:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"phenylacetate 2-hydroxylase activity","secondary_identifiers":["EC:1.14.14.54","UM-BBD_reactionID:r0036"],"synonyms":[{"name":"phenylacetate hydroxylase activity","type":"exact"}],"termid":"GO:0018631"}


id: FYPO:0005033
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the phosphorylation of one or more specific proteins, or of specific protein sites, is abnormal when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein phosphorylation","termid":"FYPO:0002677"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0002274","FYPO:0005447","FYPO:0002494"],"is_obsolete":false,"name":"abnormal protein phosphorylation during nitrogen starvation","synonyms":[{"name":"abnormal protein phosphorylation during cellular response to nitrogen starvation","type":"exact"},{"name":"abnormal protein phosphorylation during nitrogen depletion","type":"exact"},{"name":"abnormal protein phosphorylation during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0005033"}


id: PBO:0091822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Arf3/6 docking factor","termid":"PBO:0091822"}


id: PBO:0052271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine demethylase 4E","termid":"PBO:0052271"}


id: MONDO:0016019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, progressive chronic inflammation of a single cerebral hemisphere that usually affects children. It is characterized by severe seizures, loss of motor skills and speech, hemiparesis, and dementia.","definition_xrefs":["NCIT:C125384"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"immune epilepsy","termid":"MONDO:0100028"},{"relation_name":"is_a","term_name":"epilepsy","termid":"MONDO:0005027"},{"relation_name":"is_a","term_name":"postinfectious encephalitis","termid":"MONDO:0020068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"Rasmussen subacute encephalitis","secondary_identifiers":["GARD:18752","NORD:1649","UMLS:C2930868","ICD9:323.9","MEDGEN:418934","NANDO:2200900","Orphanet:1929","MESH:C535291","NANDO:2100246","NANDO:1200598","SCTID:230191005"],"synonyms":[{"name":"CFE","type":"exact"},{"name":"RE","type":"related"},{"name":"Rasmussen Encephalitis","type":"exact"},{"name":"Rasmussen encephalitis","type":"exact"},{"name":"Rasmussen syndrome","type":"exact"},{"name":"Rasmussen’s encephalitis","type":"exact"},{"name":"Rasmussen’s syndrome","type":"exact"},{"name":"chronic focal encephalitis","type":"exact"}],"termid":"MONDO:0016019","xrefs":{"Monarch":{"xref_id":"0016019"}}}


id: PBO:0109378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 9B","termid":"PBO:0109378"}


id: PBO:0089676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"major facilitator family transmembrane transporter Mug111","termid":"PBO:0089676"}


id: PR:Q9P7R6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A splicing factor 3B subunit 5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03892","PANTHER:PTHR20978:SF0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C211.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC211.05","secondary_identifiers":["UniProtKB:Q9P7R6"],"synonyms":[{"name":"Spom972h-SF3B5","type":"exact"}],"termid":"PR:Q9P7R6"}


id: PBO:0038825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 32","termid":"PBO:0038825"}


id: GO:0047401
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + trithionate = H+ + sulfate + thiosulfate.","definition_xrefs":["RHEA:21884"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid sulfur-sulfur bonds","termid":"GO:0016828"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"trithionate hydrolase activity","secondary_identifiers":["EC:3.12.1.1","KEGG_REACTION:R01930","MetaCyc:3.12.1.1-RXN"],"synonyms":[{"name":"trithionate thiosulfohydrolase activity","type":"related"}],"termid":"GO:0047401"}


id: GO:0015975
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways by which a cell derives energy from inorganic compounds; results in the oxidation of the compounds from which energy is released.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"generation of precursor metabolites and energy","termid":"GO:0006091"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"energy derivation by oxidation of reduced inorganic compounds","secondary_identifiers":["Wikipedia:Lithotrophy"],"synonyms":[{"name":"chemolithotrophie","type":"exact"},{"name":"chemolithotrophy","type":"exact"},{"name":"lithotrophy","type":"exact"}],"termid":"GO:0015975"}


id: GO:1905767
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of double-stranded telomeric DNA binding.","definition_xrefs":["PMID:18812185","GOC:BHF","GO_REF:0000059","GOC:nc","GOC:TermGenie","GOC:BHF_telomere"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of double-stranded telomeric DNA binding (obsolete GO:1905767)","termid":"GO:1905767"}


id: PBO:0063245
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin alpha 10","termid":"PBO:0063245"}


id: GO:0050984
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The sulfation of peptidyl-serine to form peptidyl-O-sulfo-L-serine.","definition_xrefs":["RESID:AA0361"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-serine sulfation (obsolete GO:0050984)","termid":"GO:0050984"}


id: GO:0102590
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: delphinidin 3-O-rutinoside + 1-O-4-hydroxybenzoyl-beta-D-glucose = delphinidin 3-O-rutinoside-7-O-glucoside + 4-hydroxybenzoic acid + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete delphinidin 3-O-rutinoside 7-O-glucosyltransferase (acyl-glucose dependent) activity (obsolete GO:0102590)","termid":"GO:0102590"}


id: MONDO:0044271
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete bone mineral density quantitative trait locus 1 (obsolete MONDO:0044271)","secondary_identifiers":["OMIM:601884"],"synonyms":[{"name":"BMND1","type":"related"},{"name":"bone mineral density quantitative trait locus 1","type":"related"},{"name":"bone mineral density variability 1","type":"exact"},{"name":"high bone Mass","type":"related"},{"name":"osteoporosis, susceptibility to","type":"related"}],"termid":"MONDO:0044271","xrefs":{"Monarch":{"xref_id":"0044271"}}}


id: PBO:0087852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcriptional activator; binds specific gene recruitment sequences and is required for DNA zip code-mediated targeting of genes to nuclear periphery; regulates proline utilization genes, constitutively binds PUT1 and PUT2 promoters as a dimer, undergoes conformational change to form active state; binds other promoters only under activating conditions; differentially phosphorylated in presence of different nitrogen sources; has a Zn(2)-Cys(6) binuclear cluster domain","termid":"PBO:0087852"}


id: PBO:0075866
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSX family pseudogene 6","termid":"PBO:0075866"}


id: PBO:0083999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Glycerol 3-phosphate/dihydroxyacetone phosphate sn-1 acyltransferase; dual substrate-specific acyltransferase of the glycerolipid biosynthesis pathway; prefers 16-carbon fatty acids; similar to Gpt2p; gene is constitutively transcribed","termid":"PBO:0083999"}


id: PBO:0040686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCAS3 microtubule associated cell migration factor","termid":"PBO:0040686"}


id: PBO:0036549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOPS/CORVET complex subunit, ubiquitin-protein ligase E3 Pep3/Vps18 (predicted)","termid":"PBO:0036549"}


id: MONDO:0700073
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any multiple acyl-CoA dehydrogenase deficiency in which the cause of the disease is a mutation in the ETFA gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple acyl-CoA dehydrogenase deficiency","termid":"MONDO:0009282"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069","MONDO:0005267","MONDO:0002525"],"is_obsolete":false,"name":"glutaric acidemia IIa","secondary_identifiers":["MEDGEN:479784","UMLS:C3278154"],"synonyms":[{"name":"ETFA deficiency","type":"exact"},{"name":"GA2A","type":"exact"},{"name":"glutaric acidemia 2A","type":"exact"},{"name":"multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFA","type":"exact"}],"termid":"MONDO:0700073","xrefs":{"Monarch":{"xref_id":"0700073"}}}


id: PBO:0047905
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(8)(q22.1)","termid":"PBO:0047905"}


id: PBO:0078285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 18-1","termid":"PBO:0078285"}


id: GO:0004555
data:
  {"annotated_genes":["SJAG_04859"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111005],"is_not":false,"summary":null,"term":"GO:0004555"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha,alpha-trehalose + H2O = 2 D-glucose.","definition_xrefs":["RHEA:32675","PMID:19897915"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trehalase activity","termid":"GO:0015927"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04859":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016798","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"alpha,alpha-trehalase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:3.2.1.28","Reactome:R-HSA-188985","MetaCyc:TREHALA-RXN"],"synonyms":[{"name":"alpha,alpha-trehalose glucohydrolase activity","type":"related"}],"termid":"GO:0004555","terms_by_termid":{"GO:0004555":null}}


id: MONDO:0012536
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any osteogenesis imperfecta in which the cause of the disease is a mutation in the CRTAP gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta and a reduction of bone mineral density.","termid":"MONDO:0800064"}],"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":"osteogenesis imperfecta type 7","secondary_identifiers":["GARD:8701","UMLS:C1853162","MEDGEN:343981","OMIM:610682","DOID:0110337","SCTID:254111008"],"synonyms":[{"name":"CRTAP osteogenesis imperfecta","type":"exact"},{"name":"OI type 7","type":"related"},{"name":"OI type VII","type":"related"},{"name":"OI, type 7","type":"related"},{"name":"OI7","type":"exact"},{"name":"osteogenesis imperfecta caused by mutation in CRTAP","type":"exact"},{"name":"osteogenesis imperfecta type 7","type":"exact"},{"name":"osteogenesis imperfecta type VII","type":"exact"},{"name":"osteogenesis imperfecta, type 7","type":"related"},{"name":"osteogenesis imperfecta, type IIb","type":"related"},{"name":"osteogenesis imperfecta, type IIb, formerly","type":"related"},{"name":"osteogenesis imperfecta, type VII","type":"related"}],"termid":"MONDO:0012536","xrefs":{"Monarch":{"xref_id":"0012536"}}}


id: PR:Q4ZGE2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC3D6.16 gene.","definition_xrefs":["UniProtKB:Q4ZGE2","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 C3D6.16 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3D6.16","synonyms":[{"name":"Spom972h-SPBC3D6.16","type":"exact"}],"termid":"PR:Q4ZGE2"}


id: FYPO:0002821
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 mitotic spindle pole body is decreased during interphase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to mitotic spindle pole body","termid":"FYPO:0000940"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to mitotic spindle pole body during interphase","synonyms":[{"name":"decreased protein localisation to mitotic spindle pole body during interphase","type":"exact"},{"name":"decreased protein localization to mitotic SPB during interphase","type":"exact"},{"name":"decreased protein localization to mitotic spindle pole body during mitotic interphase","type":"exact"},{"name":"decreased protein localization to spindle pole body during interphase during vegetative growth","type":"exact"},{"name":"reduced protein localization to mitotic spindle pole body during interphase","type":"exact"}],"termid":"FYPO:0002821"}


id: GO:0019025
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A single stranded RNA genome with the same nucleotide polarity as mRNA.","definition_xrefs":["ISBN:0121585336"],"gene_count":0,"genotype_count":0,"name":"obsolete positive sense viral genome (obsolete GO:0019025)","termid":"GO:0019025"}


id: MOD:00260
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-threonine residue and the 5'-end of DNA through a phosphodiester bond to form O-(phospho-5'-DNA)-L-threonine.","definition_xrefs":["RESID:AA0255","PubMed:3081736"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyribonucleic acid linked residue","termid":"MOD:00750"},{"relation_name":"is_a","term_name":"modified L-threonine residue","termid":"MOD:00917"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O-(phospho-5'-DNA)-L-threonine","synonyms":[{"name":"(S)-2-amino-3-(5'-deoxyribonucleic acid phosphonoxy)butanoic acid","type":"exact"},{"name":"O-(phospho-5'-DNA)-L-threonine","type":"exact"},{"name":"O3-(phospho-5'-DNA)-L-threonine","type":"exact"},{"name":"O3-L-threonine 5'-DNA phosphodiester","type":"exact"}],"termid":"MOD:00260"}


id: GO:0061786
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A peptidoglycan endopeptidase activity that acts on a stem peptide of peptidoglycan.","definition_xrefs":["GOC:dph","GOC:jh","PMID:22748813"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidoglycan endopeptidase activity","termid":"GO:0061785"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0003824","GO:0140096","GO:0008233"],"is_obsolete":false,"name":"peptidoglycan stem peptide endopeptidase activity","termid":"GO:0061786"}


id: PBO:0064180
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group XG, pseudogene","termid":"PBO:0064180"}


id: PBO:0029101
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_sulfate_import","termid":"PBO:0029101"}


id: GO:0035158
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Ensuring that a tube in an open tracheal system is of the correct diameter. When primary branches form their lumens are small (less than 2 micrometers) in caliber and must undergo regulated expansion during larval life to reach their mature size.","definition_xrefs":["PMID:14570584","GOC:mtg_sensu"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tube size, open tracheal system","termid":"GO:0035151"},{"relation_name":"is_a","term_name":"regulation of tube diameter","termid":"GO:0035296"}],"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 tube diameter, open tracheal system","synonyms":[{"name":"regulation of tracheal tube diameter","type":"exact"},{"name":"tracheal tube dilation","type":"narrow"},{"name":"tracheal tube expansion","type":"narrow"}],"termid":"GO:0035158"}


id: GO:0072359
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the circulatory system over time, from its formation to the mature structure. The circulatory system is the organ system that passes nutrients (such as amino acids and electrolytes), gases, hormones, blood cells, etc. to and from cells in the body to help fight diseases and help stabilize body temperature and pH to maintain homeostasis.","definition_xrefs":["GOC:mah","UBERON:0001009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"system development","termid":"GO:0048731"}],"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":"circulatory system development","secondary_identifiers":["GO:0072358"],"synonyms":[{"name":"cardiovascular system development","type":"narrow"}],"termid":"GO:0072359"}


id: MONDO:0030266
data:
  {"annotated_genes":["SJAG_00399"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86001],"is_not":false,"summary":null,"term":"MONDO:0030266"}]},"cv_name":"mondo","definition":"An autosomal recessive immunologic disorder with variable manifestations. One patient with infantile-onset of chronic cytomegalovirus (CMV) infection associated with severely decreased NK cells has been reported. Another family with 3 affected fetuses showing restrictive cardiomyopathy and hypoplasia of the spleen and thymus has also been reported.","definition_xrefs":["OMIM:619313"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immunodeficiency disease","termid":"MONDO:0021094"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00399":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency 80 with or without congenital cardiomyopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1786417","UMLS:C5543344"],"synonyms":[{"name":"IMD80","type":"exact"},{"name":"MCM10 deficiency","type":"exact"},{"name":"immunodeficiency 80 with or without cardiomyopathy","type":"exact"},{"name":"immunodeficiency 80 with or without congenital cardiomyopathy","type":"exact"},{"name":"immunodeficiency with or without congenital cardiomyopathy","type":"exact"}],"termid":"MONDO:0030266","terms_by_termid":{"MONDO:0030266":null},"xrefs":{"Monarch":{"xref_id":"0030266"}}}


id: PBO:0066468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"replication factor C subunit 5","termid":"PBO:0066468"}


id: GO:1900510
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of pentose catabolic process to ethanol.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of pentose catabolic process to ethanol (obsolete GO:1900510)","synonyms":[{"name":"down regulation of pentose catabolic process to ethanol","type":"exact"},{"name":"down regulation of pentose catabolism to ethanol","type":"exact"},{"name":"down-regulation of pentose catabolic process to ethanol","type":"exact"},{"name":"down-regulation of pentose catabolism to ethanol","type":"exact"},{"name":"downregulation of pentose catabolic process to ethanol","type":"exact"},{"name":"downregulation of pentose catabolism to ethanol","type":"exact"},{"name":"inhibition of pentose catabolic process to ethanol","type":"narrow"},{"name":"inhibition of pentose catabolism to ethanol","type":"exact"},{"name":"negative regulation of pentose catabolism to ethanol","type":"exact"}],"termid":"GO:1900510"}


id: PBO:0075378
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRY-box transcription factor 15","termid":"PBO:0075378"}


id: GO:0106291
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADH + 2 O2 = H+ + NAD+ + 2 superoxide.","definition_xrefs":["RHEA:63184"],"direct_ancestors":[{"relation_name":"is_a","term_name":"superoxide-generating NAD(P)H oxidase activity","termid":"GO:0016175"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"superoxide-generating NADH oxidase activity","termid":"GO:0106291"}


id: GO:0050372
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: n ATP + calmodulin + n ubiquitin = n AMP + n diphosphate + ubiquitin(n)-calmodulin.","definition_xrefs":["MetaCyc:UBIQUITIN--CALMODULIN-LIGASE-RXN"],"gene_count":0,"genotype_count":0,"name":"obsolete ubiquitin-calmodulin ligase activity (obsolete GO:0050372)","synonyms":[{"name":"calmodulin:ubiquitin ligase (AMP-forming)","type":"related"},{"name":"uCaM-synthetase activity","type":"related"},{"name":"ubiquitin-calmodulin synthetase activity","type":"related"},{"name":"ubiquityl-calmodulin synthase activity","type":"related"},{"name":"ubiquityl-calmodulin synthetase activity","type":"related"}],"termid":"GO:0050372"}


id: PBO:0053532
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 533","termid":"PBO:0053532"}


id: MOD:02017
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue amino group with an arachidonoylamino group.","direct_ancestors":[{"relation_name":"is_a","term_name":"N-acylated residue","termid":"MOD:00670"},{"relation_name":"is_a","term_name":"arachidonoylated residue","termid":"MOD:02018"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"N-arachidonoylated residue","termid":"MOD:02017"}


id: PBO:0058872
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 9983","termid":"PBO:0058872"}


id: PBO:0054029
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 1360","termid":"PBO:0054029"}


id: PBO:0029389
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_nucleoplasm_during_cellular_response_to_hydroxyurea","termid":"PBO:0029389"}


id: GO:0048857
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of a neural nucleus from its initial condition to its mature state. A neural nucleus is an anatomical structure consisting of a discrete aggregate of neuronal soma.","definition_xrefs":["GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural nucleus development","termid":"GO:0048857"}


id: GO:0002907
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of mature B cell apoptotic process.","definition_xrefs":["GOC:add","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of immune system process","termid":"GO:0002684"},{"relation_name":"is_a","term_name":"positive regulation of B cell apoptotic process","termid":"GO:0002904"},{"relation_name":"is_a","term_name":"regulation of mature B cell apoptotic process","termid":"GO:0002905"},{"relation_name":"positively_regulates","term_name":"mature B cell apoptotic process","termid":"GO:0002901"}],"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 mature B cell apoptotic process","synonyms":[{"name":"activation of mature B cell apoptosis","type":"narrow"},{"name":"positive regulation of mature B cell apoptosis","type":"narrow"},{"name":"stimulation of mature B cell apoptosis","type":"narrow"},{"name":"up regulation of mature B cell apoptosis","type":"exact"},{"name":"up-regulation of mature B cell apoptosis","type":"exact"},{"name":"upregulation of mature B cell apoptosis","type":"exact"}],"termid":"GO:0002907"}


id: GO:0140433
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of protein localization to a meiotic spindle pole body.","definition_xrefs":["PMID:22438582"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"is_a","term_name":"regulation of protein localization to spindle pole body","termid":"GO:1902363"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"protein localization to meiotic spindle pole body","termid":"GO:1902441"}],"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:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of protein localization to meiotic spindle pole body","termid":"GO:0140433"}


id: PBO:0087996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"t-SNARE protein required for retrograde vesicular traffic; involved in Sey1p-independent homotypic ER fusion; required for efficient nuclear fusion during mating; forms a complex with the SNAREs Sec22p, Sec20p and Use1p to mediate fusion of Golgi-derived vesicles at the ER","termid":"PBO:0087996"}


id: PBO:0064940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRAC1 small nuclear protein","termid":"PBO:0064940"}


id: PBO:0001287
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Graves' disease","termid":"PBO:0001287"}


id: PBO:0049681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HuR (ELAVL1) associated fibroblast migratory lncRNA","termid":"PBO:0049681"}


id: GO:0005220
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a calcium ion by a channel that opens when inositol 1,4,5-trisphosphate (IP3) has been bound by the channel complex or one of its constituent parts.","definition_xrefs":["GOC:signaling","GOC:mah","PMID:8660280","Wikipedia:Inositol_trisphosphate_receptor","PMID:28416699"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellularly gated calcium channel activity","termid":"GO:0015278"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"inositol 1,4,5-trisphosphate-gated calcium channel activity","secondary_identifiers":["GO:0008095"],"synonyms":[{"name":"IP3 receptor activity","type":"exact"},{"name":"InsP3 receptor","type":"exact"},{"name":"inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity","type":"exact"},{"name":"inositol-1,4,5-trisphosphate receptor activity","type":"exact"}],"termid":"GO:0005220"}


id: PBO:0003888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S23 (predicted)","termid":"PBO:0003888"}


id: MONDO:0003160
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An adenocarcinoma with sebaceous differentiation. It presents as a painless mass and it may be multifocal. It grows in the ocular adnexae and in the skin of head and neck, trunk, genitals, and extremities. It is characterized by the presence of malignant cells with multivesicular and clear cytoplasm. It may recur and metastasize.","definition_xrefs":["NCIT:C40310"],"gene_count":0,"genotype_count":0,"name":"obsolete sebaceous carcinoma (obsolete MONDO:0003160)","termid":"MONDO:0003160","xrefs":{"Monarch":{"xref_id":"0003160"}}}


id: FYPO:0007899
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 rate, or speed, localization of a protein to the actomyosin contractile ring is increased.","definition_xrefs":["PomBase:vw","PMID:34613787"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to actomyosin contractile ring","termid":"FYPO:0002560"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000032","FYPO:0000631","FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased rate of protein localization to actomyosin contractile ring","synonyms":[{"name":"increased rate of protein localisation to actomyosin contractile ring","type":"exact"},{"name":"increased rate of protein localization to actomyosin contractile ring during vegetative growth","type":"exact"},{"name":"increased rate of protein localization to actomyosin contractile ring involved in mitotic cytokinesis","type":"exact"},{"name":"increased rate of protein localization to cytokinetic contractile ring","type":"exact"},{"name":"increased rate of protein localization to mitotic contractile ring","type":"exact"}],"termid":"FYPO:0007899"}


id: FYPO:0002168
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing ethyl methanesulfonate.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002060"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002060","FYPO:0002058","FYPO:0000257","FYPO:0002057","FYPO:0000139"],"is_obsolete":false,"name":"normal growth on ethyl methanesulfonate","synonyms":[{"name":"normal cell population growth in presence of ethyl methanesulfonate","type":"exact"},{"name":"normal cell population growth on EMS","type":"exact"},{"name":"normal cell population growth on ethyl methanesulfonate","type":"exact"},{"name":"normal cellular response to ethyl methanesulfonate","type":"related"},{"name":"normal growth on ethyl methanesulphonate","type":"exact"},{"name":"normal vegetative cell population growth on ethyl methanesulfonate","type":"exact"}],"termid":"FYPO:0002168"}


id: MONDO:0005156
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the brain and the spinal cord.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system disorder","termid":"MONDO:0002602"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"encephalomyelitis","secondary_identifiers":["UMLS:C0014070","DOID:640","EFO:0001423","NCIT:C34580","MEDGEN:8603","MESH:D004679","ICD9:323.9","SCTID:62950007"],"synonyms":[{"name":"central nervous system inflammation","type":"exact"},{"name":"encephalitis &/or myelitis","type":"exact"},{"name":"encephalitis and/or myelitis","type":"exact"},{"name":"inflammation of central nervous system","type":"exact"}],"termid":"MONDO:0005156","xrefs":{"Monarch":{"xref_id":"0005156"}}}


id: MONDO:0014656
data:
  {"annotated_genes":["SJAG_06022"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84613],"is_not":false,"summary":null,"term":"MONDO:0014656"}]},"cv_name":"mondo","definition":"Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the RNASEH1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progressive external ophthalmoplegia with mitochondrial DNA deletions","termid":"MONDO:0000090"},{"relation_name":"is_a","term_name":"adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy","termid":"MONDO:0018002"}],"gene_count":1,"genes_by_uniquename":{"SJAG_06022":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0004069","MONDO:0002320","MONDO:0005066"],"is_obsolete":false,"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:901897","OMIM:616479","DOID:0111515","GARD:18450","UMLS:C4225312"],"synonyms":[{"name":"PEOB2","type":"related"},{"name":"RNASEH1 progressive external ophthalmoplegia with mitochondrial DNA deletions","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RNASEH1","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 2","type":"exact"},{"name":"progressive external ophthalmoplegia, autosomal recessive 2","type":"related"}],"termid":"MONDO:0014656","terms_by_termid":{"MONDO:0014656":null},"xrefs":{"Monarch":{"xref_id":"0014656"}}}


id: PBO:0061881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oocyte secreted protein family member 4A","termid":"PBO:0061881"}


id: PBO:0042781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centrosomal protein 112","termid":"PBO:0042781"}


id: PBO:0047025
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 90 member A28, pseudogene","termid":"PBO:0047025"}


id: PBO:0069000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 244, pseudogene","termid":"PBO:0069000"}


id: GO:0090724
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The center of the migrating motile tip of a growing nerve cell axon or dendrite.","definition_xrefs":["PMID:16260607","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"growth cone","termid":"GO:0030426"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"central region of growth cone","termid":"GO:0090724"}


id: PBO:0067305
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 391, pseudogene","termid":"PBO:0067305"}


id: GO:0034007
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: geranyl diphosphate + H2O = (S)-linalool + diphosphate.","definition_xrefs":["EC:4.2.3.25","RHEA:24116"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-oxygen lyase activity, acting on phosphates","termid":"GO:0016838"}],"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:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"S-linalool synthase activity","secondary_identifiers":["KEGG_REACTION:R07631","MetaCyc:4.2.3.25-RXN"],"synonyms":[{"name":"3S-linalool synthase activity","type":"related"},{"name":"LIS","type":"related"},{"name":"geranyl-diphosphate diphosphate-lyase [(3S)-linalool-forming] activity","type":"related"}],"termid":"GO:0034007"}


id: GO:0006361
data:
  {"annotated_genes":["SJAG_01744","SJAG_01712","SJAG_01562","SJAG_02747","SJAG_03956","SJAG_00421","SJAG_05331","SJAG_02813","SJAG_00692","SJAG_04766","SJAG_00202"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90840,92654,94889,95063,107175,108641,109231,109274,111425,115946],"is_not":false,"summary":null,"term":"GO:0006361"},{"annotations":[108640,63525,111424,95227],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0001188"}]},"cv_name":"biological_process","definition":"A transcription initiation process that takes place at a RNA polymerase I gene promoter. Ribosomal RNAs (rRNA) genes are transcribed by RNA polymerase I.","definition_xrefs":["GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-templated transcription initiation","termid":"GO:0006352"},{"relation_name":"part_of","term_name":"transcription by RNA polymerase I","termid":"GO:0006360"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00202":null,"SJAG_00421":null,"SJAG_00692":null,"SJAG_01562":null,"SJAG_01712":null,"SJAG_01744":null,"SJAG_02747":null,"SJAG_02813":null,"SJAG_03956":null,"SJAG_04766":null,"SJAG_05331":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006351"],"is_obsolete":false,"name":"transcription initiation at RNA polymerase I promoter","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000108":null},"secondary_identifiers":["GO:0001180","Reactome:R-HSA-73854"],"synonyms":[{"name":"transcription initiation from Pol I promoter","type":"exact"},{"name":"transcription initiation from RNA polymerase I promoter","type":"exact"},{"name":"transcription initiation from RNA polymerase I promoter for nuclear large rRNA transcript","type":"narrow"}],"termid":"GO:0006361","terms_by_termid":{"GO:0001188":null,"GO:0006361":null}}


id: GO:1901129
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of gentamycin.","definition_xrefs":["GOC:yaf","UniPathway:UPA00967","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoglycoside antibiotic catabolic process","termid":"GO:0030649"},{"relation_name":"is_a","term_name":"polyol catabolic process","termid":"GO:0046174"},{"relation_name":"is_a","term_name":"gentamycin metabolic process","termid":"GO:1901128"}],"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":"gentamycin catabolic process","synonyms":[{"name":"gentamycin breakdown","type":"exact"},{"name":"gentamycin catabolism","type":"exact"},{"name":"gentamycin degradation","type":"exact"}],"termid":"GO:1901129"}


id: MONDO:0007602
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete favism, susceptibility to (obsolete MONDO:0007602)","secondary_identifiers":["OMIM:134700"],"synonyms":[{"name":"favism, susceptibility to","type":"exact"},{"name":"moved to {300908}","type":"related"}],"termid":"MONDO:0007602","xrefs":{"Monarch":{"xref_id":"0007602"}}}


id: PBO:0091812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP citrate synthase subunit 1","termid":"PBO:0091812"}


id: MOD:00764
data:
  {"annotated_genes":["SJAG_04819","SJAG_03009","SJAG_01488"],"annotation_feature_type":"gene","cv_annotations":{"PSI-MOD":[{"annotations":[80094,80166,80089,80165,80091,80093,80168,79953,80167,80095,80169,80170,80092,79955,79954,79952,79951,80090],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MOD:00693"}]},"cv_name":"PSI-MOD","definition":"A protein modification that effectively results from forming an adduct with a carbohydrate-like group either through enzymatic formation of a glycosidic bond, or through non-enzymatic glycation formation of a Schiff-base or an Amadori ketosamine residue adduct.","definition_xrefs":["PubMed:3743566","PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01488":null,"SJAG_03009":null,"SJAG_04819":null},"genotype_count":0,"is_obsolete":false,"name":"glycoconjugated residue","references_by_uniquename":{"PMID:36408920":null},"termid":"MOD:00764","terms_by_termid":{"MOD:00693":null}}


id: GO:0090520
data:
  {"annotated_genes":["SJAG_05290"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104674],"is_not":false,"summary":null,"term":"GO:0090520"}]},"cv_name":"biological_process","definition":"The series of molecular signals mediated by a sphingolipid.","definition_xrefs":["PMID:9525917"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signal transduction","termid":"GO:0007165"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05290":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"sphingolipid mediated signaling pathway","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"ceramide 1-phosphate signaling pathway","type":"narrow"},{"name":"ceramide signaling pathway","type":"narrow"},{"name":"sphingolipid mediated signal transduction","type":"exact"},{"name":"sphingolipid signaling pathway","type":"related"},{"name":"sphingolipid-mediated signaling pathway","type":"exact"},{"name":"sphingosine signaling pathway","type":"narrow"}],"termid":"GO:0090520","terms_by_termid":{"GO:0090520":null}}


id: GO:0098549
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A stable intercellular bridge between somatic cells. Examples include the intercellular bridges between ovarian follicle cells in insects and between imaginal disc cells in insects.","definition_xrefs":["PMID:670316","GOC:dos","PMID:22135360"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intercellular bridge","termid":"GO:0045171"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"somatic ring canal","termid":"GO:0098549"}


id: MONDO:1011667
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lundehund syndrome, non-human animal","secondary_identifiers":["OMIA:002031"],"termid":"MONDO:1011667","xrefs":{"Monarch":{"xref_id":"1011667"}}}


id: PR:Q9URU2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA replication ATP-dependent helicase/nuclease DNA2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10887:SF14","OMA:SCHPO03776","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 ATP-dependent helicase/nuclease dna2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC16D10.04c","secondary_identifiers":["UniProtKB:Q9URU2"],"synonyms":[{"name":"Spom972h-DNA2","type":"exact"}],"termid":"PR:Q9URU2"}


id: PBO:0072848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"suppressor APC domain containing 2 pseudogene 3","termid":"PBO:0072848"}


id: MONDO:0013147
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the NEXN gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial dilated cardiomyopathy","termid":"MONDO:0016333"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"dilated cardiomyopathy 1CC","secondary_identifiers":["DOID:0110424","GARD:15621","MESH:C567733","OMIM:613122","UMLS:C2751084","MEDGEN:413929"],"synonyms":[{"name":"CMD1CC","type":"exact"},{"name":"NEXN familial isolated dilated cardiomyopathy","type":"exact"},{"name":"cardiomyopathy, dilated, 1CC","type":"related"},{"name":"cardiomyopathy, dilated, type 1Cc","type":"exact"},{"name":"dilated cardiomyopathy type 1CC","type":"exact"},{"name":"familial isolated dilated cardiomyopathy caused by mutation in NEXN","type":"exact"}],"termid":"MONDO:0013147","xrefs":{"Monarch":{"xref_id":"0013147"}}}


id: PBO:0053442
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 388","termid":"PBO:0053442"}


id: GO:0015230
data:
  {"annotated_genes":["SJAG_03503"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[107052],"is_not":false,"summary":null,"term":"GO:0015230"}]},"cv_name":"molecular_function","definition":"Enables the directed movement of flavin-adenine dinucleotide (FAD) from one side of a membrane to the other. FAD forms the coenzyme of the prosthetic group of various flavoprotein oxidoreductase enzymes, in which it functions as an electron acceptor by being reversibly converted to its reduced form.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"nucleotide transmembrane transporter activity","termid":"GO:0015215"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03503":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"FAD transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0005472"],"synonyms":[{"name":"FAD carrier activity","type":"related"},{"name":"FAD transporter activity","type":"broad"},{"name":"flavin adenine dinucleotide carrier activity","type":"related"},{"name":"flavin adenine dinucleotide transmembrane transporter activity","type":"exact"},{"name":"flavin-adenine dinucleotide carrier activity","type":"related"},{"name":"flavin-adenine dinucleotide transmembrane transporter activity","type":"exact"}],"termid":"GO:0015230","terms_by_termid":{"GO:0015230":null}}


id: PBO:0055946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 55","termid":"PBO:0055946"}


id: MONDO:0008685
data:
  {"annotated_genes":["SJAG_02785"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85514],"is_not":false,"summary":null,"term":"MONDO:0008685"}]},"cv_name":"mondo","definition":"A cardiac conduction disorder characterized by an electrocardiographic finding of ventricular pre-excitation, which is a short PR interval and a long QRS interval with a delta wave. Most individuals are asymptomatic; however they can experience periods of palpitations, shortness of breath or syncope during tachycardic episodes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart conduction disease","termid":"MONDO:0000992"},{"relation_name":"is_a","term_name":"PRKAG2-related cardiomyopathy","termid":"MONDO:0800484"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02785":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"Wolff-Parkinson-White syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D014927","icd11.foundation:1091030330","Orphanet:907","HP:0001716","UMLS:C0043202","DOID:384","MEDGEN:12162","EFO:1001450","NANDO:2200217","NCIT:C35132","OMIM:194200","SCTID:17869006","ICD9:426.7"],"synonyms":[{"name":"WPW","type":"exact"},{"name":"Wolff-Parkinson-White pattern","type":"exact"},{"name":"Wolff-Parkinson-White pattern (finding)","type":"exact"},{"name":"Wolff-Parkinson-White syndrome","type":"exact"},{"name":"Wolff-Parkinson-white syndrome (disease)","type":"exact"},{"name":"Wpw syndrome","type":"related"},{"name":"accessory atrioventricular pathways","type":"related"},{"name":"anomalous A-V excitation","type":"exact"},{"name":"anomalous atrioventricular excitation","type":"exact"},{"name":"preexcitation syndrome","type":"related"},{"name":"ventricular familial preexcitation syndrome","type":"exact"}],"termid":"MONDO:0008685","terms_by_termid":{"MONDO:0008685":null},"xrefs":{"Monarch":{"xref_id":"0008685"}}}


id: GO:1901280
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of D-ribose 5-phosphate.","definition_xrefs":["GOC:TermGenie","UniPathway:UPA00293","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribose phosphate biosynthetic process","termid":"GO:0046390"},{"relation_name":"is_a","term_name":"D-ribose 5-phosphate metabolic process","termid":"GO:1901278"}],"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":"D-ribose 5-phosphate biosynthetic process","synonyms":[{"name":"D-ribose 5-phosphate anabolism","type":"exact"},{"name":"D-ribose 5-phosphate biosynthesis","type":"exact"},{"name":"D-ribose 5-phosphate formation","type":"exact"},{"name":"D-ribose 5-phosphate synthesis","type":"exact"}],"termid":"GO:1901280"}


id: FYPO:0007663
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the kinetochore of a chromosome does not occur during the second meiotic nuclear division.","definition_xrefs":["PMID:11331883","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to kinetochore during meiosis","termid":"FYPO:0004762"},{"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to kinetochore during meiosis II","synonyms":[{"name":"abolished protein localisation to kinetochore during meiosis II","type":"exact"},{"name":"abolished protein localisation to kinetochore during second meiotic nuclear division","type":"exact"}],"termid":"FYPO:0007663"}


id: PBO:0054136
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 1502","termid":"PBO:0054136"}


id: PBO:0002053
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kinesin-14 family","termid":"PBO:0002053"}


id: GO:0005222
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a cation by a channel that opens when intracellular cAMP has been bound by the channel complex or one of its constituent parts.","definition_xrefs":["GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellularly cyclic nucleotide-activated monoatomic cation channel activity","termid":"GO:0005221"}],"gene_count":0,"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":"intracellularly cAMP-activated cation channel activity","synonyms":[{"name":"HCN channel activity","type":"broad"},{"name":"hyperpolarization-activated cyclic nucleotide-gated channel activity","type":"broad"},{"name":"intracellular 3',5' cAMP activated cation channel activity","type":"exact"},{"name":"intracellular 3',5'-cAMP activated cation channel activity","type":"exact"},{"name":"intracellular adenosine 3',5'-cyclophosphate activated cation channel activity","type":"exact"},{"name":"intracellular cAMP activated cation channel activity","type":"exact"},{"name":"intracellular cAMP-activated cation channel activity","type":"exact"},{"name":"intracellular cyclic AMP activated cation channel activity","type":"exact"}],"termid":"GO:0005222"}


id: GO:0001312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Replication of rDNA following its excision from the chromosome of dividing cells as they age. Extrachromosomal rDNA forms a circle that contains at least one autonomously replicating sequence (ARS), which supports replication independent of chromosomal replication.","definition_xrefs":["GOC:jh","PMID:12044934"],"gene_count":0,"genotype_count":0,"name":"obsolete replication of extrachromosomal rDNA circles involved in replicative cell aging (obsolete GO:0001312)","synonyms":[{"name":"replication of extrachromosomal rDNA circles during replicative cell ageing","type":"related"},{"name":"replication of extrachromosomal rDNA circles during replicative cell aging","type":"related"},{"name":"replication of extrachromosomal ribosomal DNA circles during replicative cell aging","type":"related"}],"termid":"GO:0001312"}


id: FYPO:0006955
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 L-glutamine measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular amino acid level","termid":"FYPO:0003986"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular glutamine level","synonyms":[{"name":"increased cellular L-glutamine level","type":"exact"},{"name":"increased cellular glutamine level during mitotic cell cycle","type":"related"},{"name":"increased cellular glutamine level during vegetative growth","type":"exact"},{"name":"increased glutamine accumulation","type":"related"}],"termid":"FYPO:0006955"}


id: GO:0071226
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 stimulus by molecules of fungal origin such as chito-octamer oligosaccharide.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to molecule of fungal origin","termid":"GO:0002238"},{"relation_name":"is_a","term_name":"cellular response to biotic stimulus","termid":"GO:0071216"}],"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 molecule of fungal origin","synonyms":[{"name":"cellular response to fungus associated molecule","type":"exact"}],"termid":"GO:0071226"}


id: GO:0009059
data:
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