# terms

id: GO:0035374
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to chondroitin sulfate, a glycosaminoglycan made up of two alternating monosaccharides: D-glucuronic acid (GlcA) and N-acetyl-D-galactosamine (GalNAc).","definition_xrefs":["ISBN:0198506732","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosaminoglycan binding","termid":"GO:0005539"},{"relation_name":"is_a","term_name":"sulfur compound binding","termid":"GO:1901681"}],"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":"chondroitin sulfate binding","termid":"GO:0035374"}


id: GO:0042421
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of norepinephrine, a hormone secreted by the adrenal medulla, and a neurotransmitter in the sympathetic peripheral nervous system and in some tracts in the central nervous system. It is also the demethylated biosynthetic precursor of epinephrine.","definition_xrefs":["ISBN:0198506732","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"norepinephrine metabolic process","termid":"GO:0042415"},{"relation_name":"is_a","term_name":"catecholamine biosynthetic process","termid":"GO:0042423"}],"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":"norepinephrine biosynthetic process","synonyms":[{"name":"levarterenol biosynthesis","type":"exact"},{"name":"levarterenol biosynthetic process","type":"exact"},{"name":"noradrenaline biosynthesis","type":"exact"},{"name":"noradrenaline biosynthetic process","type":"exact"},{"name":"norepinephrine anabolism","type":"exact"},{"name":"norepinephrine biosynthesis","type":"exact"},{"name":"norepinephrine formation","type":"exact"},{"name":"norepinephrine synthesis","type":"exact"}],"termid":"GO:0042421"}


id: PBO:0069238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 493, pseudogene","termid":"PBO:0069238"}


id: FYPO:0006295
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which macroautophagy does not occur when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah","GO:0016236"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished macroautophagy","termid":"FYPO:0000380"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abolished macroautophagy during nitrogen starvation","synonyms":[{"name":"abolished macroautophagy during cellular response to nitrogen starvation","type":"exact"},{"name":"abolished macroautophagy during nitrogen depletion","type":"exact"},{"name":"abolished macroautophagy during nitrogen deprivation","type":"exact"},{"name":"macroautophagy abolished during nitrogen starvation","type":"exact"}],"termid":"FYPO:0006295"}


id: PBO:0084898
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial translation release factor; involved in stop codon recognition and hydrolysis of the peptidyl-tRNA bond during mitochondrial translation; lack of MRF1 causes mitochondrial genome instability","termid":"PBO:0084898"}


id: PBO:0073661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SINHCAF pseudogene 1","termid":"PBO:0073661"}


id: GO:0021951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The creation and reception of signals that guide a precerebellar neuron towards their signals, where this process is involved in tangential migration.","definition_xrefs":["GO_REF:0000021","GOC:cls","GOC:jid","GOC:dgh","PMID:15157725","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive chemotaxis","termid":"GO:0050918"},{"relation_name":"part_of","term_name":"brainstem precerebellar neuron precursor migration","termid":"GO:0021949"}],"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":"chemoattraction involved in precerebellar neuron migration","synonyms":[{"name":"positive chemotaxis involved in precerebellar neuron migration","type":"exact"}],"termid":"GO:0021951"}


id: GO:0110046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A signal transduction process that contributes to cell cycle switching, mitotic to meiotic cell cycle.","definition_xrefs":["GOC:al","PMID:17674143"],"gene_count":0,"genotype_count":0,"name":"obsolete signal transduction involved in cell cycle switching, mitotic to meiotic cell cycle (obsolete GO:0110046)","termid":"GO:0110046"}


id: MONDO:0017598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Primary cutaneous anaplastic large cell lymphoma (C-ALCL) is a rare T-cell non-Hodgkin lymphoma that affects the skin and generally shows no extracutaneous involvement at presentation. It belongs to the spectrum of primary cutaneous CD30+ lymphoproliferative disorders along with lymphomatoid papulosis with which it shares overlapping clinical and histopathologic features.","definition_xrefs":["Orphanet:300865"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary cutaneous T-cell non-Hodgkin lymphoma","termid":"MONDO:0000607"},{"relation_name":"is_a","term_name":"primary cutaneous CD30+ T-cell lymphoproliferative disease","termid":"MONDO:0018897"},{"relation_name":"is_a","term_name":"anaplastic large cell lymphoma","termid":"MONDO:0020325"},{"relation_name":"is_a","term_name":"anaplastic cancer","termid":"MONDO:0020633"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"primary cutaneous anaplastic large cell lymphoma","secondary_identifiers":["icd11.foundation:1972636482","GARD:21247","ONCOTREE:PCALCL","MedDRA:10065863","MESH:D054446","MEDGEN:266255","UMLS:C1301362","NCIT:C6860"],"synonyms":[{"name":"ALCL, cutaneous","type":"exact"},{"name":"C-ALCL","type":"exact"},{"name":"anaplastic large-cell lymphoma, primary cutaneous type","type":"exact"},{"name":"primary C-ALCL","type":"exact"},{"name":"primary anaplastic large cell lymphoma of skin","type":"exact"},{"name":"primary anaplastic large cell lymphoma of the skin","type":"exact"},{"name":"primary cutaneous CD30 Positive anaplastic large cell lymphoma","type":"exact"},{"name":"primary cutaneous CD30+ ALCL","type":"exact"},{"name":"primary cutaneous CD30+ anaplastic large cell lymphoma","type":"exact"},{"name":"regressive atypical histiocytosis","type":"exact"}],"termid":"MONDO:0017598","xrefs":{"Monarch":{"xref_id":"0017598"}}}


id: SO:0001077
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Polypeptide region traversing the lipid bilayer.","definition_xrefs":["UniProt:curator_manual","EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramembrane_polypeptide_region","termid":"SO:0001075"}],"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":"transmembrane_polypeptide_region","secondary_identifiers":["BS:00158"],"synonyms":[{"name":"transmem","type":"related"},{"name":"transmembrane","type":"related"},{"name":"transmembrane polypeptide region","type":"exact"}],"termid":"SO:0001077"}


id: PBO:0071166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 5","termid":"PBO:0071166"}


id: MONDO:0001331
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"conjunctival disorder","termid":"MONDO:0006170"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"conjunctival deposit","secondary_identifiers":["SCTID:62660000","UMLS:C0162280","DOID:11653","ICD9:372.56","MEDGEN:511536"],"termid":"MONDO:0001331","xrefs":{"Monarch":{"xref_id":"0001331"}}}


id: FYPO:0006236
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells contain a normal (i.e. indistinguishable from wild type) number of monomeric ribosomes (80S monosomes) in the cytosol.","definition_xrefs":["PMID:18065650","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of macromolecular complex","termid":"FYPO:0006235"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal cytosolic monomeric ribosome level","synonyms":[{"name":"cytosolic monomeric ribosomes present at normal level","type":"exact"},{"name":"normal cytosolic 80S monosome level","type":"exact"},{"name":"normal cytosolic monomeric 80S ribosome level","type":"exact"},{"name":"normal cytosolic monomeric ribosome level during mitotic cell cycle","type":"related"},{"name":"normal cytosolic monomeric ribosome level during vegetative growth","type":"exact"},{"name":"normal cytosolic ribosome level","type":"broad"},{"name":"normal level of cytosolic monomeric ribosomes","type":"exact"}],"termid":"FYPO:0006236"}


id: GO:0047611
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N(8)-acetylspermidine + H2O = acetate + spermidine.","definition_xrefs":["RHEA:23928","EC:3.5.1.48"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"},{"relation_name":"is_a","term_name":"deacetylase activity","termid":"GO:0019213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0019213"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824","GO:0019213","GO:0016810"],"is_obsolete":false,"name":"acetylspermidine deacetylase activity","secondary_identifiers":["MetaCyc:ACETYLSPERMIDINE-DEACETYLASE-RXN","KEGG_REACTION:R07300"],"synonyms":[{"name":"8-N-acetylspermidine amidohydrolase activity","type":"related"},{"name":"N(1)-acetylspermidine amidohydrolase activity","type":"related"},{"name":"N(8)-acetylspermidine amidohydrolase activity","type":"related"},{"name":"N(8)-acetylspermidine deacetylase activity","type":"related"},{"name":"N(8)-monoacetylspermidine deacetylase activity","type":"related"},{"name":"N-acetylspermidine deacetylase activity","type":"broad"},{"name":"N1-acetylspermidine amidohydrolase activity","type":"related"},{"name":"N8-acetylspermidine amidohydrolase activity","type":"related"},{"name":"N8-acetylspermidine deacetylase activity","type":"related"},{"name":"N8-monoacetylspermidine deacetylase activity","type":"related"}],"termid":"GO:0047611"}


id: PBO:0087165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase III subunit C31","termid":"PBO:0087165"}


id: PBO:0110333
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP5PF pseudogene 3","termid":"PBO:0110333"}


id: GO:0098684
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A ribbon synapse between a retinal photoreceptor cell (rod or cone) and a retinal bipolar cell. These contain a plate-like synaptic ribbon.","definition_xrefs":["PMID:15626493"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribbon synapse","termid":"GO:0097470"}],"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":"photoreceptor ribbon synapse","termid":"GO:0098684"}


id: PBO:0000212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SEL1 repeat protein","termid":"PBO:0000212"}


id: MONDO:0010082
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subaortic stenosis-short stature syndrome","secondary_identifiers":["GARD:405","MESH:C537749","UMLS:C0795947","Orphanet:3191","OMIM:271960","MEDGEN:167085"],"synonyms":[{"name":"Onat syndrome","type":"exact"},{"name":"subaortic stenosis short stature syndrome","type":"related"},{"name":"subaortic stenosis--short stature syndrome","type":"related"}],"termid":"MONDO:0010082","xrefs":{"Monarch":{"xref_id":"0010082"}}}


id: PBO:0064987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich protein BstNI subfamily 4","termid":"PBO:0064987"}


id: PBO:0053135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM domain binding 2","termid":"PBO:0053135"}


id: PBO:0057990
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3914-2","termid":"PBO:0057990"}


id: GO:0061574
data:
  {"annotated_genes":["SJAG_05926","SJAG_00888"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[102333,113484],"is_not":false,"summary":null,"term":"GO:0061574"}]},"cv_name":"cellular_component","definition":"A protein complex involved in regulation of mRNA processing and apoptosis. It binds to RNA in a sequence-independent manner and is recruited to the EJC prior to or during the splicing process. In humans the core proteins are RNPS1, SAP18 and ACIN1.","definition_xrefs":["PMID:12665594","PMID:16314458","GOC:dph","PMID:22388736"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00888":null,"SJAG_05926":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"ASAP complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061574","terms_by_termid":{"GO:0061574":null}}


id: PBO:0088185
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zinc-finger DNA-binding transcription factor; targets strong transcriptional activator Met4p to promoters of sulfur metabolic genes; involved in transcriptional regulation of the methionine biosynthetic genes; feedforward loop controlling expression of MET32 and the lack of such a loop for MET31 may account for the differential actions of Met31p and Met32p; MET31 has a paralog, MET32, that arose from the whole genome duplication","termid":"PBO:0088185"}


id: GO:0017098
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a sulfonylurea receptor, a regulatory subunit of the ATP-sensitive potassium ion channel.","definition_xrefs":["GOC:ceb","PMID:11938023"],"direct_ancestors":[{"relation_name":"is_a","term_name":"signaling receptor binding","termid":"GO:0005102"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"sulfonylurea receptor binding","synonyms":[{"name":"sulfonylurea receptor ligand","type":"narrow"},{"name":"sulphonylurea receptor binding","type":"exact"}],"termid":"GO:0017098"}


id: PBO:0044919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DiGeorge syndrome critical region gene 5","termid":"PBO:0044919"}


id: MONDO:0957308
data:
  {"annotated_genes":["SJAG_01857"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85561],"is_not":false,"summary":null,"term":"MONDO:0957308"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01857":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"spastic paraplegia 90A, autosomal dominant","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620416","DOID:0070459","UMLS:C5830574","MEDGEN:1841210"],"termid":"MONDO:0957308","terms_by_termid":{"MONDO:0957308":null},"xrefs":{"Monarch":{"xref_id":"0957308"}}}


id: PBO:0054538
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 1938","termid":"PBO:0054538"}


id: PBO:0000199
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"previously annotated as dubious","termid":"PBO:0000199"}


id: SO:0001554
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant which changes polypeptide functioning with respect to a reference sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translational_product_function_variant","termid":"SO:0001539"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polypeptide_function_variant","synonyms":[{"name":"polypeptide function variant","type":"exact"}],"termid":"SO:0001554"}


id: MONDO:0100066
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tyrosine hydroxylase deficiency in which individuals are extremely sensitive to levodopa therapy. In this very severe form, treatment with levodopa is often limited by intolerable dyskinesias.","definition_xrefs":["PMID:20301610"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tyrosine hydroxylase deficiency","termid":"MONDO:0100064"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"TH-deficient progressive infantile encephalopathy","synonyms":[{"name":"tyrosine hydroxylase-deficient progressive infantile encephalopathy","type":"exact"}],"termid":"MONDO:0100066","xrefs":{"Monarch":{"xref_id":"0100066"}}}


id: MOD:00974
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3'-chloro-L-tyrosine","termid":"MOD:01046"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(35)Cl labeled 3'-chlorotyrosine","termid":"MOD:00974"}


id: GO:0050770
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of axonogenesis, the generation of an axon, the long process of a neuron.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neuron projection development","termid":"GO:0010975"},{"relation_name":"is_a","term_name":"regulation of anatomical structure morphogenesis","termid":"GO:0022603"},{"relation_name":"regulates","term_name":"axonogenesis","termid":"GO:0007409"}],"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 axonogenesis","termid":"GO:0050770"}


id: PR:Q9USJ6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC4B3.06c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9USJ6"],"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":"NAD(P)H-dependent FMN reductase C4B3.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC4B3.06c","synonyms":[{"name":"FMN reductase C4B3.06c (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"FMN reductase [NAD(P)H] (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPCC4B3.06c","type":"exact"},{"name":"azoreductase C4B3.06c (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9USJ6"}


id: MONDO:0018210
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Alexander disease type II (AxD type II) is an astrogliopathy and a form of Alexander disease (AxD) characterized by ataxia, bulbar symptoms, spastic paraparesis, palatal myoclonus, and autonomic symptoms.","definition_xrefs":["Orphanet:363722"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Alexander disease","termid":"MONDO:0008752"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"Alexander disease type II","secondary_identifiers":["MEDGEN:1842714","UMLS:C5679914","GARD:17573","NANDO:1200556"],"synonyms":[{"name":"AxD type II","type":"exact"}],"termid":"MONDO:0018210","xrefs":{"Monarch":{"xref_id":"0018210"}}}


id: SO:0002144
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A histone 2AZ modification where the modification is the acetylation of the residue.","definition_xrefs":["PMID:19385636","PMID:24316985","PMID:27087541"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_2A_acetylation_site","termid":"SO:0002142"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"histone_2AZ_acetylation_site","synonyms":[{"name":"H2A.Zac","type":"exact"},{"name":"H2AZac","type":"exact"},{"name":"histone 2AZ acetylation site","type":"exact"}],"termid":"SO:0002144"}


id: GO:0051106
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of DNA ligation, the re-formation of a broken phosphodiester bond in the DNA backbone, carried out by DNA ligase.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of DNA metabolic process","termid":"GO:0051054"},{"relation_name":"is_a","term_name":"regulation of DNA ligation","termid":"GO:0051105"},{"relation_name":"positively_regulates","term_name":"DNA ligation","termid":"GO:0006266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"positive regulation of DNA ligation","synonyms":[{"name":"activation of DNA ligation","type":"narrow"},{"name":"stimulation of DNA ligation","type":"narrow"},{"name":"up regulation of DNA ligation","type":"exact"},{"name":"up-regulation of DNA ligation","type":"exact"},{"name":"upregulation of DNA ligation","type":"exact"}],"termid":"GO:0051106"}


id: MONDO:0001370
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fluid collection within the pericardial sac, usually due to inflammation.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pericardium disorder","termid":"MONDO:0000474"}],"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":"pericardial effusion","secondary_identifiers":["UMLS:C0031039","SCTID:373945007","DOID:118","icd11.foundation:2002014072","HP:0001698","MESH:D010490","NCIT:C3319","MEDGEN:10653"],"synonyms":[{"name":"fluid, pericardial","type":"exact"},{"name":"pericardial effusion","type":"exact"},{"name":"pericardial effusion (disease)","type":"exact"},{"name":"pericardial fluid","type":"exact"}],"termid":"MONDO:0001370","xrefs":{"Monarch":{"xref_id":"0001370"}}}


id: PBO:0077037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THO complex subunit 5","termid":"PBO:0077037"}


id: GO:0090402
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A cellular senescence process associated with the dismantling of a cell as a response to oncogenic stress, such as the activation of the Ras oncogenic family.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular senescence","termid":"GO:0090398"}],"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":"oncogene-induced cell senescence","synonyms":[{"name":"OIS","type":"exact"}],"termid":"GO:0090402"}


id: FYECO:0000206
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which caesium chloride was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ CsCl","synonyms":[{"name":"caesium chloride added","type":"exact"},{"name":"cesium chloride added","type":"exact"}],"termid":"FYECO:0000206"}


id: MONDO:0003933
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An uncommon malignant neoplasm that arises from the chest wall bones. Representative examples include chondrosarcoma, osteosarcoma, and Ewing sarcoma/peripheral primitive neuroectodermal tumor.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"chest wall lymphoma","termid":"MONDO:0003985"},{"relation_name":"is_a","term_name":"bone cancer","termid":"MONDO:0002129"},{"relation_name":"is_a","term_name":"malignant neoplasm of chest wall","termid":"MONDO:0021323"}],"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":"chest wall bone cancer","secondary_identifiers":["MEDGEN:233148","NCIT:C6724","DOID:6579","UMLS:C1334572"],"synonyms":[{"name":"bone cancer of chest wall","type":"exact"},{"name":"chest wall bone cancer","type":"exact"},{"name":"malignant bone neoplasm of chest wall","type":"related"},{"name":"malignant bone neoplasm of the chest wall","type":"exact"},{"name":"malignant bone tumor of chest wall","type":"exact"},{"name":"malignant bone tumor of the chest wall","type":"exact"},{"name":"malignant bone tumour of chest wall","type":"exact"},{"name":"malignant bone tumour of the chest wall","type":"exact"},{"name":"malignant chest wall bone neoplasm","type":"exact"},{"name":"malignant chest wall bone tumor","type":"exact"},{"name":"malignant chest wall bone tumour","type":"exact"}],"termid":"MONDO:0003933","xrefs":{"Monarch":{"xref_id":"0003933"}}}


id: GO:0004218
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of peptide bonds. Similar to cathepsin L, but with much less activity on the terminal bond of Z-Phe-Arg-NHMec, and more activity on the terminal bond of Z-Val-Val-Arg-Xaa compounds.","definition_xrefs":["EC:3.4.22.27"],"gene_count":0,"genotype_count":0,"name":"obsolete cathepsin S activity (obsolete GO:0004218)","synonyms":[{"name":"cathepsin S activity","type":"exact"}],"termid":"GO:0004218"}


id: PBO:0091400
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein phosphatase PP2A catalytic subunit Ppa1","termid":"PBO:0091400"}


id: MONDO:0015728
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"15q overgrowth syndrome","termid":"MONDO:0017806"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal trisomy 15q","secondary_identifiers":["MESH:C538036","Orphanet:1707","UMLS:C2931705","GARD:18740","NORD:942","MEDGEN:419879"],"synonyms":[{"name":"Chromosome 15, Distal Trisomy 15q","type":"exact"},{"name":"distal duplication 15q","type":"exact"},{"name":"distal trisomy type 15q","type":"exact"},{"name":"telomeric duplication 15q","type":"exact"},{"name":"trisomy 15qter","type":"exact"}],"termid":"MONDO:0015728","xrefs":{"Monarch":{"xref_id":"0015728"}}}


id: PR:Q9USZ3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A small nuclear ribonucleoprotein E that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02989","PANTHER:PTHR11193: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":"small nuclear ribonucleoprotein E (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC11G11.06c","secondary_identifiers":["UniProtKB:Q9USZ3"],"synonyms":[{"name":"Sm protein E (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Sm-E (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SmE (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SNRPE","type":"exact"},{"name":"snRNP-E (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9USZ3"}


id: GO:0140354
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a lipid from outside of a cell into a cell. This may occur via transport across the plasma membrane or via endocytosis.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid transport","termid":"GO:0006869"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"lipid import into cell","synonyms":[{"name":"lipid uptake","type":"broad"}],"termid":"GO:0140354"}


id: PBO:0004174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER oxidoreductin Ero1a","termid":"PBO:0004174"}


id: SO:0000511
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene in germline configuration including at least one J-gene and one C-gene.","direct_ancestors":[{"relation_name":"has_part","term_name":"J_gene_segment","termid":"SO:0000470"},{"relation_name":"has_part","term_name":"C_gene_segment","termid":"SO:0000478"},{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_gene_cluster","termid":"SO:0000482"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"J_C_cluster","synonyms":[{"name":"J C cluster","type":"exact"},{"name":"J-C-CLUSTER","type":"exact"}],"termid":"SO:0000511"}


id: PBO:0042240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-C motif chemokine receptor 3","termid":"PBO:0042240"}


id: GO:0004521
data:
  {"annotated_genes":["SJAG_02547","SJAG_04527","SJAG_00955","SJAG_02553","SJAG_04916","SJAG_01948","SJAG_03796","SJAG_03328","SJAG_03234","SJAG_03952","SJAG_02039","SJAG_02156","SJAG_03425","SJAG_02374","SJAG_01551","SJAG_04198","SJAG_01463","SJAG_04006","SJAG_04435","SJAG_00997","SJAG_03962","SJAG_00772","SJAG_01433","SJAG_04519","SJAG_04587","SJAG_02790","SJAG_00400","SJAG_04907","SJAG_01623","SJAG_01260","SJAG_01476","SJAG_03689","SJAG_04582","SJAG_01884","SJAG_02621","SJAG_04091","SJAG_06022","SJAG_00754","SJAG_04019","SJAG_03539","SJAG_00306","SJAG_04885","SJAG_06613"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[87559,88244,88731,89592,89835,95031,106626,108156,112058,115467,117200],"is_not":false,"summary":null,"term":"GO:0004521"},{"annotations":[91357,109053],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042781"},{"annotations":[117223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070551"},{"annotations":[90901],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990174"},{"annotations":[102620,72897,115129,101361,108996],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004525"},{"annotations":[114531,117719,103728,93910,98688,104824,95695,104823,103945,95986,112624,114444],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000171"},{"annotations":[114445,98689,93911,103946,95987,103729,112625,101240,117720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004526"},{"annotations":[117225,91415],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016891"},{"annotations":[89439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008419"},{"annotations":[97317,87516,108279,102127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004523"},{"annotations":[99987,100525,105090,116809],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000213"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of ester linkages within ribonucleic acid by creating internal breaks.","definition_xrefs":["GOC:mah","ISBN:0198547684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endonuclease activity","termid":"GO:0004519"},{"relation_name":"is_a","term_name":"RNA nuclease activity","termid":"GO:0004540"}],"gene_count":43,"genes_by_uniquename":{"SJAG_00306":null,"SJAG_00400":null,"SJAG_00754":null,"SJAG_00772":null,"SJAG_00955":null,"SJAG_00997":null,"SJAG_01260":null,"SJAG_01433":null,"SJAG_01463":null,"SJAG_01476":null,"SJAG_01551":null,"SJAG_01623":null,"SJAG_01884":null,"SJAG_01948":null,"SJAG_02039":null,"SJAG_02156":null,"SJAG_02374":null,"SJAG_02547":null,"SJAG_02553":null,"SJAG_02621":null,"SJAG_02790":null,"SJAG_03234":null,"SJAG_03328":null,"SJAG_03425":null,"SJAG_03539":null,"SJAG_03689":null,"SJAG_03796":null,"SJAG_03952":null,"SJAG_03962":null,"SJAG_04006":null,"SJAG_04019":null,"SJAG_04091":null,"SJAG_04198":null,"SJAG_04435":null,"SJAG_04519":null,"SJAG_04527":null,"SJAG_04582":null,"SJAG_04587":null,"SJAG_04885":null,"SJAG_04907":null,"SJAG_04916":null,"SJAG_06022":null,"SJAG_06613":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016788","GO:0003824","GO:0016787","GO:0140098","GO:0003674"],"is_obsolete":false,"name":"RNA endonuclease activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-9708327","Reactome:R-HSA-9009941","Reactome:R-HSA-426520","Reactome:R-HSA-6791223","Reactome:R-HSA-5601910","Reactome:R-HSA-9023909","Reactome:R-HSA-9023912","Reactome:R-HSA-9708812","Reactome:R-HSA-927836","Reactome:R-HSA-425923","Reactome:R-HSA-5601887","Reactome:R-HSA-9009936","Reactome:R-HSA-6814555"],"synonyms":[{"name":"endonuclease G activity","type":"related"},{"name":"endoribonuclease activity","type":"exact"}],"termid":"GO:0004521","terms_by_termid":{"GO:0000171":null,"GO:0000213":null,"GO:0004521":null,"GO:0004523":null,"GO:0004525":null,"GO:0004526":null,"GO:0008419":null,"GO:0016891":null,"GO:0042781":null,"GO:0070551":null,"GO:1990174":null}}


id: GO:0050194
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + phosphonoacetaldehyde = acetaldehyde + H+ + phosphate.","definition_xrefs":["RHEA:18905"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid carbon-phosphorus bonds","termid":"GO:0016827"}],"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:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"phosphonoacetaldehyde hydrolase activity","secondary_identifiers":["EC:3.11.1.1","KEGG_REACTION:R00747","MetaCyc:PHOSPHONOACETALDEHYDE-HYDROLASE-RXN"],"synonyms":[{"name":"2-oxoethylphosphonate phosphonohydrolase activity","type":"related"},{"name":"2-phosphonoacetylaldehyde phosphonohydrolase activity","type":"related"},{"name":"phosphonatase activity","type":"related"},{"name":"phosphonoacetylaldehyde phosphonohydrolase activity","type":"related"}],"termid":"GO:0050194"}


id: GO:0003318
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a cell toward the midline that contributes to the progression of the heart over time.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration involved in heart development","termid":"GO:0060973"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell migration to the midline involved in heart development","termid":"GO:0003318"}


id: PBO:0052466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLF transcription factor 12","termid":"PBO:0052466"}


id: FYPO:0000025
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a cell has a larger volume than normal. In a swollen cell, both length and diameter are greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cell size","termid":"FYPO:0008096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000005","FYPO:0001985"],"is_obsolete":false,"name":"swollen cell","synonyms":[{"name":"cell morphology, swollen cells","type":"exact"},{"name":"enlarged cell","type":"related"},{"name":"increased cell size","type":"related"},{"name":"increased cell volume","type":"exact"},{"name":"large cell","type":"related"}],"termid":"FYPO:0000025"}


id: PBO:0113318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in sphingolipid metabolism; localizes to vacuolar contact sites with mitochondria, ER and peroxisomes; mutant has enhanced sensitivity to overexpression of mutant huntingtin; relative distribution within the vacuolar membrane changes upon DNA replication stress","termid":"PBO:0113318"}


id: PBO:0076144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUCLG2 pseudogene 3","termid":"PBO:0076144"}


id: PBO:0050470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOXA cluster antisense RNA 2","termid":"PBO:0050470"}


id: MONDO:0005526
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A serious infectious disorder that follows wound contamination by the Gram-positive bacterium Clostridium tetani. The bacteria produce a neurotoxin called tetanospasmin, which causes muscle spasm in the jaw and other anatomic sites.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"infectious disorder of the nervous system","termid":"MONDO:0020010"},{"relation_name":"is_a","term_name":"Clostridium infectious disease","termid":"MONDO:0024388"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetanus","secondary_identifiers":["MedDRA:10043376","GARD:5144","SCTID:276202003","ICD9:037","NCIT:C85185","MESH:D013742","SCTID:76902006","UMLS:C0039614","MEDGEN:21489","icd11.foundation:1793762788","DOID:11338","Orphanet:3299","EFO:0005593"],"synonyms":[{"name":"Clostridium tetani caused infectious disease of the nervous system","type":"exact"},{"name":"Clostridium tetani infectious disease of the nervous system","type":"exact"},{"name":"clostridial tetanus","type":"exact"},{"name":"infection due to Clostridium tetani","type":"exact"},{"name":"lockjaw","type":"related"}],"termid":"MONDO:0005526","xrefs":{"Monarch":{"xref_id":"0005526"}}}


id: GO:1903096
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a meiotic spindle midzone.","definition_xrefs":["GOC:kmv","PMID:12707312","GO_REF:0000087","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to meiotic spindle","termid":"GO:1905359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"protein localization to meiotic spindle midzone","synonyms":[{"name":"protein localisation in meiotic spindle midzone","type":"exact"},{"name":"protein localisation to meiotic spindle midzone","type":"exact"},{"name":"protein localization in meiotic spindle midzone","type":"exact"}],"termid":"GO:1903096"}


id: MONDO:0009311
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"grouped pigmentation of the retina","secondary_identifiers":["UMLS:C1856244","MEDGEN:341100","MESH:C565530","OMIM:233800"],"synonyms":[{"name":"grouped pigmentation of retinal pigment epithelium","type":"related"},{"name":"grouped pigmentation of the macula","type":"related"},{"name":"grouped pigmentation of the retina","type":"exact"}],"termid":"MONDO:0009311","xrefs":{"Monarch":{"xref_id":"0009311"}}}


id: GO:0004705
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: JUN + ATP = JUN phosphate + ADP. This reaction is the phosphorylation and activation of members of the JUN family, a gene family that encodes nuclear transcription factors.","definition_xrefs":["ISBN:0198506732","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"MAP kinase activity","termid":"GO:0004707"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0004672"},{"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:0140096"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003824","GO:0004672","GO:0016740","GO:0016301","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"JUN kinase activity","secondary_identifiers":["Reactome:R-HSA-205075","Reactome:R-HSA-205132","Reactome:R-HSA-168136","Reactome:R-HSA-204949","Reactome:R-HSA-9673789"],"synonyms":[{"name":"JNK","type":"exact"},{"name":"JNK3alpha1","type":"related"},{"name":"SAPK1","type":"narrow"},{"name":"c-Jun N-terminal kinase activity","type":"narrow"}],"termid":"GO:0004705"}


id: MONDO:0019565
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary von Willebrand disease (VWD) is a hereditary bleeding disorder caused by a genetic anomaly leading to quantitative, structural or functional abnormalities of the Willebrand factor (von Willebrand factor; VWF). Two major groups of VWF deficiency have been defined: quantitative and partial (type 1) or total (type 3), and qualitative (type 2) with several subtypes (2A, 2B, 2M, 2N).","definition_xrefs":["Orphanet:903"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemorrhagic disease","termid":"MONDO:0002243"},{"relation_name":"is_a","term_name":"inherited blood coagulation disorder","termid":"MONDO:0021181"},{"relation_name":"is_a","term_name":"von Willebrand disease (hereditary or acquired)","termid":"MONDO:0024574"}],"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":"hereditary von Willebrand disease","secondary_identifiers":["UMLS:C5703318","icd11.foundation:2112021600","MEDGEN:1814986","ICD9:286.4","MESH:C531844","DOID:12531","SCTID:234446004","GARD:7867","MedDRA:10047715"],"synonyms":[{"name":"congenital von willebrand disease","type":"related"},{"name":"congenital von willebrand's disease","type":"exact"},{"name":"hereditary von Willebrand disease","type":"exact"},{"name":"hereditary von Willebrand disease (hereditary or acquired)","type":"exact"},{"name":"vascular haemophilia","type":"broad"},{"name":"vascular hemophilia","type":"broad"},{"name":"vascular pseudohemophilia","type":"exact"},{"name":"von Willebrand disease","type":"broad"},{"name":"von Willebrand disorder","type":"broad"},{"name":"von Willebrand's disease","type":"related"},{"name":"von Willebrand's-Jurgens' disease","type":"broad"},{"name":"von Willebrand-Jrgens disease","type":"exact"},{"name":"von Willebrand-Jurgens disease","type":"broad"}],"termid":"MONDO:0019565","xrefs":{"Monarch":{"xref_id":"0019565"}}}


id: GO:0071655
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of production of granulocyte colony-stimulating factor.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of macrophage colony-stimulating factor production","termid":"GO:1901256"},{"relation_name":"regulates","term_name":"granulocyte colony-stimulating factor production","termid":"GO:0071611"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of granulocyte colony-stimulating factor production","synonyms":[{"name":"regulation of CSF3 production","type":"exact"},{"name":"regulation of G-CSF production","type":"exact"},{"name":"regulation of colony stimulating factor 3 (granulocyte) production","type":"exact"},{"name":"regulation of filgrastim production","type":"exact"},{"name":"regulation of granulocyte colony stimulating factor production","type":"exact"},{"name":"regulation of lenograstim production","type":"exact"},{"name":"regulation of pluripoietin production","type":"exact"}],"termid":"GO:0071655"}


id: SO:0001992
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A non-synonymous variant is an inframe, protein altering variant, resulting in a codon change.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inframe_variant","termid":"SO:0001650"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nonsynonymous_variant","synonyms":[{"name":"non_synonymous_coding","type":"exact"},{"name":"nonsynonymous variant","type":"exact"}],"termid":"SO:0001992"}


id: GO:0052874
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: FMNH2 + NAD+ = FMN + NADH + 2 H+.","definition_xrefs":["RHEA:21620"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor","termid":"GO:0016646"}],"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:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"FMN reductase (NADH) activity","secondary_identifiers":["EC:1.5.1.42","KEGG_REACTION:R05705"],"synonyms":[{"name":"NADH dehydrogenase (FMN) activity","type":"exact"},{"name":"NADH-FMN reductase activity","type":"related"},{"name":"NADH-dependent FMN reductase activity","type":"related"}],"termid":"GO:0052874"}


id: PBO:0111832
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-C5HC2 type","termid":"PBO:0111832"}


id: MOD:01194
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative -","definition_xrefs":["Unimod:264#S","PubMed:15279557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphorylation to pyridyl thiol","termid":"MOD:00586"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphorylation to pyridyl thiol - site S","synonyms":[{"name":"PET","type":"related"},{"name":"phosphorylation to pyridyl thiol","type":"related"}],"termid":"MOD:01194"}


id: MONDO:0016322
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Neuroendocrine cell hyperplasia of infancy (NCHI) is a non-lethal pediatric form of interstitial lung disease (ILD) characterized by tachypnea without respiratory failure.","definition_xrefs":["Orphanet:217560"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperplasia","termid":"MONDO:0005043"},{"relation_name":"is_a","term_name":"interstitial lung disease specific to infancy","termid":"MONDO:0017019"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroendocrine cell hyperplasia of infancy","secondary_identifiers":["NCIT:C120169","UMLS:C3161105","SCTID:707435002","GARD:20517","icd11.foundation:1641999159","MEDGEN:837309","ICD10CM:J84.841"],"synonyms":[{"name":"CTI","type":"exact"},{"name":"NCHI","type":"exact"},{"name":"NEHI","type":"exact"},{"name":"chronic tachypnoe of infancy","type":"exact"}],"termid":"MONDO:0016322","xrefs":{"Monarch":{"xref_id":"0016322"}}}


id: MONDO:0044221
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete blood group--lutheran inhibitor (obsolete MONDO:0044221)","secondary_identifiers":["OMIM:111150"],"synonyms":[{"name":"INLU","type":"related"},{"name":"blood group--Lutheran INHIBITOR","type":"related"},{"name":"dominant 50U (A-B-) phenotype","type":"related"}],"termid":"MONDO:0044221","xrefs":{"Monarch":{"xref_id":"0044221"}}}


id: GO:0002024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that results in increased metabolic rate in tissues of an organism. It is triggered by the detection of dietary excess. This process is achieved via signaling in the sympathetic nervous system.","definition_xrefs":["PMID:12161655"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adaptive thermogenesis","termid":"GO:1990845"},{"relation_name":"part_of","term_name":"response to dietary excess","termid":"GO:0002021"}],"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":"diet induced thermogenesis","termid":"GO:0002024"}


id: GO:0099515
data:
  {"annotated_genes":["SJAG_00938","SJAG_03011"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[69324,115319],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030050"}]},"cv_name":"biological_process","definition":"The transport of organelles or other particles from one location in the cell to another along actin filaments.","definition_xrefs":["GOC:dos","GOC:mah","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoskeleton-dependent intracellular transport","termid":"GO:0030705"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00938":null,"SJAG_03011":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"actin filament-based transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0099515","terms_by_termid":{"GO:0030050":null}}


id: PBO:0089959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH pyrophosphatase","termid":"PBO:0089959"}


id: PBO:0004777
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron-sulfur protein Isa2","termid":"PBO:0004777"}


id: MONDO:0017875
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bolivian hemorrhagic fever (BHF), caused by the Machupo virus (MACV), is a severe acute viral hemorrhagic fever characterized by fever, myalgia, and arthralgia followed by hemorrhagic and neurological manifestations.","definition_xrefs":["Orphanet:319229"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral hemorrhagic fever","termid":"MONDO:0018087"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bolivian hemorrhagic fever","secondary_identifiers":["MEDGEN:76386","UMLS:C0282192","SCTID:67247008","GARD:21412","DOID:0050195","icd11.foundation:1780467429","MedDRA:10005932"],"synonyms":[{"name":"Machupo hemorrhagic fever","type":"exact"}],"termid":"MONDO:0017875","xrefs":{"Monarch":{"xref_id":"0017875"}}}


id: PBO:0040772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BEN domain containing 7","termid":"PBO:0040772"}


id: FYPO:0000403
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype in which the duration of progression through the G2/M transition of the mitotic cell cycle is increased.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete increased duration of mitotic G2/M phase transition (obsolete FYPO:0000403)","synonyms":[{"name":"cell cycle progression through the G2/M phase transition: increased duration","type":"related"},{"name":"increased duration of cell cycle progression through mitotic G2/M phase transition","type":"exact"},{"name":"increased duration of mitotic G2/M phase transition during vegetative growth","type":"exact"}],"termid":"FYPO:0000403"}


id: PR:Q2L4W6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spo5 gene.","definition_xrefs":["UniProtKB:Q2L4W6","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":"sporulation-specific protein 5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC29A10.02","synonyms":[{"name":"Spom972h-spo5","type":"exact"},{"name":"meiotic RNA-binding protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"meiotically up-regulated gene 12 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q2L4W6"}


id: GO:1901272
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 2-dehydro-3-deoxy-D-gluconic acid.","definition_xrefs":["GOC:TermGenie","UniPathway:UPA00856","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monosaccharide metabolic process","termid":"GO:0005996"},{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0005975","GO:0044281"],"is_obsolete":false,"name":"2-dehydro-3-deoxy-D-gluconic acid metabolic process","synonyms":[{"name":"2-dehydro-3-deoxy-D-gluconic acid metabolism","type":"exact"}],"termid":"GO:1901272"}


id: PBO:0073757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 2 member 11","termid":"PBO:0073757"}


id: SO:0001945
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A kind of histone modification site, whereby the 56th residue (a lysine), from the start of the H3 histone protein is acetylated.","definition_xrefs":["EBI:nj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone_3_acetylation_site","termid":"SO:0001973"}],"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":"H3K56_acetylation_site","synonyms":[{"name":"H3K56 acetylation site","type":"exact"},{"name":"H3K56ac","type":"exact"}],"termid":"SO:0001945"}


id: MONDO:0054750
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amyotrophic lateral sclerosis, susceptibility to, 24","secondary_identifiers":["UMLS:C4693523","DOID:0081378","MEDGEN:1632999","OMIM:617892"],"synonyms":[{"name":"ALS24","type":"related"},{"name":"amyotrophic lateral sclerosis, susceptibility to, 24","type":"exact"}],"termid":"MONDO:0054750","xrefs":{"Monarch":{"xref_id":"0054750"}}}


id: PBO:0113384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative phosphomutase; contains a region homologous to the active site of phosphomutases; overexpression suppresses the histidine auxotrophy of an ade3 ade16 ade17 triple mutant and the temperature sensitivity of a tps2 mutant; localizes to cytosol an peroxisomes","termid":"PBO:0113384"}


id: PBO:0062940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prolyl 4-hydroxylase subunit beta","termid":"PBO:0062940"}


id: MONDO:0015478
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete paramedian facial cleft (obsolete MONDO:0015478)","secondary_identifiers":["Orphanet:155867"],"synonyms":[{"name":"Tessier number 1-1 and 2-12 facial cleft","type":"exact"}],"termid":"MONDO:0015478","xrefs":{"Monarch":{"xref_id":"0015478"}}}


id: PBO:0041797
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"caspase recruitment domain family member 6","termid":"PBO:0041797"}


id: PBO:0043725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 6C pseudogene 4","termid":"PBO:0043725"}


id: GO:1903007
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of Lys63-specific deubiquitinase activity.","definition_xrefs":["GOC:bf","GOC:PARL","GO_REF:0000059","PMID:22970133","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of peptidase activity","termid":"GO:0010952"},{"relation_name":"is_a","term_name":"positive regulation of protein K63-linked deubiquitination","termid":"GO:1903006"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0070647"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"positive regulation of Lys63-specific deubiquitinase activity","synonyms":[{"name":"activation of Lys63-specific deubiquitinase activity","type":"narrow"},{"name":"up regulation of Lys63-specific deubiquitinase activity","type":"exact"},{"name":"up-regulation of Lys63-specific deubiquitinase activity","type":"exact"},{"name":"upregulation of Lys63-specific deubiquitinase activity","type":"exact"}],"termid":"GO:1903007"}


id: PATO:0001667
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An attachment quality inhering in a bearer by virtue of the bearer's connection or association with another entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"attachment quality","termid":"PATO:0001435"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"attached to","synonyms":[{"name":"affixed to","type":"related"},{"name":"attached","type":"exact"}],"termid":"PATO:0001667"}


id: GO:0075184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of symbiont infection cushion formation.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental process","termid":"GO:0050793"},{"relation_name":"regulates","term_name":"infection cushion formation","termid":"GO:0075183"}],"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 infection cushion formation","synonyms":[{"name":"regulation of infection cushion formation on or near host","type":"exact"}],"termid":"GO:0075184"}


id: PBO:0059344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S10 pseudogene 5","termid":"PBO:0059344"}


id: PBO:0085923
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; member of the seripauperin multigene family encoded mainly in subtelomeric regions; SWAT-GFP and mCherry fusion proteins localize to the vacuole","termid":"PBO:0085923"}


id: GO:0047415
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N(2)-benzoyl-D-arginine-4-nitroanilide + H2O = 4-nitroaniline + N(2)-benzoyl-D-arginine + H+.","definition_xrefs":["EC:3.5.1.72","RHEA:14421"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016810","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"D-benzoylarginine-4-nitroanilide amidase activity","secondary_identifiers":["MetaCyc:3.5.1.72-RXN","KEGG_REACTION:R04113"],"synonyms":[{"name":"D-BAPA-ase activity","type":"related"},{"name":"N-benzoyl-D-arginine-4-nitroanilide amidohydrolase activity","type":"related"},{"name":"benzoyl-D-arginine arylamidase activity","type":"related"}],"termid":"GO:0047415"}


id: PBO:0077237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMCC2 antisense RNA 1","termid":"PBO:0077237"}


id: GO:1901116
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving cephamycin C.","definition_xrefs":["GOC:TermGenie","GOC:yaf","UniPathway:UPA00183"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"beta-lactam antibiotic metabolic process","termid":"GO:0030653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0008150"],"is_obsolete":false,"name":"cephamycin C metabolic process","synonyms":[{"name":"cephamycin C metabolism","type":"exact"}],"termid":"GO:1901116"}


id: PBO:0038483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily B member 8","termid":"PBO:0038483"}


id: MONDO:0044906
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm of the bladder that involves the transitional epithelium projecting above the surrounding epithelial surface and consisting of villous or arborescent outgrowths of fibrovascular stroma.","definition_xrefs":["NCIT:C39858"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bladder benign neoplasm","termid":"MONDO:0000384"},{"relation_name":"is_a","term_name":"non-invasive bladder papillary urothelial neoplasm","termid":"MONDO:0003822"},{"relation_name":"is_a","term_name":"urothelial papilloma","termid":"MONDO:0004041"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bladder urothelial papilloma","secondary_identifiers":["MEDGEN:237227","UMLS:C1384678"],"synonyms":[{"name":"bladder transitional cell papilloma","type":"exact"},{"name":"bladder urothelial papilloma","type":"exact"},{"name":"urinary bladder transitional cell papilloma","type":"exact"},{"name":"urinary bladder urothelial papilloma","type":"exact"}],"termid":"MONDO:0044906","xrefs":{"Monarch":{"xref_id":"0044906"}}}


id: PBO:0027838
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_localization_to_cortical_microtubule_cytoskeleton","termid":"PBO:0027838"}


id: PBO:0068601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 52, pseudogene","termid":"PBO:0068601"}


id: FYPO:0006094
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 assembly of actin filament bundles is abnormal.","definition_xrefs":["GO:0061572","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular component assembly during vegetative growth","termid":"FYPO:0001354"},{"relation_name":"is_a","term_name":"abnormal actin filament bundle organization","termid":"FYPO:0005979"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0004803"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0004803"],"is_obsolete":false,"name":"abnormal actin filament bundle assembly","synonyms":[{"name":"abnormal actin bundling","type":"exact"},{"name":"abnormal actin filament bundle assembly during mitotic cell cycle","type":"related"},{"name":"abnormal actin filament bundle assembly during vegetative growth","type":"exact"}],"termid":"FYPO:0006094"}


id: PBO:0038343
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_eggs_laid_on_by","termid":"PBO:0038343"}


id: PBO:0034642
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_phosphorylation_during_cellular_response_to_arsenite_ion","termid":"PBO:0034642"}


id: MONDO:1012590
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oculocutaneous albinism that occurs in water buffalo due to a mutation in the TYR gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oculocutaneous albinism, non-human animal","termid":"MONDO:1012579"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculocutaneous albinism, TYR-related, water buffalo","secondary_identifiers":["OMIA:000202-89462"],"synonyms":[{"name":"coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related in Bubalus bubalis (water buffalo)","type":"exact"}],"termid":"MONDO:1012590","xrefs":{"Monarch":{"xref_id":"1012590"}}}


id: GO:0046610
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The V0 domain of a proton-transporting V-type ATPase found in the lysosomal membrane.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vacuolar proton-transporting V-type ATPase, V0 domain","termid":"GO:0000220"},{"relation_name":"part_of","term_name":"lysosomal proton-transporting V-type ATPase complex","termid":"GO:0046611"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005773"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005773","GO:0005737","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"lysosomal proton-transporting V-type ATPase, V0 domain","synonyms":[{"name":"lysosomal hydrogen ion-transporting ATPase V0 domain","type":"exact"}],"termid":"GO:0046610"}


id: GO:0003344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the pericardium is generated and organized.","definition_xrefs":["PMID:18722343","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of an epithelial sheet","termid":"GO:0002011"},{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"pericardium development","termid":"GO:0060039"}],"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":"pericardium morphogenesis","termid":"GO:0003344"}


id: PBO:0077244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane and coiled-coil domains 5A","termid":"PBO:0077244"}


id: GO:1905304
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiac myofibril assembly.","definition_xrefs":["GO_REF:0000058","GOC:BHF","GOC:TermGenie","GOC:rl","PMID:16151019"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell development","termid":"GO:0060284"},{"relation_name":"is_a","term_name":"regulation of actomyosin structure organization","termid":"GO:0110020"},{"relation_name":"is_a","term_name":"regulation of organelle assembly","termid":"GO:1902115"},{"relation_name":"is_a","term_name":"regulation of supramolecular fiber organization","termid":"GO:1902903"},{"relation_name":"regulates","term_name":"cardiac myofibril assembly","termid":"GO:0055003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0030036","GO:0007010","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"regulation of cardiac myofibril assembly","synonyms":[{"name":"regulation of cardiac myofibril development","type":"exact"},{"name":"regulation of cardiac myofibril morphogenesis","type":"exact"},{"name":"regulation of heart myofibril assembly","type":"related"}],"termid":"GO:1905304"}


id: PBO:0040744
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone","termid":"PBO:0040744"}


id: PBO:0057673
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1264","termid":"PBO:0057673"}


id: PBO:0066726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 23","termid":"PBO:0066726"}


id: MOD:00327
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tryptophan residue to a 3-hydroxy-L-tryptophan.","definition_xrefs":["PubMed:10024453","RESID:AA0322","ChEBI:141794","PubMed:11457355"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monohydroxylated tryptophan","termid":"MOD:01622"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-hydroxy-L-tryptophan","synonyms":[{"name":"(2S,3S)-2-amino-3-hydroxy-3-(1H-indol-3-yl)propanoic acid","type":"exact"},{"name":"3-hydroxy-L-tryptophan","type":"exact"},{"name":"3-hydroxylated L-tryptophan","type":"exact"},{"name":"3-hydroxytryptophan","type":"exact"},{"name":"3HyTrp","type":"exact"},{"name":"MOD_RES 3-hydroxytryptophan","type":"exact"},{"name":"beta-hydroxytryptophan","type":"exact"}],"termid":"MOD:00327"}


id: PBO:0061196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NNT antisense RNA 1","termid":"PBO:0061196"}


id: GO:0048520
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of behavior, the internally coordinated responses (actions or inactions) of whole living organisms (individuals or groups) to internal or external stimuli.","definition_xrefs":["GOC:jid","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of behavior","termid":"GO:0050795"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"behavior","termid":"GO:0007610"}],"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 behavior","synonyms":[{"name":"activation of behavior","type":"narrow"},{"name":"stimulation of behavior","type":"narrow"},{"name":"up regulation of behavior","type":"exact"},{"name":"up-regulation of behavior","type":"exact"},{"name":"upregulation of behavior","type":"exact"}],"termid":"GO:0048520"}


id: GO:1990551
data:
  {"annotated_genes":["SJAG_00522"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95757],"is_not":false,"summary":null,"term":"GO:1990551"}]},"cv_name":"biological_process","definition":"The process in which 2-oxoadipate is transported across a mitochondrial membrane, into or out of the mitochondrion.","definition_xrefs":["PMID:11013234"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dicarboxylic acid transport","termid":"GO:0006835"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transport","termid":"GO:1905039"},{"relation_name":"is_a","term_name":"mitochondrial transmembrane transport","termid":"GO:1990542"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00522":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"mitochondrial 2-oxoadipate transmembrane transport","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990551","terms_by_termid":{"GO:1990551":null}}


id: MONDO:0012206
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, primary bone dysplasia disorder characterized by early-onset, progressive pseudorheumatoid arthritis, platyspondyly, and hypoplasia/dysplasia of the third and fourth metatarsals, in the absence of ophthalmologic, cleft palate, and height anomalies.","definition_xrefs":["Orphanet:137678"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"},{"relation_name":"is_a","term_name":"type 2 collagenopathy","termid":"MONDO:0022800"}],"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":"spondyloepiphyseal dysplasia with metatarsal shortening","secondary_identifiers":["SCTID:720826006","GARD:10220","UMLS:C1836683","MEDGEN:324580","OMIM:609162","MESH:C535766","NANDO:2201353"],"synonyms":[{"name":"Czech dysplasia","type":"exact"},{"name":"Czech dysplasia metatarsal type","type":"exact"},{"name":"Czech dysplasia, metatarsal type","type":"exact"},{"name":"SED with metatarsal shortening","type":"exact"},{"name":"pseudorheumatoid dysplasia progressive, with hypoplastic toes","type":"related"},{"name":"pseudorheumatoid dysplasia, progressive, with hypoplastic toes","type":"exact"},{"name":"spondyloepiphyseal dysplasia with precocious osteoarthritis","type":"exact"}],"termid":"MONDO:0012206","xrefs":{"Monarch":{"xref_id":"0012206"}}}


id: GO:0016824
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of any acid halide bond.","definition_xrefs":["EC:3.8.-.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity","termid":"GO:0016787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"hydrolase activity, acting on acid halide bonds","termid":"GO:0016824"}


id: MONDO:0012442
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the DCDC2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 66","secondary_identifiers":["MESH:C565701","MEDGEN:346659","UMLS:C1857750","OMIM:610212","DOID:0110517","GARD:22621"],"synonyms":[{"name":"DCDC2 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"DFNB66","type":"narrow"},{"name":"autosomal recessive deafness 66","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 66","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in DCDC2","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 66","type":"narrow"},{"name":"deafness, autosomal recessive 66","type":"narrow"},{"name":"deafness, autosomal recessive type 66","type":"narrow"}],"termid":"MONDO:0012442","xrefs":{"Monarch":{"xref_id":"0012442"}}}


id: MONDO:0003997
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Kaposi sarcoma arising from the colon.","definition_xrefs":["NCIT:C5516"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colon sarcoma","termid":"MONDO:0003352"},{"relation_name":"is_a","term_name":"colorectal Kaposi sarcoma","termid":"MONDO:0024659"}],"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":"colon Kaposi sarcoma","secondary_identifiers":["DOID:6804","UMLS:C1333091","MEDGEN:232378"],"synonyms":[{"name":"Kaposi's sarcoma (disease) of colon","type":"exact"},{"name":"Kaposi's sarcoma of colon","type":"exact"},{"name":"Kaposi's sarcoma of the colon","type":"exact"},{"name":"colon Kaposi sarcoma","type":"exact"},{"name":"colon Kaposi's sarcoma","type":"exact"},{"name":"colon Kaposi's sarcoma (disease)","type":"exact"},{"name":"colon Kaposis sarcoma","type":"exact"},{"name":"colonic Kaposi sarcoma","type":"exact"},{"name":"colonic Kaposi's sarcoma","type":"exact"},{"name":"colonic Kaposis sarcoma","type":"exact"}],"termid":"MONDO:0003997","xrefs":{"Monarch":{"xref_id":"0003997"}}}


id: GO:0052917
data:
  {"annotated_genes":["SJAG_00437"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104164],"is_not":false,"summary":null,"term":"GO:0052917"}]},"cv_name":"molecular_function","definition":"Catalysis of the addition of mannose to dolichyl-pyrophosphate Man7GlcNAc2 (also written as Man7GlcNAc2-PP-Dol) in alpha-(1->6) linkage, producing Man8GlcNAc2-PP-Dol.","definition_xrefs":["PMID:10336995","RHEA:29535"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-1,6-mannosyltransferase activity","termid":"GO:0000009"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00437":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:0016740"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016740","GO:0016757"],"is_obsolete":false,"name":"dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichol alpha-1,6-mannosyltransferase","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:RXN-5468","GO:0052824","EC:2.4.1.260","KEGG_REACTION:R06260"],"synonyms":[{"name":"dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase activity","type":"exact"},{"name":"dolichyl-P-mannose:Man(7)GlcNAc(2)-PP-dolichyl mannosyltransferase activity","type":"exact"},{"name":"dolichyl-pyrophosphate Man7GlcNAc2 alpha-1,6-mannosyltransferase activity","type":"exact"}],"termid":"GO:0052917","terms_by_termid":{"GO:0052917":null}}


id: GO:0033975
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-2-haloacid + H2O = (S)-2-hydroxyacid + halide.","definition_xrefs":["EC:3.8.1.9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid halide bonds, in C-halide compounds","termid":"GO:0019120"}],"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:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"(R)-2-haloacid dehalogenase activity","secondary_identifiers":["MetaCyc:RXN-6264","RHEA:22188"],"synonyms":[{"name":"(R)-2-haloacid halidohydrolase activity","type":"related"},{"name":"2-haloalkanoic acid dehalogenase activity","type":"broad"},{"name":"2-haloalkanoid acid halidohydrolase activity","type":"broad"},{"name":"D-2-haloacid dehalogenase activity","type":"related"},{"name":"D-DEX","type":"related"}],"termid":"GO:0033975"}


id: PR:P05219
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nda3 gene.","definition_xrefs":["UniProtKB:P05219","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 beta chain (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC26H8.07c","synonyms":[{"name":"Spom972h-nda3","type":"exact"},{"name":"beta-tubulin (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P05219"}


id: PBO:0036194
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitotic_spindle_elongation_without_chromosome_separation","termid":"PBO:0036194"}


id: PBO:0060366
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myogenin promoter associated myogenic regulatory antisense long non coding RNA","termid":"PBO:0060366"}


id: MOD:01936
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-oleoyl-L-lysine.","definition_xrefs":["RESID:AA0590","PubMed:20942504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"},{"relation_name":"is_a","term_name":"N-oleoylated residue","termid":"MOD:02011"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"},{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875","MOD:01155"],"is_obsolete":false,"name":"N6-oleoyl-L-lysine","synonyms":[{"name":"(2S)-2-amino-6-([(9Z)-octadec-9-enoyl]amino)hexanoic acid","type":"exact"},{"name":"N6-[(9Z)-1-oxo-9-octadecenyl]lysine","type":"exact"},{"name":"N6-oleoyl-L-lysine","type":"exact"}],"termid":"MOD:01936"}


id: GO:0032924
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by an extracellular ligand binding to an activin receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:rl","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transforming growth factor beta receptor superfamily signaling pathway","termid":"GO:0141091"}],"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":"activin receptor signaling pathway","synonyms":[{"name":"activin receptor signalling pathway","type":"exact"}],"termid":"GO:0032924"}


id: GO:0034296
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which zygospores are formed. Zygospores are characteristic of the zygomycete fungi (phylum Zygomycota) thick-walled and darkly colored, and usually heavily ornamented as well, with many spines or ridges. It is formed between two specialized organs called suspensors, which are themselves usually heavily ornamented, one from each mating partner. The zygospore forms between them and then breaks away.","definition_xrefs":["PMID:21858438","GOC:ds","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sexual sporulation resulting in formation of a cellular spore","termid":"GO:0043935"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"zygospore formation","termid":"GO:0034296"}


id: PBO:0041903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CBFA2/RUNX1 partner transcriptional co-repressor 3","termid":"PBO:0041903"}


id: PBO:0081821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 738","termid":"PBO:0081821"}


id: PBO:0011442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi Dsc E3 ligase complex subunit Dsc3","termid":"PBO:0011442"}


id: GO:0002042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of endothelial cells into the extracellular matrix in order to form new blood vessels involved in sprouting angiogenesis.","definition_xrefs":["PMID:16391003"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel endothelial cell migration","termid":"GO:0043534"},{"relation_name":"part_of","term_name":"sprouting angiogenesis","termid":"GO:0002040"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell migration involved in sprouting angiogenesis","termid":"GO:0002042"}


id: GO:0019558
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of L-histidine into other compounds, including 2-oxoglutarate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate metabolic process","termid":"GO:0006103"},{"relation_name":"is_a","term_name":"L-histidine catabolic process","termid":"GO:0006548"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0006520","GO:0044248","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"L-histidine catabolic process to 2-oxoglutarate","synonyms":[{"name":"histidine breakdown to 2-oxoglutarate","type":"exact"},{"name":"histidine catabolic process to 2-ketoglutarate","type":"exact"},{"name":"histidine catabolic process to 2-oxoglutarate","type":"broad"},{"name":"histidine catabolic process to alpha-ketoglutarate","type":"exact"},{"name":"histidine catabolic process to alpha-oxoglutarate","type":"exact"},{"name":"histidine catabolism to 2-ketoglutarate","type":"exact"},{"name":"histidine catabolism to alpha-ketoglutarate","type":"exact"},{"name":"histidine catabolism to alpha-oxoglutarate","type":"exact"},{"name":"histidine degradation to 2-oxoglutarate","type":"exact"}],"termid":"GO:0019558"}


id: GO:1903833
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cellular response to amino acid starvation.","definition_xrefs":["GO_REF:0000058","PMID:7623840","GOC:TermGenie","PMID:25002487"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of response to nutrient levels","termid":"GO:0032109"},{"relation_name":"is_a","term_name":"positive regulation of cellular process","termid":"GO:0048522"},{"relation_name":"is_a","term_name":"regulation of cellular response to amino acid starvation","termid":"GO:1903832"},{"relation_name":"positively_regulates","term_name":"cellular response to amino acid starvation","termid":"GO:0034198"}],"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 cellular response to amino acid starvation","synonyms":[{"name":"activation of cellular response to amino acid starvation","type":"narrow"},{"name":"up regulation of cellular response to amino acid starvation","type":"exact"},{"name":"up-regulation of cellular response to amino acid starvation","type":"exact"},{"name":"upregulation of cellular response to amino acid starvation","type":"exact"}],"termid":"GO:1903833"}


id: MONDO:1011967
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vertebral and spinal dysplasia, non-human animal","secondary_identifiers":["OMIA:001951"],"termid":"MONDO:1011967","xrefs":{"Monarch":{"xref_id":"1011967"}}}


id: PBO:0003957
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.2.1.3","termid":"PBO:0003957"}


id: GO:0036305
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of an ameloblast, a cylindrical epithelial cell in the innermost layer of the enamel organ.","definition_xrefs":["CL:0000059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"columnar/cuboidal epithelial cell differentiation","termid":"GO:0002065"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"ameloblast differentiation","termid":"GO:0036305"}


id: GO:1903721
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of I-kappaB phosphorylation.","definition_xrefs":["PMID:23675531","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein phosphorylation","termid":"GO:0001934"},{"relation_name":"is_a","term_name":"regulation of I-kappaB phosphorylation","termid":"GO:1903719"},{"relation_name":"positively_regulates","term_name":"I-kappaB phosphorylation","termid":"GO:0007252"}],"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 I-kappaB phosphorylation","synonyms":[{"name":"activation of I-kappaB phosphorylation","type":"narrow"},{"name":"activation of IKB phosphorylation","type":"narrow"},{"name":"activation of IkappaB phosphorylation","type":"narrow"},{"name":"activation of inhibitor of NF-kappaB phosphorylation","type":"narrow"},{"name":"activation of inhibitor of kappaB phosphorylation","type":"narrow"},{"name":"positive regulation of IKB phosphorylation","type":"exact"},{"name":"positive regulation of IkappaB phosphorylation","type":"exact"},{"name":"positive regulation of inhibitor of NF-kappaB phosphorylation","type":"exact"},{"name":"positive regulation of inhibitor of kappaB phosphorylation","type":"exact"},{"name":"up regulation of I-kappaB phosphorylation","type":"exact"},{"name":"up regulation of IKB phosphorylation","type":"exact"},{"name":"up regulation of IkappaB phosphorylation","type":"exact"},{"name":"up regulation of inhibitor of NF-kappaB phosphorylation","type":"exact"},{"name":"up regulation of inhibitor of kappaB phosphorylation","type":"exact"},{"name":"up-regulation of I-kappaB phosphorylation","type":"exact"},{"name":"up-regulation of IKB phosphorylation","type":"exact"},{"name":"up-regulation of IkappaB phosphorylation","type":"exact"},{"name":"up-regulation of inhibitor of NF-kappaB phosphorylation","type":"exact"},{"name":"up-regulation of inhibitor of kappaB phosphorylation","type":"exact"},{"name":"upregulation of I-kappaB phosphorylation","type":"exact"},{"name":"upregulation of IKB phosphorylation","type":"exact"},{"name":"upregulation of IkappaB phosphorylation","type":"exact"},{"name":"upregulation of inhibitor of NF-kappaB phosphorylation","type":"exact"},{"name":"upregulation of inhibitor of kappaB phosphorylation","type":"exact"}],"termid":"GO:1903721"}


id: MONDO:0001871
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute inflammation of the glomeruli, in which all glomeruli are affected, resulting in acute renal failure.","definition_xrefs":["NCIT:C35587"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse glomerulonephritis","termid":"MONDO:0003137"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"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":"acute diffuse glomerulonephritis","secondary_identifiers":["SCTID:197585004","UMLS:C0341689","MEDGEN:137959","DOID:14066"],"synonyms":[{"name":"acute diffuse glomerulonephritis","type":"exact"},{"name":"acute diffuse nephritis","type":"related"},{"name":"diffuse glomerulonephritis, acute","type":"exact"}],"termid":"MONDO:0001871","xrefs":{"Monarch":{"xref_id":"0001871"}}}


id: MOD:01505
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ4plex-116 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ4plex-116 reporter+balance reagent acylated residue","termid":"MOD:01499"},{"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-threonine","termid":"MOD:02004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ4plex-116 reporter+balance reagent O3-acylated threonine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"iTRAQ4plex","type":"related"}],"termid":"MOD:01505"}


id: GO:0032616
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-13 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"interleukin-13 production","secondary_identifiers":["GO:0072611","GO:0042231"],"synonyms":[{"name":"IL-13 production","type":"exact"},{"name":"interleukin-13 biosynthetic process","type":"narrow"},{"name":"interleukin-13 secretion","type":"narrow"}],"termid":"GO:0032616"}


id: PBO:0042713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell migration inducing hyaluronidase 1","termid":"PBO:0042713"}


id: SO:0001281
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"3-methylcytidine is a modified cytidine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytidine","termid":"SO:0001275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_methylcytidine","secondary_identifiers":["RNAMOD:020"],"synonyms":[{"name":"3-methylcytidine","type":"exact"},{"name":"m3C","type":"exact"},{"name":"three methylcytidine","type":"exact"}],"termid":"SO:0001281"}


id: GO:0009481
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: 4 ferrocytochrome c + O2 = 4 ferricytochrome c + 2 H2O.","definition_xrefs":["EC:1.9.3.1"],"gene_count":0,"genotype_count":0,"name":"obsolete aa3-type cytochrome c oxidase (obsolete GO:0009481)","synonyms":[{"name":"aa3-type cytochrome c oxidase","type":"exact"}],"termid":"GO:0009481"}


id: GO:1902929
data:
  {"annotated_genes":["SJAG_01388"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[98840],"is_not":false,"summary":null,"term":"GO:1902929"}]},"cv_name":"cellular_component","definition":"Any plasma membrane part that is part of a growing cell tip.","definition_xrefs":["GOC:TermGenie","PMID:17085965","GO_REF:0000064"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane of cell tip","termid":"GO:0031520"},{"relation_name":"part_of","term_name":"growing cell tip","termid":"GO:0035838"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01388":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"plasma membrane of growing cell tip","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"growing cell tip plasma membrane part","type":"exact"},{"name":"plasma membrane part of growing cell end","type":"exact"},{"name":"plasma membrane part of growing cell tip","type":"exact"}],"termid":"GO:1902929","terms_by_termid":{"GO:1902929":null}}


id: MONDO:0010952
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary hyperferritinemia with congenital cataracts is characterized by the association of early onset (although generally absent at birth) cataract with persistently raised plasma ferritin concentrations in the absence of iron overload.","definition_xrefs":["Orphanet:163"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"hereditary hyperferritinemia with congenital cataracts","secondary_identifiers":["SCTID:702398007","DOID:0111256","MEDGEN:318812","GARD:2806","ICD9:289.89","NORD:1264","OMIM:600886","UMLS:C1833213","ICD9:366.44","MESH:C538137"],"synonyms":[{"name":"Bonneau-Beaumont syndrome","type":"exact"},{"name":"HHCS","type":"exact"},{"name":"HRFTC","type":"related"},{"name":"Hyperferritinemia Cataract Syndrome","type":"exact"},{"name":"cataract-hyperferritinemia syndrome","type":"related"},{"name":"hereditary hyperferritinemia cataract syndrome","type":"related"},{"name":"hereditary hyperferritinemia-cataract syndrome","type":"exact"},{"name":"hyperferritinemia cataract syndrome","type":"related"},{"name":"hyperferritinemia with or without cataract","type":"related"},{"name":"hyperferritinemia, hereditary, with congenital cataracts","type":"related"},{"name":"hyperferritinemia-cataract syndrome","type":"related"}],"termid":"MONDO:0010952","xrefs":{"Monarch":{"xref_id":"0010952"}}}


id: FYPO:0005598
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the centromere of a chromosome is increased during the meiotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to centromere","termid":"FYPO:0006239"},{"relation_name":"is_a","term_name":"abnormal protein localization to centromere during meiotic cell cycle","termid":"FYPO:0006529"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased protein localization to centromere during meiotic cell cycle","synonyms":[{"name":"increased protein localisation to centromere during meiotic cell cycle","type":"exact"},{"name":"increased protein localisation to chromosome, centromeric region during meiotic cell cycle","type":"exact"},{"name":"increased protein localization to chromosome, centric region during meiotic cell cycle","type":"exact"},{"name":"increased protein localization to chromosome, centromeric region during meiotic cell cycle","type":"exact"}],"termid":"FYPO:0005598"}


id: GO:0032069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of nuclease activity, the hydrolysis of ester linkages within nucleic acids.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hydrolase activity","termid":"GO:0051336"},{"relation_name":"is_a","term_name":"regulation of macromolecule metabolic process","termid":"GO:0060255"}],"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 nuclease activity","synonyms":[{"name":"nuclease regulator activity","type":"related"}],"termid":"GO:0032069"}


id: GO:2000853
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of corticosterone secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of glucocorticoid secretion","termid":"GO:2000850"},{"relation_name":"is_a","term_name":"regulation of corticosterone secretion","termid":"GO:2000852"},{"relation_name":"negatively_regulates","term_name":"corticosterone secretion","termid":"GO:0035934"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"negative regulation of corticosterone secretion","termid":"GO:2000853"}


id: GO:1904314
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 methamphetamine hydrochloride stimulus.","definition_xrefs":["GO_REF:0000071","PMID:22174933","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to amine stimulus","termid":"GO:0071418"},{"relation_name":"is_a","term_name":"response to methamphetamine hydrochloride","termid":"GO:1904313"}],"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 methamphetamine hydrochloride","synonyms":[{"name":"cellular response to methamphetamine HCL","type":"exact"}],"termid":"GO:1904314"}


id: GO:0008506
data:
  {"annotated_genes":["SJAG_03960"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94968],"is_not":false,"summary":null,"term":"GO:0008506"}]},"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: sucrose(out) + H+(out) = sucrose(in) + H+(in).","definition_xrefs":["TC:2.A.1.5.3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate:proton symporter activity","termid":"GO:0005351"},{"relation_name":"is_a","term_name":"sucrose:monoatomic cation symporter activity","termid":"GO:0009669"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03960":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"sucrose:proton symporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:TRANS-RXN-244","RHEA:72187"],"synonyms":[{"name":"hydrogen/sucrose transporter activity","type":"broad"},{"name":"sucrose:hydrogen symporter activity","type":"exact"}],"termid":"GO:0008506","terms_by_termid":{"GO:0008506":null}}


id: PBO:0086013
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; SWAT-GFP and seamless-GFP fusion proteins localize to the endoplasmic reticulum; identified by gene-trapping, microarray-based expression analysis, and genome-wide homology searching","termid":"PBO:0086013"}


id: FYPO:0006535
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the cell periphery is increased when the cell is subject to nitrogen starvation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to cell periphery","termid":"FYPO:0006533"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"increased protein localization to cell periphery during nitrogen starvation","synonyms":[{"name":"increased protein localisation to cell periphery during nitrogen starvation","type":"exact"},{"name":"increased protein localization to cell periphery during nitrogen depletion","type":"exact"},{"name":"increased protein localization to cell periphery during nitrogen deprivation","type":"exact"}],"termid":"FYPO:0006535"}


id: CHEBI:49976
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc dichloride","termid":"CHEBI:49976"}


id: MONDO:0009148
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare congenital ectodermal dysplasia syndrome with a range of signs and symptoms including cleft lip or palate, mental retardation and various forms of ectodermal dysplasia. Additional symptoms may include fused eyelids, absent nails, delayed bone growth and dry skin. It is believed that this syndrome follows an autosomal dominant pattern of inheritance with incomplete penetrance, and caused by a mutation affecting the TP63 gene","definition_xrefs":["Wikipedia:Rosselli%E2%80%93Gulienetti_syndrome"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ankyloblepharon-ectodermal defects-cleft lip/palate syndrome","termid":"MONDO:0007124"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005497"],"is_obsolete":false,"name":"Rosselli-Gulienetti syndrome","secondary_identifiers":["MESH:C563117","OMIM:225000","Orphanet:90339","icd11.foundation:1430451924","UMLS:C0796139","MEDGEN:163221"],"synonyms":[{"name":"Rosselli-Gulienetti syndrome","type":"exact"}],"termid":"MONDO:0009148","xrefs":{"Monarch":{"xref_id":"0009148"}}}


id: GO:0006033
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which chitin is transported to, or maintained in, a specific location.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide localization","termid":"GO:0033037"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"chitin localization","synonyms":[{"name":"chitin localisation","type":"exact"},{"name":"establishment and maintenance of chitin localization","type":"exact"}],"termid":"GO:0006033"}


id: MONDO:0012855
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Joubert syndrome in which the cause of the disease is a mutation in the ARL13B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Joubert syndrome 8","secondary_identifiers":["DOID:0111003","OMIM:612291","MESH:C567358","GARD:15550","UMLS:C2676771","MEDGEN:436772"],"synonyms":[{"name":"ARL13B Joubert syndrome","type":"exact"},{"name":"JBTS8","type":"exact"},{"name":"Joubert syndrome 8","type":"exact"},{"name":"Joubert syndrome caused by mutation in ARL13B","type":"exact"},{"name":"Joubert syndrome type 8","type":"exact"}],"termid":"MONDO:0012855","xrefs":{"Monarch":{"xref_id":"0012855"}}}


id: PBO:0041833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer susceptibility 9","termid":"PBO:0041833"}


id: GO:0010735
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of the specifically regulated synthesis of RNA from DNA encoding a specific set of genes as a result of a transcription factor interacting with a serum response element (SRE). A serum response element is a short sequence with dyad symmetry found in the promoters of some of the cellular immediate-early genes, regulated by serum.","definition_xrefs":["GOC:tb","GOC:rl","GOC:dph","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription via serum response element binding (obsolete GO:0010735)","termid":"GO:0010735"}


id: PBO:0016942
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pombe Histone Deacetylase","termid":"PBO:0016942"}


id: PBO:0087962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transport adaptor or symportin; assembly chaperone that co-translationally associates with nascent Rpl5p, preventing aggregation; facilitates synchronized nuclear coimport of two 5S-rRNA binding proteins, Rpl5p and Rpl11p, mediated by import receptor Kap104p; required for biogenesis of the large ribosomal subunit; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and nucleus","termid":"PBO:0087962"}


id: PATO:0002067
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A spatial pattern inhering in a bearer by virtue of the bearer's layered configuration.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spatial pattern","termid":"PATO:0000060"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"stratification","termid":"PATO:0002067"}


id: GO:0045622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of T-helper cell differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of immune effector process","termid":"GO:0002697"},{"relation_name":"is_a","term_name":"regulation of CD4-positive, alpha-beta T cell differentiation","termid":"GO:0043370"},{"relation_name":"is_a","term_name":"regulation of immune response","termid":"GO:0050776"},{"relation_name":"regulates","term_name":"T-helper cell differentiation","termid":"GO:0042093"}],"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 T-helper cell differentiation","synonyms":[{"name":"regulation of T-helper cell development","type":"related"}],"termid":"GO:0045622"}


id: GO:0015488
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: glucuronide(out) + monovalent cation(out) = glucuronide(in) + monovalent cation(in).","definition_xrefs":["TC:2.A.2.3.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucuronoside transmembrane transporter activity","termid":"GO:0015164"},{"relation_name":"is_a","term_name":"glycoside-pentoside-hexuronide:cation symporter activity","termid":"GO:0015486"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"glucuronide:cation symporter activity","synonyms":[{"name":"glucuronide:monovalent cation symporter activity","type":"exact"},{"name":"glucuronoside permease activity","type":"related"}],"termid":"GO:0015488"}


id: PBO:0016989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AFG1 family mitochondrial ATPase Afg1 (predicted)","termid":"PBO:0016989"}


id: FYPO:0003006
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal during a cellular response to caffeine.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation during vegetative growth","termid":"FYPO:0001838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0002494","FYPO:0000002","FYPO:0005447","FYPO:0002274"],"is_obsolete":false,"name":"decreased protein phosphorylation during cellular response to caffeine","synonyms":[{"name":"decreased protein phosphorylation during cellular response to caffeine during mitotic cell cycle","type":"related"},{"name":"decreased protein phosphorylation during cellular response to caffeine during vegetative growth","type":"exact"},{"name":"reduced protein phosphorylation during cellular response to caffeine","type":"exact"}],"termid":"FYPO:0003006"}


id: MONDO:0005572
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polycythemia resulting from hypoxia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired secondary polycythemia","termid":"MONDO:0016541"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"polycythemia due to hypoxia","secondary_identifiers":["MEDGEN:163546","NCIT:C27312","DOID:2835","UMLS:C0856818"],"termid":"MONDO:0005572","xrefs":{"Monarch":{"xref_id":"0005572"}}}


id: MONDO:0015968
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare genetic hypothalamic or pituitary disease (obsolete MONDO:0015968)","secondary_identifiers":["Orphanet:183628"],"termid":"MONDO:0015968","xrefs":{"Monarch":{"xref_id":"0015968"}}}


id: PATO:0001734
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a plant by virtue of the bearer's disposition to being between evergeen and deciduous.","definition_xrefs":["PATOC:cjm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shedability","termid":"PATO:0001729"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"semi-deciduous(plant)","termid":"PATO:0001734"}


id: MONDO:0009033
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Temtamy syndrome is a very rare congenital genetic neurological disorder characterized by agenesis/hypoplasia of corpus callosum with developmental abnormalities, ocular disorders, and variable craniofacial and skeletal abnormalities.","definition_xrefs":["Orphanet:1777"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"temtamy syndrome","secondary_identifiers":["DOID:0111621","GARD:5688","OMIM:218340","SCTID:719947004","MEDGEN:347474","NCIT:C148371","MESH:C536959","UMLS:C1857512"],"synonyms":[{"name":"Dysmorphism, corpus callosum agenesis and colobomas","type":"related"},{"name":"TEMTAMY syndrome","type":"related"},{"name":"TEMTYS","type":"related"},{"name":"Temtamy-Shalash syndrome","type":"exact"},{"name":"craniofacial dysmorphism with ocular coloboma absent corpus callosum and aortic dilatation","type":"related"},{"name":"craniofacial dysmorphism-coloboma-corpus callosum agenesis syndrome","type":"exact"},{"name":"intellectual disability with or without craniofacial Dysmorphism, ocular coloboma, or abnormal corpus callosum","type":"related"},{"name":"mental retardation with or without craniofacial Dysmorphism, ocular coloboma, or abnormal corpus callosum","type":"related"},{"name":"temtamy syndrome","type":"exact"}],"termid":"MONDO:0009033","xrefs":{"Monarch":{"xref_id":"0009033"}}}


id: GO:0008414
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a CDP-alcohol group from one compound to another.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring phosphorus-containing groups","termid":"GO:0016772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"CDP-alcohol phosphotransferase activity","termid":"GO:0008414"}


id: PBO:0050928
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon induced transmembrane protein 5","termid":"PBO:0050928"}


id: GO:0052381
data:
  {"annotated_genes":["SJAG_01575"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95867],"is_not":false,"summary":null,"term":"GO:0052381"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: dimethylallyl diphosphate + tRNA = diphosphate + tRNA containing 6-dimethylallyladenosine.","definition_xrefs":["EC:2.5.1.75"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01575":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0140098","GO:0140101","GO:0016765","GO:0003824"],"is_obsolete":false,"name":"tRNA dimethylallyltransferase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:26482","MetaCyc:RXN0-6274","GO:0004811","Reactome:R-HSA-6784462","Reactome:R-HSA-6787567"],"synonyms":[{"name":"dimethylallyl-diphosphate:tRNA dimethylallyltransferase activity","type":"exact"},{"name":"tRNA isopentenyltransferase activity","type":"related"},{"name":"tRNA prenyltransferase activity","type":"broad"}],"termid":"GO:0052381","terms_by_termid":{"GO:0052381":null}}


id: PBO:0078084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRAPPC2L pseudogene 1","termid":"PBO:0078084"}


id: PBO:0084226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hsp90 chaperone; redundant in function with Hsc82p; required for pheromone signaling, negative regulation of Hsf1p; docks with Tom70p for mitochondrial preprotein delivery; promotes telomerase DNA binding, nucleotide addition; protein abundance increases in response to DNA replication stress; promotes solubility of chaperone-substrate complexes; HSP82 has a paralog, HSC82, that arose from the whole genome duplication; human homolog, HSP90AB1, complements null mutant","termid":"PBO:0084226"}


id: PBO:0074517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small NF90 (ILF3) associated RNA A9","termid":"PBO:0074517"}


id: FYPO:0008229
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to phosphate (Pi). Cells stop growing (and may die) at a concentration of phosphate that allows wild type cells to grow.","direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000003","FYPO:0002683","FYPO:0005447","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to phosphate (Pi)","termid":"FYPO:0008229"}


id: GO:0140646
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of the process leading up to expression of the pre-B cell receptor on the surface of pre-B cells.","definition_xrefs":["PMID:22949502"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"negatively_regulates","term_name":"pre-B cell receptor expression","termid":"GO:0002330"}],"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 pre-B cell receptor expression","termid":"GO:0140646"}


id: GO:0007245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Upregulation of MAPKKK activity in the context of transduction of mating pheromone signal, as described for Saccharomyces.","definition_xrefs":["PMID:9561267"],"gene_count":0,"genotype_count":0,"name":"obsolete activation of MAPKKK (mating sensu Saccharomyces) (obsolete GO:0007245)","synonyms":[{"name":"activation of MAPKKK (mating sensu Saccharomyces)","type":"exact"}],"termid":"GO:0007245"}


id: PBO:0003151
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eIF-5A-deoxyhypusine synthase (predicted)","termid":"PBO:0003151"}


id: PBO:0005088
data:
  {"annotation_feature_type":"gene","cv_name":"DNA_binding_specificity","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"binds CSL response element 5'-GTG[G/A]GAA-3'","termid":"PBO:0005088"}


id: MONDO:1011921
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive system disorder, non-human animal","termid":"MONDO:1011354"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyometra, non-human animal","secondary_identifiers":["OMIA:002391"],"termid":"MONDO:1011921","xrefs":{"Monarch":{"xref_id":"1011921"}}}


id: PBO:0110497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-phase kinase associated protein 1 pseudogene 4","termid":"PBO:0110497"}


id: PBO:0086116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for cytoplasm to vacuole targeting of proteins; forms a complex with Far3p and Far7p to Far11p involved in recovery from pheromone-induced cell cycle arrest; mutant has increased aneuploidy tolerance; VPS64 has a paralog, FAR10, that arose from the whole genome duplication","termid":"PBO:0086116"}


id: GO:0120206
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The distal region of the photoreceptor connecting cilium is structurally unique to the photoreceptor and is maintained by retina-specific protein, SPATA7, and its interacting partners RPGR and RPGRIP1. It is essential for photoreceptor sensory cilium stability.","definition_xrefs":["PMID:29899041","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"photoreceptor connecting cilium","termid":"GO:0032391"}],"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":"photoreceptor distal connecting cilium","synonyms":[{"name":"DCC","type":"related"},{"name":"photoreceptor DCC","type":"related"}],"termid":"GO:0120206"}


id: PBO:0049239
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GRM7 antisense RNA 3","termid":"PBO:0049239"}


id: PBO:0030218
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_alpha,alpha-trehalase_activity","termid":"PBO:0030218"}


id: PBO:0028021
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cellular_physical_quality_phenotype","termid":"PBO:0028021"}


id: PBO:0051692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"INO80 complex subunit B","termid":"PBO:0051692"}


id: PBO:0064707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peptidylprolyl isomerase A pseudogene 43","termid":"PBO:0064707"}


id: GO:0047478
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-aspartate + ATP + NH4 = L-asparagine + ADP + 2 H+ + phosphate.","definition_xrefs":["RHEA:14197","EC:6.3.1.4"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acid-ammonia (or amide) ligase activity","termid":"GO:0016880"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0016874","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"aspartate-ammonia ligase (ADP-forming) activity","secondary_identifiers":["MetaCyc:6.3.1.4-RXN","KEGG_REACTION:R00482"],"synonyms":[{"name":"L-aspartate:ammonia ligase (ADP-forming)","type":"related"},{"name":"asparagine synthetase (ADP-forming) activity","type":"related"},{"name":"asparagine synthetase (adenosine diphosphate-forming)","type":"related"}],"termid":"GO:0047478"}


id: GO:0036037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The change in morphology and behavior of a CD8-positive, alpha-beta T cell resulting from exposure to a mitogen, cytokine, chemokine, cellular ligand, or an antigen for which it is specific.","definition_xrefs":["GOC:yaf","CL:0000625"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-beta T cell activation","termid":"GO:0046631"}],"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":"CD8-positive, alpha-beta T cell activation","termid":"GO:0036037"}


id: MONDO:0008508
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"symphalangism","termid":"MONDO:0000151"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"symphalangism, C. S. Lewis type","secondary_identifiers":["MESH:C566100","OMIM:185650","UMLS:C1861404","MEDGEN:396126"],"synonyms":[{"name":"symphalangism, C. S. Lewis type","type":"exact"},{"name":"thumbs, stiff","type":"related"}],"termid":"MONDO:0008508","xrefs":{"Monarch":{"xref_id":"0008508"}}}


id: PBO:0068150
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 457","termid":"PBO:0068150"}


id: PBO:0026933
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_nucleus_during_mitotic_interphase","termid":"PBO:0026933"}


id: PBO:0076035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine kinase 32C","termid":"PBO:0076035"}


id: GO:0008983
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + protein L-glutamate = S-adenosyl-L-homocysteine + protein L-glutamate 5-methyl ester; this reaction is the methylation of peptidyl-L-glutamate to form peptidyl-L-glutamate 5-methyl ester.","definition_xrefs":["EC:2.1.1.80"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"},{"relation_name":"is_a","term_name":"protein carboxyl O-methyltransferase activity","termid":"GO:0051998"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0008276"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0016741","GO:0003674","GO:0008276","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"protein-glutamate O-methyltransferase activity","secondary_identifiers":["RESID:AA0072","RHEA:24452","MetaCyc:CHER-RXN"],"synonyms":[{"name":"MCP methyltransferase I","type":"related"},{"name":"MCP methyltransferase II","type":"related"},{"name":"S-adenosyl-L-methionine:protein-L-glutamate O-methyltransferase activity","type":"related"},{"name":"S-adenosylmethionine-glutamyl methyltransferase activity","type":"related"},{"name":"S-adenosylmethionine:protein-carboxyl O-methyltransferase activity","type":"related"},{"name":"methyl-accepting chemotaxis protein O-methyltransferase activity","type":"narrow"},{"name":"methyl-accepting chemotaxis protein methyltransferase II","type":"related"},{"name":"protein O-methyltransferase activity","type":"related"},{"name":"protein carboxyl-O-methyltransferase activity","type":"related"},{"name":"protein carboxyl-methylase activity","type":"related"},{"name":"protein carboxylmethyltransferase II","type":"related"},{"name":"protein carboxymethylase activity","type":"related"},{"name":"protein carboxymethyltransferase activity","type":"related"},{"name":"protein glutamate O-methylase activity","type":"exact"},{"name":"protein glutamate O-methyltransferase activity","type":"exact"},{"name":"protein methylase II","type":"related"},{"name":"protein(aspartate)methyltransferase activity","type":"related"},{"name":"protein(carboxyl)methyltransferase activity","type":"related"}],"termid":"GO:0008983"}


id: MONDO:0009646
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial monosomy 7 syndrome","termid":"MONDO:0044645"}],"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":"monosomy 7 myelodysplasia and leukemia syndrome 1","secondary_identifiers":["GARD:18505","OMIM:252270","UMLS:C1854978","NCIT:C176908","MEDGEN:381529","MESH:C565370"],"synonyms":[{"name":"M7MLS1","type":"exact"},{"name":"chromosome 7Q deletion","type":"exact"},{"name":"monosomy 7 of bone marrow","type":"exact"},{"name":"myelodysplasia and leukaemia syndrome with monosomy 7","type":"exact"},{"name":"myelodysplasia and leukemia syndrome with monosomy 7","type":"exact"}],"termid":"MONDO:0009646","xrefs":{"Monarch":{"xref_id":"0009646"}}}


id: GO:1905036
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of an antifungal innate immune response.","definition_xrefs":["GOC:TermGenie","PMID:22470487","GO_REF:0000058","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of innate immune response","termid":"GO:0045089"},{"relation_name":"is_a","term_name":"regulation of antifungal innate immune response","termid":"GO:1905034"},{"relation_name":"positively_regulates","term_name":"antifungal innate immune response","termid":"GO:0061760"}],"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 antifungal innate immune response","synonyms":[{"name":"activation of antifungal innate immune response","type":"narrow"},{"name":"up regulation of antifungal innate immune response","type":"exact"},{"name":"up-regulation of antifungal innate immune response","type":"exact"},{"name":"upregulation of antifungal innate immune response","type":"exact"}],"termid":"GO:1905036"}


id: MONDO:0004810
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute form of ethmoid sinusitis.","definition_xrefs":["MONDO:patterns/acute"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ethmoid sinusitis","termid":"MONDO:0005756"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute ethmoiditis","secondary_identifiers":["UMLS:C0155806","MEDGEN:510088","ICD9:461.2","SCTID:67832005","DOID:9506"],"synonyms":[{"name":"acute ethmoid sinusitis","type":"exact"},{"name":"acute ethmoidal sinusitis","type":"exact"},{"name":"ethmoid sinusitis, acute","type":"exact"},{"name":"ethmoidal sinus - acute","type":"exact"}],"termid":"MONDO:0004810","xrefs":{"Monarch":{"xref_id":"0004810"}}}


id: PBO:0061637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nudix hydrolase 16 like 1","termid":"PBO:0061637"}


id: PR:C6Y4B2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC57A7.15c gene.","definition_xrefs":["PRO:DNx","UniProtKB:C6Y4B2"],"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 C57A7.15c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC57A7.15c","synonyms":[{"name":"Spom972h-SPAC57A7.15c","type":"exact"}],"termid":"PR:C6Y4B2"}


id: PATO:0002495
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An orientation quality inhering in a bearer by virtue of the bearer having a position that is directed dorsally.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"orientation","termid":"PATO:0000133"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dorsal orientation","synonyms":[{"name":"dorsally directed","type":"exact"}],"termid":"PATO:0002495"}


id: PBO:0053956
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 1262","termid":"PBO:0053956"}


id: GO:1901921
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any phosphorylation of RNA polymerase II C-terminal domain that is involved in recruitment of 3'-end processing factors to RNA polymerase II holoenzyme complex.","definition_xrefs":["GOC:TermGenie","PMID:10594013"],"gene_count":0,"genotype_count":0,"name":"obsolete phosphorylation of RNA polymerase II C-terminal domain involved in recruitment of 3'-end processing factors to RNA polymerase II holoenzyme complex (obsolete GO:1901921)","synonyms":[{"name":"CTD domain phosphorylation of RNA polymerase II involved in recruitment of 3'-end processing factors to RNA polymerase II holoenzyme complex","type":"exact"}],"termid":"GO:1901921"}


id: FYPO:0006609
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which a protein that is normally localized intermittently to the Cdr2 medial cortical node complex is associated with the complex for periods of shorter duration than normal.","definition_xrefs":["PomBase:mah","PMID:29514920"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal intermittent protein localization to Cdr2 medial cortical node complex","termid":"FYPO:0006607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0000138","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein dwell time during intermittent localization to Cdr2 medial cortical node complex","synonyms":[{"name":"decreased duration of bursts of intermittent protein localization to Cdr2 medial cortical node complex","type":"related"},{"name":"decreased duration of protein localization bursts to Cdr2 medial cortical node complex","type":"related"},{"name":"decreased duration of protein visits to Cdr2 medial cortical node complex","type":"related"},{"name":"decreased protein dwell time during intermittent localization to Cdr2 medial cortical node complex during mitotic cell cycle","type":"related"},{"name":"decreased protein dwell time during intermittent localization to Cdr2 medial cortical node complex during vegetative growth","type":"exact"},{"name":"decreased protein dwell time during transient localization to Cdr2 medial cortical node complex","type":"exact"},{"name":"reduced protein dwell time during intermittent localization to Cdr2 medial cortical node complex","type":"exact"}],"termid":"FYPO:0006609"}


id: GO:0004258
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the release of a C-terminal amino acid with a broad specificity.","definition_xrefs":["EC:3.4.16.5"],"gene_count":0,"genotype_count":0,"name":"obsolete vacuolar carboxypeptidase Y (obsolete GO:0004258)","synonyms":[{"name":"vacuolar carboxypeptidase Y","type":"exact"}],"termid":"GO:0004258"}


id: PBO:0003452
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydropteroatesynthase/2-amino-4-hydroxy-6-hydroxymethyldihydropteridinediphosphokinase/dihydroneopterin aldolase (predicted)","termid":"PBO:0003452"}


id: PBO:0047962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FRAT regulator of WNT signaling pathway 2","termid":"PBO:0047962"}


id: PBO:0054610
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 2015","termid":"PBO:0054610"}


id: PBO:0111056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HLA complex group 22 (non-protein coding)","termid":"PBO:0111056"}


id: PBO:0091737
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sre1 and Scp1 form a functional 4:4 oligomer","termid":"PBO:0091737"}


id: GO:0035533
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of production of chemokine (C-C motif) ligand 6 (CCL6).","definition_xrefs":["GOC:add","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of chemokine production","termid":"GO:0032722"},{"relation_name":"is_a","term_name":"regulation of chemokine (C-C motif) ligand 6 production","termid":"GO:0035531"},{"relation_name":"positively_regulates","term_name":"chemokine (C-C motif) ligand 6 production","termid":"GO:0035530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of chemokine (C-C motif) ligand 6 production","secondary_identifiers":["GO:0035537"],"synonyms":[{"name":"positive regulation of CCL6 production","type":"exact"},{"name":"positive regulation of chemokine (C-C motif) ligand 6 secretion","type":"narrow"}],"termid":"GO:0035533"}


id: MONDO:0011103
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the GJB2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 3A","secondary_identifiers":["GARD:9933","MESH:C567277","UMLS:C2675750","DOID:0110564","MEDGEN:436512","OMIM:601544"],"synonyms":[{"name":"DFNA3","type":"narrow"},{"name":"DFNA3A","type":"narrow"},{"name":"GJB2 autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"NSRD1","type":"narrow"},{"name":"autosomal dominant deafness 3A","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 3A","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in GJB2","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 3A","type":"narrow"},{"name":"deafness, autosomal dominant 3A","type":"narrow"},{"name":"deafness, autosomal dominant 3a","type":"narrow"},{"name":"deafness, autosomal dominant nonsyndromic sensorineural 3","type":"narrow"},{"name":"deafness, autosomal dominant type 3A","type":"narrow"},{"name":"neurosensory nonsyndromic dominant deafness 1","type":"narrow"}],"termid":"MONDO:0011103","xrefs":{"Monarch":{"xref_id":"0011103"}}}


id: PBO:0060750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B3","termid":"PBO:0060750"}


id: PBO:0074436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 36","termid":"PBO:0074436"}


id: FYPO:0006341
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 endocytosis does not occur in the equatorial region of the cell during mitosis as in wild-type cells.","definition_xrefs":["PMID:16141239","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal endocytosis during vegetative growth","termid":"FYPO:0000034"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abolished equatorial endocytosis during mitosis","synonyms":[{"name":"abolished endocytosis to cell division site","type":"related"},{"name":"abolished equatorial endocytosis during M phase of mitotic cell cycle","type":"related"},{"name":"abolished equatorial endocytosis during cell division","type":"related"},{"name":"abolished equatorial endocytosis during mitosis during vegetative growth","type":"exact"},{"name":"abolished equatorial endocytosis during mitotic M phase","type":"related"},{"name":"endocytosis restricted to cell end during mitosis","type":"related"},{"name":"equatorial endocytosis abolished during mitosis","type":"exact"}],"termid":"FYPO:0006341"}


id: PBO:0039138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adherens junctions associated protein 1","termid":"PBO:0039138"}


id: FYPO:0001679
data:
  {"alleles_by_uniquename":{"SJAG_01050:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01050","name":"nur1delta","uniquename":"SJAG_01050:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[118387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001132"}],"single_locus_phenotype":[{"annotations":[118386],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004718"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to chromatin is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to chromosome","termid":"FYPO:0004996"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01050":null,"SJAG_01745":null,"SJAG_03892":null},"genotype_count":2,"genotypes_by_uniquename":{"nur1delta__vps4delta":{"display_name":"nur1delta vps4delta","display_uniquename":"nur1delta__vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]},"vps4delta":{"display_name":"vps4delta","display_uniquename":"vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03892","SJAG_01050"],"name":"abnormal protein localization to chromatin","references_by_uniquename":{"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_03892"],"single_locus_genotype_uniquenames":["vps4delta"],"synonyms":[{"name":"abnormal protein localisation to chromatin","type":"exact"}],"termid":"FYPO:0001679","terms_by_termid":{"FYPO:0001132":null,"FYPO:0004718":null,"FYPO_EXT:0000001":null}}


id: PBO:0039837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho GTPase activating protein 6","termid":"PBO:0039837"}


id: GO:0045444
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of an adipocyte, an animal connective tissue cell specialized for the synthesis and storage of fat.","definition_xrefs":["GOC:go_curators","CL:0000136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"}],"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":"fat cell differentiation","synonyms":[{"name":"adipocyte cell differentiation","type":"exact"},{"name":"adipocyte differentiation","type":"exact"},{"name":"adipogenesis","type":"related"},{"name":"adipose cell differentiation","type":"exact"}],"termid":"GO:0045444"}


id: MONDO:0000832
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete myeloid neoplasm (obsolete MONDO:0000832)","termid":"MONDO:0000832","xrefs":{"Monarch":{"xref_id":"0000832"}}}


id: GO:1905124
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of glucosylceramidase activity.","definition_xrefs":["GO_REF:0000059","GOC:bf","GOC:TermGenie","GOC:PARL"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of glucosylceramidase activity (obsolete GO:1905124)","synonyms":[{"name":"down regulation of D-glucosyl-N-acylsphingosine glucohydrolase activity","type":"exact"},{"name":"down regulation of GlcCer-beta-glucosidase activity","type":"exact"},{"name":"down regulation of acid beta-glucosidase activity","type":"exact"},{"name":"down regulation of beta-D-glucocerebrosidase activity","type":"exact"},{"name":"down regulation of beta-glucocerebrosidase activity","type":"exact"},{"name":"down regulation of beta-glucosylceramidase activity","type":"exact"},{"name":"down regulation of ceramide glucosidase activity","type":"exact"},{"name":"down regulation of glucocerebrosidase activity","type":"exact"},{"name":"down regulation of glucosphingosine glucosylhydrolase activity","type":"exact"},{"name":"down regulation of glucosylceramidase activity","type":"exact"},{"name":"down regulation of glucosylcerebrosidase activity","type":"exact"},{"name":"down regulation of glucosylsphingosine beta-D-glucosidase activity","type":"exact"},{"name":"down regulation of glucosylsphingosine beta-glucosidase activity","type":"exact"},{"name":"down regulation of psychosine hydrolase activity","type":"exact"},{"name":"down-regulation of D-glucosyl-N-acylsphingosine glucohydrolase activity","type":"exact"},{"name":"down-regulation of GlcCer-beta-glucosidase activity","type":"exact"},{"name":"down-regulation of acid beta-glucosidase activity","type":"exact"},{"name":"down-regulation of beta-D-glucocerebrosidase activity","type":"exact"},{"name":"down-regulation of beta-glucocerebrosidase activity","type":"exact"},{"name":"down-regulation of beta-glucosylceramidase activity","type":"exact"},{"name":"down-regulation of ceramide glucosidase activity","type":"exact"},{"name":"down-regulation of glucocerebrosidase activity","type":"exact"},{"name":"down-regulation of glucosphingosine glucosylhydrolase activity","type":"exact"},{"name":"down-regulation of glucosylceramidase activity","type":"exact"},{"name":"down-regulation of glucosylcerebrosidase activity","type":"exact"},{"name":"down-regulation of glucosylsphingosine beta-D-glucosidase activity","type":"exact"},{"name":"down-regulation of glucosylsphingosine beta-glucosidase activity","type":"exact"},{"name":"down-regulation of psychosine hydrolase activity","type":"exact"},{"name":"downregulation of D-glucosyl-N-acylsphingosine glucohydrolase activity","type":"exact"},{"name":"downregulation of GlcCer-beta-glucosidase activity","type":"exact"},{"name":"downregulation of acid beta-glucosidase activity","type":"exact"},{"name":"downregulation of beta-D-glucocerebrosidase activity","type":"exact"},{"name":"downregulation of beta-glucocerebrosidase activity","type":"exact"},{"name":"downregulation of beta-glucosylceramidase activity","type":"exact"},{"name":"downregulation of ceramide glucosidase activity","type":"exact"},{"name":"downregulation of glucocerebrosidase activity","type":"exact"},{"name":"downregulation of glucosphingosine glucosylhydrolase activity","type":"exact"},{"name":"downregulation of glucosylceramidase activity","type":"exact"},{"name":"downregulation of glucosylcerebrosidase activity","type":"exact"},{"name":"downregulation of glucosylsphingosine beta-D-glucosidase activity","type":"exact"},{"name":"downregulation of glucosylsphingosine beta-glucosidase activity","type":"exact"},{"name":"downregulation of psychosine hydrolase activity","type":"exact"},{"name":"inhibition of D-glucosyl-N-acylsphingosine glucohydrolase activity","type":"narrow"},{"name":"inhibition of GlcCer-beta-glucosidase activity","type":"narrow"},{"name":"inhibition of acid beta-glucosidase activity","type":"narrow"},{"name":"inhibition of beta-D-glucocerebrosidase activity","type":"narrow"},{"name":"inhibition of beta-glucocerebrosidase activity","type":"narrow"},{"name":"inhibition of beta-glucosylceramidase activity","type":"narrow"},{"name":"inhibition of ceramide glucosidase activity","type":"narrow"},{"name":"inhibition of glucocerebrosidase activity","type":"narrow"},{"name":"inhibition of glucosphingosine glucosylhydrolase activity","type":"narrow"},{"name":"inhibition of glucosylceramidase activity","type":"narrow"},{"name":"inhibition of glucosylcerebrosidase activity","type":"narrow"},{"name":"inhibition of glucosylsphingosine beta-D-glucosidase activity","type":"narrow"},{"name":"inhibition of glucosylsphingosine beta-glucosidase activity","type":"narrow"},{"name":"inhibition of psychosine hydrolase activity","type":"narrow"},{"name":"negative regulation of D-glucosyl-N-acylsphingosine glucohydrolase activity","type":"exact"},{"name":"negative regulation of GCase activity","type":"exact"},{"name":"negative regulation of GlcCer-beta-glucosidase activity","type":"exact"},{"name":"negative regulation of acid beta-glucosidase activity","type":"exact"},{"name":"negative regulation of beta-D-glucocerebrosidase activity","type":"exact"},{"name":"negative regulation of beta-glucocerebrosidase activity","type":"exact"},{"name":"negative regulation of beta-glucosylceramidase activity","type":"exact"},{"name":"negative regulation of ceramide glucosidase activity","type":"exact"},{"name":"negative regulation of glucocerebrosidase activity","type":"exact"},{"name":"negative regulation of glucosphingosine glucosylhydrolase activity","type":"exact"},{"name":"negative regulation of glucosylcerebrosidase activity","type":"exact"},{"name":"negative regulation of glucosylsphingosine beta-D-glucosidase activity","type":"exact"},{"name":"negative regulation of glucosylsphingosine beta-glucosidase activity","type":"exact"},{"name":"negative regulation of psychosine hydrolase activity","type":"exact"}],"termid":"GO:1905124"}


id: PBO:0002980
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino acid permease (predicted)","termid":"PBO:0002980"}


id: GO:2000328
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of T-helper 17 cell lineage commitment.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell fate commitment","termid":"GO:0010453"},{"relation_name":"is_a","term_name":"regulation of T-helper 17 cell differentiation","termid":"GO:2000319"},{"relation_name":"regulates","term_name":"T-helper 17 cell lineage commitment","termid":"GO:0072540"}],"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 T-helper 17 cell lineage commitment","synonyms":[{"name":"regulation of T-helper 17 cell fate commitment","type":"exact"},{"name":"regulation of Th17 cell lineage commitment","type":"exact"},{"name":"regulation of Th17 fate commitment","type":"exact"}],"termid":"GO:2000328"}


id: PBO:0065832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB7B, member RAS oncogene family","termid":"PBO:0065832"}


id: PBO:0086512
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved across S. cerevisiae strains; deletion decreases transcription of downstream gene ALD6; YPL062W is not an essential gene; null mutant shows decrease in terpenoid production; homozygous diploid mutant shows a decrease in glycogen accumulation","termid":"PBO:0086512"}


id: MONDO:0013839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary sensory and autonomic neuropathy in which the cause of the disease is a mutation in the DST gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary sensory and autonomic neuropathy","termid":"MONDO:0015364"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"hereditary sensory and autonomic neuropathy type 6","secondary_identifiers":["OMIM:614653","GARD:12987","DOID:0070151","MEDGEN:761278","Orphanet:314381","UMLS:C3539003"],"synonyms":[{"name":"DST hereditary sensory and autonomic neuropathy","type":"exact"},{"name":"HSAN 6","type":"related"},{"name":"HSAN6","type":"exact"},{"name":"familial dysautonomia with contractures","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy caused by mutation in DST","type":"exact"},{"name":"hereditary sensory and autonomic neuropathy type VI","type":"exact"},{"name":"neuropathy, hereditary sensory and autonomic, type 6","type":"related"},{"name":"neuropathy, hereditary sensory and autonomic, type VI","type":"related"}],"termid":"MONDO:0013839","xrefs":{"Monarch":{"xref_id":"0013839"}}}


id: GO:0060950
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized features of a glial cell of the heart.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell differentiation","termid":"GO:0010001"},{"relation_name":"is_a","term_name":"cardiocyte differentiation","termid":"GO:0035051"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cardiac glial cell differentiation","termid":"GO:0060950"}


id: PBO:0029759
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_DNA_5'-adenosine_monophosphate_hydrolase_activity","termid":"PBO:0029759"}


id: PBO:0062283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily J member 7 pseudogene","termid":"PBO:0062283"}


id: MONDO:0005733
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dirofilariasis (obsolete MONDO:0005733)","termid":"MONDO:0005733","xrefs":{"Monarch":{"xref_id":"0005733"}}}


id: MONDO:0044788
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An intrahepatic cholangiocarcinoma that arises from the intrahepatic large bile ducts.","definition_xrefs":["NCIT:C96804"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intrahepatic cholangiocarcinoma","termid":"MONDO:0003210"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"perihilar intrahepatic cholangiocarcinoma","secondary_identifiers":["ONCOTREE:PHCH"],"synonyms":[{"name":"perihilar ICC","type":"exact"},{"name":"perihilar bile duct carcinoma","type":"exact"},{"name":"perihilar cholangiocarcinoma","type":"related"},{"name":"perihilar intrahepatic cholangiocarcinoma","type":"exact"}],"termid":"MONDO:0044788","xrefs":{"Monarch":{"xref_id":"0044788"}}}


id: MONDO:1011993
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lacrimal fistula, non-human animal","secondary_identifiers":["OMIA:001693"],"termid":"MONDO:1011993","xrefs":{"Monarch":{"xref_id":"1011993"}}}


id: MONDO:0017223
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The transitional form of Pelizaeus-Merzbacher disease (PMD) is the intermediate form of PMD.","definition_xrefs":["Orphanet:280224"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Pelizeaus-Merzbacher spectrum disorder","termid":"MONDO:0010714"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"Pelizaeus-Merzbacher disease, transitional form","secondary_identifiers":["MEDGEN:199764","GARD:21074","UMLS:C0751917","icd11.foundation:1471805474"],"synonyms":[{"name":"transitional PMD","type":"exact"}],"termid":"MONDO:0017223","xrefs":{"Monarch":{"xref_id":"0017223"}}}


id: FYPO:0000015
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a daughter cell begins to grow from the lateral portion of the long axis of the cell, and at an angle to the septum or cell division site of the mother cell, resulting in the formation of a single cell that has a branch.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell shape","termid":"FYPO:0002196"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0000005"],"is_obsolete":false,"name":"branched vegetative cell","synonyms":[{"name":"branched cell","type":"exact"},{"name":"branched cell during vegetative growth","type":"exact"},{"name":"branched vegetative cell during mitotic cell cycle","type":"related"},{"name":"cell morphology, branched","type":"exact"}],"termid":"FYPO:0000015"}


id: GO:0051564
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the concentration of calcium ions in the smooth endoplasmic reticulum.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of endoplasmic reticulum calcium ion concentration","termid":"GO:0032470"},{"relation_name":"is_a","term_name":"smooth endoplasmic reticulum calcium ion homeostasis","termid":"GO:0051563"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098771"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0098771","GO:0008150"],"is_obsolete":false,"name":"positive regulation of smooth endoplasmic reticulum calcium ion concentration","synonyms":[{"name":"elevation of calcium ion concentration in smooth endoplasmic reticulum","type":"exact"},{"name":"elevation of smooth ER calcium ion concentration","type":"exact"},{"name":"elevation of smooth endoplasmic reticulum calcium ion concentration","type":"exact"},{"name":"smooth endoplasmic reticulum calcium ion concentration elevation","type":"exact"}],"termid":"GO:0051564"}


id: PBO:0048825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein subunit gamma 10 pseudogene 1","termid":"PBO:0048825"}


id: PATO:0001104
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001104 strain value (obsolete PATO:0001104)","termid":"PATO:0001104"}


id: PBO:0047377
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 8","termid":"PBO:0047377"}


id: PBO:0027267
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-RNA_absent_from_cell_during_cellular_response_to_pheromone","termid":"PBO:0027267"}


id: PBO:0039011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AFF4 pseudogene 1","termid":"PBO:0039011"}


id: GO:0007553
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving ecdysteroids, a group of polyhydroxylated ketosteroids which initiate post-embryonic development, including the metamorphosis of immature forms and the development of the reproductive system and the maturation of oocytes in adult females.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone metabolic process","termid":"GO:0010565"},{"relation_name":"is_a","term_name":"regulation of steroid metabolic process","termid":"GO:0019218"},{"relation_name":"is_a","term_name":"regulation of hormone metabolic process","termid":"GO:0032350"},{"relation_name":"regulates","term_name":"ecdysteroid metabolic process","termid":"GO:0045455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"regulation of ecdysteroid metabolic process","synonyms":[{"name":"regulation of ecdysteroid metabolism","type":"exact"}],"termid":"GO:0007553"}


id: FYPO:0002200
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetatively growing cell is inviable and has one or more septa, and the cell diameter is larger than normal and the cell length is shorter than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable stubby vegetative cell","termid":"FYPO:0002107"},{"relation_name":"is_a","term_name":"inviable septated vegetative cell with abnormal cell morphology","termid":"FYPO:0002452"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000004","FYPO:0000002","FYPO:0001320","FYPO:0000005"],"is_obsolete":false,"name":"inviable stubby septated vegetative cell","synonyms":[{"name":"inviable stubby septated cell during vegetative growth","type":"exact"},{"name":"inviable stubby septated vegetative cell during mitotic cell cycle","type":"related"},{"name":"inviable watermelon-shaped septated vegetative cell","type":"exact"},{"name":"lethal; stubby septated vegetative cell","type":"exact"},{"name":"stubby septated inviable vegetative cell","type":"exact"}],"termid":"FYPO:0002200"}


id: FYPO:0007621
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of one protein to another occurs to a lower extent than normal when the cell is subject to oxidative stress. The relevant proteins may include the one encoded by the mutated gene, or may both be encoded by different genes.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein-protein interaction","termid":"FYPO:0001571"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000702","FYPO:0000707","FYPO:0001985","FYPO:0000652"],"is_obsolete":false,"name":"increased protein-protein interaction during cellular response to oxidative stress","synonyms":[{"name":"increased protein binding during cellular response to oxidative stress","type":"exact"},{"name":"increased protein-protein interaction during oxidative stress response","type":"exact"}],"termid":"FYPO:0007621"}


id: PBO:0029380
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_stress","termid":"PBO:0029380"}


id: PBO:0054097
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 1450","termid":"PBO:0054097"}


id: PBO:0053985
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 1301","termid":"PBO:0053985"}


id: GO:0016873
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A grouping term for isomerases that cannot be more accurately categorized.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete other isomerase activity (obsolete GO:0016873)","synonyms":[{"name":"other isomerase activity","type":"exact"}],"termid":"GO:0016873"}


id: PBO:0028487
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_mitotic_spindle_pole_body_during_interphase","termid":"PBO:0028487"}


id: PBO:0089666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent chromatin remodeller/ubiquitin-protein ligase E3 Rad8","termid":"PBO:0089666"}


id: MOD:00531
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-asparagine residue to L-aspartic acid with one (18)O as the result of having been deglycosylated in (18)O water.","definition_xrefs":["PubMed:14435542","Unimod:170"],"direct_ancestors":[{"relation_name":"is_a","term_name":"1x(18)O labeled deamidated L-asparagine","termid":"MOD:01293"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(18)O labeled deglycosylated asparagine","synonyms":[{"name":"Delta:H(1)O(-1)18O(1)","type":"related"},{"name":"glycosylated asparagine 18O labeling","type":"related"}],"termid":"MOD:00531"}


id: PBO:0051867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon stimulated exonuclease gene 20 like 2","termid":"PBO:0051867"}


id: PBO:0031715
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitochondrial_transport","termid":"PBO:0031715"}


id: PBO:0053430
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 375","termid":"PBO:0053430"}


id: PBO:0079354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin alpha 1b","termid":"PBO:0079354"}


id: PBO:0066236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding motif protein 43 pseudogene 1","termid":"PBO:0066236"}


id: PBO:0114652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipid scramblase","termid":"PBO:0114652"}


id: GO:0016807
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of a single C-terminal amino acid residue from a polypeptide chain by a mechanism in which the sulfhydryl group of a cysteine residue at the active center acts as a nucleophile.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxypeptidase activity","termid":"GO:0004180"},{"relation_name":"is_a","term_name":"cysteine-type exopeptidase activity","termid":"GO:0070004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0008233"}],"interesting_parent_ids":["GO:0003824","GO:0008233","GO:0016787","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"cysteine-type carboxypeptidase activity","secondary_identifiers":["EC:3.4.18.-"],"termid":"GO:0016807"}


id: PBO:0027776
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_2-bromo-2-(((4-methylphenyl)sulfonyl)methyl)-1-indanone","termid":"PBO:0027776"}


id: PBO:0060849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nei like DNA glycosylase 3","termid":"PBO:0060849"}


id: MONDO:0016152
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete qualitative or quantitative defects of calpain (obsolete MONDO:0016152)","secondary_identifiers":["Orphanet:207104"],"termid":"MONDO:0016152","xrefs":{"Monarch":{"xref_id":"0016152"}}}


id: MONDO:0013673
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Wolfram-like syndrome is a rare endocrine disease characterized by the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy. Psychiatric (i.e. anxiety, depression, hallucinations) and sleep disorders, the only neurologic abnormalities observed in this disease, have been reported in rare cases. Unlike Wolfram syndrome, patients with Wolfram-like syndrome do not report endocrine or cardiac findings.","definition_xrefs":["Orphanet:411590"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"endocrine system disorder","termid":"MONDO:0005151"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Wolfram-like syndrome","secondary_identifiers":["SCTID:734022008","OMIM:614296","DOID:0080584","GARD:17683","UMLS:C3280358","MESH:C565631","MEDGEN:481988"],"synonyms":[{"name":"WFSL","type":"related"},{"name":"Wolfram-like syndrome","type":"exact"},{"name":"Wolfram-like syndrome, autosomal dominant","type":"related"},{"name":"hearing loss, progressive, with optic atrophy and/or impaired glucose Regulation","type":"related"}],"termid":"MONDO:0013673","xrefs":{"Monarch":{"xref_id":"0013673"}}}


id: PBO:0002906
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"26S proteasome regulatory particle assembly protein (predicted)","termid":"PBO:0002906"}


id: PBO:0080516
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WASP family member 3","termid":"PBO:0080516"}


id: PBO:0054776
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 2189","termid":"PBO:0054776"}


id: PBO:0038779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activin A receptor type 2A","termid":"PBO:0038779"}


id: PBO:0051710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin","termid":"PBO:0051710"}


id: PBO:0090312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Ddx27/Drs1","termid":"PBO:0090312"}


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


id: MONDO:0013329
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"17q23.1-q23.2 microduplication is a newly described cause of familial isolated clubfoot.","definition_xrefs":["Orphanet:238578"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial clubfoot with or without associated lower limb anomalies","termid":"MONDO:0016046"},{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome 17","termid":"MONDO:0016967"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial clubfoot due to 17q23.1q23.2 microduplication","secondary_identifiers":["OMIM:613618","MEDGEN:462230","GARD:17177","UMLS:C3150880"],"synonyms":[{"name":"chromosome 17q23.1-q23.2 DUPLICATION syndrome","type":"related"},{"name":"hereditary clubfoot due to 17q23.1-q23.2 microduplication","type":"exact"}],"termid":"MONDO:0013329","xrefs":{"Monarch":{"xref_id":"0013329"}}}


id: SO:0000800
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A multi-chromosome duplication aberration generated by reassortment of other aberration components.","definition_xrefs":["FB:gm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"assortment_derived_variation","termid":"SO:0001504"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"assortment_derived_duplication","synonyms":[{"name":"assortment derived duplication","type":"exact"}],"termid":"SO:0000800"}


id: GO:1902197
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of isovaleryl-CoA(4-).","definition_xrefs":["PMID:11231285","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty-acyl-CoA biosynthetic process","termid":"GO:0046949"},{"relation_name":"is_a","term_name":"isovaleryl-CoA(4-) metabolic process","termid":"GO:1902195"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0055086"},{"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:0055086","GO:0006790","GO:0006629","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"isovaleryl-CoA(4-) biosynthetic process","synonyms":[{"name":"isovaleryl-CoA(4-) anabolism","type":"exact"},{"name":"isovaleryl-CoA(4-) biosynthesis","type":"exact"},{"name":"isovaleryl-CoA(4-) formation","type":"exact"},{"name":"isovaleryl-CoA(4-) synthesis","type":"exact"}],"termid":"GO:1902197"}


id: PBO:0075668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine palmitoyltransferase long chain base subunit 1 pseudogene 3","termid":"PBO:0075668"}


id: PBO:0074545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sushi, nidogen and EGF like domains 1","termid":"PBO:0074545"}


id: GO:0097361
data:
  {"annotated_genes":["SJAG_02866","SJAG_02895","SJAG_00040","SJAG_02497"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[86853,88175,99218,113895],"is_not":false,"summary":null,"term":"GO:0097361"}]},"cv_name":"cellular_component","definition":"A protein complex capable of condensing two 2Fe-2S clusters into one 4Fe-4S center in the cytoplasm and nucleus. In humans it consists of MMS19, CIAO1, CIAO2A/CIAO2B, CIAO3. MMS19, CIAO1 and CIAO2A/CIAO2B form a tight 'core' complex, whereas CIAO3 is an 'external' component of this complex.","definition_xrefs":["PMID:23585563","PMID:34660592","PMID:23891004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular protein-containing complex","termid":"GO:0140535"},{"relation_name":"is_a","term_name":"iron-sulfur cluster assembly complex","termid":"GO:1990229"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00040":null,"SJAG_02497":null,"SJAG_02866":null,"SJAG_02895":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005829"}],"interesting_parent_ids":["GO:0005737","GO:0005829","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"cytosolic [4Fe-4S] assembly targeting complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"CIA complex","type":"broad"},{"name":"CIA targeting complex","type":"exact"},{"name":"cytosolic iron-sulfur protein assembly complex","type":"related"}],"termid":"GO:0097361","terms_by_termid":{"GO:0097361":null}}


id: PBO:0059495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myostatin","termid":"PBO:0059495"}


id: GO:0070286
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form an axonemal dynein complex, a dynein complex found in eukaryotic cilia and flagella, in which the motor domain heads interact with adjacent microtubules to generate a sliding force which is converted to a bending motion.","definition_xrefs":["GOC:cilia","PMID:19052621","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"part_of","term_name":"axoneme assembly","termid":"GO:0035082"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0000226"},{"rel_name":"part_of","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150","GO:0000226","GO:0007010"],"is_obsolete":false,"name":"axonemal dynein complex assembly","synonyms":[{"name":"dynein arm assembly","type":"exact"}],"termid":"GO:0070286"}


id: GO:1902794
data:
  {"annotated_genes":["SJAG_01867","SJAG_02622","SJAG_04768","SJAG_04574","SJAG_00769","SJAG_01599","SJAG_04186","SJAG_03844","SJAG_02382","SJAG_03624","SJAG_03664"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[86713,90003,103367,109631,111250,115672,117245],"is_not":false,"summary":null,"term":"GO:1902794"},{"annotations":[117242,96385,116883,99490,91064],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902801"}]},"cv_name":"biological_process","definition":"The formation of facultative heterochromatin into a heterochromatin domain, enriched in histone H3 methylated on lysine 9 (H3K9me), by a process independent of small interfering RNAs.","definition_xrefs":["PMID:22144463","PMID:24210919"],"direct_ancestors":[{"relation_name":"is_a","term_name":"facultative heterochromatin formation","termid":"GO:0140718"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00769":null,"SJAG_01599":null,"SJAG_01867":null,"SJAG_02382":null,"SJAG_02622":null,"SJAG_03624":null,"SJAG_03664":null,"SJAG_03844":null,"SJAG_04186":null,"SJAG_04574":null,"SJAG_04768":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006325"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006325","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"siRNA-independent facultative heterochromatin formation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"heterochromatin island assembly","type":"exact"},{"name":"heterochromatin island formation","type":"exact"},{"name":"siRNA-independent facultative heterochromatin assembly","type":"exact"}],"termid":"GO:1902794","terms_by_termid":{"GO:1902794":null,"GO:1902801":null}}


id: PBO:0004138
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-oxoglutarate and Fe(II) dioxygenase domain containing protein 1","termid":"PBO:0004138"}


id: GO:0006114
data:
  {"annotated_genes":["SJAG_01012","SJAG_00409"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93174,105660],"is_not":false,"summary":null,"term":"GO:0006114"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of glycerol, 1,2,3-propanetriol, a sweet, hygroscopic, viscous liquid, widely distributed in nature as a constituent of many lipids.","definition_xrefs":["ISBN:0198506732","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycerol metabolic process","termid":"GO:0006071"},{"relation_name":"is_a","term_name":"alditol biosynthetic process","termid":"GO:0019401"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00409":null,"SJAG_01012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975"],"is_obsolete":false,"name":"glycerol biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"glycerol anabolism","type":"exact"},{"name":"glycerol biosynthesis","type":"exact"},{"name":"glycerol formation","type":"exact"},{"name":"glycerol synthesis","type":"exact"}],"termid":"GO:0006114","terms_by_termid":{"GO:0006114":null}}


id: MONDO:1012422
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"exfoliative cutaneous lupus erythematosus, non-human animal","termid":"MONDO:1011756"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exfoliative cutaneous lupus erythematosus, dog","secondary_identifiers":["OMIA:001609-9615"],"termid":"MONDO:1012422","xrefs":{"Monarch":{"xref_id":"1012422"}}}


id: MONDO:0002383
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurofibroma characterized by the presence of structures which resemble Vater-Pacini corpuscles.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurofibroma","termid":"MONDO:0016755"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pacinian tumor","secondary_identifiers":["DOID:2669","NCIT:C4328","ICDO:9507/0","SCTID:404033003","ICD9:215.9","UMLS:C0334599","MEDGEN:87273"],"synonyms":[{"name":"Pacinian neurofibroma","type":"exact"},{"name":"Pacinian tumor (morphologic abnormality)","type":"exact"},{"name":"Pacinian tumour (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0002383","xrefs":{"Monarch":{"xref_id":"0002383"}}}


id: PBO:0074381
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMG1 pseudogene 7","termid":"PBO:0074381"}


id: PBO:0087969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transverse filament protein of the synaptonemal complex; required for normal levels of meiotic recombination and pairing between homologous chromosome during meiosis; required for meiotic recombination between non-allelc sites; potential Cdc28p substrate","termid":"PBO:0087969"}


id: GO:1902464
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of histone H3-K27 trimethylation.","definition_xrefs":["GOC:TermGenie","PMID:19270745"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone H3-K27 trimethylation (obsolete GO:1902464)","termid":"GO:1902464"}


id: PBO:0087987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA:pseudouridine synthase; introduces pseudouridines at position 38 or 39 in tRNA; also responsible for pseudouracil modification of some mRNAs; important for maintenance of translation efficiency and normal cell growth, localizes to both the nucleus and cytoplasm; non-essential for viability","termid":"PBO:0087987"}


id: GO:1903064
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of reverse cholesterol transport.","definition_xrefs":["PMID:23931754","GOC:rl","GOC:TermGenie","GO_REF:0000058","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cholesterol transport","termid":"GO:0032376"},{"relation_name":"is_a","term_name":"regulation of reverse cholesterol transport","termid":"GO:1903062"},{"relation_name":"positively_regulates","term_name":"reverse cholesterol transport","termid":"GO:0043691"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"positive regulation of reverse cholesterol transport","synonyms":[{"name":"activation of reverse cholesterol transport","type":"narrow"},{"name":"up regulation of reverse cholesterol transport","type":"exact"},{"name":"up-regulation of reverse cholesterol transport","type":"exact"},{"name":"upregulation of reverse cholesterol transport","type":"exact"}],"termid":"GO:1903064"}


id: GO:0016200
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a neuronal cell in a multicellular organism recognizes chemoattractant signals from, and grows towards, potential targets.","definition_xrefs":["GOC:mah","ISBN:0878932437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive chemotaxis","termid":"GO:0050918"},{"relation_name":"part_of","term_name":"synaptic target recognition","termid":"GO:0008039"}],"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":"synaptic target attraction","termid":"GO:0016200"}


id: MONDO:0020848
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant osteopetrosis","termid":"MONDO:0020645"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"osteopetrosis, autosomal dominant 3","secondary_identifiers":["MEDGEN:1648454","OMIM:618107","UMLS:C4748197"],"synonyms":[{"name":"OPTA3","type":"exact"},{"name":"OSTEOPETROSIS, autosomal dominant 3","type":"exact"}],"termid":"MONDO:0020848","xrefs":{"Monarch":{"xref_id":"0020848"}}}


id: PBO:0065270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich 32","termid":"PBO:0065270"}


id: PBO:0110167
data:
  {"annotation_feature_type":"gene","cv_name":"pubprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canto_approver_orcid","termid":"PBO:0110167"}


id: PBO:0003094
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homotetrameric","termid":"PBO:0003094"}


id: PR:P79083
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A eukaryotic translation initiation factor 3 subunit I that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR19877:SF1","PRO:DNx","OMA:SCHPO02224"],"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":"eukaryotic translation initiation factor 3 subunit I (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.05","secondary_identifiers":["UniProtKB:P79083"],"synonyms":[{"name":"Spom972h-EIF3I","type":"exact"},{"name":"eIF-3 39 kDa subunit homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eIF3 p39 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eIF3i (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"eukaryotic translation initiation factor 3 39 kDa subunit homolog (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"suppressor of uncontrolled mitosis 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P79083"}


id: MONDO:0015100
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myelodysplastic syndrome with multilineage dysplasia","termid":"MONDO:0019453"}],"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":"aregenerative anemia","secondary_identifiers":["MEDGEN:639969","Orphanet:101096","MedDRA:10054329","UMLS:C0553669","SCTID:89112009","GARD:19778"],"termid":"MONDO:0015100","xrefs":{"Monarch":{"xref_id":"0015100"}}}


id: PBO:0005073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligosaccharyltransferase delta subunit Swp1 (predicted)","termid":"PBO:0005073"}


id: PBO:0058503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5693","termid":"PBO:0058503"}


id: GO:0005674
data:
  {"annotated_genes":["SJAG_00735","SJAG_04852","SJAG_00095"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[92705,101478,114110],"is_not":false,"summary":null,"term":"GO:0005674"}]},"cv_name":"cellular_component","definition":"A general transcription initiation factor which in humans consists of a heterodimer of an alpha and a beta subunit. Helps recruit RNA polymerase II to the initiation complex and promotes translation elongation.","definition_xrefs":["GOC:jl","PMID:7597077"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription regulator complex","termid":"GO:0090575"},{"relation_name":"part_of","term_name":"RNA polymerase II, holoenzyme","termid":"GO:0016591"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00095":null,"SJAG_00735":null,"SJAG_04852":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005654"}],"interesting_parent_ids":["GO:0005654","GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"transcription factor TFIIF complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0005674","terms_by_termid":{"GO:0005674":null}}


id: GO:0061175
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Terminal inflated portion of the axon of a non-glutamatergic neuron, containing the specialized apparatus necessary to release neurotransmitters at a regulatory synapse. The axon terminus is considered to be the whole region of thickening and the terminal bouton is a specialized region of it.","definition_xrefs":["GOC:dph","GOC:mc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"terminal bouton","termid":"GO:0043195"}],"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":"type II terminal bouton","synonyms":[{"name":"type II terminal button","type":"exact"}],"termid":"GO:0061175"}


id: PBO:0079034
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Val (anticodon AAC) 3-1","termid":"PBO:0079034"}


id: PBO:0072922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small Cajal body-specific RNA 3","termid":"PBO:0072922"}


id: GO:1990592
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A protein ufmylation process in which a polymer of the ubiquitin-like protein UFM1 is formed by linkages between lysine residues at position 69 of the UFM1 monomers, is added to a protein.","definition_xrefs":["PMID:25219498"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein polyufmylation","termid":"GO:1990564"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"protein K69-linked ufmylation","termid":"GO:1990592"}


id: PBO:0088207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zn-ribbon protein that co-purifies with Dph1 and Dph2; forms a complex required for synthesis of diphthamide on translation factor eEF2 and with Elongator subunits Iki3p, Elp2p, and Elp3p; involved in modification of wobble nucleosides in tRNAs; forms a stable heterodimer with Ats1p","termid":"PBO:0088207"}


id: PBO:0001997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJ domain protein Erj5 (predicted)","termid":"PBO:0001997"}


id: GO:0033501
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A homeostatic process involved in the maintenance of an internal steady state of galactose within an organism or cell.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete galactose homeostasis (obsolete GO:0033501)","termid":"GO:0033501"}


id: PBO:0069424
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 687, pseudogene","termid":"PBO:0069424"}


id: GO:1902000
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of homogentisate.","definition_xrefs":["GOC:TermGenie","PMID:22980205"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"},{"relation_name":"is_a","term_name":"homogentisate metabolic process","termid":"GO:1901999"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0044248"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0044248"],"is_obsolete":false,"name":"homogentisate catabolic process","synonyms":[{"name":"homogentisate breakdown","type":"exact"},{"name":"homogentisate catabolism","type":"exact"},{"name":"homogentisate degradation","type":"exact"}],"termid":"GO:1902000"}


id: MONDO:0007104
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"amyotrophic lateral sclerosis-parkinsonism-dementia complex","secondary_identifiers":["GARD:9239","MEDGEN:107775","OMIM:105500","Orphanet:90020","UMLS:C0543859","ICD10CM:G12.2","DOID:0111246"],"synonyms":[{"name":"ALS-pDC","type":"related"},{"name":"Guam disease","type":"exact"},{"name":"Lytico-Bodig disease","type":"exact"},{"name":"Lytigo-Bodig disease","type":"exact"},{"name":"PDALS","type":"exact"},{"name":"Parkinsonism-dementia-ALS complex","type":"exact"},{"name":"amyotrophic lateral sclerosis, Parkinsonism/dementia complex of Guam","type":"related"},{"name":"amyotrophic lateral sclerosis-PARKINSONISM/dementia complex 1","type":"related"},{"name":"amyotrophic lateral sclerosis-Parkinsonism/dementia Complex of Guam","type":"related"},{"name":"amyotrophic lateral sclerosis-Parkinsonism/dementia Complex type 1","type":"exact"},{"name":"amyotrophic lateral sclerosis-parkinsonism-dementia of Guam syndrome","type":"exact"},{"name":"amyotrophic lateral sclerosis-parkinsonism/dementia complex, susceptibility to","type":"related"}],"termid":"MONDO:0007104","xrefs":{"Monarch":{"xref_id":"0007104"}}}


id: GO:0072218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a metanephric ascending thin limb over time, from its formation to the mature structure. The metanephric ascending thin limb is a segment of a nephron tubule in the metanephros lying in the inner medulla that is permeable to ions but not to water and has a simple epithelium; active transepithelial solute transport is absent.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ascending thin limb development","termid":"GO:0072021"},{"relation_name":"is_a","term_name":"metanephric nephron tubule development","termid":"GO:0072234"},{"relation_name":"part_of","term_name":"metanephric loop of Henle development","termid":"GO:0072236"}],"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 ascending thin limb development","termid":"GO:0072218"}


id: GO:0120316
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly and organization of the sperm flagellum, the microtubule-based axoneme and associated structures that are part of a sperm flagellum (or cilium).","definition_xrefs":["PMID:32791035","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"motile cilium assembly","termid":"GO:0044458"},{"relation_name":"part_of","term_name":"spermatid development","termid":"GO:0007286"},{"relation_name":"part_of","term_name":"flagellated sperm motility","termid":"GO:0030317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150"],"is_obsolete":false,"name":"sperm flagellum assembly","termid":"GO:0120316"}


id: PBO:0082451
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C2H2-type zinc finger protein required for ribosome assembly; shuttling factor which associates with pre-60S particles in the nucleus, accompanying them to the cytoplasm; cytoplasmic dissociation of Bud20p requires Drg1p; N-terminus harbors a nuclear localization signal (NLS) and a nuclear export signal (NES); cytoplasmic Bud20p is reimported by Kap123-dependent pathway; involved in bud-site selection; diploid mutants display a random budding pattern; similar to human ZNF593","termid":"PBO:0082451"}


id: PBO:0079048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Val (anticodon CAC) 4-1","termid":"PBO:0079048"}


id: PBO:0002692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"20S proteasome component beta 6","termid":"PBO:0002692"}


id: PBO:0046453
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPS8 like 1","termid":"PBO:0046453"}


id: PBO:0085609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in cytochrome c oxidase (Complex IV) assembly; involved in delivery of copper to Complex IV; also required for efficient formation of respiratory supercomplexes comprised of Complexes III and IV; localizes to the mitochondrial intermembrane space; ortholog implicated in cardiac defects in zebrafish and human; transcription is induced in response to the DNA-damaging agent MMS; protein abundance increases in response to DNA replication stress","termid":"PBO:0085609"}


id: GO:0072186
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the metanephric cap are generated and organized. The metanephric cap is formed by the condensation of metanephric mesenchymal cells surrounding the ureteric bud tip.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metanephric mesenchyme morphogenesis","termid":"GO:0072133"},{"relation_name":"part_of","term_name":"metanephric cap development","termid":"GO:0072185"}],"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 cap morphogenesis","termid":"GO:0072186"}


id: GO:0007215
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of glutamate to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","PMID:9131252","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway","termid":"GO:0007166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"glutamate receptor signaling pathway","synonyms":[{"name":"glutamate signaling pathway","type":"exact"},{"name":"glutamate signalling pathway","type":"exact"}],"termid":"GO:0007215"}


id: GO:0030355
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete small nucleolar ribonucleoprotein (obsolete GO:0030355)","synonyms":[{"name":"small nucleolar ribonucleoprotein","type":"exact"},{"name":"snoRNP","type":"exact"}],"termid":"GO:0030355"}


id: FYPO:0000664
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which a specified catalytic activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"},{"relation_name":"is_a","term_name":"abolished molecular function","termid":"FYPO:0005446"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000654","FYPO:0000707","FYPO:0001985","FYPO:0000652"],"is_obsolete":false,"name":"abolished catalytic activity","synonyms":[{"name":"catalytic activity abolished","type":"exact"}],"termid":"FYPO:0000664"}


id: PBO:0074541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synuclein gamma","termid":"PBO:0074541"}


id: PBO:0082383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Beta 3 subunit of the 20S proteasome; involved in ubiquitin-dependent catabolism; human homolog is subunit C10","termid":"PBO:0082383"}


id: GO:0010644
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that mediates signaling interactions between one cell and another cell by transfer of current between their adjacent cytoplasms via intercellular protein channels.","definition_xrefs":["GOC:dph","GOC:kmv","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell communication","termid":"GO:0007154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell communication by electrical coupling","termid":"GO:0010644"}


id: PATO:0001906
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physical quality inhering in a bearer by virtue of the bearer's participation in movement.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physical quality","termid":"PATO:0001018"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"movement quality","termid":"PATO:0001906"}


id: FYPO:0003787
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells form mitotic spindle microtubules that are longer than normal, and extend beyond the spindle pole body. The protruding spindle microtubules are surrounded by an extension of the nuclear envelope.","definition_xrefs":["PomBase:mah","PMID:17486116"],"direct_ancestors":[{"relation_name":"has_part","term_name":"nuclear envelope protrusion present during mitosis","termid":"FYPO:0003788"},{"relation_name":"is_a","term_name":"long microtubules","termid":"FYPO:0000055"},{"relation_name":"is_a","term_name":"long mitotic spindle","termid":"FYPO:0000733"},{"relation_name":"is_a","term_name":"nuclear envelope protrusion present during mitosis","termid":"FYPO:0003788"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0002403","FYPO:0002399","FYPO:0000054","FYPO:0000120","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"long mitotic spindle microtubules protruding beyond spindle pole body","synonyms":[{"name":"elongated mitotic spindle microtubules protruding from spindle pole body","type":"exact"},{"name":"elongated mitotic spindle microtubules protruding from spindle pole body during M-phase","type":"exact"},{"name":"long mitotic spindle microtubules protruding beyond spindle pole body, with nuclear envelope deformation","type":"related"},{"name":"long mitotic spindle microtubules protruding beyond spindle pole body, with nuclear envelope protrusion","type":"exact"},{"name":"long mitotic spindle microtubules protruding from SPB","type":"exact"},{"name":"long mitotic spindle microtubules protruding from spindle pole body during mitotic cell cycle","type":"related"},{"name":"long mitotic spindle microtubules protruding from spindle pole body during vegetative growth","type":"exact"},{"name":"mitotic spindle microtubules protruding beyond spindle pole body","type":"broad"},{"name":"nuclear envelope protrusion with long mitotic spindle microtubules protruding beyond spindle pole body","type":"exact"}],"termid":"FYPO:0003787"}


id: MONDO:0004697
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare condition that usually affects the middle-to-distal esophagus in middle-aged and elderly people. There is usually a history of tobacco smoking or alcohol intake. Dysphagia is the presenting symptom. Morphologically, the lesions are well-demarcated and are characterized by epithelial hyperplasia, thickened basal layer, prominent granular cell layer, and hyperorthokeratosis. In a minority of patients this condition is associated with adjacent high-grade squamous dysplasia and/or squamous cell carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"esophageal disorder","termid":"MONDO:0003749"},{"relation_name":"is_a","term_name":"leukoplakia","termid":"MONDO:0043243"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"esophageal leukoplakia","secondary_identifiers":["HP:0012859","DOID:9021","ICD9:530.83","MEDGEN:75628","NCIT:C3953","SCTID:89057003","UMLS:C0267095"],"synonyms":[{"name":"esophageal epidermoid metaplasia","type":"exact"},{"name":"esophageal leukoplakia","type":"exact"},{"name":"esophageal leukoplakia (disease)","type":"exact"},{"name":"esophagus leukoplakia","type":"exact"},{"name":"leukoplakia of esophagus","type":"exact"},{"name":"leukoplakia of oesophagus","type":"exact"},{"name":"leukoplakia of the esophagus","type":"exact"},{"name":"leukoplakia of the oesophagus","type":"exact"},{"name":"oesophagus leukoplakia","type":"exact"}],"termid":"MONDO:0004697","xrefs":{"Monarch":{"xref_id":"0004697"}}}


id: GO:0039675
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of the viral genome or a viral particle out of the host cell nucleus through the nuclear pore.","definition_xrefs":["PMID:12921991","VZ:1953"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exit of virus from host cell nucleus","termid":"GO:0039674"}],"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":"exit of virus from host cell nucleus through nuclear pore","synonyms":[{"name":"exit of virus from host cell nucleus through nuclear pore complex","type":"exact"},{"name":"nuclear pore exit of virus","type":"exact"},{"name":"viral enome export through nuclear pore","type":"exact"}],"termid":"GO:0039675"}


id: PBO:0038637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA thioesterase 2","termid":"PBO:0038637"}


id: MONDO:0007555
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A basal subtype of epidermolysis bullosa simplex (EBS) characterized by sometimes widespread, primarily acral blistering.","definition_xrefs":["Orphanet:79401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolysis bullosa simplex","termid":"MONDO:0017610"}],"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":"pidermolysis bullosa simplex 5A, Ogna type","secondary_identifiers":["UMLS:C0432317","MEDGEN:98488","SCTID:398071000","OMIM:131950","DOID:0060736","ICD9:757.39","MESH:C535962","GARD:2148"],"synonyms":[{"name":"EBS-O","type":"exact"},{"name":"EBS-Og","type":"exact"},{"name":"EBSOG","type":"exact"},{"name":"epidermolysis bullosa simplex 5A, Ogna type","type":"exact"},{"name":"epidermolysis bullosa simplex, Ogna type","type":"exact"}],"termid":"MONDO:0007555","xrefs":{"Monarch":{"xref_id":"0007555"}}}


id: PBO:0005571
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA dihydrouridine synthase Dus4 (predicted)","termid":"PBO:0005571"}


id: MONDO:1012228
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progressive retinal atrophy, non-human animal","termid":"MONDO:1011977"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive retinal atrophy, sheep","secondary_identifiers":["OMIA:000830-9940"],"termid":"MONDO:1012228","xrefs":{"Monarch":{"xref_id":"1012228"}}}


id: FYPO:0000747
data:
  {"alleles_by_uniquename":{"SJAG_01081:allele-1":{"allele_type":"nonsense_mutation","description":"S427>stop","gene_uniquename":"SJAG_01081","name":"ade6-domE","uniquename":"SJAG_01081:allele-1"},"SJAG_01081:allele-2":{"allele_type":"amino_acid_mutation","description":"Q262A","gene_uniquename":"SJAG_01081","name":"ade6-domK","uniquename":"SJAG_01081:allele-2"},"SJAG_01081:allele-3":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01081","name":"ade6delta","uniquename":"SJAG_01081:allele-3"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118505,118506,118507,118742],"is_not":false,"summary":null,"term":"FYPO:0000747"}]},"cv_name":"fission_yeast_phenotype","definition":"Auxotrophy in which a cell is unable to synthesize adenine, and therefore requires adenine in the medium for vegetative cell growth.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxotrophy","termid":"FYPO:0000128"},{"relation_name":"is_a","term_name":"abnormal cellular physical quality phenotype","termid":"FYPO:0004638"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01081":null},"genotype_count":3,"genotypes_by_uniquename":{"ade6-domE-S427>stop-nonsense_mutation-expression-not_assayed_or_wild_type":{"display_name":"ade6-domE(S427>stop)","display_uniquename":"ade6-domE-S427>stop-nonsense_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01081:allele-1","expression":"Not assayed or wild type"}]}]},"ade6-domK-Q262A-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"ade6-domK(Q262A aa)","display_uniquename":"ade6-domK-Q262A-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01081:allele-2","expression":"Not assayed or wild type"}]}]},"ade6delta":{"display_name":"ade6delta","display_uniquename":"ade6delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01081:allele-3","expression":"Null"}]}]}},"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":"growth auxotrophic for adenine","references_by_uniquename":{"PMID:19330769":null,"PMID:21905090":null},"single_locus_annotated_genes":["SJAG_01081"],"single_locus_genotype_uniquenames":["ade6-domE-S427>stop-nonsense_mutation-expression-not_assayed_or_wild_type","ade6delta","ade6-domK-Q262A-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"adenine auxotrophy","type":"exact"},{"name":"growth auxotrophic for adenine during mitotic cell cycle","type":"related"},{"name":"growth auxotrophic for adenine during vegetative growth","type":"exact"}],"termid":"FYPO:0000747","terms_by_termid":{"FYPO:0000747":null}}


id: GO:0035091
data:
  {"annotated_genes":["SJAG_01564","SJAG_00368","SJAG_03756","SJAG_02912","SJAG_01748","SJAG_01516","SJAG_02468","SJAG_01324","SJAG_04963","SJAG_03405","SJAG_02572","SJAG_02728","SJAG_05245","SJAG_04221","SJAG_00152","SJAG_00971","SJAG_04219","SJAG_00173","SJAG_03250","SJAG_00216","SJAG_01143","SJAG_04275","SJAG_01519","SJAG_04644","SJAG_02613","SJAG_05179","SJAG_01309","SJAG_04960","SJAG_02989","SJAG_00314","SJAG_04010","SJAG_00821","SJAG_04077","SJAG_02587","SJAG_01783","SJAG_01382","SJAG_02852","SJAG_02248","SJAG_00053","SJAG_01769","SJAG_00118","SJAG_00638","SJAG_00970","SJAG_00115","SJAG_00117","SJAG_00907","SJAG_01945","SJAG_03721","SJAG_02492","SJAG_01722","SJAG_02166","SJAG_02392","SJAG_03170","SJAG_03851","SJAG_02657","SJAG_01794","SJAG_01135","SJAG_04024","SJAG_00663"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[62360,89623,91492,92677,96651,98176,100903,103557,104138,106531,106788,107895,111999,113907,114338,115379,116683,117123,118142],"is_not":false,"summary":null,"term":"GO:0035091"},{"annotations":[105185,107360],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005545"},{"annotations":[95056],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901981"},{"annotations":[87273,116594,101609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005547"},{"annotations":[97807,98522,96802,99473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0080025"},{"annotations":[107809,111594,97808,104000,98896,108795,109145,89789,102610,99031,95129,99474,90711,99032,100898,96803,114359,108946],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032266"},{"annotations":[116170,98485,105187,114018,87205,89958,105756,100954,100945,116662,118100,101107],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005546"},{"annotations":[97917,101610,98486,93707,99308,111635],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070273"}]},"cv_name":"molecular_function","definition":"Binding to an inositol-containing glycerophospholipid, i.e. phosphatidylinositol (PtdIns) and its phosphorylated derivatives.","definition_xrefs":["ISBN:0198506732","PMID:11395417","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid binding","termid":"GO:0005543"}],"gene_count":59,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00115":null,"SJAG_00117":null,"SJAG_00118":null,"SJAG_00152":null,"SJAG_00173":null,"SJAG_00216":null,"SJAG_00314":null,"SJAG_00368":null,"SJAG_00638":null,"SJAG_00663":null,"SJAG_00821":null,"SJAG_00907":null,"SJAG_00970":null,"SJAG_00971":null,"SJAG_01135":null,"SJAG_01143":null,"SJAG_01309":null,"SJAG_01324":null,"SJAG_01382":null,"SJAG_01516":null,"SJAG_01519":null,"SJAG_01564":null,"SJAG_01722":null,"SJAG_01748":null,"SJAG_01769":null,"SJAG_01783":null,"SJAG_01794":null,"SJAG_01945":null,"SJAG_02166":null,"SJAG_02248":null,"SJAG_02392":null,"SJAG_02468":null,"SJAG_02492":null,"SJAG_02572":null,"SJAG_02587":null,"SJAG_02613":null,"SJAG_02657":null,"SJAG_02728":null,"SJAG_02852":null,"SJAG_02912":null,"SJAG_02989":null,"SJAG_03170":null,"SJAG_03250":null,"SJAG_03405":null,"SJAG_03721":null,"SJAG_03756":null,"SJAG_03851":null,"SJAG_04010":null,"SJAG_04024":null,"SJAG_04077":null,"SJAG_04219":null,"SJAG_04221":null,"SJAG_04275":null,"SJAG_04644":null,"SJAG_04960":null,"SJAG_04963":null,"SJAG_05179":null,"SJAG_05245":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008289"}],"interesting_parent_ids":["GO:0008289","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"phosphatidylinositol binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"phosphoinositide binding","type":"exact"}],"termid":"GO:0035091","terms_by_termid":{"GO:0005545":null,"GO:0005546":null,"GO:0005547":null,"GO:0032266":null,"GO:0035091":null,"GO:0070273":null,"GO:0080025":null,"GO:1901981":null}}


id: FYPO:0006061
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 septin ring assembly is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein-containing complex assembly","termid":"FYPO:0000447"},{"relation_name":"is_a","term_name":"abnormal cytoskeleton organization during vegetative growth","termid":"FYPO:0001328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abnormal septin ring assembly during vegetative growth","synonyms":[{"name":"abnormal septin ring assembly during mitotic cell cycle","type":"related"},{"name":"abnormal septin ring formation during vegetative growth","type":"exact"}],"termid":"FYPO:0006061"}


id: GO:0047224
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-O-N-acetyl-D-galactosalaminyl-[protein] + UDP-N-acetyl-D-glucosamine = 3-O-N-acetyl-beta-D-glucosaminyl-1,3-N-acetyl-D-galactosaminyl-[protein] + UDP. Linkage of the glycan to the protein occurs via the oxygen atom in the side chain of an L-serine or L-threonine residue.","definition_xrefs":["EC:2.4.1.147"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylglucosaminyltransferase activity","termid":"GO:0008375"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a glycoprotein","termid":"GO:0140103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0140096","GO:0016757","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"acetylgalactosaminyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase activity","secondary_identifiers":["MetaCyc:2.4.1.147-RXN"],"synonyms":[{"name":"O-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase III activity","type":"related"},{"name":"UDP-N-acetyl-D-glucosamine:O-glycosyl-glycoprotein (N-acetyl-D-glucosamine to N-acetyl-D-galactosaminyl-R) beta-1,3-N-acetyl-D-glucosaminyltransferase activity","type":"related"},{"name":"core 3-beta-GlcNAc-transferase activity","type":"related"},{"name":"core 3beta-GlcNAc-transferase activity","type":"related"},{"name":"mucin core 3 beta3-GlcNAc-transferase activity","type":"related"},{"name":"uridine diphosphoacetylglucosamine-mucin beta(1->3)-acetylglucosaminyltransferase activity","type":"related"}],"termid":"GO:0047224"}


id: GO:0036497
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of a phosphate group from the translation initiation factor eIF2alpha, as a result of endoplasmic reticulum stress.","definition_xrefs":["GOC:PARL","PMID:16835242","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of translation initiation in response to endoplasmic reticulum stress","termid":"GO:0036491"},{"relation_name":"is_a","term_name":"regulation of translational initiation by eIF2 alpha dephosphorylation","termid":"GO:0036496"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"eIF2alpha dephosphorylation in response to endoplasmic reticulum stress","synonyms":[{"name":"eIF2alpha dephosphorylation in response to ER stress","type":"exact"},{"name":"regulation of translation initiation by eIF2alpha dephosphorylation in response to endoplasmic reticulum stress","type":"exact"}],"termid":"GO:0036497"}


id: PBO:0058604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6736","termid":"PBO:0058604"}


id: PR:Q09795
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An Xaa-Pro aminopeptidase 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO00285"],"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 peptidase C22G7.01c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22G7.01c","secondary_identifiers":["UniProtKB:Q09795"],"synonyms":[{"name":"Spom972h-XPNPEP1","type":"exact"}],"termid":"PR:Q09795"}


id: MONDO:0850096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondylometaphyseal dysplasia","termid":"MONDO:0016763"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SBDS-related severe neonatal spondylometaphyseal dysplasia","secondary_identifiers":["UMLS:C5680412","GARD:22491","MEDGEN:1843152","Orphanet:622934"],"termid":"MONDO:0850096","xrefs":{"Monarch":{"xref_id":"0850096"}}}


id: PBO:0060010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 30","termid":"PBO:0060010"}


id: GO:0043800
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-arabino-3-hexulose 6-phosphate = D-fructose 6-phosphate.","definition_xrefs":["MetaCyc:R12-RXN","PMID:11839305"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isomerase activity","termid":"GO:0016853"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"hexulose-6-phosphate isomerase activity","secondary_identifiers":["EC:5.3.1.27","RHEA:25900"],"synonyms":[{"name":"HUMPI","type":"exact"}],"termid":"GO:0043800"}


id: PBO:0076464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TAMALIN antisense RNA 1","termid":"PBO:0076464"}


id: GO:0033068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways leading to the formation of macrolides, any of a large group of polyketide compounds that contain a large lactone ring with few or no double bonds and no nitrogen atoms, linked glycosidically to one or more sugar groups. The macrolides include the carbomycins, the erythromycins, oleandomycin, oligomycins, and the spiramycins, and act as antibiotics, mainly against Gram-positive bacteria.","definition_xrefs":["ISBN:0198506732","PMID:17298179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"antibiotic biosynthetic process","termid":"GO:0017000"},{"relation_name":"is_a","term_name":"polyketide biosynthetic process","termid":"GO:0030639"},{"relation_name":"is_a","term_name":"macrolide metabolic process","termid":"GO:0033067"},{"relation_name":"is_a","term_name":"lactone biosynthetic process","termid":"GO:1901336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"macrolide biosynthetic process","synonyms":[{"name":"macrolide anabolism","type":"exact"},{"name":"macrolide biosynthesis","type":"exact"},{"name":"macrolide formation","type":"exact"},{"name":"macrolide synthesis","type":"exact"}],"termid":"GO:0033068"}


id: FYPO:0003155
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 cells grow from one end, and do not grow continuously, but instead oscillate between periods of growth and pauses during which no growth occurs.","definition_xrefs":["PMID:24146635","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell growth","termid":"FYPO:0003154"}],"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:0005447","FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"intermittent monopolar cell growth","synonyms":[{"name":"intermittent monopolar vegetative cell growth","type":"exact"}],"termid":"FYPO:0003155"}


id: MONDO:0009408
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase","secondary_identifiers":["MEDGEN:383794","MESH:C565489","UMLS:C1855884","OMIM:240000"],"synonyms":[{"name":"hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase","type":"exact"}],"termid":"MONDO:0009408","xrefs":{"Monarch":{"xref_id":"0009408"}}}


id: GO:0032578
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding an aleurone grain.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoplasmic vesicle membrane","termid":"GO:0030659"},{"relation_name":"is_a","term_name":"bounding membrane of organelle","termid":"GO:0098588"},{"relation_name":"part_of","term_name":"aleurone grain","termid":"GO:0033095"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0031410","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"aleurone grain membrane","termid":"GO:0032578"}


id: GO:0061407
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of a hydrogen peroxide (H2O2) stimulus.","definition_xrefs":["GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter in response to hydrogen peroxide (obsolete GO:0061407)","termid":"GO:0061407"}


id: PBO:0080977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZBTB11 antisense RNA 1","termid":"PBO:0080977"}


id: PBO:0108992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RecQ type DNA helicase, N-terminal truncated compared to other tlh genes","termid":"PBO:0108992"}


id: PR:000045542
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cyclin-dependent kinase 1 (Schizosaccharomyces pombe) that has been phosphorylated on a Thr residue (Thr-167) within the T-Loop, and Thr-14 and Tyr-15 within the ATP binding region. UniProtKB:P04551, Thr-14/Thr-167, MOD:00047|Tyr-15, MOD:00048.","definition_xrefs":["PomBase:MAH","PMID:26131711","PRO:CNA"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclin-dependent kinase 1 (Schizosaccharomyces pombe)","termid":"PR:000036301"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cdc2/Phos:(T14,Y15,T167)","pombase_gene_id":"SPBC11B10.09","synonyms":[{"name":"Cdc2 phosphorylated 3","type":"related"},{"name":"Cdc2-Hf","type":"exact"},{"name":"PomBase_original_PRO_term_name: cyclin-dependent kinase 1 phosphorylated 3 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-cdc2/Phos:3","type":"exact"},{"name":"UniProtKB:P04551, Thr-14/Thr-167, MOD:00047|Tyr-15, MOD:00048","type":"exact"},{"name":"cdc2/Phos:(T14,Y15,T167)","type":"exact"}],"termid":"PR:000045542"}


id: GO:2000555
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of T-helper 1 cell cytokine production.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell cytokine production","termid":"GO:0002725"},{"relation_name":"is_a","term_name":"negative regulation of T-helper 1 type immune response","termid":"GO:0002826"},{"relation_name":"is_a","term_name":"regulation of T-helper 1 cell cytokine production","termid":"GO:2000554"},{"relation_name":"negatively_regulates","term_name":"T-helper 1 cell cytokine production","termid":"GO:0035744"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of T-helper 1 cell cytokine production","synonyms":[{"name":"negative regulation of Th1 cell cytokine production","type":"exact"}],"termid":"GO:2000555"}


id: GO:0048818
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hair follicle maturation.","definition_xrefs":["GOC:devbiol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hair follicle maturation","termid":"GO:0048819"},{"relation_name":"is_a","term_name":"positive regulation of hair follicle development","termid":"GO:0051798"},{"relation_name":"positively_regulates","term_name":"hair follicle maturation","termid":"GO:0048820"}],"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 hair follicle maturation","synonyms":[{"name":"activation of hair follicle maturation","type":"narrow"},{"name":"stimulation of hair follicle maturation","type":"narrow"},{"name":"up regulation of hair follicle maturation","type":"exact"},{"name":"up-regulation of hair follicle maturation","type":"exact"},{"name":"upregulation of hair follicle maturation","type":"exact"}],"termid":"GO:0048818"}


id: PBO:0061787
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OCRL inositol polyphosphate-5-phosphatase","termid":"PBO:0061787"}


id: MONDO:0060533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microcephaly, short stature, and limb abnormalities","secondary_identifiers":["MEDGEN:1613834","OMIM:617604","GARD:18655","Orphanet:572773","UMLS:C4539873","DOID:0081431"],"synonyms":[{"name":"MISSLA","type":"related"},{"name":"microcephaly, short stature, and limb abnormalities","type":"exact"}],"termid":"MONDO:0060533","xrefs":{"Monarch":{"xref_id":"0060533"}}}


id: MONDO:0002384
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete transitional cell carcinoma (obsolete MONDO:0002384)","termid":"MONDO:0002384","xrefs":{"Monarch":{"xref_id":"0002384"}}}


id: PBO:0075423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm associated antigen 9","termid":"PBO:0075423"}


id: GO:0090440
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of abscisic acid from one side of a membrane to the other.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transmembrane transporter activity","termid":"GO:0008028"},{"relation_name":"is_a","term_name":"alcohol transmembrane transporter activity","termid":"GO:0015665"},{"relation_name":"is_a","term_name":"lipid transmembrane transporter activity","termid":"GO:0170055"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"abscisic acid transmembrane transporter activity","synonyms":[{"name":"abscisic acid transporter activity","type":"exact"}],"termid":"GO:0090440"}


id: GO:0032253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a dense core granule is transported to, and/or maintained in, a specific location within the cell.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secretory granule localization","termid":"GO:0032252"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"dense core granule localization","synonyms":[{"name":"dense core granule clustering","type":"related"},{"name":"dense core granule localisation","type":"exact"},{"name":"dense core vesicle localization","type":"exact"}],"termid":"GO:0032253"}


id: GO:0044001
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directional movement of an organism from one place to another within its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:cc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process involved in interaction with host","termid":"GO:0051701"}],"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":"migration in host","synonyms":[{"name":"migration within host","type":"exact"}],"termid":"GO:0044001"}


id: GO:0002322
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of a B cell population by cell division following B cell activation during an immune response.","definition_xrefs":["GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell activation involved in immune response","termid":"GO:0002312"},{"relation_name":"is_a","term_name":"B cell proliferation","termid":"GO:0042100"}],"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":"B cell proliferation involved in immune response","synonyms":[{"name":"B cell proliferation during immune response","type":"related"},{"name":"B lymphocyte proliferation during immune response","type":"related"},{"name":"B-cell proliferation during immune response","type":"related"},{"name":"B-lymphocyte proliferation during immune response","type":"related"}],"termid":"GO:0002322"}


id: GO:1901410
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of tetrapyrrole biosynthetic process from glutamate.","definition_xrefs":["GOC:TermGenie","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tetrapyrrole biosynthetic process","termid":"GO:1901463"},{"relation_name":"is_a","term_name":"regulation of glutamate metabolic process","termid":"GO:2000211"},{"relation_name":"regulates","term_name":"tetrapyrrole biosynthetic process from glutamate","termid":"GO:0033526"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0044281","GO:0033013"],"is_obsolete":false,"name":"regulation of tetrapyrrole biosynthetic process from glutamate","synonyms":[{"name":"regulation of tetrapyrrole anabolism from glutamate","type":"exact"},{"name":"regulation of tetrapyrrole biosynthesis from glutamate","type":"exact"},{"name":"regulation of tetrapyrrole formation from glutamate","type":"exact"},{"name":"regulation of tetrapyrrole synthesis from glutamate","type":"exact"}],"termid":"GO:1901410"}


id: PBO:0079144
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetraspanin 6","termid":"PBO:0079144"}


id: GO:2001236
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of extrinsic apoptotic signaling pathway.","definition_xrefs":["GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of apoptotic signaling pathway","termid":"GO:2001233"},{"relation_name":"regulates","term_name":"extrinsic apoptotic signaling pathway","termid":"GO:0097191"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of extrinsic apoptotic signaling pathway","synonyms":[{"name":"regulation of extrinsic apoptosis","type":"narrow"},{"name":"regulation of extrinsic apoptotic signalling pathway","type":"exact"}],"termid":"GO:2001236"}


id: PBO:0066067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RARA antisense RNA 1","termid":"PBO:0066067"}


id: PBO:0084352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Late endosomal protein involved in late endosome to vacuole transport; functional homolog of human obesity receptor gene-related protein (OB-RGRP)","termid":"PBO:0084352"}


id: GO:0052005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts the normal execution of the ethylene-mediated defense response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated suppression of host defenses","termid":"GO:0044414"},{"relation_name":"is_a","term_name":"modulation by symbiont of host ethylene-mediated defense response","termid":"GO:0052084"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host ethylene-mediated defense response","secondary_identifiers":["GO:0052070","GO:0052254","GO:0052268"],"synonyms":[{"name":"down regulation by symbiont of host ethylene-mediated defense response","type":"exact"},{"name":"down-regulation by symbiont of host ethylene-mediated defense response","type":"exact"},{"name":"downregulation by symbiont of host ethylene-mediated defense response","type":"exact"},{"name":"inhibition by symbiont of host ethylene-mediated defense response","type":"narrow"},{"name":"negative regulation by organism of defense-related ethylene-mediated signal transduction pathway in other organism involved in symbiotic interaction","type":"broad"},{"name":"negative regulation by organism of ethylene-mediated defense response of other organism involved in symbiotic interaction","type":"broad"},{"name":"negative regulation by symbiont of defense-related host ethylene-mediated signal transduction pathway","type":"broad"},{"name":"negative regulation by symbiont of host ethylene-mediated defense response","type":"exact"},{"name":"suppression by organism of host ethylene-mediated defense response","type":"exact"},{"name":"suppression by symbiont of host ethylene-mediated defense response","type":"exact"}],"termid":"GO:0052005"}


id: SO:0001983
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A 5' UTR variant where a premature start codon is introduced, moved or lost.","definition_xrefs":["SANGER:am"],"direct_ancestors":[{"relation_name":"is_a","term_name":"5_prime_UTR_variant","termid":"SO:0001623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5_prime_UTR_premature_start_codon_variant","synonyms":[{"name":"5' UTR premature start codon variant","type":"exact"}],"termid":"SO:0001983"}


id: MONDO:0016207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intraocular inflammation occurring after extracapsular cataract extraction; probably an immune reaction to the patient's liberated lenticular proteins.","direct_ancestors":[{"relation_name":"is_a","term_name":"non-infectious anterior uveitis","termid":"MONDO:0017634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"phacoanaphylactic uveitis","secondary_identifiers":["SCTID:410494003","GARD:20443","MEDGEN:731803","Orphanet:209959","UMLS:C1444621"],"synonyms":[{"name":"Phacoallergic endophthalmitis","type":"exact"},{"name":"Phacoantigenic endophthalmitis","type":"exact"},{"name":"Phako-anaphylactic endophthalmitis","type":"exact"},{"name":"endophthalmitis phacoanaphylactica","type":"exact"},{"name":"lens-induced endophthalmitis","type":"exact"},{"name":"lens-induced iridocyclitis","type":"related"},{"name":"lens-induced uveitis","type":"exact"}],"termid":"MONDO:0016207","xrefs":{"Monarch":{"xref_id":"0016207"}}}


id: SO:0000417
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A structurally or functionally defined protein region. In proteins with multiple domains, the combination of the domains determines the function of the protein. A region which has been shown to recur throughout evolution.","definition_xrefs":["EBIBS:GAR"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_structural_region","termid":"SO:0001070"},{"relation_name":"is_a","term_name":"polypeptide_conserved_region","termid":"SO:0100021"}],"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":"polypeptide_domain","secondary_identifiers":["SO:0001069","BS:00134","BS:00012"],"synonyms":[{"name":"domain","type":"broad"},{"name":"polypeptide domain","type":"exact"},{"name":"polypeptide_structural_domain","type":"exact"},{"name":"structural domain","type":"broad"}],"termid":"SO:0000417"}


id: MONDO:0008572
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome is a rare, genetic dysostosis syndrome, with marked inter- and intra-familial variation, typically characterized by triphalangeal thumbs, hand and/or foot polysyndactyly and/or absent/hypoplastic tibiae (associated with duplication of fibulae in some cases), although isolated triphalangeal thumbs have also been reported. It is often accompanied with remarkable short stature and additional features may include radio-ulnar synostosis and hand oligodactyly, as well as abnormal carpal and metatarsal bones.","definition_xrefs":["Orphanet:988"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"},{"relation_name":"is_a","term_name":"congenital limb malformation","termid":"MONDO:0019054"},{"relation_name":"is_a","term_name":"non-syndromic limb reduction defect","termid":"MONDO:0019713"}],"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":"tibia, hypoplasia or aplasia of, with polydactyly","secondary_identifiers":["MEDGEN:348786","DOID:0111564","SCTID:716741008","MESH:C566046","UMLS:C1861098","OMIM:188740","MESH:C535564","Orphanet:3332","GARD:8309"],"synonyms":[{"name":"THYP","type":"related"},{"name":"Werner mesomelic syndrome","type":"exact"},{"name":"absence of tibia with polydactyly","type":"related"},{"name":"absent tibia-polydactyly syndrome","type":"exact"},{"name":"hypoplastic or aplastic tibia with polydactyly","type":"exact"},{"name":"hypoplastic tibiae-postaxial polydactyly syndrome","type":"exact"},{"name":"polydactyly with absent tibia","type":"related"},{"name":"tibia, hypoplasia or aplasia of, with polydactyly","type":"exact"},{"name":"tibial hemimelia-polydactyly-triphalangeal thumbs with fibular dimelia","type":"related"},{"name":"tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome","type":"related"}],"termid":"MONDO:0008572","xrefs":{"Monarch":{"xref_id":"0008572"}}}


id: MONDO:1010270
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Alkaptonuria that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"metabolic disease, non-human animal","termid":"MONDO:1011331"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alkaptonuria, non-human animal","secondary_identifiers":["OMIA:001243"],"termid":"MONDO:1010270","xrefs":{"Monarch":{"xref_id":"1010270"}}}


id: MONDO:0008712
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acrocraniofacial dysostosis is a very rare form of acrofacial dyosotosis, reported in two sisters to date, characterized by short stature, acrocephaly, ocular hypertelorism, ptosis of eyelids, ocular proptosis, downslanting palpebral fissures, high nasal bridge, anteverted nostrils, short philtrum, cleft palate, micrognathia, abnormal external ears, preauricular pits, mixed hearing loss, bulbous digits, metatarsus varus, pectus excavatum and various radiological abnormalities. Features of this syndrome were reported to overlap with otopalatodigital syndrome types 1 and 2. There have been no further descriptions in the literature since 1988.","definition_xrefs":["Orphanet:949"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"acrofacial dysostosis","termid":"MONDO:0018237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"acrocraniofacial dysostosis","secondary_identifiers":["MESH:C536892","OMIM:201050","SCTID:720418008","MEDGEN:349738","GARD:3075","UMLS:C1860145"],"synonyms":[{"name":"Kaplan Plauchu Fitch syndrome","type":"related"},{"name":"Kaplan-Plauchu-Fitch syndrome","type":"exact"},{"name":"acrocraniofacial dysostosis","type":"exact"}],"termid":"MONDO:0008712","xrefs":{"Monarch":{"xref_id":"0008712"}}}


id: PBO:0046250
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELOVL fatty acid elongase 6","termid":"PBO:0046250"}


id: PBO:0062837
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oligosaccharyltransferase complex subunit pseudogene 3","termid":"PBO:0062837"}


id: PBO:0005034
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.8.1.6","termid":"PBO:0005034"}


id: PBO:0116196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"yippee-like protein, Moh1","termid":"PBO:0116196"}


id: GO:0102487
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: dUTP + 2 H2O = dUMP + 2 hydrogenphosphate + 2 H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete dUTP phosphohydrolase activity (obsolete GO:0102487)","termid":"GO:0102487"}


id: PBO:0056399
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAPRE3 antisense RNA 1","termid":"PBO:0056399"}


id: MONDO:0003835
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from glandular epithelial cells of the cardia of stomach.","direct_ancestors":[{"relation_name":"is_a","term_name":"gastric cardia carcinoma","termid":"MONDO:0003834"},{"relation_name":"is_a","term_name":"gastric adenocarcinoma","termid":"MONDO:0005036"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992"],"is_obsolete":false,"name":"gastric cardia adenocarcinoma","secondary_identifiers":["DOID:6271","NCIT:C5247","MEDGEN:232543","UMLS:C1333762"],"synonyms":[{"name":"adenocarcinoma of cardia of stomach","type":"exact"},{"name":"adenocarcinoma of gastric cardia","type":"related"},{"name":"adenocarcinoma of the cardia of the stomach","type":"exact"},{"name":"adenocarcinoma of the gastric cardia","type":"exact"},{"name":"cardia of stomach adenocarcinoma","type":"exact"}],"termid":"MONDO:0003835","xrefs":{"Monarch":{"xref_id":"0003835"}}}


id: PBO:0051364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 3-25 (pseudogene)","termid":"PBO:0051364"}


id: MOD:00614
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom of an amino acid residue or of a modifying group with a fucose (6-deoxy-D-galactose) group through a glycosidic bond.","definition_xrefs":["Unimod:295","PubMed:11344537","PubMed:15189151"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deoxyhexosylated","termid":"MOD:00736"}],"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":"fucosylated","synonyms":[{"name":"Fuc","type":"exact"},{"name":"Fucose","type":"related"},{"name":"dHex","type":"related"}],"termid":"MOD:00614"}


id: PBO:0073538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 and PX domains 2B","termid":"PBO:0073538"}


id: FYPO:0000251
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is decreased relative to normal in a medium containing galactose as the carbon source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased vegetative cell population growth","termid":"FYPO:0001355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0002057","FYPO:0002058","FYPO:0001985","FYPO:0002060","FYPO:0000003"],"is_obsolete":false,"name":"decreased cell population growth on galactose carbon source","synonyms":[{"name":"decreased growth on galactose carbon source","type":"broad"},{"name":"decreased vegetative cell growth on galactose carbon source","type":"exact"},{"name":"growth defects, growth inhibition in galactose-based medium","type":"related"},{"name":"reduced cell growth on galactose carbon source","type":"exact"},{"name":"slow cell growth on galactose carbon source","type":"narrow"}],"termid":"FYPO:0000251"}


id: FYPO:0006339
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell has one nucleus that is not in the normal location.","definition_xrefs":["PMID:15937127","PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"has_part","term_name":"mononucleate vegetative cell","termid":"FYPO:0000060"},{"relation_name":"has_part","term_name":"mislocalized nucleus","termid":"FYPO:0002069"},{"relation_name":"is_a","term_name":"mononucleate vegetative cell","termid":"FYPO:0000060"},{"relation_name":"is_a","term_name":"mislocalized nucleus","termid":"FYPO:0002069"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001320"],"is_obsolete":false,"name":"mononucleate vegetative cell with mislocalized nucleus","synonyms":[{"name":"lethal; mononucleate vegetative cell with mislocalized nucleus","type":"exact"},{"name":"mononucleate cell with abnormal nucleus location","type":"exact"},{"name":"mononucleate cell with abnormal nucleus position","type":"exact"},{"name":"mononucleate cell with asymmetrically localized nucleus","type":"exact"},{"name":"mononucleate cell with displaced nucleus","type":"exact"},{"name":"mononucleate cell with mislocalised nucleus","type":"exact"},{"name":"mononucleate cell with mislocalized nucleus during vegetative growth","type":"exact"},{"name":"mononucleate cell with misplaced nucleus","type":"exact"},{"name":"mononucleate vegetative cell with mislocalized nucleus during mitotic cell cycle","type":"related"},{"name":"vegetative cell with mislocalized mononucleus","type":"exact"}],"termid":"FYPO:0006339"}


id: MOD:01391
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-cysteine residue and an L-valine residue, and C-5 methoxymethylates to form L-valine 5-(methoxymethyl)thiazole-4-carboxylic acid.","definition_xrefs":["PubMed:1880060","PubMed:7844053","PubMed:10625477","RESID:AA0468"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thiazole/thiazoline ring crosslinked residues","termid":"MOD:01420"},{"relation_name":"is_a","term_name":"didehydrogenated residue","termid":"MOD:01888"},{"relation_name":"is_a","term_name":"crosslinked L-valine residue","termid":"MOD:02059"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-valine 5-(methoxymethyl)thiazole-4-carboxylic acid","synonyms":[{"name":"2-[(1S)-1-amino-2-methylpropyl]-5-(methoxymethyl)-1,3-thiazole-4-carboxylic acid","type":"exact"},{"name":"2-[1-azanyl-2-methylpropyl]-5-(methoxymethyl)-1,3-thiazole-4-carboxylic acid","type":"exact"},{"name":"CROSSLNK 5-(methoxymethyl)thiazole-4-carboxylic acid (Val-Cys)","type":"exact"},{"name":"L-valine 5-(methoxymethyl)thiazole-4-carboxylic acid","type":"exact"}],"termid":"MOD:01391"}


id: GO:1904004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of sebum secreting cell proliferation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:16901790","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell population proliferation","termid":"GO:0008284"},{"relation_name":"is_a","term_name":"regulation of sebum secreting cell proliferation","termid":"GO:1904002"},{"relation_name":"positively_regulates","term_name":"sebum secreting cell proliferation","termid":"GO:1990654"}],"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 sebum secreting cell proliferation","synonyms":[{"name":"activation of sebocyte proliferation","type":"related"},{"name":"activation of sebum secreting cell proliferation","type":"narrow"},{"name":"positive regulation of sebocyte proliferation","type":"related"},{"name":"up regulation of sebocyte proliferation","type":"related"},{"name":"up regulation of sebum secreting cell proliferation","type":"exact"},{"name":"up-regulation of sebocyte proliferation","type":"related"},{"name":"up-regulation of sebum secreting cell proliferation","type":"exact"},{"name":"upregulation of sebocyte proliferation","type":"related"},{"name":"upregulation of sebum secreting cell proliferation","type":"exact"}],"termid":"GO:1904004"}


id: GO:0002368
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that contributes to cytokine production by a B cell.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production involved in immune response","termid":"GO:0002367"},{"relation_name":"is_a","term_name":"B cell mediated immunity","termid":"GO:0019724"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"B cell cytokine production","synonyms":[{"name":"B lymphocyte cytokine production","type":"exact"},{"name":"B-cell cytokine production","type":"exact"},{"name":"B-lymphocyte cytokine production","type":"exact"}],"termid":"GO:0002368"}


id: PBO:0077779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane O-methyltransferase","termid":"PBO:0077779"}


id: PBO:0069221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 476, pseudogene","termid":"PBO:0069221"}


id: MONDO:1012781
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any paroxysmal dyskinesia that occurs in dogs due to a mutation in the PIGN gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paroxysmal dyskinesia, dog","termid":"MONDO:1010422"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paroxysmal dyskinesia, PIGN-related, dog","secondary_identifiers":["OMIA:002084-9615"],"termid":"MONDO:1012781","xrefs":{"Monarch":{"xref_id":"1012781"}}}


id: PBO:0005029
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4.99.1.1","termid":"PBO:0005029"}


id: PBO:0043613
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COMM domain containing 4 pseudogene 1","termid":"PBO:0043613"}


id: FYPO:0003272
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 sodium hypochlorite.","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:0000257"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002057","FYPO:0002058","FYPO:0000257","FYPO:0002060","FYPO:0000003"],"is_obsolete":false,"name":"normal growth on sodium hypochlorite","synonyms":[{"name":"normal cell population growth in presence of sodium hypochlorite","type":"exact"},{"name":"normal cell population growth on NaOCl","type":"exact"},{"name":"normal cell population growth on sodium hypochlorite","type":"exact"},{"name":"normal cellular response to sodium hypochlorite","type":"related"},{"name":"normal vegetative cell population growth on sodium hypochlorite","type":"exact"}],"termid":"FYPO:0003272"}


id: GO:0036404
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which double-stranded small interfering RNA (ds siRNA) molecules are converted to single-stranded small interfering RNA (ss siRNA).","definition_xrefs":["GOC:vw"],"gene_count":0,"genotype_count":0,"name":"obsolete conversion of ds siRNA to ss siRNA (obsolete GO:0036404)","synonyms":[{"name":"conversion of double-stranded small interfering RNA to single-stranded small interfering RNA","type":"related"}],"termid":"GO:0036404"}


id: PBO:0088897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell wall glycoside hydrolase, family 5","termid":"PBO:0088897"}


id: PBO:0028536
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_cell_tip,_with_protein_distributed_in_plasma_membrane_or_cortex","termid":"PBO:0028536"}


id: GO:0036358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a D-alanyl ester of lipoteichoic acid by transfer of D-Ala onto a membrane-associated lipoteichoic acid (LTA).","definition_xrefs":["GOC:crds","PMID:22750871","PMID:8682792"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teichoic acid D-alanylation","termid":"GO:0070400"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0071554","GO:0044281","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"lipoteichoic acid D-alanylation","synonyms":[{"name":"D-alanyl LTA formation","type":"exact"},{"name":"D-alanyl lipoteichoic acid formation","type":"exact"},{"name":"LTA D-alanylation","type":"exact"}],"termid":"GO:0036358"}


id: PBO:0038448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alanyl-tRNA synthetase 1","termid":"PBO:0038448"}


id: PBO:0005221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COPII cargo receptor subunit Sec23a (predicted)","termid":"PBO:0005221"}


id: GO:0060191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lipase activity, the hydrolysis of a lipid or phospholipid.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hydrolase activity","termid":"GO:0051336"}],"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 lipase activity","termid":"GO:0060191"}


id: FYPO:0003715
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 Skb1-containing lateral cortical nodes is abolished, and the protein is instead detected distributed throughout the plasma membrane and/or cell cortex.","definition_xrefs":["PMID:25009287","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to lateral cortical node","termid":"FYPO:0003713"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abolished protein localization to lateral cortical node, with protein distributed in plasma membrane or cortex","synonyms":[{"name":"abolished protein localisation to lateral cortical node, with protein distributed in plasma membrane or cortex","type":"exact"},{"name":"abolished protein localization to lateral cortical node, with protein distributed in cell cortex","type":"narrow"},{"name":"abolished protein localization to lateral cortical node, with protein distributed in plasma membrane","type":"narrow"},{"name":"abolished protein localization to lateral cortical node, with protein distributed in plasma membrane or cortex, during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to lateral cortical node, with protein distributed in plasma membrane or cortex, during vegetative growth","type":"exact"},{"name":"protein localization to lateral cortical node abolished, with protein distributed in plasma membrane or cortex","type":"exact"}],"termid":"FYPO:0003715"}


id: MONDO:0031376
data:
  {"annotated_genes":["SJAG_03227"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0800044"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03227":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"congenital disorder of deglycosylation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:815321","OMIMPS:615273","UMLS:C3808991"],"termid":"MONDO:0031376","terms_by_termid":{"MONDO:0800044":null},"xrefs":{"Monarch":{"xref_id":"0031376"}}}


id: PR:O59813
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC794.03 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59813"],"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 amino-acid permease C794.03 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC794.03","synonyms":[{"name":"Spom972h-SPCC794.03","type":"exact"}],"termid":"PR:O59813"}


id: GO:0070062
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A vesicle that is released into the extracellular region by fusion of the limiting endosomal membrane of a multivesicular body with the plasma membrane. Extracellular exosomes, also simply called exosomes, have a diameter of about 40-100 nm.","definition_xrefs":["PMID:15908444","GOC:vesicles","PMID:22418571","PMID:24009894","GOC:mah","PMID:19498381","PMID:17641064","GOC:BHF","PMID:19442504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular vesicle","termid":"GO:1903561"},{"relation_name":"part_of","term_name":"extracellular space","termid":"GO:0005615"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"}],"interesting_parent_ids":["GO:0005576","GO:0005575"],"is_obsolete":false,"name":"extracellular exosome","synonyms":[{"name":"exosome","type":"exact"},{"name":"extracellular vesicular exosome","type":"exact"}],"termid":"GO:0070062"}


id: PBO:0036032
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-septation_following_abnormal_mitotic_chromosome_segregation_during_cellular_response_to_hydroxyurea","termid":"PBO:0036032"}


id: GO:0045940
data:
  {"annotated_genes":["SJAG_04018"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[109003],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070452"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving steroids.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of steroid metabolic process","termid":"GO:0019218"},{"relation_name":"is_a","term_name":"positive regulation of lipid metabolic process","termid":"GO:0045834"},{"relation_name":"positively_regulates","term_name":"steroid metabolic process","termid":"GO:0008202"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"positive regulation of steroid metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of steroid metabolic process","type":"narrow"},{"name":"positive regulation of steroid metabolism","type":"exact"},{"name":"stimulation of steroid metabolic process","type":"narrow"},{"name":"up regulation of steroid metabolic process","type":"exact"},{"name":"up-regulation of steroid metabolic process","type":"exact"},{"name":"upregulation of steroid metabolic process","type":"exact"}],"termid":"GO:0045940","terms_by_termid":{"GO:0070452":null}}


id: GO:0060880
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The change in form (cell shape and size) that occurs when a semicircular canal epithelial cell acquires the structural features that allow it to contribute to the process of semicircular canal fusion.","definition_xrefs":["GOC:tb","GOC:sdb_2009","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell morphogenesis","termid":"GO:0000902"},{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"semicircular canal fusion","termid":"GO:0060879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell morphogenesis involved in semicircular canal fusion","termid":"GO:0060880"}


id: GO:1990640
data:
  {"annotated_genes":["SJAG_00063"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[107453],"is_not":false,"summary":null,"term":"GO:1990640"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol 2,4,5-trisphosphate + H2O = 1D-myo-inositol 2,4-bisphosphate + phosphate.","definition_xrefs":["PMID:15316017"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol trisphosphate phosphatase activity","termid":"GO:0046030"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00063":null},"genotype_count":0,"interesting_parent_details":[{"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:0016788"}],"interesting_parent_ids":["GO:0003824","GO:0016788","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"inositol-2,4,5-triphosphate 5-phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990640","terms_by_termid":{"GO:1990640":null}}


id: PBO:0036151
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H2A_phosphorylation_at_G4_motif_during_vegetative_growth","termid":"PBO:0036151"}


id: MOD:01998
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue alpha-amino- or alpha-imino-hydrogen with a butanoyl group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-butanoylated residue","termid":"MOD:01997"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-amino butanoylated residue","synonyms":[{"name":"N2ButRes","type":"exact"}],"termid":"MOD:01998"}


id: GO:1905788
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of detection of mechanical stimulus involved in sensory perception of touch.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:8692859"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of nervous system process","termid":"GO:0031645"},{"relation_name":"is_a","term_name":"negative regulation of response to external stimulus","termid":"GO:0032102"},{"relation_name":"is_a","term_name":"regulation of detection of mechanical stimulus involved in sensory perception of touch","termid":"GO:1905787"},{"relation_name":"negatively_regulates","term_name":"detection of mechanical stimulus involved in sensory perception of touch","termid":"GO:0050976"}],"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 detection of mechanical stimulus involved in sensory perception of touch","synonyms":[{"name":"down regulation of detection of mechanical stimulus involved in sensory perception of touch","type":"exact"},{"name":"down regulation of perception of touch, detection of mechanical stimulus","type":"exact"},{"name":"down regulation of perception of touch, sensory detection of mechanical stimulus","type":"exact"},{"name":"down regulation of perception of touch, sensory transduction of mechanical stimulus","type":"exact"},{"name":"down regulation of sensory detection of mechanical stimulus during perception of touch","type":"exact"},{"name":"down regulation of sensory transduction of mechanical stimulus during perception of touch","type":"exact"},{"name":"down regulation of tactition, sensory detection of mechanical stimulus","type":"exact"},{"name":"down-regulation of detection of mechanical stimulus involved in sensory perception of touch","type":"exact"},{"name":"down-regulation of perception of touch, detection of mechanical stimulus","type":"exact"},{"name":"down-regulation of perception of touch, sensory detection of mechanical stimulus","type":"exact"},{"name":"down-regulation of perception of touch, sensory transduction of mechanical stimulus","type":"exact"},{"name":"down-regulation of sensory detection of mechanical stimulus during perception of touch","type":"exact"},{"name":"down-regulation of sensory transduction of mechanical stimulus during perception of touch","type":"exact"},{"name":"down-regulation of tactition, sensory detection of mechanical stimulus","type":"exact"},{"name":"downregulation of detection of mechanical stimulus involved in sensory perception of touch","type":"exact"},{"name":"downregulation of perception of touch, detection of mechanical stimulus","type":"exact"},{"name":"downregulation of perception of touch, sensory detection of mechanical stimulus","type":"exact"},{"name":"downregulation of perception of touch, sensory transduction of mechanical stimulus","type":"exact"},{"name":"downregulation of sensory detection of mechanical stimulus during perception of touch","type":"exact"},{"name":"downregulation of sensory transduction of mechanical stimulus during perception of touch","type":"exact"},{"name":"downregulation of tactition, sensory detection of mechanical stimulus","type":"exact"},{"name":"inhibition of detection of mechanical stimulus involved in sensory perception of touch","type":"narrow"},{"name":"inhibition of perception of touch, detection of mechanical stimulus","type":"narrow"},{"name":"inhibition of perception of touch, sensory detection of mechanical stimulus","type":"narrow"},{"name":"inhibition of perception of touch, sensory transduction of mechanical stimulus","type":"narrow"},{"name":"inhibition of sensory detection of mechanical stimulus during perception of touch","type":"narrow"},{"name":"inhibition of sensory transduction of mechanical stimulus during perception of touch","type":"narrow"},{"name":"inhibition of tactition, sensory detection of mechanical stimulus","type":"narrow"},{"name":"negative regulation of perception of touch, detection of mechanical stimulus","type":"exact"},{"name":"negative regulation of perception of touch, sensory detection of mechanical stimulus","type":"exact"},{"name":"negative regulation of perception of touch, sensory transduction of mechanical stimulus","type":"exact"},{"name":"negative regulation of sensory detection of mechanical stimulus during perception of touch","type":"exact"},{"name":"negative regulation of sensory transduction of mechanical stimulus during perception of touch","type":"exact"},{"name":"negative regulation of tactition, sensory detection of mechanical stimulus","type":"exact"}],"termid":"GO:1905788"}


id: MOD:01425
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that crosslinks three residues by formation of a pyridinyl ring, such as pyridine-2,5-dicarboxylic acid or 5-aminopiperideine-2,5-dicarboxylic acid.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked residues","termid":"MOD:00033"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridinyl ring crosslinked residues","termid":"MOD:01425"}


id: GO:0010681
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of cinnamic acid, 3-phenyl-2-propenoic acid, which is then utilized in the metabolism of stilbene.","definition_xrefs":["GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete cinnamic acid biosynthetic process involved in stilbene metabolism (obsolete GO:0010681)","termid":"GO:0010681"}


id: PBO:0036047
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_histone_H3-K14_acetylation_at_centromere_outer_repeat_during_vegetative_growth","termid":"PBO:0036047"}


id: PBO:0114435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPATA31 subfamily B member 2, pseudogene","termid":"PBO:0114435"}


id: GO:0015571
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of N-acetylgalactosamine from one side of a membrane to the other. N-acetylgalactosamine, 2-acetamido-2-deoxygalactopyranose, is the n-acetyl derivative of galactosamine.","definition_xrefs":["GOC:ai","GOC:mtg_transport","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"galactosamine transmembrane transporter activity","termid":"GO:0019196"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"N-acetylgalactosamine transmembrane transporter activity","secondary_identifiers":["GO:0015590"],"synonyms":[{"name":"N-acetylgalactosamine permease activity","type":"exact"}],"termid":"GO:0015571"}


id: GO:0060253
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or decreases the rate or extent of glial cell proliferation.","definition_xrefs":["GOC:tb","GOC:dph","GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell population proliferation","termid":"GO:0008285"},{"relation_name":"is_a","term_name":"negative regulation of gliogenesis","termid":"GO:0014014"},{"relation_name":"is_a","term_name":"regulation of glial cell proliferation","termid":"GO:0060251"},{"relation_name":"negatively_regulates","term_name":"glial cell proliferation","termid":"GO:0014009"}],"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 glial cell proliferation","termid":"GO:0060253"}


id: PBO:0083197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps the verified gene KNS1","termid":"PBO:0083197"}


id: PBO:0029984
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_prospore_membrane_formation","termid":"PBO:0029984"}


id: GO:2001263
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of C-C chemokine binding.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein binding","termid":"GO:0043393"}],"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 C-C chemokine binding","termid":"GO:2001263"}


id: PBO:0065327
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 51","termid":"PBO:0065327"}


id: SO:0001454
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A negatively charged, hydorophilic amino acid encoded by the codons GAA and GAG.","direct_ancestors":[{"relation_name":"is_a","term_name":"amino_acid","termid":"SO:0001237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamic_acid","synonyms":[{"name":"E","type":"exact"},{"name":"Glu","type":"exact"},{"name":"glutamic acid","type":"exact"}],"termid":"SO:0001454"}


id: PBO:0069097
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 344, pseudogene","termid":"PBO:0069097"}


id: GO:0044593
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of iron-sulfur-molybdenum cofactor, the cofactor located at the active site of the molybdenum nitrogenase.","definition_xrefs":["GOC:tt","PMID:18429691","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron-sulfur cluster assembly","termid":"GO:0016226"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0016226"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0016226"],"is_obsolete":false,"name":"iron-sulfur-molybdenum cofactor assembly","synonyms":[{"name":"FeMoco assembly","type":"exact"},{"name":"FeMoco biosynthetic process","type":"exact"},{"name":"iron molybdenum cofactor assembly","type":"exact"},{"name":"iron molybdenum cofactor biosynthesis","type":"exact"},{"name":"iron molybdenum cofactor biosynthetic process","type":"exact"}],"termid":"GO:0044593"}


id: FYPO:0004601
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the S-phase DNA damage checkpoint (also known as the intra-S phase DNA damage checkpoint) is normal (i.e. indistinguishable from wild type) when the cell is exposed to hydroxyurea. The S phase DNA damage checkpoint slows progression through S phase in response to DNA damage.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cell cycle regulation during cellular response to hydroxyurea","termid":"FYPO:0001929"},{"relation_name":"is_a","term_name":"normal S-phase DNA damage checkpoint","termid":"FYPO:0003530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001312","FYPO:0000298","FYPO:0000257","FYPO:0001320","FYPO:0000631"],"is_obsolete":false,"name":"normal S-phase DNA damage checkpoint during cellular response to hydroxyurea","synonyms":[{"name":"normal S-phase DNA damage checkpoint activation during cellular response to hydroxyurea","type":"exact"},{"name":"normal S-phase DNA damage checkpoint during cellular response to HU","type":"exact"},{"name":"normal S-phase DNA damage checkpoint during cellular response to hydroxyurea during mitotic cell cycle","type":"exact"},{"name":"normal S-phase DNA damage checkpoint during cellular response to hydroxyurea during vegetative growth","type":"exact"},{"name":"normal intra-S phase DNA damage checkpoint during cellular response to hydroxyurea","type":"exact"},{"name":"normal mitotic S-phase DNA damage checkpoint during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0004601"}


id: PBO:0031338
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_amiodarone","termid":"PBO:0031338"}


id: PBO:0069386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 646, pseudogene","termid":"PBO:0069386"}


id: PR:O13710
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A structural maintenance of chromosomes protein 5 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR19306:SF1","OMA:SCHPO02171","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":"structural maintenance of chromosomes protein 5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC14C4.02c","secondary_identifiers":["UniProtKB:O13710"],"synonyms":[{"name":"DNA repair protein spr18 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SMC partner of rad18 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SMC5","type":"exact"}],"termid":"PR:O13710"}


id: GO:0009996
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that restricts, stops or prevents a cell from adopting a specific cell fate.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell fate commitment","termid":"GO:0010454"},{"relation_name":"is_a","term_name":"regulation of cell fate specification","termid":"GO:0042659"},{"relation_name":"negatively_regulates","term_name":"cell fate specification","termid":"GO:0001708"}],"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 cell fate specification","synonyms":[{"name":"down regulation of cell fate specification","type":"exact"},{"name":"down-regulation of cell fate specification","type":"exact"},{"name":"downregulation of cell fate specification","type":"exact"},{"name":"inhibition of cell fate specification","type":"narrow"},{"name":"suppression of cell fate","type":"exact"}],"termid":"GO:0009996"}


id: MONDO:0007107
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anal sphincter myopathy, internal","secondary_identifiers":["MESH:C566287","UMLS:C1862935","OMIM:105565","MEDGEN:349633"],"synonyms":[{"name":"anal sphincter myopathy, internal","type":"exact"},{"name":"proctalgia fugax due to anal sphincter myopathy","type":"related"}],"termid":"MONDO:0007107","xrefs":{"Monarch":{"xref_id":"0007107"}}}


id: PR:Q9US51
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mtf1 gene.","definition_xrefs":["UniProtKB:Q9US51","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":"mitochondrial transcription factor 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1002.08c","synonyms":[{"name":"Spom972h-mtf1","type":"exact"}],"termid":"PR:Q9US51"}


id: GO:0046760
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A viral budding that starts with formation of a membrane curvature in the host Golgi membrane.","definition_xrefs":["VZ:1947","ISBN:0072370319","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral budding","termid":"GO:0046755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"viral budding from Golgi membrane","secondary_identifiers":["GO:0046763","GO:0046750"],"synonyms":[{"name":"Golgi membrane viral budding","type":"exact"},{"name":"Golgi membrane viral budding during viral capsid envelopment","type":"related"},{"name":"viral budding from Golgi membrane by viral capsid envelopment","type":"related"},{"name":"viral budding from Golgi membrane during viral capsid envelopment","type":"related"},{"name":"virus budding from Golgi membrane","type":"exact"},{"name":"virus budding from Golgi membrane by viral capsid envelopment","type":"related"},{"name":"virus budding from Golgi membrane during viral capsid envelopment","type":"related"}],"termid":"GO:0046760"}


id: MONDO:0002208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete vulva adenocarcinoma (obsolete MONDO:0002208)","termid":"MONDO:0002208","xrefs":{"Monarch":{"xref_id":"0002208"}}}


id: SO:0001618
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that causes the inactivation of a catalytic site with respect to a reference sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inactive_ligand_binding_site","termid":"SO:0001560"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inactive_catalytic_site","synonyms":[{"name":"inactive catalytic site","type":"exact"}],"termid":"SO:0001618"}


id: GO:0050051
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: leukotriene B4 + O2 + reduced [NADPH-hemoprotein reductase] = 20-hydroxy-leukotriene B4 + H+ + H2O + oxidized [NADPH-hemoprotein reductase].","definition_xrefs":["PMID:9675028","PMID:11461919","PMID:8486631","PMID:15364545","RHEA:22176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"leukotriene-B4 20-monooxygenase activity","secondary_identifiers":["MetaCyc:LEUKOTRIENE-B4-20-MONOOXYGENASE-RXN","Reactome:R-HSA-211873","EC:1.14.14.94"],"synonyms":[{"name":"LTB(4) 20-hydroxylase activity","type":"related"},{"name":"LTB(4) omega-hydroxylase activity","type":"related"},{"name":"LTB4 20-hydroxylase activity","type":"related"},{"name":"LTB4 omega-hydroxylase activity","type":"related"},{"name":"leukotriene-B4 20-hydroxylase activity","type":"related"},{"name":"leukotriene-B4 omega-hydroxylase activity","type":"related"}],"termid":"GO:0050051"}


id: PATO:0000557
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000557 thermosensitive (obsolete PATO:0000557)","termid":"PATO:0000557"}


id: GO:0046187
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of acetaldehyde, a colorless, flammable liquid intermediate in the metabolism of alcohol.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetaldehyde metabolic process","termid":"GO:0006117"},{"relation_name":"is_a","term_name":"aldehyde catabolic process","termid":"GO:0046185"}],"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":"acetaldehyde catabolic process","synonyms":[{"name":"acetaldehyde breakdown","type":"exact"},{"name":"acetaldehyde catabolism","type":"exact"},{"name":"acetaldehyde degradation","type":"exact"}],"termid":"GO:0046187"}


id: GO:0004551
data:
  {"annotated_genes":["SJAG_03091","SJAG_00705"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[110979],"is_not":false,"summary":null,"term":"GO:0004551"},{"annotations":[104278],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000210"},{"annotations":[104279],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035529"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a dinucleotide + H2O = 2 mononucleotides.","definition_xrefs":["PMID:2848456","PMID:4405504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00705":null,"SJAG_03091":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"dinucleotide phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-196955"],"synonyms":[{"name":"dinucleotide nucleotidohydrolase activity","type":"related"},{"name":"nucleotide diphosphatase activity","type":"broad"},{"name":"nucleotide pyrophosphatase activity","type":"exact"}],"termid":"GO:0004551","terms_by_termid":{"GO:0000210":null,"GO:0004551":null,"GO:0035529":null}}


id: PBO:0086514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved across S. cerevisiae strains; large-scale analyses show mRNA expression increases under anaerobic conditions and two-hybrid interactions with Sst2p","termid":"PBO:0086514"}


id: PR:000050457
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protection of telomeres protein tpz1 (Schizosaccharomyces pombe 972h-) that has been post-translationally modified to include sumoylated lysine at position 242 of the amino acid sequence represented by UniProtKB:Q13426. UniProtKB:O14246, Lys-242, MOD:01149.","definition_xrefs":["PMID:24925530","PomBase:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sumoylated protein","termid":"PR:000037078"},{"relation_name":"is_a","term_name":"protection of telomeres protein tpz1 (Schizosaccharomyces pombe 972h-)","termid":"PR:O14246"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tpz1/Sumo(K242)","pombase_gene_id":"SPAC6F6.16c","synonyms":[{"name":"PomBase_original_PRO_term_name: protection of telomeres protein tpz1 sumoylated 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"tpz1/Sumo(K242)","type":"exact"}],"termid":"PR:000050457"}


id: PBO:0078273
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Cys (anticodon GCA) 9-1","termid":"PBO:0078273"}


id: PR:O42972
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC20F10.02c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O42972"],"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":"UPF0588 membrane protein C20F10.02c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC20F10.02c","synonyms":[{"name":"Spom972h-SPBC20F10.02c","type":"exact"}],"termid":"PR:O42972"}


id: PBO:0084344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lanosterol synthase; an essential enzyme that catalyzes the cyclization of squalene 2,3-epoxide, a step in ergosterol biosynthesis; human LSS functionally complements the lethality of the erg7 null mutation","termid":"PBO:0084344"}


id: PATO:0000292
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000292 mobility value (obsolete PATO:0000292)","termid":"PATO:0000292"}


id: PBO:0067981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 283","termid":"PBO:0067981"}


id: PBO:0027098
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_number_of_Rad52_foci_at_rDNA_replication_origins","termid":"PBO:0027098"}


id: GO:1901830
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of zeaxanthin bis(beta-D-glucoside).","definition_xrefs":["GOC:yaf","MetaCyc:PWY-6288","PMID:20075616","UniPathway:UPA00798","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carotenoid biosynthetic process","termid":"GO:0016117"},{"relation_name":"is_a","term_name":"beta-glucoside biosynthetic process","termid":"GO:1901806"},{"relation_name":"is_a","term_name":"zeaxanthin bis(beta-D-glucoside) metabolic process","termid":"GO:1901828"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"zeaxanthin bis(beta-D-glucoside) biosynthetic process","synonyms":[{"name":"zeaxanthin bis(beta-D-glucoside) anabolism","type":"exact"},{"name":"zeaxanthin bis(beta-D-glucoside) biosynthesis","type":"exact"},{"name":"zeaxanthin bis(beta-D-glucoside) formation","type":"exact"},{"name":"zeaxanthin bis(beta-D-glucoside) synthesis","type":"exact"},{"name":"zeaxanthin diglucoside anabolism","type":"exact"},{"name":"zeaxanthin diglucoside biosynthesis","type":"exact"},{"name":"zeaxanthin diglucoside formation","type":"exact"},{"name":"zeaxanthin diglucoside synthesis","type":"exact"}],"termid":"GO:1901830"}


id: MONDO:0017873
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Ebola hemorrhagic fever (obsolete MONDO:0017873)","termid":"MONDO:0017873","xrefs":{"Monarch":{"xref_id":"0017873"}}}


id: GO:1903229
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of xanthosine.","definition_xrefs":["PMID:7007809","PMID:7559336","GO_REF:0000068","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine ribonucleoside biosynthetic process","termid":"GO:0046129"},{"relation_name":"is_a","term_name":"xanthosine metabolic process","termid":"GO:1903227"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0055086","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"xanthosine biosynthetic process","synonyms":[{"name":"xanthosine anabolism","type":"exact"},{"name":"xanthosine biosynthesis","type":"exact"},{"name":"xanthosine formation","type":"exact"},{"name":"xanthosine synthesis","type":"exact"}],"termid":"GO:1903229"}


id: GO:2000312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of kainate selective glutamate receptor activity.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neurotransmitter receptor activity","termid":"GO:0099601"},{"relation_name":"is_a","term_name":"regulation of potassium ion transmembrane transporter activity","termid":"GO:1901016"},{"relation_name":"is_a","term_name":"regulation of sodium ion transmembrane transporter activity","termid":"GO:2000649"},{"relation_name":"is_a","term_name":"regulation of cation channel activity","termid":"GO:2001257"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0055085","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"regulation of kainate selective glutamate receptor activity","termid":"GO:2000312"}


id: PBO:0057765
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 2054","termid":"PBO:0057765"}


id: MONDO:0859279
data:
  {"annotated_genes":["SJAG_05289"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85104],"is_not":false,"summary":null,"term":"MONDO:0859279"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neuronopathy, distal hereditary motor, autosomal recessive","termid":"MONDO:0015363"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05289":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0006025","MONDO:0005244"],"is_obsolete":false,"name":"spinal muscular atrophy, distal, autosomal recessive, 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0081425","UMLS:C5774201","MEDGEN:1823974","OMIM:620011"],"synonyms":[{"name":"DSMA6","type":"exact"}],"termid":"MONDO:0859279","terms_by_termid":{"MONDO:0859279":null},"xrefs":{"Monarch":{"xref_id":"0859279"}}}


id: PBO:0006187
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_upstream_target","termid":"PBO:0006187"}


id: PBO:0030888
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_DNA_replication_initiation","termid":"PBO:0030888"}


id: GO:0060415
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of muscle tissue are generated and organized. Muscle tissue consists of a set of cells that are part of an organ and carry out a contractive function.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue morphogenesis","termid":"GO:0048729"},{"relation_name":"part_of","term_name":"muscle organ morphogenesis","termid":"GO:0048644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"muscle tissue morphogenesis","termid":"GO:0060415"}


id: GO:1901951
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of anterograde dense core granule transport.","definition_xrefs":["GOC:kmv","GOC:TermGenie","PMID:23358451"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vesicle transport along microtubule","termid":"GO:1901608"},{"relation_name":"is_a","term_name":"regulation of dense core granule transport","termid":"GO:1904809"},{"relation_name":"regulates","term_name":"anterograde neuronal dense core vesicle transport","termid":"GO:1990048"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of anterograde dense core granule transport","termid":"GO:1901951"}


id: FYPO:0001516
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of mercury ions than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002682","FYPO:0001985","FYPO:0005447","FYPO:0000003","FYPO:0000139"],"is_obsolete":false,"name":"resistance to mercury","synonyms":[{"name":"resistance to mercury during mitotic cell cycle","type":"related"},{"name":"resistance to mercury during vegetative growth","type":"exact"},{"name":"resistance to mercury ion","type":"exact"},{"name":"resistance to mercury ions","type":"exact"},{"name":"resistant to mercury","type":"exact"}],"termid":"FYPO:0001516"}


id: MONDO:0001980
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Wolman disease (obsolete MONDO:0001980)","termid":"MONDO:0001980","xrefs":{"Monarch":{"xref_id":"0001980"}}}


id: FYPO:0008043
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in which the localization of a protein to the nucleus is increased during stationary phase.","definition_xrefs":["PMID:36174923"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to nucleus","termid":"FYPO:0004456"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"increased protein localization to nucleus during stationary phase","termid":"FYPO:0008043"}


id: GO:2000275
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of oxidative phosphorylation uncoupler activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of proton transport","termid":"GO:0010155"},{"relation_name":"is_a","term_name":"regulation of transmembrane transporter activity","termid":"GO:0022898"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0055085"],"is_obsolete":false,"name":"regulation of oxidative phosphorylation uncoupler activity","synonyms":[{"name":"regulation of mitochondrial uncoupling protein activity","type":"related"},{"name":"regulation of uncoupling protein activity","type":"related"}],"termid":"GO:2000275"}


id: PBO:0029283
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_mitotic_spindle_pole_body","termid":"PBO:0029283"}


id: GO:0032364
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A homeostatic process involved in the maintenance of a steady state level of oxygen within a cell.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular chemical homeostasis","termid":"GO:0055082"}],"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":"intracellular oxygen homeostasis","synonyms":[{"name":"cellular oxygen homeostasis","type":"exact"},{"name":"oxygen homeostasis","type":"broad"}],"termid":"GO:0032364"}


id: MONDO:0018393
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Male infertility with azoospermia or oligospermia due to single gene mutation is a rare, genetic male infertility due to sperm disorder characterized by the absence of a measurable amount of spermatozoa in the ejaculate (azoospermia), or a number of sperm in the ejaculate inferior to 15 million/mL (oligozoospermia), resulting from a mutation in a single gene known to cause azoo- or oligo-spermia. Sperm morphology may be normal.","definition_xrefs":["Orphanet:399805"],"gene_count":0,"genotype_count":0,"name":"obsolete male infertility with azoospermia or oligozoospermia due to single gene mutation (obsolete MONDO:0018393)","termid":"MONDO:0018393","xrefs":{"Monarch":{"xref_id":"0018393"}}}


id: GO:1903487
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lactation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:19563620","GOC:mr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of body fluid levels","termid":"GO:0050878"},{"relation_name":"is_a","term_name":"regulation of secretion","termid":"GO:0051046"},{"relation_name":"is_a","term_name":"regulation of multicellular organismal development","termid":"GO:2000026"},{"relation_name":"regulates","term_name":"lactation","termid":"GO:0007595"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of lactation","termid":"GO:1903487"}


id: GO:0070994
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events in which a stimulus indicating oxidative stress is received and converted into a molecular signal.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to oxidative stress","termid":"GO:0006979"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"detection of oxidative stress","termid":"GO:0070994"}


id: GO:0150020
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a dendritic tree are generated on the basal neuron side and organized into dendritic branches.","definition_xrefs":["GOC:bc","PMID:22683681","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dendrite arborization","termid":"GO:0140059"},{"relation_name":"is_a","term_name":"basal dendrite morphogenesis","termid":"GO:0150019"}],"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":"basal dendrite arborization","termid":"GO:0150020"}


id: PBO:0049015
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycoprotein M6B","termid":"PBO:0049015"}


id: PBO:0017440
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_transcription_of","termid":"PBO:0017440"}


id: MONDO:0034979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A rare congenital optic disk excavation characterized by deep fundus excavation of chorioretinal atrophy surrounding a relatively normal appearing optic disk. Retinal vasculature is normal, and retinochoroidal coloboma and glial anomalies are absent. Patients present with mostly unilateral markedly reduced visual acuity. Association with other congenital defects or systemic diseases is uncommon. [Orphanet:519400]","definition_xrefs":["Orphanet:519400"],"gene_count":0,"genotype_count":0,"name":"obsolete peripapillary staphyloma (obsolete MONDO:0034979)","secondary_identifiers":["ICD10CM:Q14.2"],"termid":"MONDO:0034979","xrefs":{"Monarch":{"xref_id":"0034979"}}}


id: PBO:0084108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HDEL receptor; an integral membrane protein that binds to the HDEL motif in proteins destined for retention in the endoplasmic reticulum; has a role in maintenance of normal levels of ER-resident proteins","termid":"PBO:0084108"}


id: GO:0016872
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The catalysis of certain rearrangements of a molecule to break or form a ring.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isomerase activity","termid":"GO:0016853"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674"],"is_obsolete":false,"name":"intramolecular lyase activity","secondary_identifiers":["EC:5.5.1.-"],"termid":"GO:0016872"}


id: MOD:01795
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-methionine residue containing common isotopes to 1x(13)C,3x(2)H C(6)-labeled L-methionine.","definition_xrefs":["PubMed:18688235","PubMed:15782174"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(2)H deuterium labeled residue","termid":"MOD:00839"},{"relation_name":"is_a","term_name":"modified L-methionine residue","termid":"MOD:00913"},{"relation_name":"is_a","term_name":"1x(13)C,3x(2)H labeled monomethylated residue","termid":"MOD:01794"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1x(13)C,3x(2)H C(6)-labeled L-methionine","synonyms":[{"name":"Methyl:2H(3)13C(1)","type":"related"}],"termid":"MOD:01795"}


id: GO:0010550
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the chemical reactions and pathways resulting in the breakdown of one or more components of the light-harvesting complex of photosystem II.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein catabolic process","termid":"GO:0042176"},{"relation_name":"regulates","term_name":"PSII associated light-harvesting complex II catabolic process","termid":"GO:0010304"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0030163"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0030163"],"is_obsolete":false,"name":"regulation of PSII associated light-harvesting complex II catabolic process","synonyms":[{"name":"regulation of LHCII catabolism","type":"exact"},{"name":"regulation of LHCII degradation","type":"exact"}],"termid":"GO:0010550"}


id: MONDO:0100472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lissencephaly spectrum disorder that manifests as posterior predominant pachygyria (ranging from mild severity to classic lissencephaly) and brainstem malformations which include brainstem dysplasia (typically with reduced anteroposterior thickness and transverse broadening of the pons/medulla) and midline crossing defects (anterior commissure, transverse pontine fibers, pyramidal tract, callosum hypoplasia).","direct_ancestors":[{"relation_name":"is_a","term_name":"lissencephaly spectrum disorders","termid":"MONDO:0018838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"lissencephaly spectrum disorder with complex brainstem malformation","termid":"MONDO:0100472","xrefs":{"Monarch":{"xref_id":"0100472"}}}


id: MONDO:0000336
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tertiary neurosyphilis that results in inflammation located in arteries of the brain or located in arteries of spinal cord. The infection has symptom headache, has symptom neck stiffness, has symptom dizziness, has symptom behavioral abnormalities, has symptom poor concentration, has symptom memory loss, has symptom lassitude, has symptom insomnia, has symptom blurred vision, has symptom weakness and wasting of shoulder-girdle and arm muscles, has symptom slowly progressive leg weakness with urinary or fecal incontinence or both, and has symptom paralysis of the legs due to thrombosis of spinal arteries.","definition_xrefs":["DOID:0050491"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurosyphilis","termid":"MONDO:0004944"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meningovascular neurosyphilis","termid":"MONDO:0000336","xrefs":{"Monarch":{"xref_id":"0000336"}}}


id: GO:1902191
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of 2-methylbutanoyl-CoA(4-).","definition_xrefs":["GOC:TermGenie","PMID:15574432"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty-acyl-CoA biosynthetic process","termid":"GO:0046949"},{"relation_name":"is_a","term_name":"2-methylbutanoyl-CoA(4-) metabolic process","termid":"GO:1902189"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006790","GO:0006629","GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"2-methylbutanoyl-CoA(4-) biosynthetic process","synonyms":[{"name":"2-methylbutanoyl-CoA(4-) anabolism","type":"exact"},{"name":"2-methylbutanoyl-CoA(4-) biosynthesis","type":"exact"},{"name":"2-methylbutanoyl-CoA(4-) formation","type":"exact"},{"name":"2-methylbutanoyl-CoA(4-) synthesis","type":"exact"}],"termid":"GO:1902191"}


id: GO:0048073
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of establishment of a pattern of pigment in the eye of an organism.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental pigmentation","termid":"GO:0048070"},{"relation_name":"regulates","term_name":"eye pigmentation","termid":"GO:0048069"}],"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 eye pigmentation","termid":"GO:0048073"}


id: GO:0019990
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of pteridine, pyrazino(2,3-dipyrimidine), the parent structure of pterins and the pteroyl group.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pteridine metabolic process","termid":"GO:0019889"},{"relation_name":"is_a","term_name":"pteridine-containing compound catabolic process","termid":"GO:0042560"}],"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":"pteridine catabolic process","synonyms":[{"name":"pteridine breakdown","type":"exact"},{"name":"pteridine catabolism","type":"exact"},{"name":"pteridine degradation","type":"exact"}],"termid":"GO:0019990"}


id: MONDO:0007403
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia.","definition_xrefs":["Orphanet:282166"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Creutzfeldt Jacob disease","termid":"MONDO:0005357"},{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"inherited neurodegenerative disorder","termid":"MONDO:0024237"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"inherited Creutzfeldt-Jakob disease","secondary_identifiers":["GARD:17307","NANDO:1200189","SCTID:715807002","UMLS:C0751254","icd11.foundation:607607042","OMIM:123400","MEDGEN:155837"],"synonyms":[{"name":"CJD","type":"related"},{"name":"Creutzfeldt-Jakob disease","type":"related"},{"name":"Creutzfeldt-Jakob disease, Heidenhain variant","type":"related"},{"name":"Creutzfeldt-Jakob disease, familial","type":"related"},{"name":"Creutzfeldt-Jakob disease, sporadic","type":"related"},{"name":"Creutzfeldt-Jakob disease, variant","type":"related"},{"name":"Creutzfeldt-Jakob disease, variant, resistance to","type":"exact"},{"name":"hereditary Creutzfeldt Jacob disease","type":"exact"},{"name":"inherited CJD","type":"exact"}],"termid":"MONDO:0007403","xrefs":{"Monarch":{"xref_id":"0007403"}}}


id: PBO:0043681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CORO7-PAM16 readthrough","termid":"PBO:0043681"}


id: MONDO:0003909
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign neoplasm that arises from the Bartholin gland and is characterized by the presence of a fibromuscular stroma and glands lined by mucin-secreting epithelial cells, arranged in a lobular architecture.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bartholin gland benign neoplasm","termid":"MONDO:0002193"},{"relation_name":"is_a","term_name":"vulvar glandular neoplasm","termid":"MONDO:0002198"},{"relation_name":"is_a","term_name":"adenomyoma","termid":"MONDO:0005635"},{"relation_name":"is_a","term_name":"benign epithelial neoplasm","termid":"MONDO:0036976"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bartholin gland adenomyoma","secondary_identifiers":["UMLS:C1511049","DOID:6518","MEDGEN:307248","NCIT:C40300"],"synonyms":[{"name":"Bartholin gland adenomyoma","type":"exact"},{"name":"adenomyoma of major vestibular gland","type":"exact"},{"name":"major vestibular gland adenomyoma","type":"exact"}],"termid":"MONDO:0003909","xrefs":{"Monarch":{"xref_id":"0003909"}}}


id: GO:0007366
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Allocation of cells to parasegments in the embryo, through the action of overlapping series of pair rule gene activities.","definition_xrefs":["ISBN:0632030488","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"periodic partitioning","termid":"GO:0007365"},{"relation_name":"is_a","term_name":"anterior/posterior pattern specification","termid":"GO:0009952"}],"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":"periodic partitioning by pair rule gene","termid":"GO:0007366"}


id: PBO:0051909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"integrin subunit alpha M","termid":"PBO:0051909"}


id: PBO:0017455
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-input_of","termid":"PBO:0017455"}


id: MONDO:0005123
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Hibiscus chlorotic ringspot virus infection (obsolete MONDO:0005123)","termid":"MONDO:0005123","xrefs":{"Monarch":{"xref_id":"0005123"}}}


id: PBO:0041593
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"carbonic anhydrase 5B","termid":"PBO:0041593"}


id: MONDO:0100576
data:
  {"annotated_genes":["SJAG_03536"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85949],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014517"}]},"cv_name":"mondo","definition":"An instance of generalized epilepsy that is caused by an inherited genomic modification in an individual.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"},{"relation_name":"is_a","term_name":"genetic generalized epilepsy","termid":"MONDO:0100575"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03536":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"hereditary generalized epilepsy","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0100576","terms_by_termid":{"MONDO:0014517":null},"xrefs":{"Monarch":{"xref_id":"0100576"}}}


id: GO:0043385
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving a mycotoxin, any poisonous substance produced by a fungus.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxin metabolic process","termid":"GO:0009404"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"mycotoxin metabolic process","synonyms":[{"name":"mycotoxin metabolism","type":"exact"}],"termid":"GO:0043385"}


id: GO:0050273
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-succinylglutathione + H2O = glutathione + H+ + succinate.","definition_xrefs":["EC:3.1.2.13","RHEA:16713"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thiolester hydrolase activity","termid":"GO:0016790"}],"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:0016788"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016788","GO:0016787"],"is_obsolete":false,"name":"S-succinylglutathione hydrolase activity","secondary_identifiers":["KEGG_REACTION:R00499","MetaCyc:S-SUCCINYLGLUTATHIONE-HYDROLASE-RXN"],"termid":"GO:0050273"}


id: PATO:0001092
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001092 flux value (obsolete PATO:0001092)","termid":"PATO:0001092"}


id: GO:0052626
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: benzoate + L-glutamate + ATP = N-benzoyl-L-glutamate + AMP + diphosphate + H+.","definition_xrefs":["MetaCyc:RXN-10886","PMID:19189963"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016874","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"N-benzoyl-L-glutamate synthetase activity","synonyms":[{"name":"benzoate amino acid synthetase activity","type":"broad"},{"name":"benzoyl amino acid synthetase activity","type":"exact"}],"termid":"GO:0052626"}


id: MONDO:0008365
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Recombinant 8 (rec(8)) syndrome, also known as San Luis Valley syndrome, is a complex chromosomal disorder that is due to a parental pericentric inversion of chromosome 8 and is characterized by major congenital heart anomalies, urogenital malformations, moderate to severe intellectual deficiency and mild craniofacial dysmorphism.","definition_xrefs":["Orphanet:96167"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"recombinant 8 syndrome","secondary_identifiers":["UMLS:C0795822","MESH:C535296","MEDGEN:167070","GARD:9698","OMIM:179613","SCTID:718189004"],"synonyms":[{"name":"Duplication 8q/deletion 8p","type":"exact"},{"name":"RECOMBINANT chromosome 8 syndrome","type":"related"},{"name":"Rec(8) syndrome","type":"exact"},{"name":"Rec8 syndrome","type":"exact"},{"name":"Recombinant chromosome 8 syndrome","type":"exact"},{"name":"San Luis Valley recombinant chromosome 8 syndrome","type":"related"},{"name":"San Luis Valley syndrome","type":"exact"},{"name":"chromosome 8Q22.1-qter Duplication and 8Pter-p23.1 deletion","type":"related"}],"termid":"MONDO:0008365","xrefs":{"Monarch":{"xref_id":"0008365"}}}


id: PBO:0058447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5047","termid":"PBO:0058447"}


id: PBO:0065448
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, ATPase 5","termid":"PBO:0065448"}


id: FYPO:0004199
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 occurrence of protein degradation is increased during mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein degradation during vegetative growth","termid":"FYPO:0000847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"increased protein degradation during mitosis","synonyms":[{"name":"increased protein breakdown during mitosis","type":"exact"},{"name":"increased protein catabolic process during mitosis","type":"exact"},{"name":"increased protein catabolism during mitosis","type":"exact"},{"name":"increased protein degradation during mitosis during mitotic cell cycle","type":"related"},{"name":"increased protein degradation during mitosis during vegetative growth","type":"exact"},{"name":"increased protein degradation during mitotic M phase","type":"related"},{"name":"increased protein degradation during mitotic nuclear division","type":"exact"}],"termid":"FYPO:0004199"}


id: PBO:0030824
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mating_cassette_duplication","termid":"PBO:0030824"}


id: PBO:0080537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WASH and IL9R antisense RNA 2","termid":"PBO:0080537"}


id: MONDO:0850078
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"craniosynostosis","termid":"MONDO:0015469"}],"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":"non-syndromic non-specific multisutural craniosynostosis","secondary_identifiers":["MEDGEN:1842261","Orphanet:620158","UMLS:C5680398","GARD:22475"],"termid":"MONDO:0850078","xrefs":{"Monarch":{"xref_id":"0850078"}}}


id: PBO:0044125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CTAGE family member 11, pseudogene","termid":"PBO:0044125"}


id: PBO:0055845
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat, Ig-like and transmembrane domains 1","termid":"PBO:0055845"}


id: PBO:0071077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 79","termid":"PBO:0071077"}


id: PBO:0070493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L5 pseudogene 28","termid":"PBO:0070493"}


id: FYPO:0000766
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 N-ethylmaleimide 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:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002682"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002682","FYPO:0000139","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"resistance to N-ethylmaleimide","synonyms":[{"name":"resistance to N-ethylmaleimide during mitotic cell cycle","type":"related"},{"name":"resistance to N-ethylmaleimide during vegetative growth","type":"exact"},{"name":"resistant to N-ethylmaleimide","type":"exact"}],"termid":"FYPO:0000766"}


id: PBO:0028508
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_transposable_element-derived_small_RNA_level","termid":"PBO:0028508"}


id: MONDO:0002207
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An uncommon intraepithelial malignant neoplasm of eccrine or apocrine origin, arising from the vulva. It usually affects post-menopausal women. In approximately 10-20% of the cases there is an associated anorectal, or urothelial carcinoma or a skin appendage adenocarcinoma identified. It presents as a red, eczematous lesion. Microscopically, it is characterized by the presence of the typical Paget cells which are large, round cells with abundant cytoplasm and prominent nuclei.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extramammary Paget disease","termid":"MONDO:0008177"},{"relation_name":"is_a","term_name":"vulvar adenocarcinoma","termid":"MONDO:0024336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"vulval Paget disease","secondary_identifiers":["UMLS:C1275217","MEDGEN:266154","SCTID:254898001","NCIT:C4027","DOID:2097","ICD9:233.39"],"synonyms":[{"name":"Paget disease of the vulva","type":"exact"},{"name":"Paget's disease of the vulva","type":"exact"},{"name":"Paget's disease of vulva","type":"exact"},{"name":"mammalian vulva Paget disease","type":"exact"},{"name":"vulva Paget's disease","type":"exact"},{"name":"vulval Paget disease","type":"exact"},{"name":"vulval Paget's disease","type":"exact"},{"name":"vulvar Paget's disease","type":"exact"}],"termid":"MONDO:0002207","xrefs":{"Monarch":{"xref_id":"0002207"}}}


id: GO:1904774
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of ubiquinone biosynthetic process.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:8125303"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"regulation of ubiquinone biosynthetic process","termid":"GO:0010795"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"negatively_regulates","term_name":"ubiquinone biosynthetic process","termid":"GO:0006744"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006744"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006744"}],"interesting_parent_ids":["GO:0006744","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"negative regulation of ubiquinone biosynthetic process","synonyms":[{"name":"down regulation of coenzyme Q biosynthesis","type":"exact"},{"name":"down regulation of coenzyme Q biosynthetic process","type":"exact"},{"name":"down regulation of coenzyme Q10 biosynthesis","type":"narrow"},{"name":"down regulation of coenzyme Q10 biosynthetic process","type":"narrow"},{"name":"down regulation of coenzyme Q6 biosynthesis","type":"narrow"},{"name":"down regulation of coenzyme Q6 biosynthetic process","type":"narrow"},{"name":"down regulation of coenzyme Q8 biosynthesis","type":"narrow"},{"name":"down regulation of coenzyme Q8 biosynthetic process","type":"narrow"},{"name":"down regulation of coenzyme Q9 biosynthesis","type":"narrow"},{"name":"down regulation of coenzyme Q9 biosynthetic process","type":"narrow"},{"name":"down regulation of ubiquinone anabolism","type":"exact"},{"name":"down regulation of ubiquinone biosynthesis","type":"exact"},{"name":"down regulation of ubiquinone biosynthetic process","type":"exact"},{"name":"down regulation of ubiquinone formation","type":"exact"},{"name":"down regulation of ubiquinone synthesis","type":"exact"},{"name":"down-regulation of coenzyme Q biosynthesis","type":"exact"},{"name":"down-regulation of coenzyme Q biosynthetic process","type":"exact"},{"name":"down-regulation of coenzyme Q10 biosynthesis","type":"narrow"},{"name":"down-regulation of coenzyme Q10 biosynthetic process","type":"narrow"},{"name":"down-regulation of coenzyme Q6 biosynthesis","type":"narrow"},{"name":"down-regulation of coenzyme Q6 biosynthetic process","type":"narrow"},{"name":"down-regulation of coenzyme Q8 biosynthesis","type":"narrow"},{"name":"down-regulation of coenzyme Q8 biosynthetic process","type":"narrow"},{"name":"down-regulation of coenzyme Q9 biosynthesis","type":"narrow"},{"name":"down-regulation of coenzyme Q9 biosynthetic process","type":"narrow"},{"name":"down-regulation of ubiquinone anabolism","type":"exact"},{"name":"down-regulation of ubiquinone biosynthesis","type":"exact"},{"name":"down-regulation of ubiquinone biosynthetic process","type":"exact"},{"name":"down-regulation of ubiquinone formation","type":"exact"},{"name":"down-regulation of ubiquinone synthesis","type":"exact"},{"name":"downregulation of coenzyme Q biosynthesis","type":"exact"},{"name":"downregulation of coenzyme Q biosynthetic process","type":"exact"},{"name":"downregulation of coenzyme Q10 biosynthesis","type":"narrow"},{"name":"downregulation of coenzyme Q10 biosynthetic process","type":"narrow"},{"name":"downregulation of coenzyme Q6 biosynthesis","type":"narrow"},{"name":"downregulation of coenzyme Q6 biosynthetic process","type":"narrow"},{"name":"downregulation of coenzyme Q8 biosynthesis","type":"narrow"},{"name":"downregulation of coenzyme Q8 biosynthetic process","type":"narrow"},{"name":"downregulation of coenzyme Q9 biosynthesis","type":"narrow"},{"name":"downregulation of coenzyme Q9 biosynthetic process","type":"narrow"},{"name":"downregulation of ubiquinone anabolism","type":"exact"},{"name":"downregulation of ubiquinone biosynthesis","type":"exact"},{"name":"downregulation of ubiquinone biosynthetic process","type":"exact"},{"name":"downregulation of ubiquinone formation","type":"exact"},{"name":"downregulation of ubiquinone synthesis","type":"exact"},{"name":"inhibition of coenzyme Q biosynthesis","type":"narrow"},{"name":"inhibition of coenzyme Q biosynthetic process","type":"narrow"},{"name":"inhibition of coenzyme Q10 biosynthesis","type":"narrow"},{"name":"inhibition of coenzyme Q10 biosynthetic process","type":"narrow"},{"name":"inhibition of coenzyme Q6 biosynthesis","type":"narrow"},{"name":"inhibition of coenzyme Q6 biosynthetic process","type":"narrow"},{"name":"inhibition of coenzyme Q8 biosynthesis","type":"narrow"},{"name":"inhibition of coenzyme Q8 biosynthetic process","type":"narrow"},{"name":"inhibition of coenzyme Q9 biosynthesis","type":"narrow"},{"name":"inhibition of coenzyme Q9 biosynthetic process","type":"narrow"},{"name":"inhibition of ubiquinone anabolism","type":"narrow"},{"name":"inhibition of ubiquinone biosynthesis","type":"narrow"},{"name":"inhibition of ubiquinone biosynthetic process","type":"narrow"},{"name":"inhibition of ubiquinone formation","type":"narrow"},{"name":"inhibition of ubiquinone synthesis","type":"narrow"},{"name":"negative regulation of coenzyme Q biosynthesis","type":"exact"},{"name":"negative regulation of coenzyme Q biosynthetic process","type":"exact"},{"name":"negative regulation of coenzyme Q10 biosynthesis","type":"narrow"},{"name":"negative regulation of coenzyme Q10 biosynthetic process","type":"narrow"},{"name":"negative regulation of coenzyme Q6 biosynthesis","type":"narrow"},{"name":"negative regulation of coenzyme Q6 biosynthetic process","type":"narrow"},{"name":"negative regulation of coenzyme Q8 biosynthesis","type":"narrow"},{"name":"negative regulation of coenzyme Q8 biosynthetic process","type":"narrow"},{"name":"negative regulation of coenzyme Q9 biosynthesis","type":"narrow"},{"name":"negative regulation of coenzyme Q9 biosynthetic process","type":"narrow"},{"name":"negative regulation of ubiquinone anabolism","type":"exact"},{"name":"negative regulation of ubiquinone biosynthesis","type":"exact"},{"name":"negative regulation of ubiquinone formation","type":"exact"},{"name":"negative regulation of ubiquinone synthesis","type":"exact"}],"termid":"GO:1904774"}


id: MONDO:0014032
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any brachydactyly type A1 in which the cause of the disease is a mutation in the GDF5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"brachydactyly type A1","termid":"MONDO:0007215"},{"relation_name":"is_a","term_name":"brachydactyly","termid":"MONDO:0021004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brachydactyly type A1C","secondary_identifiers":["GARD:15903","DOID:0110977","UMLS:C3554446","OMIM:615072","MEDGEN:767360"],"synonyms":[{"name":"BDA1C","type":"exact"},{"name":"GDF5 brachydactyly type A1","type":"exact"},{"name":"brachydactyly type A1 caused by mutation in GDF5","type":"exact"},{"name":"brachydactyly, type A1, C","type":"related"}],"termid":"MONDO:0014032","xrefs":{"Monarch":{"xref_id":"0014032"}}}


id: PBO:0044236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cullin 4B","termid":"PBO:0044236"}


id: PBO:0046627
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group W member 8","termid":"PBO:0046627"}


id: FYECO:0000102
data:
  {"alleles_by_uniquename":{"SJAG_04312:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04312","name":"pka1delta","uniquename":"SJAG_04312:allele-1"}},"annotation_feature_type":"gene","cv_annotations":{"fission_yeast_phenotype_condition":[{"annotations":[118615],"is_not":false,"summary":null,"term":"FYECO:0000102"}]},"cv_name":"fission_yeast_phenotype_condition","definition":"Cells were grown on agar plates.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping growth medium","termid":"FYECO:0000009"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04312":null},"genotype_count":1,"genotypes_by_uniquename":{"pka1delta":{"display_name":"pka1delta","display_uniquename":"pka1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04312:allele-1","expression":"Null"}]}]}},"is_obsolete":false,"name":"agar plates","references_by_uniquename":{"PMID:27678009":null},"single_locus_annotated_genes":["SJAG_04312"],"single_locus_genotype_uniquenames":["pka1delta"],"synonyms":[{"name":"solid agar plates","type":"exact"}],"termid":"FYECO:0000102","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000102":null,"FYECO:0000137":null,"FYPO_EXT:0000003":null}}


id: PBO:0080847
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Y-box binding protein 2","termid":"PBO:0080847"}


id: PBO:0087074
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L36B; binds to 5.8 S rRNA; homologous to mammalian ribosomal protein L36, no bacterial homolog; RPL36B has a paralog, RPL36A, that arose from the whole genome duplication","termid":"PBO:0087074"}


id: PBO:0030055
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_adenylyl_cyclase_activity","termid":"PBO:0030055"}


id: GO:0015419
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 + sulfate(out) = ADP + phosphate + sulfate(in).","definition_xrefs":["RHEA:10192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfate transmembrane transporter activity","termid":"GO:0015116"},{"relation_name":"is_a","term_name":"ATPase-coupled inorganic anion transmembrane transporter activity","termid":"GO:0043225"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"ABC-type sulfate transporter activity","secondary_identifiers":["MetaCyc:ABC-70-RXN"],"synonyms":[{"name":"ATPase-coupled sulfate transmembrane transporter activity","type":"related"},{"name":"sulfate ABC transporter","type":"exact"},{"name":"sulfate transmembrane-transporting ATPase activity","type":"related"},{"name":"sulfate-transporting ATPase activity","type":"related"},{"name":"sulfate/thiosulfate porter activity","type":"broad"},{"name":"sulphate transporting ATPase activity","type":"related"}],"termid":"GO:0015419"}


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


id: MONDO:0042979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypokalemic periodic paralysis","termid":"MONDO:0008223"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"hypokalemic periodic paralysis, type 1","secondary_identifiers":["OMIM:170400","MEDGEN:811387","UMLS:C3714580"],"synonyms":[{"name":"HOKPP1","type":"related"},{"name":"hypokalemic periodic paralysis, type 1","type":"exact"}],"termid":"MONDO:0042979","xrefs":{"Monarch":{"xref_id":"0042979"}}}


id: FYPO:0007650
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to pericentric heterochromatin is abolished during prophase of the first meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:14730319"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to chromatin","termid":"FYPO:0001678"},{"relation_name":"is_a","term_name":"abolished protein localization to centromere during meiotic prophase II","termid":"FYPO:0006530"},{"relation_name":"is_a","term_name":"abnormal protein localization to pericentric heterochromatin","termid":"FYPO:0007648"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to pericentric heterochromatin during meiotic prophase I","synonyms":[{"name":"abolished protein localization to centromeric heterochromatin during meiotic prophase I","type":"exact"},{"name":"abolished protein localization to nuclear centromeric heterochromatin during meiotic prophase I","type":"exact"},{"name":"abolished protein localization to pericentric heterochromatin during prophase of meiosis I","type":"exact"}],"termid":"FYPO:0007650"}


id: FYPO:0003119
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 polyadenylated messenger RNA (mRNA) measured in the nucleus is higher than normal. Total mRNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased nuclear RNA level during vegetative growth","termid":"FYPO:0000911"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002403","FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0006551","FYPO:0001320"],"is_obsolete":false,"name":"increased nuclear polyadenylated mRNA level during vegetative growth","synonyms":[{"name":"increased nuclear poly(A)+ mRNA level during vegetative growth","type":"exact"},{"name":"increased nuclear polyadenylated mRNA accumulation during vegetative growth","type":"related"},{"name":"increased nuclear polyadenylated mRNA level during mitotic cell cycle","type":"related"},{"name":"increased nuclear polyadenylated mRNA transcript level during vegetative growth","type":"exact"},{"name":"increased nuclear polyadenylated messenger RNA level during vegetative growth","type":"exact"},{"name":"nuclear poly(A)+ mRNA accumulation","type":"related"},{"name":"nuclear poly-A mRNA accumulation","type":"related"}],"termid":"FYPO:0003119"}


id: FYPO:0006770
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which kinetochore disassembly is abnormal during prophase of meiosis I. Normally, outer kinetochore components delocalize from the centromere during bouquet formation in meiotic prophase I.","definition_xrefs":["PMID:27611693","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiosis I","termid":"FYPO:0003603"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000631"],"is_obsolete":false,"name":"abnormal kinetochore disassembly during meiotic prophase I","synonyms":[{"name":"abnormal kinetochore disassembly during prophase I","type":"exact"},{"name":"abnormal kinetochore disassembly during prophase of meiosis I","type":"exact"},{"name":"defective kinetochore disassembly during meiotic prophase I","type":"exact"}],"termid":"FYPO:0006770"}


id: GO:0099184
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action of a molecule that contributes to the structural integrity of a postsynaptic intermediate filament cytoskeleton.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structural constituent of cytoskeleton","termid":"GO:0005200"},{"relation_name":"is_a","term_name":"structural constituent of postsynapse","termid":"GO:0099186"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005198"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005198","GO:0003674"],"is_obsolete":false,"name":"structural constituent of postsynaptic intermediate filament cytoskeleton","termid":"GO:0099184"}


id: GO:1904925
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of autophagy of the mitochondrion in response to mitochondrial depolarization.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:22020285","GOC:pad","GOC:PARL"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of autophagy of mitochondrion in response to mitochondrial depolarization (obsolete GO:1904925)","termid":"GO:1904925"}


id: GO:0047595
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,4,5,6-tetrahydro-6-oxonicotinate + oxidized ferredoxin = 6-hydroxynicotinate + reduced ferredoxin.","definition_xrefs":["MetaCyc:6-HYDROXYNICOTINATE-REDUCTASE-RXN","EC:1.3.7.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, iron-sulfur protein as acceptor","termid":"GO:0016636"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"6-hydroxynicotinate reductase activity","secondary_identifiers":["RHEA:17225"],"synonyms":[{"name":"1,4,5,6-tetrahydro-6-oxonicotinate:ferredoxin oxidoreductase activity","type":"related"},{"name":"6-hydroxynicotinic reductase activity","type":"related"},{"name":"6-oxo-1,4,5,6-tetrahydronicotinate:ferredoxin oxidoreductase activity","type":"related"},{"name":"6-oxotetrahydro-nicotinate dehydrogenase activity","type":"related"},{"name":"6-oxotetrahydronicotinate dehydrogenase activity","type":"related"},{"name":"HNA reductase activity","type":"related"}],"termid":"GO:0047595"}


id: PBO:0091782
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bromodomain containing protein","termid":"PBO:0091782"}


id: MONDO:0850415
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A myopathy that is characterized by muscle breakdown (rhabdomyolysis), heat and exertion-related muscle pain (myalgia) and cramping symptoms, severe muscle pain, sudden elevation and subsequent fall of serum creatine phosphokinase levels and products of muscle breakdown in the urine (myoglobinuria). Associated with RYR1 variations. Rhabdomyolysis is associated with a range of external triggers, including strenuous exercise beyond the limit of fatigue, heat stress, illicit drug or alcohol abuse, use of supplements or certain medications, recent viral illness or muscle trauma.","definition_xrefs":["DOID:0080992"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RYR1-related myopathy","termid":"MONDO:0100150"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"rhabdomyolysis-myalgia syndrome","termid":"MONDO:0850415","xrefs":{"Monarch":{"xref_id":"0850415"}}}


id: PBO:0057075
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 154","termid":"PBO:0057075"}


id: PBO:0012583
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G Protein Beta gene","termid":"PBO:0012583"}


id: PBO:0066119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAS like family 12","termid":"PBO:0066119"}


id: MONDO:1011270
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetic cataract that occurs in degu.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diabetic cataract, non-human animal","termid":"MONDO:1010343"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diabetic cataract, degu","secondary_identifiers":["OMIA:001865-10160"],"termid":"MONDO:1011270","xrefs":{"Monarch":{"xref_id":"1011270"}}}


id: MONDO:0042727
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A teratoma that is found at the base of the coccyx. It is the most commonly seen tumor in newborns.","definition_xrefs":["NCIT:C99055"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vertebral column disorder","termid":"MONDO:0000812"},{"relation_name":"is_a","term_name":"teratoma","termid":"MONDO:0002601"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sacrococcygeal teratoma","secondary_identifiers":["NANDO:2100216","SCTID:281561000","UMLS:C0559459","NANDO:2200816","HP:0030736","MEDGEN:107852","Orphanet:494421","NANDO:2201287","NORD:1685","GARD:319"],"synonyms":[{"name":"pre-sacral teratoma","type":"exact"},{"name":"presacral teratoma","type":"exact"},{"name":"sacrococcygeal teratoma","type":"exact"}],"termid":"MONDO:0042727","xrefs":{"Monarch":{"xref_id":"0042727"}}}


id: PBO:0028840
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-heterochromatin_assembly_beyond_boundary_element_IRR","termid":"PBO:0028840"}


id: FYPO:0007388
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the mitotic spindle is assembled in an incorrect orientation. Normally, the spindle is parallel to the long axis of the cell.","definition_xrefs":["PMID:18495844","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic spindle","termid":"FYPO:0000338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000054","FYPO:0000120","FYPO:0001320","FYPO:0000002","FYPO:0002399","FYPO:0005447"],"is_obsolete":false,"name":"misoriented mitotic spindle","synonyms":[{"name":"abnormal angle of mitotic spindle orientation","type":"related"},{"name":"abnormal mitotic spindle orientation","type":"exact"},{"name":"misoriented mitotic spindle during mitotic cell cycle","type":"related"},{"name":"misoriented mitotic spindle during vegetative growth","type":"exact"}],"termid":"FYPO:0007388"}


id: FYPO:0004628
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which premeiotic DNA replication begins later than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal premeiotic DNA replication","termid":"FYPO:0000625"}],"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:0000293"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000293","FYPO:0000631","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"delayed onset of premeiotic DNA replication","synonyms":[{"name":"delayed premeiotic DNA replication","type":"exact"}],"termid":"FYPO:0004628"}


id: MONDO:0002436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the nose.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"upper respiratory tract disorder","termid":"MONDO:0004867"},{"relation_name":"is_a","term_name":"otorhinolaryngologic disease","termid":"MONDO:0024623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nasal disorder","secondary_identifiers":["DOID:2825","MEDGEN:10385","SCTID:89488007","MESH:D009668","UMLS:C0028432","ICD9:478.19"],"synonyms":[{"name":"disease of nose","type":"exact"},{"name":"disease or disorder of nose","type":"exact"},{"name":"disorder of nose","type":"exact"},{"name":"disorder of the nose","type":"exact"},{"name":"nasal disorder","type":"exact"},{"name":"nose disease","type":"exact"},{"name":"nose disease or disorder","type":"exact"}],"termid":"MONDO:0002436","xrefs":{"Monarch":{"xref_id":"0002436"}}}


id: PBO:0070172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 86 pseudogene","termid":"PBO:0070172"}


id: PBO:0069268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 524, pseudogene","termid":"PBO:0069268"}


id: MONDO:0100117
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. An instance of sudden cardiac death that is caused by an inherited genomic modification in an individual.","definition_xrefs":["MONDO:patterns/hereditary"],"gene_count":0,"genotype_count":0,"name":"obsolete familial sudden death (obsolete MONDO:0100117)","synonyms":[{"name":"familial sudden death syndrome","type":"exact"}],"termid":"MONDO:0100117","xrefs":{"Monarch":{"xref_id":"0100117"}}}


id: GO:0043105
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops or reduces the activity of the enzyme GTP cyclohydrolase I.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of GTP cyclohydrolase I activity (obsolete GO:0043105)","synonyms":[{"name":"down regulation of GTP cyclohydrolase I activity","type":"exact"},{"name":"down-regulation of GTP cyclohydrolase I activity","type":"exact"},{"name":"downregulation of GTP cyclohydrolase I activity","type":"exact"},{"name":"inhibition of GTP cyclohydrolase I activity","type":"narrow"}],"termid":"GO:0043105"}


id: GO:0015673
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of silver (Ag+) ions into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion transport","termid":"GO:0000041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"silver ion transport","synonyms":[{"name":"silver transport","type":"exact"}],"termid":"GO:0015673"}


id: GO:0003200
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A transition where an endocardial cell loses apical/basolateral polarity, severs intercellular adhesive junctions, degrades basement membrane components and becomes a migratory mesenchymal cell that will contribute to the formation of the heart septum.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocardial cushion to mesenchymal transition","termid":"GO:0090500"},{"relation_name":"part_of","term_name":"cardiac septum morphogenesis","termid":"GO:0060411"}],"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":"endocardial cushion to mesenchymal transition involved in heart chamber septation","termid":"GO:0003200"}


id: MONDO:0006747
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disease caused by the liberation of exotoxins of clostridium perfringens in the intestines of sheep, goats, cattle, foals, and piglets. Type B enterotoxemia in lambs is lamb dysentery; type C enterotoxemia in mature sheep produces 'struck', and in calves, lambs and piglets it produces hemorrhagic enterotoxemia; type D enterotoxemia in sheep and goats is pulpy-kidney disease or overeating disease.","definition_xrefs":["MESH:D004767"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cattle disease","termid":"MONDO:0024913"},{"relation_name":"is_a","term_name":"horse disease","termid":"MONDO:0024950"},{"relation_name":"is_a","term_name":"sheep disease","termid":"MONDO:0024985"},{"relation_name":"is_a","term_name":"swine disease","termid":"MONDO:0024990"},{"relation_name":"is_a","term_name":"goat disease","termid":"MONDO:0025003"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enterotoxemia","secondary_identifiers":["ICD9:799.89","EFO:1000922","SCTID:370514003"],"termid":"MONDO:0006747","xrefs":{"Monarch":{"xref_id":"0006747"}}}


id: PR:Q09783
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tim8 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09783"],"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":"mitochondrial import inner membrane translocase subunit tim8 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13G6.04","synonyms":[{"name":"Spom972h-tim8","type":"exact"}],"termid":"PR:Q09783"}


id: GO:0052487
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism stops, prevents, or reduces the frequency, rate or extent of the jasmonic acid-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 negative regulation by organism of symbiont jasmonic acid-mediated defense response (obsolete GO:0052487)","synonyms":[{"name":"negative regulation by organism of symbiont jasmonic acid-mediated defense response","type":"exact"},{"name":"suppression by organism of symbiont JA-mediated defense response","type":"exact"}],"termid":"GO:0052487"}


id: PBO:0032706
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_level_during_cellular_response_to_methyl_methanesulfonate","termid":"PBO:0032706"}


id: GO:2000866
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of estradiol secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of steroid hormone secretion","termid":"GO:2000833"},{"relation_name":"is_a","term_name":"regulation of estradiol secretion","termid":"GO:2000864"},{"relation_name":"positively_regulates","term_name":"estradiol secretion","termid":"GO:0035938"}],"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"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of estradiol secretion","synonyms":[{"name":"positive regulation of oestradiol secretion","type":"exact"}],"termid":"GO:2000866"}


id: MONDO:1010448
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dilated cardiomyopathy that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dilated cardiomyopathy, non-human animal","termid":"MONDO:1010011"},{"relation_name":"is_a","term_name":"cardiomyopathy, dog","termid":"MONDO:1010441"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dilated cardiomyopathy, dog","secondary_identifiers":["OMIA:000162-9615"],"termid":"MONDO:1010448","xrefs":{"Monarch":{"xref_id":"1010448"}}}


id: MONDO:1011122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent Mullerian duct syndrome that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"persistent Mullerian duct syndrome, non-human animal","termid":"MONDO:1010278"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent Mullerian duct syndrome, dog","secondary_identifiers":["OMIA:000791-9615"],"termid":"MONDO:1011122","xrefs":{"Monarch":{"xref_id":"1011122"}}}


id: MONDO:0021908
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Aplasia cutis congenita with with autosomal dominant inheritance with reduced penetrance.","definition_xrefs":["PMID:3906608"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aplasia cutis congenita","termid":"MONDO:0007145"}],"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":"aplasia cutis congenita dominant","secondary_identifiers":["GARD:751"],"termid":"MONDO:0021908","xrefs":{"Monarch":{"xref_id":"0021908"}}}


id: PBO:0084172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"High-mobility group (HMG) protein; binds to and remodels nucleosomes; involved in recruiting FACT and other chromatin remodelling complexes to the chromosomes; functionally redundant with Nhp6Ap; required for transcriptional initiation fidelity of some tRNA genes; homologous to mammalian HMGB1 and HMGB2; NHP6B has a paralog, NHP6A, that arose from the whole genome duplication","termid":"PBO:0084172"}


id: PBO:0053617
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 658","termid":"PBO:0053617"}


id: GO:0052829
data:
  {"annotated_genes":["SJAG_01702"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[114677],"is_not":false,"summary":null,"term":"GO:0052829"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-myo-inositol 1,3,4-trisphosphate + H2O = myo-inositol 3,4-bisphosphate + phosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol trisphosphate phosphatase activity","termid":"GO:0046030"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01702":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"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:0003674","GO:0003824","GO:0016787","GO:0016788"],"is_obsolete":false,"name":"inositol-1,3,4-trisphosphate 1-phosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-1855232"],"termid":"GO:0052829","terms_by_termid":{"GO:0052829":null}}


id: PBO:0057238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 425","termid":"PBO:0057238"}


