# terms

id: GO:0090090
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of the Wnt signaling pathway through beta-catenin, the series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of Wnt signaling pathway","termid":"GO:0030178"},{"relation_name":"is_a","term_name":"regulation of canonical Wnt signaling pathway","termid":"GO:0060828"},{"relation_name":"negatively_regulates","term_name":"canonical Wnt signaling pathway","termid":"GO:0060070"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of canonical Wnt signaling pathway","secondary_identifiers":["Reactome:R-HSA-4641258","GO:0035414","Reactome:R-HSA-3772470"],"synonyms":[{"name":"negative regulation of Wnt receptor signaling pathway through beta-catenin","type":"exact"},{"name":"negative regulation of canonical Wnt receptor signaling pathway","type":"exact"},{"name":"negative regulation of canonical Wnt receptor signalling pathway","type":"exact"},{"name":"negative regulation of canonical Wnt-activated signaling pathway","type":"exact"},{"name":"negative regulation of catenin import into nucleus","type":"narrow"},{"name":"negative regulation of catenin protein nuclear translocation","type":"narrow"}],"termid":"GO:0090090"}


id: MONDO:0003717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A papillary tumor originating in the renal pelvis.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"papillary urothelial neoplasm","termid":"MONDO:0003443"},{"relation_name":"is_a","term_name":"renal pelvis neoplasm","termid":"MONDO:0003719"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"renal pelvis papillary tumor","secondary_identifiers":["DOID:5975","MEDGEN:163120","UMLS:C0853688","NCIT:C8603"],"synonyms":[{"name":"papillary neoplasm of renal pelvis","type":"exact"},{"name":"papillary neoplasm of the renal pelvis","type":"exact"},{"name":"papillary tumor of renal pelvis","type":"exact"},{"name":"papillary tumor of the renal pelvis","type":"exact"},{"name":"papillary tumour of renal pelvis","type":"exact"},{"name":"papillary tumour of the renal pelvis","type":"exact"},{"name":"renal pelvis papillary tumor","type":"exact"},{"name":"renal pelvis papillary urothelial neoplasm","type":"exact"}],"termid":"MONDO:0003717","xrefs":{"Monarch":{"xref_id":"0003717"}}}


id: MONDO:0004326
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that arises from the ciliated respiratory mucosa that lines the sphenoid sinus. It results from the invagination and proliferation of epithelial cells in the underlying stroma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inverted papilloma","termid":"MONDO:0002537"},{"relation_name":"is_a","term_name":"sphenoid sinus Schneiderian papilloma","termid":"MONDO:0004327"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sphenoid sinus inverted papilloma","secondary_identifiers":["NCIT:C6841","UMLS:C1336037","DOID:7678","MEDGEN:236834"],"synonyms":[{"name":"inverted papilloma of sphenoid sinus","type":"exact"},{"name":"inverted papilloma of the sphenoid sinus","type":"exact"},{"name":"sphenoidal sinus inverted papilloma","type":"exact"}],"termid":"MONDO:0004326","xrefs":{"Monarch":{"xref_id":"0004326"}}}


id: PATO:0001636
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A necessity quality (continuant) inhering in a bearer by virtue of the bearer's being non-essential or dispensable.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"necessity (continuant)","termid":"PATO:0001634"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unnecessary (continuant)","termid":"PATO:0001636"}


id: PBO:0048130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fucosyltransferase 10","termid":"PBO:0048130"}


id: MONDO:0958205
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Yuksel-Vogel-Bauer syndrome","secondary_identifiers":["MEDGEN:1847314","OMIM:620703","UMLS:C5882751"],"termid":"MONDO:0958205","xrefs":{"Monarch":{"xref_id":"0958205"}}}


id: MONDO:0009535
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lymphedema, congenital recessive (obsolete MONDO:0009535)","secondary_identifiers":["MESH:C565432","OMIM:247440"],"synonyms":[{"name":"lymphedema, congenital recessive","type":"exact"}],"termid":"MONDO:0009535","xrefs":{"Monarch":{"xref_id":"0009535"}}}


id: PBO:0046713
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eva-1 homolog B","termid":"PBO:0046713"}


id: SO:0001788
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An U-box is a conserved T-rich region upstream of a retroviral polypurine tract that is involved in PPT primer creation during reverse transcription.","definition_xrefs":["PMID:9649446","PMID:11577982","PMID:10556309"],"direct_ancestors":[{"relation_name":"is_a","term_name":"conserved_region","termid":"SO:0000330"},{"relation_name":"part_of","term_name":"LTR_retrotransposon","termid":"SO:0000186"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U_box","synonyms":[{"name":"U-box","type":"exact"}],"termid":"SO:0001788"}


id: PBO:0036515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GET complex (ER membrane insertion) subunit Get4 (predicted)","termid":"PBO:0036515"}


id: GO:0050988
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The carboxylation of the N-terminal methionine of proteins to form the derivative N-carboxy-L-methionine.","definition_xrefs":["RESID:AA0363"],"gene_count":0,"genotype_count":0,"name":"obsolete N-terminal peptidyl-methionine carboxylation (obsolete GO:0050988)","termid":"GO:0050988"}


id: FYECO:0000010
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"The experimental conditions included the absence of a chemical.","definition_xrefs":["PomBase:al"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE FYECO:0000010 absence of chemical (obsolete FYECO:0000010)","termid":"FYECO:0000010"}


id: GO:1901345
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a L-thialysine stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to amino acid","termid":"GO:0043200"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to L-thialysine","synonyms":[{"name":"response to thialysine","type":"broad"}],"termid":"GO:1901345"}


id: GO:0071947
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of one or more ubiquitin groups from a protein as part of a process of ubiquitin-dependent protein catabolism.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein deubiquitination","termid":"GO:0016579"},{"relation_name":"part_of","term_name":"ubiquitin-dependent protein catabolic process","termid":"GO:0006511"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0030163"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0008150","GO:0030163","GO:0070647"],"is_obsolete":false,"name":"protein deubiquitination involved in ubiquitin-dependent protein catabolic process","termid":"GO:0071947"}


id: FYPO:0006895
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the cell tip is decreased during one or both meiotic nuclear divisions.","definition_xrefs":["PomBase:mah","PMID:30649994"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during meiosis","termid":"FYPO:0003549"},{"relation_name":"is_a","term_name":"abnormal protein localization to cell tip","termid":"FYPO:0005987"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein localization to cell tip during meiosis","synonyms":[{"name":"decreased protein localisation to cell tip during meiosis","type":"exact"},{"name":"decreased protein localization to cell end during meiosis","type":"exact"},{"name":"decreased protein localization to cell tip during meiotic nuclear division","type":"exact"},{"name":"reduced protein localization to cell tip during meiosis","type":"exact"}],"termid":"FYPO:0006895"}


id: FYPO:0003708
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A conjugation phenotype in which a normal proportion of cells in the population undergoes conjugation with wild type h+ cells.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal conjugation frequency","termid":"FYPO:0003797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000301"},{"rel_name":"part_of","termid":"FYPO:0000257"},{"rel_name":"part_of","termid":"FYPO:0000301"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000301"],"is_obsolete":false,"name":"normal frequency of conjugation with h+ cells","synonyms":[{"name":"normal conjugation with WT h+ cells","type":"exact"},{"name":"normal frequency of conjugation with h plus cells","type":"exact"},{"name":"normal frequency of mating with h+ cells","type":"exact"}],"termid":"FYPO:0003708"}


id: PR:O14041
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC2C4.08 gene.","definition_xrefs":["UniProtKB:O14041","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized nucleolar protein C2C4.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC2C4.08","synonyms":[{"name":"Spom972h-SPAC2C4.08","type":"exact"}],"termid":"PR:O14041"}


id: MONDO:0034099
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete SYNGAP1-related developmental and epileptic encephalopathy (obsolete MONDO:0034099)","secondary_identifiers":["GARD:22232"],"termid":"MONDO:0034099","xrefs":{"Monarch":{"xref_id":"0034099"}}}


id: PBO:0061889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OPCML intronic transcript 2","termid":"PBO:0061889"}


id: MONDO:0001908
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hypophosphatasia (obsolete MONDO:0001908)","termid":"MONDO:0001908","xrefs":{"Monarch":{"xref_id":"0001908"}}}


id: PBO:0026869
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-K9_methylation_at_telomere","termid":"PBO:0026869"}


id: GO:0052787
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The breakdown of large alpha-linked polysaccharides by hydrolysis of (1->4)-alpha-D-glucosidic linkages to yield maltopentaose.","definition_xrefs":["PMID:7511484","PMID:9406414","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polysaccharide catabolic process","termid":"GO:0000272"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"alpha-linked polysaccharide catabolism to maltopentaose","synonyms":[{"name":"alpha-amylase-mediated polysaccharide catabolism, producing maltopentaose","type":"exact"},{"name":"maltopentaose-forming alpha-amylase activity","type":"related"}],"termid":"GO:0052787"}


id: GO:0002348
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process leading to positive selection of B cells in the bone marrow. Positive selection is the process in which B or T cells are selected to survive based on signaling through their antigen receptors.","definition_xrefs":["GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central B cell selection","termid":"GO:0002340"},{"relation_name":"is_a","term_name":"B cell positive selection","termid":"GO:0002346"}],"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":"central B cell positive selection","synonyms":[{"name":"central B lymphocyte positive selection","type":"exact"},{"name":"central B-cell positive selection","type":"exact"},{"name":"central B-lymphocyte positive selection","type":"exact"}],"termid":"GO:0002348"}


id: GO:0051524
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell switches from bipolar cell growth to monopolar cell growth.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of monopolar cell polarity","termid":"GO:0061162"},{"relation_name":"is_a","term_name":"regulation of direction of cell growth","termid":"GO:0061389"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007163"}],"interesting_parent_ids":["GO:0008150","GO:0007163"],"is_obsolete":false,"name":"cell growth mode switching, bipolar to monopolar","termid":"GO:0051524"}


id: SO:0000254
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A tRNA sequence that has an alanine anticodon, and a 3' alanine binding region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"alanine_tRNA_primary_transcript","termid":"SO:0000211"},{"relation_name":"is_a","term_name":"tRNA","termid":"SO:0000253"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alanyl_tRNA","synonyms":[{"name":"alanyl tRNA","type":"exact"},{"name":"alanyl-transfer RNA","type":"exact"},{"name":"alanyl-transfer ribonucleic acid","type":"exact"}],"termid":"SO:0000254"}


id: PBO:0045232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ heat shock protein family (Hsp40) member C19","termid":"PBO:0045232"}


id: GO:0120320
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The myosin-based contraction and retraction of a lateral pseudopodium.","definition_xrefs":["PMID:12953059","PMID:17623773","GOC:krc","GOC:pf","PMID:15483055"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pseudopodium retraction","termid":"GO:0031270"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lateral pseudopodium retraction","synonyms":[{"name":"lateral pseudopodium suppression","type":"related"}],"termid":"GO:0120320"}


id: GO:0030603
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + oxaloacetate = acetate + H+ + oxalate.","definition_xrefs":["RHEA:24432","EC:3.7.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid carbon-carbon bonds, in ketonic substances","termid":"GO:0016823"}],"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":"oxaloacetase activity","secondary_identifiers":["MetaCyc:OXALOACETASE-RXN","KEGG_REACTION:R00338"],"synonyms":[{"name":"oxalacetic hydrolase activity","type":"related"},{"name":"oxaloacetate acetylhydrolase activity","type":"related"}],"termid":"GO:0030603"}


id: GO:0032915
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of production of transforming growth factor-beta2.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transforming growth factor beta2 production","termid":"GO:0032909"},{"relation_name":"is_a","term_name":"positive regulation of transforming growth factor beta production","termid":"GO:0071636"},{"relation_name":"positively_regulates","term_name":"transforming growth factor beta2 production","termid":"GO:0032906"}],"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 transforming growth factor beta2 production","synonyms":[{"name":"activation of transforming growth factor-beta2 production","type":"narrow"},{"name":"positive regulation of TGF-B2 production","type":"exact"},{"name":"positive regulation of TGFB2 production","type":"exact"},{"name":"positive regulation of transforming growth factor-beta2 production","type":"exact"},{"name":"stimulation of transforming growth factor-beta2 production","type":"narrow"},{"name":"up regulation of transforming growth factor-beta2 production","type":"exact"},{"name":"up-regulation of transforming growth factor-beta2 production","type":"exact"},{"name":"upregulation of transforming growth factor-beta2 production","type":"exact"}],"termid":"GO:0032915"}


id: PBO:0091656
data:
  {"annotation_feature_type":"gene","cv_name":"cat_act","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydrolysis rate of PNPG to glucose is 20.3 (uM min-1 ml-2)","termid":"PBO:0091656"}


id: PBO:0087241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Serine protease and general molecular chaperone; cleaves Roq1p, which modifies the substrate specificity of the Ubr1p Ub-ligase, promoting the stress-induced homeostatically-regulated protein degradation (SHRED) of misfolded and native ER-membrane and cytosolic proteins; chaperone activity involved in the heat stress response; promotes apoptosis through proteolysis of Bir1p; role in lipid homeostasis; mammalian Omi/HtrA2 serine protease family member","termid":"PBO:0087241"}


id: PR:Q10281
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A guanine nucleotide-binding protein subunit beta-2-like 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR19868:SF0","OMA:SCHPO01018","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":"guanine nucleotide-binding protein subunit beta-like protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6B12.15","secondary_identifiers":["UniProtKB:Q10281"],"synonyms":[{"name":"Spom972h-GNB2L1","type":"exact"},{"name":"receptor of activated protein kinase C (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q10281"}


id: GO:0062200
data:
  {"annotated_genes":["SJAG_00317","SJAG_00333","SJAG_04461","SJAG_03637","SJAG_00661","SJAG_00236"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[92953,102001,107188,114331,114904,120668],"is_not":false,"summary":null,"term":"GO:0062200"}]},"cv_name":"biological_process","definition":"An intracellular signaling cascade that starts with the activation of S. cerevisiae Kic1p, which activate Mob2p and Cbk1p. Cbk1p phosphorylates Ace2p, which results in its nuclear translocation, where it regulates transcription of genes involved in polarity and morphogenesis.","definition_xrefs":["PMID:23212898","PMID:22629372","PMID:21246752","PMID:16096637","PMID:15731009","PMID:20805322","PMID:20826805"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular signal transduction","termid":"GO:0035556"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00236":null,"SJAG_00317":null,"SJAG_00333":null,"SJAG_00661":null,"SJAG_03637":null,"SJAG_04461":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"RAM/MOR signaling","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"MOR signaling pathway","type":"narrow"},{"name":"RAM signaling pathway","type":"narrow"},{"name":"RAM/MOR signaling pathway","type":"exact"},{"name":"morphogenesis Orb6 network","type":"exact"}],"termid":"GO:0062200","terms_by_termid":{"GO:0062200":null}}


id: FYPO:0004219
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which methylation of lysine at position 20 of histone H4 is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone methylation during vegetative growth","termid":"FYPO:0000861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal histone H4-K20 methylation during vegetative growth","synonyms":[{"name":"normal histone H4 K20 methylation during vegetative growth","type":"exact"},{"name":"normal histone H4-K20 methylation during mitotic cell cycle","type":"related"},{"name":"normal histone H4K20me during vegetative growth","type":"exact"},{"name":"normal histone lysine H4 K20 methylation during vegetative growth","type":"exact"}],"termid":"FYPO:0004219"}


id: PBO:0059838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial fission regulator 2","termid":"PBO:0059838"}


id: PBO:0114376
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane calcium permeable gated cation channel","termid":"PBO:0114376"}


id: PR:Q9P3V5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC1348.05 gene.","definition_xrefs":["UniProtKB:Q9P3V5","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized transporter C1348.05 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1348.05","synonyms":[{"name":"Spom972h-SPBC1348.05","type":"exact"}],"termid":"PR:Q9P3V5"}


id: FYPO:0006514
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which chromosome structure is normal (i.e. indistinguishable from wild type) at the telomeric regions. Telomere structure refers to the position, shape, arrangement and connectivity of DNA and associated proteins in the telomeric region.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal telomere morphology","termid":"FYPO:0006512"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal telomere structure","synonyms":[{"name":"normal chromosome structure at telomere","type":"exact"},{"name":"normal chromosome structure at telomeric region","type":"exact"},{"name":"normal telomeric region structure","type":"exact"}],"termid":"FYPO:0006514"}


id: PBO:0078029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 19 (non-functional)","termid":"PBO:0078029"}


id: MONDO:0971009
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyloid neuropathy","termid":"MONDO:0007100"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0021179"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0021179","MONDO:0005066"],"is_obsolete":false,"name":"amyloidosis, hereditary systemic 5","secondary_identifiers":["MEDGEN:1859086","UMLS:C5935572","OMIM:620658"],"termid":"MONDO:0971009","xrefs":{"Monarch":{"xref_id":"0971009"}}}


id: GO:1903162
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any serine transmembrane transporter activity that is involved in serine import into cell.","definition_xrefs":["GO_REF:0000061","GOC:TermGenie","ISBN:0-8249-3695-6"],"gene_count":0,"genotype_count":0,"name":"obsolete serine transmembrane transporter activity involved in serine import into cell (obsolete GO:1903162)","synonyms":[{"name":"serine transmembrane transporter activity involved in serine import into cell","type":"exact"}],"termid":"GO:1903162"}


id: MONDO:0003781
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute or chronic inflammatory process affecting the bronchi.","definition_xrefs":["NCIT:C2911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bronchial disorder","termid":"MONDO:0001358"},{"relation_name":"is_a","term_name":"tracheobronchitis","termid":"MONDO:0021925"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bronchitis","secondary_identifiers":["MEDGEN:2736","ICD9:491","ICD9:466.0","DOID:6132","icd11.foundation:11753425","ICD9:490","ICD9:491.9","SCTID:32398004","MESH:D001991","UMLS:C0006277","CSP:2596-1500","EFO:0009661"],"synonyms":[{"name":"CI - chest infection","type":"exact"},{"name":"acute bronchitis","type":"narrow"},{"name":"acute bronchitis and bronchiolitis","type":"related"},{"name":"bronchial infection","type":"exact"},{"name":"bronchus inflammation","type":"exact"},{"name":"chest cold","type":"related"},{"name":"chest infection","type":"related"},{"name":"chronic bronchitis","type":"narrow"},{"name":"inflammation of bronchus","type":"exact"},{"name":"recurrent wheezy bronchitis","type":"related"}],"termid":"MONDO:0003781","xrefs":{"Monarch":{"xref_id":"0003781"}}}


id: PBO:0030846
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_localization_to_cell_tip,_with_protein_distributed_in_plasma_membrane_or_cortex","termid":"PBO:0030846"}


id: PBO:0084873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial ribosomal protein of the small subunit; MRP17 exhibits genetic interactions with PET122, encoding a COX3-specific translational activator","termid":"PBO:0084873"}


id: GO:0052892
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: an aromatic (S)-hydroxynitrile = an aromatic aldehyde + cyanide.","definition_xrefs":["RHEA:54660"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(S)-hydroxynitrile lyase activity","termid":"GO:0047606"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"aromatic (S)-hydroxynitrile lyase activity","secondary_identifiers":["MetaCyc:RXN-11732","KEGG_REACTION:R09359"],"termid":"GO:0052892"}


id: PBO:0052503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch like family member 15","termid":"PBO:0052503"}


id: PBO:0045588
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"double homeobox 3","termid":"PBO:0045588"}


id: GO:0031686
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an A1 adenosine receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenosine receptor binding","termid":"GO:0031685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"A1 adenosine receptor binding","synonyms":[{"name":"A1 adenosine receptor ligand","type":"narrow"}],"termid":"GO:0031686"}


id: PBO:0082125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Acid trehalase required for utilization of extracellular trehalose; involved in intracellular trehalose degradation during growth recovery after saline stress","termid":"PBO:0082125"}


id: GO:0051663
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of the nucleus to a specific location within a cell during the establishment and maintenance of the dorsal/ventral axis of the oocyte.","definition_xrefs":["GOC:dph","GOC:tb","GOC:mtg_sensu","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleus localization","termid":"GO:0051647"},{"relation_name":"part_of","term_name":"oocyte dorsal/ventral axis specification","termid":"GO:0007310"}],"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":"oocyte nucleus localization involved in oocyte dorsal/ventral axis specification","secondary_identifiers":["GO:0051662"],"synonyms":[{"name":"establishment and maintenance of oocyte nucleus localization during oocyte axis determination","type":"exact"},{"name":"oocyte axis determination, oocyte nucleus localization","type":"exact"},{"name":"oocyte nucleus localisation involved in oocyte dorsal/ventral axis specification","type":"exact"},{"name":"oocyte nucleus localization during oocyte axis determination","type":"related"},{"name":"oocyte nucleus localization involved in oocyte dorsal-ventral axis specification","type":"exact"},{"name":"oocyte nucleus localization involved in oocyte dorsal/ventral axis determination","type":"exact"},{"name":"oocyte nucleus localization involved in oocyte dorsoventral axis specification","type":"exact"}],"termid":"GO:0051663"}


id: MONDO:0005501
data:
  {"annotated_genes":["SJAG_03054","SJAG_01459","SJAG_00041","SJAG_03865","SJAG_02211","SJAG_04096","SJAG_06514","SJAG_03158","SJAG_03552","SJAG_01940","SJAG_04363","SJAG_01071","SJAG_01960","SJAG_00578","SJAG_04697"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88559],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012637"},{"annotations":[87978],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013281"},{"annotations":[88844],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013325"},{"annotations":[88243],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013810"},{"annotations":[88739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012635"},{"annotations":[88149],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957540"},{"annotations":[88029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957820"},{"annotations":[88688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054559"},{"annotations":[87340],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859356"},{"annotations":[87339],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859357"},{"annotations":[87398],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009953"},{"annotations":[88376],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011629"},{"annotations":[88724],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010478"},{"annotations":[87942],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013870"},{"annotations":[87567],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014790"}]},"cv_name":"mondo","definition":"A congenital disorder of glycosylation that involves malfunctioning trimming/processing of the protein-bound oligosaccharide chain.","definition_xrefs":["DOID:0050571"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital disorder of glycosylation","termid":"MONDO:0015286"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00041":null,"SJAG_00578":null,"SJAG_01071":null,"SJAG_01459":null,"SJAG_01940":null,"SJAG_01960":null,"SJAG_02211":null,"SJAG_03054":null,"SJAG_03158":null,"SJAG_03552":null,"SJAG_03865":null,"SJAG_04096":null,"SJAG_04363":null,"SJAG_04697":null,"SJAG_06514":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"congenital disorder of glycosylation type II","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["EFO:0005546","MEDGEN:1812737","OMIMPS:212066","MESH:C535747","UMLS:C5574948"],"synonyms":[{"name":"B4GALT1-CDG","type":"related"},{"name":"B4GALT1-CDG (CDG-2d)","type":"related"},{"name":"MGAT2-CDG","type":"related"},{"name":"MGAT2-CDG (CDG-2a)","type":"related"},{"name":"MOGS-CDG","type":"related"},{"name":"MOGS-CDG (CDG-2b)","type":"related"},{"name":"congenital disorder of glycosylation type II","type":"exact"},{"name":"congenital disorders of glycosylation, type II","type":"exact"}],"termid":"MONDO:0005501","terms_by_termid":{"MONDO:0009953":null,"MONDO:0010478":null,"MONDO:0011629":null,"MONDO:0012635":null,"MONDO:0012637":null,"MONDO:0013281":null,"MONDO:0013325":null,"MONDO:0013810":null,"MONDO:0013870":null,"MONDO:0014790":null,"MONDO:0054559":null,"MONDO:0859356":null,"MONDO:0859357":null,"MONDO:0957540":null,"MONDO:0957820":null},"xrefs":{"Monarch":{"xref_id":"0005501"}}}


id: SO:0001462
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A collection of contigs.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_part","term_name":"contig","termid":"SO:0000149"},{"relation_name":"is_a","term_name":"sequence_conflict","termid":"SO:0001085"},{"relation_name":"is_a","term_name":"sequence_collection","termid":"SO:0001260"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"contig_collection","synonyms":[{"name":"contig collection","type":"exact"}],"termid":"SO:0001462"}


id: PBO:0080408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS37B subunit of ESCRT-I","termid":"PBO:0080408"}


id: PBO:0070988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L19 pseudogene 12","termid":"PBO:0070988"}


id: GO:0001190
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Binding to an RNA polymerase II transcription factor, which may be a single protein or a complex, in order to increase the frequency, rate or extent of transcription from an RNA polymerase II promoter. A protein binding transcription factor may or may not also interact with the template nucleic acid (either DNA or RNA) as well.","definition_xrefs":["GOC:txnOH"],"gene_count":0,"genotype_count":0,"name":"obsolete transcriptional activator activity, RNA polymerase II transcription factor binding (obsolete GO:0001190)","synonyms":[{"name":"RNA polymerase II transcription factor binding transcription activator activity","type":"exact"},{"name":"RNA polymerase II transcription factor binding transcription factor activity involved in positive regulation of transcription","type":"exact"}],"termid":"GO:0001190"}


id: MONDO:0003461
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, benign, asymptomatic neoplasm that arises from the fallopian tube. The majority of cases are incidental findings during operation for an unrelated gynecologic disorder. The tumors are round and solitary and contain connective tissue and papillary or tubular structures lined by serous-type epithelium.","definition_xrefs":["NCIT:C40113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fallopian tube benign neoplasm","termid":"MONDO:0000645"},{"relation_name":"is_a","term_name":"serous adenofibroma","termid":"MONDO:0024886"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fallopian tube serous adenofibroma","secondary_identifiers":["MEDGEN:309125","DOID:5478","UMLS:C1517109"],"synonyms":[{"name":"fallopian tube adenofibroma","type":"exact"},{"name":"fallopian tube serous adenofibroma","type":"exact"},{"name":"serous adenofibroma of fallopian tube","type":"exact"}],"termid":"MONDO:0003461","xrefs":{"Monarch":{"xref_id":"0003461"}}}


id: GO:0009023
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: L-cysteine + activated-tRNA = L-serine + tRNA containing a thionucleotide.","definition_xrefs":["EC:2.8.1.4","GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete tRNA sulfurtransferase (obsolete GO:0009023)","synonyms":[{"name":"tRNA sulfurtransferase","type":"exact"},{"name":"tRNA sulphurtransferase activity","type":"exact"}],"termid":"GO:0009023"}


id: GO:0110052
data:
  {"annotated_genes":["SJAG_00419","SJAG_04953","SJAG_00365"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97382,101825,108440],"is_not":false,"summary":null,"term":"GO:0110052"}]},"cv_name":"biological_process","definition":"A cellular process that, through single- or multi-step enzymatic reactions, repairs toxic endogenous compounds, formed as by-products of primary metabolism, by converting them into useful metabolites.","definition_xrefs":["GOC:ka","PMID:23334546","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolite repair","termid":"GO:0110051"},{"relation_name":"is_a","term_name":"cellular detoxification","termid":"GO:1990748"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00365":null,"SJAG_00419":null,"SJAG_04953":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0098754","GO:0008150"],"is_obsolete":false,"name":"toxic metabolite repair","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0110052","terms_by_termid":{"GO:0110052":null}}


id: PBO:0034203
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-determined_by_part_of","termid":"PBO:0034203"}


id: GO:1990865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an episodic stimulus indicating lowered oxygen tension.","definition_xrefs":["PMID:24055447"],"gene_count":0,"genotype_count":0,"name":"obsolete response to intermittent hypoxia (obsolete GO:1990865)","termid":"GO:1990865"}


id: RO:0002225
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x develops from part of y if and only if there exists some z such that x develops from z and z is part of y","direct_ancestors":[{"relation_name":"is_a","term_name":"develops_from","termid":"RO:0002202"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"develops_from_part_of","termid":"RO:0002225"}


id: PBO:0087539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of protein phosphatase PP4 complex; Pph3p and Psy2p form the active complex, Psy4p may provide additional substrate specificity; regulates recovery from the DNA damage checkpoint, the gene conversion- and single-strand annealing-mediated pathways of meiotic double-strand break repair and efficient Non-Homologous End-Joining (NHEJ) pathway; Pph3p and Psy2p localize to foci on meiotic chromosomes; putative homolog of mammalian R3","termid":"PBO:0087539"}


id: PBO:0041558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 19 open reading frame 48, pseudogene","termid":"PBO:0041558"}


id: GO:0034971
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by addition of a methyl group to arginine at position 17 of the histone.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-R17 methylation (obsolete GO:0034971)","synonyms":[{"name":"histone H3 R17 methylation","type":"exact"},{"name":"histone H3R17me","type":"exact"},{"name":"histone lysine H3 R17 methylation","type":"exact"}],"termid":"GO:0034971"}


id: MONDO:0011952
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"}],"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 type 7","secondary_identifiers":["GARD:10500","MESH:C564300","MEDGEN:334136","OMIM:608031","UMLS:C1842674","DOID:0060199"],"synonyms":[{"name":"ALS7","type":"exact"},{"name":"amyotrophic lateral sclerosis 7","type":"exact"}],"termid":"MONDO:0011952","xrefs":{"Monarch":{"xref_id":"0011952"}}}


id: MONDO:1010337
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Myopia that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of orbital region, non-human animal","termid":"MONDO:1011315"},{"relation_name":"is_a","term_name":"disorder of visual system, non-human animal","termid":"MONDO:1011316"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myopia, non-human animal","secondary_identifiers":["OMIA:001487"],"termid":"MONDO:1010337","xrefs":{"Monarch":{"xref_id":"1010337"}}}


id: PBO:0015220
data:
  {"annotation_feature_type":"gene","cv_name":"subunit_composition","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homooligomeric","termid":"PBO:0015220"}


id: PBO:0001358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho family GTPase Rho5","termid":"PBO:0001358"}


id: PBO:0050325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 27","termid":"PBO:0050325"}


id: GO:0036402
data:
  {"annotated_genes":["SJAG_01131","SJAG_00712","SJAG_01544","SJAG_00766","SJAG_04477","SJAG_01489"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75444,78641,79861,80191,80928,81312],"is_not":false,"summary":null,"term":"GO:0036402"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2O = ADP + phosphate, which promotes unfolding of protein substrates, and channel opening of the core proteasome.","definition_xrefs":["PMID:11430818","GOC:rb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide conformation or assembly isomerase activity","termid":"GO:0120544"},{"relation_name":"is_a","term_name":"ATP-dependent activity","termid":"GO:0140657"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00712":null,"SJAG_00766":null,"SJAG_01131":null,"SJAG_01489":null,"SJAG_01544":null,"SJAG_04477":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:0016853"}],"interesting_parent_ids":["GO:0003824","GO:0016853","GO:0003674"],"is_obsolete":false,"name":"proteasome-activating activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["EC:5.6.1.5"],"synonyms":[{"name":"ATPase involved in positive regulation of proteasomal protein catabolic process","type":"exact"},{"name":"proteasomal ATPase activity","type":"exact"},{"name":"proteasome channel gating activity","type":"narrow"},{"name":"proteasome channel opening activity","type":"narrow"},{"name":"proteasome-activating ATPase activity","type":"exact"}],"termid":"GO:0036402","terms_by_termid":{"GO:0036402":null}}


id: MONDO:0021072
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant paraganglioma arising from the chromaffin cells of the paraganglia that are located along the sympathetic nerves. It includes extra-adrenal paragangliomas and paragangliomas that arise from the adrenal medulla. The latter are commonly referred to as pheochromocytomas. Representative examples of extra-adrenal sympathetic paragangliomas include the bladder, and superior and inferior paraaortic paragangliomas. Clinical signs are related to the secretion of catecholamines resulting in hypertension.","definition_xrefs":["NCIT:C4216"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paraganglioma","termid":"MONDO:0000448"},{"relation_name":"is_a","term_name":"epithelial neoplasm","termid":"MONDO:0005626"},{"relation_name":"is_a","term_name":"sympathetic nervous system disorder","termid":"MONDO:0044993"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sympathetic paraganglioma","secondary_identifiers":["UMLS:C0334415","MEDGEN:137758","ICDO:8681/1","SCTID:399343007","MESH:C531777"],"synonyms":[{"name":"Chromaffinoma","type":"exact"},{"name":"chromaffin neoplasm","type":"exact"},{"name":"chromaffin tumor","type":"exact"},{"name":"chromaffin tumour","type":"exact"},{"name":"paraganglioma of sympathetic nervous system","type":"exact"},{"name":"sympathetic Paraganglionic neoplasm","type":"exact"},{"name":"sympathetic nervous system paraganglioma","type":"exact"},{"name":"sympathetic paraganglioma","type":"exact"}],"termid":"MONDO:0021072","xrefs":{"Monarch":{"xref_id":"0021072"}}}


id: PBO:0081428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 282","termid":"PBO:0081428"}


id: GO:0085041
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Highly branched symbiont haustoria within host root cortex cells, responsible for nutrient exchange.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"haustorium","termid":"GO:0085035"}],"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":"arbuscule","termid":"GO:0085041"}


id: PBO:0046182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongation factor for RNA polymerase II 2 pseudogene 3","termid":"PBO:0046182"}


id: PBO:0077813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tumor protein p53 pathway corepressor 1","termid":"PBO:0077813"}


id: MONDO:0003518
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A teratoma that involves the mediastinum.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teratoma","termid":"MONDO:0002601"},{"relation_name":"is_a","term_name":"extragonadal non-dysgerminomatous germ cell tumor","termid":"MONDO:0020539"},{"relation_name":"is_a","term_name":"mediastinal germ cell tumor","termid":"MONDO:0021067"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediastinum teratoma","secondary_identifiers":["DOID:5568","MEDGEN:233175","UMLS:C1334682","NCIT:C6438"],"synonyms":[{"name":"mediastinum teratoma","type":"exact"},{"name":"teratoma of mediastinum","type":"exact"}],"termid":"MONDO:0003518","xrefs":{"Monarch":{"xref_id":"0003518"}}}


id: PBO:0089825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"18S rRNA dimethylase Cdh1","termid":"PBO:0089825"}


id: GO:0000958
data:
  {"annotated_genes":["SJAG_02526"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115743],"is_not":false,"summary":null,"term":"GO:0000958"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of mRNA transcribed from the mitochondrial genome and occurring in the mitochondrion.","definition_xrefs":["GOC:krc","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial RNA catabolic process","termid":"GO:0000957"},{"relation_name":"is_a","term_name":"mRNA catabolic process","termid":"GO:0006402"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02526":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0016071","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"mitochondrial mRNA catabolic process","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0000958","terms_by_termid":{"GO:0000958":null}}


id: GO:0141176
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A small RNA-based gene silencing process in which Piwi-associated RNAs (piRNAs) guide de novo DNA methylation. This results in a heterochromatin assembly, a chromatin conformation that is refractory to transcription.","definition_xrefs":["PMID:38359823","PMID:32674113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA methylation-dependent constitutive heterochromatin formation","termid":"GO:0006346"},{"relation_name":"is_a","term_name":"piRNA-mediated heterochromatin formation","termid":"GO:0140966"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006325"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006325"],"is_obsolete":false,"name":"gene silencing by piRNA-directed DNA methylation","termid":"GO:0141176"}


id: MONDO:0009330
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An uncommon malignant neoplasm arising from pericytes. Distinction between benign and malignant hemangiopericytoma may be difficult or even impossible on morphologic grounds alone.","definition_xrefs":["NCIT:C4301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangiopericytoma","termid":"MONDO:0005094"},{"relation_name":"is_a","term_name":"solitary fibrous tumor","termid":"MONDO:0016238"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemangiopericytoma, malignant","secondary_identifiers":["GARD:2627","MESH:C562740","OMIM:234820","UMLS:C0334542","ICDO:9150/3","MEDGEN:90803"],"synonyms":[{"name":"hemangiopericytoma, malignant","type":"exact"},{"name":"malignant hemangiopericytoma","type":"exact"}],"termid":"MONDO:0009330","xrefs":{"Monarch":{"xref_id":"0009330"}}}


id: PBO:0055441
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 2872","termid":"PBO:0055441"}


id: GO:0017111
data:
  {"annotated_genes":["SJAG_02824","SJAG_00930","SJAG_02704","SJAG_01024","SJAG_03785","SJAG_03471","SJAG_01731","SJAG_00768","SJAG_03496","SJAG_00378","SJAG_01653","SJAG_01595","SJAG_00947","SJAG_02738","SJAG_03866","SJAG_01669","SJAG_03320","SJAG_02605","SJAG_02295","SJAG_02180","SJAG_02943","SJAG_00212","SJAG_01546","SJAG_03534","SJAG_05332","SJAG_00447","SJAG_02601","SJAG_04599","SJAG_02516","SJAG_00136","SJAG_00645","SJAG_01471","SJAG_01620","SJAG_03502","SJAG_02897","SJAG_02457","SJAG_05313","SJAG_03371","SJAG_00457","SJAG_16455","SJAG_02656","SJAG_01339","SJAG_01152","SJAG_01530","SJAG_01613","SJAG_00851","SJAG_01391","SJAG_01500","SJAG_04003","SJAG_03732","SJAG_02061","SJAG_02906","SJAG_03011","SJAG_01769","SJAG_02373","SJAG_03036","SJAG_01817","SJAG_03850","SJAG_04940","SJAG_02382","SJAG_04531","SJAG_02394","SJAG_02242","SJAG_02610","SJAG_02957","SJAG_02926","SJAG_02339","SJAG_02872","SJAG_01489","SJAG_02595","SJAG_00587","SJAG_02399","SJAG_03161","SJAG_02353","SJAG_00757","SJAG_03137","SJAG_02082","SJAG_01405","SJAG_03832","SJAG_01913","SJAG_00604","SJAG_02233","SJAG_04203","SJAG_04470","SJAG_02598","SJAG_03688","SJAG_03948","SJAG_01129","SJAG_00065","SJAG_03345","SJAG_00705","SJAG_01615","SJAG_03237","SJAG_02366","SJAG_00516","SJAG_03461","SJAG_00906","SJAG_00659","SJAG_01354","SJAG_03684","SJAG_03896","SJAG_00231","SJAG_00599","SJAG_01297","SJAG_01400","SJAG_04147","SJAG_02084","SJAG_02265","SJAG_02384","SJAG_03798","SJAG_03892","SJAG_01851","SJAG_00414","SJAG_01010","SJAG_00466","SJAG_01438","SJAG_02171","SJAG_04477","SJAG_00332","SJAG_04154","SJAG_02561","SJAG_01449","SJAG_04118","SJAG_05213","SJAG_04167","SJAG_01945","SJAG_00790","SJAG_05032","SJAG_03358","SJAG_01410","SJAG_00871","SJAG_02267","SJAG_03923","SJAG_03406","SJAG_00330","SJAG_01397","SJAG_00344","SJAG_00938","SJAG_01456","SJAG_04258","SJAG_04375","SJAG_01944","SJAG_03682","SJAG_00773","SJAG_04001","SJAG_00857","SJAG_03676","SJAG_03950","SJAG_05019","SJAG_01095","SJAG_04862","SJAG_05030","SJAG_03050","SJAG_01179","SJAG_01558","SJAG_04004","SJAG_02226","SJAG_01879","SJAG_00984","SJAG_01662","SJAG_03886","SJAG_02748","SJAG_01240","SJAG_01379","SJAG_04355","SJAG_02292","SJAG_01447","SJAG_02521","SJAG_02132","SJAG_01807","SJAG_02782","SJAG_03780","SJAG_05295","SJAG_02199","SJAG_03415","SJAG_04157","SJAG_03982","SJAG_02606","SJAG_01774","SJAG_03927","SJAG_00884","SJAG_05294","SJAG_03560","SJAG_03515","SJAG_03072","SJAG_02575","SJAG_03342","SJAG_04187","SJAG_03567","SJAG_02563","SJAG_00272","SJAG_00669","SJAG_00541","SJAG_00018","SJAG_04566","SJAG_02684","SJAG_02187","SJAG_02571","SJAG_00729","SJAG_03451","SJAG_03703","SJAG_02994","SJAG_02182","SJAG_02302","SJAG_00244","SJAG_03495","SJAG_04038","SJAG_04277","SJAG_01510","SJAG_04150","SJAG_04114","SJAG_00923","SJAG_02023","SJAG_04666","SJAG_01344","SJAG_02074","SJAG_00390","SJAG_02331","SJAG_03453","SJAG_00853","SJAG_02077","SJAG_02848","SJAG_00031","SJAG_02431","SJAG_04064","SJAG_01677","SJAG_03613","SJAG_00424","SJAG_04511","SJAG_03497","SJAG_00226","SJAG_00712","SJAG_04343","SJAG_01277","SJAG_00806","SJAG_00878","SJAG_00564","SJAG_00863","SJAG_04509","SJAG_02604","SJAG_02619","SJAG_03915","SJAG_04488","SJAG_05209","SJAG_04596","SJAG_04055","SJAG_02558","SJAG_04955","SJAG_01816","SJAG_00111","SJAG_04692","SJAG_01696","SJAG_02378","SJAG_01544","SJAG_02895","SJAG_04210","SJAG_02708","SJAG_04755","SJAG_04745","SJAG_03570","SJAG_00430","SJAG_04351","SJAG_02997","SJAG_00983","SJAG_02286","SJAG_02825","SJAG_01831","SJAG_00589","SJAG_04121","SJAG_03846","SJAG_01002","SJAG_01435","SJAG_01131","SJAG_04874","SJAG_02336","SJAG_04679","SJAG_03436","SJAG_04757","SJAG_01655","SJAG_00475","SJAG_01186","SJAG_01499","SJAG_02602","SJAG_02444","SJAG_03909","SJAG_01874","SJAG_04015","SJAG_02545","SJAG_00663","SJAG_03363","SJAG_00500","SJAG_00766","SJAG_02640","SJAG_02114","SJAG_03374","SJAG_01419","SJAG_02581","SJAG_00650","SJAG_02856","SJAG_01402","SJAG_01929","SJAG_03658","SJAG_00609","SJAG_01664"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72253,72352],"is_not":false,"summary":null,"term":"GO:0017111"},{"annotations":[58727,74024,60660,62560,60109,109082,100754,100735,63571,107424,67930,111720,58792,82066,98135,61543,68349,70364,115178,103512,114385,104495,114102,110109,60118,69451,72385,77677,92339,90991,66695,113258,101766,91665,57095,113243,117775,76309,60809,91620,64037,100799,70342,116917,98431,119456,72697,72547,62976,115282,102958,67856,90771,71256,74996,63141,58422,102373,77932,59145,67391,101052,89577,60522,66333,90939,101711,67853,68468,92342,102456,60895,113100,70863,82182,92104,76070,61344,58835,90148,75774,64917,120059,66860,65672,71177,58909,92340,101859,90411,92346,108266,92338,92341,72554,61829,98028,107020,101153,94671,104321,98734,60244,118389,92344,92343,117144,68262,75203,120610,75578,74311,66466,89852,101360,92345,69011,104160,71299,115821,92708,70296,117627,115715,61760,58519,74411,80753,59626,91977,109427,120804,96595,97878,103459,67345,105690,106686,66500,61190,62256,108027,69639,98591,100846,57825,79871,62759,102406,100881,105352,93783,62099,93531,70495,76354,77346,105570,107905,65265,71829,62765,73905,73152,68855,70661,115038,81124,64842,68828,69833,70526,69790,93870,98699,67390,61513,73472,105732,113906,97468,62912,62542,106916,58029,58396,58703,59128,63380,63897,68605,102548,104017,92017,89728,100378,114135,119098,94495,66963,61186,72033,75786,57129,101837,78198,59291,68416,80577,60824,67877,68049,112405,90868,57602,105107,66042,62068,75056,64282,109633,63712,109404,77707,76804,70224,71924],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016887"},{"annotations":[92666,71133],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003925"},{"annotations":[70840,60953,78181,77606,71789,79190,66756,75037,74111,76650,58250,71763,77293,77893,74269,71092,61592,68979,109277,65354,66426,76165,97913,72050,100111,103060,79567,78813,75068,75781,73123,59973,81536,75947,72545,78135,76937,81083,73253,82122,79068,77636,105396,81445,74441,115824,74080,72468,76155,82139,62168,67648,78791,73206,79544,76386,76530,80130,101457,73440,68967,72794,79217,68124,74615,120362,82195,81858,79242,79684,68192,63829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003924"},{"annotations":[106486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061791"},{"annotations":[101786,104594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990606"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a ribonucleoside triphosphate + H2O = a ribonucleoside diphosphate + H+ + phosphate.","definition_xrefs":["RHEA:23680"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":304,"genes_by_uniquename":{"SJAG_00018":null,"SJAG_00031":null,"SJAG_00065":null,"SJAG_00111":null,"SJAG_00136":null,"SJAG_00212":null,"SJAG_00226":null,"SJAG_00231":null,"SJAG_00244":null,"SJAG_00272":null,"SJAG_00330":null,"SJAG_00332":null,"SJAG_00344":null,"SJAG_00378":null,"SJAG_00390":null,"SJAG_00414":null,"SJAG_00424":null,"SJAG_00430":null,"SJAG_00447":null,"SJAG_00457":null,"SJAG_00466":null,"SJAG_00475":null,"SJAG_00500":null,"SJAG_00516":null,"SJAG_00541":null,"SJAG_00564":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00599":null,"SJAG_00604":null,"SJAG_00609":null,"SJAG_00645":null,"SJAG_00650":null,"SJAG_00659":null,"SJAG_00663":null,"SJAG_00669":null,"SJAG_00705":null,"SJAG_00712":null,"SJAG_00729":null,"SJAG_00757":null,"SJAG_00766":null,"SJAG_00768":null,"SJAG_00773":null,"SJAG_00790":null,"SJAG_00806":null,"SJAG_00851":null,"SJAG_00853":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00871":null,"SJAG_00878":null,"SJAG_00884":null,"SJAG_00906":null,"SJAG_00923":null,"SJAG_00930":null,"SJAG_00938":null,"SJAG_00947":null,"SJAG_00983":null,"SJAG_00984":null,"SJAG_01002":null,"SJAG_01010":null,"SJAG_01024":null,"SJAG_01095":null,"SJAG_01129":null,"SJAG_01131":null,"SJAG_01152":null,"SJAG_01179":null,"SJAG_01186":null,"SJAG_01240":null,"SJAG_01277":null,"SJAG_01297":null,"SJAG_01339":null,"SJAG_01344":null,"SJAG_01354":null,"SJAG_01379":null,"SJAG_01391":null,"SJAG_01397":null,"SJAG_01400":null,"SJAG_01402":null,"SJAG_01405":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01435":null,"SJAG_01438":null,"SJAG_01447":null,"SJAG_01449":null,"SJAG_01456":null,"SJAG_01471":null,"SJAG_01489":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01510":null,"SJAG_01530":null,"SJAG_01544":null,"SJAG_01546":null,"SJAG_01558":null,"SJAG_01595":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01620":null,"SJAG_01653":null,"SJAG_01655":null,"SJAG_01662":null,"SJAG_01664":null,"SJAG_01669":null,"SJAG_01677":null,"SJAG_01696":null,"SJAG_01731":null,"SJAG_01769":null,"SJAG_01774":null,"SJAG_01807":null,"SJAG_01816":null,"SJAG_01817":null,"SJAG_01831":null,"SJAG_01851":null,"SJAG_01874":null,"SJAG_01879":null,"SJAG_01913":null,"SJAG_01929":null,"SJAG_01944":null,"SJAG_01945":null,"SJAG_02023":null,"SJAG_02061":null,"SJAG_02074":null,"SJAG_02077":null,"SJAG_02082":null,"SJAG_02084":null,"SJAG_02114":null,"SJAG_02132":null,"SJAG_02171":null,"SJAG_02180":null,"SJAG_02182":null,"SJAG_02187":null,"SJAG_02199":null,"SJAG_02226":null,"SJAG_02233":null,"SJAG_02242":null,"SJAG_02265":null,"SJAG_02267":null,"SJAG_02286":null,"SJAG_02292":null,"SJAG_02295":null,"SJAG_02302":null,"SJAG_02331":null,"SJAG_02336":null,"SJAG_02339":null,"SJAG_02353":null,"SJAG_02366":null,"SJAG_02373":null,"SJAG_02378":null,"SJAG_02382":null,"SJAG_02384":null,"SJAG_02394":null,"SJAG_02399":null,"SJAG_02431":null,"SJAG_02444":null,"SJAG_02457":null,"SJAG_02516":null,"SJAG_02521":null,"SJAG_02545":null,"SJAG_02558":null,"SJAG_02561":null,"SJAG_02563":null,"SJAG_02571":null,"SJAG_02575":null,"SJAG_02581":null,"SJAG_02595":null,"SJAG_02598":null,"SJAG_02601":null,"SJAG_02602":null,"SJAG_02604":null,"SJAG_02605":null,"SJAG_02606":null,"SJAG_02610":null,"SJAG_02619":null,"SJAG_02640":null,"SJAG_02656":null,"SJAG_02684":null,"SJAG_02704":null,"SJAG_02708":null,"SJAG_02738":null,"SJAG_02748":null,"SJAG_02782":null,"SJAG_02824":null,"SJAG_02825":null,"SJAG_02848":null,"SJAG_02856":null,"SJAG_02872":null,"SJAG_02895":null,"SJAG_02897":null,"SJAG_02906":null,"SJAG_02926":null,"SJAG_02943":null,"SJAG_02957":null,"SJAG_02994":null,"SJAG_02997":null,"SJAG_03011":null,"SJAG_03036":null,"SJAG_03050":null,"SJAG_03072":null,"SJAG_03137":null,"SJAG_03161":null,"SJAG_03237":null,"SJAG_03320":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03358":null,"SJAG_03363":null,"SJAG_03371":null,"SJAG_03374":null,"SJAG_03406":null,"SJAG_03415":null,"SJAG_03436":null,"SJAG_03451":null,"SJAG_03453":null,"SJAG_03461":null,"SJAG_03471":null,"SJAG_03495":null,"SJAG_03496":null,"SJAG_03497":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03534":null,"SJAG_03560":null,"SJAG_03567":null,"SJAG_03570":null,"SJAG_03613":null,"SJAG_03658":null,"SJAG_03676":null,"SJAG_03682":null,"SJAG_03684":null,"SJAG_03688":null,"SJAG_03703":null,"SJAG_03732":null,"SJAG_03780":null,"SJAG_03785":null,"SJAG_03798":null,"SJAG_03832":null,"SJAG_03846":null,"SJAG_03850":null,"SJAG_03866":null,"SJAG_03886":null,"SJAG_03892":null,"SJAG_03896":null,"SJAG_03909":null,"SJAG_03915":null,"SJAG_03923":null,"SJAG_03927":null,"SJAG_03948":null,"SJAG_03950":null,"SJAG_03982":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04004":null,"SJAG_04015":null,"SJAG_04038":null,"SJAG_04055":null,"SJAG_04064":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04147":null,"SJAG_04150":null,"SJAG_04154":null,"SJAG_04157":null,"SJAG_04167":null,"SJAG_04187":null,"SJAG_04203":null,"SJAG_04210":null,"SJAG_04258":null,"SJAG_04277":null,"SJAG_04343":null,"SJAG_04351":null,"SJAG_04355":null,"SJAG_04375":null,"SJAG_04470":null,"SJAG_04477":null,"SJAG_04488":null,"SJAG_04509":null,"SJAG_04511":null,"SJAG_04531":null,"SJAG_04566":null,"SJAG_04596":null,"SJAG_04599":null,"SJAG_04666":null,"SJAG_04679":null,"SJAG_04692":null,"SJAG_04745":null,"SJAG_04755":null,"SJAG_04757":null,"SJAG_04862":null,"SJAG_04874":null,"SJAG_04940":null,"SJAG_04955":null,"SJAG_05019":null,"SJAG_05030":null,"SJAG_05032":null,"SJAG_05209":null,"SJAG_05213":null,"SJAG_05294":null,"SJAG_05295":null,"SJAG_05313":null,"SJAG_05332":null,"SJAG_16455":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:0016787","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"ribonucleoside triphosphate phosphatase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["EC:3.6.1.15","Reactome:R-HSA-8851089","MetaCyc:NUCLEOSIDE-TRIPHOSPHATASE-RXN","Reactome:R-HSA-8851234","Reactome:R-HSA-8851494","Reactome:R-HSA-8851538","Reactome:R-HSA-8851110","Reactome:R-HSA-8850846"],"synonyms":[{"name":"NTPase activity","type":"exact"},{"name":"apyrase activity","type":"broad"},{"name":"nucleoside 5-triphosphatase activity","type":"broad"},{"name":"nucleoside triphosphatase activity","type":"broad"},{"name":"nucleoside triphosphate hydrolase activity","type":"broad"},{"name":"nucleoside triphosphate phosphatase activity","type":"broad"},{"name":"nucleoside triphosphate phosphohydrolase activity","type":"related"},{"name":"nucleoside-5-triphosphate phosphohydrolase activity","type":"related"},{"name":"nucleoside-triphosphatase activity","type":"broad"}],"termid":"GO:0017111","terms_by_termid":{"GO:0003924":null,"GO:0003925":null,"GO:0016887":null,"GO:0017111":null,"GO:0061791":null,"GO:1990606":null}}


id: PBO:0001425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Utp11 (predicted)","termid":"PBO:0001425"}


id: PBO:0074440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 41","termid":"PBO:0074440"}


id: FYPO:0006205
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 dGTP measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular dNTP level","termid":"FYPO:0005753"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal cellular dGTP level","synonyms":[{"name":"normal cellular dGTP level during mitotic cell cycle","type":"related"},{"name":"normal cellular dGTP level during vegetative growth","type":"exact"},{"name":"normal dGTP accumulation","type":"related"}],"termid":"FYPO:0006205"}


id: GO:0006073
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways involving glucans, polysaccharides consisting only of glucose residues, occurring at the level of an individual cell.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete cellular glucan metabolic process (obsolete GO:0006073)","synonyms":[{"name":"cellular glucan metabolism","type":"exact"}],"termid":"GO:0006073"}


id: GO:0007395
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Dorsally-directed movement of a cell at the leading edge of the epithelium over the amnioserosa.","definition_xrefs":["PMID:12147138","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"},{"relation_name":"part_of","term_name":"dorsal closure","termid":"GO:0007391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"dorsal closure, spreading of leading edge cells","termid":"GO:0007395"}


id: PBO:0047671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"filaggrin","termid":"PBO:0047671"}


id: PR:O59757
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spc7 gene.","definition_xrefs":["UniProtKB:O59757","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":"kinetochore protein spc7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1020.02","synonyms":[{"name":"NMS complex subunit spc7 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-spc7","type":"exact"}],"termid":"PR:O59757"}


id: FYPO:0008403
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the degradation of a protein is normal (i.e. indistinguishable from wild type) during meiosis. Protein degradation, also known as protein catabolism, is any metabolic process that results in the destruction of the native, active configuration of a protein, with or without the hydrolysis of peptide bonds.","definition_xrefs":["PomBase:pc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein degradation","termid":"FYPO:0002799"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein degradation during meiosis","termid":"FYPO:0008403"}


id: FYPO:0000356
data:
  {"alleles_by_uniquename":{"SJAG_00426:allele-1":{"allele_type":"amino_acid_mutation","description":"P363S","gene_uniquename":"SJAG_00426","name":"bbl1-P363S","uniquename":"SJAG_00426:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121082],"is_not":false,"summary":null,"term":"FYPO:0000356"}]},"cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the size, shape, or structure of lipid droplets is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"output_of","term_name":"abnormal lipid droplet organization","termid":"FYPO:0000808"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00426":null},"genotype_count":1,"genotypes_by_uniquename":{"bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"bbl1-P363S(aa)","display_uniquename":"bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00426:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"abnormal lipid droplet morphology","references_by_uniquename":{"PMID:25318672":null},"single_locus_annotated_genes":["SJAG_00426"],"single_locus_genotype_uniquenames":["bbl1-P363S-P363S-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"abnormal lipid droplet morphology during mitotic cell cycle","type":"related"},{"name":"abnormal lipid droplet morphology during vegetative growth","type":"exact"},{"name":"abnormal lipid particle morphology","type":"exact"},{"name":"lipid particle morphology: abnormal","type":"related"}],"termid":"FYPO:0000356","terms_by_termid":{"FYECO:0000004":null,"FYECO:0000162":null,"FYPO:0000356":null,"FYPO_EXT:0000001":null}}


id: GO:0008039
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a neuronal cell in a multicellular organism interprets signals produced by potential target cells, with which it may form synapses.","definition_xrefs":["GOC:mah","ISBN:0878932437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron recognition","termid":"GO:0008038"}],"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 recognition","synonyms":[{"name":"neuronal targeting","type":"exact"}],"termid":"GO:0008039"}


id: FYPO:0000666
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a peptidase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0001985","FYPO:0000652","FYPO:0000654","FYPO:0000707"],"is_obsolete":false,"name":"abnormal peptidase activity","synonyms":[{"name":"abnormal protease activity","type":"exact"}],"termid":"FYPO:0000666"}


id: PBO:0065648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein tyrosine phosphatase receptor type B","termid":"PBO:0065648"}


id: PBO:0071309
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L26 pseudogene 32","termid":"PBO:0071309"}


id: GO:0035930
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The regulated release of any corticosteroid hormone into the circulatory system.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid hormone secretion","termid":"GO:0035929"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0051179","GO:0023052","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"corticosteroid hormone secretion","synonyms":[{"name":"corticosteroid secretion","type":"broad"}],"termid":"GO:0035930"}


id: PBO:0048300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceraldehyde-3-phosphate dehydrogenase","termid":"PBO:0048300"}


id: MONDO:0004382
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic or neoplastic disorder that affects the larynx. Representative examples include laryngitis, vocal cord polyp, squamous papilloma, and carcinoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"upper respiratory tract disorder","termid":"MONDO:0004867"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laryngeal disorder","secondary_identifiers":["NCIT:C26810","SCTID:60600009","MESH:D007818","MEDGEN:7268","DOID:786","ICD9:478.70","EFO:0009673","UMLS:C0023051"],"synonyms":[{"name":"disease of larynx","type":"exact"},{"name":"disease or disorder of larynx","type":"exact"},{"name":"disorder of larynx","type":"exact"},{"name":"disorder of the larynx","type":"exact"},{"name":"laryngeal disease","type":"exact"},{"name":"laryngeal disorder","type":"exact"},{"name":"larynx disease","type":"exact"},{"name":"larynx disease or disorder","type":"exact"}],"termid":"MONDO:0004382","xrefs":{"Monarch":{"xref_id":"0004382"}}}


id: MONDO:0018206
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"myopathy, proximal, and ophthalmoplegia","termid":"MONDO:0011577"},{"relation_name":"is_a","term_name":"hereditary inclusion-body myopathy","termid":"MONDO:0016112"}],"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":"childhood-onset autosomal recessive myopathy with external ophthalmoplegia","secondary_identifiers":["UMLS:C5192594","GARD:17568","MEDGEN:1673410","Orphanet:363677"],"termid":"MONDO:0018206","xrefs":{"Monarch":{"xref_id":"0018206"}}}


id: GO:0035099
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a hemocyte within the embryo. Hemocytes are blood cells associated with a hemocoel (the cavity containing most of the major organs of the arthropod body) which are involved in defense and clotting of hemolymph, but not involved in transport of oxygen. In Drosophila, embryonic hemocytes originate from the head mesoderm as a cluster of cells. The cluster splits into two and one group of cells crosses the amnioserosa. Both populations then spread toward the middle of the embryo and then disperse evenly throughout the embryo.","definition_xrefs":["GOC:mtg_sensu","PMID:12885551","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"},{"relation_name":"part_of","term_name":"embryonic hemopoiesis","termid":"GO:0035162"}],"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":"hemocyte migration","synonyms":[{"name":"arthropod blood cell migration","type":"exact"},{"name":"hemocyte cell migration","type":"exact"}],"termid":"GO:0035099"}


id: MONDO:0000780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A allergy involving a Prunus armeniaca.","definition_xrefs":["MONDO:patterns/allergy"],"gene_count":0,"genotype_count":0,"name":"obsolete apricot allergy (obsolete MONDO:0000780)","secondary_identifiers":["DOID:0060505"],"synonyms":[{"name":"Prunus armeniaca allergic disease","type":"exact"},{"name":"Prunus armeniaca caused allergic disease","type":"exact"},{"name":"Prunus armeniaca fruit allergy","type":"exact"},{"name":"allergy of Prunus armeniaca","type":"exact"}],"termid":"MONDO:0000780","xrefs":{"Monarch":{"xref_id":"0000780"}}}


id: MONDO:1012562
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondromatosis, non-human animal","termid":"MONDO:1011972"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteochondromatosis, horse","secondary_identifiers":["OMIA:002555-9796"],"termid":"MONDO:1012562","xrefs":{"Monarch":{"xref_id":"1012562"}}}


id: PBO:0082224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-arrestin involved in ubiquitin-dependent endocytosis; activating dephosphorylation relays glucose signaling to transporter endocytosis; calcineurin dephosphorylation is required for Rsp5p-dependent internalization of agonist-occupied Ste2p, as part of signal desensitization; recruits Rsp5p to Ste2p via its 2 PPXY motifs; protein abundance increases in response to DNA replication stress; ROD1 has a paralog, ROG3, that arose from the whole genome duplication","termid":"PBO:0082224"}


id: MONDO:0001441
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An eating disorder characterized by the persistent eating of nonnutritive substances such as clay or soil; this behavior must be inappropriate to the level of the individual's development.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eating disorder","termid":"MONDO:0005451"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pica disease","secondary_identifiers":["NCIT:C92566","ICD9:307.52","DOID:12128","MEDGEN:45917","SCTID:14077003","UMLS:C0031873","MESH:D010842"],"synonyms":[{"name":"Pica","type":"exact"},{"name":"Pica eating disorder","type":"exact"}],"termid":"MONDO:0001441","xrefs":{"Monarch":{"xref_id":"0001441"}}}


id: PBO:0057408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 548j","termid":"PBO:0057408"}


id: GO:0160103
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: guanosine(26)/guanosine(27) in tRNA + 4 S-adenosyl-L-methionine = 4 H+ + N(2)-dimethylguanosine(26)/N(2)-dimethylguanosine(27) in tRNA + 4 S-adenosyl-L-homocysteine.","definition_xrefs":["EC:2.1.1.215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-methyltransferase activity","termid":"GO:0008170"},{"relation_name":"is_a","term_name":"tRNA (guanine) methyltransferase activity","termid":"GO:0016423"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140101"}],"interesting_parent_ids":["GO:0016741","GO:0003674","GO:0003824","GO:0140101","GO:0016740","GO:0140098"],"is_obsolete":false,"name":"tRNA (guanine(26)-N2/guanine(27)-N2)-dimethyltransferase activity","secondary_identifiers":["RHEA:43136"],"synonyms":[{"name":"tRNA (guanine(26)-N(2)/guanine(27)-N(2))-dimethyltransferase activity","type":"exact"},{"name":"tRNA (guanosine(26)-N(2)/guanosine(27)-N(2))-dimethyltransferase activity","type":"exact"}],"termid":"GO:0160103"}


id: MONDO:0012562
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any holoprosencephaly in which the cause of the disease is a mutation in the PTCH1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"holoprosencephaly","termid":"MONDO:0016296"}],"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":"holoprosencephaly 7","secondary_identifiers":["OMIM:610828","MEDGEN:372134","MESH:C563660","UMLS:C1835820","DOID:0110876"],"synonyms":[{"name":"HPE7","type":"exact"},{"name":"PTCH1 holoprosencephaly","type":"exact"},{"name":"holoprosencephaly 7","type":"exact"},{"name":"holoprosencephaly caused by mutation in PTCH1","type":"exact"},{"name":"holoprosencephaly type 7","type":"exact"}],"termid":"MONDO:0012562","xrefs":{"Monarch":{"xref_id":"0012562"}}}


id: GO:0042065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Growth of glial cells, non-neuronal cells that provide support and nutrition, maintain homeostasis, form myelin, and participate in signal transmission in the nervous system.","definition_xrefs":["GOC:jid","GOC:isa_complete","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental cell growth","termid":"GO:0048588"},{"relation_name":"part_of","term_name":"gliogenesis","termid":"GO:0042063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"glial cell growth","termid":"GO:0042065"}


id: GO:0046022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of transcription from an RNA polymerase II promoter that occurs during the mitotic cell cycle.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter during mitotic cell cycle (obsolete GO:0046022)","synonyms":[{"name":"activation of transcription from RNA polymerase II promoter during mitosis","type":"narrow"},{"name":"mitotic activation of transcription from Pol II promoter","type":"exact"},{"name":"positive regulation of transcription from Pol II promoter during mitosis","type":"exact"},{"name":"positive regulation of transcription from RNA polymerase II promoter, mitotic","type":"exact"},{"name":"stimulation of transcription from RNA polymerase II promoter during mitosis","type":"narrow"},{"name":"up regulation of transcription from RNA polymerase II promoter during mitosis","type":"exact"},{"name":"up-regulation of transcription from RNA polymerase II promoter during mitosis","type":"exact"},{"name":"upregulation of transcription from RNA polymerase II promoter during mitosis","type":"exact"}],"termid":"GO:0046022"}


id: FYPO:0003294
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 UDP-galactose transmembrane transport is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal transport","termid":"FYPO:0001071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001312","FYPO:0001320","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"normal UDP-galactose transmembrane transport","synonyms":[{"name":"normal UDP-galactose transmembrane transport during mitotic cell cycle","type":"related"},{"name":"normal UDP-galactose transmembrane transport during vegetative growth","type":"exact"}],"termid":"FYPO:0003294"}


id: SO:0000992
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of DNA that has been inserted into the bacterial genome using a bacterial artificial chromosome.","direct_ancestors":[{"relation_name":"derives_from","term_name":"BAC","termid":"SO:0000153"},{"relation_name":"is_a","term_name":"cloned_genomic_insert","termid":"SO:0000914"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAC_cloned_genomic_insert","synonyms":[{"name":"BAC cloned genomic insert","type":"exact"}],"termid":"SO:0000992"}


id: PBO:0053148
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lactate dehydrogenase A pseudogene 4","termid":"PBO:0053148"}


id: MOD:00471
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["Unimod:93"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EDT-maleimide-PEO-biotin","synonyms":[{"name":"EDT-maleimide-PEO-biotin","type":"related"}],"termid":"MOD:00471"}


id: GO:0015614
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + D-xylose(out) = ADP + phosphate + D-xylose(in).","definition_xrefs":["RHEA:29899"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-xylose transmembrane transporter activity","termid":"GO:0015148"},{"relation_name":"is_a","term_name":"ABC-type monosaccharide transporter activity","termid":"GO:0015407"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"ABC-type D-xylose transporter activity","secondary_identifiers":["EC:7.5.2.10","MetaCyc:ABC-33-RXN"],"synonyms":[{"name":"ATPase-coupled D-xylose transmembrane transporter activity","type":"related"},{"name":"D-xylose porter activity","type":"broad"},{"name":"D-xylose-importing ATPase activity","type":"related"}],"termid":"GO:0015614"}


id: PBO:0045538
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual oxidase 2","termid":"PBO:0045538"}


id: PBO:0046888
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAM9C pseudogene 1","termid":"PBO:0046888"}


id: GO:0000091
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle phase during which the kinetochore microtubules shorten as chromosomes move toward the spindle poles as part of mitosis.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitotic anaphase","termid":"GO:0000090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0000087"},{"rel_name":"is_a","termid":"GO:0000090"}],"interesting_parent_ids":["GO:0000087","GO:0008150","GO:0000090"],"is_obsolete":false,"name":"mitotic anaphase A","termid":"GO:0000091"}


id: PBO:0073638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sialic acid binding Ig like lectin 25, pseudogene","termid":"PBO:0073638"}


id: GO:0022601
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of physiological phases, occurring in the endometrium during the menstrual cycle that recur at regular intervals during the reproductive years. The menstrual cycle is an ovulation cycle where the endometrium is shed if pregnancy does not occur.","definition_xrefs":["GOC:jid","GOC:isa_complete","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological phase","termid":"GO:0044848"}],"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":"menstrual cycle phase","termid":"GO:0022601"}


id: PBO:0034225
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_phenotype","termid":"PBO:0034225"}


id: GO:0035235
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by glutamate binding to a glutamate receptor on the surface of the target cell, followed by the movement of ions through a channel in the receptor complex, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutamate receptor signaling pathway","termid":"GO:0007215"},{"relation_name":"is_a","term_name":"ligand-gated ion channel signaling pathway","termid":"GO:1990806"}],"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:0023052","GO:0008150"],"is_obsolete":false,"name":"ionotropic glutamate receptor signaling pathway","synonyms":[{"name":"ionotropic glutamate receptor signalling pathway","type":"exact"}],"termid":"GO:0035235"}


id: GO:0009675
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: sulfate(out) + H+(out) = sulfate(in) + H+(in). In high-affinity transport the transporter is able to bind the solute even if it is only present at very low concentrations.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfate:proton symporter activity","termid":"GO:0008512"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"high-affinity sulfate:proton symporter activity","synonyms":[{"name":"high affinity sulfate:hydrogen symporter activity","type":"exact"},{"name":"high affinity sulfate:proton symporter activity","type":"exact"},{"name":"high affinity sulphate:hydrogen symporter activity","type":"exact"}],"termid":"GO:0009675"}


id: GO:0002711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of T cell mediated immunity.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lymphocyte mediated immunity","termid":"GO:0002708"},{"relation_name":"is_a","term_name":"regulation of T cell mediated immunity","termid":"GO:0002709"},{"relation_name":"is_a","term_name":"positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains","termid":"GO:0002824"},{"relation_name":"positively_regulates","term_name":"T cell mediated immunity","termid":"GO:0002456"}],"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 T cell mediated immunity","synonyms":[{"name":"activation of T cell mediated immunity","type":"narrow"},{"name":"positive regulation of T lymphocyte mediated immunity","type":"exact"},{"name":"positive regulation of T-cell mediated immunity","type":"exact"},{"name":"positive regulation of T-lymphocyte mediated immunity","type":"exact"},{"name":"stimulation of T cell mediated immunity","type":"narrow"},{"name":"up regulation of T cell mediated immunity","type":"exact"},{"name":"up-regulation of T cell mediated immunity","type":"exact"},{"name":"upregulation of T cell mediated immunity","type":"exact"}],"termid":"GO:0002711"}


id: MOD:01377
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-isoleucine residue to a (2S,3R,4S)-4-hydroxyisoleucine.","definition_xrefs":["RESID:AA0448","ChEBI:141844","PubMed:363352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monohydroxylated isoleucine","termid":"MOD:01415"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(2S,3R,4S)-4-hydroxyisoleucine","synonyms":[{"name":"(2S,3R,4S)-2-amino-3-methyl-4-hydroxyvaleric acid","type":"exact"},{"name":"(2S,3R,4S)-2-amino-4-hydroxy-3-methylpentanoic acid","type":"exact"},{"name":"(2S,3R,4S)-4-hydroxyisoleucine","type":"exact"},{"name":"(3R,4S)-4-hydroxyisoleucine","type":"exact"},{"name":"MOD_RES (3R,4S)-4-hydroxyisoleucine","type":"exact"},{"name":"gamma-hydroxyisoleucine","type":"exact"}],"termid":"MOD:01377"}


id: GO:0047151
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5,10-methylenetetrahydrofolate + tRNA containing uridine at position 54 + FADH + H+ = tetrahydrofolate + tRNA containing ribothymidine at position 54 + FAD+.","definition_xrefs":["MetaCyc:2.1.1.74-RXN","EC:2.1.1.74"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA (uridine) methyltransferase activity","termid":"GO:0016300"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140101"}],"interesting_parent_ids":["GO:0016740","GO:0016741","GO:0003824","GO:0140098","GO:0003674","GO:0140101"],"is_obsolete":false,"name":"tRNA (uracil(54)-C5)-methyltransferase activity, 5,10-methylenetetrahydrofolate-dependent","secondary_identifiers":["KEGG_REACTION:R03704","RHEA:16873"],"synonyms":[{"name":"5,10-methylenetetrahydrofolate:tRNA (uracil-5-)-methyltransferase activity","type":"related"},{"name":"5,10-methylenetetrahydrofolate:tRNA-UPsiC (uracil-5-)-methyl-transferase activity","type":"related"},{"name":"folate-dependent ribothymidyl synthase activity","type":"related"},{"name":"methylenetetrahydrofolate-tRNA-(uracil-5-)-methyltransferase (FADH-oxidizing) activity","type":"exact"},{"name":"methylenetetrahydrofolate-transfer ribonucleate uracil 5-methyltransferase activity","type":"related"},{"name":"tRNA (uracil(54)-C(5))-methyltransferase activity, 5,10-methylenetetrahydrofolate-dependent","type":"exact"}],"termid":"GO:0047151"}


id: PBO:0069156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 408, pseudogene","termid":"PBO:0069156"}


id: GO:0180064
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A glycoprotein biosynthetic process starting with the covalent linkage of a xylose via a beta-glycosidic bond to the oxygen atom of a serine or a threonine side chain in a protein, which can be further elongated with the sequential addition of sugar units resulting in the formation of a protein O-linked glycan.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein O-linked glycosylation","termid":"GO:0006493"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"protein O-linked xylosylation","termid":"GO:0180064"}


id: GO:0050946
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of xanthophore differentiation.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of xanthophore differentiation","termid":"GO:0050938"},{"relation_name":"is_a","term_name":"positive regulation of pigment cell differentiation","termid":"GO:0050942"},{"relation_name":"positively_regulates","term_name":"xanthophore differentiation","termid":"GO:0050936"}],"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 xanthophore differentiation","synonyms":[{"name":"activation of xanthophore differentiation","type":"narrow"},{"name":"stimulation of xanthophore differentiation","type":"narrow"},{"name":"up regulation of xanthophore differentiation","type":"exact"},{"name":"up-regulation of xanthophore differentiation","type":"exact"},{"name":"upregulation of xanthophore differentiation","type":"exact"}],"termid":"GO:0050946"}


id: MONDO:0015723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy 12p is an extremely rare chromosomal disorder (over 30 cases reported worldwide) characterized by craniofacial malformations (round face, prominent cheeks, high bulging forehead, broad and flat nasal bridge, short nose with anteverted nostrils, long philtrum, prominent and everted lower lip, low-set ears, abnormally folded helix, protuberant antihelix), postnatal growth retardation, mental and psychomotor retardation, generalized hypotonia, abnormally short wide hands and/or other abnormalities.","definition_xrefs":["Orphanet:1699"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"epilepsy","termid":"MONDO:0005027"},{"relation_name":"is_a","term_name":"partial trisomy/tetrasomy of the short arm of chromosome 12","termid":"MONDO:0016933"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trisomy 12p","secondary_identifiers":["UMLS:C0795845","MEDGEN:162880","GARD:5305","MESH:C538299"],"synonyms":[{"name":"12p duplication","type":"related"},{"name":"12p trisomy","type":"related"},{"name":"Duplication 12p","type":"exact"},{"name":"chromosome 12p duplication","type":"related"},{"name":"partial trisomy 12p","type":"related"},{"name":"trisomy type 12p","type":"exact"}],"termid":"MONDO:0015723","xrefs":{"Monarch":{"xref_id":"0015723"}}}


id: MONDO:0000521
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from the major or minor salivary glands. Representative examples include carcinoma ex pleomorphic adenoma, adenocarcinoma, adenoid cystic carcinoma, and mucoepidermoid carcinoma.","definition_xrefs":["NCIT:C9272"],"direct_ancestors":[{"relation_name":"is_a","term_name":"salivary gland cancer","termid":"MONDO:0004669"},{"relation_name":"is_a","term_name":"oral cavity carcinoma","termid":"MONDO:0044925"}],"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":"salivary gland carcinoma","secondary_identifiers":["UMLS:C0948750","MEDGEN:215302","DOID:0050904","NANDO:2200076","ONCOTREE:SACA"],"synonyms":[{"name":"carcinoma of saliva-secreting gland","type":"exact"},{"name":"carcinoma of salivary gland","type":"exact"},{"name":"carcinoma of the salivary gland","type":"exact"},{"name":"saliva-secreting gland carcinoma","type":"exact"},{"name":"salivary carcinoma","type":"related"},{"name":"salivary gland cancer","type":"broad"},{"name":"salivary gland carcinoma","type":"exact"}],"termid":"MONDO:0000521","xrefs":{"Monarch":{"xref_id":"0000521"}}}


id: PBO:0064895
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 2 regulatory subunit B'alpha","termid":"PBO:0064895"}


id: GO:0045146
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The activation, by acetate, of the chemical reactions and pathways resulting in the breakdown of acetate.","definition_xrefs":["PMID:11741859"],"direct_ancestors":[{"relation_name":"is_a","term_name":"initiation of acetate catabolic process","termid":"GO:0043077"},{"relation_name":"part_of","term_name":"response to acetate","termid":"GO:0010034"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"initiation of acetate catabolic process by acetate","synonyms":[{"name":"initiation of acetate breakdown by acetate","type":"exact"},{"name":"initiation of acetate degradation by acetate","type":"exact"}],"termid":"GO:0045146"}


id: GO:0021850
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The division of glioblasts in the subpallium. These cells will give rise to oligodendrocytes.","definition_xrefs":["GO_REF:0000021","GOC:dgh","GOC:jid","GOC:cls","PMID:12626695","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glioblast division","termid":"GO:0048860"},{"relation_name":"part_of","term_name":"subpallium cell proliferation in forebrain","termid":"GO:0022012"}],"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":"subpallium glioblast cell division","synonyms":[{"name":"glioblast cell division in subpallium","type":"exact"},{"name":"glioblast division in ventral telencephalon","type":"exact"}],"termid":"GO:0021850"}


id: FYPO:0002319
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 lanosterol measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular sterol level","termid":"FYPO:0002327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular lanosterol level","synonyms":[{"name":"increased cellular lanosterol level during mitotic cell cycle","type":"related"},{"name":"increased cellular lanosterol level during vegetative growth","type":"exact"},{"name":"increased lanosterol accumulation","type":"related"}],"termid":"FYPO:0002319"}


id: MONDO:0004757
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the ethmoid sinus that typically lasts beyond eight weeks. It is caused by infections, allergies, and the presence of sinus polyps or a deviated septum. Signs and symptoms include headache, nasal discharge, swelling in the face, dizziness, and breathing difficulties.","definition_xrefs":["NCIT:C34472"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ethmoid sinusitis","termid":"MONDO:0005756"},{"relation_name":"is_a","term_name":"chronic rhinosinusitis","termid":"MONDO:0006031"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic ethmoidal sinusitis","secondary_identifiers":["SCTID:73237007","DOID:9312","UMLS:C0008681","ICD9:473.2","ICD10CM:J32.2","MEDGEN:3454","icd11.foundation:1076459084"],"synonyms":[{"name":"chronic ethmoid sinusitis","type":"exact"},{"name":"chronic ethmoidal sinusitis","type":"exact"},{"name":"chronic ethmoiditis","type":"related"},{"name":"ethmoid sinusitis, chronic","type":"exact"},{"name":"ethmoidal sinusitis - chronic","type":"exact"}],"termid":"MONDO:0004757","xrefs":{"Monarch":{"xref_id":"0004757"}}}


id: GO:0052024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The increase by an organism of the levels of hormones or growth regulators in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by symbiont of hormone or growth regulator levels in host (obsolete GO:0052024)","synonyms":[{"name":"activation by symbiont of hormone or growth regulator levels in host","type":"narrow"},{"name":"positive modulation of hormone or growth regulator levels in host","type":"exact"},{"name":"positive regulation by organism of hormone or growth regulator levels in other organism involved in symbiotic interaction","type":"broad"},{"name":"stimulation by symbiont of hormone or growth regulator levels in host","type":"narrow"},{"name":"up regulation by symbiont of hormone or growth regulator levels in host","type":"exact"},{"name":"up-regulation by symbiont of hormone or growth regulator levels in host","type":"exact"},{"name":"upregulation by symbiont of hormone or growth regulator levels in host","type":"exact"}],"termid":"GO:0052024"}


id: PBO:0067325
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 416, pseudogene","termid":"PBO:0067325"}


id: GO:0016541
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Intervening protein sequence excised from a protein precursor in protein splicing; inteins catalyze their own excision and many also possess endonuclease activity.","definition_xrefs":["GOC:mah","PMID:8165123"],"gene_count":0,"genotype_count":0,"name":"obsolete intein (obsolete GO:0016541)","synonyms":[{"name":"intein","type":"exact"}],"termid":"GO:0016541"}


id: _global:has_role
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"a relation between an independent continuant (the bearer) and a role, in which the role specifically depends on the bearer for its existence","direct_ancestors":[{"relation_name":"is_a","term_name":"has_characteristic","termid":"_global:has_characteristic"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"has_role","secondary_identifiers":["RO:0000087"],"termid":"_global:has_role"}


id: PBO:0045359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DPEP2 neighbor","termid":"PBO:0045359"}


id: PBO:0063711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PGM5 antisense RNA 1","termid":"PBO:0063711"}


id: MONDO:0012532
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hemorrhagic telangiectasia","termid":"MONDO:0019180"}],"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":"hereditary hemorrhagic telangiectasia type 4","secondary_identifiers":["UMLS:C1857688","GARD:10615","MEDGEN:341824","OMIM:610655","MESH:C565691"],"synonyms":[{"name":"HHT4","type":"related"},{"name":"telangiectasia, hereditary hemorrhagic, type 4","type":"related"}],"termid":"MONDO:0012532","xrefs":{"Monarch":{"xref_id":"0012532"}}}


id: PBO:0082196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Allantoate permease; ureidosuccinate permease; also transports dipeptides, though with lower affinity than for allantoate and ureidosuccinate; expression is constitutive but sensitive to nitrogen catabolite repression","termid":"PBO:0082196"}


id: GO:0015759
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of beta-glucosides into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore. Beta-glucosides are glycosides in which the sugar group is a glucose residue, and the anomeric carbon of the bond is in a beta configuration.","definition_xrefs":["GOC:jl","ISBN:0198506732","PMID:6756954","PMID:3034860"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucoside transport","termid":"GO:0042946"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"beta-glucoside transport","termid":"GO:0015759"}


id: GO:0002868
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of B cell deletion.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of B cell tolerance induction","termid":"GO:0002662"},{"relation_name":"is_a","term_name":"regulation of acute inflammatory response","termid":"GO:0002673"},{"relation_name":"is_a","term_name":"regulation of B cell deletion","termid":"GO:0002867"},{"relation_name":"is_a","term_name":"negative regulation of B cell apoptotic process","termid":"GO:0002903"},{"relation_name":"is_a","term_name":"negative regulation of apoptotic process involved in development","termid":"GO:1904746"},{"relation_name":"negatively_regulates","term_name":"B cell deletion","termid":"GO:0002516"}],"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 B cell deletion","synonyms":[{"name":"down regulation of B cell deletion","type":"exact"},{"name":"down-regulation of B cell deletion","type":"exact"},{"name":"downregulation of B cell deletion","type":"exact"},{"name":"inhibition of B cell deletion","type":"narrow"},{"name":"negative regulation of B lymphocyte deletion","type":"exact"},{"name":"negative regulation of B-cell deletion","type":"exact"},{"name":"negative regulation of B-lymphocyte deletion","type":"exact"}],"termid":"GO:0002868"}


id: PBO:0092761
data:
  {"annotation_feature_type":"gene","cv_name":"feature_relationshipprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_throughput_type","termid":"PBO:0092761"}


id: MONDO:0020568
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"myiasis","termid":"MONDO:0019147"}],"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":"cutaneous myiasis","secondary_identifiers":["Orphanet:99983","SCTID:240877000","UMLS:C0027031","GARD:19723","ICD10CM:B87.0","icd11.foundation:1342682193","MEDGEN:507962"],"termid":"MONDO:0020568","xrefs":{"Monarch":{"xref_id":"0020568"}}}


id: GO:0062154
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H+ + H2O + N6-methyl-AMP = IMP + methylamine. Can also use N6-methyl-dAMP as a substrate.","definition_xrefs":["RHEA:16001","PMID:29884623"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deaminase activity","termid":"GO:0019239"}],"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"},{"rel_name":"is_a","termid":"GO:0016810"}],"interesting_parent_ids":["GO:0003674","GO:0016787","GO:0016810","GO:0003824"],"is_obsolete":false,"name":"N6-methyl-AMP deaminase activity","secondary_identifiers":["Reactome:R-HSA-2161195","Reactome:R-HSA-2161187","Reactome:R-HSA-9731661"],"synonyms":[{"name":"MAPDA","type":"exact"},{"name":"N6-mAMP deaminase activity","type":"exact"},{"name":"N6-methyl-AMP/dAMP aminohydrolase","type":"exact"}],"termid":"GO:0062154"}


id: GO:0050410
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-oxododecanoate + H+ = 2-undecanone + CO2. Also decarboxylates other C14 to C16 oxo acids.","definition_xrefs":["EC:4.1.1.56","RHEA:13385"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016829","GO:0003674"],"is_obsolete":false,"name":"3-oxolaurate decarboxylase activity","secondary_identifiers":["MetaCyc:3-OXOLAURATE-DECARBOXYLASE-RXN","KEGG_REACTION:R03747"],"synonyms":[{"name":"3-oxododecanoate carboxy-lyase (2-undecanone-forming)","type":"related"},{"name":"3-oxododecanoate carboxy-lyase activity","type":"related"},{"name":"beta-ketoacyl decarboxylase activity","type":"related"},{"name":"beta-ketolaurate decarboxylase activity","type":"related"}],"termid":"GO:0050410"}


id: PBO:0051376
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 3/OR22-2 (pseudogene)","termid":"PBO:0051376"}


id: GO:0006470
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of removing one or more phosphoric residues from a protein.","definition_xrefs":["GOC:hb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dephosphorylation","termid":"GO:0016311"},{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"}],"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":"protein dephosphorylation","synonyms":[{"name":"protein amino acid dephosphorylation","type":"exact"}],"termid":"GO:0006470"}


id: PBO:0005825
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nitrilase family protein, omega-amidase related (predicted)","termid":"PBO:0005825"}


id: GO:1904041
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of cystathionine beta-synthase activity.","definition_xrefs":["PMID:24416422","GO_REF:0000059","GOC:TermGenie","GOC:hal","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cystathionine beta-synthase activity (obsolete GO:1904041)","synonyms":[{"name":"regulation of L-serine hydro-lyase (adding homocysteine)","type":"exact"},{"name":"regulation of L-serine hydro-lyase (adding homocysteine; L-cystathionine-forming)","type":"exact"},{"name":"regulation of beta-thionase activity","type":"exact"},{"name":"regulation of methylcysteine synthase activity","type":"exact"},{"name":"regulation of serine sulfhydrase activity","type":"exact"},{"name":"regulation of serine sulfhydrylase activity","type":"exact"}],"termid":"GO:1904041"}


id: GO:0008386
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cholesterol + reduced adrenal ferredoxin + O2 = pregnenolone + 4-methylpentanal + oxidized adrenal ferredoxin + H2O.","definition_xrefs":["EC:1.14.15.6"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid hydroxylase activity","termid":"GO:0008395"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016713"}],"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:0003674","GO:0003824"],"is_obsolete":false,"name":"cholesterol monooxygenase (side-chain-cleaving) activity","secondary_identifiers":["Reactome:R-HSA-193065","MetaCyc:1.14.15.6-RXN","Reactome:R-HSA-193101","RHEA:35739","Reactome:R-HSA-193054"],"synonyms":[{"name":"C27-side chain cleavage enzyme","type":"related"},{"name":"Cyp11a1","type":"narrow"},{"name":"cholesterol 20-22-desmolase activity","type":"related"},{"name":"cholesterol C(20-22) desmolase activity","type":"related"},{"name":"cholesterol C20-22 desmolase activity","type":"related"},{"name":"cholesterol desmolase activity","type":"related"},{"name":"cholesterol side-chain cleavage enzyme activity","type":"related"},{"name":"cholesterol side-chain-cleaving enzyme activity","type":"related"},{"name":"cholesterol,reduced-adrenal-ferredoxin:oxygen oxidoreductase (side-chain-cleaving)","type":"related"},{"name":"cytochrome P-450(scc) activity","type":"narrow"},{"name":"cytochrome P-450scc","type":"related"},{"name":"cytochrome p450(scc) activity","type":"narrow"},{"name":"cytochrome p450scc","type":"related"},{"name":"desmolase, steroid 20-22","type":"related"},{"name":"enzymes, cholesterol side-chain-cleaving","type":"related"},{"name":"steroid 20-22 desmolase activity","type":"broad"},{"name":"steroid 20-22-lyase activity","type":"broad"}],"termid":"GO:0008386"}


id: PBO:0078722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Leu (anticodon TAG) 2-1","termid":"PBO:0078722"}


id: PBO:0091412
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae GRX5","termid":"PBO:0091412"}


id: PR:O13895
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A COP9 signalosome complex subunit 4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10855:SF2","PRO:DNx","OMA:SCHPO00467"],"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":"COP9 signalosome complex subunit 4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC22A12.03c","secondary_identifiers":["UniProtKB:O13895"],"synonyms":[{"name":"CSN complex subunit 4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SGN4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-COPS4","type":"exact"}],"termid":"PR:O13895"}


id: GO:0005096
data:
  {"annotated_genes":["SJAG_04498","SJAG_02277","SJAG_04724","SJAG_01011","SJAG_04910","SJAG_01184","SJAG_03655","SJAG_00092","SJAG_02390","SJAG_03153","SJAG_00028","SJAG_04074","SJAG_01048","SJAG_00551","SJAG_00824","SJAG_01600","SJAG_02520","SJAG_04462","SJAG_02539","SJAG_02278","SJAG_03338","SJAG_05346","SJAG_02765","SJAG_04733","SJAG_03268","SJAG_04938","SJAG_04548","SJAG_04522","SJAG_01114","SJAG_04013","SJAG_02666","SJAG_03021","SJAG_00990","SJAG_00991","SJAG_04080","SJAG_04765","SJAG_04776","SJAG_04391","SJAG_04400","SJAG_02379","SJAG_01386","SJAG_03085","SJAG_01526","SJAG_00467","SJAG_04943","SJAG_02012","SJAG_03748","SJAG_00289","SJAG_00864","SJAG_02231"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[59025,60663,66475,66944,67222,67705,67827,69468,69968,70804,71850,71921,71931,72098,72396,72570,72642,72979,73282,73363,73581,74064,74535,74645,74907,75164,75285,76664,76744,77376,78481,78522,78841,79159,79347,79350,80011,80153,80963,81399,89347,95137,95145,95787,97687,97918,98373,107120,112813,116862],"is_not":false,"summary":null,"term":"GO:0005096"}]},"cv_name":"molecular_function","definition":"Binds to and increases the activity of a GTPase, an enzyme that catalyzes the hydrolysis of GTP.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme activator activity","termid":"GO:0008047"},{"relation_name":"is_a","term_name":"GTPase regulator activity","termid":"GO:0030695"}],"gene_count":50,"genes_by_uniquename":{"SJAG_00028":null,"SJAG_00092":null,"SJAG_00289":null,"SJAG_00467":null,"SJAG_00551":null,"SJAG_00824":null,"SJAG_00864":null,"SJAG_00990":null,"SJAG_00991":null,"SJAG_01011":null,"SJAG_01048":null,"SJAG_01114":null,"SJAG_01184":null,"SJAG_01386":null,"SJAG_01526":null,"SJAG_01600":null,"SJAG_02012":null,"SJAG_02231":null,"SJAG_02277":null,"SJAG_02278":null,"SJAG_02379":null,"SJAG_02390":null,"SJAG_02520":null,"SJAG_02539":null,"SJAG_02666":null,"SJAG_02765":null,"SJAG_03021":null,"SJAG_03085":null,"SJAG_03153":null,"SJAG_03268":null,"SJAG_03338":null,"SJAG_03655":null,"SJAG_03748":null,"SJAG_04013":null,"SJAG_04074":null,"SJAG_04080":null,"SJAG_04391":null,"SJAG_04400":null,"SJAG_04462":null,"SJAG_04498":null,"SJAG_04522":null,"SJAG_04548":null,"SJAG_04724":null,"SJAG_04733":null,"SJAG_04765":null,"SJAG_04776":null,"SJAG_04910":null,"SJAG_04938":null,"SJAG_04943":null,"SJAG_05346":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0140677","GO:0098772","GO:0003674","GO:0030234"],"is_obsolete":false,"name":"GTPase activator activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-5638007","Reactome:R-HSA-392513","Reactome:R-HSA-428522","Reactome:R-HSA-9017488","GO:0005098","GO:0005100","Reactome:R-HSA-9013161","Reactome:R-HSA-9018806","GO:0005097","GO:0017123","Reactome:R-HSA-416559","Reactome:R-HSA-4093339","Reactome:R-HSA-9013111","Reactome:R-HSA-9013022","GO:0005099","Reactome:R-HSA-9693282","Reactome:R-HSA-416546","Reactome:R-HSA-8985594","GO:0046582","GO:0005101","GO:0008060","Reactome:R-HSA-9013437","Reactome:R-HSA-428533","Reactome:R-HSA-9013144","Reactome:R-HSA-399935","Reactome:R-HSA-9014434","Reactome:R-HSA-9624893","GO:0030675","Reactome:R-HSA-8981637","Reactome:R-HSA-9014295","Reactome:R-HSA-9018745"],"synonyms":[{"name":"ARF GAP activity","type":"narrow"},{"name":"ARF GTPase activator activity","type":"narrow"},{"name":"GAP activity","type":"exact"},{"name":"Rab GAP activity","type":"narrow"},{"name":"Rab GTPase activator activity","type":"narrow"},{"name":"Rac GAP activity","type":"narrow"},{"name":"Rac GTPase activator activity","type":"narrow"},{"name":"Ral GAP activity","type":"narrow"},{"name":"Ral GTPase activator activity","type":"narrow"},{"name":"Ran GAP activity","type":"narrow"},{"name":"Ran GTPase activator activity","type":"narrow"},{"name":"RanGAP","type":"narrow"},{"name":"Rap GAP activity","type":"narrow"},{"name":"Rap GTPase activator activity","type":"narrow"},{"name":"Ras GAP activity","type":"narrow"},{"name":"Ras GTPase activator activity","type":"narrow"},{"name":"Rho GAP activity","type":"narrow"},{"name":"Rho GTPase activator activity","type":"narrow"},{"name":"Sar GAP activity","type":"narrow"},{"name":"Sar GTPase activator activity","type":"narrow"}],"termid":"GO:0005096","terms_by_termid":{"GO:0005096":null}}


id: PBO:0068954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 198, pseudogene","termid":"PBO:0068954"}


id: PBO:0012036
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPCC663.03, pmd1 is more closely related to S. cerevisiae STE6","termid":"PBO:0012036"}


id: PBO:0030682
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-vegetative_cell,_abnormal_cell_shape,_normal_cell_size","termid":"PBO:0030682"}


id: MONDO:0007412
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A severe form of syndromic craniosynostosis, characterized by a variable degree of craniosynostosis, with cloverleaf skull reported in over 50% of cases, cutis gyrata, corduroy-like linear striations in the skin, acanthosis nigricans, skin tags, and choanal stenosis or atresia. Additional features include facial features similar to Crouzon disease, ear defects (conductive hearing loss, posteriorly angulated ears, stenotic auditory canals, preauricular furrows, and narrow ear canals), hirsutism, a prominent umbilical stump, and genitorurinary anomalies (anteriorly placed anus, hypoplasic labia, hypospadias). BSS is associated with a poor outcome as patients present an elevated risk for sudden death in their first year of life. Significant developmental delay and intellectual disability are observed in most patients who survive infancy.","definition_xrefs":["Orphanet:1555"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"excluded_subClassOf","term_name":"dermis disorder","termid":"MONDO:0021154"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005497"],"is_obsolete":false,"name":"Beare-Stevenson cutis gyrata syndrome","secondary_identifiers":["DOID:0050660","MEDGEN:377668","MESH:C565129","ICD9:759.89","SCTID:703528008","OMIM:123790","NCIT:C123813","GARD:332","UMLS:C1852406","icd11.foundation:947865461"],"synonyms":[{"name":"BSTVS","type":"related"},{"name":"Beare Stevenson syndrome","type":"related"},{"name":"Beare-Stevenson cutis gyrata syndrome","type":"exact"},{"name":"Beare-Stevenson syndrome","type":"related"},{"name":"cutis gyrata - acanthosis nigricans - craniosynostosis","type":"related"},{"name":"cutis gyrata syndrome of Beare and Stevenson","type":"related"},{"name":"cutis gyrata-acanthosis nigricans-craniosynostosis syndrome","type":"related"}],"termid":"MONDO:0007412","xrefs":{"Monarch":{"xref_id":"0007412"}}}


id: MONDO:0007192
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":"beta-amino acids, renal transport of","secondary_identifiers":["MEDGEN:349470","OMIM:109660","UMLS:C1862289"],"synonyms":[{"name":"AABT","type":"exact"},{"name":"BETA-amino acids, renal TRANSPORT OF","type":"related"},{"name":"taurine renal reabsorption","type":"related"}],"termid":"MONDO:0007192","xrefs":{"Monarch":{"xref_id":"0007192"}}}


id: MONDO:0008764
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Leber congenital amaurosis in which the cause of the disease is a mutation in the GUCY2D gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Leber congenital amaurosis","termid":"MONDO:0018998"},{"relation_name":"is_a","term_name":"GUCY2D-related recessive retinopathy","termid":"MONDO:0100453"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005328","MONDO:0006025"],"is_obsolete":false,"name":"Leber congenital amaurosis 1","secondary_identifiers":["DOID:0110078","UMLS:C2931258","ICD10CM:H35.5","MEDGEN:419026","GARD:635","OMIM:204000"],"synonyms":[{"name":"CRB","type":"related"},{"name":"GUCY2D Leber congenital amaurosis","type":"exact"},{"name":"LCA","type":"related"},{"name":"LCA1","type":"exact"},{"name":"Leber congenital amaurosis 1","type":"exact"},{"name":"Leber congenital amaurosis caused by mutation in GUCY2D","type":"exact"},{"name":"Leber congenital amaurosis type 1","type":"exact"},{"name":"amaurosis congenita of Leber 1","type":"related"},{"name":"amaurosis congenita of Leber I","type":"exact"},{"name":"amaurosis congenita of Leber, type 1","type":"related"},{"name":"retinal blindness, congenital","type":"related"}],"termid":"MONDO:0008764","xrefs":{"Monarch":{"xref_id":"0008764"}}}


id: GO:0010572
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate or frequency of platelet activation. Platelet activation is a series of progressive, overlapping events triggered by exposure of the platelets to subendothelial tissue.","definition_xrefs":["GOC:dph","GOC:sl","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of platelet activation","termid":"GO:0010543"},{"relation_name":"is_a","term_name":"positive regulation of cell activation","termid":"GO:0050867"},{"relation_name":"positively_regulates","term_name":"platelet activation","termid":"GO:0030168"}],"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 platelet activation","termid":"GO:0010572"}


id: PBO:0058169
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4464","termid":"PBO:0058169"}


id: GO:1904023
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of glucose catabolic process to lactate via pyruvate.","definition_xrefs":["GO_REF:0000058","GOC:dph","GOC:TermGenie","PMID:20935145"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of glucose metabolic process","termid":"GO:0010906"},{"relation_name":"is_a","term_name":"regulation of fermentation","termid":"GO:0043465"},{"relation_name":"is_a","term_name":"regulation of carbohydrate catabolic process","termid":"GO:0043470"},{"relation_name":"regulates","term_name":"glucose catabolic process to lactate via pyruvate","termid":"GO:0019661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006091"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0044281","GO:0005975","GO:0008150","GO:0006091"],"is_obsolete":false,"name":"regulation of glucose catabolic process to lactate via pyruvate","synonyms":[{"name":"regulation of glucose fermentation to lactate via pyruvate","type":"exact"},{"name":"regulation of homofermentation","type":"exact"},{"name":"regulation of homofermentative lactate fermentation","type":"exact"},{"name":"regulation of homofermentative pathway","type":"exact"},{"name":"regulation of homolactate fermentation","type":"exact"},{"name":"regulation of homolactic fermentation","type":"exact"}],"termid":"GO:1904023"}


id: GO:0071712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of misfolded proteins transported from the endoplasmic reticulum and targeted to cytoplasmic proteasomes for degradation.","definition_xrefs":["PMID:19520858","PMID:14607247"],"gene_count":0,"genotype_count":0,"name":"obsolete ER-associated misfolded protein catabolic process (obsolete GO:0071712)","synonyms":[{"name":"endoplasmic reticulum-associated misfolded protein catabolism","type":"exact"}],"termid":"GO:0071712"}


id: PBO:0057261
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 487a","termid":"PBO:0057261"}


id: PBO:0029932
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_RNA_level_during_cellular_response_to_non-ionic_osmotic_stress","termid":"PBO:0029932"}


id: MONDO:0013883
data:
  {"annotated_genes":["SJAG_00924"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87956],"is_not":false,"summary":null,"term":"MONDO:0013883"}]},"cv_name":"mondo","definition":"Any congenital myasthenic syndromes with glycosylation defect in which the cause of the disease is a mutation in the DPAGT1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myasthenic syndrome with tubular aggregates","termid":"MONDO:0000182"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00924":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"congenital myasthenic syndrome 13","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:614750","DOID:0110676","UMLS:C3553645","GARD:18452","MEDGEN:766559"],"synonyms":[{"name":"CMS13","type":"exact"},{"name":"CMSTA2","type":"exact"},{"name":"DPAGT1 congenital myasthenic syndromes with glycosylation defect","type":"exact"},{"name":"congenital myasthenic syndrome 13 with tubular aggregates","type":"exact"},{"name":"congenital myasthenic syndrome type 13","type":"exact"},{"name":"congenital myasthenic syndrome with tubular aggregates 2","type":"exact"},{"name":"congenital myasthenic syndromes with glycosylation defect caused by mutation in DPAGT1","type":"exact"},{"name":"myasthenic syndrome, congenital, 13","type":"related"},{"name":"myasthenic syndrome, congenital, 13, with tubular aggregates","type":"exact"},{"name":"myasthenic syndrome, congenital, type 13","type":"exact"},{"name":"myasthenic syndrome, congenital, with tubular aggregates 2","type":"related"}],"termid":"MONDO:0013883","terms_by_termid":{"MONDO:0013883":null},"xrefs":{"Monarch":{"xref_id":"0013883"}}}


id: GO:1903368
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of foraging behavior.","definition_xrefs":["GO_REF:0000058","GOC:mr","GOC:TermGenie","PMID:8677262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of behavior","termid":"GO:0050795"},{"relation_name":"regulates","term_name":"foraging behavior","termid":"GO:0060756"}],"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 foraging behavior","termid":"GO:1903368"}


id: PBO:0060682
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NDRG family member 2","termid":"PBO:0060682"}


id: GO:0016605
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A class of nuclear body; they react against SP100 auto-antibodies (PML, promyelocytic leukemia); cells typically contain 10-30 PML bodies per nucleus; alterations in the localization of PML bodies occurs after viral infection.","definition_xrefs":["GOC:ma","PMID:10944585"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear body","termid":"GO:0016604"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005654"}],"interesting_parent_ids":["GO:0005654","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"PML body","synonyms":[{"name":"ND10","type":"exact"},{"name":"PML NB","type":"exact"},{"name":"PML nuclear body","type":"exact"},{"name":"nuclear dot","type":"related"}],"termid":"GO:0016605"}


id: PBO:0052155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium inwardly rectifying channel subfamily J member 4","termid":"PBO:0052155"}


id: PBO:0039435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin and armadillo repeat containing","termid":"PBO:0039435"}


id: GO:0047291
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cytolipin-H + CMP-N-acetylneuraminate = alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,4-beta-D-glucosylceramide + CMP. Alpha-N-acetylneuraminyl-2,3-beta-D-galactosyl-1,4-beta-D-glucosylceramide is also known as GM3.","definition_xrefs":["MetaCyc:2.4.99.9-RXN","EC:2.4.3.9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sialyltransferase activity","termid":"GO:0008373"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016757","GO:0003824"],"is_obsolete":false,"name":"lactosylceramide alpha-2,3-sialyltransferase activity","secondary_identifiers":["RHEA:18417"],"synonyms":[{"name":"CMP-acetylneuraminate-lactosylceramide-sialyltransferase","type":"broad"},{"name":"GM3 synthase activity","type":"related"},{"name":"cytidine monophosphoacetylneuraminate-lactosylceramide alpha2,3- sialyltransferase activity","type":"related"},{"name":"cytidine monophosphoacetylneuraminate-lactosylceramide sialyltransferase","type":"broad"},{"name":"ganglioside GM3 synthase activity","type":"related"}],"termid":"GO:0047291"}


id: PBO:0076914
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor AP-2 beta","termid":"PBO:0076914"}


id: GO:1904903
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of an ESCRT III complex into its constituent components.","definition_xrefs":["GOC:TermGenie","GO_REF:0000079","GOC:PARL","GOC:pad","PMID:20588296"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ESCRT complex disassembly","termid":"GO:1904896"}],"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":"ESCRT III complex disassembly","termid":"GO:1904903"}


id: PBO:0031623
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_sporulation_frequency","termid":"PBO:0031623"}


id: GO:0050502
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: cis-zeatin + UDP-D-glucose = O-beta-D-glucosyl-cis-zeatin + H+ + UDP.","definition_xrefs":["RHEA:20681","EC:2.4.1.215"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016757","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"cis-zeatin O-beta-D-glucosyltransferase activity","secondary_identifiers":["MetaCyc:RXN-4735","KEGG_REACTION:R07260"],"synonyms":[{"name":"UDP-glucose:cis-zeatin O-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:cis-zeatin O-beta-D-glucosyltransferase activity","type":"related"},{"name":"cis-zeatin O-b-D-glucosyltransferase activity","type":"exact"}],"termid":"GO:0050502"}


id: GO:1990110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process by which a callus is formed at a wound site. A plant callus is a portion of plant tissue that consists of mass of undifferentiated plant cells. It consists primarily of parenchyma cells but possibly contains other cell types as the callus begins to differentiate.","definition_xrefs":["ISBN:0070187517"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multicellular organismal process","termid":"GO:0032501"},{"relation_name":"part_of","term_name":"wound healing","termid":"GO:0042060"}],"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":"callus formation","termid":"GO:1990110"}


id: PBO:0039887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARHGAP42 pseudogene 4","termid":"PBO:0039887"}


id: PR:Q9UTC4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- reg1 gene.","definition_xrefs":["UniProtKB:Q9UTC4","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C227.15 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC227.15","synonyms":[{"name":"Spom972h-reg1","type":"exact"}],"termid":"PR:Q9UTC4"}


id: MONDO:0003836
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, hormonally functioning or non-functioning pituitary gland adenocarcinoma that produces thyrotropin.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TSH producing pituitary tumor","termid":"MONDO:0003837"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malignant thyroid stimulating hormone producing neoplasm of pituitary gland","secondary_identifiers":["DOID:6274","UMLS:C1334627","NCIT:C5965","MEDGEN:277341"],"synonyms":[{"name":"TSH producing pituitary gland carcinoma","type":"exact"},{"name":"TSH-producing pituitary gland carcinoma","type":"exact"},{"name":"malignant TSH producing neoplasm of pituitary","type":"exact"},{"name":"malignant TSH producing neoplasm of pituitary gland","type":"exact"},{"name":"malignant TSH producing neoplasm of the pituitary","type":"exact"},{"name":"malignant TSH producing neoplasm of the pituitary gland","type":"exact"},{"name":"malignant TSH producing pituitary gland neoplasm","type":"exact"},{"name":"malignant TSH producing pituitary gland tumor","type":"exact"},{"name":"malignant TSH producing pituitary gland tumour","type":"exact"},{"name":"malignant TSH producing pituitary neoplasm","type":"exact"},{"name":"malignant TSH producing pituitary tumor","type":"exact"},{"name":"malignant TSH producing pituitary tumour","type":"exact"},{"name":"malignant TSH producing tumor of pituitary","type":"exact"},{"name":"malignant TSH producing tumor of pituitary gland","type":"exact"},{"name":"malignant TSH producing tumor of the pituitary","type":"exact"},{"name":"malignant TSH producing tumor of the pituitary gland","type":"exact"},{"name":"malignant TSH producing tumour of pituitary","type":"exact"},{"name":"malignant TSH producing tumour of pituitary gland","type":"exact"},{"name":"malignant TSH producing tumour of the pituitary","type":"exact"},{"name":"malignant TSH producing tumour of the pituitary gland","type":"exact"},{"name":"malignant TSH secreting neoplasm of pituitary","type":"exact"},{"name":"malignant TSH secreting neoplasm of pituitary gland","type":"exact"},{"name":"malignant TSH secreting neoplasm of the pituitary","type":"exact"},{"name":"malignant TSH secreting neoplasm of the pituitary gland","type":"exact"},{"name":"malignant TSH secreting pituitary gland neoplasm","type":"exact"},{"name":"malignant TSH secreting pituitary gland tumor","type":"exact"},{"name":"malignant TSH secreting pituitary gland tumour","type":"exact"},{"name":"malignant TSH secreting pituitary neoplasm","type":"exact"},{"name":"malignant TSH secreting pituitary tumor","type":"exact"},{"name":"malignant TSH secreting pituitary tumour","type":"exact"},{"name":"malignant TSH secreting tumor of pituitary","type":"exact"},{"name":"malignant TSH secreting tumor of pituitary gland","type":"exact"},{"name":"malignant TSH secreting tumor of the pituitary","type":"exact"},{"name":"malignant TSH secreting tumor of the pituitary gland","type":"exact"},{"name":"malignant TSH secreting tumour of pituitary","type":"exact"},{"name":"malignant TSH secreting tumour of pituitary gland","type":"exact"},{"name":"malignant TSH secreting tumour of the pituitary","type":"exact"},{"name":"malignant TSH secreting tumour of the pituitary gland","type":"exact"},{"name":"malignant pituitary gland thyrotropinoma","type":"exact"},{"name":"malignant pituitary thyrotropinoma","type":"exact"},{"name":"malignant thyroid stimulating hormone producing neoplasm of pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone producing neoplasm of pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone producing neoplasm of the pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone producing neoplasm of the pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone producing pituitary gland neoplasm","type":"exact"},{"name":"malignant thyroid stimulating hormone producing pituitary gland tumor","type":"exact"},{"name":"malignant thyroid stimulating hormone producing pituitary gland tumour","type":"exact"},{"name":"malignant thyroid stimulating hormone producing pituitary neoplasm","type":"exact"},{"name":"malignant thyroid stimulating hormone producing pituitary tumor","type":"exact"},{"name":"malignant thyroid stimulating hormone producing pituitary tumour","type":"exact"},{"name":"malignant thyroid stimulating hormone producing tumor","type":"exact"},{"name":"malignant thyroid stimulating hormone producing tumor of pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone producing tumor of pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone producing tumor of the pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone producing tumor of the pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone producing tumour","type":"exact"},{"name":"malignant thyroid stimulating hormone producing tumour of pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone producing tumour of pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone producing tumour of the pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone producing tumour of the pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting neoplasm of pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting neoplasm of pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting neoplasm of the pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting neoplasm of the pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting pituitary gland neoplasm","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting pituitary gland tumor","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting pituitary gland tumour","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting pituitary neoplasm","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting pituitary tumor","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting pituitary tumour","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting tumor of pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting tumor of pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting tumor of the pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting tumor of the pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting tumour of pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting tumour of pituitary gland","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting tumour of the pituitary","type":"exact"},{"name":"malignant thyroid stimulating hormone secreting tumour of the pituitary gland","type":"exact"},{"name":"malignant thyrotropinoma","type":"exact"},{"name":"malignant thyrotropinoma of pituitary","type":"exact"},{"name":"malignant thyrotropinoma of pituitary gland","type":"exact"},{"name":"malignant thyrotropinoma of the pituitary","type":"exact"},{"name":"malignant thyrotropinoma of the pituitary gland","type":"exact"},{"name":"thyrotropin producing pituitary gland carcinoma","type":"exact"}],"termid":"MONDO:0003836","xrefs":{"Monarch":{"xref_id":"0003836"}}}


id: GO:0042773
data:
  {"annotated_genes":["SJAG_01190","SJAG_00755","SJAG_01763","SJAG_MIT03","SJAG_02646","SJAG_01490","SJAG_01077","SJAG_01355","SJAG_05629","SJAG_07007","SJAG_04152","SJAG_00601","SJAG_MIT04","SJAG_02744","SJAG_07006","SJAG_02504","SJAG_MIT13","SJAG_00080","SJAG_00260","SJAG_02398","SJAG_03490","SJAG_MIT20","SJAG_03920","SJAG_01671","SJAG_00976"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75992,73580,78190,80627,110126,120964,117321,120934,62548,116089,120912],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006123"},{"annotations":[114715],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006120"},{"annotations":[90629,91000,118618,115054],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006121"},{"annotations":[77425,73917,77507,119550,120939,62514,115260,75503,105898,78189],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006122"}]},"cv_name":"biological_process","definition":"The transfer of electrons through a series of electron donors and acceptors, generating energy that is ultimately used for synthesis of ATP.","definition_xrefs":["ISBN:0716731363"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory electron transport chain","termid":"GO:0022904"},{"relation_name":"part_of","term_name":"oxidative phosphorylation","termid":"GO:0006119"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00080":null,"SJAG_00260":null,"SJAG_00601":null,"SJAG_00755":null,"SJAG_00976":null,"SJAG_01077":null,"SJAG_01190":null,"SJAG_01355":null,"SJAG_01490":null,"SJAG_01671":null,"SJAG_01763":null,"SJAG_02398":null,"SJAG_02504":null,"SJAG_02646":null,"SJAG_02744":null,"SJAG_03490":null,"SJAG_03920":null,"SJAG_04152":null,"SJAG_05629":null,"SJAG_07006":null,"SJAG_07007":null,"SJAG_MIT03":null,"SJAG_MIT04":null,"SJAG_MIT13":null,"SJAG_MIT20":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150"],"is_obsolete":false,"name":"ATP synthesis coupled electron transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"termid":"GO:0042773","terms_by_termid":{"GO:0006120":null,"GO:0006121":null,"GO:0006122":null,"GO:0006123":null}}


id: MONDO:0007809
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"keratinopathic ichthyosis","termid":"MONDO:0017266"},{"relation_name":"is_a","term_name":"ichthyosis hystrix","termid":"MONDO:0859383"}],"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":"ichthyosis histrix, Lambert type","secondary_identifiers":["MESH:C536087","GARD:9497","SCTID:254174005","Orphanet:79504","OMIM:146600","ICD10CM:Q80.0","UMLS:C0432311","ICD9:757.39","MEDGEN:98487"],"synonyms":[{"name":"Lambert type ichthyosis","type":"related"},{"name":"ichthyosis hystrix gravior","type":"exact"},{"name":"ichthyosis, Lambert type","type":"exact"},{"name":"porcupine Man","type":"related"}],"termid":"MONDO:0007809","xrefs":{"Monarch":{"xref_id":"0007809"}}}


id: GO:0140368
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A receptor complex that recognizes, binds and sequesters a specific receptor ligand to prevent it from binding to its regular receptor. May be soluble or membrane bound.","definition_xrefs":["PMID:30621730","GOC:bhm","PMID:9168977"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor complex","termid":"GO:0043235"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"decoy receptor complex","synonyms":[{"name":"osteoclastogenesis inhibitory factor","type":"narrow"},{"name":"osteoprotegerin complex","type":"narrow"}],"termid":"GO:0140368"}


id: PBO:0060244
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYC binding protein","termid":"PBO:0060244"}


id: SO:0001641
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that encodes a long, intervening non-coding RNA.","definition_xrefs":["SO:ke","PMID:23463798"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lncRNA_gene","termid":"SO:0002127"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lincRNA_gene","synonyms":[{"name":"lincRNA gene","type":"exact"}],"termid":"SO:0001641"}


id: GO:0004911
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with interleukin-2 and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:jl","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor activity","termid":"GO:0004896"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"interleukin-2 receptor activity","synonyms":[{"name":"IL-2 receptor activity","type":"exact"},{"name":"IL-2R","type":"exact"}],"termid":"GO:0004911"}


id: PBO:0091489
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"accumulation and persistence of Sfr1 foci in rad54delta cells","termid":"PBO:0091489"}


id: FYPO:0006397
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 cytoplasmic microtubules become detached from the nuclear envelope (NE). Normally, some cytoplasmic microtubules are nucleated at the NE and remain attached.","definition_xrefs":["PMID:16481403","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton morphology during vegetative growth","termid":"FYPO:0001418"},{"relation_name":"is_a","term_name":"abnormal cytoplasmic microtubules","termid":"FYPO:0004088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"output_of","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0002399","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"cytoplasmic microtubules detached from nuclear envelope","synonyms":[{"name":"cytoplasmic microtubules detached from nuclear envelope during mitotic cell cycle","type":"related"},{"name":"cytoplasmic microtubules detached from nuclear envelope during vegetative growth","type":"exact"},{"name":"cytoplasmic microtubules dissociated from nuclear envelope","type":"exact"}],"termid":"FYPO:0006397"}


id: _global:finishes
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"X finishes Y if X is part_of Y and X and Y share a 3' or C terminal boundary.","definition_xrefs":["PMID:20226267"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"finishes","termid":"_global:finishes"}


id: GO:1904511
data:
  {"annotated_genes":["SJAG_02761","SJAG_00113","SJAG_01196","SJAG_03052","SJAG_03540","SJAG_02336","SJAG_00851","SJAG_02695","SJAG_00140","SJAG_00723"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[91434,98783,102185,104139,105701,115897,120529],"is_not":false,"summary":null,"term":"GO:1904511"},{"annotations":[99385,97018,105562],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903754"}]},"cv_name":"cellular_component","definition":"Any microtubule plus-end that is part of a cytoplasmic microtubule.","definition_xrefs":["GO_REF:0000064","GOC:TermGenie","PMID:15772152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule plus-end","termid":"GO:0035371"},{"relation_name":"part_of","term_name":"cytoplasmic microtubule","termid":"GO:0005881"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00113":null,"SJAG_00140":null,"SJAG_00723":null,"SJAG_00851":null,"SJAG_01196":null,"SJAG_02336":null,"SJAG_02695":null,"SJAG_02761":null,"SJAG_03052":null,"SJAG_03540":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0015630","GO:0005737"],"is_obsolete":false,"name":"cytoplasmic microtubule plus-end","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"growing microtubule plus end of cytoplasmic microtubule","type":"exact"},{"name":"growing microtubule plus end of non-spindle-associated astral microtubule","type":"narrow"},{"name":"microtubule plus end of cytoplasmic microtubule","type":"exact"},{"name":"microtubule plus end of non-spindle-associated astral microtubule","type":"narrow"},{"name":"microtubule plus-end of cytoplasmic microtubule","type":"exact"},{"name":"microtubule plus-end of non-spindle-associated astral microtubule","type":"narrow"}],"termid":"GO:1904511","terms_by_termid":{"GO:1903754":null,"GO:1904511":null}}


id: FYPO:0004283
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of oxanine DNA N-glycosylase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA N-glycosylase activity","termid":"FYPO:0008216"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0001985","FYPO:0000707","FYPO:0000652","FYPO:0000654"],"is_obsolete":false,"name":"abnormal oxanine DNA N-glycosylase activity","termid":"FYPO:0004283"}


id: GO:0005920
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A septate junction that lacks the regular arrays of electron-dense septae found in pleated septate junctions.","definition_xrefs":["PMID:11700298"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septate junction","termid":"GO:0005918"}],"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":"smooth septate junction","synonyms":[{"name":"zonula continua","type":"exact"}],"termid":"GO:0005920"}


id: GO:0015448
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. This term was not defined before being made obsolete.","definition_xrefs":["GOC:mtg_transport"],"gene_count":0,"genotype_count":0,"name":"obsolete type III protein (virulence-related) secretor activity (obsolete GO:0015448)","synonyms":[{"name":"type III protein (virulence-related) secretor activity","type":"exact"}],"termid":"GO:0015448"}


id: MONDO:0850419
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A diffuse large B-cell lymphoma that is characterized by the expression of CD10, BCL-6, A-myb, and LMO2 genes, BCL-2 translocation, and c-REL amplification.","definition_xrefs":["DOID:0080997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diffuse large B-cell lymphoma","termid":"MONDO:0018905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"diffuse large B-cell lymphoma germinal center B-cell type","secondary_identifiers":["UMLS:C1333295","MEDGEN:234202","NCIT:C36080"],"termid":"MONDO:0850419","xrefs":{"Monarch":{"xref_id":"0850419"}}}


id: MONDO:0044344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An infection that is caused by Schistosoma japonicum.","definition_xrefs":["NCIT:C35001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"schistosomiasis","termid":"MONDO:0015254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schistosoma japonicum infectious disease","secondary_identifiers":["MESH:D012554","SCTID:268058007"],"synonyms":[{"name":"Asiatic schistosomiasis","type":"related"},{"name":"Katamaya fever","type":"related"},{"name":"Katamaya syndrome","type":"related"},{"name":"Katayama disease","type":"related"},{"name":"Schistosoma japonicum caused disease or disorder","type":"exact"},{"name":"Schistosoma japonicum disease or disorder","type":"exact"},{"name":"Schistosoma japonicum infection","type":"exact"},{"name":"schistosomiasis japonicum","type":"related"}],"termid":"MONDO:0044344","xrefs":{"Monarch":{"xref_id":"0044344"}}}


id: PBO:0047624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FIGNL2 divergent transcript","termid":"PBO:0047624"}


id: PBO:0073522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 domain binding protein 5","termid":"PBO:0073522"}


id: PBO:0058495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR5689 host gene","termid":"PBO:0058495"}


id: GO:1990212
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism activates, maintains or increases the frequency, rate or extent of the ethylene levels in the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:16167902","GOC:ml"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by symbiont of ethylene levels in host (obsolete GO:1990212)","termid":"GO:1990212"}


id: PBO:0079217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thiosulfate sulfurtransferase like domain containing 2","termid":"PBO:0079217"}


id: GO:0061099
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of protein tyrosine kinase activity.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein kinase activity","termid":"GO:0006469"},{"relation_name":"is_a","term_name":"negative regulation of peptidyl-tyrosine phosphorylation","termid":"GO:0050732"},{"relation_name":"is_a","term_name":"regulation of protein tyrosine kinase activity","termid":"GO:0061097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein tyrosine kinase activity","termid":"GO:0061099"}


id: GO:2000465
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of glycogen (starch) synthase activity.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transferase activity","termid":"GO:0051338"}],"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 glycogen (starch) synthase activity","synonyms":[{"name":"regulation of UDP-glucose-glycogen glucosyltransferase activity","type":"exact"},{"name":"regulation of UDP-glucose:glycogen 4-alpha-D-glucosyltransferase activity","type":"exact"},{"name":"regulation of UDP-glycogen synthase activity","type":"exact"},{"name":"regulation of UDPG-glycogen synthetase activity","type":"exact"},{"name":"regulation of UDPG-glycogen transglucosylase activity","type":"exact"},{"name":"regulation of UDPglucose:glycogen 4-alpha-D-glucosyltransferase activity","type":"exact"},{"name":"regulation of glycogen (starch) synthetase activity","type":"exact"},{"name":"regulation of uridine diphosphoglucose-glycogen glucosyltransferase activity","type":"exact"}],"termid":"GO:2000465"}


id: PBO:0083873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein required for both the G1/S and G2/M phase transitions; modular substrate specificity factor which associates with core SCF (Cdc53p, Skp1p and Hrt1p/Rbx1p) to form the SCFCdc4 complex; SCFCdc4 acts as a ubiquitin-protein ligase directing ubiquitination of cyclin-dependent kinase (CDK) phosphorylated substrates, such as: Sic1p, Far1p, Cdc6p, Clb6p, and Cln3p","termid":"PBO:0083873"}


id: PBO:0081342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 142","termid":"PBO:0081342"}


id: MONDO:0008322
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pseudoachondroplasia is characterized by severe growth deficiency and deformations such as bow legs and hyperlordosis.","definition_xrefs":["Orphanet:750"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"},{"relation_name":"is_a","term_name":"COMP-related skeletal dysplasia","termid":"MONDO:0100593"}],"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":"pseudoachondroplasia","secondary_identifiers":["DOID:0080047","MEDGEN:98378","OMIM:177170","GARD:4540","icd11.foundation:1192649257","MESH:C535819","ICD9:756.9","NCIT:C118635","NANDO:2201018","NORD:1625","UMLS:C0410538","SCTID:22567005"],"synonyms":[{"name":"PSACH","type":"related"},{"name":"Pseudoachondroplastic dysplasia","type":"exact"},{"name":"Pseudoachondroplastic spondyloepiphyseal dysplasia","type":"exact"},{"name":"Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome","type":"related"},{"name":"pseudoachondroplasia","type":"exact"},{"name":"pseudoachondroplastic dysplasia","type":"exact"},{"name":"spondyloepiphyseal dysplasia, PSEUDOACHONDROPLASTIC","type":"exact"},{"name":"spondyloepiphyseal dysplasia, Pseudoachondroplastic","type":"related"}],"termid":"MONDO:0008322","xrefs":{"Monarch":{"xref_id":"0008322"}}}


id: GO:0010130
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of ethylbenzene, a benzene derivative with an ethyl group attached to the ring, which occurs in the absence of oxygen.","definition_xrefs":["GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ethylbenzene catabolic process","termid":"GO:0018915"}],"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":"anaerobic ethylbenzene catabolic process","secondary_identifiers":["UM-BBD_pathwayID:ethb","MetaCyc:PWY-481"],"synonyms":[{"name":"anaerobic ethylbenzene breakdown","type":"exact"},{"name":"anaerobic ethylbenzene catabolism","type":"exact"},{"name":"anaerobic ethylbenzene degradation","type":"exact"}],"termid":"GO:0010130"}


id: PBO:0031044
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_concentration_of_substance_in_growth_medium","termid":"PBO:0031044"}


id: PBO:0087829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFIIIB B-related factor; one of three subunits of RNA polymerase III transcription initiation factor TFIIIB, binds TFIIIC and TBP and recruits RNA pol III to promoters, amino-terminal half is homologous to TFIIB; mutations in human homolog are associated with autosomal recessive cerebellar-facial-dental syndrome","termid":"PBO:0087829"}


id: MONDO:0008800
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microphthalmia with limb anomalies, also known as ophthalmo-acromelic syndrome (OAS), is a rare developmental disorder characterized by bilateral microphthalmia or anophthalmia, synostosis, syndactyly, oligodactyly and/or polydactyly.","definition_xrefs":["Orphanet:1106"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"microphthalmia with limb anomalies","secondary_identifiers":["OMIM:206920","GARD:722","UMLS:C0599973","DOID:0060861","MEDGEN:154638","ICD9:755.8","SCTID:703403003","MESH:C537769"],"synonyms":[{"name":"MLA","type":"exact"},{"name":"OAS","type":"exact"},{"name":"Ophthalmoacromelic syndrome","type":"exact"},{"name":"Waardenburg anophthalmia syndrome","type":"exact"},{"name":"anophthalmia Waardenburg syndrome","type":"related"},{"name":"anophthalmia-syndactyly","type":"related"},{"name":"anophthalmia-syndactyly syndrome","type":"exact"},{"name":"anophthalmos with limb anomalies","type":"related"},{"name":"anophthalmos-syndactyly","type":"related"},{"name":"microphthalmia with limb anomalies","type":"exact"},{"name":"ophthalmoacromelic syndrome","type":"exact"}],"termid":"MONDO:0008800","xrefs":{"Monarch":{"xref_id":"0008800"}}}


id: GO:0044692
data:
  {"annotated_genes":["SJAG_04682","SJAG_00686"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91517,106752],"is_not":false,"summary":null,"term":"GO:0044692"}]},"cv_name":"molecular_function","definition":"Binds to and increases the activity of an exoribonuclease.","definition_xrefs":["GOC:rb","PMID:22570495"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribonuclease activator activity","termid":"GO:0170054"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00686":null,"SJAG_04682":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0140677","GO:0003674","GO:0030234","GO:0098772"],"is_obsolete":false,"name":"exoribonuclease activator activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0044692","terms_by_termid":{"GO:0044692":null}}


id: GO:0102001
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-isoleucine + 2 O2 + 2 NADPH(4-) + 2 H+ = (E)-2-methylbutanal oxime + 2 NADP(3-) + carbon dioxide + 3 H2O.","definition_xrefs":["EC:1.14.14.39"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"isoleucine N-monooxygenase (oxime forming) activity","secondary_identifiers":["MetaCyc:1.14.13.117-RXN","RHEA:28602"],"termid":"GO:0102001"}


id: PBO:0027913
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_level_during_cellular_response_to_ionizing_radiation","termid":"PBO:0027913"}


id: GO:0016231
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of terminal non-reducing N-acetyl-D-glucosamine residues in N-acetyl-beta-D-glucosaminides.","definition_xrefs":["PMID:37590576","PMID:29143882"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-N-acetylhexosaminidase activity","termid":"GO:0004563"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"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:0016798","GO:0003824","GO:0016787"],"is_obsolete":false,"name":"beta-N-acetylglucosaminidase activity","termid":"GO:0016231"}


id: MONDO:0009508
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":"Lambotte syndrome","secondary_identifiers":["MEDGEN:343380","UMLS:C1855550","MESH:C537549","OMIM:245552"],"synonyms":[{"name":"Lambotte syndrome","type":"exact"},{"name":"microcephaly, holoprosencephaly, and intrauterine Growth retardation","type":"related"}],"termid":"MONDO:0009508","xrefs":{"Monarch":{"xref_id":"0009508"}}}


id: PBO:0073893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 12 member 9","termid":"PBO:0073893"}


id: SO:1000158
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An intrachromosomal transposition whereby the segment between the first two breaks listed is removed and inserted at the third break; the insertion is in cytologically inverted orientation with respect to its flanking segments.","definition_xrefs":["FB:reference_manual"],"direct_ancestors":[{"relation_name":"has_part","term_name":"inversion","termid":"SO:1000036"},{"relation_name":"is_a","term_name":"inversion_cum_translocation","termid":"SO:1000148"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inverted_intrachromosomal_transposition","synonyms":[{"name":"(Drosophila)iTp","type":"related"},{"name":"inverted intrachromosomal transposition","type":"exact"}],"termid":"SO:1000158"}


id: GO:0090560
data:
  {"annotated_genes":["SJAG_01058","SJAG_04085"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[67997,69744],"is_not":false,"summary":null,"term":"GO:0090560"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction S-adenosyl-L-methionine + L-histidine-[translation elongation factor 2] = S-methyl-5-thioadenosine + 2-[(3S)-3-amino-3-carboxypropyl]-L-histidine-[translation elongation factor 2].","definition_xrefs":["RHEA:36783","GOC:pde","PMID:15485916"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring alkyl or aryl (other than methyl) groups","termid":"GO:0016765"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01058":null,"SJAG_04085":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016765"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016765","GO:0016740"],"is_obsolete":false,"name":"2-(3-amino-3-carboxypropyl)histidine synthase activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["Reactome:R-HSA-5358494","MetaCyc:RXN-11371","EC:2.5.1.108"],"termid":"GO:0090560","terms_by_termid":{"GO:0090560":null}}


id: PR:P0CT63
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rps3002 gene.","definition_xrefs":["UniProtKB:P0CT63","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":"40S ribosomal protein S30-B (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19G7.03c","synonyms":[{"name":"Spom972h-rps3002","type":"exact"}],"termid":"PR:P0CT63"}


id: GO:1904502
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of lipophagy.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:25383539","GOC:dph","GOC:autophagy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of macroautophagy","termid":"GO:0016241"},{"relation_name":"regulates","term_name":"lipophagy","termid":"GO:0061724"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006914"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006914","GO:0008150"],"is_obsolete":false,"name":"regulation of lipophagy","termid":"GO:1904502"}


id: PBO:0081661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF584 divergent transcript","termid":"PBO:0081661"}


id: GO:1900312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of maltohexaose transport.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hexasaccharide transport","termid":"GO:1900297"},{"relation_name":"regulates","term_name":"maltohexaose transport","termid":"GO:2001103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of maltohexaose transport","termid":"GO:1900312"}


id: PR:Q9URT4
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ams2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9URT4"],"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":"CENP-A multicopy suppressor protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC290.04","synonyms":[{"name":"Spom972h-ams2","type":"exact"}],"termid":"PR:Q9URT4"}


id: PBO:0049756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HCCS divergent transcript","termid":"PBO:0049756"}


id: MONDO:0022645
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":"cardioencephalomyopathy","termid":"MONDO:0022645","xrefs":{"Monarch":{"xref_id":"0022645"}}}


id: GO:0097076
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that possesses protein kinase activity and activates the I-kappa B kinase complex (IKK) and mitogen-activated protein (MAP) kinases in response to TRAF6 signaling. It comprises the catalytic subunit TAK1 complexed to the regulatory subunits, termed TABs (TAK1-binding subunits).","definition_xrefs":["PMID:16410796","PMID:17496917","GOC:cna","PMID:18021073"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase complex","termid":"GO:1902911"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"transforming growth factor beta activated kinase 1 complex","synonyms":[{"name":"TAK1 kinase complex","type":"exact"}],"termid":"GO:0097076"}


id: MONDO:0044627
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinal disorder","termid":"MONDO:0005283"},{"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:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"acute macular neuroretinopathy","secondary_identifiers":["GARD:22000","icd11.foundation:1081365759","MEDGEN:1678428","Orphanet:488239","UMLS:C5200735"],"synonyms":[{"name":"AMNR","type":"exact"}],"termid":"MONDO:0044627","xrefs":{"Monarch":{"xref_id":"0044627"}}}


id: GO:0052723
data:
  {"annotated_genes":["SJAG_00244"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58721],"is_not":false,"summary":null,"term":"GO:0052723"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 1D-myo-inositol hexakisphosphate + ATP = 1-diphospho-1D-myo-inositol 2,3,4,5,6-pentakisphosphate + ADP.","definition_xrefs":["RHEA:37459","PMID:18981179"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol hexakisphosphate kinase activity","termid":"GO:0000828"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00244":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016301","GO:0016740"],"is_obsolete":false,"name":"inositol hexakisphosphate 1-kinase activity","references_by_uniquename":{"GO_REF:0000117":null},"secondary_identifiers":["MetaCyc:RXN-10972","KEGG_REACTION:R05799"],"termid":"GO:0052723","terms_by_termid":{"GO:0052723":null}}


id: PBO:0053214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galectin 9D, pseudogene","termid":"PBO:0053214"}


id: GO:0019571
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of D-arabinose, the D-enantiomer of arabino-pentose.","definition_xrefs":["GOC:mah","GOC:jsg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arabinose catabolic process","termid":"GO:0019568"},{"relation_name":"is_a","term_name":"D-arabinose metabolic process","termid":"GO:0046372"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0005975"],"is_obsolete":false,"name":"D-arabinose catabolic process","synonyms":[{"name":"D-arabinose breakdown","type":"exact"},{"name":"D-arabinose catabolism","type":"exact"},{"name":"D-arabinose degradation","type":"exact"}],"termid":"GO:0019571"}


id: PBO:0069615
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 892, pseudogene","termid":"PBO:0069615"}


id: PR:Q9P7N5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cell division cycle protein 123 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR15323:SF6","PRO:DNx","OMA:SCHPO00652"],"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":"cell division cycle protein 123 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAP27G11.03","secondary_identifiers":["UniProtKB:Q9P7N5"],"synonyms":[{"name":"Spom972h-CDC123","type":"exact"}],"termid":"PR:Q9P7N5"}


id: MOD:01071
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes a diphenylmethyl group for a hydrogen atom.","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diphenylmethyl modified residue","synonyms":[{"name":"Dpm","type":"exact"}],"termid":"MOD:01071"}


id: GO:0018630
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 3-hydroxytoluene + NADH + O2 = NAD+ + OH- + 3-hydroxybenzyl alcohol.","definition_xrefs":["UM-BBD_reactionID:r0081"],"gene_count":0,"genotype_count":0,"name":"obsolete 3,5-xylenol methylhydroxylase activity (obsolete GO:0018630)","termid":"GO:0018630"}


id: PBO:0080553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WBP1L pseudogene 12","termid":"PBO:0080553"}


id: MONDO:0018030
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tetrasomy 9p is a rare autosomal anomaly characterized by pre- and postnatal growth retardation, psychomotor delay, mild to moderate intellectual disability, hypotonia, microcephaly, dysmorphic features (ocular hypertelorism, low-set, malformed ears, bulbous/beaked nose, microretrognathia, enophthalmos/micropthalmia, epicanthus, strabismus), cleft lip/palate, skeletal abnormalities (hypoplastic nails/distal phalanges, short stature, short neck, contractures), congenital heart defects, renal and urogenital malformations (renal hypoplasia, genital hypoplasia, cryptorchidism).","definition_xrefs":["Orphanet:3310"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal duplication of the short arm of chromosome 9","termid":"MONDO:0700043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetrasomy 9p","secondary_identifiers":["MEDGEN:162876","icd11.foundation:1426428869","MESH:C538027","SCTID:715530004","GARD:42","NORD:964","UMLS:C0795832"],"synonyms":[{"name":"Chromosome 9, Tetrasomy 9p","type":"exact"},{"name":"Isochromosome 9p","type":"exact"},{"name":"Mosaic tetrasomy 9p","type":"related"},{"name":"chromosome 9p tetrasomy","type":"related"},{"name":"tetrasomy of short arm of chromosome 9","type":"related"},{"name":"tetrasomy type 9p","type":"exact"}],"termid":"MONDO:0018030","xrefs":{"Monarch":{"xref_id":"0018030"}}}


id: PBO:0052479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch domain containing 7A","termid":"PBO:0052479"}


id: MONDO:0004958
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma arising from the oral cavity. It affects predominantly adults in their fifth and sixth decades of life and is associated with alcohol and tobacco use. Human papillomavirus is present in approximately half of the cases. It is characterized by a tendency to metastasize early to the lymph nodes. When the tumor is small, patients are often asymptomatic. Physical examination may reveal erythematous or white lesions or plaques. The majority of patients present with signs and symptoms of locally advanced disease including mucosal ulceration, pain, difficulty with speaking, chewing, and swallowing, bleeding, weight loss, and neck swelling. Patients may also present with swollen neck lymph nodes without any symptoms from the oropharyngeal tumor. The most significant prognostic factors are the size of the tumor and the lymph nodes status.","definition_xrefs":["NCIT:C4833"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lip and oral cavity squamous cell carcinoma","termid":"MONDO:0044710"},{"relation_name":"is_a","term_name":"oral cavity carcinoma","termid":"MONDO:0044925"}],"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":"oral cavity squamous cell carcinoma","secondary_identifiers":["MEDGEN:108436","ONCOTREE:OCSC","Orphanet:502363","DOID:0050866","GARD:17932","SCTID:307502000","UMLS:C0585362","EFO:0000199"],"synonyms":[{"name":"OCSC","type":"related"},{"name":"mouth scc","type":"exact"},{"name":"mouth squamous cell carcinoma","type":"exact"},{"name":"oral cavity scc","type":"exact"},{"name":"oral cavity squamous cell cancer","type":"exact"},{"name":"oral cavity squamous cell carcinoma","type":"exact"},{"name":"oral squamous cell carcinoma","type":"related"},{"name":"scc of mouth","type":"exact"},{"name":"scc of oral cavity","type":"exact"},{"name":"scc of the mouth","type":"exact"},{"name":"scc of the oral cavity","type":"exact"},{"name":"squamous cell carcinoma of mouth","type":"exact"},{"name":"squamous cell carcinoma of oral cavity","type":"exact"},{"name":"squamous cell carcinoma of the mouth","type":"exact"},{"name":"squamous cell carcinoma of the oral cavity","type":"exact"}],"termid":"MONDO:0004958","xrefs":{"Monarch":{"xref_id":"0004958"}}}


id: GO:0045574
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of sterigmatocystin, a carcinogenic mycotoxin produced in high yields by strains of the common molds.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"toxin catabolic process","termid":"GO:0009407"},{"relation_name":"is_a","term_name":"sterigmatocystin metabolic process","termid":"GO:0045460"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0098754"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0098754","GO:0019748","GO:0008150"],"is_obsolete":false,"name":"sterigmatocystin catabolic process","synonyms":[{"name":"sterigmatocystin breakdown","type":"exact"},{"name":"sterigmatocystin catabolism","type":"exact"},{"name":"sterigmatocystin degradation","type":"exact"}],"termid":"GO:0045574"}


id: PBO:0071160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23","termid":"PBO:0071160"}


id: PBO:0001427
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bowen Conradi syndrome","termid":"PBO:0001427"}


id: PBO:0085578
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in 3' mRNA processing; interacts with Ref2p; APCC(Cdh1) substrate; potential Cdc28p substrate","termid":"PBO:0085578"}


id: GO:0009051
data:
  {"annotated_genes":["SJAG_03852","SJAG_00633","SJAG_02696","SJAG_02297","SJAG_01824"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74800,82111,98705,98795,100000],"is_not":false,"summary":null,"term":"GO:0009051"}]},"cv_name":"biological_process","definition":"The branch of the pentose-phosphate shunt which involves the oxidation of glucose 6-P and produces ribulose 5-P, reduced NADP+ and carbon dioxide (CO2).","definition_xrefs":["MetaCyc:OXIDATIVEPENT-PWY","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"NADPH regeneration","termid":"GO:0006740"},{"relation_name":"is_a","term_name":"carbohydrate derivative metabolic process","termid":"GO:1901135"},{"relation_name":"part_of","term_name":"pentose-phosphate shunt","termid":"GO:0006098"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00633":null,"SJAG_01824":null,"SJAG_02297":null,"SJAG_02696":null,"SJAG_03852":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"part_of","termid":"GO:0044281"},{"rel_name":"part_of","termid":"GO:0055086"},{"rel_name":"part_of","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150","GO:0006091"],"is_obsolete":false,"name":"pentose-phosphate shunt, oxidative branch","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"oxidative branch, pentose pathway","type":"exact"},{"name":"oxidative pentose phosphate pathway","type":"exact"},{"name":"pentose phosphate pathway, oxidative branch","type":"exact"},{"name":"pentose phosphate shunt, oxidative branch","type":"exact"},{"name":"pentose-phosphate pathway, oxidative branch","type":"exact"}],"termid":"GO:0009051","terms_by_termid":{"GO:0009051":null}}


id: GO:0034574
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: didemethylisoproturon + H2O = 4'-(2-hydroxyisopropyl)phenylurea + 2 H+ + 2 e-.","definition_xrefs":["UM-BBD_reactionID:r0899"],"gene_count":0,"genotype_count":0,"name":"obsolete didemethylisoproturon dehydrogenase activity (obsolete GO:0034574)","termid":"GO:0034574"}


id: PBO:0068966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 210, pseudogene","termid":"PBO:0068966"}


id: GO:0014910
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of smooth muscle cell migration.","definition_xrefs":["CL:0000192","GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell migration","termid":"GO:0030334"},{"relation_name":"regulates","term_name":"smooth muscle cell migration","termid":"GO:0014909"}],"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 smooth muscle cell migration","termid":"GO:0014910"}


id: MONDO:0033486
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"leukodystrophy, hypomyelinating, 14","secondary_identifiers":["GARD:16266","MEDGEN:1635255","UMLS:C4693535","OMIM:617899","DOID:0080296"],"synonyms":[{"name":"HLD14","type":"related"},{"name":"hypomyelinating leukodystrophy 14","type":"related"},{"name":"leukodystrophy, hypomyelinating, 14","type":"exact"}],"termid":"MONDO:0033486","xrefs":{"Monarch":{"xref_id":"0033486"}}}


id: MONDO:0700178
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oral squamous cell carcinoma that occurs in a cat.","definition_xrefs":["NCIT:C132824"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carcinoma, non-human animal","termid":"MONDO:0700101"},{"relation_name":"is_a","term_name":"feline neoplasm","termid":"MONDO:0700175"},{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"},{"relation_name":"is_a","term_name":"mouth disorder, non-human animal","termid":"MONDO:1011333"},{"relation_name":"is_a","term_name":"otorhinolaryngologic disease, non-human animal","termid":"MONDO:1011342"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"feline oral squamous cell carcinoma","termid":"MONDO:0700178","xrefs":{"Monarch":{"xref_id":"0700178"}}}


id: PATO:0001538
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A solubility quality inhering in a substance by virtue of the bearer's inability of a substance to dissolve in a liquid.","definition_xrefs":["edp:edp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"solubility","termid":"PATO:0001536"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insoluble in","synonyms":[{"name":"insoluble","type":"exact"}],"termid":"PATO:0001538"}


id: MONDO:0001614
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lymph node cancer","termid":"MONDO:0001082"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0004992"],"is_obsolete":false,"name":"intra-abdominal lymph node mast cell malignancy","secondary_identifiers":["DOID:13005","ICD9:202.63","SCTID:188664008","MEDGEN:509471","UMLS:C0153844"],"synonyms":[{"name":"malignant mast cell tumors involving intra-abdominal lymph nodes","type":"exact"},{"name":"malignant mast cell tumours involving intra-abdominal lymph nodes","type":"exact"},{"name":"mast cell malignancy of intra-abdominal lymph nodes","type":"exact"}],"termid":"MONDO:0001614","xrefs":{"Monarch":{"xref_id":"0001614"}}}


id: PBO:0111937
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulator of Heat Sensitivity","termid":"PBO:0111937"}


id: GO:0003042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is triggered by carotid body-vasomotor excitation and results in a decrease in the diameter of an artery during the chemoreceptor response to decreased blood pressure.","definition_xrefs":["ISBN:0323031951"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vasoconstriction of artery involved in chemoreceptor response to lowering of systemic arterial blood pressure","termid":"GO:0002012"},{"relation_name":"part_of","term_name":"regulation of systemic arterial blood pressure by carotid body chemoreceptor signaling","termid":"GO:0003027"}],"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":"vasoconstriction of artery involved in carotid body chemoreceptor response to lowering of systemic arterial blood pressure","synonyms":[{"name":"vasoconstriction of artery during carotid body chemoreceptor response to lowering of systemic arterial blood pressure","type":"related"}],"termid":"GO:0003042"}


id: PBO:0070544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 10","termid":"PBO:0070544"}


id: PBO:0029293
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_nucleus_during_meiosis","termid":"PBO:0029293"}


id: PBO:0040155
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acid sensing ion channel subunit 1","termid":"PBO:0040155"}


id: PBO:0034306
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-preys_on","termid":"PBO:0034306"}


id: GO:0061132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The close range interaction of two or more cells or tissues that causes the cells of the gut to change their fates and specify the development of the pancreas.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organ induction","termid":"GO:0001759"},{"relation_name":"is_a","term_name":"regulation of morphogenesis of a branching structure","termid":"GO:0060688"},{"relation_name":"is_a","term_name":"positive regulation of epithelial tube formation","termid":"GO:1905278"},{"relation_name":"positively_regulates","term_name":"pancreas field specification","termid":"GO:0061131"}],"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":"pancreas induction","termid":"GO:0061132"}


id: GO:0106024
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate of onset of pupariation.","definition_xrefs":["PMID:26510564"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of post-embryonic development","termid":"GO:0048581"},{"relation_name":"is_a","term_name":"regulation of pupariation","termid":"GO:0106023"},{"relation_name":"negatively_regulates","term_name":"pupariation","termid":"GO:0035073"}],"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 pupariation","termid":"GO:0106024"}


id: GO:0052831
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: inositol-1,3,4,6-tetrakisphosphate + H2O = inositol-3,4,6-trisphosphate + phosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol tetrakisphosphate phosphatase activity","termid":"GO:0052743"}],"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:0016788"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0003674","GO:0016788"],"is_obsolete":false,"name":"inositol-1,3,4,6-tetrakisphosphate 1-phosphatase activity","secondary_identifiers":["Reactome:R-HSA-1855159"],"termid":"GO:0052831"}


id: PBO:0076546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TatD DNase domain containing 1","termid":"PBO:0076546"}


id: MONDO:0043073
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":"Zadik-Barak-Levin syndrome","secondary_identifiers":["MESH:C536721","UMLS:C2931298","MEDGEN:444023"],"synonyms":[{"name":"dermoid cysts, hypothyroidism, cleft palate and hypodontia","type":"related"},{"name":"dermoid cysts, hypothyroidism, cleft palate, and hypodontia","type":"related"}],"termid":"MONDO:0043073","xrefs":{"Monarch":{"xref_id":"0043073"}}}


id: FYPO:0007722
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of nucleosome-dependent ATPase activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nucleosome-dependent ATPase activity","termid":"FYPO:0005519"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000661","FYPO:0000652","FYPO:0000654","FYPO:0001985"],"is_obsolete":false,"name":"decreased nucleosome-dependent ATPase activity","synonyms":[{"name":"reduced nucleosome-dependent ATPase activity","type":"exact"}],"termid":"FYPO:0007722"}


id: PBO:0080831
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"YAP1 pseudogene 2","termid":"PBO:0080831"}


id: PBO:0048852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GNRHR2 pseudogene 1","termid":"PBO:0048852"}


id: PBO:0054751
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 2161","termid":"PBO:0054751"}


id: GO:0033954
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of the 1,3-alpha-L-galactosidic linkages of neoagaro-oligosaccharides that are smaller than a hexamer, yielding 3,6-anhydro-L-galactose and D-galactose.","definition_xrefs":["EC:3.2.1.159"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0016798","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"alpha-neoagaro-oligosaccharide hydrolase activity","secondary_identifiers":["MetaCyc:3.2.1.159-RXN"],"synonyms":[{"name":"alpha-NAOS hydrolase activity","type":"related"},{"name":"alpha-neoagaro-oligosaccharide 3-glycohydrolase activity","type":"related"},{"name":"alpha-neoagarooligosaccharide hydrolase activity","type":"related"}],"termid":"GO:0033954"}


id: PBO:0054084
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 1435","termid":"PBO:0054084"}


id: PBO:0067479
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 612, pseudogene","termid":"PBO:0067479"}


id: MONDO:0018518
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete adenocarcinoma of the anal canal (obsolete MONDO:0018518)","termid":"MONDO:0018518","xrefs":{"Monarch":{"xref_id":"0018518"}}}


id: FYPO:0005794
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a cell is bent along the long axis when the cell undergoes transition from G0 phase to G1. In a bent cell, the long axis has one or more angles, rather than following a straight line.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bent cell","termid":"FYPO:0005793"}],"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:0001985","FYPO:0000002","FYPO:0000005"],"is_obsolete":false,"name":"bent cell during G0 to G1 transition","synonyms":[{"name":"bent cell during cell cycle re-entry at G1","type":"exact"},{"name":"bent cell during cell quiescence to G1 transition","type":"exact"},{"name":"bent cell during exit from cell quiescence into G1","type":"exact"},{"name":"bent cell during quiescence to G1 transition","type":"exact"},{"name":"bent cell during recovery from quiescence following G1 arrest","type":"exact"},{"name":"bent cell during recovery from quiescence into G1","type":"exact"}],"termid":"FYPO:0005794"}


id: PBO:0030377
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_diamide","termid":"PBO:0030377"}


id: PBO:0058411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4780","termid":"PBO:0058411"}


id: SO:0002216
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A promoter element with consensus sequence [5'-TCG(G/C)(A/T)xxTTxAA], bound by the transcription factor Pho7.","definition_xrefs":["PMID:28811350"],"direct_ancestors":[{"relation_name":"is_a","term_name":"promoter_element","termid":"SO:0001659"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pho7_binding_site","synonyms":[{"name":"Pho7 binding site","type":"exact"}],"termid":"SO:0002216"}


id: PBO:0046660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"espin","termid":"PBO:0046660"}


id: SO:0000076
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An attribute to describe a gene when the 3' region overlaps with another gene's 5' region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"overlapping","termid":"SO:0000068"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_five_prime_overlap","synonyms":[{"name":"5' 3' overlap","type":"exact"},{"name":"three prime five prime overlap","type":"exact"}],"termid":"SO:0000076"}


id: PBO:0112994
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adenylate kinase, required for purine metabolism; controls ATP homeostasis; localized to the cytoplasm and the mitochondria; lacks cleavable signal sequence; protein abundance increases in response to DNA replication stress; mutations affecting Adk1p catalytic activity deregulate expression of phosphate utilization genes PHO5 and PHO84; human homolog AK1 can complement yeast adk1 mutant","termid":"PBO:0112994"}


id: PBO:0003576
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial GIDA family tRNA uridine 5-carboxymethylaminomethyl modification enzyme (predicted)","termid":"PBO:0003576"}


id: GO:0009080
data:
  {"annotated_genes":["SJAG_04145","SJAG_00944"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[70209],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042853"},{"annotations":[74829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006574"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of any amino acid that requires pyruvate for its synthesis, e.g. alanine.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate family amino acid metabolic process","termid":"GO:0009078"},{"relation_name":"is_a","term_name":"L-amino acid catabolic process","termid":"GO:0170035"},{"relation_name":"is_a","term_name":"proteinogenic amino acid catabolic process","termid":"GO:0170040"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00944":null,"SJAG_04145":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0044281"],"is_obsolete":false,"name":"pyruvate family amino acid catabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null},"synonyms":[{"name":"pyruvate family amino acid breakdown","type":"exact"},{"name":"pyruvate family amino acid catabolism","type":"exact"},{"name":"pyruvate family amino acid degradation","type":"exact"}],"termid":"GO:0009080","terms_by_termid":{"GO:0006574":null,"GO:0042853":null}}


id: PBO:0031038
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_Golgi_organization","termid":"PBO:0031038"}


id: PBO:0028762
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cytoplasmic_translational_initiation","termid":"PBO:0028762"}


id: MONDO:0004133
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An epithelial neoplasm of the anterior pituitary gland in which the neoplastic cells stain positive with acidic and basic dyes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pituitary gland adenoma","termid":"MONDO:0006373"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pituitary gland mixed eosinophil-basophil adenoma","secondary_identifiers":["UMLS:C0334312","ICDO:8281/0","DOID:7179","MEDGEN:87215","NCIT:C4148"],"synonyms":[{"name":"mixed acidophil-basophil adenoma","type":"exact"},{"name":"mixed acidophil-basophil adenoma (morphologic abnormality)","type":"exact"},{"name":"mixed eosinophil-basophil adenoma","type":"related"},{"name":"pituitary gland mixed acidophil-basophil adenoma","type":"exact"}],"termid":"MONDO:0004133","xrefs":{"Monarch":{"xref_id":"0004133"}}}


id: PBO:0029202
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_micafungin","termid":"PBO:0029202"}


id: GO:0046255
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of 2,4,6-trinitrotoluene, 1-methyl-2,4,6-trinitrobenzene.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete 2,4,6-trinitrotoluene biosynthetic process (obsolete GO:0046255)","synonyms":[{"name":"2,4,6-trinitrotoluene anabolism","type":"exact"},{"name":"2,4,6-trinitrotoluene biosynthesis","type":"exact"},{"name":"2,4,6-trinitrotoluene biosynthetic process","type":"exact"},{"name":"2,4,6-trinitrotoluene formation","type":"exact"},{"name":"2,4,6-trinitrotoluene synthesis","type":"exact"}],"termid":"GO:0046255"}


id: PBO:0060775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B8 pseudogene 1","termid":"PBO:0060775"}


id: PBO:0088653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome base subcomplex ATPase subunit Rpt4","termid":"PBO:0088653"}


id: PBO:0075987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STAU2 pseudogene 1","termid":"PBO:0075987"}


id: GO:0051315
data:
  {"annotated_genes":["SJAG_03989","SJAG_05319","SJAG_02624","SJAG_04623","SJAG_00646","SJAG_00302","SJAG_00794","SJAG_00418","SJAG_00918","SJAG_01837","SJAG_01297","SJAG_02761","SJAG_05266","SJAG_01082","SJAG_04412","SJAG_02045","SJAG_05290","SJAG_01805","SJAG_01775","SJAG_03217","SJAG_04884","SJAG_05220","SJAG_00930","SJAG_04280","SJAG_02286","SJAG_04040","SJAG_01370","SJAG_00335","SJAG_01601","SJAG_02731","SJAG_03048","SJAG_00082","SJAG_03327","SJAG_03220","SJAG_03540","SJAG_02451","SJAG_02336","SJAG_03126","SJAG_04140","SJAG_00768","SJAG_01211","SJAG_04076","SJAG_02346","SJAG_04259","SJAG_03437","SJAG_00207","SJAG_01278","SJAG_00678","SJAG_03543","SJAG_01371","SJAG_01224"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[66733,70180,73754,74680,77460,89569,89817,91854,92805,93197,97376,99719,102198,107302,112162,112208,113538,118387],"is_not":false,"summary":null,"term":"GO:0051315"},{"annotations":[110095],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0099607"},{"annotations":[104258,91563,95645,79728,96009,102342,110729,114479,100438,115956,116360,118779,100938,64638,105365,90956,105718,91176,92793,114478,109342,115087,120573,110100,111739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990758"},{"annotations":[104184],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:1902424"},{"annotations":[107011,117870,113816],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1902425"},{"annotations":[113056,104204,91816,95619,118541],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0140429"}]},"cv_name":"biological_process","definition":"The cellular process in which spindle microtubules become physically associated with the proteins making up the kinetochore complex in mitosis.","definition_xrefs":["GOC:clt","PMID:26705896","GOC:dph","GOC:ai","PMID:26258632","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"attachment of spindle microtubules to kinetochore","termid":"GO:0008608"},{"relation_name":"is_a","term_name":"mitotic cell cycle process","termid":"GO:1903047"},{"relation_name":"part_of","term_name":"mitotic metaphase chromosome alignment","termid":"GO:0007080"}],"gene_count":51,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00207":null,"SJAG_00302":null,"SJAG_00335":null,"SJAG_00418":null,"SJAG_00646":null,"SJAG_00678":null,"SJAG_00768":null,"SJAG_00794":null,"SJAG_00918":null,"SJAG_00930":null,"SJAG_01082":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01278":null,"SJAG_01297":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01601":null,"SJAG_01775":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_02045":null,"SJAG_02286":null,"SJAG_02336":null,"SJAG_02346":null,"SJAG_02451":null,"SJAG_02624":null,"SJAG_02731":null,"SJAG_02761":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03327":null,"SJAG_03437":null,"SJAG_03540":null,"SJAG_03543":null,"SJAG_03989":null,"SJAG_04040":null,"SJAG_04076":null,"SJAG_04140":null,"SJAG_04259":null,"SJAG_04280":null,"SJAG_04412":null,"SJAG_04623":null,"SJAG_04884":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05290":null,"SJAG_05319":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0000070"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150","GO:0000070"],"is_obsolete":false,"name":"attachment of mitotic spindle microtubules to kinetochore","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0051314"],"synonyms":[{"name":"attachment of spindle microtubules to kinetochore during mitosis","type":"related"},{"name":"attachment of spindle microtubules to kinetochore involved in mitosis","type":"exact"},{"name":"attachment of spindle microtubules to kinetochore involved in mitotic sister chromatid segregation","type":"exact"},{"name":"attachment of spindle microtubules to mitotic chromosome","type":"exact"},{"name":"mitotic bipolar attachment","type":"related"}],"termid":"GO:0051315","terms_by_termid":{"GO:0051315":null,"GO:0099607":null,"GO:0140429":null,"GO:1902424":null,"GO:1902425":null,"GO:1990758":null}}


id: MONDO:0009292
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Glycogen branching enzyme (GBE) deficiency (Andersen's disease or amylopectinosis), or glycogen storage disease type 4 (GSD4), is a rare and severe form of glycogen storage disease which accounts for approximately 3% of all the glycogen storage diseases.","definition_xrefs":["Orphanet:367"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete muscular glycogenosis (obsolete MONDO:0016118)","termid":"MONDO:0016118"},{"relation_name":"excluded_subClassOf","term_name":"familial dilated cardiomyopathy","termid":"MONDO:0016333"},{"relation_name":"is_a","term_name":"disorder of glycogen metabolism","termid":"MONDO:0002412"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792"],"is_obsolete":false,"name":"glycogen storage disease due to glycogen branching enzyme deficiency","secondary_identifiers":["NANDO:2200540","NCIT:C84737","OMIM:232500","NANDO:1200850","UMLS:C0017923","MedDRA:10053249","NANDO:1200827","DOID:2750","NORD:770","SCTID:124267007","GARD:2520","ICD9:277.6","MEDGEN:6642"],"synonyms":[{"name":"Andersen Disease (GSD IV)","type":"exact"},{"name":"Andersen disease","type":"exact"},{"name":"Andersen's disease","type":"exact"},{"name":"GBE1 glycogen storage disease","type":"exact"},{"name":"GSD 4","type":"related"},{"name":"GSD IV","type":"related"},{"name":"GSD IV, classic hepatic","type":"related"},{"name":"GSD IV, neuromuscular form, adult, with isolated myopathy","type":"related"},{"name":"GSD IV, neuromuscular form, childhood","type":"related"},{"name":"GSD IV, neuromuscular form, congenital","type":"related"},{"name":"GSD IV, neuromuscular form, fatal perinatal","type":"related"},{"name":"GSD IV, nonprogressive hepatic","type":"related"},{"name":"GSD due to glycogen branching enzyme deficiency","type":"exact"},{"name":"GSD type 4","type":"exact"},{"name":"GSD type IV","type":"exact"},{"name":"GSD4","type":"related"},{"name":"Gbe1 deficiency","type":"related"},{"name":"amylopectinosis","type":"exact"},{"name":"brancher deficiency","type":"related"},{"name":"brancher deficiency glycogenosis","type":"exact"},{"name":"branching-transferase deficiency glycogenosis","type":"exact"},{"name":"cirrhosis, familial, with deposition of abnormal glycogen","type":"related"},{"name":"deficiency of 1,4-alpha-glucan branching enzyme","type":"exact"},{"name":"glycogen branching enzyme deficiency","type":"related"},{"name":"glycogen storage disease 4","type":"related"},{"name":"glycogen storage disease IV","type":"related"},{"name":"glycogen storage disease caused by mutation in GBE1","type":"exact"},{"name":"glycogen storage disease due to glycogen branching enzyme deficiency","type":"exact"},{"name":"glycogen storage disease type 4","type":"exact"},{"name":"glycogen storage disease type IV","type":"exact"},{"name":"glycogen storage disease, type IV","type":"exact"},{"name":"glycogenosis 4","type":"related"},{"name":"glycogenosis due to glycogen branching enzyme deficiency","type":"exact"},{"name":"glycogenosis type 4","type":"exact"},{"name":"glycogenosis type IV","type":"exact"}],"termid":"MONDO:0009292","xrefs":{"Monarch":{"xref_id":"0009292"}}}


id: PATO:0001730
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's disposition to shed body parts.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shedability","termid":"PATO:0001729"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deciduous (generic)","termid":"PATO:0001730"}


id: PBO:0088754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate decarboxylase","termid":"PBO:0088754"}


id: PBO:0039717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apolipoprotein B mRNA editing enzyme catalytic subunit 3A","termid":"PBO:0039717"}


id: GO:0062102
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Division of a female germline stem cell to produce two germline stem cells of the same type as the parent.","definition_xrefs":["PMID:30248087","GOC:ha"],"direct_ancestors":[{"relation_name":"is_a","term_name":"germline stem cell symmetric division","termid":"GO:0098729"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"female germline stem cell symmetric division","termid":"GO:0062102"}


id: PBO:0043447
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calponin 2 pseudogene 8","termid":"PBO:0043447"}


id: GO:0015753
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which D-xylose is transported across a lipid bilayer, from one side of a membrane to the other. D-xylose (the naturally occurring enantiomer is always D-) is a constituent of plant polysaccharides.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentose transmembrane transport","termid":"GO:0015750"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"D-xylose transmembrane transport","synonyms":[{"name":"D-xylose transport","type":"related"}],"termid":"GO:0015753"}


id: GO:1990571
data:
  {"annotated_genes":["SJAG_03540","SJAG_01805","SJAG_00794","SJAG_01613","SJAG_04076","SJAG_02814","SJAG_03683","SJAG_02761","SJAG_02624"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[66730,70177,95610,97130,101036,102200,104257,110985,117786],"is_not":false,"summary":null,"term":"GO:1990571"}]},"cv_name":"biological_process","definition":"The process by which centromeres/kinetochores attach to and migrate along microtubules to become localized to clusters at the spindle pole body during a meiotic prometaphase I.","definition_xrefs":["PMID:9009280","PMID:10366596"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic chromosome movement towards spindle pole","termid":"GO:0016344"},{"relation_name":"is_a","term_name":"chromosome organization involved in meiotic cell cycle","termid":"GO:0070192"},{"relation_name":"is_a","term_name":"centromere clustering","termid":"GO:0098653"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00794":null,"SJAG_01613":null,"SJAG_01805":null,"SJAG_02624":null,"SJAG_02761":null,"SJAG_02814":null,"SJAG_03540":null,"SJAG_03683":null,"SJAG_04076":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0140013"}],"interesting_parent_ids":["GO:0140013","GO:0051179","GO:0008150","GO:0007049"],"is_obsolete":false,"name":"meiotic centromere clustering","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"centromere clustering during meiosis","type":"exact"},{"name":"homologous chromosome movement towards spindle pole in meiosis I prometaphase","type":"exact"}],"termid":"GO:1990571","terms_by_termid":{"GO:1990571":null}}


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:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0000138"],"is_obsolete":false,"name":"increased protein localization to nucleus during stationary phase","termid":"FYPO:0008043"}


id: PR:O74856
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- caf1 gene.","definition_xrefs":["UniProtKB:O74856","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":"poly(A) ribonuclease pop2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC18.06c","synonyms":[{"name":"CCR4-associated factor 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-caf1","type":"exact"}],"termid":"PR:O74856"}


id: PBO:0085878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; induced by ketoconazole; promoter region contains sterol regulatory element motif, which has been identified as a Upc2p-binding site; overexpression complements function of Nce102p in NCE102 deletion strain; FHN1 has a paralog, NCE102, that arose from the whole genome duplication","termid":"PBO:0085878"}


id: GO:0005248
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transmembrane transfer of a sodium ion by a voltage-gated channel. A voltage-gated channel is a channel whose open state is dependent on the voltage across the membrane in which it is embedded.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sodium channel activity","termid":"GO:0005272"}],"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:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"voltage-gated sodium channel activity","secondary_identifiers":["Reactome:R-HSA-5576895"],"synonyms":[{"name":"voltage gated sodium channel activity","type":"exact"},{"name":"voltage-dependent sodium channel activity","type":"exact"},{"name":"voltage-gated sodium ion channel activity","type":"exact"},{"name":"voltage-sensitive sodium channel","type":"exact"}],"termid":"GO:0005248"}


id: PBO:0091159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methionine aminopeptidase Fma2","termid":"PBO:0091159"}


id: FYPO:0007109
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which centromere clustering is normal (i.e. indistinguishable from wild type during meiotic prometaphase I.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"},{"relation_name":"is_a","term_name":"normal meiotic cell cycle process","termid":"FYPO:0007078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal meiotic centromere clustering during meiotic prometaphase I","synonyms":[{"name":"normal centromere clustering during meiotic prometaphase I","type":"exact"},{"name":"normal chromosome retrieval during meiotic prometaphase I","type":"related"},{"name":"normal kinetochore retrieval during meiotic prometaphase I","type":"related"},{"name":"normal meiotic centromere clustering during prometaphase I","type":"exact"}],"termid":"FYPO:0007109"}


id: MONDO:0010197
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Freeman-Sheldon syndrome","termid":"MONDO:0008675"}],"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":"whistling face syndrome, recessive form","secondary_identifiers":["MEDGEN:376364","DOID:0111606","GARD:10024","MESH:C536699","OMIM:277720","UMLS:C1848470"],"synonyms":[{"name":"whistling face syndrome, recessive form","type":"exact"}],"termid":"MONDO:0010197","xrefs":{"Monarch":{"xref_id":"0010197"}}}


id: MOD:01932
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links two lysine residues with a carbon-nitrogen bond to form L-lysinonorleucine..","definition_xrefs":["PubMed:6030254","PubMed:5117030","RESID:AA0586","PubMed:5817620","PubMed:5879466"],"direct_ancestors":[{"relation_name":"is_a","term_name":"crosslinked residues with loss of ammonia","termid":"MOD:00946"},{"relation_name":"is_a","term_name":"crosslinked L-lysine residue","termid":"MOD:02051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-lysinonorleucine","synonyms":[{"name":"(2S)-2-amino-6-([(5S)-5-amino-5-carboxypentyl]amino)hexanoic acid","type":"exact"},{"name":"(2S,2'S)-6,6'-iminobis(2-aminohexanoic acid)","type":"exact"},{"name":"6-(N6-L-lysino)-L-norleucine","type":"exact"},{"name":"L-lysinonorleucine","type":"exact"},{"name":"N6-[(5S)-5-amino-5-carboxypentyl]-L-lysine","type":"exact"},{"name":"lysinonorleucine","type":"exact"},{"name":"lysinorleucine [misspelling]","type":"exact"},{"name":"lysylnorleucine","type":"exact"}],"termid":"MOD:01932"}


id: GO:0042242
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the conversion of cobyrinic acid to cobyrinic acid a,c-diamide via the intermediate formation of cobyrinic acid c-monoamide.","definition_xrefs":["PMID:2172209","RHEA:26289"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-nitrogen ligase activity, with glutamine as amido-N-donor","termid":"GO:0016884"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016874","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"cobyrinic acid a,c-diamide synthase activity","secondary_identifiers":["EC:6.3.5.11","GO:0043775"],"synonyms":[{"name":"CobB","type":"narrow"},{"name":"cobyrinate a c diamide synthase activity","type":"exact"},{"name":"cobyrinate a c-diamide synthase activity","type":"exact"},{"name":"cobyrinate a,c diamide synthase activity","type":"exact"},{"name":"cobyrinate a,c-diamide synthase activity","type":"exact"}],"termid":"GO:0042242"}


id: MONDO:0016644
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Logopenic progressive aphasia (lv-PPA) is a form of primary progressive aphasia (PPA), characterized by impaired single-word retrieval and naming and impaired repetition with spared single-word comprehension and object knowledge.","definition_xrefs":["Orphanet:250831"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary progressive aphasia","termid":"MONDO:0019806"}],"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":"logopenic progressive aphasia","secondary_identifiers":["UMLS:C4274665","MEDGEN:907332","GARD:10791","SCTID:716380002","DOID:0081389"],"synonyms":[{"name":"LPA","type":"exact"},{"name":"Logopenic primary progressive aphasia","type":"exact"},{"name":"Logopenic variant PPA","type":"exact"}],"termid":"MONDO:0016644","xrefs":{"Monarch":{"xref_id":"0016644"}}}


id: PBO:0072600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RSF1 intronic transcript 1","termid":"PBO:0072600"}


id: GO:0015016
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3'-phosphoadenylyl sulfate + alpha-D-glucosaminyl-[heparan sulfate](n) = adenosine 3',5'-bisphosphate + 2 H+ + N-sulfo-alpha-D-glucosaminyl-[heparan sulfate](n).","definition_xrefs":["RHEA:21980","EC:2.8.2.8"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heparan sulfate sulfotransferase activity","termid":"GO:0034483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0016782","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"heparan sulfate N-sulfotransferase activity","secondary_identifiers":["MetaCyc:HEPARITIN-SULFOTRANSFERASE-RXN","GO:0051910","Reactome:R-HSA-2022860","GO:0015022","GO:0004393"],"synonyms":[{"name":"3'-phosphoadenylyl-sulfate:N-desulfoheparin N-sulfotransferase activity","type":"related"},{"name":"3'-phosphoadenylyl-sulfate:[heparan sulfate]-glucosamine N-sulfotransferase activity","type":"related"},{"name":"3'-phosphoadenylyl-sulfate:heparitin N-sulfotransferase activity","type":"related"},{"name":"3'-phosphoadenylylsulfate:N-desulfoheparin sulfotransferase activity","type":"related"},{"name":"N-HSST activity","type":"related"},{"name":"N-desulfoheparin sulfotransferase activity","type":"related"},{"name":"N-heparan sulfate sulfotransferase activity","type":"related"},{"name":"PAPS:DSH sulfotransferase activity","type":"related"},{"name":"PAPS:N-desulfoheparin sulfotransferase activity","type":"related"},{"name":"[heparan sulfate]-glucosamine N-sulfotransferase activity","type":"exact"},{"name":"[heparan sulphate]-glucosamine N-sulphotransferase activity","type":"exact"},{"name":"desulfoheparin sulfotransferase activity","type":"exact"},{"name":"glucosaminyl N-deacetylase/N-sulfotransferase activity","type":"related"},{"name":"heparan sulfate 2-N-sulfotransferase activity","type":"related"},{"name":"heparan sulfate N-deacetylase/N-sulfotransferase activity","type":"related"},{"name":"heparin N-deacetylase/N-sulfotransferase activity","type":"related"},{"name":"heparin N-deacetylase/N-sulphotransferase activity","type":"related"},{"name":"heparin N-sulfotransferase activity","type":"related"},{"name":"heparin-glucosamine N-sulfotransferase activity","type":"exact"},{"name":"heparitin N-sulfotransferase activity","type":"exact"},{"name":"heparitin N-sulphotransferase activity","type":"exact"},{"name":"heparitin sulfotransferase activity","type":"exact"}],"termid":"GO:0015016"}


id: PBO:0030516
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_4-nitroquinoline_N-oxide","termid":"PBO:0030516"}


id: PBO:0078612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 64C","termid":"PBO:0078612"}


id: PBO:0091669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial DUF1772 family protein, multimembrane spanning anthrone oxygenase-like","termid":"PBO:0091669"}


id: MONDO:0012714
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial dilated cardiomyopathy","termid":"MONDO:0016333"},{"relation_name":"is_a","term_name":"autosomal recessive titinopathy","termid":"MONDO:0100493"},{"relation_name":"is_a","term_name":"hereditary neuromuscular disease","termid":"MONDO:0100546"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0002320","MONDO:0005336","MONDO:0005267"],"is_obsolete":false,"name":"early-onset myopathy with fatal cardiomyopathy","secondary_identifiers":["DOID:0081341","MESH:C567129","Orphanet:289377","OMIM:611705","MEDGEN:435983","SCTID:702343002","GARD:17324","UMLS:C2673677"],"synonyms":[{"name":"EOMFC","type":"related"},{"name":"SALMY","type":"related"},{"name":"Salih myopathy","type":"exact"},{"name":"myopathy, early-onset, with fatal cardiomyopathy","type":"related"}],"termid":"MONDO:0012714","xrefs":{"Monarch":{"xref_id":"0012714"}}}


id: MONDO:0013268
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Frontonasal dysplasia with alopecia and genital anomaly is a new phenotype of frontonasal dysplasia associated with total alopecia and hypogonadism.","definition_xrefs":["Orphanet:228390"],"direct_ancestors":[{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"frontonasal dysplasia","termid":"MONDO:0016643"}],"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":"frontonasal dysplasia with alopecia and genital anomaly","secondary_identifiers":["DOID:0081046","OMIM:613451","UMLS:C3150703","GARD:12641","SCTID:725029001","MEDGEN:462053"],"synonyms":[{"name":"ALX4-related FNDAG","type":"exact"},{"name":"FND2","type":"related"},{"name":"craniofrontonasal dysplasia with alopecia and hypogonadism","type":"exact"},{"name":"frontonasal dysplasia 2","type":"related"},{"name":"frontonasal dysplasia type 2","type":"exact"},{"name":"frontonasal dysplasia with alopecia and genital abnomality","type":"exact"}],"termid":"MONDO:0013268","xrefs":{"Monarch":{"xref_id":"0013268"}}}


id: MONDO:0018446
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"},{"relation_name":"is_a","term_name":"monogenic epilepsy","termid":"MONDO:0015653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0005027","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome","secondary_identifiers":["Orphanet:404481","GARD:21719","MEDGEN:1843349","UMLS:C5681145"],"termid":"MONDO:0018446","xrefs":{"Monarch":{"xref_id":"0018446"}}}


id: MONDO:0009869
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pierre-Robin syndrome (or Pierre-Robin sequence) is characterized by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft.","definition_xrefs":["Orphanet:718"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome or malformation associated with head and neck malformations (obsolete MONDO:0015501)","termid":"MONDO:0015501"},{"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":"isolated Pierre-Robin syndrome","secondary_identifiers":["icd11.foundation:136361299","MESH:D010855","OMIM:261800","SCTID:4602007","MEDGEN:19310","GARD:4347","UMLS:C0031900","NCIT:C85010","NORD:1579"],"synonyms":[{"name":"PRBNS","type":"related"},{"name":"Pierre Robin Sequence","type":"exact"},{"name":"Pierre Robin sequence","type":"related"},{"name":"Pierre Robin syndrome","type":"related"},{"name":"Pierre Robin syndrome skeletal dysplasia polydactyly","type":"related"},{"name":"Pierre Robin's sequence","type":"related"},{"name":"Pierre Robins sequence","type":"related"},{"name":"Pierre-Robin syndrome","type":"related"},{"name":"Robin sequence","type":"related"},{"name":"Robin syndrome, Pierre","type":"related"},{"name":"glossoptosis, micrognathia, and cleft palate","type":"related"},{"name":"isolated Pierre Robin sequence","type":"exact"},{"name":"isolated Pierre Robin syndrome","type":"related"},{"name":"isolated Pierre-Robin syndrome","type":"exact"},{"name":"sequence, Pierre Robin","type":"related"},{"name":"sequence, Pierre Robin's","type":"related"},{"name":"sequence, Robin","type":"related"},{"name":"syndrome, Pierre Robin","type":"related"},{"name":"syndrome, Pierre-Robin","type":"related"}],"termid":"MONDO:0009869","xrefs":{"Monarch":{"xref_id":"0009869"}}}


id: PBO:0046712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EVA1A antisense RNA","termid":"PBO:0046712"}


id: GO:0015279
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A ligand-gated ion channel activity which transports calcium in response to emptying of intracellular calcium stores.","definition_xrefs":["GOC:dph","PMID:15788710","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"calcium channel activity","termid":"GO:0005262"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"store-operated calcium channel activity","secondary_identifiers":["Reactome:R-HSA-434798"],"termid":"GO:0015279"}


id: PBO:0082159
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Adenine phosphoribosyltransferase; catalyzes the formation of AMP from adenine and 5-phosphoribosylpyrophosphate; involved in the salvage pathway of purine nucleotide biosynthesis; APT1 has a paralog, APT2, that arose from the whole genome duplication","termid":"PBO:0082159"}


id: MONDO:0010041
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disorder characterized by early-onset cerebellar ataxia with spasticity, a pyramidal syndrome and peripheral neuropathy.","definition_xrefs":["Orphanet:98"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cerebellar ataxia","termid":"MONDO:0015244"},{"relation_name":"is_a","term_name":"autosomal recessive spastic ataxia","termid":"MONDO:0017847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0006025"],"is_obsolete":false,"name":"Charlevoix-Saguenay spastic ataxia","secondary_identifiers":["GARD:4910","DOID:0050946","MESH:C536787","SCTID:702445005","MEDGEN:338620","OMIM:270550","UMLS:C1849140"],"synonyms":[{"name":"ARSACS","type":"exact"},{"name":"Charlevoix-Saguenay spastic ataxia","type":"exact"},{"name":"SPAX6","type":"exact"},{"name":"autosomal recessive spastic ataxia of Charlevoix-Saguenay","type":"related"},{"name":"autosomal recessive spastic ataxia type 6","type":"exact"},{"name":"sacs","type":"related"},{"name":"spastic ataxia 6, autosomal recessive","type":"related"},{"name":"spastic ataxia Charlevoix-Saguenay type","type":"related"},{"name":"spastic ataxia of Charlevoix-Saguenay","type":"related"},{"name":"spastic ataxia, Charlevoix-Saguenay type","type":"related"}],"termid":"MONDO:0010041","xrefs":{"Monarch":{"xref_id":"0010041"}}}


id: GO:0043682
data:
  {"annotated_genes":["SJAG_02399"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79574],"is_not":false,"summary":null,"term":"GO:0043682"}]},"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 + Cu2+(in) = ADP + phosphate + Cu2+(out).","definition_xrefs":["RHEA:10376"],"direct_ancestors":[{"relation_name":"is_a","term_name":"copper ion transmembrane transporter activity","termid":"GO:0005375"},{"relation_name":"is_a","term_name":"P-type ion transporter activity","termid":"GO:0015662"},{"relation_name":"is_a","term_name":"ATPase-coupled monoatomic cation transmembrane transporter activity","termid":"GO:0019829"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02399":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"P-type divalent copper transporter activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["GO:0004008","EC:7.2.2.9","Reactome:R-HSA-936802","MetaCyc:TRANS-RXN-178","Reactome:R-HSA-6803545","Reactome:R-HSA-936895","Reactome:R-HSA-3697838"],"synonyms":[{"name":"Cu(2+)-exporting ATPase activity","type":"related"},{"name":"Cu2+-exporting ATPase activity","type":"related"},{"name":"copper exporting ATPase activity","type":"broad"},{"name":"copper transmembrane transporter activity, phosphorylative mechanism","type":"broad"},{"name":"copper-exporting ATPase activity","type":"narrow"},{"name":"copper-translocating P-type ATPase activity","type":"broad"},{"name":"copper-transporting ATPase activity","type":"broad"}],"termid":"GO:0043682","terms_by_termid":{"GO:0043682":null}}


id: FYPO:0002268
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which glutamate-ammonia ligase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished catalytic activity","termid":"FYPO:0000664"},{"relation_name":"is_a","term_name":"abnormal glutamate-ammonia ligase activity","termid":"FYPO:0002267"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0000654","FYPO:0000661","FYPO:0001985"],"is_obsolete":false,"name":"abolished glutamate-ammonia ligase activity","synonyms":[{"name":"abolished GS activity","type":"exact"},{"name":"abolished glutamine synthetase activity","type":"exact"},{"name":"abolished glutamylhydroxamic synthetase activity","type":"exact"},{"name":"glutamate-ammonia ligase activity abolished","type":"exact"}],"termid":"FYPO:0002268"}


id: PBO:0053524
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 519","termid":"PBO:0053524"}


id: PBO:0000078
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"no apparent orthologs","termid":"PBO:0000078"}


id: PBO:0066620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RIB43A domain with coiled-coils 2","termid":"PBO:0066620"}


id: PBO:0013839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"controlled curation, orthologous to S. cerevisiae YIL026C","termid":"PBO:0013839"}


id: MONDO:0035350
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"letrozole toxicity","secondary_identifiers":["MEDGEN:1826119","Orphanet:529831","UMLS:C5681461"],"termid":"MONDO:0035350","xrefs":{"Monarch":{"xref_id":"0035350"}}}


id: MONDO:0015796
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition of lung damage that is characterized by bilateral pulmonary infiltrates (pulmonary edema) rich in neutrophils, and in the absence of clinical heart failure. This can represent a spectrum of pulmonary lesions, endothelial and epithelial, due to numerous factors (physical, chemical, or biological).","definition_xrefs":["MESH:D055371"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lung disorder","termid":"MONDO:0005275"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"injury","termid":"MONDO:0021178"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute lung injury","secondary_identifiers":["Orphanet:178320","EFO:0004610","GARD:20146","MedDRA:10069351","NCIT:C155766","SCTID:315345002"],"termid":"MONDO:0015796","xrefs":{"Monarch":{"xref_id":"0015796"}}}


id: PBO:0091044
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy associated protein Aut12","termid":"PBO:0091044"}


id: MONDO:1011947
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":"muscle contracture and chondrodysplasia, non-human animal","secondary_identifiers":["OMIA:000675"],"termid":"MONDO:1011947","xrefs":{"Monarch":{"xref_id":"1011947"}}}


id: GO:0042186
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of o-xylene, (1,2-dimethylbenzene) a colorless, liquid aromatic hydrocarbon.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"o-xylene metabolic process","termid":"GO:0018950"},{"relation_name":"is_a","term_name":"xylene catabolic process","termid":"GO:0042184"}],"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":"o-xylene catabolic process","synonyms":[{"name":"o-xylene breakdown","type":"exact"},{"name":"o-xylene catabolism","type":"exact"},{"name":"o-xylene degradation","type":"exact"},{"name":"ortho-xylene catabolic process","type":"exact"},{"name":"ortho-xylene catabolism","type":"exact"}],"termid":"GO:0042186"}


id: GO:0141156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An intracellular signaling cassette that starts with production of cyclic AMP (cAMP) by adenylate cyclase (either transmembrane or soluble), which activates protein kinase A, and ends with activation of downstream effectors such as the transcription factor CREB that further transmit the signal within the cell.","definition_xrefs":["PMID:23209152"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular signaling cassette","termid":"GO:0141124"}],"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":"cAMP/PKA signal transduction","synonyms":[{"name":"PKA signaling","type":"broad"},{"name":"cAMP signaling","type":"broad"},{"name":"cAMP/PKA signaling cassette","type":"exact"},{"name":"protein kinase A signaling","type":"broad"}],"termid":"GO:0141156"}


id: PBO:0042268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chaperonin containing TCP1 subunit 6 pseudogene 3","termid":"PBO:0042268"}


id: MONDO:0015343
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Secondary acute transverse myelitis (ATM) is characterized by focal inflammation within the spinal cord due to a known cause, usually an inflammatory disease.","definition_xrefs":["Orphanet:139420"],"gene_count":0,"genotype_count":0,"name":"obsolete secondary acute transverse myelitis (obsolete MONDO:0015343)","synonyms":[{"name":"disease-associated transverse myelitis","type":"exact"}],"termid":"MONDO:0015343","xrefs":{"Monarch":{"xref_id":"0015343"}}}


id: GO:0070634
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of ammonium ions from one side of an epithelium to the other.","definition_xrefs":["GOC:mah","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transepithelial transport","termid":"GO:0070633"},{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"}],"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:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"transepithelial ammonium transport","termid":"GO:0070634"}


id: PATO:0000786
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000786 neural function value (obsolete PATO:0000786)","termid":"PATO:0000786"}


id: PBO:0027858
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_kinase_activity_during_mitotic_S_phase_during_cellular_response_to_DNA_damage","termid":"PBO:0027858"}


id: PATO:0000882
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000882 litter size value (obsolete PATO:0000882)","termid":"PATO:0000882"}


id: GO:0018350
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The addition of an ester group to a protein amino acid.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete protein esterification (obsolete GO:0018350)","synonyms":[{"name":"protein amino acid esterification","type":"exact"}],"termid":"GO:0018350"}


id: PBO:0049209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate ionotropic receptor NMDA type subunit 2C","termid":"PBO:0049209"}


id: PBO:0030478
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_glutamine_level","termid":"PBO:0030478"}


id: MONDO:0800377
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ACTH-independent Cushing syndrome","termid":"MONDO:0020529"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACTH-independent adrenal Cushing syndrome, somatic","termid":"MONDO:0800377","xrefs":{"Monarch":{"xref_id":"0800377"}}}


id: PBO:0076670
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRPM8 channel associated factor 2C","termid":"PBO:0076670"}


id: FYECO:0000427
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in rich medium containing fructose as the carbon source, yeast extract and other components. The concentration of fructose is typically around 2%.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping rich medium","termid":"FYECO:0000080"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fructose YE","synonyms":[{"name":"fructose rich medium","type":"broad"}],"termid":"FYECO:0000427"}


id: MONDO:0006164
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polyp that arises from the colon or rectum. It is characterized by the presence of serrated glands and the absence of generalized dysplasia. Some authors have suggested that it is a precursor lesion for some colorectal adenocarcinomas with microsatellite instability.","definition_xrefs":["NCIT:C83176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colorectal adenoma","termid":"MONDO:0005484"}],"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":"colorectal sessile serrated adenoma/polyp","secondary_identifiers":["MEDGEN:415420","EFO:1000197","UMLS:C2826783"],"synonyms":[{"name":"colorectal SSA","type":"exact"},{"name":"colorectal SSA/P","type":"exact"},{"name":"colorectal SSP","type":"exact"},{"name":"colorectal mixed hyperplastic adenomatous polyp","type":"exact"},{"name":"colorectal mixed hyperplastic adenomatous polyp/serrated adenoma","type":"exact"},{"name":"colorectal sessile serrated adenoma","type":"exact"},{"name":"colorectal sessile serrated adenoma/polyp","type":"exact"},{"name":"colorectal sessile serrated polyp","type":"exact"}],"termid":"MONDO:0006164","xrefs":{"Monarch":{"xref_id":"0006164"}}}


id: PBO:0075384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SOX30 pseudogene 1","termid":"PBO:0075384"}


id: MOD:00108
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tyrosine residue to L-tyrosine amide.","definition_xrefs":["RESID:AA0099","PubMed:3562898","PubMed:1377792","PubMed:6509012"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C1-amidated residue","termid":"MOD:00883"},{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-tyrosine amide","synonyms":[{"name":"(2S)-2-amino-3-(4-hydoxyphenyl)propanamide","type":"exact"},{"name":"L-tyrosine amide","type":"exact"},{"name":"MOD_RES Tyrosine amide","type":"exact"},{"name":"TyrN","type":"exact"},{"name":"amidated L-tyrosine","type":"exact"},{"name":"tyrosinamide","type":"exact"}],"termid":"MOD:00108"}


id: PBO:0050365
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 68","termid":"PBO:0050365"}


id: PBO:0055710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"limb development membrane protein 1 like","termid":"PBO:0055710"}


id: MONDO:0008642
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"VACTERL/VATER is an association of congenital malformations typically characterized by the presence of at least three of the following: vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities.","definition_xrefs":["Orphanet:887"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VACTERL/vater association","secondary_identifiers":["OMIM:192350","MedDRA:10066022","MEDGEN:902479","ICD9:759.89","NORD:1818","DOID:14679","SCTID:27742002","NANDO:2200983","icd11.foundation:1452617987","MedDRA:10053665","NANDO:1200657","NCIT:C99105","GARD:5443","UMLS:C4225671"],"synonyms":[{"name":"VACTERL Association","type":"exact"},{"name":"VACTERL association","type":"exact"},{"name":"VATER association","type":"exact"},{"name":"VATER syndrome","type":"related"},{"name":"VATER/VACTERL association","type":"related"},{"name":"vertebral abnormalities, anal atresia, Cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome","type":"exact"}],"termid":"MONDO:0008642","xrefs":{"Monarch":{"xref_id":"0008642"}}}


id: PBO:0017790
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Golgi GDP-mannose transmembrane transporter Vrg4 (predicted)","termid":"PBO:0017790"}


id: GO:0043381
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of memory T cell differentiation.","definition_xrefs":["ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of immune effector process","termid":"GO:0002698"},{"relation_name":"is_a","term_name":"regulation of memory T cell differentiation","termid":"GO:0043380"},{"relation_name":"is_a","term_name":"negative regulation of T cell differentiation","termid":"GO:0045581"},{"relation_name":"is_a","term_name":"negative regulation of immune response","termid":"GO:0050777"},{"relation_name":"negatively_regulates","term_name":"memory T cell differentiation","termid":"GO:0043379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of memory T cell differentiation","synonyms":[{"name":"down regulation of memory T cell differentiation","type":"exact"},{"name":"down-regulation of memory T cell differentiation","type":"exact"},{"name":"downregulation of memory T cell differentiation","type":"exact"},{"name":"inhibition of memory T cell differentiation","type":"narrow"},{"name":"negative regulation of memory T cell development","type":"related"},{"name":"negative regulation of memory T lymphocyte differentiation","type":"exact"},{"name":"negative regulation of memory T-cell differentiation","type":"exact"},{"name":"negative regulation of memory T-lymphocyte differentiation","type":"exact"}],"termid":"GO:0043381"}


id: GO:0005868
data:
  {"annotated_genes":["SJAG_00113","SJAG_01370","SJAG_02286","SJAG_01662","SJAG_02561"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[67236,67427,79100,81496,92797],"is_not":false,"summary":null,"term":"GO:0005868"}]},"cv_name":"cellular_component","definition":"Any dynein complex with a homodimeric dynein heavy chain core that catalyzes movement along a microtubule. Cytoplasmic dynein complexes participate in many cytoplasmic transport activities in eukaryotes, such as mRNA localization, intermediate filament transport, nuclear envelope breakdown, apoptosis, transport of centrosomal proteins, mitotic spindle assembly, virus transport, kinetochore functions, and movement of signaling and spindle checkpoint proteins. Some complexes participate in intraflagellar transport. Subunits associated with the dynein heavy chain mediate association between dynein heavy chain and cargoes, and may include light chains and light intermediate chains.","definition_xrefs":["GOC:mah","GOC:krc","GOC:cilia","GOC:hla","PMID:12600311"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dynein complex","termid":"GO:0030286"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00113":null,"SJAG_01370":null,"SJAG_01662":null,"SJAG_02286":null,"SJAG_02561":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:0015630"}],"interesting_parent_ids":["GO:0015630","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"cytoplasmic dynein complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"cytoplasmic dynein heavy chain","type":"narrow"},{"name":"cytoplasmic dynein intermediate chain","type":"narrow"},{"name":"cytoplasmic dynein intermediate light chain","type":"narrow"},{"name":"cytoplasmic dynein light chain","type":"narrow"}],"termid":"GO:0005868","terms_by_termid":{"GO:0005868":null}}


id: GO:0042372
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phylloquinone, vitamin K1, a quinone-derived compound synthesized by green plants.","definition_xrefs":["GOC:jl","PMID:27337968","PMID:23821151"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin K biosynthetic process","termid":"GO:0042371"},{"relation_name":"is_a","term_name":"phylloquinone metabolic process","termid":"GO:0042374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0006766","GO:0008150"],"is_obsolete":false,"name":"phylloquinone biosynthetic process","secondary_identifiers":["MetaCyc:PWY-5027"],"synonyms":[{"name":"phylloquinone anabolism","type":"exact"},{"name":"phylloquinone biosynthesis","type":"exact"},{"name":"phylloquinone formation","type":"exact"},{"name":"phylloquinone synthesis","type":"exact"},{"name":"phytomenadione biosynthesis","type":"exact"},{"name":"phytomenadione biosynthetic process","type":"exact"},{"name":"phytonadione biosynthesis","type":"exact"},{"name":"phytonadione biosynthetic process","type":"exact"},{"name":"phytylmenaquinone biosynthesis","type":"exact"},{"name":"phytylmenaquinone biosynthetic process","type":"exact"},{"name":"vitamin K1 biosynthesis","type":"exact"},{"name":"vitamin K1 biosynthetic process","type":"exact"}],"termid":"GO:0042372"}


id: PBO:0029783
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_vegetative_cell_population_with_abnormal_cell_morphology_(obsolete_FYPO:0002454)","termid":"PBO:0029783"}


id: GO:1990916
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The outermost layers of the spore wall, as described in Schizosaccharomyces pombe.","definition_xrefs":["PMID:24623719"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"ascospore wall","termid":"GO:0005619"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005618"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005618","GO:0005575"],"is_obsolete":false,"name":"Isp3 layer of spore wall","termid":"GO:1990916"}


id: PBO:0030868
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_actin_cytoskeleton_organization","termid":"PBO:0030868"}


id: MONDO:1012786
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ichthyosis that occurs in dogs due to a mutation in the ASPRV1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"ichthyosis, dog","termid":"MONDO:1012978"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ichthyosis, ASPRV1-related, dog","secondary_identifiers":["OMIA:002099-9615"],"termid":"MONDO:1012786","xrefs":{"Monarch":{"xref_id":"1012786"}}}


id: MONDO:0020179
data:
  {"annotated_genes":["SJAG_03453"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87667],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008097"}]},"cv_name":"mondo","definition":"A melanocytic nevus that involves the skin of eyelid.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"},{"relation_name":"is_a","term_name":"benign tumor of palpebral epidermis","termid":"MONDO:0020173"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005328"],"is_obsolete":false,"name":"palpebral nevus","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:231827008","Orphanet:98588","MEDGEN:65985","UMLS:C0239460","NCIT:C3880"],"synonyms":[{"name":"eyelid nevus","type":"exact"},{"name":"melanocytic nevus of skin of eyelid","type":"exact"},{"name":"nevus of eyelid","type":"exact"},{"name":"nevus of the eyelid","type":"exact"},{"name":"skin of eyelid melanocytic nevus","type":"exact"}],"termid":"MONDO:0020179","terms_by_termid":{"MONDO:0008097":null},"xrefs":{"Monarch":{"xref_id":"0020179"}}}


id: PBO:0068245
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 28S ribosomal 2","termid":"PBO:0068245"}


id: PBO:0071581
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L36","termid":"PBO:0071581"}


id: PBO:0045524
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DTW domain containing 1","termid":"PBO:0045524"}


id: PBO:0056610
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"malic enzyme 2 pseudogene 1","termid":"PBO:0056610"}


id: MONDO:1012309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"degenerative myeloencephalopathy, non-human animal","termid":"MONDO:1011866"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"degenerative myeloencephalopathy, horse","secondary_identifiers":["OMIA:001163-9796"],"termid":"MONDO:1012309","xrefs":{"Monarch":{"xref_id":"1012309"}}}


id: PBO:0078863
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transient receptor potential cation channel subfamily C member 7","termid":"PBO:0078863"}


id: PR:000037486
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cdc2 gene or a 1:1 ortholog thereof.","definition_xrefs":["PRO:CNA","UniProtKB:P04551"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fungal-type cyclin-dependent kinase 1","pombase_gene_id":"SPBC11B10.09","synonyms":[{"name":"Cell division control protein 2","type":"exact"},{"name":"Cell division protein kinase 1","type":"exact"},{"name":"cdc2","type":"exact"},{"name":"p34 protein kinase","type":"exact"}],"termid":"PR:000037486"}


id: GO:1904778
data:
  {"annotated_genes":["SJAG_03602"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[100244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120047"}]},"cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein localization to cell cortex.","definition_xrefs":["PMID:17115027","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein localization to cell periphery","termid":"GO:1904377"},{"relation_name":"is_a","term_name":"regulation of protein localization to cell cortex","termid":"GO:1904776"},{"relation_name":"positively_regulates","term_name":"protein localization to cell cortex","termid":"GO:0072697"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03602":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of protein localization to cell cortex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"activation of protein localisation to cell cortex","type":"narrow"},{"name":"activation of protein localization to cell cortex","type":"narrow"},{"name":"positive regulation of protein localisation to cell cortex","type":"exact"},{"name":"up regulation of protein localisation to cell cortex","type":"exact"},{"name":"up regulation of protein localization to cell cortex","type":"exact"},{"name":"up-regulation of protein localisation to cell cortex","type":"exact"},{"name":"up-regulation of protein localization to cell cortex","type":"exact"},{"name":"upregulation of protein localisation to cell cortex","type":"exact"},{"name":"upregulation of protein localization to cell cortex","type":"exact"}],"termid":"GO:1904778","terms_by_termid":{"GO:0120047":null}}


id: RO:0002467
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","direct_ancestors":[{"relation_name":"is_a","term_name":"is_symbiosis","termid":"RO:0002465"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_mutualism","termid":"RO:0002467"}


id: PR:O74774
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An HBS1-like protein that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongation factor 1 alpha-like protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC25B2.01","secondary_identifiers":["UniProtKB:O74774"],"synonyms":[{"name":"SPBC25B2.01","type":"related"},{"name":"Spom972h-HBS1L","type":"exact"}],"termid":"PR:O74774"}


id: GO:0001717
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification process that results in the conversion of serine, carried by a specialized tRNA(ser) (which can read a UGA anticodon), to selenocysteine.","definition_xrefs":["ISBN:155581073X"],"direct_ancestors":[{"relation_name":"is_a","term_name":"charged-tRNA amino acid modification","termid":"GO:0019988"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006399"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006399"],"is_obsolete":false,"name":"conversion of seryl-tRNAsec to selenocys-tRNAsec","termid":"GO:0001717"}


id: MONDO:0957524
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cytochrome-c oxidase deficiency disease characterized by localization to tissues of the skeletal muscles.","definition_xrefs":["DOID:0081377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn mitochondrial myopathy","termid":"MONDO:0009637"},{"relation_name":"is_a","term_name":"mitochondrial complex IV deficiency, nuclear-type","termid":"MONDO:0033885"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005066","MONDO:0004069"],"is_obsolete":false,"name":"COX deficiency, benign infantile mitochondrial myopathy","termid":"MONDO:0957524","xrefs":{"Monarch":{"xref_id":"0957524"}}}


id: PBO:0055145
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 2564","termid":"PBO:0055145"}


id: PBO:0075813
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SSBP3 pseudogene 2","termid":"PBO:0075813"}


id: PBO:0085056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Non-essential protein of unknown function; null mutation results in a decrease in plasma membrane electron transport","termid":"PBO:0085056"}


id: MONDO:0014042
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any left ventricular noncompaction in which the cause of the disease is a mutation in the MIB1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"left ventricular noncompaction","termid":"MONDO:0018901"}],"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":"left ventricular noncompaction 7","secondary_identifiers":["GARD:15906","MEDGEN:767410","UMLS:C3554496","NCIT:C157266","OMIM:615092"],"synonyms":[{"name":"LVNC7","type":"related"},{"name":"MIB1 left ventricular noncompaction","type":"exact"},{"name":"left ventricular noncompaction 7","type":"exact"},{"name":"left ventricular noncompaction caused by mutation in MIB1","type":"exact"},{"name":"left ventricular noncompaction type 7","type":"exact"}],"termid":"MONDO:0014042","xrefs":{"Monarch":{"xref_id":"0014042"}}}


id: MONDO:1010850
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any glycogen storage disease that occurs in dogs due to a mutation in the GAA gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycogen storage disease, non-human animal","termid":"MONDO:1011419"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycogen storage disease, GAA-related, dog","secondary_identifiers":["OMIA:000419-9615"],"synonyms":[{"name":"glycogen storage disease II, dog","type":"related"}],"termid":"MONDO:1010850","xrefs":{"Monarch":{"xref_id":"1010850"}}}


id: GO:0102261
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADP+ + reduced coenzyme F420-(gamma-L-Glu)(n) = 2 H+ + NADPH + oxidized coenzyme F420-(gamma-L-Glu)(n).","definition_xrefs":["RHEA:31363","PMID:11726492"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"8-hydroxy-5-deazaflavin:NADPH oxidoreductase activity","secondary_identifiers":["MetaCyc:RXN-12450","EC:1.5.1.40"],"synonyms":[{"name":"F420-dependent NADP reductase activity","type":"broad"}],"termid":"GO:0102261"}


id: GO:0031659
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of cyclin-dependent protein serine/threonine kinase activity contributing to the G1/S transition of the cell cycle.","definition_xrefs":["GOC:pr","GOC:mah","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cyclin-dependent protein serine/threonine kinase activity involved in G1/S transition of mitotic cell cycle (obsolete GO:0031659)","synonyms":[{"name":"G1/S-specific activation of cyclin-dependent protein kinase activity","type":"narrow"},{"name":"G1/S-specific positive regulation of cyclin-dependent protein kinase activity","type":"exact"},{"name":"G1/S-specific stimulation of cyclin-dependent protein kinase activity","type":"narrow"},{"name":"G1/S-specific up regulation of cyclin-dependent protein kinase activity","type":"exact"},{"name":"G1/S-specific up-regulation of cyclin-dependent protein kinase activity","type":"exact"},{"name":"G1/S-specific upregulation of cyclin-dependent protein kinase activity","type":"exact"},{"name":"positive regulation of cyclin-dependent protein kinase activity during G1/S","type":"related"},{"name":"positive regulation of cyclin-dependent protein kinase activity involved in G1/S","type":"broad"}],"termid":"GO:0031659"}


id: GO:0009925
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region of the plasma membrane located at the basal end of the cell. Often used in reference to animal polarized epithelial membranes, where the basal membrane is the part attached to the extracellular matrix, or in plant cells, where the basal membrane is defined with respect to the zygotic axis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane region","termid":"GO:0098590"},{"relation_name":"part_of","term_name":"basal part of cell","termid":"GO:0045178"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0005575"],"is_obsolete":false,"name":"basal plasma membrane","termid":"GO:0009925"}


id: PBO:0077030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"threonine synthase like 1","termid":"PBO:0077030"}


id: PBO:0043973
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"citrate synthase","termid":"PBO:0043973"}


id: PBO:0002742
data:
  {"annotation_feature_type":"gene","cv_name":"ex_tools","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"structure","termid":"PBO:0002742"}


id: GO:0033688
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of osteoblast proliferation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell population proliferation","termid":"GO:0042127"},{"relation_name":"regulates","term_name":"osteoblast proliferation","termid":"GO:0033687"}],"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 osteoblast proliferation","termid":"GO:0033688"}


id: GO:0003174
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the mitral valve over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrioventricular valve development","termid":"GO:0003171"}],"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":"mitral valve development","termid":"GO:0003174"}


id: MONDO:0009862
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dihydropteridine reductase (DHPR) deficiency is a severe form of hyperphenylalaninemia (HPA) due to impaired regeneration of tetrahydrobiopterin (BH4), leading to decreased levels of neurotransmitters (dopamine, serotonin) and folate in cerebrospinal fluid, and causing neurological symptoms such as psychomotor delay, hypotonia, seizures, abnormal movements, hypersalivation, and swallowing difficulties.","definition_xrefs":["Orphanet:226"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperphenylalaninemia due to tetrahydrobiopterin deficiency","termid":"MONDO:0016543"},{"relation_name":"is_a","term_name":"tetrahydrobiopterin metabolic process disease","termid":"MONDO:0045014"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"dihydropteridine reductase deficiency","secondary_identifiers":["GARD:4319","MEDGEN:75682","NCIT:C138173","DOID:0081130","OMIM:261630","SCTID:58256000","UMLS:C0268465","icd11.foundation:1931239861"],"synonyms":[{"name":"6,7-dihydropteridine reductase activity disease","type":"exact"},{"name":"DHPR deficiency","type":"related"},{"name":"HPABH4C","type":"related"},{"name":"PKU type 2","type":"exact"},{"name":"Qdpr deficiency","type":"related"},{"name":"dihydropteridine reductase deficiency","type":"exact"},{"name":"disorder of 6,7-dihydropteridine reductase activity","type":"exact"},{"name":"hyperphenylalaninemia due to dihydropteridine reductase deficiency","type":"exact"},{"name":"hyperphenylalaninemia, BH-4-deficient, C","type":"related"},{"name":"hyperphenylalaninemia, BH4-deficient C","type":"exact"},{"name":"hyperphenylalaninemia, BH4-deficient, C","type":"related"},{"name":"hyperphenylalaninemia, Bh4-deficient, type C","type":"exact"},{"name":"hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to DHPR deficiency","type":"related"},{"name":"phenylketonuria type 2","type":"exact"},{"name":"quinoid dihydropteridine reductase deficiency","type":"related"}],"termid":"MONDO:0009862","xrefs":{"Monarch":{"xref_id":"0009862"}}}


id: MONDO:0007498
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":"ear exostoses","secondary_identifiers":["MEDGEN:56363","OMIM:128300","UMLS:C0155411"],"synonyms":[{"name":"ear exostoses","type":"exact"},{"name":"exostoses of external auditory canal","type":"related"}],"termid":"MONDO:0007498","xrefs":{"Monarch":{"xref_id":"0007498"}}}


id: PBO:0076738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"t-complex 11","termid":"PBO:0076738"}


id: MONDO:0010846
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary multiple osteochondromas","termid":"MONDO:0005508"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exostoses, multiple, type III","secondary_identifiers":["GARD:2206","OMIM:600209","UMLS:C1838420","MEDGEN:333090","MESH:C563975"],"synonyms":[{"name":"EXT3","type":"exact"},{"name":"exostoses, multiple, type 3","type":"related"},{"name":"exostoses, multiple, type III","type":"exact"}],"termid":"MONDO:0010846","xrefs":{"Monarch":{"xref_id":"0010846"}}}


id: GO:0102622
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: linuron + H2O = N,O-dimethylhydroxylamine + carbon dioxide + 3,4-dichloroaniline.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete linuron hydrolase activity (obsolete GO:0102622)","termid":"GO:0102622"}


id: PBO:0065338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteinase 3","termid":"PBO:0065338"}


id: PBO:0075465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spermatogenesis associated 17","termid":"PBO:0075465"}


id: GO:0102025
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 + thiosulfate(out) = ADP + phosphate + thiosulfate(in).","definition_xrefs":["GOC:pz","GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thiosulfate transmembrane transporter activity","termid":"GO:0015117"},{"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:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"ABC-type thiosulfate transporter activity","secondary_identifiers":["RHEA:29871","MetaCyc:ABC-7-RXN","GO:0032146"],"synonyms":[{"name":"ATPase-coupled thiosulfate transmembrane transporter activity","type":"related"},{"name":"thiosulfate transmembrane-transporting ATPase activity","type":"related"},{"name":"thiosulphate ABC transporter activity","type":"exact"}],"termid":"GO:0102025"}


id: GO:0017022
data:
  {"annotated_genes":["SJAG_04781","SJAG_01665"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[81717,73394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032036"}]},"cv_name":"molecular_function","definition":"Binding to a myosin; myosins are any of a superfamily of molecular motor proteins that bind to actin and use the energy of ATP hydrolysis to generate force and movement along actin filaments.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytoskeletal protein binding","termid":"GO:0008092"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01665":null,"SJAG_04781":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:0005515"},{"rel_name":"is_a","termid":"GO:0008092"}],"interesting_parent_ids":["GO:0003674","GO:0008092","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"myosin binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"myosin phosphatase myosin binding","type":"narrow"}],"termid":"GO:0017022","terms_by_termid":{"GO:0032036":null}}


id: PBO:0120282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAML3 antisense RNA 1","termid":"PBO:0120282"}


id: GO:0097727
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An intracellular non-membrane-bounded organelle found in multi-ciliated sperm cells of some primitive land plants, and consisting of many radially arranged ninefold symmetric cylinders. The blepharoplast is involved in de novo formation of multiple centrioles; it enlarges and then disintegrates into many procentrioles, which elongate and ultimately nucleate cilia on the surface of the sperm cell.","definition_xrefs":["GOC:tb","PMID:22691130","GOC:cilia","PMID:25047614"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular membraneless organelle","termid":"GO:0043232"}],"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":"blepharoplast","termid":"GO:0097727"}


id: PBO:0090182
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial TOM complex subunit Tom7","termid":"PBO:0090182"}


id: PR:Q00619
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mam2 gene.","definition_xrefs":["UniProtKB:Q00619","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":"pheromone P-factor receptor (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11H11.04","synonyms":[{"name":"Spom972h-mam2","type":"exact"}],"termid":"PR:Q00619"}


id: GO:0071580
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of zinc ions (Zn2+) from one side of a membrane to the other.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of zinc ion transport","termid":"GO:0071579"},{"relation_name":"is_a","term_name":"regulation of monoatomic cation transmembrane transport","termid":"GO:1904062"},{"relation_name":"regulates","term_name":"zinc ion transmembrane transport","termid":"GO:0071577"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"regulation of zinc ion transmembrane transport","synonyms":[{"name":"regulation of zinc ion membrane transport","type":"exact"}],"termid":"GO:0071580"}


id: GO:0062146
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-chloro-L-lysine + AH2 + O2 = A + formaldehyde + H2O + L-2-amino-4-chloropent-4-enoate + NH4(+).","definition_xrefs":["RHEA:59888","PMID:30867596"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"4-chloro-allylglycine synthase activity","termid":"GO:0062146"}


id: PBO:0053716
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 926","termid":"PBO:0053716"}


id: GO:0018271
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ATP + biotin + protein = AMP + diphosphate + biotin-protein.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete biotin-protein ligase activity (obsolete GO:0018271)","secondary_identifiers":["Reactome:R-HSA-2993802","Reactome:R-HSA-4167511","Reactome:R-HSA-2993447","Reactome:R-HSA-9035987","Reactome:R-HSA-2993799","Reactome:R-HSA-9035988","Reactome:R-HSA-9035990","Reactome:R-HSA-3323184","Reactome:R-HSA-2993814"],"synonyms":[{"name":"biotin-apoprotein ligase activity","type":"exact"}],"termid":"GO:0018271"}


id: MONDO:0000071
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete myopathy, myofibrillar (obsolete MONDO:0000071)","termid":"MONDO:0000071","xrefs":{"Monarch":{"xref_id":"0000071"}}}


id: MONDO:0012999
data:
  {"annotated_genes":["SJAG_02271"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87242],"is_not":false,"summary":null,"term":"MONDO:0012999"}]},"cv_name":"mondo","definition":"A creatine deficiency syndrome characterized by global developmental delay/intellectual disability (DD/ID), prominent speech delay, autistic/hyperactive behavioral disorders, seizures, and various types of pyramidal and/or extra-pyramidal manifestations.","definition_xrefs":["Orphanet:382"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral creatine deficiency syndrome","termid":"MONDO:0000456"},{"relation_name":"is_a","term_name":"creatine biosynthetic process disease","termid":"MONDO:0045018"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02271":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"guanidinoacetate methyltransferase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NORD:1967","DOID:0050799","ICD9:277.6","NANDO:2201300","OMIM:612736","SCTID:124239003","UMLS:C0574080","GARD:2578","icd11.foundation:1811642217","MEDGEN:154356","MESH:C537622","NANDO:1201034"],"synonyms":[{"name":"CCDS2","type":"related"},{"name":"GAMT deficiency","type":"exact"},{"name":"cerebral creatine deficiency syndrome 2","type":"exact"},{"name":"cerebral creatine deficiency syndrome type 2","type":"exact"},{"name":"creatine deficiency syndrome due to GAMT deficiency","type":"related"},{"name":"disorder of guanidinoacetate N-methyltransferase activity","type":"exact"},{"name":"guanidinoacetate N-methyltransferase activity disease","type":"exact"},{"name":"guanidinoacetate methyltransferase deficiency","type":"exact"}],"termid":"MONDO:0012999","terms_by_termid":{"MONDO:0012999":null},"xrefs":{"Monarch":{"xref_id":"0012999"}}}


id: MONDO:0006498
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polypoid adenoma that arises from and protrudes into the lumen of the colon. Epithelial dysplasia is always present. According to the architectural pattern it is classified as tubular, tubulovillous, or villous.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colon adenoma","termid":"MONDO:0000527"},{"relation_name":"is_a","term_name":"polyp of colon","termid":"MONDO:0021400"}],"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":"adenomatous colon polyp","secondary_identifiers":["MEDGEN:163407","UMLS:C0850572","EFO:1000633","NCIT:C96479","SCTID:428054006","HP:0005227"],"synonyms":[{"name":"adenomatous polyp of colon","type":"exact"},{"name":"adenomatous polyp of the colon","type":"exact"},{"name":"colon adenomatous polyp","type":"exact"},{"name":"colonic adenomatous polyp","type":"exact"}],"termid":"MONDO:0006498","xrefs":{"Monarch":{"xref_id":"0006498"}}}


id: PBO:0113220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA-binding protein; binds to the 3'UTR of cell wall-related mRNAs and stabilizes these mRNAs, acting in parallel to cell wall integrity signaling to maintain expression of cell wall genes during stress; acts antagonistically to Nab6p; deletion mutants display increased sensitivity to some cell wall disrupting agents; expression negatively regulated by cAMP","termid":"PBO:0113220"}


id: GO:0034198
data:
  {"annotated_genes":["SJAG_02424","SJAG_02026","SJAG_01184","SJAG_02389","SJAG_04873","SJAG_00209","SJAG_02292","SJAG_00169","SJAG_02973","SJAG_02331"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[62914,73275,73874,75393,75737,77642,96493,97040],"is_not":false,"summary":null,"term":"GO:0034198"},{"annotations":[68126,71094],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903833"}]},"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 deprivation of amino acids.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to starvation","termid":"GO:0009267"},{"relation_name":"is_a","term_name":"response to amino acid starvation","termid":"GO:1990928"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00169":null,"SJAG_00209":null,"SJAG_01184":null,"SJAG_02026":null,"SJAG_02292":null,"SJAG_02331":null,"SJAG_02389":null,"SJAG_02424":null,"SJAG_02973":null,"SJAG_04873":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to amino acid starvation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-9633012","Reactome:R-HSA-9639288"],"synonyms":[{"name":"GAAC response","type":"narrow"},{"name":"general amino acid control response","type":"narrow"}],"termid":"GO:0034198","terms_by_termid":{"GO:0034198":null,"GO:1903833":null}}


id: PBO:0001207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uracil phosphoribosyltransferase (predicted)","termid":"PBO:0001207"}


id: GO:0103072
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: a (R)-2-hydroxy even numbered straight chain 2,3,4-saturated fatty acyl CoA = formyl-CoA + an odd numbered straight chain 2,3,4-saturated fatty aldehyde.","definition_xrefs":["MetaCyc:RXN66-475","GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete straight chain (R)-2-hydroxy fatty acyl-CoA lyase activity (obsolete GO:0103072)","termid":"GO:0103072"}


id: MONDO:0008113
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Schilbach-Rott syndrome (SRS) is an autosomal dominant dysmorphic disorder that is characterized by dysmorphic facies with hypotelorism, blepharophimosis, and cleft palate, and the frequent occurrence of hypospadias in males.","definition_xrefs":["Orphanet:2353"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schilbach-Rott syndrome","secondary_identifiers":["GARD:2930","MEDGEN:371716","MESH:C563509","OMIM:164220","SCTID:721902002","UMLS:C1834038"],"synonyms":[{"name":"BRSS","type":"exact"},{"name":"Schilbach-Rott syndrome","type":"exact"},{"name":"blepharofacioskeletal syndrome","type":"related"},{"name":"cleft palate, hypotelorism, and hypospadias","type":"related"},{"name":"hypotelorism cleft palate hypospadias","type":"related"},{"name":"hypotelorism-cleft palate-hypospadias syndrome","type":"exact"},{"name":"ocular hypotelorism, submucosal cleft palate, and hypospadias","type":"related"}],"termid":"MONDO:0008113","xrefs":{"Monarch":{"xref_id":"0008113"}}}


id: MONDO:0015064
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the jejunum.","definition_xrefs":["NCIT:C135090"],"direct_ancestors":[{"relation_name":"is_a","term_name":"jejunal neoplasm","termid":"MONDO:0002564"},{"relation_name":"is_a","term_name":"small intestine neuroendocrine tumor, well differentiated, low or intermediate grade","termid":"MONDO:0002995"}],"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":"jejunal neuroendocrine tumor, well differentiated, low or intermediate grade","secondary_identifiers":["Orphanet:100077","UMLS:C4525626","MEDGEN:1619460","GARD:19752"],"synonyms":[{"name":"jejunal neuroendocrine neoplasm","type":"exact"},{"name":"jejunal neuroendocrine tumor","type":"related"},{"name":"jejunal neuroendocrine tumour","type":"related"}],"termid":"MONDO:0015064","xrefs":{"Monarch":{"xref_id":"0015064"}}}


id: PBO:0086683
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; identified by homology to <i>Ashbya gossypii</i>","termid":"PBO:0086683"}


id: GO:0071589
data:
  {"annotated_genes":["SJAG_03096"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71652],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071590"},{"annotations":[71653],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071592"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of any pyridine nucleoside, one of a family of organic molecules consisting of a pyridine base covalently bonded to a sugar, usually ribose.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside biosynthetic process","termid":"GO:0009163"},{"relation_name":"is_a","term_name":"pyridine nucleoside metabolic process","termid":"GO:0070637"},{"relation_name":"is_a","term_name":"pyridine-containing compound biosynthetic process","termid":"GO:0072525"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03096":null},"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:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"pyridine nucleoside biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"pyridine nucleoside anabolism","type":"exact"},{"name":"pyridine nucleoside biosynthesis","type":"exact"},{"name":"pyridine nucleoside formation","type":"exact"},{"name":"pyridine nucleoside synthesis","type":"exact"}],"termid":"GO:0071589","terms_by_termid":{"GO:0071590":null,"GO:0071592":null}}


id: PBO:0087342
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Spermidine synthase; involved in biosynthesis of spermidine and also in biosynthesis of pantothenic acid; spermidine is required for growth of wild-type cells","termid":"PBO:0087342"}


id: GO:0044646
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant modulation of complement activation in the bitten/stung organism.","definition_xrefs":["GOC:jl","PMID:20837040","GOC:fj"],"gene_count":0,"genotype_count":0,"name":"obsolete envenomation resulting in modulation of complement activation in another organism (obsolete GO:0044646)","synonyms":[{"name":"envenomation resulting in modulation of complement activation in other organism","type":"exact"},{"name":"envenomation resulting in regulation of complement activation in other organism","type":"exact"}],"termid":"GO:0044646"}


id: GO:2000225
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of testosterone biosynthetic process.","definition_xrefs":["GOC:obol","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of steroid biosynthetic process","termid":"GO:0010894"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"regulation of testosterone biosynthetic process","termid":"GO:2000224"},{"relation_name":"negatively_regulates","term_name":"testosterone biosynthetic process","termid":"GO:0061370"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"negative regulation of testosterone biosynthetic process","termid":"GO:2000225"}


id: PBO:0078781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 6-1","termid":"PBO:0078781"}


id: GO:0006855
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a xenobiotic, a compound foreign to the organism exposed to it, is transported across a membrane. It may be synthesized by another organism (like ampicilin) or it can be a synthetic chemical.","definition_xrefs":["GOC:krc","GOC:ai","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xenobiotic transport","termid":"GO:0042908"},{"relation_name":"is_a","term_name":"transmembrane transport","termid":"GO:0055085"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"xenobiotic transmembrane transport","synonyms":[{"name":"drug membrane transport","type":"exact"},{"name":"drug transmembrane transport","type":"related"},{"name":"multidrug transport","type":"related"}],"termid":"GO:0006855"}


id: PBO:0061032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NINJ2 antisense RNA 1","termid":"PBO:0061032"}


id: MOD:01644
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively removes or replaces an L-phenylalanine.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-phenylalanine residue","termid":"MOD:00914"},{"relation_name":"is_a","term_name":"natural, standard, encoded residue removal","termid":"MOD:01651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-phenylalanine removal","termid":"MOD:01644"}


id: PBO:0063962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol-4-phosphate 5-kinase like 1","termid":"PBO:0063962"}


id: MONDO:0012637
data:
  {"annotated_genes":["SJAG_00041"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88559],"is_not":false,"summary":null,"term":"MONDO:0012637"}]},"cv_name":"mondo","definition":"COG1-CDG is an extremely rare form of CDG syndrome characterized clinically in the few cases reported to date by variable signs including microcephaly, growth retardation, psychomotor retardation and facial dysmorphism.","definition_xrefs":["Orphanet:263508"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"congenital disorder of glycosylation type II","termid":"MONDO:0005501"},{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"defect in conserved oligomeric Golgi complex","termid":"MONDO:0017750"},{"relation_name":"is_a","term_name":"cardiogenetic disease","termid":"MONDO:0100547"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00041":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"},{"rel_name":"is_a","termid":"MONDO:0024322"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005066","MONDO:0024322"],"is_obsolete":false,"name":"COG1-congenital disorder of glycosylation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:611209","DOID:0070259","GARD:10226","MESH:C535756","SCTID:718750004","UMLS:C2931011","MEDGEN:443957"],"synonyms":[{"name":"CDG 2G","type":"related"},{"name":"CDG IIg","type":"related"},{"name":"CDG syndrome type IIg","type":"exact"},{"name":"CDG-IIg","type":"exact"},{"name":"CDG2G","type":"exact"},{"name":"COG1-CDG","type":"exact"},{"name":"COG1-CDG (CDG-IIg)","type":"related"},{"name":"COG1-congenital disorder of glycosylation","type":"exact"},{"name":"Cdgii/Cog1 Cerebrocostomandibular-like syndrome","type":"related"},{"name":"carbohydrate deficient glycoprotein syndrome type IIg","type":"exact"},{"name":"congenital disorder of glycosylation type 2g","type":"exact"},{"name":"congenital disorder of glycosylation type IIg","type":"exact"},{"name":"congenital disorder of glycosylation, type IIg","type":"related"}],"termid":"MONDO:0012637","terms_by_termid":{"MONDO:0012637":null},"xrefs":{"Monarch":{"xref_id":"0012637"}}}


id: PBO:0089738
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CENP-H ortholog Fta3","termid":"PBO:0089738"}


id: PBO:0068409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNFT1 divergent transcript","termid":"PBO:0068409"}


id: MOD:01750
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 Proteome Sciences TMT6plex-129 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TMT6plex reporter+balance reagent O-acylated residue","termid":"MOD:01719"},{"relation_name":"is_a","term_name":"TMT6plex-129 reporter+balance reagent acylated residue","termid":"MOD:01744"},{"relation_name":"is_a","term_name":"O3-acylated L-threonine","termid":"MOD:02004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMT6plex-129 reporter+balance reagent O3-acylated threonine","synonyms":[{"name":"3-[(2,6-dimethylpiperidin-1-yl)acetyl]amino)propanoyl","type":"exact"},{"name":"Sixplex Tandem Mass Tag(TM)","type":"related"},{"name":"TMT6plex","type":"related"}],"termid":"MOD:01750"}


id: PBO:0051955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ITPR2 and SSPN antisense RNA 1","termid":"PBO:0051955"}


id: GO:0060347
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of creating a trabecula in the heart. A trabecula is a tissue element in the form of a small beam, strut or rod.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trabecula formation","termid":"GO:0060343"},{"relation_name":"part_of","term_name":"cardiac chamber morphogenesis","termid":"GO:0003206"},{"relation_name":"part_of","term_name":"heart trabecula morphogenesis","termid":"GO:0061384"}],"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":"heart trabecula formation","synonyms":[{"name":"cardiac trabecula formation","type":"exact"},{"name":"cardiac trabeculation","type":"exact"},{"name":"heart trabecula biogenesis","type":"related"},{"name":"heart trabeculation","type":"exact"}],"termid":"GO:0060347"}


id: MONDO:0018068
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trisomy 13 is a chromosomal anomaly caused by the presence of an extra chromosome 13 and is characterized by brain malformations (holoprosencephaly), facial dysmorphism, ocular anomalies, postaxial polydactyly, visceral malformations (cardiopathy) and severe psychomotor retardation.","definition_xrefs":["Orphanet:3378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"excluded_subClassOf","term_name":"obsolete chromosomal anomaly with cataract (obsolete MONDO:0020226)","termid":"MONDO:0020226"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"congenital vitreoretinal dysplasia","termid":"MONDO:0020247"},{"relation_name":"is_a","term_name":"chromosome 13 disorder","termid":"MONDO:0700020"},{"relation_name":"is_a","term_name":"trisomy","termid":"MONDO:0700065"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0002320"],"is_obsolete":false,"name":"trisomy 13","secondary_identifiers":["UMLS:C0152095","MedDRA:10044686","MEDGEN:56261","ICD9:758.1","NCIT:C101223","MESH:C536305","NCIT:C36529","NANDO:2200964","NORD:1796","icd11.foundation:1435958084","DOID:11665","GARD:7341","SCTID:21111006"],"synonyms":[{"name":"D trisomy syndrome (formerly)","type":"related"},{"name":"D1 trisomy","type":"related"},{"name":"Patau syndrome","type":"exact"},{"name":"Patau's syndrome","type":"exact"},{"name":"Trisomy 13 Syndrome","type":"exact"},{"name":"chromosome 13, trisomy 13 complete","type":"related"},{"name":"trisomy 13","type":"exact"},{"name":"trisomy type 13","type":"exact"}],"termid":"MONDO:0018068","xrefs":{"Monarch":{"xref_id":"0018068"}}}


id: GO:1905810
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of excitatory synapse pruning.","definition_xrefs":["PMID:27779093","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synapse pruning","termid":"GO:1905806"},{"relation_name":"regulates","term_name":"excitatory synapse pruning","termid":"GO:1905805"}],"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 excitatory synapse pruning","synonyms":[{"name":"regulation of synapse clearance","type":"broad"},{"name":"regulation of synapse disassembly","type":"broad"},{"name":"regulation of synapse elimination","type":"broad"},{"name":"regulation of synapse removal","type":"broad"}],"termid":"GO:1905810"}


id: MONDO:0800418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast cancer, familial, susceptibility to, 1","termid":"MONDO:0800418","xrefs":{"Monarch":{"xref_id":"0800418"}}}


id: MONDO:0011695
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"uveal melanoma","termid":"MONDO:0006486"},{"relation_name":"is_a","term_name":"susceptibility to uveal melanoma","termid":"MONDO:0007966"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanoma, uveal, susceptibility to, 1","secondary_identifiers":["MEDGEN:376198","OMIM:606660","UMLS:C1847724"],"synonyms":[{"name":"UVM1","type":"exact"},{"name":"melanoma, uveal, susceptibility to, 1","type":"exact"},{"name":"melanoma, uveal, susceptibility to, type 1","type":"exact"}],"termid":"MONDO:0011695","xrefs":{"Monarch":{"xref_id":"0011695"}}}


id: PBO:0041024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BPI fold containing family B member 9, pseudogene","termid":"PBO:0041024"}


id: MONDO:0034671
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete non-syndromic complex polydactyly (obsolete MONDO:0034671)","secondary_identifiers":["Orphanet:498470"],"termid":"MONDO:0034671","xrefs":{"Monarch":{"xref_id":"0034671"}}}


id: MONDO:0010114
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thanatophoric dysplasia","termid":"MONDO:0017042"}],"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":"thanatophoric dysplasia, Glasgow variant","secondary_identifiers":["UMLS:C1848865","GARD:5165","MEDGEN:376457","Orphanet:93275","MESH:C536506","OMIM:273680"],"synonyms":[{"name":"neonatally lethal short-limb skeletal dysplasia, Glasgow type","type":"related"},{"name":"thanatophoric dysplasia, Glasgow variant","type":"exact"}],"termid":"MONDO:0010114","xrefs":{"Monarch":{"xref_id":"0010114"}}}


id: PBO:0031365
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_5-azacytidine","termid":"PBO:0031365"}


id: FYPO:0005692
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A microtubule cytoskeleton organization phenotype observed in the vegetative growth phase of the life cycle in which nucleation of microtubules from one or more microtubule organizing centers (MTOCs) is abnormal.","definition_xrefs":["PMID:19001497","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 microtubule dynamics during vegetative growth","termid":"FYPO:0000901"},{"relation_name":"is_a","term_name":"abnormal microtubule nucleation","termid":"FYPO:0007484"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"abnormal microtubule nucleation during vegetative growth","synonyms":[{"name":"abnormal microtubule nucleation during mitotic cell cycle","type":"related"},{"name":"microtubule nucleation defects during vegetative growth","type":"exact"}],"termid":"FYPO:0005692"}


id: GO:0102988
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (9Z,12Z)-hexadecadienoyl-CoA + O2 + a reduced electron acceptor = 9,12,15-cis-hexadecatrienoyl-CoA + 2 H2O + an oxidized electron acceptor.","definition_xrefs":["EC:1.14.19.13"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyl-CoA desaturase activity","termid":"GO:0016215"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"acyl-CoA 15-desaturase activity","secondary_identifiers":["MetaCyc:RXN-9617","RHEA:46232"],"synonyms":[{"name":"9,12-cis-hexadecadienoic acid delta 15 desaturase activity","type":"exact"}],"termid":"GO:0102988"}


id: PBO:0116692
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR548BA host gene","termid":"PBO:0116692"}


id: PBO:0058735
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6860","termid":"PBO:0058735"}


id: PBO:0067033
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 47, pseudogene","termid":"PBO:0067033"}


id: GO:0042437
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of indole-3-acetic acid, a compound which functions as a growth regulator in plants.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"indoleacetic acid metabolic process","termid":"GO:0009683"},{"relation_name":"is_a","term_name":"auxin catabolic process","termid":"GO:0009852"},{"relation_name":"is_a","term_name":"indole-containing compound catabolic process","termid":"GO:0042436"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"indoleacetic acid catabolic process","synonyms":[{"name":"IAA catabolic process","type":"exact"},{"name":"indole acetic acid catabolic process","type":"exact"},{"name":"indole acetic acid catabolism","type":"exact"},{"name":"indoleacetic acid breakdown","type":"exact"},{"name":"indoleacetic acid catabolism","type":"exact"},{"name":"indoleacetic acid degradation","type":"exact"}],"termid":"GO:0042437"}


id: PBO:0029253
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_negative_regulation_of_DNA_replication_during_cellular_response_to_methyl_methanesulfonate","termid":"PBO:0029253"}


id: PBO:0053684
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 871","termid":"PBO:0053684"}


id: PBO:0000373
data:
  {"annotation_feature_type":"gene","cv_name":"DNA_binding_specificity","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"binds IDP (GATA) 5'-[AT]GATAA-3'","termid":"PBO:0000373"}


id: GO:0018341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-lysine to form peptidyl-N6-pyruvic acid 2-iminyl-L-lysine.","definition_xrefs":["PSI-MOD:00292"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-lysine modification to peptidyl-N6-pyruvic acid 2-iminyl-L-lysine (obsolete GO:0018341)","synonyms":[{"name":"peptidyl-N6-pyruvic acid 2-iminyl-L-lysine anabolism","type":"exact"},{"name":"peptidyl-N6-pyruvic acid 2-iminyl-L-lysine biosynthesis","type":"exact"},{"name":"peptidyl-N6-pyruvic acid 2-iminyl-L-lysine biosynthetic process","type":"exact"},{"name":"peptidyl-N6-pyruvic acid 2-iminyl-L-lysine formation","type":"exact"},{"name":"peptidyl-N6-pyruvic acid 2-iminyl-L-lysine synthesis","type":"exact"}],"termid":"GO:0018341"}


id: PBO:0012282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cdc48-Npl4-Ufd1 complex subunit Npl4 (predicted)","termid":"PBO:0012282"}


id: GO:0045897
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of transcription that occurs during the mitotic cell cycle.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription during mitotic cell cycle (obsolete GO:0045897)","synonyms":[{"name":"activation of transcription during mitosis","type":"narrow"},{"name":"mitotic activation of transcription","type":"exact"},{"name":"positive regulation of transcription, mitotic","type":"exact"},{"name":"stimulation of transcription during mitosis","type":"narrow"},{"name":"up regulation of transcription during mitosis","type":"exact"},{"name":"up-regulation of transcription during mitosis","type":"exact"},{"name":"upregulation of transcription during mitosis","type":"exact"}],"termid":"GO:0045897"}


id: FYPO:0004589
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 localization of the gamma-tubulin complex to the spindle pole body is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein complex localization","termid":"FYPO:0001440"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0005447","FYPO:0000002","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"abnormal gamma-tubulin complex localization to mitotic spindle pole body","synonyms":[{"name":"abnormal gamma-tubulin complex localisation to mitotic spindle pole body","type":"exact"},{"name":"abnormal gamma-tubulin complex localization to mitotic SPB","type":"exact"},{"name":"abnormal gamma-tubulin complex localization to mitotic spindle pole body during vegetative growth","type":"exact"},{"name":"abnormal gamma-tubulin complex localization to spindle pole body during mitotic cell cycle","type":"related"}],"termid":"FYPO:0004589"}


id: GO:0004221
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ubiquitin C-terminal thioester + H2O = ubiquitin + a thiol.","definition_xrefs":["GOC:jh2","EC:3.1.2.15"],"gene_count":0,"genotype_count":0,"name":"obsolete ubiquitin thiolesterase activity (obsolete GO:0004221)","synonyms":[{"name":"ubiquitin C-terminal hydrolase activity","type":"related"},{"name":"ubiquitin carboxy-terminal esterase activity","type":"related"},{"name":"ubiquitin carboxy-terminal hydrolase activity","type":"related"},{"name":"ubiquitin thioesterase activity","type":"related"},{"name":"ubiquitin thiolesterase activity","type":"exact"},{"name":"ubiquitin-C-terminal-thioester hydrolase activity","type":"related"},{"name":"ubiquitinyl hydrolase 1 activity","type":"narrow"}],"termid":"GO:0004221"}


id: PBO:0055742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LMX1A antisense RNA 2","termid":"PBO:0055742"}


id: GO:0099106
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Modulates the activity of a channel via direct interaction with it. A channel catalyzes energy-independent facilitated diffusion, mediated by passage of a solute through a transmembrane aqueous pore or channel.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"channel regulator activity","termid":"GO:0016247"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0098772","GO:0003674"],"is_obsolete":false,"name":"ion channel regulator activity","termid":"GO:0099106"}


id: PBO:0072189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S17 pseudogene 6","termid":"PBO:0072189"}


id: GO:0046615
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The resumption of the Saccharomyces mitotic cell division cycle by pheromone-arrested cells that have not mated.","definition_xrefs":["PMID:9927449","GOC:krc"],"gene_count":0,"genotype_count":0,"name":"obsolete re-entry into mitotic cell cycle after pheromone arrest (sensu Saccharomyces) (obsolete GO:0046615)","synonyms":[{"name":"re-entry into mitotic cell cycle after pheromone arrest (sensu Saccharomyces)","type":"exact"}],"termid":"GO:0046615"}


id: GO:1902455
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of stem cell population maintenance.","definition_xrefs":["GOC:TermGenie","GOC:hjd","PMID:22969033"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of stem cell population maintenance","termid":"GO:2000036"},{"relation_name":"negatively_regulates","term_name":"stem cell population maintenance","termid":"GO:0019827"}],"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 stem cell population maintenance","synonyms":[{"name":"down regulation of maintenance of pluripotency","type":"related"},{"name":"down regulation of stem cell maintenance","type":"exact"},{"name":"down-regulation of maintenance of pluripotency","type":"related"},{"name":"down-regulation of stem cell maintenance","type":"exact"},{"name":"downregulation of maintenance of pluripotency","type":"related"},{"name":"downregulation of stem cell maintenance","type":"exact"},{"name":"inhibition of maintenance of pluripotency","type":"related"},{"name":"inhibition of stem cell maintenance","type":"narrow"},{"name":"negative regulation of maintenance of pluripotency","type":"related"}],"termid":"GO:1902455"}


id: RO:0002527
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"x does not overlaps the sequence of x if and only if there is no z such that x has a subsequence z and z is a subsequence of y.","direct_ancestors":[{"relation_name":"is_a","term_name":"sequentially_related_to","termid":"RO:0002514"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"does_not_overlap_sequence_of","termid":"RO:0002527"}


id: MONDO:0002255
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cervix disorder","termid":"MONDO:0002256"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypertrophic elongation of cervix","secondary_identifiers":["DOID:2251","ICD9:622.6","SCTID:198353000","MEDGEN:507825","UMLS:C0020561"],"termid":"MONDO:0002255","xrefs":{"Monarch":{"xref_id":"0002255"}}}


id: GO:0090230
data:
  {"annotated_genes":["SJAG_03048","SJAG_00718","SJAG_04638","SJAG_01837"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[119812],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905560"},{"annotations":[104198,91467,118537],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905561"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of centromere complex assembly, the aggregation, arrangement and bonding together of proteins and centromeric DNA molecules to form a centromeric protein-DNA complex.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chromosome organization","termid":"GO:0033044"},{"relation_name":"is_a","term_name":"regulation of protein-containing complex assembly","termid":"GO:0043254"},{"relation_name":"regulates","term_name":"centromere complex assembly","termid":"GO:0034508"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00718":null,"SJAG_01837":null,"SJAG_03048":null,"SJAG_04638":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of centromere complex assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"centromere licensing","type":"related"}],"termid":"GO:0090230","terms_by_termid":{"GO:1905560":null,"GO:1905561":null}}


id: GO:2000220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of pseudohyphal growth.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell growth","termid":"GO:0001558"},{"relation_name":"is_a","term_name":"regulation of growth of unicellular organism as a thread of attached cells","termid":"GO:0070784"},{"relation_name":"regulates","term_name":"pseudohyphal growth","termid":"GO:0007124"}],"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 pseudohyphal growth","termid":"GO:2000220"}


id: SO:0001824
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An inframe increase in cds length that inserts one or more codons into the coding sequence within an existing codon.","definition_xrefs":["EBI:gr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inframe_insertion","termid":"SO:0001821"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disruptive_inframe_insertion","secondary_identifiers":["http://snpeff.sourceforge.net/SnpEff_manual.html"],"synonyms":[{"name":"Jannovar:disruptive_inframe_insertion","type":"exact"},{"name":"disruptive increase in CDS length","type":"exact"},{"name":"disruptive inframe insertion","type":"exact"},{"name":"snpEff:CODON_CHANGE_PLUS_CODON_INSERTION","type":"exact"}],"termid":"SO:0001824"}


id: GO:0060016
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a granulosa cell over time, from its formation to the mature structure. Cell development does not include the steps involved in committing a cell to a granulosa cell fate.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell development","termid":"GO:0002064"},{"relation_name":"part_of","term_name":"granulosa cell differentiation","termid":"GO:0060014"}],"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":"granulosa cell development","termid":"GO:0060016"}


id: GO:1901352
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of phosphatidylglycerol biosynthetic process.","definition_xrefs":["PMID:12869188","GOC:dgf","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of phospholipid biosynthetic process","termid":"GO:0071072"},{"relation_name":"is_a","term_name":"regulation of phosphatidylglycerol biosynthetic process","termid":"GO:1901351"},{"relation_name":"negatively_regulates","term_name":"phosphatidylglycerol biosynthetic process","termid":"GO:0006655"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"negative regulation of phosphatidylglycerol biosynthetic process","synonyms":[{"name":"down regulation of phosphatidylglycerol anabolism","type":"exact"},{"name":"down regulation of phosphatidylglycerol biosynthesis","type":"exact"},{"name":"down regulation of phosphatidylglycerol biosynthetic process","type":"exact"},{"name":"down regulation of phosphatidylglycerol formation","type":"exact"},{"name":"down regulation of phosphatidylglycerol synthesis","type":"exact"},{"name":"down-regulation of phosphatidylglycerol anabolism","type":"exact"},{"name":"down-regulation of phosphatidylglycerol biosynthesis","type":"exact"},{"name":"down-regulation of phosphatidylglycerol biosynthetic process","type":"exact"},{"name":"down-regulation of phosphatidylglycerol formation","type":"exact"},{"name":"down-regulation of phosphatidylglycerol synthesis","type":"exact"},{"name":"downregulation of phosphatidylglycerol anabolism","type":"exact"},{"name":"downregulation of phosphatidylglycerol biosynthesis","type":"exact"},{"name":"downregulation of phosphatidylglycerol biosynthetic process","type":"exact"},{"name":"downregulation of phosphatidylglycerol formation","type":"exact"},{"name":"downregulation of phosphatidylglycerol synthesis","type":"exact"},{"name":"inhibition of phosphatidylglycerol anabolism","type":"narrow"},{"name":"inhibition of phosphatidylglycerol biosynthesis","type":"narrow"},{"name":"inhibition of phosphatidylglycerol biosynthetic process","type":"narrow"},{"name":"inhibition of phosphatidylglycerol formation","type":"narrow"},{"name":"inhibition of phosphatidylglycerol synthesis","type":"narrow"},{"name":"negative regulation of phosphatidylglycerol anabolism","type":"exact"},{"name":"negative regulation of phosphatidylglycerol biosynthesis","type":"exact"},{"name":"negative regulation of phosphatidylglycerol formation","type":"exact"},{"name":"negative regulation of phosphatidylglycerol synthesis","type":"exact"}],"termid":"GO:1901352"}


id: PBO:0074899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 73A","termid":"PBO:0074899"}


id: PBO:0032772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"riboflavin synthase Rib5","termid":"PBO:0032772"}


id: PBO:0043843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CPVL antisense RNA 1","termid":"PBO:0043843"}


id: MONDO:0013981
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic movement disorder characterized by autosomal dominant, adult-onset, slowly progressive, multifocal, cortical myoclonus. Patients present somatosensory-evoked, brief, jerky, involuntary movements in the face, arms and legs, associated in most of cases with sustained, multiple, sudden falls without loss of consciousness. Seizures or other neurological deficits, aside from mild cerebellar ataxia late in the course of the illness, are absent.","definition_xrefs":["Orphanet:319189"],"direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myoclonus, familial","secondary_identifiers":["OMIMPS:614937","SCTID:763770005","GARD:17444"],"synonyms":[{"name":"FCM","type":"related"},{"name":"familial cortical myoclonus","type":"exact"},{"name":"familial myoclonus","type":"exact"},{"name":"myoclonus, familial cortical","type":"exact"}],"termid":"MONDO:0013981","xrefs":{"Monarch":{"xref_id":"0013981"}}}


id: GO:0034738
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: acyl-CoA + lanosterol = CoA + lanosterol ester.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sterol O-acyltransferase activity","termid":"GO:0004772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"lanosterol O-acyltransferase activity","termid":"GO:0034738"}


id: PBO:0089657
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPS15 repeat family actin cortical patch component Ede1","termid":"PBO:0089657"}


id: MONDO:0017949
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Arctic type is a form of HCHWA characterized by an age of onset of 54-61 years and progressive Alzheimer's disease-like dementia, without intracerebral hemorrhages.","definition_xrefs":["Orphanet:324723"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral amyloid angiopathy, APP-related","termid":"MONDO:0011583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0021179"}],"interesting_parent_ids":["MONDO:0021179","MONDO:0005066"],"is_obsolete":false,"name":"ABeta amyloidosis, Arctic type","secondary_identifiers":["ICD10EXP:E85.4+","ICD10EXP:I68.0*","MEDGEN:414032","GARD:17493","UMLS:C2751494"],"synonyms":[{"name":"ABetaE22G amyloidosis","type":"exact"},{"name":"HCHWA, Arctic type","type":"exact"},{"name":"cerebral amyloid angiopathy, APP-related, Arctic variant","type":"exact"},{"name":"hereditary cerebral haemorrhage with amyloidosis, Arctic type","type":"exact"},{"name":"hereditary cerebral hemorrhage with amyloidosis, Arctic type","type":"exact"}],"termid":"MONDO:0017949","xrefs":{"Monarch":{"xref_id":"0017949"}}}


id: GO:0018297
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of a protein-FAD linkage via 1'-(8-alpha-FAD)-L-histidine.","definition_xrefs":["RESID:AA0221"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-FAD linkage via 1'-(8alpha-FAD)-L-histidine (obsolete GO:0018297)","termid":"GO:0018297"}


id: GO:0098988
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with glutamate and transmitting a signal from one side of the membrane to the other by activating an associated G-protein, initiating a change in cell activity.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor activity","termid":"GO:0004930"},{"relation_name":"is_a","term_name":"glutamate receptor activity","termid":"GO:0008066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"G protein-coupled glutamate receptor activity","synonyms":[{"name":"G-protein coupled glutamate receptor activity","type":"exact"}],"termid":"GO:0098988"}


id: FYPO:0007483
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which meiotic spindle pole body duplication is abnormal during the first meiotic nuclear division.","definition_xrefs":["PMID:27889481","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic spindle pole body duplication","termid":"FYPO:0007258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000054","FYPO:0001985","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"abnormal meiotic spindle pole body duplication during meiosis I","synonyms":[{"name":"abnormal meiotic SPB duplication during meiosis I","type":"exact"},{"name":"abnormal meiotic spindle pole body duplication during first meiotic nuclear division","type":"exact"},{"name":"abnormal spindle pole body duplication during meiosis I","type":"exact"}],"termid":"FYPO:0007483"}


id: GO:0070674
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: hypoxanthine + NAD+ + H2O = xanthine + NADH + H+.","definition_xrefs":["GOC:mah","GOC:pde"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH or CH2 groups, NAD or NADP as acceptor","termid":"GO:0016726"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"hypoxanthine dehydrogenase activity","secondary_identifiers":["Reactome:R-HSA-9727347"],"synonyms":[{"name":"NAD-hypoxanthine dehydrogenase activity","type":"related"},{"name":"hypoxanthine oxidoreductase activity","type":"broad"},{"name":"hypoxanthine-NAD oxidoreductase activity","type":"related"},{"name":"hypoxanthine/NAD(+) oxidoreductase activity","type":"related"},{"name":"hypoxanthine/NAD+ oxidoreductase activity","type":"related"},{"name":"hypoxanthine:NAD+ oxidoreductase activity","type":"related"}],"termid":"GO:0070674"}


id: PBO:0084680
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial beta-keto-acyl synthase; possible role in fatty acid synthesis; required for mitochondrial respiration; human homolog OXSM can complement yeast cem1 null mutant","termid":"PBO:0084680"}


id: GO:0070606
data:
  {"annotated_genes":["SJAG_00610","SJAG_00424","SJAG_02278","SJAG_04666"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104671,94240,96756,91254],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070610"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of (1->3)-alpha-D-glucans, compounds composed of glucose residues linked by (1->3)-alpha-D-glucosidic bonds.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of alpha-glucan biosynthetic process","termid":"GO:0032949"},{"relation_name":"is_a","term_name":"regulation of (1->3)-alpha-glucan metabolic process","termid":"GO:0070605"},{"relation_name":"regulates","term_name":"(1->3)-alpha-glucan biosynthetic process","termid":"GO:0070596"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00424":null,"SJAG_00610":null,"SJAG_02278":null,"SJAG_04666":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"regulation of (1->3)-alpha-glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of 1,3-alpha-glucan anabolism","type":"exact"},{"name":"regulation of 1,3-alpha-glucan biosynthesis","type":"exact"},{"name":"regulation of 1,3-alpha-glucan biosynthetic process","type":"exact"},{"name":"regulation of 1,3-alpha-glucan formation","type":"exact"},{"name":"regulation of 1,3-alpha-glucan synthesis","type":"exact"},{"name":"regulation of alpha-1,3 glucan anabolism","type":"exact"},{"name":"regulation of alpha-1,3 glucan biosynthesis","type":"exact"},{"name":"regulation of alpha-1,3 glucan biosynthetic process","type":"exact"},{"name":"regulation of alpha-1,3 glucan formation","type":"exact"},{"name":"regulation of alpha-1,3 glucan synthesis","type":"exact"}],"termid":"GO:0070606","terms_by_termid":{"GO:0070610":null}}


id: PATO:0000144
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000144 solid substance (obsolete PATO:0000144)","termid":"PATO:0000144"}


id: MONDO:0006288
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pheochromocytoma that metastasizes to other anatomic sites. Common sites of metastasis include lymph nodes, bones, liver, and lung. Morphologic features associated with malignant pheochromocytomas include: atypical mitotic figures, capsular and vascular invasion, tumor cell necrosis, and high mitotic activity.","definition_xrefs":["NCIT:C4220"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuroendocrine carcinoma","termid":"MONDO:0002120"},{"relation_name":"is_a","term_name":"central nervous system cancer","termid":"MONDO:0002714"},{"relation_name":"is_a","term_name":"adrenal medulla carcinoma","termid":"MONDO:0004202"},{"relation_name":"is_a","term_name":"adrenal gland pheochromocytoma","termid":"MONDO:0004974"},{"relation_name":"is_a","term_name":"peripheral nervous system cancer","termid":"MONDO:0021089"}],"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":"malignant adrenal gland pheochromocytoma","secondary_identifiers":["ICDO:8700/3","SCTID:21851000119103","UMLS:C0334419","MEDGEN:87238","DOID:0080347","EFO:1000348"],"synonyms":[{"name":"adrenal gland pheochromocytoma, malignant","type":"exact"},{"name":"malignant adrenal gland Chromaffinoma","type":"exact"},{"name":"malignant adrenal gland chromaffin neoplasm","type":"exact"},{"name":"malignant adrenal gland chromaffin paraganglioma","type":"exact"},{"name":"malignant adrenal gland chromaffin tumor","type":"exact"},{"name":"malignant adrenal gland chromaffin tumour","type":"exact"},{"name":"malignant adrenal gland paraganglioma","type":"exact"},{"name":"malignant adrenal gland pheochromocytoma","type":"exact"},{"name":"malignant adrenal medullary paraganglioma","type":"exact"},{"name":"malignant adrenal medullary pheochromocytoma","type":"exact"},{"name":"malignant adrenal pheochromocytoma","type":"exact"},{"name":"malignant pheochromocytoma","type":"exact"},{"name":"pheochromoblastoma","type":"exact"},{"name":"pheochromocytoma, malignant","type":"exact"}],"termid":"MONDO:0006288","xrefs":{"Monarch":{"xref_id":"0006288"}}}


id: PBO:0073934
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC17A6 divergent transcript","termid":"PBO:0073934"}


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


id: MONDO:0022457
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":"ankyloblepharon filiforme imperforate anus","termid":"MONDO:0022457","xrefs":{"Monarch":{"xref_id":"0022457"}}}


id: PBO:0047354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box and leucine rich repeat protein 7","termid":"PBO:0047354"}


id: PBO:0029824
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_curved_vegetative_cell_population_(obsolete_FYPO:0002413)","termid":"PBO:0029824"}


id: PBO:0078995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Thr (anticodon AGT) 2-2","termid":"PBO:0078995"}


id: MONDO:0015167
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of sporadic congenital anomalies, that occur in association with amniotic bands, involving the limbs, craniofacial regions, spine and trunk with a highly variable clinical spectrum ranging from simple digital band constriction (or amputation) to complex craniofacial, central nervous system and visceral anomalies.","definition_xrefs":["Orphanet:1034"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"},{"relation_name":"is_a","term_name":"dysostosis","termid":"MONDO:0018234"}],"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":"amniotic band syndrome","secondary_identifiers":["MEDGEN:66322","NORD:766","GARD:429","MESH:D000652","NCIT:C84552","icd11.foundation:1033549095","OMIM:217100","SCTID:440214006","Orphanet:295000","UMLS:C0220724"],"synonyms":[{"name":"Adam Complex","type":"related"},{"name":"Adam syndrome","type":"exact"},{"name":"CONSTRICTING bands, congenital","type":"related"},{"name":"Streeter anomaly","type":"related"},{"name":"Streeter dysplasia","type":"exact"},{"name":"amniotic band constriction","type":"exact"},{"name":"amniotic band sequence","type":"related"},{"name":"amniotic bands","type":"exact"},{"name":"amniotic bands sequence","type":"related"},{"name":"amniotic deformity-adhesion-mutilation syndrome","type":"exact"},{"name":"amputation, congenital","type":"related"},{"name":"congenital constricting bands","type":"related"},{"name":"congenital ring constrictions","type":"exact"},{"name":"constriction band syndrome","type":"exact"},{"name":"constriction rings syndrome","type":"exact"},{"name":"deformity due to amniotic band","type":"exact"},{"name":"familial amniotic bands","type":"related"},{"name":"terminal transverse defects of arm","type":"related"}],"termid":"MONDO:0015167","xrefs":{"Monarch":{"xref_id":"0015167"}}}


id: PBO:0080083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 45","termid":"PBO:0080083"}


id: PBO:0120224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosome large subunit assembly GTPase Mtg2","termid":"PBO:0120224"}


id: PATO:0001082
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001082 damage value (obsolete PATO:0001082)","termid":"PATO:0001082"}


id: GO:0060376
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of mast cell differentiation, the process in which a relatively unspecialized myeloid precursor cell acquires the specialized features of a mast cell. A mast cell is a cell that is found in almost all tissues containing numerous basophilic granules and capable of releasing large amounts of histamine and heparin upon activation.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of myeloid leukocyte differentiation","termid":"GO:0002763"},{"relation_name":"is_a","term_name":"regulation of mast cell differentiation","termid":"GO:0060375"},{"relation_name":"positively_regulates","term_name":"mast cell differentiation","termid":"GO:0060374"}],"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 mast cell differentiation","termid":"GO:0060376"}


id: SO:0001754
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A SL2_acceptor_site which appends the SL9 RNA leader sequence to the 5' end of an mRNA. SL9 acceptor sites occur in genes in internal segments of polycistronic transcripts.","definition_xrefs":["SO:nlw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SL2_acceptor_site","termid":"SO:0000709"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SL9_acceptor_site","synonyms":[{"name":"SL9 acceptor site","type":"exact"}],"termid":"SO:0001754"}


id: MONDO:0002145
data:
  {"annotated_genes":["SJAG_04337","SJAG_00630"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88740],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009916"},{"annotations":[87998],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010814"}]},"cv_name":"mondo","definition":"A congenital disorder characterized by abnormalities in the development of the sexual characteristics.","definition_xrefs":["NCIT:C103186"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gonadal disorder","termid":"MONDO:0002259"},{"relation_name":"is_a","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00630":null,"SJAG_04337":null},"genotype_count":0,"is_obsolete":false,"name":"disorder of sexual differentiation","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:1923","GTR:AN1172969","UMLS:C2930619","MEDGEN:415936","MESH:D012734","NANDO:2100140","SCTID:39179006","Orphanet:90771","MedDRA:10070597"],"synonyms":[{"name":"CARD","type":"broad"},{"name":"DSD","type":"broad"},{"name":"conditions affecting reproductive development","type":"exact"},{"name":"differences of sex development","type":"exact"},{"name":"disorder of sex development","type":"exact"},{"name":"disorder of sex differentiation","type":"exact"},{"name":"disorder of sexual differentiation","type":"exact"},{"name":"disorders of sex development","type":"exact"},{"name":"disorders of sex development (DSD)","type":"related"},{"name":"intersex","type":"exact"},{"name":"intersex conditions","type":"exact"},{"name":"sex differentiation disease","type":"exact"},{"name":"sex differentiation disorder","type":"exact"},{"name":"sexual differentiation disorder","type":"exact"}],"termid":"MONDO:0002145","terms_by_termid":{"MONDO:0009916":null,"MONDO:0010814":null},"xrefs":{"Monarch":{"xref_id":"0002145"}}}


id: GO:0047041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-carnitine + NAD+ = 3-dehydrocarnitine + H+ + NADH.","definition_xrefs":["EC:1.1.1.254","RHEA:11556"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"(S)-carnitine 3-dehydrogenase activity","secondary_identifiers":["MetaCyc:1.1.1.254-RXN","KEGG_REACTION:R01921"],"synonyms":[{"name":"(S)-carnitine:NAD+ oxidoreductase activity","type":"related"},{"name":"D-carnitine dehydrogenase activity","type":"related"}],"termid":"GO:0047041"}


id: PBO:0090849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial tRNA N6-threonyl-carbamoyl-adenosine (t6A) Sua5","termid":"PBO:0090849"}


id: FYPO:0006630
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetative cell is inviable, elongated, has no septum, and contains four nuclei.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated multinucleate aseptate vegetative cell","termid":"FYPO:0002024"},{"relation_name":"is_a","term_name":"elongated tetranucleate vegetative cell","termid":"FYPO:0004044"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0000631","FYPO:0000004","FYPO:0000002","FYPO:0001985","FYPO:0000032","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"inviable elongated tetranucleate aseptate vegetative cell","synonyms":[{"name":"elongated tetranucleate aseptate inviable vegetative cell","type":"exact"},{"name":"inviable elongated tetranucleate aseptate cell during vegetative growth","type":"exact"},{"name":"inviable elongated tetranucleate aseptate vegetative cell during mitotic cell cycle","type":"related"},{"name":"lethal; elongated tetranucleate aseptate vegetative cell","type":"exact"}],"termid":"FYPO:0006630"}


id: PBO:0045546
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 1","termid":"PBO:0045546"}


id: PBO:0110361
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJC2 pseudogene 1","termid":"PBO:0110361"}


id: PBO:0027901
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_spliced_cen-dg_RNA_level","termid":"PBO:0027901"}


id: PBO:0042002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCDC54 antisense RNA 1","termid":"PBO:0042002"}


id: GO:0001406
data:
  {"annotated_genes":["SJAG_00232","SJAG_05325","SJAG_03644"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104420,104421,104422],"is_not":false,"summary":null,"term":"GO:0001406"}]},"cv_name":"molecular_function","definition":"Enables the transfer of glycerophosphodiesters from one side of a membrane to the other. Glycerophosphodiesters are small molecules composed of glycerol-3-phosphate and an alcohol, for example, glycerophosphoinositol.","definition_xrefs":["PMID:12912892","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"organophosphate ester transmembrane transporter activity","termid":"GO:0015605"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00232":null,"SJAG_03644":null,"SJAG_05325":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"glycerophosphodiester transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0001406","terms_by_termid":{"GO:0001406":null}}


id: GO:0098567
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of a plasma membrane that faces the periplasm, and all proteins embedded in it or attached to its surface.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"external side of plasma membrane","termid":"GO:0009897"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0009986"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0009986"],"is_obsolete":false,"name":"periplasmic side of plasma membrane","termid":"GO:0098567"}


id: GO:0098550
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The side (leaflet) of the early endosome membrane that faces the lumen.","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lumenal side of endosome membrane","termid":"GO:0098565"},{"relation_name":"part_of","term_name":"early endosome membrane","termid":"GO:0031901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005768","GO:0005575","GO:0005737","GO:0031410"],"is_obsolete":false,"name":"lumenal side of early endosome membrane","synonyms":[{"name":"internal leaflet of early endosome membrane","type":"exact"},{"name":"internal side of early endosome membrane","type":"exact"}],"termid":"GO:0098550"}


id: GO:1904591
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of protein import.","definition_xrefs":["PMID:11406629","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein transport","termid":"GO:0051222"},{"relation_name":"is_a","term_name":"regulation of protein import","termid":"GO:1904589"},{"relation_name":"positively_regulates","term_name":"protein import","termid":"GO:0017038"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"positively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"positive regulation of protein import","synonyms":[{"name":"activation of protein import","type":"narrow"},{"name":"activation of protein uptake","type":"narrow"},{"name":"positive regulation of protein uptake","type":"exact"},{"name":"up regulation of protein import","type":"exact"},{"name":"up regulation of protein uptake","type":"exact"},{"name":"up-regulation of protein import","type":"exact"},{"name":"up-regulation of protein uptake","type":"exact"},{"name":"upregulation of protein import","type":"exact"},{"name":"upregulation of protein uptake","type":"exact"}],"termid":"GO:1904591"}


id: GO:0070555
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interleukin-1 stimulus.","definition_xrefs":["GOC:BHF","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cytokine","termid":"GO:0034097"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to interleukin-1","synonyms":[{"name":"response to IL-1","type":"exact"}],"termid":"GO:0070555"}


id: PBO:0081515
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 423","termid":"PBO:0081515"}


id: PR:000050521
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-binding protein scr1 (Schizosaccharomyces pombe) that has not been phosphorylated at positions equivalent to Ser-235, Ser-332, Ser-333, Ser-408, and Ser-410 of the amino acid sequence represented by UniProtKB:O14335. Example: UniProtKB:O14335, Ser-235/Ser-332/Ser-333/Ser-408/Ser-410, PR:000026291.","definition_xrefs":["PMID:22140232","PomBase:VW","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA-binding protein scr1 (Schizosaccharomyces pombe)","termid":"PR:000050519"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"scr1/UnPhos:(S236,S332,S333,S408,S410)","pombase_gene_id":"SPBC1D7.02c","synonyms":[{"name":"PomBase_original_PRO_term_name: DNA-binding protein scr1 unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-scr1/Phos:1","type":"exact"},{"name":"UniProtKB:O14335, Ser-235/Ser-332/Ser-333/Ser-408/Ser-410, PR:000026291","type":"narrow"},{"name":"scr1/UnPhos:(S236,S332,S333,S408,S410)","type":"exact"}],"termid":"PR:000050521"}


id: MONDO:0012903
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 1q43-q44.","definition_xrefs":["DOID:0110502","PMID:18325041"],"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 45","secondary_identifiers":["GARD:22628","OMIM:612433","UMLS:C3888030","MEDGEN:854732"],"synonyms":[{"name":"DFNB45","type":"narrow"},{"name":"autosomal recessive deafness 45","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 45","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 45","type":"narrow"},{"name":"deafness, autosomal recessive 45","type":"narrow"}],"termid":"MONDO:0012903","xrefs":{"Monarch":{"xref_id":"0012903"}}}


id: GO:0008237
data:
  {"annotated_genes":["SJAG_03744","SJAG_00479","SJAG_03429","SJAG_02809","SJAG_01004","SJAG_03752","SJAG_01896","SJAG_00720","SJAG_00662","SJAG_04497","SJAG_04651","SJAG_02900","SJAG_01179","SJAG_01430","SJAG_03686","SJAG_01816","SJAG_04858","SJAG_01281","SJAG_02244","SJAG_03407","SJAG_04215","SJAG_03586","SJAG_03393","SJAG_02397","SJAG_00795","SJAG_04514","SJAG_03648","SJAG_00406","SJAG_03009","SJAG_01542","SJAG_00764","SJAG_04103","SJAG_01838","SJAG_00451","SJAG_01088","SJAG_01321","SJAG_00546","SJAG_01312","SJAG_00730","SJAG_04533","SJAG_02033","SJAG_06636","SJAG_01528","SJAG_00181","SJAG_02419","SJAG_00742","SJAG_00969","SJAG_00762","SJAG_00573","SJAG_03396","SJAG_03022","SJAG_04641","SJAG_02341","SJAG_03147","SJAG_02503"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[63221,65529,68064,73965,78121,100627,104028,108808,116509],"is_not":false,"summary":null,"term":"GO:0008237"},{"annotations":[115484,107632,117030,64306,69821,57408,116673,112185,97119,117102,75959,90310,98358,95951,101691,106447,107464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140492"},{"annotations":[76213,99657,65601,60678,57978,64808,74382,116314],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070006"},{"annotations":[76137,58448],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004181"},{"annotations":[61015,61993],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070573"},{"annotations":[71817,109916,111044,77613,78616,79374,79931,76639,57146,100122,60525,68515,79046,99139,71397],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004222"},{"annotations":[70771,69459],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008235"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of peptide bonds by a mechanism in which water acts as a nucleophile, one or two metal ions hold the water molecule in place, and charged amino acid side chains are ligands for the metal ions.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidase activity","termid":"GO:0008233"}],"gene_count":55,"genes_by_uniquename":{"SJAG_00181":null,"SJAG_00406":null,"SJAG_00451":null,"SJAG_00479":null,"SJAG_00546":null,"SJAG_00573":null,"SJAG_00662":null,"SJAG_00720":null,"SJAG_00730":null,"SJAG_00742":null,"SJAG_00762":null,"SJAG_00764":null,"SJAG_00795":null,"SJAG_00969":null,"SJAG_01004":null,"SJAG_01088":null,"SJAG_01179":null,"SJAG_01281":null,"SJAG_01312":null,"SJAG_01321":null,"SJAG_01430":null,"SJAG_01528":null,"SJAG_01542":null,"SJAG_01816":null,"SJAG_01838":null,"SJAG_01896":null,"SJAG_02033":null,"SJAG_02244":null,"SJAG_02341":null,"SJAG_02397":null,"SJAG_02419":null,"SJAG_02503":null,"SJAG_02809":null,"SJAG_02900":null,"SJAG_03009":null,"SJAG_03022":null,"SJAG_03147":null,"SJAG_03393":null,"SJAG_03396":null,"SJAG_03407":null,"SJAG_03429":null,"SJAG_03586":null,"SJAG_03648":null,"SJAG_03686":null,"SJAG_03744":null,"SJAG_03752":null,"SJAG_04103":null,"SJAG_04215":null,"SJAG_04497":null,"SJAG_04514":null,"SJAG_04533":null,"SJAG_04641":null,"SJAG_04651":null,"SJAG_04858":null,"SJAG_06636":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0003824","GO:0003674","GO:0008233","GO:0016787"],"is_obsolete":false,"name":"metallopeptidase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-9662837","Reactome:R-HSA-9604264","Reactome:R-HSA-157629","Reactome:R-HSA-2220976","Reactome:R-HSA-5211387","Reactome:R-HSA-2220944","Reactome:R-HSA-8986181","Reactome:R-HSA-9013284","Reactome:R-HSA-9759522","Reactome:R-HSA-2730752","Reactome:R-HSA-5211400","Reactome:R-HSA-5211356","Reactome:R-HSA-193679","Reactome:R-HSA-2022393","Reactome:R-HSA-2022396","Reactome:R-HSA-5211405","Reactome:R-HSA-2022368","Reactome:R-HSA-157632","Reactome:R-HSA-2666278","Reactome:R-HSA-3928660","Reactome:R-HSA-2022399","Reactome:R-HSA-5211340","Reactome:R-HSA-5211391"],"synonyms":[{"name":"metalloprotease activity","type":"narrow"},{"name":"metalloproteinase activity","type":"narrow"}],"termid":"GO:0008237","terms_by_termid":{"GO:0004181":null,"GO:0004222":null,"GO:0008235":null,"GO:0008237":null,"GO:0070006":null,"GO:0070573":null,"GO:0140492":null}}


id: MONDO:0004723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign smooth muscle neoplasm arising from the liver. It is characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern.","definition_xrefs":["NCIT:C5753"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign endocrine neoplasm","termid":"MONDO:0000627"},{"relation_name":"is_a","term_name":"leiomyoma","termid":"MONDO:0001572"},{"relation_name":"is_a","term_name":"liver and intrahepatic bile duct neoplasm","termid":"MONDO:0024477"},{"relation_name":"is_a","term_name":"hepatobiliary benign neoplasm","termid":"MONDO:0859689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"liver leiomyoma","secondary_identifiers":["DOID:917","MEDGEN:232276","UMLS:C1333968"],"synonyms":[{"name":"hepatic leiomyoma","type":"exact"},{"name":"leiomyoma of liver","type":"exact"},{"name":"leiomyoma of the liver","type":"exact"},{"name":"liver leiomyoma","type":"exact"}],"termid":"MONDO:0004723","xrefs":{"Monarch":{"xref_id":"0004723"}}}


id: PBO:0087915
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcription factor involved in regulating gluconeogenesis; also involved in the regulation of glyoxylate cycle genes; member of the zinc cluster family of proteins; confers resistance to ketoconazole","termid":"PBO:0087915"}


id: GO:0160075
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a non-canonical inflammasome complex.","definition_xrefs":["PMID:27291964"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0065003"],"is_obsolete":false,"name":"non-canonical inflammasome complex assembly","termid":"GO:0160075"}


id: GO:0005803
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A small subcellular vesicle, or granule, surrounded by a single-layered membrane; formed from the Golgi apparatus and contains a highly concentrated protein destined for secretion.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete secretory vesicle (obsolete GO:0005803)","synonyms":[{"name":"secretory vesicle","type":"exact"},{"name":"transition vesicle","type":"narrow"}],"termid":"GO:0005803"}


id: FYPO:0007369
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which a cell's redox status differs from normal, as measured by the ratios of reduced to oxidized forms of one or more metabolites (e.g. NAD+:NADH).","definition_xrefs":["PMID:32319721","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal vegetative cell phenotype","termid":"FYPO:0003755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"altered cellular redox status","termid":"FYPO:0007369"}


id: PBO:0058562
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6504","termid":"PBO:0058562"}


id: PBO:0054532
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 1932","termid":"PBO:0054532"}


id: FYPO:0000816
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the concentration of a substance released into the growth medium by cells is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered effect on growth medium","termid":"FYPO:0001155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001155"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001155","FYPO:0001985"],"is_obsolete":false,"name":"decreased concentration of substance in growth medium","synonyms":[{"name":"decreased accumulation of substance in growth medium","type":"related"},{"name":"decreased level of substance in growth medium","type":"exact"},{"name":"decreased release of substance into growth medium","type":"related"},{"name":"reduced concentration of substance in growth medium","type":"exact"}],"termid":"FYPO:0000816"}


id: PBO:0068514
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 105, pseudogene","termid":"PBO:0068514"}


id: GO:1905160
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of Factor XII activation.","definition_xrefs":["PMID:617517","GO_REF:0000058","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of Factor XII activation (obsolete GO:1905160)","synonyms":[{"name":"activation of Factor XII activation","type":"narrow"},{"name":"activation of Hageman factor activation","type":"narrow"},{"name":"positive regulation of Hageman factor activation","type":"exact"},{"name":"up regulation of Factor XII activation","type":"exact"},{"name":"up regulation of Hageman factor activation","type":"exact"},{"name":"up-regulation of Factor XII activation","type":"exact"},{"name":"up-regulation of Hageman factor activation","type":"exact"},{"name":"upregulation of Factor XII activation","type":"exact"},{"name":"upregulation of Hageman factor activation","type":"exact"}],"termid":"GO:1905160"}


id: MONDO:0014218
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin disorder","termid":"MONDO:0005093"},{"relation_name":"excluded_subClassOf","term_name":"allergic disease","termid":"MONDO:0005271"},{"relation_name":"excluded_subClassOf","term_name":"hyper-IgE syndrome","termid":"MONDO:0018037"},{"relation_name":"excluded_subClassOf","term_name":"epidermal disease","termid":"MONDO:0019268"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"severe dermatitis-multiple allergies-metabolic wasting syndrome","secondary_identifiers":["UMLS:C3809719","GARD:17594","MEDGEN:816049","OMIM:615508","Orphanet:369992"],"synonyms":[{"name":"EPKHE","type":"related"},{"name":"SAM syndrome","type":"exact"},{"name":"Sam syndrome","type":"related"},{"name":"congenital erythroderma-hypotrichosis-recurrent infections-multiple food allergies syndrome","type":"exact"},{"name":"erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE","type":"exact"},{"name":"erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-IgE","type":"related"},{"name":"severe dermatitis, multiple allergies, and metabolic wasting syndrome","type":"related"}],"termid":"MONDO:0014218","xrefs":{"Monarch":{"xref_id":"0014218"}}}


