# terms

id: PBO:0044646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dendrocyte expressed seven transmembrane protein","termid":"PBO:0044646"}


id: PBO:0059775
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 1","termid":"PBO:0059775"}


id: PBO:0074267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMC5-SMC6 complex localization factor 2","termid":"PBO:0074267"}


id: GO:1904038
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of export of iron ions from inside of a cell, across the plasma membrane and into the extracellular region.","definition_xrefs":["GO_REF:0000058","PMID:15514116","GOC:BHF","GOC:kom","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of iron ion transmembrane transport","termid":"GO:0034759"},{"relation_name":"regulates","term_name":"iron ion export across plasma membrane","termid":"GO:1903988"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of iron export across plasma membrane","synonyms":[{"name":"regulation of ferrous iron export","type":"narrow"},{"name":"regulation of iron(2+) export","type":"narrow"}],"termid":"GO:1904038"}


id: GO:1900115
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any regulation of signal transduction that takes place in the extracellular region.","definition_xrefs":["GOC:signaling","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"extracellular regulation of signal transduction","synonyms":[{"name":"regulation of signaling pathway in extracellular region","type":"exact"},{"name":"regulation of signalling pathway in extracellular region","type":"exact"}],"termid":"GO:1900115"}


id: PBO:0052638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 6","termid":"PBO:0052638"}


id: PBO:0067348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 445, pseudogene","termid":"PBO:0067348"}


id: PBO:0085589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in axial bud site selection; prevents repolarization of cells at previous division sites; recruited by Aim44p and Nap1p to the cell cortex and to cytokinesis remnants (bud scars) where it prevents Rsr1p-mediated activation of Cdc24p, the Cdc42p GEF; localizes to the cytoplasm, and the cell division site prior to being stably recruited to cytokinesis remnants; establishes the transient localization of Rga1p, a Cdc42p GAP, at bud scars along with Nis1p; potential Cdc28p substrate","termid":"PBO:0085589"}


id: PBO:0068964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 208, pseudogene","termid":"PBO:0068964"}


id: MONDO:0007652
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare premalignant hyperproliferative gastropathy characterized by massive overgrowth of foveolar cells in the gastric lining, resulting in large gastric folds, and manifesting with epigastric pain, nausea, vomiting, peripheral edema and, less commonly, anorexia and weight loss.","definition_xrefs":["Orphanet:2494"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"gastritis","termid":"MONDO:0004966"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"gastric mucosal hypertrophy","secondary_identifiers":["GARD:2436","icd11.foundation:1343994188","UMLS:C0017155","EFO:1000946","ICD9:535.2","ICD9:535.20","MedDRA:10017868","OMIM:137280","DOID:8757","MESH:D005758","MEDGEN:4844","ICD9:535.21","NORD:1432","MedDRA:10017807","NCIT:C67277","SCTID:60002000"],"synonyms":[{"name":"MENETRIER disease","type":"exact"},{"name":"Menetrier Disease","type":"exact"},{"name":"Menetrier disease","type":"exact"},{"name":"Menetrier's disease","type":"exact"},{"name":"Ménétrier disease","type":"exact"},{"name":"familial giant hypertrophic gastritis","type":"exact"},{"name":"gastritis, familial giant hypertrophic","type":"related"},{"name":"gastroenteropathy, protein losing","type":"related"},{"name":"giant hypertrophic gastritis","type":"exact"},{"name":"giant hypertrophic gastropathy","type":"related"},{"name":"giant hypertrophy of the gastric mucosa","type":"related"},{"name":"giant rugal hypertrophy of stomach","type":"exact"},{"name":"hypertrophic gastritis","type":"exact"},{"name":"hypertrophic gastropathy","type":"exact"},{"name":"hypoproteinemic hypertrophic gastropathy","type":"exact"}],"termid":"MONDO:0007652","xrefs":{"Monarch":{"xref_id":"0007652"}}}


id: PR:000050599
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A serine/threonine-protein phosphatase PP1-1 (Schizosaccharomyces pombe) that has not been phosphorylated at the position equivalent to Thr-316 of the amino acid sequence represented by UniProtKB:P13681. Example: UniProtKB:P13681, Thr-316, PR:000026291.","definition_xrefs":["PRO:DAN","PMID:7957097","PMID:29899453","PomBase:VW"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine/threonine-protein kinase sid2 (Schizosaccharomyces pombe)","termid":"PR:000050482"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dis2/UnPhos(T316)","pombase_gene_id":"SPBC776.02c","synonyms":[{"name":"PomBase_original_PRO_term_name: serine/threonine-protein phosphatase PP1-1 unphosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-dis2/UnPhos:1","type":"exact"},{"name":"UniProtKB:P13681, Thr-316, PR:000026291","type":"narrow"},{"name":"dis2/UnPhos(T316)","type":"exact"}],"termid":"PR:000050599"}


id: GO:0099160
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The intermediate filament cytoskeleton that is part of a postsynapse.","definition_xrefs":["GOC:dos","PMID:25869803"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate filament cytoskeleton","termid":"GO:0045111"},{"relation_name":"is_a","term_name":"postsynaptic cytoskeleton","termid":"GO:0099571"}],"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":"postsynaptic intermediate filament cytoskeleton","termid":"GO:0099160"}


id: PBO:0047945
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, distamycin A type, rare, fra(16)(q22.1)","termid":"PBO:0047945"}


id: MONDO:1011289
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dacryocystitis that occurs in rabbit.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dacryocystitis, non-human animal","termid":"MONDO:1010360"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dacryocystitis, rabbit","secondary_identifiers":["OMIA:002610-9986"],"termid":"MONDO:1011289","xrefs":{"Monarch":{"xref_id":"1011289"}}}


id: GO:0033557
data:
  {"annotated_genes":["SJAG_05180","SJAG_05237"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[61113,67775],"is_not":false,"summary":null,"term":"GO:0033557"}]},"cv_name":"cellular_component","definition":"A heterodimeric protein complex that possesses an endonuclease activity that specifically cleaves certain types of branched DNA structures; because such structures often form during the replication ribosomal DNA (rDNA) repeats, the complex plays a role in the maintenance of rDNA. The subunits are known as Slx1 and Slx 4 in budding and fission yeasts, and are conserved in eukaryotes.","definition_xrefs":["PMID:14528010","PMID:16467377"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"part_of","term_name":"nuclear chromosome","termid":"GO:0000228"}],"gene_count":2,"genes_by_uniquename":{"SJAG_05180":null,"SJAG_05237":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005694","GO:0005575"],"is_obsolete":false,"name":"Slx1-Slx4 complex","references_by_uniquename":{"GO_REF:0000002":null},"termid":"GO:0033557","terms_by_termid":{"GO:0033557":null}}


id: PBO:0076518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 20","termid":"PBO:0076518"}


id: PBO:0027915
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_nucleus_during_cellular_response_to_hydroxyurea","termid":"PBO:0027915"}


id: PBO:0089618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"threonine aldolase Gly1","termid":"PBO:0089618"}


id: PBO:0041294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C2 calcium dependent domain containing 2","termid":"PBO:0041294"}


id: MONDO:0015581
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete bile acid synthesis defect with cholestasis and malabsorption (obsolete MONDO:0015581)","secondary_identifiers":["Orphanet:163631","icd11.foundation:1295299670"],"termid":"MONDO:0015581","xrefs":{"Monarch":{"xref_id":"0015581"}}}


id: PBO:0053297
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM zinc finger domain containing 3","termid":"PBO:0053297"}


id: PBO:0120056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier, inorganic phosphate/copper, Mir1","termid":"PBO:0120056"}


id: GO:0072136
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of cells, resulting in the expansion of a metanephric mesenchymal cell population.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney mesenchymal cell proliferation","termid":"GO:0072135"},{"relation_name":"is_a","term_name":"cell proliferation involved in metanephros development","termid":"GO:0072203"},{"relation_name":"part_of","term_name":"metanephric mesenchyme development","termid":"GO:0072075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric mesenchymal cell proliferation involved in metanephros development","termid":"GO:0072136"}


id: PR:Q10495
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC26F1.08c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q10495"],"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 C26F1.08c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26F1.08c","synonyms":[{"name":"Spom972h-SPAC26F1.08c","type":"exact"}],"termid":"PR:Q10495"}


id: GO:0106381
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process which produces a purine deoxyribonucleotide from derivatives of it, without de novo synthesis.","definition_xrefs":["PMID:6605343"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine deoxyribonucleotide biosynthetic process","termid":"GO:0009153"},{"relation_name":"is_a","term_name":"purine nucleotide salvage","termid":"GO:0032261"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"purine deoxyribonucleotide salvage","termid":"GO:0106381"}


id: PBO:0031142
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-lagging_mitotic_chromosomes","termid":"PBO:0031142"}


id: GO:0097059
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that is composed of two soluble ciliary neurotrophic factor receptor alpha subunits (product of the CNTFR gene) and two molecules of cardiotrophin-like cytokine factor 1 (product of the CLCF1 gene). The complex is secreted into the extracellular space.","definition_xrefs":["GOC:BHF","PMID:11285233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"extracellular region","termid":"GO:0005576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005576","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"CNTFR-CLCF1 complex","synonyms":[{"name":"sCNTFR-CLC complex","type":"narrow"}],"termid":"GO:0097059"}


id: PBO:0057922
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3648-1","termid":"PBO:0057922"}


id: PBO:0039662
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adaptor related protein complex 2 subunit sigma 1","termid":"PBO:0039662"}


id: GO:0160108
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any developmental process whose specific outcome is the progression of a gross anatomical part of an animal from an initial immature state, to a later, more mature state.","definition_xrefs":["GOC:pg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process","termid":"GO:0032502"}],"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":"animal gross anatomical part developmental process","synonyms":[{"name":"animal development","type":"related"}],"termid":"GO:0160108"}


id: PBO:0083542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified ORF YRF1-4/YLR466W","termid":"PBO:0083542"}


id: PBO:0050583
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heparan sulfate 6-O-sulfotransferase 1","termid":"PBO:0050583"}


id: MONDO:0009647
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mucopolysaccharidosis type 4","termid":"MONDO:0018938"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0002561"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0002561","MONDO:0037792","MONDO:0005066"],"is_obsolete":false,"name":"Morquio syndrome C","secondary_identifiers":["GARD:7059","UMLS:C2931140","MEDGEN:443986","OMIM:252300","MESH:C536247"],"synonyms":[{"name":"Morquio syndrome C","type":"exact"},{"name":"Morquio syndrome type C","type":"exact"},{"name":"Morquio syndrome, Nonkeratosulfate-Excreting type","type":"related"}],"termid":"MONDO:0009647","xrefs":{"Monarch":{"xref_id":"0009647"}}}


id: PBO:0073432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing factor 3b subunit 2","termid":"PBO:0073432"}


id: GO:0048080
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of establishment of a pattern of pigment in the cuticle of an organism.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cuticle pigmentation","termid":"GO:0048079"},{"relation_name":"is_a","term_name":"negative regulation of developmental pigmentation","termid":"GO:0048086"},{"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":"negatively_regulates","term_name":"cuticle pigmentation","termid":"GO:0048067"}],"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 cuticle pigmentation","synonyms":[{"name":"down regulation of cuticle pigmentation","type":"exact"},{"name":"down-regulation of cuticle pigmentation","type":"exact"},{"name":"downregulation of cuticle pigmentation","type":"exact"},{"name":"inhibition of cuticle pigmentation","type":"narrow"}],"termid":"GO:0048080"}


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


id: PBO:0026814
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_RNA_level_during_meiotic_cell_cycle","termid":"PBO:0026814"}


id: GO:0033599
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mammary gland epithelial cell proliferation.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of epithelial cell proliferation","termid":"GO:0050678"},{"relation_name":"regulates","term_name":"mammary gland epithelial cell proliferation","termid":"GO:0033598"}],"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 mammary gland epithelial cell proliferation","termid":"GO:0033599"}


id: GO:0052417
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by an organism involving protein macromolecules within the symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete metabolism by host of symbiont protein (obsolete GO:0052417)","termid":"GO:0052417"}


id: GO:0038119
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by the binding of the C-C chemokine CCL19 to a C-C chemokine type 7 receptor (CCR7) on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:nhn","PMID:15059845","GOC:signaling"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine (C-C motif) ligand 19 signaling pathway","termid":"GO:0038115"},{"relation_name":"is_a","term_name":"C-C chemokine receptor CCR7 signaling pathway","termid":"GO:0038118"}],"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":"CCL19-activated CCR7 signaling pathway","synonyms":[{"name":"CCL19-activated CCR7 signalling pathway","type":"exact"}],"termid":"GO:0038119"}


id: PBO:0052427
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIT proto-oncogene, receptor tyrosine kinase","termid":"PBO:0052427"}


id: PR:Q09847
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- nup146 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q09847"],"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":"nucleoporin nup146 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23D3.06c","synonyms":[{"name":"Spom972h-nup146","type":"exact"},{"name":"nuclear pore protein nup146 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q09847"}


id: _global:depends_on
data:
  {"annotation_feature_type":"gene","cv_name":"external","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"depends_on","secondary_identifiers":["RO:0002502"],"termid":"_global:depends_on"}


id: MONDO:1011046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nephrolithiasis that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephrolithiasis, non-human animal","termid":"MONDO:1010260"},{"relation_name":"is_a","term_name":"urolithiasis, domestic cat","termid":"MONDO:1011080"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nephrolithiasis, domestic cat","secondary_identifiers":["OMIA:000709-9685"],"termid":"MONDO:1011046","xrefs":{"Monarch":{"xref_id":"1011046"}}}


id: GO:1990161
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A homohexameric protein complex that possesses DNA helicase activity; functions during DNA replication and repair.","definition_xrefs":["PMID:17947583","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA helicase complex","termid":"GO:0033202"}],"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":"DnaB helicase complex","synonyms":[{"name":"DnaB hexamer","type":"exact"}],"termid":"GO:1990161"}


id: GO:1901082
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of relaxation of smooth muscle.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of relaxation of muscle","termid":"GO:1901079"},{"relation_name":"is_a","term_name":"regulation of relaxation of smooth muscle","termid":"GO:1901080"},{"relation_name":"positively_regulates","term_name":"relaxation of smooth muscle","termid":"GO:0044557"}],"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 relaxation of smooth muscle","synonyms":[{"name":"activation of relaxation of smooth muscle","type":"narrow"},{"name":"activation of smooth muscle relaxation","type":"exact"},{"name":"positive regulation of smooth muscle relaxation","type":"exact"},{"name":"up regulation of relaxation of smooth muscle","type":"exact"},{"name":"up regulation of smooth muscle relaxation","type":"exact"},{"name":"up-regulation of relaxation of smooth muscle","type":"exact"},{"name":"up-regulation of smooth muscle relaxation","type":"exact"},{"name":"upregulation of relaxation of smooth muscle","type":"exact"},{"name":"upregulation of smooth muscle relaxation","type":"exact"}],"termid":"GO:1901082"}


id: MOD:01874
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-alanine residue to N-carboxy-L-valine.","definition_xrefs":["PubMed:18688235","PubMed:4593770","PubMed:4647257","PubMed:8312270"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-valine residue","termid":"MOD:00920"},{"relation_name":"is_a","term_name":"carboxylated residue","termid":"MOD:01152"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-carboxy-L-valine","synonyms":[{"name":"(S)-2-carboxyamino-propanoic acid","type":"exact"},{"name":"2-carbamic-propanoic acid","type":"exact"},{"name":"N-carboxymethionine","type":"exact"}],"termid":"MOD:01874"}


id: GO:0070849
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 epidermal growth factor stimulus.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to growth factor","termid":"GO:0070848"}],"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 epidermal growth factor","synonyms":[{"name":"response to EGF stimulus","type":"exact"},{"name":"response to epidermal growth factor stimulus","type":"exact"}],"termid":"GO:0070849"}


id: MONDO:0018352
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A squamous cell carcinoma arising from the penis. It occurs chiefly in the squamous epithelium of the glans, coronal sulcus, and foreskin. Etiologic factors include phimosis, lichen sclerosus, smoking, ultraviolet irradiation, history of warts or condylomas, and lack of circumcision. Human papilloma virus is present in a subset of penile squamous cell carcinomas. Patients may present with an exophytic or flat ulcerative mass in the glans or a large primary tumor with inguinal nodal and skin metastases. Morphologic variants include the basaloid carcinoma, warty (condylomatous) carcinoma, verrucous carcinoma, and sarcomatoid (spindle cell) carcinoma. (WHO, 2004)","definition_xrefs":["NCIT:C7729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma","termid":"MONDO:0005096"},{"relation_name":"is_a","term_name":"penile carcinoma","termid":"MONDO:0006360"}],"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":"squamous cell carcinoma of penis","secondary_identifiers":["GARD:21639","DOID:5518","Orphanet:398058","MEDGEN:116057","UMLS:C0238348","SCTID:403468003","icd11.foundation:186592209","ONCOTREE:PSCC"],"synonyms":[{"name":"PSCC","type":"related"},{"name":"epidermoid carcinoma of penis","type":"exact"},{"name":"epidermoid carcinoma of the penis","type":"exact"},{"name":"epidermoid cell carcinoma of penis","type":"exact"},{"name":"epidermoid cell carcinoma of the penis","type":"exact"},{"name":"penile epidermoid carcinoma","type":"exact"},{"name":"penile epidermoid cell carcinoma","type":"exact"},{"name":"penile squamous car.(epidermoid)","type":"exact"},{"name":"penile squamous carcinoma (epidermoid)","type":"exact"},{"name":"penile squamous cell cancer","type":"exact"},{"name":"penile squamous cell carcinoma","type":"exact"},{"name":"penis squamous cell carcinoma","type":"exact"},{"name":"squamous cell carcinoma of penis","type":"exact"},{"name":"squamous cell carcinoma of the penis","type":"exact"}],"termid":"MONDO:0018352","xrefs":{"Monarch":{"xref_id":"0018352"}}}


id: SO:0002088
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript variant occurring within the splice region (1-3 bases of the exon or 3-8 bases of the intron) of a non coding transcript.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non_coding_transcript_variant","termid":"SO:0001619"},{"relation_name":"is_a","term_name":"splice_region_variant","termid":"SO:0001630"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non_coding_transcript_splice_region_variant","synonyms":[{"name":"ANNOVAR:ncRNA_splicing","type":"narrow"}],"termid":"SO:0002088"}


id: MONDO:0010905
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cone-rod dystrophy","termid":"MONDO:0015993"}],"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":"cone-rod dystrophy 1","secondary_identifiers":["MEDGEN:371596","UMLS:C1833564","OMIM:600624","DOID:0111009","GARD:10651","MESH:C563469"],"synonyms":[{"name":"CORD1","type":"exact"},{"name":"CRD1","type":"exact"},{"name":"Crd1","type":"related"},{"name":"cone-rod dystrophy 1","type":"exact"},{"name":"cone-rod dystrophy type 1","type":"exact"},{"name":"cone-rod retinal dystrophy-1","type":"exact"}],"termid":"MONDO:0010905","xrefs":{"Monarch":{"xref_id":"0010905"}}}


id: GO:0015996
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of chlorophyll, any compound of magnesium complexed in a porphyrin (tetrapyrrole) ring and which functions as a photosynthetic pigment, into less complex products.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porphyrin-containing compound catabolic process","termid":"GO:0006787"},{"relation_name":"is_a","term_name":"chlorophyll metabolic process","termid":"GO:0015994"},{"relation_name":"is_a","term_name":"pigment catabolic process","termid":"GO:0046149"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0033013","GO:0008150"],"is_obsolete":false,"name":"chlorophyll catabolic process","synonyms":[{"name":"chlorophyll breakdown","type":"exact"},{"name":"chlorophyll catabolism","type":"exact"},{"name":"chlorophyll degradation","type":"exact"}],"termid":"GO:0015996"}


id: MONDO:0014744
data:
  {"annotated_genes":["SJAG_04622"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87672],"is_not":false,"summary":null,"term":"MONDO:0014744"}]},"cv_name":"mondo","definition":"An autosomal recessive cerebellar ataxia that has material basis in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.","definition_xrefs":["DOID:0111155"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive syndromic cerebellar ataxia","termid":"MONDO:0020047"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04622":null},"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":"acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:17833","OMIM:616719","Orphanet:466794","UMLS:C5569084","MEDGEN:1800507"],"synonyms":[{"name":"SCAR21","type":"exact"},{"name":"acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia 21","type":"related"},{"name":"autosomal recessive spinocerebellar ataxia 21 with hepatopathy","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia type 21","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 21","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 21, with hepatopathy","type":"related"},{"name":"spinocerebellar ataxia, autosomal recessive type 21","type":"exact"}],"termid":"MONDO:0014744","terms_by_termid":{"MONDO:0014744":null},"xrefs":{"Monarch":{"xref_id":"0014744"}}}


id: PBO:0062085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily A member 16","termid":"PBO:0062085"}


id: PBO:0116665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARF like GTPase 5A","termid":"PBO:0116665"}


id: MONDO:0001123
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the sphenoid 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:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sphenoid sinusitis","termid":"MONDO:0005964"},{"relation_name":"is_a","term_name":"chronic rhinosinusitis","termid":"MONDO:0006031"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic sphenoidal sinusitis","secondary_identifiers":["SCTID:38961000","DOID:10793","ICD10CM:J32.3","ICD9:473.3","NCIT:C34480","icd11.foundation:627227610","UMLS:C0008712","MEDGEN:3087"],"synonyms":[{"name":"chronic sphenoid sinusitis","type":"exact"},{"name":"sphenoid sinusitis, chronic","type":"exact"},{"name":"sphenoidal sinus-chr.","type":"exact"}],"termid":"MONDO:0001123","xrefs":{"Monarch":{"xref_id":"0001123"}}}


id: PBO:0063988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 22","termid":"PBO:0063988"}


id: MONDO:0015668
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. The hereditary dentin disorders, dentinogenesis imperfecta (DGI) and dentin dysplasia (DD), comprise a group of conditions characterized by abnormal dentin structure affecting either the primary or both the primary and secondary dentitions.","definition_xrefs":["Orphanet:167759"],"gene_count":0,"genotype_count":0,"name":"obsolete hereditary dentin defect (obsolete MONDO:0015668)","termid":"MONDO:0015668","xrefs":{"Monarch":{"xref_id":"0015668"}}}


id: FYPO:0000687
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase 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:0001985"},{"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:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0001985","FYPO:0000661","FYPO:0000654","FYPO:0000707"],"is_obsolete":false,"name":"abnormal peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase activity","termid":"FYPO:0000687"}


id: PBO:0001337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitinated histone-like protein Uhp1","termid":"PBO:0001337"}


id: PBO:0082489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Catalytically inactive alanine transaminase; expression is repressed in the presence of alanine and repression is mediated by Nrg1p; ALT2 has a paralog, ALT1, that arose from the whole genome duplication","termid":"PBO:0082489"}


id: FYPO:0004795
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the meiotic nuclear divisions are normal (i.e. indistinguishable from wild type) during a cycle of zygotic meiosis and sporulation. Zygotic meiosis and sporulation take place under conditions of continuous nitrogen starvation, in which haploid cells of the opposite mating types conjugate to form diploid zygotes that proceed immediately to undergo meiosis and sporulation.","definition_xrefs":["PMID:22558440","PMID:25891897","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal meiosis","termid":"FYPO:0000478"}],"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 zygotic meiosis","synonyms":[{"name":"normal meiosis during zygotic meiosis","type":"exact"},{"name":"normal zygotic meiotic nuclear division","type":"exact"}],"termid":"FYPO:0004795"}


id: PBO:0073406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SET pseudogene 9","termid":"PBO:0073406"}


id: PBO:0018119
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Defective In Sister chromatid disjoining","termid":"PBO:0018119"}


id: GO:0048077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of establishment of a pattern of pigment in the compound eye.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of eye pigmentation","termid":"GO:0048074"},{"relation_name":"is_a","term_name":"regulation of compound eye pigmentation","termid":"GO:0048076"},{"relation_name":"negatively_regulates","term_name":"compound eye pigmentation","termid":"GO:0048072"}],"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 compound eye pigmentation","synonyms":[{"name":"down regulation of eye pigmentation","type":"broad"},{"name":"down-regulation of eye pigmentation","type":"broad"},{"name":"downregulation of eye pigmentation","type":"broad"},{"name":"inhibition of eye pigmentation","type":"broad"},{"name":"negative regulation of eye pigmentation","type":"broad"}],"termid":"GO:0048077"}


id: GO:0140872
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of viridicatumtoxin, a tetracycline-like fungal meroterpenoid with a unique, fused spirobicyclic ring system.","definition_xrefs":["PMID:20534346","PMID:24161266"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyketide biosynthetic process","termid":"GO:0030639"},{"relation_name":"is_a","term_name":"ketone biosynthetic process","termid":"GO:0042181"},{"relation_name":"is_a","term_name":"mycotoxin biosynthetic process","termid":"GO:0043386"},{"relation_name":"is_a","term_name":"amide biosynthetic process","termid":"GO:0043604"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"olefinic compound biosynthetic process","termid":"GO:0120255"},{"relation_name":"is_a","term_name":"ether biosynthetic process","termid":"GO:1901503"},{"relation_name":"is_a","term_name":"tertiary alcohol biosynthetic process","termid":"GO:1902645"},{"relation_name":"is_a","term_name":"secondary alcohol biosynthetic process","termid":"GO:1902653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"viridicatumtoxin biosynthetic process","secondary_identifiers":["MetaCyc:PWY-7659"],"synonyms":[{"name":"viridicatumtoxin anabolism","type":"exact"},{"name":"viridicatumtoxin biosynthesis","type":"exact"},{"name":"viridicatumtoxin formation","type":"exact"},{"name":"viridicatumtoxin synthesis","type":"exact"}],"termid":"GO:0140872"}


id: GO:0021575
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structure of the hindbrain is generated and organized. The hindbrain is the region consisting of the medulla, pons and cerebellum. Areas of the hindbrain control motor and autonomic functions.","definition_xrefs":["ISBN:0838580343","GO_REF:0000021","GOC:dgh","GOC:cls","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"hindbrain development","termid":"GO:0030902"}],"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":"hindbrain morphogenesis","synonyms":[{"name":"rhombencephalon morphogenesis","type":"related"}],"termid":"GO:0021575"}


id: PBO:0088856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"palmitoyltransferase Akr1","termid":"PBO:0088856"}


id: PBO:0044172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"catenin alpha 1 pseudogene 1","termid":"PBO:0044172"}


id: PBO:0074640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 32","termid":"PBO:0074640"}


id: FYPO:0006952
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 N2-acetyl-L-lysine measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"increased cellular N2-acetyl-L-lysine level","synonyms":[{"name":"increased N2-acetyl-L-lysine accumulation","type":"related"},{"name":"increased cellular N2-acetyl-L-lysine level during mitotic cell cycle","type":"related"},{"name":"increased cellular N2-acetyl-L-lysine level during vegetative growth","type":"exact"},{"name":"increased cellular N2-acetyl-lysine level","type":"exact"}],"termid":"FYPO:0006952"}


id: GO:2000473
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hematopoietic stem cell migration.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell migration","termid":"GO:0030335"},{"relation_name":"is_a","term_name":"regulation of hematopoietic stem cell migration","termid":"GO:2000471"},{"relation_name":"positively_regulates","term_name":"hematopoietic stem cell migration","termid":"GO:0035701"}],"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 hematopoietic stem cell migration","synonyms":[{"name":"positive regulation of hemopoietic stem cell migration","type":"exact"}],"termid":"GO:2000473"}


id: GO:0042898
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of fosmidomycin, a phosphonic acid derivative with potent activity against Gram-negative organisms, from one side of a membrane to the other.","definition_xrefs":["PMID:12543685","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amide transmembrane transporter activity","termid":"GO:0042887"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"fosmidomycin transmembrane transporter activity","synonyms":[{"name":"fosmidomycin transporter activity","type":"related"}],"termid":"GO:0042898"}


id: PBO:0053356
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 260","termid":"PBO:0053356"}


id: PBO:0002559
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by Ste11","termid":"PBO:0002559"}


id: PBO:0067779
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 79","termid":"PBO:0067779"}


id: PBO:0028371
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_GT_repeat_stability","termid":"PBO:0028371"}


id: PBO:0000085
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"possible horizontal transfer","termid":"PBO:0000085"}


id: PBO:0052259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine demethylase 1B","termid":"PBO:0052259"}


id: PBO:0040833
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"baculoviral IAP repeat containing 7","termid":"PBO:0040833"}


id: GO:0102479
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: quercetin-7-olate + UDP-D-galactose = quercetin 3-O-beta-D-galactopyranoside + UDP(3-) + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete quercetin 3-O-beta:-D-galactosyltransferase activity (obsolete GO:0102479)","termid":"GO:0102479"}


id: MONDO:1012702
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked form of progressive retinal atrophy that occurs in dogs due to a mutation in the RPGR gene and is characterized by severe manifestation during early retinal development.","definition_xrefs":["PMID:32176262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progressive retinal atrophy, dog","termid":"MONDO:1012226"},{"relation_name":"is_a","term_name":"X-linked disease, non-human animal","termid":"MONDO:1012575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-linked progressive retinal atrophy 2, RPGR-related, dog","secondary_identifiers":["OMIA:001518-9615"],"synonyms":[{"name":"XLPRA2","type":"exact"},{"name":"progressive retinal atrophy, X-linked, type 2, dog","type":"related"}],"termid":"MONDO:1012702","xrefs":{"Monarch":{"xref_id":"1012702"}}}


id: PBO:0061091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NK3 homeobox 2","termid":"PBO:0061091"}


id: MONDO:0006211
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A poorly circumscribed neoplasm arising from the soft tissues in infants. It is characterized by the presence of bland fibroblastic spindle cells, collagenous stroma formation, primitive mesenchymal round cells, and mature fat cells. These components combined form a distinct organoid pattern.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mesenchymal hamartoma","termid":"MONDO:0024478"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrous hamartoma of infancy","secondary_identifiers":["UMLS:C0265979","EFO:1000257","icd11.foundation:1496992098","NCIT:C3942","ICD9:215.9","MEDGEN:120562","SCTID:56364004"],"synonyms":[{"name":"fibrous hamartoma","type":"exact"},{"name":"fibrous hamartoma of infancy","type":"exact"},{"name":"infantile fibrous hamartoma","type":"exact"}],"termid":"MONDO:0006211","xrefs":{"Monarch":{"xref_id":"0006211"}}}


id: GO:0010514
data:
  {"annotated_genes":["SJAG_02723","SJAG_04026","SJAG_03802","SJAG_03081","SJAG_03309","SJAG_02730","SJAG_02066","SJAG_01113","SJAG_04009","SJAG_03735","SJAG_02773","SJAG_05153","SJAG_06638","SJAG_00526","SJAG_04312","SJAG_02266","SJAG_01254","SJAG_00256","SJAG_04813","SJAG_00210","SJAG_03486","SJAG_01311","SJAG_00781","SJAG_03501","SJAG_02592","SJAG_03346","SJAG_00472","SJAG_02785","SJAG_03067","SJAG_00975","SJAG_02472","SJAG_01699","SJAG_01718","SJAG_04206","SJAG_00600","SJAG_01084","SJAG_02444"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89842,91027,108105,118001,118342,120096],"is_not":false,"summary":null,"term":"GO:0010514"},{"annotations":[100228],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031141"},{"annotations":[117448],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031142"},{"annotations":[103667,96038,116329,108679,107637,107734,94740,117394,117929,106323,102358,108329,110855,96180,108483,90019,93221],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0010515"},{"annotations":[102316,103210,106263,105184,89667,108884,118136,110647,120973,101314,120974,110413],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1900237"}]},"cv_name":"biological_process","definition":"The process in which a cell initiates conjugation with cellular fusion. Conjugation with cellular fusion is the process that results in the union of cellular and genetic information from compatible mating types.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of conjugation with cellular fusion","termid":"GO:0031139"}],"gene_count":37,"genes_by_uniquename":{"SJAG_00210":null,"SJAG_00256":null,"SJAG_00472":null,"SJAG_00526":null,"SJAG_00600":null,"SJAG_00781":null,"SJAG_00975":null,"SJAG_01084":null,"SJAG_01113":null,"SJAG_01254":null,"SJAG_01311":null,"SJAG_01699":null,"SJAG_01718":null,"SJAG_02066":null,"SJAG_02266":null,"SJAG_02444":null,"SJAG_02472":null,"SJAG_02592":null,"SJAG_02723":null,"SJAG_02730":null,"SJAG_02773":null,"SJAG_02785":null,"SJAG_03067":null,"SJAG_03081":null,"SJAG_03309":null,"SJAG_03346":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03735":null,"SJAG_03802":null,"SJAG_04009":null,"SJAG_04026":null,"SJAG_04206":null,"SJAG_04312":null,"SJAG_04813":null,"SJAG_05153":null,"SJAG_06638":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"positively_regulates","termid":"GO:0000747"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0000747"}],"interesting_parent_ids":["GO:0008150","GO:0000747"],"is_obsolete":false,"name":"induction of conjugation with cellular fusion","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0010514","terms_by_termid":{"GO:0010514":null,"GO:0010515":null,"GO:0031141":null,"GO:0031142":null,"GO:1900237":null}}


id: GO:1900400
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A regulation of transcription from RNA polymerase II promoter that results in regulation of iron ion import.","definition_xrefs":["PMID:18622392","GOC:mah","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of iron ion import into cell by regulation of transcription from RNA polymerase II promoter (obsolete GO:1900400)","synonyms":[{"name":"regulation of iron import by regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of iron ion import by regulation of transcription from RNA polymerase II promoter","type":"related"},{"name":"regulation of iron ion transport by regulation of transcription from RNA polymerase II promoter","type":"broad"}],"termid":"GO:1900400"}


id: MONDO:0013511
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":"cyanosis, transient neonatal","secondary_identifiers":["OMIM:613977","UMLS:C3151421","MEDGEN:462771"],"synonyms":[{"name":"TNCY","type":"related"},{"name":"cyanosis, transient neonatal","type":"exact"}],"termid":"MONDO:0013511","xrefs":{"Monarch":{"xref_id":"0013511"}}}


id: GO:0102186
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4alpha-formyl,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3beta-ol + NADH(2-) + O2 = 4alpha-carboxy,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3beta-ol + NAD(1-) + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 4alpha-formyl,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3beta-ol-4alpha-methyl oxidase activity (obsolete GO:0102186)","termid":"GO:0102186"}


id: MONDO:0022202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"locational disease characteristic","termid":"MONDO:0045040"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disseminated","termid":"MONDO:0022202","xrefs":{"Monarch":{"xref_id":"0022202"}}}


id: PBO:0049174
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growth factor receptor bound protein 7","termid":"PBO:0049174"}


id: MONDO:0011631
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of rare hemochromatosis (HC) characterized by increased transferrin saturation and hepatocellular iron deposition with distribution patterns and clinical features indistinguishable from patients with other types of HC.","definition_xrefs":["Orphanet:647834"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hemochromatosis","termid":"MONDO:0006507"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"hemochromatosis type 4","secondary_identifiers":["MEDGEN:340044","Orphanet:648562","NORD:1137","OMIM:606069","SCTID:719975002","UMLS:C1853733","MESH:C537249","DOID:0111028","Orphanet:139491","GARD:10094"],"synonyms":[{"name":"Ferroportin Disease","type":"exact"},{"name":"HFE4","type":"exact"},{"name":"SLC40A1 hereditary hemochromatosis","type":"exact"},{"name":"autosomal dominant hereditary hemochromatosis","type":"exact"},{"name":"ferroportin disease","type":"exact"},{"name":"hemochromatosis due to defect in ferroportin","type":"exact"},{"name":"hemochromatosis, autosomal dominant","type":"related"},{"name":"hemochromatosis, type 4","type":"related"},{"name":"hereditary hemochromatosis caused by mutation in SLC40A1","type":"exact"}],"termid":"MONDO:0011631","xrefs":{"Monarch":{"xref_id":"0011631"}}}


id: GO:0004394
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3'-phosphoadenosine 5'-phosphosulfate + heparan sulfate = adenosine 3',5'-bisphosphate + heparan sulfate 2-O-sulfate; results in 2-O-sulfation of iduronic acid residues in heparan sulfate.","definition_xrefs":["PMID:9153262"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016782"}],"interesting_parent_ids":["GO:0016782","GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"heparan sulfate 2-sulfotransferase activity","secondary_identifiers":["Reactome:R-HSA-2076508","MetaCyc:RXN-11558"],"synonyms":[{"name":"heparan sulfate 2-O-sulfotransferase activity","type":"exact"},{"name":"heparan-sulfate 2-O-sulphotransferase activity","type":"exact"},{"name":"heparin 2-sulfotransferase activity","type":"related"},{"name":"heparin-sulphate 2-sulphotransferase activity","type":"related"}],"termid":"GO:0004394"}


id: PATO:0002414
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality of duration having progressive course of indefinite duration with active, acute-like elements.","definition_xrefs":["PATOC:MPATH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic","termid":"PATO:0001863"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chronic-active","termid":"PATO:0002414"}


id: PBO:0071014
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 16","termid":"PBO:0071014"}


id: FYPO:0001220
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein measured in a cell during a cellular response to a pheromone is higher than normal. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level","termid":"FYPO:0000836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased protein level during cellular response to pheromone","synonyms":[{"name":"increased protein accumulation during cellular response to pheromone","type":"related"},{"name":"increased protein level during cellular response to pheromone during mitotic cell cycle","type":"related"},{"name":"increased protein level during cellular response to pheromone during vegetative growth","type":"exact"}],"termid":"FYPO:0001220"}


id: PBO:0046581
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K member 23","termid":"PBO:0046581"}


id: GO:0004969
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with histamine to initiate a change in cell activity. Histamine is a physiologically active amine, found in plant and animal tissue and released from mast cells as part of an allergic reaction in humans.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled amine receptor activity","termid":"GO:0008227"}],"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":"histamine receptor activity","termid":"GO:0004969"}


id: FYPO:0005054
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular response phenotype observed in the vegetative growth phase of the life cycle in which the regulation of the mitotic cell cycle in response to latrunculin A is normal (i.e. indistinguishable from wild type). Normally, cell cycle progression is slowed or arrested transiently following exposure to latrunculin A.","definition_xrefs":["PMID:15537703","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal regulation of mitotic cell cycle","termid":"FYPO:0001928"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001312","FYPO:0000257"],"is_obsolete":false,"name":"normal cell cycle regulation during cellular response to latrunculin A","synonyms":[{"name":"normal cell cycle delay following latrunculin A exposure","type":"narrow"},{"name":"normal cell cycle regulation during cellular response to LatA","type":"exact"},{"name":"normal cell cycle regulation during cellular response to latrunculin A during mitotic cell cycle","type":"related"},{"name":"normal cell cycle regulation during cellular response to latrunculin A during vegetative growth","type":"exact"},{"name":"normal cell cycle regulation in response to latrunculin A","type":"exact"},{"name":"normal mitotic cell cycle regulation during cellular response to latrunculin A","type":"exact"}],"termid":"FYPO:0005054"}


id: GO:1904069
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving ascaroside.","definition_xrefs":["GO_REF:0000068","GOC:TermGenie","PMID:25775534","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycoside metabolic process","termid":"GO:0016137"}],"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":"ascaroside metabolic process","synonyms":[{"name":"ascaroside metabolism","type":"exact"}],"termid":"GO:1904069"}


id: PBO:0053521
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 515","termid":"PBO:0053521"}


id: GO:0106309
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: O2 + progesterone + reduced [NADPH--hemoprotein reductase] = 21-hydroxyprogesterone + H+ + H2O + oxidized [NADPH--hemoprotein reductase].","definition_xrefs":["RHEA:50304","PMID:25855791"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid 21-monooxygenase activity","termid":"GO:0004509"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"progesterone 21-hydroxylase activity","secondary_identifiers":["Reactome:R-HSA-193964","Reactome:R-HSA-193981"],"termid":"GO:0106309"}


id: FYPO:0003248
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 histone H3 measured at centromere inner repeat regions is higher than normal.","definition_xrefs":["PomBase:mah","PMID:22291963"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level during vegetative growth","termid":"FYPO:0001327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0006551","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"increased level of histone H3 at centromere inner repeat","synonyms":[{"name":"increased level of histone H3 at centromere imr","type":"exact"},{"name":"increased level of histone H3 at centromere inner repeat during mitotic cell cycle","type":"related"},{"name":"increased level of histone H3 at centromere inner repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0003248"}


id: GO:0042789
data:
  {"annotated_genes":["SJAG_01713"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79835],"is_not":false,"summary":null,"term":"GO:0042789"}]},"cv_name":"biological_process","definition":"The cellular synthesis of messenger RNA (mRNA) from a DNA template by RNA polymerase II, originating at an RNA polymerase II promoter.","definition_xrefs":["GOC:jl","ISBN:0321000382"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription by RNA polymerase II","termid":"GO:0006366"},{"relation_name":"is_a","term_name":"mRNA transcription","termid":"GO:0009299"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01713":null},"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:0016071"},{"rel_name":"is_a","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0016071","GO:0006351","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"mRNA transcription by RNA polymerase II","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"mRNA transcription from Pol II promoter","type":"exact"},{"name":"mRNA transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:0042789","terms_by_termid":{"GO:0042789":null}}


id: PBO:0044855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 136","termid":"PBO:0044855"}


id: PBO:0073659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SIN3 transcription regulator family member B","termid":"PBO:0073659"}


id: MONDO:0000748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the mucosal lining of the mastoid antrum and mastoid air cell system of the mastoid process.","definition_xrefs":["NCIT:C128368"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone inflammation disease","termid":"MONDO:0002614"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mastoiditis","secondary_identifiers":["UMLS:C0024904","MEDGEN:7480","HP:0000265","ICD9:383.9","DOID:0060322","MESH:D008417","SCTID:52404001"],"synonyms":[{"name":"inflammation of mastoid process of temporal bone","type":"exact"},{"name":"mastoid process of temporal bone inflammation","type":"exact"},{"name":"mastoid process of temporal boneitis","type":"exact"},{"name":"mastoiditis","type":"exact"},{"name":"mastoiditis (disease)","type":"exact"}],"termid":"MONDO:0000748","xrefs":{"Monarch":{"xref_id":"0000748"}}}


id: MONDO:0007693
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypertrichosis cubiti is a rare hair anomaly characterized by symmetrical, congenital or early-onset, bilateral hypertrychosis localized on the externsor surfaces of the upper extremities (especially the elbows). Short stature, or other abnormalities, such as developmental delay, facial anomalies and intellectual disability, may or may not be associated.","definition_xrefs":["Orphanet:2220"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrichosis","termid":"MONDO:0019280"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"hypertrichosis cubiti-short stature syndrome","secondary_identifiers":["MedDRA:10068636","GARD:143","MEDGEN:870835","MESH:C535618","OMIM:139600","UMLS:C4025295"],"synonyms":[{"name":"MacDermot-Patton-Williams syndrome","type":"exact"},{"name":"hairy elbows","type":"exact"},{"name":"hairy elbows syndrome","type":"exact"},{"name":"hypertrichosis cubiti","type":"related"}],"termid":"MONDO:0007693","xrefs":{"Monarch":{"xref_id":"0007693"}}}


id: PBO:0108620
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IGBP1 pseudogene 3","termid":"PBO:0108620"}


id: PBO:0085834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; green fluorescent protein (GFP)-fusion protein localizes to the cell periphery; protein abundance increases in response to DNA replication stress; has potential orthologs in Saccharomyces species and in Yarrowia lipolytica","termid":"PBO:0085834"}


id: GO:0016814
data:
  {"annotated_genes":["SJAG_00106","SJAG_04123","SJAG_02400","SJAG_04189","SJAG_04380","SJAG_01997","SJAG_00376","SJAG_01054","SJAG_04156","SJAG_04711","SJAG_03771","SJAG_03275","SJAG_01673","SJAG_04681"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78138],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003876"},{"annotations":[71557],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004126"},{"annotations":[71646],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004132"},{"annotations":[119038],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008835"},{"annotations":[71622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003934"},{"annotations":[60666,59012],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003935"},{"annotations":[80786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008892"},{"annotations":[71659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003937"},{"annotations":[78326,77439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004477"},{"annotations":[60471],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004635"},{"annotations":[75551],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052717"},{"annotations":[73361],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043829"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of any non-peptide carbon-nitrogen bond in a cyclic amidine, a compound of the form R-C(=NH)-NH2.","definition_xrefs":["EC:3.5.4.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds","termid":"GO:0016810"}],"gene_count":14,"genes_by_uniquename":{"SJAG_00106":null,"SJAG_00376":null,"SJAG_01054":null,"SJAG_01673":null,"SJAG_01997":null,"SJAG_02400":null,"SJAG_03275":null,"SJAG_03771":null,"SJAG_04123":null,"SJAG_04156":null,"SJAG_04189":null,"SJAG_04380":null,"SJAG_04681":null,"SJAG_04711":null},"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:0016810"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0016810","GO:0003824"],"is_obsolete":false,"name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amidines","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0016814","terms_by_termid":{"GO:0003876":null,"GO:0003934":null,"GO:0003935":null,"GO:0003937":null,"GO:0004126":null,"GO:0004132":null,"GO:0004477":null,"GO:0004635":null,"GO:0008835":null,"GO:0008892":null,"GO:0043829":null,"GO:0052717":null}}


id: GO:0016667
data:
  {"annotated_genes":["SJAG_04953","SJAG_03653","SJAG_01199","SJAG_01038","SJAG_00196","SJAG_02489","SJAG_04399","SJAG_04060","SJAG_01162","SJAG_03992","SJAG_03414","SJAG_03290","SJAG_06468","SJAG_01417","SJAG_00419","SJAG_00489","SJAG_04125","SJAG_02495","SJAG_00288","SJAG_02599","SJAG_01647","SJAG_01292","SJAG_00822","SJAG_02827","SJAG_04539","SJAG_00365","SJAG_04904","SJAG_04046","SJAG_01693","SJAG_04632","SJAG_05027","SJAG_00614","SJAG_02016"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73492],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004148"},{"annotations":[120282],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015036"},{"annotations":[58258,65553],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016971"},{"annotations":[63028,77598,68810,80270,75317],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015038"},{"annotations":[80837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004362"},{"annotations":[97382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036456"},{"annotations":[96867],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016668"},{"annotations":[78769],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033743"},{"annotations":[61117],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008113"},{"annotations":[81664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004604"},{"annotations":[60842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047134"},{"annotations":[79618,80060,94125,77951,91221,102590,73689,94300,92703,103432,119240,81959,81557,79628],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015035"},{"annotations":[78007],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070224"},{"annotations":[78563],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032542"},{"annotations":[80070,71918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004783"},{"annotations":[70677,100304,59914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016972"},{"annotations":[74990,81372],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004791"}]},"cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which a sulfur-containing group acts as a hydrogen or electron donor and reduces a hydrogen or electron acceptor.","definition_xrefs":["GOC:ai","EC:1.8.-.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity","termid":"GO:0016491"}],"gene_count":33,"genes_by_uniquename":{"SJAG_00196":null,"SJAG_00288":null,"SJAG_00365":null,"SJAG_00419":null,"SJAG_00489":null,"SJAG_00614":null,"SJAG_00822":null,"SJAG_01038":null,"SJAG_01162":null,"SJAG_01199":null,"SJAG_01292":null,"SJAG_01417":null,"SJAG_01647":null,"SJAG_01693":null,"SJAG_02016":null,"SJAG_02489":null,"SJAG_02495":null,"SJAG_02599":null,"SJAG_02827":null,"SJAG_03290":null,"SJAG_03414":null,"SJAG_03653":null,"SJAG_03992":null,"SJAG_04046":null,"SJAG_04060":null,"SJAG_04125":null,"SJAG_04399":null,"SJAG_04539":null,"SJAG_04632":null,"SJAG_04904":null,"SJAG_04953":null,"SJAG_05027":null,"SJAG_06468":null},"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":"oxidoreductase activity, acting on a sulfur group of donors","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":["Reactome:R-HSA-2213240"],"synonyms":[{"name":"oxidoreductase activity, acting on sulfur group of donors, other acceptors","type":"narrow"},{"name":"oxidoreductase activity, acting on sulphur group of donors","type":"exact"}],"termid":"GO:0016667","terms_by_termid":{"GO:0004148":null,"GO:0004362":null,"GO:0004604":null,"GO:0004783":null,"GO:0004791":null,"GO:0008113":null,"GO:0015035":null,"GO:0015036":null,"GO:0015038":null,"GO:0016668":null,"GO:0016971":null,"GO:0016972":null,"GO:0032542":null,"GO:0033743":null,"GO:0036456":null,"GO:0047134":null,"GO:0070224":null}}


id: MONDO:0859293
data:
  {"annotated_genes":["SJAG_02285"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87550],"is_not":false,"summary":null,"term":"MONDO:0859293"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1823998","UMLS:C5774225","OMIM:620066"],"termid":"MONDO:0859293","terms_by_termid":{"MONDO:0859293":null},"xrefs":{"Monarch":{"xref_id":"0859293"}}}


id: PBO:0043438
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chondromodulin","termid":"PBO:0043438"}


id: FYECO:0000411
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which egtazic acid was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:mlr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ egtazic acid","synonyms":[{"name":"+ EGTA","type":"exact"},{"name":"EGTA added","type":"exact"},{"name":"egtazic acid added","type":"exact"}],"termid":"FYECO:0000411"}


id: PBO:0027951
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_pyridoxal_level","termid":"PBO:0027951"}


id: PBO:0043758
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase subunit 8B, pseudogene","termid":"PBO:0043758"}


id: MONDO:1010660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Thrombocytopenia that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thrombocytopenia, non-human animal","termid":"MONDO:1010080"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombocytopenia, domestic cat","secondary_identifiers":["OMIA:001001-9685"],"termid":"MONDO:1010660","xrefs":{"Monarch":{"xref_id":"1010660"}}}


id: MONDO:0006663
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder caused by a lack of blood flow or gas exchange to or from the fetus in the period immediately before, during, or after the birth process.","direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder","termid":"MONDO:0005087"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"perinatal asphyxia","secondary_identifiers":["DOID:11088","icd11.foundation:1281282034","GARD:19875","Orphanet:137577","MESH:D001238","ICD9:768.9","UMLS:C0004045","SCTID:28314004","MEDGEN:2469","NCIT:C116313","EFO:1000824"],"synonyms":[{"name":"HIE","type":"exact"},{"name":"asphyxia - birth","type":"exact"},{"name":"asphyxia neonatorum","type":"exact"},{"name":"asphyxia, in liveborn infant","type":"exact"},{"name":"birth asphyxia","type":"exact"},{"name":"birth depression","type":"exact"},{"name":"fetal asphyxia","type":"exact"},{"name":"foetal asphyxia","type":"exact"},{"name":"hypoxia neonatorum","type":"exact"},{"name":"hypoxic and ischaemic brain injury in the newborn","type":"related"},{"name":"hypoxic and ischemic brain injury in the newborn","type":"related"},{"name":"hypoxic-ischemic encephalopathy","type":"exact"},{"name":"intrapartum asphyxia","type":"exact"},{"name":"neonatal hypoxic and ischaemic brain injury","type":"related"},{"name":"neonatal hypoxic and ischemic brain injury","type":"related"},{"name":"perinatal asphyxia","type":"exact"},{"name":"perinatal depression","type":"exact"},{"name":"perinatal hypoxia","type":"exact"},{"name":"postnatal asphyxia","type":"exact"}],"termid":"MONDO:0006663","xrefs":{"Monarch":{"xref_id":"0006663"}}}


id: PBO:0048835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein nucleolar 2 pseudogene 1","termid":"PBO:0048835"}


id: GO:2000472
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of hematopoietic stem cell migration.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell migration","termid":"GO:0030336"},{"relation_name":"is_a","term_name":"regulation of hematopoietic stem cell migration","termid":"GO:2000471"},{"relation_name":"negatively_regulates","term_name":"hematopoietic stem cell migration","termid":"GO:0035701"}],"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 hematopoietic stem cell migration","synonyms":[{"name":"negative regulation of hemopoietic stem cell migration","type":"exact"}],"termid":"GO:2000472"}


id: GO:0050872
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a white adipocyte, an animal connective tissue cell involved in energy storage. White adipocytes have cytoplasmic lipids arranged in a unique vacuole.","definition_xrefs":["PMID:12508945"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fat cell differentiation","termid":"GO:0045444"}],"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":"white fat cell differentiation","secondary_identifiers":["Reactome:R-HSA-381340"],"synonyms":[{"name":"white adipocyte cell differentiation","type":"exact"},{"name":"white adipocyte differentiation","type":"exact"}],"termid":"GO:0050872"}


id: _global:existence_starts_and_ends_during
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"x exists during y if and only if: 1) the time point at which x begins to exist is after or equal to the time point at which y begins and 2) the time point at which x ceases to exist is before or equal to the point at which y ends. Formally: x existence starts and ends during y iff α(x) >= α(y) & α(x) <= ω(y) & ω(x) <= ω(y) & ω(x) >= α(y)","direct_ancestors":[{"relation_name":"is_a","term_name":"existence_ends_during","termid":"_global:existence_ends_during"},{"relation_name":"is_a","term_name":"existence_starts_during","termid":"_global:existence_starts_during"},{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"existence_starts_and_ends_during","secondary_identifiers":["RO:0002491"],"synonyms":[{"name":"exists during","type":"exact"}],"termid":"_global:existence_starts_and_ends_during"}


id: FYPO:0006800
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of centromeres and associated kinetochores into a cluster at the nuclear periphery is decreased during interphase of the mitotic cell cycle. Centromere-kinetochore complexes normally cluster near the old spindle pole body during mitotic interphase.","definition_xrefs":["PMID:29180432","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal centromere clustering at nuclear periphery during vegetative growth","termid":"FYPO:0001779"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000138","FYPO:0000002","FYPO:0001985","FYPO:0000631","FYPO:0005447"],"is_obsolete":false,"name":"decreased centromere clustering at nuclear periphery during mitotic interphase","synonyms":[{"name":"centromere declustering during mitotic interphase","type":"exact"},{"name":"decreased centromere clustering at SPB during mitotic interphase","type":"related"},{"name":"decreased centromere clustering at nuclear periphery during interphase during vegetative growth","type":"exact"},{"name":"decreased centromere clustering at nuclear periphery during interphase of mitotic cell cycle","type":"related"},{"name":"decreased centromere clustering at spindle pole body during mitotic interphase","type":"related"},{"name":"decreased centromere-SPB clustering during mitotic interphase","type":"related"},{"name":"decreased inter-centromere connection during mitotic interphase","type":"exact"},{"name":"decreased kinetochore clustering at SPB during mitotic interphase","type":"related"},{"name":"decreased kinetochore clustering at old mitotic spindle pole body during mitotic interphase","type":"related"},{"name":"decreased kinetochore clustering at spindle pole body during mitotic interphase","type":"related"},{"name":"decreased kinetochore localization at spindle pole body during mitotic interphase","type":"related"},{"name":"decreased mitotic centromere clustering at nuclear periphery during mitotic interphase","type":"exact"}],"termid":"FYPO:0006800"}


id: PBO:0077349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 88B","termid":"PBO:0077349"}


id: PR:Q9UT45
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- eng1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9UT45"],"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":"endo-1,3(4)-beta-glucanase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC821.09","synonyms":[{"name":"Spom972h-eng1","type":"exact"},{"name":"endo-1,3-beta-glucanase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"endo-1,4-beta-glucanase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"laminarinase-1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UT45"}


id: GO:1901558
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 metformin stimulus.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"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 metformin","termid":"GO:1901558"}


id: GO:0110061
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the angiotensin-activated signaling pathway.","definition_xrefs":["GOC:lf","PMID:28784619"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of G protein-coupled receptor signaling pathway","termid":"GO:0008277"},{"relation_name":"regulates","term_name":"angiotensin-activated signaling pathway","termid":"GO:0038166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of angiotensin-activated signaling pathway","termid":"GO:0110061"}


id: PBO:0056834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase","termid":"PBO:0056834"}


id: PBO:0081326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 117","termid":"PBO:0081326"}


id: MONDO:1012302
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spondylosis deformans, non-human animal","termid":"MONDO:1011955"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spondylosis deformans, domestic cat","secondary_identifiers":["OMIA:001132-9685"],"termid":"MONDO:1012302","xrefs":{"Monarch":{"xref_id":"1012302"}}}


id: GO:0002322
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of a B cell population by cell division following B cell activation during an immune response.","definition_xrefs":["GOC:jal"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell activation involved in immune response","termid":"GO:0002312"},{"relation_name":"is_a","term_name":"B cell proliferation","termid":"GO:0042100"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"B cell proliferation involved in immune response","synonyms":[{"name":"B cell proliferation during immune response","type":"related"},{"name":"B lymphocyte proliferation during immune response","type":"related"},{"name":"B-cell proliferation during immune response","type":"related"},{"name":"B-lymphocyte proliferation during immune response","type":"related"}],"termid":"GO:0002322"}


id: PBO:0051303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1D-43","termid":"PBO:0051303"}


id: PBO:0034168
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-in_between-species_paralogy_relationship_with","termid":"PBO:0034168"}


id: PBO:0061413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuropeptide VF precursor","termid":"PBO:0061413"}


id: MONDO:0056817
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An unusual rectal carcinoma characterized by the presence of glandular and squamous carcinomatous components. The two carcinomatous components may be admixed within the tumor, or the two may appear separately in different areas.","definition_xrefs":["NCIT:C43594"],"direct_ancestors":[{"relation_name":"is_a","term_name":"colorectal adenosquamous carcinoma","termid":"MONDO:0006157"},{"relation_name":"is_a","term_name":"squamous cell carcinoma of rectum","termid":"MONDO:0018515"}],"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:0004992","MONDO:0004335"],"is_obsolete":false,"name":"rectal adenosquamous carcinoma","secondary_identifiers":["MEDGEN:313658","UMLS:C1709865"],"synonyms":[{"name":"rectal adenosquamous cancer","type":"exact"},{"name":"rectal adenosquamous carcinoma","type":"exact"}],"termid":"MONDO:0056817","xrefs":{"Monarch":{"xref_id":"0056817"}}}


id: GO:0015334
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of oligopeptide from one side of a membrane to the other. In high-affinity transport the transporter is able to bind the solute even if it is only present at very low concentrations. Oligopeptides are molecules that contain a small number (2 to 20) of amino-acid residues connected by peptide linkages.","definition_xrefs":["GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligopeptide transmembrane transporter activity","termid":"GO:0035673"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"high-affinity oligopeptide transmembrane transporter activity","synonyms":[{"name":"high affinity oligopeptide transporter activity","type":"exact"},{"name":"high-affinity oligopeptide transporter activity","type":"related"}],"termid":"GO:0015334"}


id: GO:1904052
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein targeting to vacuole involved in autophagy.","definition_xrefs":["GOC:pad","GOC:PARL","GOC:TermGenie","PMID:22020285","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of intracellular protein transport","termid":"GO:0090317"},{"relation_name":"is_a","term_name":"negative regulation of vacuolar transport","termid":"GO:1903336"},{"relation_name":"is_a","term_name":"regulation of protein targeting to vacuole involved in autophagy","termid":"GO:1904051"},{"relation_name":"negatively_regulates","term_name":"protein targeting to vacuole involved in autophagy","termid":"GO:0071211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006605"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006605"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0006605","GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein targeting to vacuole involved in autophagy","synonyms":[{"name":"down regulation of protein targeting to vacuole involved in autophagy","type":"exact"},{"name":"down-regulation of protein targeting to vacuole involved in autophagy","type":"exact"},{"name":"downregulation of protein targeting to vacuole involved in autophagy","type":"exact"},{"name":"inhibition of protein targeting to vacuole involved in autophagy","type":"narrow"}],"termid":"GO:1904052"}


id: GO:1902224
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving ketone body.","definition_xrefs":["GOC:TermGenie","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"generation of precursor metabolites and energy","termid":"GO:0006091"},{"relation_name":"is_a","term_name":"small molecule metabolic process","termid":"GO:0044281"},{"relation_name":"is_a","term_name":"fatty acid derivative metabolic process","termid":"GO:1901568"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006091"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0044281","GO:0008150","GO:0006091"],"is_obsolete":false,"name":"ketone body metabolic process","synonyms":[{"name":"ketone body metabolism","type":"exact"}],"termid":"GO:1902224"}


id: GO:0160007
data:
  {"annotated_genes":["SJAG_03577"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[114989],"is_not":false,"summary":null,"term":"GO:0160007"}]},"cv_name":"biological_process","definition":"The process in which glutathione is transported from the cytosol into the mitochondrial matrix.","definition_xrefs":["PMID:34707288"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glutathione transmembrane transport","termid":"GO:0034775"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03577":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"glutathione import into mitochondrion","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0160007","terms_by_termid":{"GO:0160007":null}}


id: PBO:0056187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAGE family member A1","termid":"PBO:0056187"}


id: MONDO:0013729
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any pregnancy loss, recurrent, susceptibility in which the cause of the disease is a mutation in the ANXA5 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pregnancy loss, recurrent, susceptibility","termid":"MONDO:0000144"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pregnancy loss, recurrent, susceptibility to, 3","secondary_identifiers":["MEDGEN:482304","OMIM:614391","UMLS:C3280674"],"synonyms":[{"name":"ANXA5 pregnancy loss, recurrent, susceptibility","type":"exact"},{"name":"RPRGL3","type":"related"},{"name":"pregnancy loss, recurrent, susceptibility caused by mutation in ANXA5","type":"exact"},{"name":"pregnancy loss, recurrent, susceptibility to, 3","type":"exact"},{"name":"pregnancy loss, recurrent, susceptibility to, type 3","type":"exact"}],"termid":"MONDO:0013729","xrefs":{"Monarch":{"xref_id":"0013729"}}}


id: PBO:0108612
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adhesion G protein-coupled receptor F2, pseudogene","termid":"PBO:0108612"}


id: GO:0003065
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the secretion of epinephrine into the bloodstream or released from nerve endings increases the rate of heart muscle contraction.","definition_xrefs":["GOC:mtg_cardio","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heart rate by chemical signal","termid":"GO:0003062"},{"relation_name":"is_a","term_name":"positive regulation of heart rate","termid":"GO:0010460"},{"relation_name":"part_of","term_name":"positive regulation of heart rate by epinephrine-norepinephrine","termid":"GO:0001996"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of heart rate by epinephrine","synonyms":[{"name":"adrenaline cardiac chronotropy","type":"exact"},{"name":"adrenaline regulation of the rate of heart muscle contraction","type":"exact"},{"name":"epinephrine cardiac chronotropy","type":"exact"},{"name":"positive regulation of heart contraction rate by epinephrine","type":"related"},{"name":"positive regulation of heart rate by adrenaline","type":"related"}],"termid":"GO:0003065"}


id: PBO:0110421
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIAL1 pseudogene","termid":"PBO:0110421"}


id: GO:0080166
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the stomium over time, from its formation to the mature structure. A stomium is a fissure or pore in the anther lobe through which the pollen is released.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"cellular process involved in reproduction in multicellular organism","termid":"GO:0022412"},{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"anther development","termid":"GO:0048653"}],"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":"stomium development","termid":"GO:0080166"}


id: FYPO:0005169
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 9 of histone H3 at the centromere central core occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H3-K9 methylation at centromere during vegetative growth","termid":"FYPO:0005066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0002274"],"is_obsolete":false,"name":"increased histone H3-K9 methylation at centromere central core during vegetative growth","synonyms":[{"name":"increased histone H3 K9 methylation at centromere central core during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 methylation at centromere central core during mitotic cell cycle","type":"related"},{"name":"increased histone H3K9 methylation at centromere central core during vegetative growth","type":"exact"},{"name":"increased histone H3K9me at centromere central core during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K9 methylation at centromere central core during vegetative growth","type":"exact"}],"termid":"FYPO:0005169"}


id: PR:O59764
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ER membrane protein complex subunit 6 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04440","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":"ER membrane protein complex subunit 6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1020.11c","secondary_identifiers":["UniProtKB:O59764"],"synonyms":[{"name":"Spom972h-EMC6","type":"exact"}],"termid":"PR:O59764"}


id: PR:Q9P329
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of any of the following genes in Schizosaccharomyces pombe 972h-: pfl6/SPBC1348.08c.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P329"],"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 agglutination protein C1348.08c/C977.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1348.08c","synonyms":[{"name":"Spom972h-SPBC1348.08c","type":"exact"}],"termid":"PR:Q9P329"}


id: PBO:0091023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mating-type homeobox protein Pi","termid":"PBO:0091023"}


id: GO:0050356
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADP+ + tropine = H+ + NADPH + tropinone.","definition_xrefs":["RHEA:18357","EC:1.1.1.206"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"tropine dehydrogenase activity","secondary_identifiers":["KEGG_REACTION:R02832","MetaCyc:TROPINE-DEHYDROGENASE-RXN"],"synonyms":[{"name":"tropine:NADP+ 3alpha-oxidoreductase activity","type":"related"}],"termid":"GO:0050356"}


id: PBO:0051818
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 1 receptor associated kinase 3","termid":"PBO:0051818"}


id: PBO:0047851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(1)(p22)","termid":"PBO:0047851"}


id: GO:0042556
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Modulates the activity of the enzyme eukaryotic elongation factor-2 kinase.","definition_xrefs":["GOC:jl","PMID:11904175"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase regulator activity","termid":"GO:0019887"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0030234"}],"interesting_parent_ids":["GO:0098772","GO:0030234","GO:0003674"],"is_obsolete":false,"name":"eukaryotic elongation factor-2 kinase regulator activity","synonyms":[{"name":"eEF-2 kinase regulator","type":"exact"}],"termid":"GO:0042556"}


id: GO:0008406
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the gonad over time, from its formation to the mature structure. The gonad is an animal organ that produces gametes; in some species it also produces hormones.","definition_xrefs":["ISBN:0198506732","GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ development","termid":"GO:0048513"},{"relation_name":"is_a","term_name":"reproductive structure development","termid":"GO:0048608"},{"relation_name":"part_of","term_name":"development of primary sexual characteristics","termid":"GO:0045137"}],"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":"gonad development","synonyms":[{"name":"gonadogenesis","type":"exact"}],"termid":"GO:0008406"}


id: MONDO:0007540
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Multiple endocrine neoplasia Type 1 (MEN1) is a frequent form of MEN, a rare inherited cancer syndrome, characterized by the development of neuroendocrine tumors of the parathyroid, pancreas, and anterior pituitary gland, and less commonly the adrenal cortical gland, with other non-endocrine tumors in some patients.","definition_xrefs":["Orphanet:652"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"familial primary hyperparathyroidism","termid":"MONDO:0016365"},{"relation_name":"is_a","term_name":"multiple endocrine neoplasia","termid":"MONDO:0017169"},{"relation_name":"is_a","term_name":"adrenal gland neoplasm","termid":"MONDO:0021227"}],"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":"multiple endocrine neoplasia type 1","secondary_identifiers":["ICD10CM:E31.21","NCIT:C3225","MedDRA:10028190","MEDGEN:9957","ICD9:237.4","MESH:D018761","NANDO:2200405","SCTID:30664006","UMLS:C0025267","ICD9:258.01","OMIM:131100","GARD:3829","NORD:1466","icd11.foundation:1638765741","DOID:10017"],"synonyms":[{"name":"MEA 1","type":"related"},{"name":"MEA type 1","type":"exact"},{"name":"MEA type I","type":"exact"},{"name":"MEN1","type":"exact"},{"name":"MEN1 multiple endocrine neoplasia","type":"exact"},{"name":"MEN1 somatic mutations","type":"related"},{"name":"MEN1 syndrome","type":"exact"},{"name":"Wermer syndrome","type":"exact"},{"name":"Wermer's syndrome","type":"exact"},{"name":"endocrine adenomatosis multiple","type":"related"},{"name":"endocrine adenomatosis, multiple","type":"related"},{"name":"men 1","type":"exact"},{"name":"men type 1","type":"exact"},{"name":"men type I","type":"exact"},{"name":"multiple endocrine adenomatosis","type":"broad"},{"name":"multiple endocrine adenomatosis type 1","type":"exact"},{"name":"multiple endocrine adenomatosis type I","type":"exact"},{"name":"multiple endocrine adenomatosis, type I","type":"exact"},{"name":"multiple endocrine neoplasia 1","type":"exact"},{"name":"multiple endocrine neoplasia caused by mutation in MEN1","type":"exact"},{"name":"multiple endocrine neoplasia type 1","type":"exact"},{"name":"multiple endocrine neoplasia type 1 syndrome","type":"exact"},{"name":"multiple endocrine neoplasia type I","type":"exact"},{"name":"multiple endocrine neoplasia, type 1","type":"related"},{"name":"multiple endocrine neoplasia, type I","type":"exact"}],"termid":"MONDO:0007540","xrefs":{"Monarch":{"xref_id":"0007540"}}}


id: PBO:0079814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UHRF1BP1L divergent transcript","termid":"PBO:0079814"}


id: GO:0006390
data:
  {"annotated_genes":["SJAG_03289","SJAG_00634","SJAG_03014"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89225,99989,96955],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006391"}]},"cv_name":"biological_process","definition":"The synthesis of RNA from a mitochondrial DNA template, usually by a specific mitochondrial RNA polymerase.","definition_xrefs":["GOC:jl","PMID:23632312"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial RNA metabolic process","termid":"GO:0000959"},{"relation_name":"is_a","term_name":"DNA-templated transcription","termid":"GO:0006351"},{"relation_name":"part_of","term_name":"mitochondrial gene expression","termid":"GO:0140053"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00634":null,"SJAG_03014":null,"SJAG_03289":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006351"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0140053"}],"interesting_parent_ids":["GO:0010467","GO:0140053","GO:0008150","GO:0006351"],"is_obsolete":false,"name":"mitochondrial transcription","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-75944"],"synonyms":[{"name":"transcription from mitochondrial promoter","type":"exact"}],"termid":"GO:0006390","terms_by_termid":{"GO:0006391":null}}


id: FYPO:0007912
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 mitochondrial localization is normal.","definition_xrefs":["PMID:10641037","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal organelle localization","termid":"FYPO:0007913"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0001312","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"normal mitochondrial distribution","synonyms":[{"name":"normal mitochondrial localization","type":"exact"}],"termid":"FYPO:0007912"}


id: MONDO:1010609
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Exocrine pancreatic insufficiency that occurs in tiger.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"exocrine pancreatic insufficiency, non-human animal","termid":"MONDO:1010058"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocrine pancreatic insufficiency, tiger","secondary_identifiers":["OMIA:000765-9694"],"termid":"MONDO:1010609","xrefs":{"Monarch":{"xref_id":"1010609"}}}


id: PBO:0064638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pro-platelet basic protein pseudogene 1","termid":"PBO:0064638"}


id: PBO:0088320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial DDHD family phospholipase","termid":"PBO:0088320"}


id: PR:P87051
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A peptidyl-prolyl cis-trans isomerase-like 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO00551","PRO:DNx","PANTHER:PTHR11071:SF41"],"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":"peptidyl-prolyl cis-trans isomerase ppi1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC57A10.03","secondary_identifiers":["UniProtKB:P87051"],"synonyms":[{"name":"PPIase ppi1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-PPIL1","type":"exact"},{"name":"cyclophilin ppi1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"rotamase ppi1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P87051"}


id: GO:0097399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by interleukin-32 binding to its receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["PMID:21602493","GOC:ic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"},{"relation_name":"part_of","term_name":"cellular response to interleukin-32","termid":"GO:0097397"}],"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":"interleukin-32-mediated signaling pathway","synonyms":[{"name":"IL-32-mediated signaling pathway","type":"exact"},{"name":"IL-32-mediated signalling pathway","type":"exact"},{"name":"interleukin-32-mediated signalling pathway","type":"exact"}],"termid":"GO:0097399"}


id: MOD:00363
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links an L-cysteine residue and an L-selenocysteine residues to form L-cysteinyl-L-selenocystine.","definition_xrefs":["PubMed:12911312","RESID:AA0358#SEC"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-cysteinyl-L-selenocysteine","termid":"MOD:01627"},{"relation_name":"is_a","term_name":"crosslinked L-selenocysteine residue","termid":"MOD:02061"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-cysteinyl-L-selenocysteine (Cys-Sec)","synonyms":[{"name":"(R,R)-2-amino-3-[3-(2-aminopropanoic acid)sulfanyl]selanylpropanoic acid","type":"exact"},{"name":"CROSSLNK Cysteinyl-selenocysteine (Cys-Sec)","type":"exact"},{"name":"CROSSLNK Cysteinyl-selenocysteine (Sec-Cys)","type":"exact"},{"name":"L-cysteinyl-L-selenocysteine","type":"exact"}],"termid":"MOD:00363"}


id: MONDO:0018926
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Prion diseases are a group of rare transmissible disorders characterized by progressive debilitating neurological manifestations due to spongiform changes with an invariably fatal course. The disorders all involve accumulation of an abnormal prion protein in the central nervous system with no specific immunological response. Sporadic Creutzfeldt-Jakob disease (CJD) is the most frequent form accounting for about 85% of prion disease cases. The other forms of prion disease are genetic (5-15%) and include inherited CJD, fatal familial insomnia (FFI), and Familial Alzheimer-like prion disease. Acquired forms (< 5%) include iatrogenic CJD and variant CJD (vCDJ).","definition_xrefs":["Orphanet:56970"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegenerative disease","termid":"MONDO:0005559"},{"relation_name":"is_a","term_name":"central nervous system infectious disorder","termid":"MONDO:0024619"}],"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":"human prion disease","secondary_identifiers":["ICD10CM:A81.1","GARD:18851"],"synonyms":[{"name":"TSE","type":"exact"},{"name":"transmissible spongiform encephalopathy","type":"exact"}],"termid":"MONDO:0018926","xrefs":{"Monarch":{"xref_id":"0018926"}}}


id: GO:1905504
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of motile cilium assembly.","definition_xrefs":["PMID:25294941","GO_REF:0000058","GOC:TermGenie","GOC:cilia","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cilium assembly","termid":"GO:1902018"},{"relation_name":"is_a","term_name":"regulation of motile cilium assembly","termid":"GO:1905503"},{"relation_name":"negatively_regulates","term_name":"motile cilium assembly","termid":"GO:0044458"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"negative regulation of motile cilium assembly","synonyms":[{"name":"down regulation of motile primary cilia assembly","type":"related"},{"name":"down regulation of motile primary cilia formation","type":"related"},{"name":"down regulation of motile primary cilium assembly","type":"related"},{"name":"down regulation of motile primary cilium formation","type":"related"},{"name":"down regulation of nodal cilium assembly","type":"related"},{"name":"down regulation of nodal cilium formation","type":"related"},{"name":"down-regulation of motile primary cilia assembly","type":"related"},{"name":"down-regulation of motile primary cilia formation","type":"related"},{"name":"down-regulation of motile primary cilium assembly","type":"related"},{"name":"down-regulation of motile primary cilium formation","type":"related"},{"name":"down-regulation of nodal cilium assembly","type":"related"},{"name":"down-regulation of nodal cilium formation","type":"related"},{"name":"downregulation of motile primary cilia assembly","type":"related"},{"name":"downregulation of motile primary cilia formation","type":"related"},{"name":"downregulation of motile primary cilium assembly","type":"related"},{"name":"downregulation of motile primary cilium formation","type":"related"},{"name":"downregulation of nodal cilium assembly","type":"related"},{"name":"downregulation of nodal cilium formation","type":"related"},{"name":"inhibition of motile primary cilia assembly","type":"narrow"},{"name":"inhibition of motile primary cilia formation","type":"narrow"},{"name":"inhibition of motile primary cilium assembly","type":"narrow"},{"name":"inhibition of motile primary cilium formation","type":"narrow"},{"name":"inhibition of nodal cilium assembly","type":"related"},{"name":"inhibition of nodal cilium formation","type":"related"},{"name":"negative regulation of motile primary cilia assembly","type":"related"},{"name":"negative regulation of motile primary cilia formation","type":"related"},{"name":"negative regulation of motile primary cilium assembly","type":"related"},{"name":"negative regulation of motile primary cilium formation","type":"related"},{"name":"negative regulation of nodal cilium assembly","type":"related"},{"name":"negative regulation of nodal cilium formation","type":"related"}],"termid":"GO:1905504"}


id: GO:0047862
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: diisopropyl fluorophosphate + H2O = diisopropyl phosphate + fluoride + 2 H+.","definition_xrefs":["RHEA:24100"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid halide bonds","termid":"GO:0016824"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"diisopropyl-fluorophosphatase activity","secondary_identifiers":["EC:3.8.2.2","KEGG_REACTION:R01533","MetaCyc:DIISOPROPYL-FLUOROPHOSPHATASE-RXN"],"synonyms":[{"name":"DFPase activity","type":"related"},{"name":"OPA anhydrase activity","type":"related"},{"name":"OPAA activity","type":"related"},{"name":"dialkylfluorophosphatase activity","type":"related"},{"name":"diisopropyl phosphorofluoridate hydrolase activity","type":"related"},{"name":"diisopropyl-fluorophosphate fluorohydrolase activity","type":"related"},{"name":"diisopropylfluorophosphonate dehalogenase activity","type":"related"},{"name":"diisopropylphosphofluoridase activity","type":"related"},{"name":"isopropylphosphorofluoridase activity","type":"related"},{"name":"organophosphate acid anhydrase activity","type":"related"},{"name":"organophosphorus acid anhydrolase activity","type":"related"},{"name":"somanase activity","type":"related"},{"name":"tabunase activity","type":"related"}],"termid":"GO:0047862"}


id: GO:1904620
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a dimethyl sulfoxide stimulus.","definition_xrefs":["GO_REF:0000071","PMID:12873812","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to chemical stimulus","termid":"GO:0070887"},{"relation_name":"is_a","term_name":"response to dimethyl sulfoxide","termid":"GO:1904619"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to dimethyl sulfoxide","synonyms":[{"name":"cellular response to DMSO","type":"exact"}],"termid":"GO:1904620"}


id: PBO:0070969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18 pseudogene 7","termid":"PBO:0070969"}


id: GO:0140134
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which an organism alters or subverts the circulation of blood in another organism via the action of a venom.","definition_xrefs":["PMID:31370142"],"direct_ancestors":[{"relation_name":"is_a","term_name":"venom-mediated perturbation of biological process","termid":"GO:0035738"}],"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":"venom-mediated perturbation of blood circulation","synonyms":[{"name":"venom-mediated perturbation of cardiovascular system","type":"broad"},{"name":"venom-mediated perturbation of circulatory system process","type":"broad"}],"termid":"GO:0140134"}


id: PBO:0061115
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NLR family pyrin domain containing 6","termid":"PBO:0061115"}


id: PBO:0041718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calreticulin 3","termid":"PBO:0041718"}


id: GO:0098815
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of excitatory postsynaptic potential (EPSP). EPSP is a process that leads to a temporary increase in postsynaptic potential due to the flow of positively charged ions into the postsynaptic cell. The flow of ions that causes an EPSP is an excitatory postsynaptic current (EPSC) and makes it easier for the neuron to fire an action potential.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of signal transduction","termid":"GO:0009966"},{"relation_name":"is_a","term_name":"regulation of nervous system process","termid":"GO:0031644"},{"relation_name":"is_a","term_name":"regulation of membrane potential","termid":"GO:0042391"},{"relation_name":"is_a","term_name":"modulation of chemical synaptic transmission","termid":"GO:0050804"},{"relation_name":"regulates","term_name":"excitatory postsynaptic potential","termid":"GO:0060079"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"modulation of excitatory postsynaptic potential","termid":"GO:0098815"}


id: GO:0031989
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway initiated by a bombesin binding to its receptor, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled receptor signaling pathway","termid":"GO:0007186"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"bombesin receptor signaling pathway","synonyms":[{"name":"bombesin receptor signalling pathway","type":"exact"}],"termid":"GO:0031989"}


id: PBO:0060387
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"marginal zone B and B1 cell specific protein","termid":"PBO:0060387"}


id: MONDO:0010391
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"angioma serpiginosum","termid":"MONDO:0019803"}],"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":"angioma serpiginosum, X-linked","secondary_identifiers":["MESH:C536366","MEDGEN:1648301","UMLS:C4721404","GARD:10188","OMIM:300652"],"synonyms":[{"name":"angio serpiginosum, X-linked dominant","type":"exact"},{"name":"angioma serpiginosum, X-linked","type":"exact"}],"termid":"MONDO:0010391","xrefs":{"Monarch":{"xref_id":"0010391"}}}


id: GO:1900046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of hemostasis.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological process","termid":"GO:0050789"},{"relation_name":"is_a","term_name":"regulation of body fluid levels","termid":"GO:0050878"},{"relation_name":"regulates","term_name":"hemostasis","termid":"GO:0007599"}],"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 hemostasis","termid":"GO:1900046"}


id: GO:0031400
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the covalent alteration of one or more amino acid residues within a protein.","definition_xrefs":["GOC:tb","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein modification process","termid":"GO:0031399"},{"relation_name":"is_a","term_name":"negative regulation of protein metabolic process","termid":"GO:0051248"},{"relation_name":"negatively_regulates","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":"negative regulation of protein modification process","synonyms":[{"name":"down regulation of protein modification","type":"exact"},{"name":"down-regulation of protein modification","type":"exact"},{"name":"downregulation of protein modification","type":"exact"},{"name":"inhibition of protein modification","type":"narrow"}],"termid":"GO:0031400"}


id: PBO:0057060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 144","termid":"PBO:0057060"}


id: FYPO:0001056
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 L-arginine import into the cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal amino acid import","termid":"FYPO:0001596"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0000138","FYPO:0001312"],"is_obsolete":false,"name":"normal arginine import","synonyms":[{"name":"normal L-arginine import","type":"exact"},{"name":"normal L-arginine import across plasma membrane","type":"exact"},{"name":"normal L-arginine uptake","type":"exact"},{"name":"normal arginine import during mitotic cell cycle","type":"related"},{"name":"normal arginine import during vegetative growth","type":"exact"},{"name":"normal arginine import into cell","type":"exact"}],"termid":"FYPO:0001056"}


id: PBO:0058152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4447","termid":"PBO:0058152"}


id: MONDO:0002564
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant neoplasm that affects the wall of the jejunum. Representative examples include adenoma, carcinoma, and lymphoma.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small intestine neoplasm","termid":"MONDO:0004251"}],"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 neoplasm","secondary_identifiers":["UMLS:C0022374","DOID:3218","MESH:D007580","NCIT:C8401","MEDGEN:7187","SCTID:126834003"],"synonyms":[{"name":"jejunal tumor","type":"exact"},{"name":"jejunal tumour","type":"exact"},{"name":"jejunum neoplasm","type":"exact"},{"name":"jejunum neoplasm (disease)","type":"exact"},{"name":"jejunum tumor","type":"exact"},{"name":"jejunum tumour","type":"exact"},{"name":"neoplasm of jejunum","type":"exact"},{"name":"neoplasm of the jejunum","type":"exact"},{"name":"tumor of jejunum","type":"exact"},{"name":"tumor of the jejunum","type":"exact"},{"name":"tumour of jejunum","type":"exact"},{"name":"tumour of the jejunum","type":"exact"}],"termid":"MONDO:0002564","xrefs":{"Monarch":{"xref_id":"0002564"}}}


id: MONDO:0975829
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital dyserythropoietic anemia","termid":"MONDO:0019403"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"anemia, congenital dyserythropoietic, type IVb","secondary_identifiers":["OMIM:620969"],"termid":"MONDO:0975829","xrefs":{"Monarch":{"xref_id":"0975829"}}}


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


id: PBO:0086078
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function with similarity to globins; has a functional heme-binding domain; mutant has aneuploidy tolerance; transcription induced by stress conditions; may be involved in glucose signaling or metabolism; regulated by Rgt1","termid":"PBO:0086078"}


id: PBO:0089953
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Dhx37","termid":"PBO:0089953"}


id: GO:0021502
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the lateral borders of the neural plate begin to migrate upwards to form the neural folds, caused by the proliferation of the underlying mesoderm.","definition_xrefs":["PMID:15806586","GOC:dgh","GOC:dph","GOC:cls","GO_REF:0000021","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure formation involved in morphogenesis","termid":"GO:0048646"},{"relation_name":"part_of","term_name":"neural fold formation","termid":"GO:0001842"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural fold elevation formation","termid":"GO:0021502"}


id: GO:1901144
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of insulin.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete insulin biosynthetic process (obsolete GO:1901144)","synonyms":[{"name":"insulin anabolism","type":"exact"},{"name":"insulin biosynthesis","type":"exact"},{"name":"insulin biosynthetic process","type":"exact"},{"name":"insulin formation","type":"exact"},{"name":"insulin synthesis","type":"exact"}],"termid":"GO:1901144"}


id: PBO:0075924
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ST13, Hsp70 interacting protein pseudogene 16","termid":"PBO:0075924"}


id: PBO:0078164
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha variable 41","termid":"PBO:0078164"}


id: PBO:0040237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"activating transcription factor 7","termid":"PBO:0040237"}


id: GO:0031799
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 2 metabotropic glutamate receptor.","definition_xrefs":["GOC:mah","GOC:nln"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled glutamate receptor binding","termid":"GO:0035256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"type 2 metabotropic glutamate receptor binding","synonyms":[{"name":"type 2 metabotropic glutamate receptor ligand","type":"narrow"}],"termid":"GO:0031799"}


id: GO:0003976
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-N-acetyl-D-glucosamine + lysosomal-enzyme D-mannose = UMP + lysosomal-enzyme N-acetyl-D-glucosaminyl-phospho-D-mannose.","definition_xrefs":["EC:2.7.8.17"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, for other substituted phosphate groups","termid":"GO:0016780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016780"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016780","GO:0003824"],"is_obsolete":false,"name":"UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase activity","secondary_identifiers":["MetaCyc:2.7.8.17-RXN","RHEA:13581"],"synonyms":[{"name":"N-acetylglucosaminyl phosphotransferase activity","type":"related"},{"name":"N-acetylglucosaminylphosphotransferase activity","type":"related"},{"name":"UDP-GlcNAc:glycoprotein N-acetylglucosamine-1-phosphotransferase activity","type":"related"},{"name":"UDP-N-acetyl-D-glucosamine:lysosomal-enzyme N-acetylglucosaminephosphotransferase activity","type":"related"},{"name":"UDP-N-acetylglucosamine:glycoprotein N-acetylglucosamine-1-phosphotransferase activity","type":"related"},{"name":"UDP-N-acetylglucosamine:glycoprotein N-acetylglucosaminyl-1-phosphotransferase activity","type":"related"},{"name":"UDP-N-acetylglucosamine:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase activity","type":"related"},{"name":"lysosomal enzyme precursor acetylglucosamine-1-phosphotransferase activity","type":"related"}],"termid":"GO:0003976"}


id: GO:0035010
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Events resulting in the formation of a multilayered cellular sheath surrounding an invader and thus preventing its development. This defense mechanism is often seen in insects in response to nematodes or parasitoids, which are too large to be phagocytosed by individual hemocytes. In some organisms the capsule is blackened due to melanization.","definition_xrefs":["GOC:bf","PMID:11846478","GO_REF:0000022","PMID:12225920"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune effector process","termid":"GO:0002252"}],"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":"encapsulation of foreign target","termid":"GO:0035010"}


id: PBO:0047198
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 216 member A","termid":"PBO:0047198"}


id: MONDO:0019445
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Trichofolliculoma is a rare benign follicular hamartoma that develops primarily on the face of adults, with a particular predilection for the back of the nose, but also on the neck or scalp. It presents as a solitary hemispheric flesh-colored nodule with a central pore or black dot that may contain a tuft of hair.","definition_xrefs":["Orphanet:864"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare skin tumor or hamartoma (obsolete MONDO:0019300)","termid":"MONDO:0019300"},{"relation_name":"is_a","term_name":"hamartoma of skin appendage","termid":"MONDO:0021539"}],"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":"trichofolliculoma","secondary_identifiers":["NCIT:C4112","GARD:5263","ICDO:8101/0","MedDRA:10044611","MEDGEN:87202","MESH:C536553","UMLS:C0334262","SCTID:274899008"],"termid":"MONDO:0019445","xrefs":{"Monarch":{"xref_id":"0019445"}}}


id: PBO:0081619
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 548","termid":"PBO:0081619"}


id: GO:0004760
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-serine + pyruvate = 3-hydroxypyruvate + L-alanine.","definition_xrefs":["EC:2.6.1.51","RHEA:22852"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016769","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"L-serine-pyruvate transaminase activity","secondary_identifiers":["MetaCyc:SERINE--PYRUVATE-AMINOTRANSFERASE-RXN","GO:0004762","GO:0004761","KEGG_REACTION:R00585","GO:0004763"],"synonyms":[{"name":"L-serine:pyruvate aminotransferase activity","type":"related"},{"name":"SPT","type":"related"},{"name":"hydroxypyruvate:L-alanine transaminase activity","type":"related"},{"name":"serine--pyruvate aminotransferase activity","type":"related"},{"name":"serine-pyruvate aminotransferase activity","type":"exact"},{"name":"serine-pyruvate aminotransferase, type 1","type":"narrow"},{"name":"serine-pyruvate aminotransferase, type 2A","type":"narrow"},{"name":"serine-pyruvate aminotransferase, type 2B","type":"narrow"}],"termid":"GO:0004760"}


id: PBO:0045202
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJB12 pseudogene 1","termid":"PBO:0045202"}


id: MONDO:0011987
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cone-rod dystrophy in which the cause of the disease is a mutation in the RPGRIP1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cone-rod dystrophy","termid":"MONDO:0015993"}],"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":"cone-rod dystrophy 13","secondary_identifiers":["MESH:C567698","OMIM:608194","UMLS:C2750720","DOID:0111016","GARD:15426","MEDGEN:413025"],"synonyms":[{"name":"CORD13","type":"exact"},{"name":"RPGRIP1 cone-rod dystrophy","type":"exact"},{"name":"cone-rod dystrophy 13","type":"exact"},{"name":"cone-rod dystrophy caused by mutation in RPGRIP1","type":"exact"},{"name":"cone-rod dystrophy type 13","type":"exact"}],"termid":"MONDO:0011987","xrefs":{"Monarch":{"xref_id":"0011987"}}}


id: PBO:0088046
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin-conjugating enzyme that regulates gluconeogenesis; negatively regulates gluconeogenesis by mediating the glucose-induced ubiquitination of fructose-1,6-bisphosphatase (FBPase); cytoplasmic enzyme that catalyzes the ubiquitination of histones in vitro","termid":"PBO:0088046"}


id: MONDO:1012162
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital melanoma, non-human animal","termid":"MONDO:1011811"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital melanoma, pig","secondary_identifiers":["OMIA:000634-9823"],"termid":"MONDO:1012162","xrefs":{"Monarch":{"xref_id":"1012162"}}}


id: MONDO:0010825
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrioventricular defect-blepharophimosis-radial and anal defect syndrome is a rare, genetic multiple congenital anomaly syndrome characterized by atrioventricular septal defects and blepharophimosis, in addition to radial (e.g. aplastic radius, shortened ulna, fifth finger clinodactyly, absent first metacarpal and thumb) and anal (e.g. imperforate or anteriorly place anus, rectovaginal fistula) defects.","definition_xrefs":["Orphanet:1352"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"disorder of visual system","termid":"MONDO:0024458"}],"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":"atrioventricular defect-blepharophimosis-radial and anal defect syndrome","secondary_identifiers":["OMIM:600123","GARD:2742","UMLS:C1838606","MEDGEN:374010","MESH:C563994"],"synonyms":[{"name":"Houlston-Ironton-Temple syndrome","type":"exact"},{"name":"atrioventricular septal defect with blepharophimosis and anal and radial defects","type":"related"}],"termid":"MONDO:0010825","xrefs":{"Monarch":{"xref_id":"0010825"}}}


id: GO:0045889
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of transcription of homeotic genes of the Polycomb group.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription of homeotic gene (Polycomb group) (obsolete GO:0045889)","synonyms":[{"name":"positive regulation of transcription of homeotic gene (Polycomb group)","type":"exact"}],"termid":"GO:0045889"}


id: GO:1904005
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of phospholipase D activity.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","PMID:11211872"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of phospholipase D activity (obsolete GO:1904005)","synonyms":[{"name":"regulation of choline phosphatase activity","type":"exact"},{"name":"regulation of lecithinase D activity","type":"exact"},{"name":"regulation of lipophosphodiesterase II activity","type":"exact"},{"name":"regulation of phosphatidylcholine phosphatidohydrolase activity","type":"exact"}],"termid":"GO:1904005"}


id: PBO:0109230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLF7 pseudogene 1","termid":"PBO:0109230"}


id: PBO:0081545
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 461","termid":"PBO:0081545"}


id: MONDO:0011690
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Camurati-Engelmann Disease not associated with TGFB1. This is an n-of-1 use case where only one patient or family has been described with this disorder.","definition_xrefs":["Wikipedia:Camurati%E2%80%93Engelmann_disease#Classification"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Camurati-Engelmann disease, type 2","secondary_identifiers":["UMLS:C2931683","MESH:C537978","MEDGEN:419470","OMIM:606631"],"synonyms":[{"name":"CAEND2","type":"related"},{"name":"Camurati Engelmann disease, type 2","type":"related"},{"name":"Camurati-Engelmann disease, type 2","type":"exact"},{"name":"progressive diaphyseal dysplasia with striations of the bones","type":"related"}],"termid":"MONDO:0011690","xrefs":{"Monarch":{"xref_id":"0011690"}}}


id: PBO:0080344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 108 pseudogene","termid":"PBO:0080344"}


id: MONDO:0002439
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete stress polycythemia (obsolete MONDO:0002439)","termid":"MONDO:0002439","xrefs":{"Monarch":{"xref_id":"0002439"}}}


id: MONDO:0014368
data:
  {"annotated_genes":["SJAG_02194"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88216],"is_not":false,"summary":null,"term":"MONDO:0014368"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"familial melanoma","termid":"MONDO:0018961"},{"relation_name":"excluded_subClassOf","term_name":"susceptibility to familial cutaneous melanoma","termid":"MONDO:0024462"},{"relation_name":"is_a","term_name":"susceptibility to familial cutaneous melanoma","termid":"MONDO:0024462"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02194":null},"genotype_count":0,"is_obsolete":false,"name":"tumor predisposition syndrome 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:615848","UMLS:C4014476","MEDGEN:862913","GARD:18582","OMIM:616568"],"synonyms":[{"name":"CMM10","type":"exact"},{"name":"GLM9","type":"exact"},{"name":"glioma susceptibility 9","type":"exact"},{"name":"glioma susceptibility type 9","type":"exact"},{"name":"malignant glioma caused by mutation in POT1","type":"exact"},{"name":"melanoma, cutaneous malignant, susceptibility to, 10","type":"exact"},{"name":"melanoma, cutaneous malignant, susceptibility to, type 10","type":"exact"},{"name":"susceptibility to cutaneous malignant melanoma 10","type":"exact"}],"termid":"MONDO:0014368","terms_by_termid":{"MONDO:0014368":null},"xrefs":{"Monarch":{"xref_id":"0014368"}}}


id: MONDO:0004000
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pilocytic astrocytoma that occurs during childhood.","definition_xrefs":["NCIT:C4048"],"direct_ancestors":[{"relation_name":"is_a","term_name":"childhood astrocytic tumor","termid":"MONDO:0002505"},{"relation_name":"is_a","term_name":"pilocytic astrocytoma","termid":"MONDO:0016691"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"childhood pilocytic astrocytoma","secondary_identifiers":["UMLS:C1332995","MEDGEN:232355","NANDO:2200084","DOID:6812"],"synonyms":[{"name":"childhood pilocytic astrocytoma","type":"exact"},{"name":"paediatric pilocytic astrocytoma","type":"exact"},{"name":"pediatric pilocytic astrocytoma","type":"exact"},{"name":"pilocytic astrocytoma","type":"broad"},{"name":"pilocytic astrocytoma of childhood","type":"exact"}],"termid":"MONDO:0004000","xrefs":{"Monarch":{"xref_id":"0004000"}}}


id: PR:P09988
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H3 that is a translation product of any of the following genes in Schizosaccharomyces pombe 972h-: hht1/hht2.","definition_xrefs":["UniProtKB:P09988","PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"},{"relation_name":"is_a","term_name":"core histone (Schizosaccharomyces pombe)","termid":"PR:000041293"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"histone H3.1/H3.2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1834.04","synonyms":[{"name":"SPAC1834.04","type":"related"},{"name":"Spom972h-hht[1/2]","type":"exact"},{"name":"pi060","type":"related"}],"termid":"PR:P09988"}


id: PBO:0036237
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eRF1 methyltransferase complex and tRNA (m2G10) methyltransferase complex regulatory subunit Trm112 (predicted)","termid":"PBO:0036237"}


id: MONDO:0021783
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the throat due to Streptococcus pyogenes.","definition_xrefs":["NCIT:C116003"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pharyngitis","termid":"MONDO:0002258"},{"relation_name":"is_a","term_name":"streptococcal infection","termid":"MONDO:0021680"},{"relation_name":"is_a","term_name":"respiratory tract infectious disorder","termid":"MONDO:0024355"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"streptococcal sore throat","secondary_identifiers":["MEDGEN:508129","ICD10CM:J02.0","UMLS:C0036689","SCTID:43878008","ICD9:034.0"],"synonyms":[{"name":"Septic sore throat","type":"related"},{"name":"Strep throat","type":"related"},{"name":"Strept throat","type":"related"},{"name":"Streptococcal Pharyngitis","type":"related"},{"name":"Streptococcal angina","type":"related"},{"name":"Streptococcal pharyngitis","type":"related"},{"name":"Streptococcal sore throat","type":"related"},{"name":"strep throat","type":"exact"},{"name":"streptococcal pharyngitis","type":"exact"}],"termid":"MONDO:0021783","xrefs":{"Monarch":{"xref_id":"0021783"}}}


id: PBO:0012241
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial pyrimidine nucleotide transporter (predicted)","termid":"PBO:0012241"}


id: PBO:0057720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1302-5","termid":"PBO:0057720"}


id: MONDO:0015279
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete hereditary predisposition to infections (obsolete MONDO:0015979)","termid":"MONDO:0015979"},{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"chronic mucocutaneous candidiasis","secondary_identifiers":["GARD:1077","UMLS:C0006845","NANDO:2200764","DOID:2058","NCIT:C34444","Orphanet:1334","HP:0002728","icd11.foundation:2120780687","MEDGEN:2426","MedDRA:10009007","MESH:D002178","NANDO:1200363","OMIMPS:114580","SCTID:234568006"],"synonyms":[{"name":"CANDF","type":"exact"},{"name":"CMC","type":"exact"},{"name":"chronic mucocutaneous candidiasis","type":"exact"},{"name":"chronic mucocutaneous candidiasis (disease)","type":"exact"},{"name":"familial CMC","type":"exact"},{"name":"familial candidiasis","type":"exact"},{"name":"familial chronic mucocutaneous candidiasis","type":"exact"}],"termid":"MONDO:0015279","xrefs":{"Monarch":{"xref_id":"0015279"}}}


id: MOD:01274
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that is produced by formation of an adduct with 4-(2-aminoethyl)benzenesulfonyl fluoride, AEBS, and an L-histidine residue.","definition_xrefs":["Unimod:276#H","PubMed:8597590"],"direct_ancestors":[{"relation_name":"is_a","term_name":"4-(2-aminoethyl)benzenesulfonyl fluoride derivatized residue","termid":"MOD:00596"},{"relation_name":"is_a","term_name":"modified L-histidine residue","termid":"MOD:00909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N'-[4-(2-aminoethyl)benzenesulfonyl] derivatized histidine","synonyms":[{"name":"AEBS","type":"related"},{"name":"Aminoethylbenzenesulfonylation","type":"related"}],"termid":"MOD:01274"}


id: GO:2000292
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of defecation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of digestive system process","termid":"GO:0044058"},{"relation_name":"is_a","term_name":"regulation of excretion","termid":"GO:0044062"},{"relation_name":"regulates","term_name":"defecation","termid":"GO:0030421"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of defecation","termid":"GO:2000292"}


id: PBO:0088828
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CMP deaminase family/ methyltransferase bifunctional enzyme involved in riboflavin biosynthesis and tRNA pseudouridine biosynthesis Rib2","termid":"PBO:0088828"}


id: MONDO:0007286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cataract that has material basis in heterozygous mutation in the VIM gene on chromosome 10p13.","definition_xrefs":["PMID:19126778","DOID:0110248"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset partial cataract","termid":"MONDO:0020377"}],"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":"cataract 30","secondary_identifiers":["MESH:C566157","UMLS:C3805411","MEDGEN:811741","OMIM:116300"],"synonyms":[{"name":"CTRCT30","type":"exact"},{"name":"cataract 30","type":"exact"},{"name":"cataract 30 pulverulent","type":"exact"},{"name":"cataract 30, multiple types","type":"related"},{"name":"cataract 30, pulverulent","type":"related"},{"name":"cataract Coppock-like","type":"exact"},{"name":"cataract type 30","type":"exact"}],"termid":"MONDO:0007286","xrefs":{"Monarch":{"xref_id":"0007286"}}}


id: MONDO:0002055
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A very rare, benign sweat gland neoplasm that affects the breast. It is characterized by the proliferation of basaloid epithelial cells.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast benign neoplasm","termid":"MONDO:0000620"},{"relation_name":"is_a","term_name":"benign spiradenoma","termid":"MONDO:0003448"}],"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":"benign eccrine breast spiradenoma","secondary_identifiers":["UMLS:C1332492","DOID:1616","NCIT:C5193","MEDGEN:231933"],"synonyms":[{"name":"benign breast eccrine spiradenoma","type":"exact"},{"name":"benign eccrine breast spiradenoma","type":"exact"},{"name":"benign eccrine spiradenoma of breast","type":"exact"},{"name":"benign eccrine spiradenoma of the breast","type":"exact"}],"termid":"MONDO:0002055","xrefs":{"Monarch":{"xref_id":"0002055"}}}


id: PBO:0040067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cAMP regulated phosphoprotein 21","termid":"PBO:0040067"}


id: GO:0016925
data:
  {"annotated_genes":["SJAG_00604","SJAG_01776","SJAG_02082","SJAG_03843","SJAG_05032","SJAG_02503","SJAG_00727"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74242,74260,77192,77300,77417,99570,116505],"is_not":false,"summary":null,"term":"GO:0016925"}]},"cv_name":"biological_process","definition":"The process in which a SUMO protein (small ubiquitin-related modifier) is conjugated to a target protein via an isopeptide bond between the carboxy-terminus of SUMO with an epsilon-amino group of a lysine residue of the target protein.","definition_xrefs":["GOC:jl","PMID:11265250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidyl-lysine modification","termid":"GO:0018205"},{"relation_name":"is_a","term_name":"protein modification by small protein conjugation","termid":"GO:0032446"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00604":null,"SJAG_00727":null,"SJAG_01776":null,"SJAG_02082":null,"SJAG_02503":null,"SJAG_03843":null,"SJAG_05032":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0070647"}],"interesting_parent_ids":["GO:0070647","GO:0008150"],"is_obsolete":false,"name":"protein sumoylation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0016927","GO:0019951","GO:0019947","Reactome:R-HSA-2990846","Wikipedia:SUMO_protein","GO:0006485"],"synonyms":[{"name":"SUMO-protein conjugation","type":"exact"},{"name":"Smt3-protein conjugation","type":"related"},{"name":"Smt3p-protein conjugation","type":"related"},{"name":"protein sumolation","type":"exact"},{"name":"small ubiquitin-related protein 1 conjugation","type":"exact"},{"name":"sumoylation","type":"exact"}],"termid":"GO:0016925","terms_by_termid":{"GO:0016925":null}}


id: MOD:01247
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:00813 after formula correction. Remap to MOD:00813.","definition_xrefs":["Unimod:295#T","PubMed:11344537","PubMed:11857757","PubMed:15189151"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01247 fucosylated -site T (obsolete MOD:01247)","synonyms":[{"name":"Fucose","type":"related"},{"name":"dHex","type":"related"}],"termid":"MOD:01247"}


id: PBO:0004154
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJ protein Caj1/Djp1-type (predicted)","termid":"PBO:0004154"}


id: PBO:0077102
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocase of inner mitochondrial membrane 9","termid":"PBO:0077102"}


id: FYPO:0002134
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which an interaction between a protein and RNA is decreased. One of the relevant gene products may be encoded by the mutated gene, or both the RNA and protein may be encoded by genes other than the mutated one.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein-RNA interaction","termid":"FYPO:0002132"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0002131"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0002131","FYPO:0001985","FYPO:0000652"],"is_obsolete":false,"name":"decreased protein-RNA interaction","synonyms":[{"name":"decreased RNA binding","type":"exact"},{"name":"decreased RNA-protein interaction","type":"exact"},{"name":"reduced RNA binding","type":"exact"}],"termid":"FYPO:0002134"}


id: PBO:0005382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase activating protein Gyp2 (predicted)","termid":"PBO:0005382"}


id: PBO:0066019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAN binding protein 1","termid":"PBO:0066019"}


id: GO:0007508
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the larval heart over time, from its formation to the mature structure. In Drosophila the larval heart (dorsal vessel) is a continuous tube of mesodormal cells that runs beneath the dorsal midline of the epidermis, divided into an anterior aorta and a posterior heart proper.","definition_xrefs":["ISBN:0879694238","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart development","termid":"GO:0007507"},{"relation_name":"part_of","term_name":"larval development","termid":"GO:0002164"}],"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":"larval heart development","termid":"GO:0007508"}


id: PBO:0028468
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-curved_cytoplasmic_microtubules","termid":"PBO:0028468"}


id: PBO:0120337
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TRIM41 antisense RNA 1","termid":"PBO:0120337"}


id: MOD:00066
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a glycine residue to N-formylglycine.","definition_xrefs":["PubMed:5139483","RESID:AA0057"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-formylated residue","termid":"MOD:00409"},{"relation_name":"is_a","term_name":"modified glycine residue","termid":"MOD:00908"},{"relation_name":"is_a","term_name":"alpha-amino acylated residue","termid":"MOD:01696"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-formylglycine","synonyms":[{"name":"(formylamino)acetic acid","type":"exact"},{"name":"(formylamino)ethanoic acid","type":"exact"},{"name":"(formylazanyl)ethanoic acid","type":"exact"},{"name":"2-formamidoacetic acid","type":"exact"},{"name":"2-formamidoethanoic acid","type":"exact"},{"name":"MOD_RES N-formylglycine","type":"exact"},{"name":"N(alpha)-formylglycine","type":"exact"},{"name":"N-formylated glycine","type":"exact"},{"name":"N-formylglycine","type":"exact"},{"name":"NFoGly","type":"exact"}],"termid":"MOD:00066"}


id: PBO:0077234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMCC1 divergent transcript","termid":"PBO:0077234"}


id: GO:0018978
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane (DDT), a chlorinated, broad spectrum, contact insecticide, in the absence of oxygen.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane metabolic process","termid":"GO:0018977"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"anaerobic 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane metabolic process","secondary_identifiers":["UM-BBD_pathwayID:ddt2"],"synonyms":[{"name":"anaerobic 1,1,1-trichloro-2,2-bis-(4-chlorophenyl)ethane metabolism","type":"exact"},{"name":"anaerobic DDT metabolic process","type":"exact"},{"name":"anaerobic DDT metabolism","type":"exact"}],"termid":"GO:0018978"}


id: GO:0045303
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + L-2,4-diaminobutyrate = L-aspartate 4-semialdehyde + L-glutamate.","definition_xrefs":["EC:2.6.1.76","RHEA:11160"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016769","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"diaminobutyrate-2-oxoglutarate transaminase activity","secondary_identifiers":["KEGG_REACTION:R06977","MetaCyc:R101-RXN"],"synonyms":[{"name":"2,4-diaminobutyrate 4-aminotransferase activity","type":"related"},{"name":"DAB aminotransferase activity","type":"related"},{"name":"DABA aminotransferase activity","type":"related"},{"name":"EctB","type":"related"},{"name":"L-2,4-diaminobutanoate:2-oxoglutarate 4-aminotransferase activity","type":"related"},{"name":"L-2,4-diaminobutyrate:2-ketoglutarate 4-aminotransferase activity","type":"related"},{"name":"L-2,4-diaminobutyrate:2-oxoglutarate 4-aminotransferase activity","type":"related"},{"name":"diaminibutyric acid aminotransferase activity","type":"related"},{"name":"diaminobutyrate transaminase activity","type":"related"},{"name":"diaminobutyrate--2-oxoglutarate aminotransferase activity","type":"related"}],"termid":"GO:0045303"}


id: PBO:0005323
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAGA complex subunit Ada2","termid":"PBO:0005323"}


id: PR:Q9USM5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ubp1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9USM5"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin carboxyl-terminal hydrolase Ubp1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC16A11.12c","synonyms":[{"name":"SPCC16A11.12c","type":"related"},{"name":"Spom972h-ubp1","type":"exact"},{"name":"deubiquitinating enzyme 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin carboxyl-terminal hydrolase 1 (Schizosaccharomyces pombe 972h-)","type":"related"},{"name":"ubiquitin thioesterase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"ubiquitin-specific-processing protease 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9USM5"}


id: PR:P0CT40
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- Tf2-9 gene.","definition_xrefs":["UniProtKB:P0CT40","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":"transposon Tf2-9 polyprotein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC9B6.02c","synonyms":[{"name":"Spom972h-Tf2-9","type":"exact"},{"name":"retrotransposable element Tf2 155 kDa protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P0CT40"}


id: MONDO:0003632
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the endocervix.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cervicitis","termid":"MONDO:0002345"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endocervicitis","secondary_identifiers":["NCIT:C26762","UMLS:C0014127","icd11.foundation:803236221","SCTID:31354001","MEDGEN:4942","DOID:5757"],"synonyms":[{"name":"endocervix inflammation","type":"exact"},{"name":"inflammation of endocervix","type":"exact"}],"termid":"MONDO:0003632","xrefs":{"Monarch":{"xref_id":"0003632"}}}


id: PBO:0038651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acid phosphatase 1","termid":"PBO:0038651"}


id: PBO:0109391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed transcript, Y-linked 20","termid":"PBO:0109391"}


id: GO:0051346
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops or reduces the rate of hydrolase activity, the catalysis of the hydrolysis of various bonds.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of catalytic activity","termid":"GO:0043086"},{"relation_name":"is_a","term_name":"regulation of hydrolase activity","termid":"GO:0051336"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of hydrolase activity","synonyms":[{"name":"down regulation of hydrolase activity","type":"exact"},{"name":"down-regulation of hydrolase activity","type":"exact"},{"name":"downregulation of hydrolase activity","type":"exact"},{"name":"hydrolase inhibitor","type":"exact"},{"name":"inhibition of hydrolase activity","type":"narrow"}],"termid":"GO:0051346"}


id: PBO:0079248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TTC21B antisense RNA 1","termid":"PBO:0079248"}


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:23821151","PMID:27337968"],"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:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006766"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006766"],"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:0080624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WDR70 pseudogene 1","termid":"PBO:0080624"}


id: PBO:0034448
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_level_during_cell_cycle_arrest_in_mitotic_G1_phase_in_response_to_nitrogen_starvation","termid":"PBO:0034448"}


id: PBO:0088197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Zinc finger transcription factor involved in multidrug resistance; Zn(2)-Cys(6) zinc finger transcription factor; activates genes involved in multidrug resistance; paralog of Yrr1p, acting on an overlapping set of target genes","termid":"PBO:0088197"}


id: GO:0044406
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of a symbiont to its host via either adhesion molecules, general stickiness, or other mechanisms. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:jl","GOC:dos","GOC:bf","GOC:cc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process involved in interaction with host","termid":"GO:0051701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"adhesion of symbiont to host","secondary_identifiers":["GO:0051825","GO:0051856"],"synonyms":[{"name":"adhesion to host","type":"related"},{"name":"adhesion to other organism during symbiotic interaction","type":"related"},{"name":"adhesion to other organism involved in symbiotic interaction","type":"exact"},{"name":"host adhesion","type":"narrow"}],"termid":"GO:0044406"}


id: GO:0044812
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The fermentation of organic substances with a net release of hydrogen.","definition_xrefs":["GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fermentation","termid":"GO:0006113"},{"relation_name":"is_a","term_name":"hydrogen biosynthetic process","termid":"GO:1902422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0008150","GO:0006091"],"is_obsolete":false,"name":"fermentative hydrogen production","secondary_identifiers":["Wikipedia:Fermentative_hydrogen_production"],"synonyms":[{"name":"carbohydrate fermentation","type":"exact"}],"termid":"GO:0044812"}


id: MONDO:0024889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign epithelial neoplasm of the female reproductive system arising from mesonephric remnants.","definition_xrefs":["NCIT:C4294"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"benign reproductive system neoplasm","termid":"MONDO:0000383"},{"relation_name":"is_a","term_name":"kidney benign neoplasm","termid":"MONDO:0002513"},{"relation_name":"is_a","term_name":"mesonephric neoplasm","termid":"MONDO:0024888"},{"relation_name":"is_a","term_name":"benign epithelial neoplasm","termid":"MONDO:0036976"}],"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":"benign mesonephroma","secondary_identifiers":["DOID:2616","ICDO:9110/0","MEDGEN:87259","UMLS:C0334530"],"synonyms":[{"name":"Mesonephroma, benign","type":"exact"},{"name":"Mesonephroma, benign (morphologic abnormality)","type":"exact"},{"name":"Wolffian duct adenoma","type":"exact"},{"name":"benign Mesonephroma","type":"exact"},{"name":"benign mesonephric neoplasm","type":"exact"},{"name":"mesonephric adenoma","type":"exact"},{"name":"mesonephric duct adenoma","type":"exact"},{"name":"mesonephric neoplasm, benign","type":"exact"}],"termid":"MONDO:0024889","xrefs":{"Monarch":{"xref_id":"0024889"}}}


id: PBO:0040854
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BLOC1S6 pseudogene 1","termid":"PBO:0040854"}


id: GO:0075275
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that leads to the development of a telium, which is a teliospore-bearing sorus of the rust fungi.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spore-bearing structure development","termid":"GO:0075259"}],"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":"telium development","termid":"GO:0075275"}


id: PBO:0043324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC like kinase 2","termid":"PBO:0043324"}


id: PBO:0108605
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-regulates_characteristic","termid":"PBO:0108605"}


id: MONDO:0017966
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete 46,XY disorder of gonadal development (obsolete MONDO:0017966)","secondary_identifiers":["Orphanet:325118"],"termid":"MONDO:0017966","xrefs":{"Monarch":{"xref_id":"0017966"}}}


id: FYPO:0004253
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of a nuclease activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal nuclease activity","termid":"FYPO:0003163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000654","FYPO:0000707","FYPO:0001985","FYPO:0000661"],"is_obsolete":false,"name":"decreased nuclease activity","synonyms":[{"name":"reduced nuclease activity","type":"exact"}],"termid":"FYPO:0004253"}


id: GO:0047203
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 13-hydroxylupanine + 2-methylcrotonoyl-CoA = 13-(2-methylcrotonoyloxy)lupanine + CoA.","definition_xrefs":["RHEA:12360"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acyltransferase activity, transferring groups other than amino-acyl groups","termid":"GO:0016747"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016746","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"13-hydroxylupinine O-tigloyltransferase activity","secondary_identifiers":["MetaCyc:RXN-8694","KEGG_REACTION:R04205","EC:2.3.1.93"],"synonyms":[{"name":"(E)-2-methylcrotonoyl-CoA:13-hydroxylupinine O-2-methylcrotonoyltransferase activity","type":"related"},{"name":"13-hydroxylupanine acyltransferase activity","type":"related"},{"name":"tigloyl-CoA:13-hydroxylupanine O-tigloyltransferase activity","type":"related"}],"termid":"GO:0047203"}


id: PBO:0001062
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrialtRNA(5-methylaminomethyl-2-thiouridylate)-methyltransferase(predicted)","termid":"PBO:0001062"}


id: PBO:0067725
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 23","termid":"PBO:0067725"}


id: PBO:0063232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protocadherin 18","termid":"PBO:0063232"}


id: GO:0050113
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: myo-inositol + O2 = D-glucuronate + H2O + H+.","definition_xrefs":["RHEA:23696"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen","termid":"GO:0016701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"inositol oxygenase activity","secondary_identifiers":["EC:1.13.99.1","Reactome:R-HSA-5678327","MetaCyc:MYO-INOSITOL-OXYGENASE-RXN","KEGG_REACTION:R01184"],"synonyms":[{"name":"MOO activity","type":"related"},{"name":"meso-inositol oxygenase activity","type":"related"},{"name":"myo-inositol oxygenase activity","type":"exact"},{"name":"myo-inositol:oxygen oxidoreductase activity","type":"related"}],"termid":"GO:0050113"}


id: SO:0001823
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 between existing codons.","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":"conservative_inframe_insertion","synonyms":[{"name":"conservative increase in CDS length","type":"exact"},{"name":"conservative inframe insertion","type":"exact"}],"termid":"SO:0001823"}


id: PBO:0087941
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Translation elongation factor 3; contains two ABC cassettes; binds and hydrolyzes ATP; interacts with mRNA independently of translation; YEF3 has a paralog, HEF3, that arose from the whole genome duplication","termid":"PBO:0087941"}


id: PBO:0075307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"suppressor of cytokine signaling 4","termid":"PBO:0075307"}


id: GO:0002230
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any host process that results in the promotion of antiviral immune response mechanisms, thereby limiting viral replication.","definition_xrefs":["GOC:add","GOC:dph","GOC:tb","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of defense response to virus by host","termid":"GO:0050691"}],"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 defense response to virus by host","synonyms":[{"name":"activation of antiviral response by host","type":"narrow"},{"name":"positive regulation of antiviral response by host","type":"exact"},{"name":"stimulation of antiviral response by host","type":"narrow"},{"name":"up regulation of antiviral response by host","type":"exact"},{"name":"up-regulation of antiviral response by host","type":"exact"},{"name":"upregulation of antiviral response by host","type":"exact"}],"termid":"GO:0002230"}


id: GO:1904847
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell chemotaxis to fibroblast growth factor.","definition_xrefs":["PMID:23233752","GOC:rph","GO_REF:0000058","GOC:BHF","GOC:BHF_miRNA","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell migration","termid":"GO:0030334"},{"relation_name":"is_a","term_name":"regulation of chemotaxis","termid":"GO:0050920"},{"relation_name":"is_a","term_name":"regulation of cellular response to growth factor stimulus","termid":"GO:0090287"},{"relation_name":"regulates","term_name":"cell chemotaxis to fibroblast growth factor","termid":"GO:0035766"}],"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 cell chemotaxis to fibroblast growth factor","termid":"GO:1904847"}


id: MONDO:0100094
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome of cyclic vomiting associated with cannabis use. Fourteen diagnostic characteristics have been identified, and the frequency of major characteristics is as follows: history of regular cannabis for any duration of time (100%), cyclic nausea and vomiting (100%), resolution of symptoms after stopping cannabis (96.8%), compulsive hot baths with symptom relief (92.3%), male predominance (72.9%), abdominal pain (85.1%), and at least weekly cannabis use (97.4%). Supportive care with intravenous fluids, dopamine antagonists, topical capsaicin cream, and avoidance of narcotic medications has shown some benefit in the acute setting. Cannabis cessation appears to be the best treatment.","definition_xrefs":["Wikipedia:Cannabinoid_hyperemesis_syndrome","PMID:28000146"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cannabinoid hyperemesis syndrome","secondary_identifiers":["MEDGEN:1829968","icd11.foundation:908145983","UMLS:C5243764"],"synonyms":[{"name":"CHS","type":"exact"}],"termid":"MONDO:0100094","xrefs":{"Monarch":{"xref_id":"0100094"}}}


id: PBO:0072139
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 16","termid":"PBO:0072139"}


id: GO:0021944
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The changes in adhesion between a neuronal cell and a glial cell as a component of the process of hindbrain glial-mediated radial cell migration.","definition_xrefs":["GO_REF:0000021","GOC:jid","GOC:dgh","GOC:cls","GOC:dph","PMID:15157725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion","termid":"GO:0098609"},{"relation_name":"part_of","term_name":"hindbrain radial glia guided cell migration","termid":"GO:0021932"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"neuronal-glial interaction involved in hindbrain glial-mediated radial cell migration","termid":"GO:0021944"}


id: GO:0010901
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate, frequency or extent of very-low-density lipoprotein particle remodeling. Very-low-density lipoprotein particle remodeling is the acquisition, loss or modification of a protein or lipid within a very-low-density lipoprotein particle, including the hydrolysis of triglyceride by hepatic lipase or lipoprotein lipase and the subsequent loss of free fatty acid.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"very-low-density lipoprotein particle remodeling","termid":"GO:0034372"}],"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 very-low-density lipoprotein particle remodeling","synonyms":[{"name":"regulation of VLDL remodeling","type":"exact"},{"name":"regulation of VLDL remodelling","type":"exact"},{"name":"regulation of very-low-density lipoprotein particle remodelling","type":"exact"}],"termid":"GO:0010901"}


id: PBO:0026883
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_chromatin_binding_during_cellular_response_to_nitrogen_starvation","termid":"PBO:0026883"}


id: PBO:0041958
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell cycle and apoptosis regulator 2","termid":"PBO:0041958"}


id: PBO:0117160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDH4 antisense RNA 2","termid":"PBO:0117160"}


id: GO:0055126
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein complex that forms part of the nuclear pore complex. It forms a subcomplex with Nup159p and Nsp1p, interacts with Nup116p, and is required for proper localization of Nup116p. In Saccharomyces cerevisiae this complex contains Nup82p, Nsp1p, Nup159p, Nup116p, and Gle2p.","definition_xrefs":["PMID:12791264","GOC:jh","PMID:15741174"],"gene_count":0,"genotype_count":0,"name":"obsolete Nup82 complex (obsolete GO:0055126)","synonyms":[{"name":"Nup82 complex","type":"exact"}],"termid":"GO:0055126"}


id: FYPO:0001271
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic sister chromatid segregation stops before completing separation of chromosomes; some, but not all, DNA may be moved towards the ends of an elongated mitotic spindle. Chromosomes do not segregate into two equal masses.","definition_xrefs":["PMID:22711988","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unequal mitotic sister chromatid segregation","termid":"FYPO:0003241"},{"relation_name":"is_a","term_name":"incomplete mitotic sister chromatid segregation","termid":"FYPO:0003757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000641","FYPO:0000631","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000337"],"is_obsolete":false,"name":"incomplete, unequal mitotic sister chromatid segregation","synonyms":[{"name":"incomplete, unequal mitotic chromosome segregation","type":"exact"},{"name":"incomplete, unequal mitotic sister chromatid segregation during vegetative growth","type":"exact"},{"name":"incomplete, unequal mitotic sister chromatid separation","type":"related"},{"name":"incomplete, unequal sister chromatid segregation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0001271"}


id: PR:O13748
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tae1 gene.","definition_xrefs":["UniProtKB:O13748","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":"alpha N-terminal protein methyltransferase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16E8.14c","synonyms":[{"name":"NTM1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-tae1","type":"exact"},{"name":"X-Pro-Lys N-terminal protein methyltransferase 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"translation associated element 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13748"}


id: PBO:0000265
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptional corepressor Tup11","termid":"PBO:0000265"}


id: PBO:0056527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"melanocortin 4 receptor","termid":"PBO:0056527"}


id: GO:0048448
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the stamen are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"floral organ morphogenesis","termid":"GO:0048444"},{"relation_name":"part_of","term_name":"stamen development","termid":"GO:0048443"}],"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":"stamen morphogenesis","secondary_identifiers":["GO:0048426"],"termid":"GO:0048448"}


id: PATO:0001516
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An optical quality where light rays originating from a point on the object converge.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Focus_(optics)"],"direct_ancestors":[{"relation_name":"is_a","term_name":"optical quality","termid":"PATO:0001300"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"focus","termid":"PATO:0001516"}


id: GO:0097504
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Nuclear bodies frequently found near or associated with Cajal bodies (also called coiled bodies or CBs). Gemini of coiled bodies, or 'gems', are similar in size and shape to CBs, and often indistinguishable under the microscope. Unlike CBs, gems do not contain small nuclear ribonucleoproteins (snRNPs); they contain a protein called survivor of motor neurons (SMN) whose function relates to snRNP biogenesis. Gems are believed to assist CBs in snRNP biogenesis, and to play a role in the etiology of spinal muscular atrophy (SMA).","definition_xrefs":["PMID:9683623","Wikipedia:Cell_nucleus#Cajal_bodies_and_gems","PMID:11031238","GOC:pr"],"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:0005654"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005654","GO:0005575","GO:0005634"],"is_obsolete":false,"name":"Gemini of Cajal bodies","synonyms":[{"name":"Gemini of coiled bodies","type":"exact"},{"name":"Gems","type":"exact"}],"termid":"GO:0097504"}


id: GO:0033468
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of CMP-keto-3-deoxy-D-manno-octulosonic acid, a substance composed of the acidic sugar 3-deoxy-D-manno-octulosonic acid in glycosidic linkage with cytidine monophosphate.","definition_xrefs":["GOC:mah","MetaCyc:PWY-1269"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar biosynthetic process","termid":"GO:0009226"},{"relation_name":"is_a","term_name":"CMP-keto-3-deoxy-D-manno-octulosonic acid metabolic process","termid":"GO:0033467"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"CMP-keto-3-deoxy-D-manno-octulosonic acid biosynthetic process","synonyms":[{"name":"CMP-KDO biosynthesis","type":"exact"},{"name":"CMP-KDO biosynthetic process","type":"exact"},{"name":"CMP-keto-3-deoxy-D-manno-octulosonic acid anabolism","type":"exact"},{"name":"CMP-keto-3-deoxy-D-manno-octulosonic acid biosynthesis","type":"exact"},{"name":"CMP-keto-3-deoxy-D-manno-octulosonic acid formation","type":"exact"},{"name":"CMP-keto-3-deoxy-D-manno-octulosonic acid synthesis","type":"exact"},{"name":"CMP-ketodeoxyoctanoate biosynthetic process","type":"related"}],"termid":"GO:0033468"}


id: PBO:0072135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S15a pseudogene 12","termid":"PBO:0072135"}


id: PATO:0000212
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000212 neural function (obsolete PATO:0000212)","termid":"PATO:0000212"}


id: MONDO:0010879
data:
  {"annotated_genes":["SJAG_00984"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88814],"is_not":false,"summary":null,"term":"MONDO:0010879"}]},"cv_name":"mondo","definition":"Codas syndrome is a multiple congenital anomalies syndrome characterized by Cerebral, Ocular, Dental, Auricular and Skeletal anomalies.","definition_xrefs":["Orphanet:1458"],"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"},{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00984":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"CODAS syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:C536434","SCTID:717772000","MEDGEN:333031","GARD:1418","NCIT:C126744","OMIM:600373","UMLS:C1838180","DOID:0111274"],"synonyms":[{"name":"CODAS syndrome","type":"exact"},{"name":"cerebral, ocular, dental, auricular, and skeletal anomalies syndrome","type":"related"},{"name":"cerebral, ocular, dental, auricular, and skeletal syndrome","type":"related"},{"name":"cerebro-oculo-dento-auriculo-skeletal syndrome","type":"related"},{"name":"cerebrooculodentoauriculoskeletal syndrome","type":"exact"}],"termid":"MONDO:0010879","terms_by_termid":{"MONDO:0010879":null},"xrefs":{"Monarch":{"xref_id":"0010879"}}}


id: PATO:0002116
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A composition quality inhering in exudate by virtue of the bearer's containing fibrin.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"composition","termid":"PATO:0000025"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibrinopurulent","termid":"PATO:0002116"}


id: PBO:0055458
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 2890","termid":"PBO:0055458"}


id: GO:0072111
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of cells, resulting in the expansion of the population in the kidney.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population proliferation","termid":"GO:0008283"},{"relation_name":"part_of","term_name":"kidney development","termid":"GO:0001822"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell proliferation involved in kidney development","termid":"GO:0072111"}


id: SO:0000329
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An mRNA with a plus 2 frameshift.","definition_xrefs":["SO:xp"],"direct_ancestors":[{"relation_name":"has_quality","term_name":"plus_2_framshift","termid":"SO:0000869"},{"relation_name":"is_a","term_name":"mRNA_with_frameshift","termid":"SO:0000108"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA_with_plus_2_frameshift","synonyms":[{"name":"mRNA with plus 2 frameshift","type":"exact"}],"termid":"SO:0000329"}


id: MONDO:0976125
data:
  {"annotated_genes":["SJAG_03570"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86847],"is_not":false,"summary":null,"term":"MONDO:0976125"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03570":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with speech or visual impairment and brain hypomyelination","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:621034"],"termid":"MONDO:0976125","terms_by_termid":{"MONDO:0976125":null},"xrefs":{"Monarch":{"xref_id":"0976125"}}}


id: MONDO:1012075
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple exostoses, non-human animal","termid":"MONDO:1011944"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple exostoses, pig","secondary_identifiers":["OMIA:000354-9823"],"termid":"MONDO:1012075","xrefs":{"Monarch":{"xref_id":"1012075"}}}


id: GO:0080122
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of AMP, adenosine monophosphate, from one side of a membrane to the other.","definition_xrefs":["PMID:18923018"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenine nucleotide transmembrane transporter activity","termid":"GO:0000295"},{"relation_name":"is_a","term_name":"purine ribonucleotide transmembrane transporter activity","termid":"GO:0005346"},{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"AMP transmembrane transporter activity","synonyms":[{"name":"adenosine monophosphate transmembrane transporter activity","type":"exact"}],"termid":"GO:0080122"}


id: GO:0052150
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont gene product affects host apoptosis, leading to a change in the frequency, rate or extent of apoptosis in the host cell. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of killing of cells of another organism","termid":"GO:0051709"},{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host programmed cell death","termid":"GO:0052040"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host apoptosis","secondary_identifiers":["VZ:1518"],"synonyms":[{"name":"modulation by organism of host apoptotic programmed cell death","type":"exact"},{"name":"modulation by symbiont of host apoptosis","type":"narrow"},{"name":"modulation by symbiont of host apoptotic process","type":"exact"},{"name":"modulation by virus of host apoptosis","type":"narrow"},{"name":"regulation by virus of host apoptosis","type":"narrow"}],"termid":"GO:0052150"}


id: GO:0102561
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: alpha-D-ribose 1,2-cyclic phosphate 5-phosphate + H2O = D-ribose 2,5-bisphosphate + H+.","definition_xrefs":["EC:3.1.4.57"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphoric diester hydrolase activity","termid":"GO:0008081"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016788"},{"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:0016788","GO:0003674"],"is_obsolete":false,"name":"phosphoribosyl 1,2-cyclic phosphate 1,2-diphosphodiesterase activity","secondary_identifiers":["MetaCyc:RXN-14996"],"synonyms":[{"name":"D-ribose 2,5-bisphosphate 2-phosphohydrolase activity","type":"related"},{"name":"cyclic phosphate dihydrolase activity","type":"related"}],"termid":"GO:0102561"}


id: PBO:0062294
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 5 subfamily M member 5 pseudogene","termid":"PBO:0062294"}


id: MONDO:1012922
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any centronuclear myopathy that occurs in dogs due to a mutation in the DNM2 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital myopathy, dog","termid":"MONDO:1010918"},{"relation_name":"is_a","term_name":"centronuclear myopathy, non-human animal","termid":"MONDO:1012963"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centronuclear myopathy, DNM2-related, dog","secondary_identifiers":["OMIA:002534-9615"],"synonyms":[{"name":"ADCNM","type":"exact"},{"name":"autosomal dominant centronuclear myopathy","type":"related"},{"name":"centronuclear myopathy 1, DNM2-related, dog","type":"exact"}],"termid":"MONDO:1012922","xrefs":{"Monarch":{"xref_id":"1012922"}}}


id: PBO:0074697
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 70G","termid":"PBO:0074697"}


id: MONDO:0859614
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A low grade glioma that is characterized by a gene alteration that results in a MAPK pathway abnormality, with morphological features of astrocytoma or oligodendroglioma.","definition_xrefs":["DOID:0081260"],"direct_ancestors":[{"relation_name":"is_a","term_name":"low grade glioma","termid":"MONDO:0021637"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diffuse low-grade glioma, MAPK pathway–altered","secondary_identifiers":["NCIT:C185218"],"termid":"MONDO:0859614","xrefs":{"Monarch":{"xref_id":"0859614"}}}


id: GO:0061037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency, or extent of cartilage development, the process whose specific outcome is the progression of the cartilage over time, from its formation to the mature structure. Cartilage is a connective tissue dominated by extracellular matrix containing collagen type II and large amounts of proteoglycan, particularly chondroitin sulfate.","definition_xrefs":["GOC:dph"],"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 cartilage development","termid":"GO:0061035"},{"relation_name":"negatively_regulates","term_name":"cartilage development","termid":"GO:0051216"}],"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 cartilage development","termid":"GO:0061037"}


id: GO:0047662
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4(or 2)-aminobenzoate = aniline + CO2.","definition_xrefs":["EC:4.1.1.24","MetaCyc:AMINOBENZOATE-DECARBOXYLASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxy-lyase activity","termid":"GO:0016831"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"aminobenzoate decarboxylase activity","secondary_identifiers":["RHEA:24200"],"synonyms":[{"name":"aminobenzoate carboxy-lyase (aniline-forming)","type":"related"},{"name":"aminobenzoate carboxy-lyase activity","type":"related"}],"termid":"GO:0047662"}


id: PBO:0079886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uroplakin 3B like 3, pseudogene","termid":"PBO:0079886"}


id: PBO:0061724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear VCP like","termid":"PBO:0061724"}


id: SO:0001007
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A remnant of an integrated prophage in the host genome or an \\\"island\\\" in the host genome that includes phage like-genes.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genomic_island","termid":"SO:0000772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cryptic_prophage","secondary_identifiers":["http://ecoliwiki.net/colipedia/index.php/Category\\:Cryptic_Prophage.w"],"synonyms":[{"name":"cryptic prophage","type":"exact"}],"termid":"SO:0001007"}


id: GO:1904729
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of intestinal lipid absorption.","definition_xrefs":["GOC:TermGenie","PMID:18768481","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intestinal absorption","termid":"GO:1904478"},{"relation_name":"regulates","term_name":"intestinal lipid absorption","termid":"GO:0098856"}],"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 intestinal lipid absorption","termid":"GO:1904729"}


id: FYPO:0002505
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the palmitoylation of one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein modification","termid":"FYPO:0002498"},{"relation_name":"is_a","term_name":"abnormal protein palmitoylation","termid":"FYPO:0002503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002274","FYPO:0001985","FYPO:0000002","FYPO:0002494"],"is_obsolete":false,"name":"decreased protein palmitoylation","synonyms":[{"name":"reduced protein palmitoylation","type":"exact"}],"termid":"FYPO:0002505"}


id: GO:2000190
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of regulation of transcription from RNA polymerase II promoter by nuclear hormone receptor.","definition_xrefs":["GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of regulation of transcription from RNA polymerase II promoter by nuclear hormone receptor (obsolete GO:2000190)","synonyms":[{"name":"negative regulation of regulation of transcription from RNA polymerase II promoter by nuclear hormone receptor","type":"exact"}],"termid":"GO:2000190"}


id: PBO:0064017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 51","termid":"PBO:0064017"}


id: PBO:0070605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 73","termid":"PBO:0070605"}


id: MONDO:1011534
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hyperadrenocorticism that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperadrenocorticism, non-human animal","termid":"MONDO:1011403"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyperadrenocorticism, horse","secondary_identifiers":["OMIA:000494-9796"],"termid":"MONDO:1011534","xrefs":{"Monarch":{"xref_id":"1011534"}}}


id: PBO:0030430
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_eisosome_filament","termid":"PBO:0030430"}


id: PBO:0028178
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_vanadate","termid":"PBO:0028178"}


id: MONDO:0016640
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete fibrous dysplasia of bone (obsolete MONDO:0016640)","termid":"MONDO:0016640","xrefs":{"Monarch":{"xref_id":"0016640"}}}


id: GO:0019490
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The removal of the sulfonate group from 2-aminobenzenesulfonate, an aromatic sulfonate used in organic synthesis and in the manufacture of various dyes and medicines.","definition_xrefs":["MetaCyc:2ASDEG-PWY"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-aminobenzenesulfonate metabolic process","termid":"GO:0018868"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006790"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006790"],"is_obsolete":false,"name":"2-aminobenzenesulfonate desulfonation","secondary_identifiers":["UM-BBD_pathwayID:abs"],"synonyms":[{"name":"2-aminobenzenesulphonate desulphonation","type":"exact"}],"termid":"GO:0019490"}


id: PBO:0080486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"von Willebrand factor A domain containing 5B1","termid":"PBO:0080486"}


id: PBO:0082879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cullin; structural protein of SCF complexes (which also contain Skp1p, Cdc34p, Hrt1p and an F-box protein) involved in ubiquitination; SCF promotes the G1-S transition by targeting G1 cyclins and the Cln-CDK inhibitor Sic1p for degradation; human homolog CUL1 can complement yeast cdc53 null mutant","termid":"PBO:0082879"}


id: PBO:0055398
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 2828","termid":"PBO:0055398"}


id: PBO:0056774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase like 24","termid":"PBO:0056774"}


id: PATO:0000591
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A thickness which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"increased size","termid":"PATO:0000586"},{"relation_name":"is_a","term_name":"thickness","termid":"PATO:0000915"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased thickness","synonyms":[{"name":"high thickness","type":"exact"},{"name":"stout","type":"exact"},{"name":"thick","type":"related"},{"name":"thickened","type":"exact"}],"termid":"PATO:0000591"}


id: GO:0045005
data:
  {"annotated_genes":["SJAG_02610","SJAG_02822","SJAG_05237","SJAG_05372","SJAG_03843","SJAG_02992","SJAG_02079","SJAG_02198","SJAG_03898","SJAG_03097","SJAG_00727","SJAG_01185","SJAG_01410","SJAG_02039","SJAG_01221","SJAG_01832","SJAG_01572","SJAG_01374","SJAG_02439","SJAG_06022","SJAG_04855","SJAG_00623","SJAG_02465","SJAG_00573","SJAG_01076","SJAG_03780","SJAG_02818","SJAG_01584","SJAG_03997","SJAG_04671","SJAG_02908","SJAG_02724","SJAG_05180","SJAG_00177","SJAG_01044","SJAG_02299","SJAG_01644","SJAG_00935","SJAG_02698","SJAG_00247","SJAG_03728","SJAG_05012","SJAG_01677","SJAG_04971","SJAG_04272","SJAG_04183","SJAG_02214","SJAG_02294","SJAG_03300"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98961,114596],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902298"},{"annotations":[76826,75753],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045004"},{"annotations":[110966,113611],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990505"},{"annotations":[97995,111401,118664,114374,90983,100056,109564,100763,96886,96645,109588,65122,110922,97829,92762],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990426"},{"annotations":[118276,90813,107961],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0120292"},{"annotations":[105048],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902681"},{"annotations":[110354,101174,108467,105049],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0011000"},{"annotations":[104095,101175,116884],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031582"},{"annotations":[101176],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090001"},{"annotations":[104096],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071807"},{"annotations":[101096,102990,71423,109985,119308,96422,99309,107566,63112,108468,81052,81258,102467],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031297"},{"annotations":[114378,77337],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071932"},{"annotations":[99932],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990516"},{"annotations":[111403,117378,93352,116145,111811,100876,118666,98499,90986,100765,91414,97997],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0120290"}]},"cv_name":"biological_process","definition":"A DNA metabolic process that prevents or corrects errors to ensure that DNA is replicated accurately. Errors can be corrected either by intrinsic DNA polymerase proofreading activity or via mismatch repair.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA metabolic process","termid":"GO:0006259"},{"relation_name":"part_of","term_name":"DNA-templated DNA replication","termid":"GO:0006261"}],"gene_count":49,"genes_by_uniquename":{"SJAG_00177":null,"SJAG_00247":null,"SJAG_00573":null,"SJAG_00623":null,"SJAG_00727":null,"SJAG_00935":null,"SJAG_01044":null,"SJAG_01076":null,"SJAG_01185":null,"SJAG_01221":null,"SJAG_01374":null,"SJAG_01410":null,"SJAG_01572":null,"SJAG_01584":null,"SJAG_01644":null,"SJAG_01677":null,"SJAG_01832":null,"SJAG_02039":null,"SJAG_02079":null,"SJAG_02198":null,"SJAG_02214":null,"SJAG_02294":null,"SJAG_02299":null,"SJAG_02439":null,"SJAG_02465":null,"SJAG_02610":null,"SJAG_02698":null,"SJAG_02724":null,"SJAG_02818":null,"SJAG_02822":null,"SJAG_02908":null,"SJAG_02992":null,"SJAG_03097":null,"SJAG_03300":null,"SJAG_03728":null,"SJAG_03780":null,"SJAG_03843":null,"SJAG_03898":null,"SJAG_03997":null,"SJAG_04183":null,"SJAG_04272":null,"SJAG_04671":null,"SJAG_04855":null,"SJAG_04971":null,"SJAG_05012":null,"SJAG_05180":null,"SJAG_05237":null,"SJAG_05372":null,"SJAG_06022":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0006260"],"is_obsolete":false,"name":"DNA-templated DNA replication maintenance of fidelity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"DNA-dependent DNA replication maintenance of fidelity","type":"exact"},{"name":"maintenance of fidelity during DNA-dependent DNA replication","type":"related"},{"name":"maintenance of fidelity involved in DNA-dependent DNA replication","type":"exact"}],"termid":"GO:0045005","terms_by_termid":{"GO:0011000":null,"GO:0031297":null,"GO:0031582":null,"GO:0045004":null,"GO:0071807":null,"GO:0071932":null,"GO:0090001":null,"GO:0120290":null,"GO:0120292":null,"GO:1902298":null,"GO:1902681":null,"GO:1990426":null,"GO:1990505":null,"GO:1990516":null}}


id: PBO:0030856
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_calcium_level_during_cellular_response_to_salt_stress","termid":"PBO:0030856"}


id: PBO:0060742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase complex assembly factor 7","termid":"PBO:0060742"}


id: FYPO:0007007
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype in which the frequency of DNA recombination is normal (i.e. indistinguishable from wild type) downstream of DNA replication fork barriers.","definition_xrefs":["PomBase:mah","PMID:30667359"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0001312"],"is_obsolete":false,"name":"normal DNA recombination frequency downstream of mitotic DNA replication fork barriers","synonyms":[{"name":"normal DNA recombination frequency downstream of mitotic DNA replication fork barriers during mitotic cell cycle","type":"related"},{"name":"normal DNA recombination frequency downstream of mitotic DNA replication fork barriers during vegetative growth","type":"exact"},{"name":"normal template switching recombination frequency downstream of mitotic DNA replication fork barriers","type":"exact"}],"termid":"FYPO:0007007"}


id: CHEBI:17234
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucose","termid":"CHEBI:17234"}


id: MONDO:0016573
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute fatty liver of pregnancy is a rare but severe complication occurring in the third trimester of pregnancy or in early postpartum period bearing a risk for perinatal and maternal mortality and characterized by jaundice, rise of hepatic injuries and evolving to acute liver failure and encephalopathy.","definition_xrefs":["Orphanet:243367"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"},{"relation_name":"is_a","term_name":"pregnancy disorder","termid":"MONDO:0024575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute fatty liver of pregnancy","secondary_identifiers":["SCTID:716379000","UMLS:C1455728","GARD:9578","MedDRA:10000746","icd11.foundation:1226221530","MEDGEN:264102","MESH:C537957"],"synonyms":[{"name":"AFLP","type":"exact"},{"name":"acute fatty liver, gestational","type":"related"}],"termid":"MONDO:0016573","xrefs":{"Monarch":{"xref_id":"0016573"}}}


id: RO:0002258
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Candidate definition: x developmentally related to y if and only if there exists some developmental process (GO:0032502) p such that x and y both participates in p, and x is the output of p and y is the input of p","direct_ancestors":[{"relation_name":"is_a","term_name":"developmentally_related_to","termid":"RO:0002324"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"developmentally_preceded_by","termid":"RO:0002258"}


id: GO:0010415
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving the mannan backbone, the unsubstituted polymer of D-mannose units.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mannan metabolic process","termid":"GO:0010412"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0008150","GO:0071554","GO:0005975"],"is_obsolete":false,"name":"unsubstituted mannan metabolic process","synonyms":[{"name":"unsubstituted mannan metabolism","type":"exact"}],"termid":"GO:0010415"}


id: PBO:0089518
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynein heavy chain, minus-end directed microtubule motor Dhc1","termid":"PBO:0089518"}


id: GO:0102932
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + (-)-medicarpin + NADPH = (+)-vestitol + NADP.","definition_xrefs":["EC:1.3.1.-","GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete pterocarpan reductase activity (obsolete GO:0102932)","termid":"GO:0102932"}


id: PBO:0066801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 100","termid":"PBO:0066801"}


id: PBO:0031001
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_mercaptoethanol","termid":"PBO:0031001"}


id: PBO:0043341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chloride nucleotide-sensitive channel 1A","termid":"PBO:0043341"}


id: MONDO:0008372
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Leber congenital amaurosis","termid":"MONDO:0018998"}],"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":"retinal aplasia","secondary_identifiers":["MESH:C566720","UMLS:C1867331","GARD:15109","OMIM:179900","MEDGEN:356752"],"synonyms":[{"name":"amaurosis congenita","type":"related"},{"name":"retinal aplasia","type":"exact"}],"termid":"MONDO:0008372","xrefs":{"Monarch":{"xref_id":"0008372"}}}


id: PBO:0064814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory inhibitor subunit 2 pseudogene 5","termid":"PBO:0064814"}


id: MONDO:0009536
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chronic mucocutaneous candidiasis","termid":"MONDO:0015279"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"chronic mucocutaneous candidiasis due to intrinsic defect in lymphoblastic transformation","secondary_identifiers":["MEDGEN:340881","OMIM:247450","UMLS:C1855474","MESH:C565431"],"synonyms":[{"name":"lymphoblastic transformation, intrinsic defect IN","type":"related"},{"name":"lymphoblastic transformation, intrinsic defect type 1N","type":"exact"}],"termid":"MONDO:0009536","xrefs":{"Monarch":{"xref_id":"0009536"}}}


id: MONDO:0006636
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with bacteria of the genus actinobacillus.","definition_xrefs":["MESH:D000189"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Actinobacillus infectious disease","synonyms":[{"name":"Actinobacillus caused disease or disorder","type":"exact"},{"name":"Actinobacillus disease or disorder","type":"exact"},{"name":"Actinobacillus infection","type":"related"},{"name":"infection, Actinobacillus","type":"related"},{"name":"infections, Actinobacillus","type":"related"}],"termid":"MONDO:0006636","xrefs":{"Monarch":{"xref_id":"0006636"}}}


id: MONDO:0100235
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any anterior segment dysgenesis in which the cause of the disease is a mutation in the FOXC1 gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"iridogoniodysgenesis","termid":"MONDO:0011119"}],"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":"FOXC1-related anterior segment dysgenesis","termid":"MONDO:0100235","xrefs":{"Monarch":{"xref_id":"0100235"}}}


id: PBO:0081263
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF32 antisense RNA 1","termid":"PBO:0081263"}


id: PATO:0002113
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Perforated like a sieve.","definition_xrefs":["merriam-webster:merriam-webster"],"direct_ancestors":[{"relation_name":"is_a","term_name":"perforate","termid":"PATO:0002112"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cribriform","termid":"PATO:0002113"}


id: PBO:0048661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerol kinase 3","termid":"PBO:0048661"}


id: MONDO:0000191
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete renal hypodysplasia/aplasia (obsolete MONDO:0000191)","termid":"MONDO:0000191","xrefs":{"Monarch":{"xref_id":"0000191"}}}


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:0041116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"brain specific homeobox","termid":"PBO:0041116"}


id: GO:0006544
data:
  {"annotated_genes":["SJAG_02450","SJAG_03914","SJAG_02901","SJAG_03641","SJAG_03861","SJAG_01766"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[73862],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006545"},{"annotations":[75074,73814],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019264"},{"annotations":[79794,98226,75916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019464"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving glycine, aminoethanoic acid.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"serine family amino acid metabolic process","termid":"GO:0009069"},{"relation_name":"is_a","term_name":"proteinogenic amino acid metabolic process","termid":"GO:0170039"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01766":null,"SJAG_02450":null,"SJAG_02901":null,"SJAG_03641":null,"SJAG_03861":null,"SJAG_03914":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0006520"],"is_obsolete":false,"name":"glycine metabolic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"glycine metabolism","type":"exact"}],"termid":"GO:0006544","terms_by_termid":{"GO:0006545":null,"GO:0019264":null,"GO:0019464":null}}


id: MOD:00392
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to O-decanoyl-L-threonine.","definition_xrefs":["Unimod:449#T","PubMed:11546772","RESID:AA0387"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-decanoylated residue","termid":"MOD:00668"},{"relation_name":"is_a","term_name":"O3-acylated L-threonine","termid":"MOD:02004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"O-decanoyl-L-threonine","synonyms":[{"name":"(2S)-2-amino-3-(decanoyloxy)propanoic acid","type":"exact"},{"name":"Decanoyl","type":"related"},{"name":"L-threonine decanoate ester","type":"exact"},{"name":"LIPID O-decanoyl threonine","type":"exact"},{"name":"O-decanoyl-L-threonine","type":"exact"},{"name":"O-decanoylated L-threonine","type":"exact"},{"name":"O3-decanoyl-L-threonine","type":"exact"},{"name":"ODecThr","type":"exact"},{"name":"lipid","type":"related"}],"termid":"MOD:00392"}


id: MONDO:0011921
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary otorhinolaryngologic disease","termid":"MONDO:0018751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aural atresia, congenital","secondary_identifiers":["MESH:C564321","UMLS:C1842937","OMIM:607842","MEDGEN:375051","GARD:18275"],"synonyms":[{"name":"CAA","type":"related"},{"name":"aural atresia, congenital","type":"exact"},{"name":"aural atresia, congenital, with hyposmia","type":"related"}],"termid":"MONDO:0011921","xrefs":{"Monarch":{"xref_id":"0011921"}}}


id: MONDO:0033638
data:
  {"annotated_genes":["SJAG_03550"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87522],"is_not":false,"summary":null,"term":"MONDO:0033638"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex IV deficiency, nuclear-type","termid":"MONDO:0033885"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03550":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex 4 deficiency, nuclear type 8","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070495","GARD:16407","OMIM:619052","MEDGEN:1765544","UMLS:C5436689"],"synonyms":[{"name":"MC4DN8","type":"exact"},{"name":"mitochondrial complex IV deficiency, nuclear type 8","type":"exact"}],"termid":"MONDO:0033638","terms_by_termid":{"MONDO:0033638":null},"xrefs":{"Monarch":{"xref_id":"0033638"}}}


id: GO:0000921
data:
  {"annotated_genes":["SJAG_04375","SJAG_00663","SJAG_02683"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[61108,74127,105740],"is_not":false,"summary":null,"term":"GO:0000921"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of septins and associated proteins to form an organized structure resembling a ring at the cell cortex.","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septin ring organization","termid":"GO:0031106"},{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"is_a","term_name":"membraneless organelle assembly","termid":"GO:0140694"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00663":null,"SJAG_02683":null,"SJAG_04375":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"septin ring assembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"septin assembly and septum biosynthesis","type":"broad"},{"name":"septin assembly and septum formation","type":"broad"}],"termid":"GO:0000921","terms_by_termid":{"GO:0000921":null}}


id: GO:0000439
data:
  {"annotated_genes":["SJAG_01207","SJAG_00758","SJAG_00512","SJAG_03206","SJAG_00995","SJAG_04368","SJAG_00901"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[57488,63171,71877,77904,80462,92068,93983],"is_not":false,"summary":null,"term":"GO:0000439"}]},"cv_name":"cellular_component","definition":"The 7 subunit core of TFIIH that is a part of either the general transcription factor holo-TFIIH or the nucleotide-excision repair factor 3 complex. In S. cerevisiae/humans the complex is composed of: Ssl2/XPB, Tfb1/p62, Tfb2/p52, Ssl1/p44, Tfb4/p34, Tfb5/p8 and Rad3/XPD.","definition_xrefs":["PMID:22572993","GOC:krc","PMID:23028141","PMID:7813015","GOC:ew","PMID:14500720","PMID:17215295","PMID:22308316"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription regulator complex","termid":"GO:0090575"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00512":null,"SJAG_00758":null,"SJAG_00901":null,"SJAG_00995":null,"SJAG_01207":null,"SJAG_03206":null,"SJAG_04368":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:0005634"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"transcription factor TFIIH core complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0000441"],"synonyms":[{"name":"SSL2-core TFIIH complex","type":"exact"},{"name":"core TFIIH complex","type":"exact"}],"termid":"GO:0000439","terms_by_termid":{"GO:0000439":null}}


id: PBO:0062104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily C member 2 pseudogene","termid":"PBO:0062104"}


id: PBO:0083461
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene KNS1","termid":"PBO:0083461"}


id: MONDO:0030937
data:
  {"annotated_genes":["SJAG_02398"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87369],"is_not":false,"summary":null,"term":"MONDO:0030937"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial complex II deficiency, nuclear type","termid":"MONDO:0031230"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02398":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004069"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0005336","MONDO:0005066"],"is_obsolete":false,"name":"mitochondrial complex 2 deficiency, nuclear type 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5436934","GARD:16430","MEDGEN:1751884","OMIM:619167"],"synonyms":[{"name":"MC2DN3","type":"exact"},{"name":"mitochondrial complex 2 deficiency, nuclear type 3","type":"exact"},{"name":"mitochondrial complex II deficiency, nuclear type 3","type":"exact"}],"termid":"MONDO:0030937","terms_by_termid":{"MONDO:0030937":null},"xrefs":{"Monarch":{"xref_id":"0030937"}}}


id: MOD:00784
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-phenylalanine residue to N-acetyl-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":"alpha-amino acetylated residue","termid":"MOD:01458"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00408"}],"interesting_parent_ids":["MOD:00408"],"is_obsolete":false,"name":"N-acetyl-L-phenylalanine","synonyms":[{"name":"AcPhe","type":"exact"}],"termid":"MOD:00784"}


id: MONDO:0011003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the SCN5A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"dilated cardiomyopathy 1E","secondary_identifiers":["OMIM:601154","MEDGEN:331341","UMLS:C1832680","GARD:5644","DOID:0110433","MESH:C563384"],"synonyms":[{"name":"CDCD2","type":"exact"},{"name":"CMD1E","type":"exact"},{"name":"SCN5A familial isolated dilated cardiomyopathy","type":"exact"},{"name":"cardiomyopathy dilated with conduction defect type 2","type":"exact"},{"name":"cardiomyopathy, dilated, 1E","type":"exact"},{"name":"cardiomyopathy, dilated, type 1E","type":"exact"},{"name":"cardiomyopathy, dilated, with conduction defect 2","type":"exact"},{"name":"cardiomyopathy, dilated, with conduction disorder and arrhythmia","type":"exact"},{"name":"dilated cardiomyopathy type 1E","type":"exact"},{"name":"dilated cardiomyopathy with conduction defect 2","type":"exact"},{"name":"dilated cardiomyopathy with conduction disorder and arrhythmia","type":"exact"},{"name":"familial isolated dilated cardiomyopathy caused by mutation in SCN5A","type":"exact"}],"termid":"MONDO:0011003","xrefs":{"Monarch":{"xref_id":"0011003"}}}


id: MONDO:0020156
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndromic ankyloblepharon (obsolete MONDO:0020156)","secondary_identifiers":["Orphanet:98565"],"termid":"MONDO:0020156","xrefs":{"Monarch":{"xref_id":"0020156"}}}


id: PBO:0043083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholinergic receptor nicotinic beta 3 subunit","termid":"PBO:0043083"}


id: PBO:0082234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alpha-glucosidase; weak, but broad substrate specificity for alpha-1,4- and alpha-1,6-glucosides; member of IMA isomaltase family; not required for isomaltose utilization, but Ima4p overexpression allows the ima1 null mutant to grow on isomaltose; identical to IMA3","termid":"PBO:0082234"}


id: PR:P22192
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pac1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P22192"],"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":"double-strand-specific pac1 ribonuclease (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC119.11c","synonyms":[{"name":"Spom972h-pac1","type":"exact"},{"name":"protein hcs (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P22192"}


id: PBO:0087054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L26A; binds to 5.8S rRNA; non-essential even when paralog is also deleted; deletion has minimal affections on ribosome biosynthesis; homologous to mammalian ribosomal protein L26 and bacterial L24; RPL26A has a paralog, RPL26B, that arose from the whole genome duplication","termid":"PBO:0087054"}


id: GO:0061835
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The surface of a migrating cell that is in contact with the substratum or cell layer.","definition_xrefs":["PMID:11598004"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cell surface","termid":"GO:0009986"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0009986"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0009986"],"is_obsolete":false,"name":"ventral surface of cell","termid":"GO:0061835"}


id: PBO:0034717
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endosulfine Igo1","termid":"PBO:0034717"}


id: MONDO:0004024
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neuroblastoma that affects the spinal cord.","definition_xrefs":["NCIT:C5155"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system primitive neuroectodermal neoplasm","termid":"MONDO:0000640"},{"relation_name":"is_a","term_name":"extracranial neuroblastoma","termid":"MONDO:0002749"},{"relation_name":"is_a","term_name":"spinal cord cancer","termid":"MONDO:0003544"}],"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":"spinal cord neuroblastoma","secondary_identifiers":["UMLS:C1336046","DOID:6871","MEDGEN:234803"],"synonyms":[{"name":"neuroblastoma of spinal cord","type":"exact"},{"name":"neuroblastoma of the spinal cord","type":"exact"},{"name":"spinal cord neuroblastoma","type":"exact"}],"termid":"MONDO:0004024","xrefs":{"Monarch":{"xref_id":"0004024"}}}


id: PBO:0027661
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cut_during_cellular_response_to_methyl_methanesulfonate","termid":"PBO:0027661"}


id: PR:Q9P7F8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATPase ASNA1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10803:SF0","PRO:DNx","OMA:SCHPO01516"],"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":"ATPase get3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1142.06","secondary_identifiers":["UniProtKB:Q9P7F8"],"synonyms":[{"name":"Golgi to ER traffic protein 3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ASNA1","type":"exact"},{"name":"arsenical pump-driving ATPase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"arsenite-stimulated ATPase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"guided entry of tail-anchored proteins 3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P7F8"}


id: PR:Q9Y7P6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- mug72 gene.","definition_xrefs":["UniProtKB:Q9Y7P6","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":"meiotically up-regulated gene 72 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1902.02","synonyms":[{"name":"Spom972h-mug72","type":"exact"}],"termid":"PR:Q9Y7P6"}


id: GO:1903456
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of androst-4-ene-3,17-dione biosynthetic process.","definition_xrefs":["GO_REF:0000058","GOC:mr","GOC:TermGenie","PMID:24399684"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of steroid biosynthetic process","termid":"GO:0010893"},{"relation_name":"is_a","term_name":"positive regulation of small molecule metabolic process","termid":"GO:0062013"},{"relation_name":"is_a","term_name":"regulation of androst-4-ene-3,17-dione biosynthetic process","termid":"GO:1903454"},{"relation_name":"positively_regulates","term_name":"androst-4-ene-3,17-dione biosynthetic process","termid":"GO:1903449"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"positive regulation of androst-4-ene-3,17-dione biosynthetic process","synonyms":[{"name":"activation of androst-4-ene-3,17-dione anabolism","type":"narrow"},{"name":"activation of androst-4-ene-3,17-dione biosynthesis","type":"narrow"},{"name":"activation of androst-4-ene-3,17-dione biosynthetic process","type":"narrow"},{"name":"activation of androst-4-ene-3,17-dione formation","type":"narrow"},{"name":"activation of androst-4-ene-3,17-dione synthesis","type":"narrow"},{"name":"activation of androstenedione","type":"narrow"},{"name":"positive regulation of androst-4-ene-3,17-dione anabolism","type":"exact"},{"name":"positive regulation of androst-4-ene-3,17-dione biosynthesis","type":"exact"},{"name":"positive regulation of androst-4-ene-3,17-dione formation","type":"exact"},{"name":"positive regulation of androst-4-ene-3,17-dione synthesis","type":"exact"},{"name":"positive regulation of androstenedione biosynthetic process","type":"exact"},{"name":"up regulation of androst-4-ene-3,17-dione anabolism","type":"exact"},{"name":"up regulation of androst-4-ene-3,17-dione biosynthesis","type":"exact"},{"name":"up regulation of androst-4-ene-3,17-dione biosynthetic process","type":"exact"},{"name":"up regulation of androst-4-ene-3,17-dione formation","type":"exact"},{"name":"up regulation of androst-4-ene-3,17-dione synthesis","type":"exact"},{"name":"up regulation of androstenedione biosynthetic process","type":"exact"},{"name":"up-regulation of androst-4-ene-3,17-dione anabolism","type":"exact"},{"name":"up-regulation of androst-4-ene-3,17-dione biosynthesis","type":"exact"},{"name":"up-regulation of androst-4-ene-3,17-dione biosynthetic process","type":"exact"},{"name":"up-regulation of androst-4-ene-3,17-dione formation","type":"exact"},{"name":"up-regulation of androst-4-ene-3,17-dione synthesis","type":"exact"},{"name":"up-regulation of androstenedione biosynthetic process","type":"exact"},{"name":"upregulation of androst-4-ene-3,17-dione anabolism","type":"exact"},{"name":"upregulation of androst-4-ene-3,17-dione biosynthesis","type":"exact"},{"name":"upregulation of androst-4-ene-3,17-dione biosynthetic process","type":"exact"},{"name":"upregulation of androst-4-ene-3,17-dione formation","type":"exact"},{"name":"upregulation of androst-4-ene-3,17-dione synthesis","type":"exact"},{"name":"upregulation of androstenedione biosynthetic process","type":"exact"}],"termid":"GO:1903456"}


id: PBO:0071988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 pseudogene 17","termid":"PBO:0071988"}


id: PBO:0035733
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_acetylation_during_vegetative_growth","termid":"PBO:0035733"}


id: MONDO:1012616
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inherited microphthalmia that occurs in female chickens.","definition_xrefs":["PMID:1578107"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microphthalmia, chicken","termid":"MONDO:1011237"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microphthalmia-4, chicken","secondary_identifiers":["OMIA:000650-9031"],"termid":"MONDO:1012616","xrefs":{"Monarch":{"xref_id":"1012616"}}}


id: GO:0060931
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a sinoatrial (SA) node cell over time, from its formation to the mature state. SA node cells are pacemaker cells that are found in the sinoatrial node.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac pacemaker cell development","termid":"GO:0060926"},{"relation_name":"part_of","term_name":"sinoatrial node cell differentiation","termid":"GO:0060921"}],"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":"sinoatrial node cell development","synonyms":[{"name":"SA node cell development","type":"exact"},{"name":"SAN cell development","type":"exact"},{"name":"sinus node cell development","type":"narrow"}],"termid":"GO:0060931"}


id: PBO:0116740
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 16 (gene/pseudogene)","termid":"PBO:0116740"}


id: PBO:0034024
data:
  {"annotation_feature_type":"gene","cv_name":"pubprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canto_approver_name","termid":"PBO:0034024"}


id: GO:1902362
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any apoptotic process in a melanocyte, the main structural component of the epidermis.","definition_xrefs":["PMID:20530876","GOC:TermGenie","GOC:ic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apoptotic process","termid":"GO:0006915"}],"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":"melanocyte apoptotic process","synonyms":[{"name":"melanocyte apoptosis","type":"narrow"},{"name":"melanophore apoptosis","type":"narrow"},{"name":"melanophore apoptotic process","type":"narrow"}],"termid":"GO:1902362"}


id: GO:0071355
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an interleukin-9 stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to interleukin-9","termid":"GO:0071104"},{"relation_name":"is_a","term_name":"cellular response to cytokine stimulus","termid":"GO:0071345"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to interleukin-9","synonyms":[{"name":"cellular response to IL-9","type":"exact"}],"termid":"GO:0071355"}


id: GO:0035842
data:
  {"annotated_genes":["SJAG_02838"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[112609],"is_not":false,"summary":null,"term":"GO:0035842"}]},"cv_name":"cellular_component","definition":"A cell tip which has existed for at least one complete cell cycle, and at which polarized growth occurs, which is part of a cell that has activated bipolar cell growth (i.e. in which new end take-off, NETO, has taken place). For example, in fission yeast the cell end that existed prior to cell division grows immediately after division, and contains a distinctive complement of proteins including actin cytoskeletal structures.","definition_xrefs":["GOC:mah","GOC:expert_jd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"old growing cell tip","termid":"GO:0035840"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02838":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"old cell tip after activation of bipolar cell growth","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"post-NETO old cell end","type":"exact"},{"name":"post-NETO old cell tip","type":"exact"},{"name":"post-new end take-off old cell tip","type":"exact"}],"termid":"GO:0035842","terms_by_termid":{"GO:0035842":null}}


id: GO:0070603
data:
  {"annotated_genes":["SJAG_01611","SJAG_04005","SJAG_02798","SJAG_00746","SJAG_03033","SJAG_03576","SJAG_03839","SJAG_02466","SJAG_03944","SJAG_02447","SJAG_01111","SJAG_00739","SJAG_04213","SJAG_05313","SJAG_05192","SJAG_02778","SJAG_01016","SJAG_03579","SJAG_02872","SJAG_03145","SJAG_03036","SJAG_02869","SJAG_05020","SJAG_00873","SJAG_02589","SJAG_02549","SJAG_03787","SJAG_03844","SJAG_00743","SJAG_05282","SJAG_04355","SJAG_02303","SJAG_00934","SJAG_03758","SJAG_00045","SJAG_02254","SJAG_01465","SJAG_02990","SJAG_04755","SJAG_03982","SJAG_04989","SJAG_02571","SJAG_04596","SJAG_04097","SJAG_01622","SJAG_02500","SJAG_00735","SJAG_03694","SJAG_00440","SJAG_02385"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[110896,71639,114999,74663,73907,95816,58017,89614,117257,73507,103378,61755,74371,73386,78030,90683,68162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031011"},{"annotations":[114983,94107,75430,89969,95818,81391,81528,59098,67724,72339,89471,95961,97706,74715],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016586"},{"annotations":[73400,113957,109995,115145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070824"},{"annotations":[109277,114984,71638,78788,79421,74428,95943,73072,116867,78092,97707,89472],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016514"},{"annotations":[115002,116572,75410,78697,94184,110904,115173,98460,100775,71831,81765,74662,109714,119312,100046,78029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000812"}]},"cv_name":"cellular_component","definition":"A protein complex that contains an ortholog of the Saccharomyces ATPase Swi2/Snf2 as one of the catalytic subunit components (ATPase) and mediates assembly of nucleosomes, changes to the spacing or structure of nucleosomes, or some combination of those activities in a manner that requires ATP.","definition_xrefs":["GOC:mah","GOC:bhm","PMID:16155938","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"},{"relation_name":"is_a","term_name":"ATPase complex","termid":"GO:1904949"},{"relation_name":"part_of","term_name":"chromatin","termid":"GO:0000785"}],"gene_count":50,"genes_by_uniquename":{"SJAG_00045":null,"SJAG_00440":null,"SJAG_00735":null,"SJAG_00739":null,"SJAG_00743":null,"SJAG_00746":null,"SJAG_00873":null,"SJAG_00934":null,"SJAG_01016":null,"SJAG_01111":null,"SJAG_01465":null,"SJAG_01611":null,"SJAG_01622":null,"SJAG_02254":null,"SJAG_02303":null,"SJAG_02385":null,"SJAG_02447":null,"SJAG_02466":null,"SJAG_02500":null,"SJAG_02549":null,"SJAG_02571":null,"SJAG_02589":null,"SJAG_02778":null,"SJAG_02798":null,"SJAG_02869":null,"SJAG_02872":null,"SJAG_02990":null,"SJAG_03033":null,"SJAG_03036":null,"SJAG_03145":null,"SJAG_03576":null,"SJAG_03579":null,"SJAG_03694":null,"SJAG_03758":null,"SJAG_03787":null,"SJAG_03839":null,"SJAG_03844":null,"SJAG_03944":null,"SJAG_03982":null,"SJAG_04005":null,"SJAG_04097":null,"SJAG_04213":null,"SJAG_04355":null,"SJAG_04596":null,"SJAG_04755":null,"SJAG_04989":null,"SJAG_05020":null,"SJAG_05192":null,"SJAG_05282":null,"SJAG_05313":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"part_of","termid":"GO:0005694"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005694","GO:0005634"],"is_obsolete":false,"name":"SWI/SNF superfamily-type complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["GO:0090544"],"synonyms":[{"name":"BAF-type complex","type":"exact"},{"name":"SWI-SNF global transcription activator complex","type":"related"},{"name":"SWI-SNF-type complex","type":"exact"},{"name":"SWI/SNF-type complex","type":"related"},{"name":"SWI2/SNF2 superfamily ATP-dependent chromatin remodeling complex","type":"related"}],"termid":"GO:0070603","terms_by_termid":{"GO:0000812":null,"GO:0016514":null,"GO:0016586":null,"GO:0031011":null,"GO:0070824":null}}


id: PBO:0034034
data:
  {"annotation_feature_type":"gene","cv_name":"pubprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pubmed_publication_date","termid":"PBO:0034034"}


id: MONDO:0002871
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tumor that arises from the testis and is composed of neoplastic trophoblastic cells. The vast majority of cases are choriocarcinomas.","definition_xrefs":["NCIT:C39934"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trophoblastic neoplasm","termid":"MONDO:0002872"},{"relation_name":"is_a","term_name":"testicular pure germ cell tumor","termid":"MONDO:0002874"},{"relation_name":"is_a","term_name":"testicular non-seminomatous germ cell tumor","termid":"MONDO:0006447"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testicular trophoblastic tumor","secondary_identifiers":["MEDGEN:272844","UMLS:C1515301","DOID:4084"],"synonyms":[{"name":"testicular trophoblastic tumor","type":"exact"}],"termid":"MONDO:0002871","xrefs":{"Monarch":{"xref_id":"0002871"}}}


id: FYPO:0003564
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which generation of double-strand breaks at defined hotspots throughout the genome during meiosis I is abnormal.","definition_xrefs":["GO:0042138","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic recombination","termid":"FYPO:0000008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"abnormal meiotic DNA double-strand break formation","termid":"FYPO:0003564"}


id: PBO:0083408
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the dubious ORF YLR364C-A","termid":"PBO:0083408"}


id: GO:0031450
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of slow-twitch skeletal muscle contraction.","definition_xrefs":["GOC:dph","GOC:mtg_muscle","GOC:tb","GOC:ef","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of slow-twitch skeletal muscle fiber contraction","termid":"GO:0031449"},{"relation_name":"is_a","term_name":"negative regulation of striated muscle contraction","termid":"GO:0045988"},{"relation_name":"negatively_regulates","term_name":"slow-twitch skeletal muscle fiber contraction","termid":"GO:0031444"}],"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 slow-twitch skeletal muscle fiber contraction","synonyms":[{"name":"down regulation of slow-twitch skeletal muscle contraction","type":"exact"},{"name":"down-regulation of slow-twitch skeletal muscle contraction","type":"exact"},{"name":"downregulation of slow-twitch skeletal muscle contraction","type":"exact"},{"name":"inhibition of slow-twitch skeletal muscle contraction","type":"narrow"},{"name":"negative regulation of slow-twitch skeletal muscle contraction","type":"exact"}],"termid":"GO:0031450"}


id: PBO:0091959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate-1-semialdehyde 2,1-aminomutase","termid":"PBO:0091959"}


id: PBO:0030445
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cell_separation_after_cytokinesis","termid":"PBO:0030445"}


id: GO:0051757
data:
  {"annotated_genes":["SJAG_02104","SJAG_04457"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[95693,112028],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051755"}]},"cv_name":"biological_process","definition":"The process in which sister chromatids are physically detached from each other during meiosis.","definition_xrefs":["PMID:14730319","GOC:ai","PMID:16325576"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic chromosome separation","termid":"GO:0051307"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02104":null,"SJAG_04457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0140013"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0008150","GO:0007049","GO:0140013"],"is_obsolete":false,"name":"meiotic sister chromatid separation","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"meiotic sister chromatid resolution","type":"exact"}],"termid":"GO:0051757","terms_by_termid":{"GO:0051755":null}}


id: FYPO:0003137
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the mitotic spindle pole bodies are normal (i.e. indistinguishable from wild type) with respect to structure, composition, location, and orientation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component during vegetative growth","termid":"FYPO:0001313"},{"relation_name":"is_a","term_name":"normal spindle pole body","termid":"FYPO:0005379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal mitotic spindle pole body","synonyms":[{"name":"normal mitotic SPB","type":"exact"},{"name":"normal mitotic spindle pole body during mitotic cell cycle","type":"related"},{"name":"normal spindle pole body during mitosis","type":"exact"},{"name":"normal spindle pole body during vegetative growth","type":"exact"}],"termid":"FYPO:0003137"}


id: FYPO:0006718
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the duration of protein phosphorylation is longer than normal during a cellular response to osmotic stress. All phosphorylation may be affected, or only phosphorylation of specific proteins, or even specific sites within specific proteins.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased duration of protein modification during vegetative growth","termid":"FYPO:0000548"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0002494","FYPO:0002274","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased duration of protein phosphorylation during cellular response to osmotic stress","synonyms":[{"name":"increased duration of protein phosphorylation during cellular response to osmotic stress during mitotic cell cycle","type":"related"},{"name":"increased duration of protein phosphorylation during cellular response to osmotic stress during vegetative growth","type":"exact"},{"name":"prolonged protein phosphorylation during cellular response to osmotic stress","type":"exact"}],"termid":"FYPO:0006718"}


id: PBO:0040122
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat and SOCS box containing 9","termid":"PBO:0040122"}


id: GO:0051200
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the chemical reactions and pathways involving a prosthetic group.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of prosthetic group metabolic process (obsolete GO:0051200)","synonyms":[{"name":"activation of prosthetic group metabolic process","type":"narrow"},{"name":"positive regulation of coenzyme and prosthetic group metabolic process","type":"broad"},{"name":"positive regulation of coenzyme and prosthetic group metabolism","type":"broad"},{"name":"positive regulation of prosthetic group metabolism","type":"exact"},{"name":"stimulation of prosthetic group metabolic process","type":"narrow"},{"name":"up regulation of prosthetic group metabolic process","type":"exact"},{"name":"up-regulation of prosthetic group metabolic process","type":"exact"},{"name":"upregulation of prosthetic group metabolic process","type":"exact"}],"termid":"GO:0051200"}


id: PR:O43001
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- syj1 gene.","definition_xrefs":["UniProtKB:O43001","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":"inositol-1,4,5-trisphosphate 5-phosphatase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2G2.02","synonyms":[{"name":"Spom972h-syj1","type":"exact"},{"name":"synaptojanin-like protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O43001"}


id: GO:0047483
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-phospho-alpha-D-ribose 1-diphosphate + ATP + H2O + imidazol-4-ylacetate = 1-(5-phosphoribosyl)imidazol-4-ylacetate + ADP + diphosphate + 2 H+ + phosphate.","definition_xrefs":["EC:6.3.4.8","RHEA:16485"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity, forming carbon-nitrogen bonds","termid":"GO:0016879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"imidazoleacetate-phosphoribosyldiphosphate ligase activity","secondary_identifiers":["KEGG_REACTION:R04068","MetaCyc:6.3.4.8-RXN"],"synonyms":[{"name":"5-phosphoribosylimidazoleacetate synthetase activity","type":"related"},{"name":"imidazoleacetate:5-phosphoribosyl-diphosphate ligase (ADP- and diphosphate-forming)","type":"related"}],"termid":"GO:0047483"}


id: PBO:0083088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA binding protein that recognizes oligo(dA).oligo(dT) tracts; Arg side chain in its N-terminal pentad Gly-Arg-Lys-Pro-Gly repeat is required for DNA-binding; relocalizes to the cytosol in response to hypoxia; not essential for viability","termid":"PBO:0083088"}


id: PBO:0065386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PC4 and SRSF1 interacting protein 1","termid":"PBO:0065386"}


id: GO:0010521
data:
  {"annotated_genes":["SJAG_02194"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78792],"is_not":false,"summary":null,"term":"GO:0010521"}]},"cv_name":"molecular_function","definition":"Binds to and stops, prevents or reduces the activity of telomerase.","definition_xrefs":["GOC:tb","GOC:krc","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme inhibitor activity","termid":"GO:0004857"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02194":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140678"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004857"}],"interesting_parent_ids":["GO:0004857","GO:0140678","GO:0098772","GO:0003674","GO:0030234"],"is_obsolete":false,"name":"telomerase inhibitor activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0010521","terms_by_termid":{"GO:0010521":null}}


id: PBO:0051625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inflammation and lipid regulator with UBA-like and NBR1-like domains","termid":"PBO:0051625"}


id: MONDO:0045004
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease or disorder that involves the skeletal ligament.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal system disorder","termid":"MONDO:0005172"},{"relation_name":"is_a","term_name":"ligament disorder","termid":"MONDO:0045044"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"skeletal ligament disorder","synonyms":[{"name":"disease of skeletal ligament","type":"exact"},{"name":"disease or disorder of skeletal ligament","type":"exact"},{"name":"disorder of skeletal ligament","type":"exact"},{"name":"skeletal ligament disease or disorder","type":"exact"}],"termid":"MONDO:0045004","xrefs":{"Monarch":{"xref_id":"0045004"}}}


id: FYPO:0002675
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 dTDP measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular dTDP level","synonyms":[{"name":"increased cellular dTDP level during mitotic cell cycle","type":"related"},{"name":"increased cellular dTDP level during vegetative growth","type":"exact"},{"name":"increased dTDP accumulation","type":"related"}],"termid":"FYPO:0002675"}


id: PBO:0088586
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial cytosine-mismatch binding protein 1, candidate TFAM ortholog","termid":"PBO:0088586"}


id: GO:0010212
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 ionizing radiation stimulus. Ionizing radiation is radiation with sufficient energy to remove electrons from atoms and may arise from spontaneous decay of unstable isotopes, resulting in alpha and beta particles and gamma rays. Ionizing radiation also includes X-rays.","definition_xrefs":["PMID:12509526"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to radiation","termid":"GO:0009314"}],"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 ionizing radiation","synonyms":[{"name":"response to ionising radiation","type":"exact"},{"name":"response to ionizing radiation stimulus","type":"exact"}],"termid":"GO:0010212"}


id: GO:1902948
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of tau-protein kinase activity.","definition_xrefs":["PMID:22986780","GOC:sjp","PMID:15897157","GOC:TermGenie","GO_REF:0000059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein serine/threonine kinase activity","termid":"GO:0071901"},{"relation_name":"is_a","term_name":"regulation of tau-protein kinase activity","termid":"GO:1902947"}],"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 tau-protein kinase activity","synonyms":[{"name":"down regulation of CDK5/p23","type":"related"},{"name":"down regulation of GSK","type":"related"},{"name":"down regulation of STK31","type":"related"},{"name":"down regulation of TPK","type":"related"},{"name":"down regulation of TPK I","type":"related"},{"name":"down regulation of TPK II","type":"related"},{"name":"down regulation of TTK","type":"related"},{"name":"down regulation of [Tau protein] kinase activity","type":"exact"},{"name":"down regulation of brain protein kinase PK40erk activity","type":"narrow"},{"name":"down regulation of cdk5/p20","type":"related"},{"name":"down regulation of glycogen synthase kinase-3beta activity","type":"exact"},{"name":"down regulation of protein tau kinase activity","type":"exact"},{"name":"down regulation of tau kinase activity","type":"exact"},{"name":"down regulation of tau protein kinase activity","type":"exact"},{"name":"down regulation of tau-protein kinase I activity","type":"narrow"},{"name":"down regulation of tau-protein kinase II activity","type":"narrow"},{"name":"down regulation of tau-protein kinase activity","type":"exact"},{"name":"down regulation of tau-tubulin kinase activity","type":"narrow"},{"name":"down-regulation of CDK5/p23","type":"related"},{"name":"down-regulation of GSK","type":"related"},{"name":"down-regulation of STK31","type":"related"},{"name":"down-regulation of TPK","type":"related"},{"name":"down-regulation of TPK I","type":"related"},{"name":"down-regulation of TPK II","type":"related"},{"name":"down-regulation of TTK","type":"related"},{"name":"down-regulation of [Tau protein] kinase activity","type":"exact"},{"name":"down-regulation of brain protein kinase PK40erk activity","type":"narrow"},{"name":"down-regulation of cdk5/p20","type":"related"},{"name":"down-regulation of glycogen synthase kinase-3beta activity","type":"exact"},{"name":"down-regulation of protein tau kinase activity","type":"exact"},{"name":"down-regulation of tau kinase activity","type":"exact"},{"name":"down-regulation of tau protein kinase activity","type":"exact"},{"name":"down-regulation of tau-protein kinase I activity","type":"narrow"},{"name":"down-regulation of tau-protein kinase II activity","type":"narrow"},{"name":"down-regulation of tau-protein kinase activity","type":"exact"},{"name":"down-regulation of tau-tubulin kinase activity","type":"narrow"},{"name":"downregulation of CDK5/p23","type":"related"},{"name":"downregulation of GSK","type":"related"},{"name":"downregulation of STK31","type":"related"},{"name":"downregulation of TPK","type":"related"},{"name":"downregulation of TPK I","type":"related"},{"name":"downregulation of TPK II","type":"related"},{"name":"downregulation of TTK","type":"related"},{"name":"downregulation of [Tau protein] kinase activity","type":"exact"},{"name":"downregulation of brain protein kinase PK40erk activity","type":"narrow"},{"name":"downregulation of cdk5/p20","type":"related"},{"name":"downregulation of glycogen synthase kinase-3beta activity","type":"exact"},{"name":"downregulation of protein tau kinase activity","type":"exact"},{"name":"downregulation of tau kinase activity","type":"exact"},{"name":"downregulation of tau protein kinase activity","type":"exact"},{"name":"downregulation of tau-protein kinase I activity","type":"narrow"},{"name":"downregulation of tau-protein kinase II activity","type":"narrow"},{"name":"downregulation of tau-protein kinase activity","type":"exact"},{"name":"downregulation of tau-tubulin kinase activity","type":"narrow"},{"name":"inhibition of CDK5/p23","type":"related"},{"name":"inhibition of GSK","type":"related"},{"name":"inhibition of STK31","type":"related"},{"name":"inhibition of TPK","type":"related"},{"name":"inhibition of TPK I","type":"related"},{"name":"inhibition of TPK II","type":"related"},{"name":"inhibition of TTK","type":"related"},{"name":"inhibition of [Tau protein] kinase activity","type":"narrow"},{"name":"inhibition of brain protein kinase PK40erk activity","type":"narrow"},{"name":"inhibition of cdk5/p20","type":"related"},{"name":"inhibition of glycogen synthase kinase-3beta activity","type":"narrow"},{"name":"inhibition of protein tau kinase activity","type":"narrow"},{"name":"inhibition of tau kinase activity","type":"narrow"},{"name":"inhibition of tau protein kinase activity","type":"narrow"},{"name":"inhibition of tau-protein kinase I activity","type":"narrow"},{"name":"inhibition of tau-protein kinase II activity","type":"narrow"},{"name":"inhibition of tau-protein kinase activity","type":"narrow"},{"name":"inhibition of tau-tubulin kinase activity","type":"narrow"},{"name":"negative regulation of CDK5/p23","type":"related"},{"name":"negative regulation of GSK","type":"related"},{"name":"negative regulation of STK31","type":"related"},{"name":"negative regulation of TPK","type":"related"},{"name":"negative regulation of TPK I","type":"related"},{"name":"negative regulation of TPK II","type":"related"},{"name":"negative regulation of TTK","type":"related"},{"name":"negative regulation of [Tau protein] kinase activity","type":"exact"},{"name":"negative regulation of brain protein kinase PK40erk activity","type":"narrow"},{"name":"negative regulation of cdk5/p20","type":"related"},{"name":"negative regulation of glycogen synthase kinase-3beta activity","type":"exact"},{"name":"negative regulation of protein tau kinase activity","type":"exact"},{"name":"negative regulation of tau kinase activity","type":"exact"},{"name":"negative regulation of tau protein kinase activity","type":"exact"},{"name":"negative regulation of tau-protein kinase I activity","type":"narrow"},{"name":"negative regulation of tau-protein kinase II activity","type":"narrow"},{"name":"negative regulation of tau-tubulin kinase activity","type":"narrow"}],"termid":"GO:1902948"}


id: GO:0036213
data:
  {"annotated_genes":["SJAG_01894","SJAG_04887","SJAG_04776","SJAG_04498","SJAG_04077","SJAG_04597","SJAG_03936","SJAG_00268","SJAG_00845","SJAG_03703","SJAG_01665","SJAG_03581","SJAG_02431","SJAG_02700","SJAG_03379","SJAG_03631","SJAG_02645"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[100714,90075,102518,97106,99843,58837,99463,102750,104242,114162],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902404"},{"annotations":[105515],"is_not":false,"rel_names":["negatively_regulates","regulates"],"summary":null,"term":"GO:1903472"},{"annotations":[96224,89342,96394,112373,115219],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:1903473"},{"annotations":[79949],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0031991"}]},"cv_name":"biological_process","definition":"The process of an actomyosin ring getting smaller in diameter.","definition_xrefs":["GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokinetic process","termid":"GO:0032506"},{"relation_name":"part_of","term_name":"cytoskeleton-dependent cytokinesis","termid":"GO:0061640"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00268":null,"SJAG_00845":null,"SJAG_01665":null,"SJAG_01894":null,"SJAG_02431":null,"SJAG_02645":null,"SJAG_02700":null,"SJAG_03379":null,"SJAG_03581":null,"SJAG_03631":null,"SJAG_03703":null,"SJAG_03936":null,"SJAG_04077":null,"SJAG_04498":null,"SJAG_04597":null,"SJAG_04776":null,"SJAG_04887":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"contractile ring contraction","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"contractile ring constriction","type":"exact"}],"termid":"GO:0036213","terms_by_termid":{"GO:0031991":null,"GO:1902404":null,"GO:1903472":null,"GO:1903473":null}}


id: PBO:0030563
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_cellular_phenylalanine_level","termid":"PBO:0030563"}


id: FYPO:0005894
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin is normal (i.e. indistinguishable from wild type) during G1 phase of the mitotic cell cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin during vegetative growth","termid":"FYPO:0001509"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001312","FYPO:0000257","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to chromatin during mitotic G1 phase","synonyms":[{"name":"normal protein localisation to chromatin during mitotic G1 phase","type":"exact"},{"name":"normal protein localization to chromatin during G1 phase during vegetative growth","type":"exact"},{"name":"normal protein localization to chromatin during G1 phase of mitotic cell cycle","type":"exact"}],"termid":"FYPO:0005894"}


id: MONDO:0001901
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A classification of dysgammaglobulinemias characterized by low or undetectable serum levels of one of the four immunoglobulin class G (IgG) subclasses. Selective IgG1 deficiency is rare and primarily decreases the immune response to bacterial protein antigens. Selective IgG2 deficiency is the most common subclass deficiency among children and primarily leads to an inadequate response to bacterial polysaccharide antigens. Selective IgG3 deficiency is the most common subclass deficiency among adults and also primarily lowers the response to bacterial proteins. Selective IgG4 deficiency may be a clinically insignificant developmental variant, as IgG4 is a subclass that is virtually undetectable until the end of the first decade of life. Low levels of any IgG subclass will reduce the immune system's effectiveness and thus the clinical presentation of these diseases is usually recurrent infection, particularly by encapsulated bacteria.","definition_xrefs":["NCIT:C27024"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"dysgammaglobulinemia","termid":"MONDO:0001342"},{"relation_name":"is_a","term_name":"immunoglobulin heavy chain deficiency","termid":"MONDO:0015697"},{"relation_name":"is_a","term_name":"selective IgG immunodeficiency","termid":"MONDO:0045045"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"selective IgG subclass deficiency","secondary_identifiers":["ICD9:279.03","MEDGEN:56446","MESH:D017099","UMLS:C0162539","DOID:14176","SCTID:190981001"],"synonyms":[{"name":"Immunoglobin G subclass deficiency","type":"exact"},{"name":"selective IgG deficiency disease","type":"related"},{"name":"selective IgG immunodeficiency","type":"related"},{"name":"selective Immunoglobulin G subclass deficiency","type":"exact"},{"name":"selective deficiency of IgG","type":"exact"},{"name":"selective immunoglobulin G deficiency","type":"exact"}],"termid":"MONDO:0001901","xrefs":{"Monarch":{"xref_id":"0001901"}}}


id: GO:0036493
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, or increases the frequency, rate or extent of translation as a result of endoplasmic reticulum stress.","definition_xrefs":["GOC:bf","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of translation in response to stress","termid":"GO:0032056"},{"relation_name":"is_a","term_name":"regulation of translation in response to endoplasmic reticulum stress","termid":"GO:0036490"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_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 translation in response to endoplasmic reticulum stress","synonyms":[{"name":"positive regulation of translation in response to ER stress","type":"exact"}],"termid":"GO:0036493"}


id: GO:0038106
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to choriogonadotropin hormone, a heterodimer, with an alpha subunit identical to that of luteinizing hormone (LH), follicle-stimulating hormone (FSH) and thyroid-stimulating hormone (TSH), and a unique beta subunit.","definition_xrefs":["Wikipedia:Human_chorionic_gonadotropin","GOC:BHF","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone binding","termid":"GO:0042562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"choriogonadotropin hormone binding","synonyms":[{"name":"chorionic gonadotrophin binding","type":"exact"},{"name":"chorionic gonadotropin binding","type":"exact"}],"termid":"GO:0038106"}


id: PBO:0089213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP 3'tRNA nucleotidyltransferase Cca2","termid":"PBO:0089213"}


id: GO:0021945
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process that increases the extent of granule cell motility using intracellular calcium signaling mechanisms during radial migration.","definition_xrefs":["GOC:tb","GOC:dph","GO_REF:0000021","GOC:cls","GOC:jid","PMID:15157725","GOC:dgh"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of cerebellar granule cell migration by calcium (obsolete GO:0021945)","synonyms":[{"name":"calcium-mediated activation of granule cell migration","type":"narrow"},{"name":"calcium-mediated positive regulation of granule cell migration","type":"exact"},{"name":"calcium-mediated stimulation of granule cell migration","type":"narrow"},{"name":"calcium-mediated up regulation of granule cell migration","type":"exact"},{"name":"calcium-mediated up-regulation of granule cell migration","type":"exact"},{"name":"calcium-mediated upregulation of granule cell migration","type":"exact"}],"termid":"GO:0021945"}


id: PBO:0057681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1270","termid":"PBO:0057681"}


id: MONDO:0001746
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Optic disk bodies composed primarily of acid mucopolysaccharides that may produce pseudopapilledema (elevation of the optic disk without associated intracranial hypertension) and visual field deficits. Drusen may also occur in the retina (see retinal drusen). (Miller et al., Clinical Neuro-Ophthalmology, 4th ed, p355)","definition_xrefs":["MESH:D015594"],"direct_ancestors":[{"relation_name":"is_a","term_name":"optic nerve disorder","termid":"MONDO:0002135"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"optic disk drusen","secondary_identifiers":["ICD10CM:H47.32","MEDGEN:14495","ICD9:377.21","DOID:13561","UMLS:C0029128","SCTID:33629003"],"synonyms":[{"name":"drusen of optic disc","type":"exact"},{"name":"drusen of optic disk","type":"exact"},{"name":"optic nerve head drusen","type":"exact"}],"termid":"MONDO:0001746","xrefs":{"Monarch":{"xref_id":"0001746"}}}


id: MONDO:0019150
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Familial restrictive cardiomyopathy is a genetic form of heart disease, in which the heart muscle is stiff and cannot fully relax after each contraction. Impaired muscle relaxation causes blood to back up in the atria and lungs, which reduces the amount of blood in the ventricles.","gene_count":0,"genotype_count":0,"name":"obsolete familial isolated restrictive cardiomyopathy (obsolete MONDO:0019150)","secondary_identifiers":["Orphanet:75249"],"synonyms":[{"name":"familial or idiopathic restrictive cardiomyopathy","type":"exact"}],"termid":"MONDO:0019150","xrefs":{"Monarch":{"xref_id":"0019150"}}}


id: GO:0120155
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A trimeric complex involved in cytokinesis. Proposed to bridge actomyosin ring contraction and septum synthesis in yeast, resulting in the coordination of these processes, and leading to plasma membrane ingression and fusion. In the yeast Saccharomyces cerevisiae this complex consists of Mlc1p, Iqg1p and Hof1p proteins.","definition_xrefs":["PMID:24413167","GOC:rn","PMID:24895401"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cellular bud neck","termid":"GO:0005935"}],"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":"MIH complex","synonyms":[{"name":"Mlc1p-Iqg1p-Hof1p complex","type":"exact"}],"termid":"GO:0120155"}


id: GO:0070682
data:
  {"annotated_genes":["SJAG_00954","SJAG_04844","SJAG_02570"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[81835,101297,117598],"is_not":false,"summary":null,"term":"GO:0070682"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a mature, active proteasome regulatory particle complex.","definition_xrefs":["PMID:19412159","GOC:rb","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proteasome assembly","termid":"GO:0043248"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00954":null,"SJAG_02570":null,"SJAG_04844":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0065003","GO:0044085"],"is_obsolete":false,"name":"proteasome regulatory particle assembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"proteasome regulatory complex assembly","type":"exact"}],"termid":"GO:0070682","terms_by_termid":{"GO:0070682":null}}


id: GO:0015217
data:
  {"annotated_genes":["SJAG_02050"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[59186],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005471"}]},"cv_name":"molecular_function","definition":"Enables the transfer of ADP, adenosine diphosphate, from one side of a membrane to the other.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenine nucleotide transmembrane transporter activity","termid":"GO:0000295"},{"relation_name":"is_a","term_name":"purine ribonucleotide transmembrane transporter activity","termid":"GO:0005346"},{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02050":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"ADP transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000002":null},"termid":"GO:0015217","terms_by_termid":{"GO:0005471":null}}


id: PBO:0044491
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 51 subfamily A member 1","termid":"PBO:0044491"}


id: GO:0047333
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + dihydrostreptomycin 6-phosphate = ADP + dihydrostreptomycin 3'alpha,6-bisphosphate + 2 H+.","definition_xrefs":["EC:2.7.1.88","RHEA:16281"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aminoglycoside phosphotransferase activity","termid":"GO:0034071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"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:0003824","GO:0003674","GO:0016740","GO:0016301"],"is_obsolete":false,"name":"dihydrostreptomycin-6-phosphate 3'-alpha-kinase activity","secondary_identifiers":["KEGG_REACTION:R03395","MetaCyc:2.7.1.88-RXN"],"synonyms":[{"name":"ATP:dihydrostreptomycin-6-P 3'alpha-phosphotransferase activity","type":"related"},{"name":"ATP:dihydrostreptomycin-6-phosphate 3'alpha-phosphotransferase activity","type":"related"},{"name":"dihydrostreptomycin 6-phosphate kinase (phosphorylating)","type":"related"},{"name":"dihydrostreptomycin-6-phosphate 3'alpha-kinase activity","type":"related"}],"termid":"GO:0047333"}


id: PBO:0050622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hydroxysteroid 17-beta dehydrogenase 14","termid":"PBO:0050622"}


id: PBO:0039214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldo-keto reductase family 1 member C5, pseudogene","termid":"PBO:0039214"}


id: PBO:0028348
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_CENP-A_containing_chromatin","termid":"PBO:0028348"}


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


id: PBO:0046786
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"enhancer of zeste 1 polycomb repressive complex 2 subunit","termid":"PBO:0046786"}


id: GO:0034191
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an apolipoprotein A-I receptor.","definition_xrefs":["GOC:rl","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apolipoprotein receptor binding","termid":"GO:0034190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"apolipoprotein A-I receptor binding","termid":"GO:0034191"}


id: PBO:0031685
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_peroxisome_degradation","termid":"PBO:0031685"}


id: GO:0000785
data:
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id: PBO:0050391
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id: PBO:0078386
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id: MONDO:0015129
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id: GO:0009509
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id: GO:1900129
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of G-protein activated inward rectifier potassium channel activity.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of G-protein activated inward rectifier potassium channel activity (obsolete GO:1900129)","synonyms":[{"name":"activation of G protein activated inward rectifier potassium channel activity","type":"narrow"},{"name":"activation of G protein enhanced inward rectifier potassium channel activity","type":"narrow"},{"name":"activation of G-protein activated inward rectifier potassium channel activity","type":"narrow"},{"name":"activation of G-protein enhanced inward rectifier potassium channel activity","type":"narrow"},{"name":"activation of G-protein-activated inward rectifier potassium channel activity","type":"narrow"},{"name":"activation of G-protein-enhanced inward rectifier potassium channel activity","type":"narrow"},{"name":"positive regulation of G protein activated inward rectifier potassium channel activity","type":"exact"},{"name":"positive regulation of G protein enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"positive regulation of G-protein enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"positive regulation of G-protein-activated inward rectifier potassium channel activity","type":"exact"},{"name":"positive regulation of G-protein-enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"up regulation of G protein activated inward rectifier potassium channel activity","type":"exact"},{"name":"up regulation of G protein enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"up regulation of G-protein activated inward rectifier potassium channel activity","type":"exact"},{"name":"up regulation of G-protein enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"up regulation of G-protein-activated inward rectifier potassium channel activity","type":"exact"},{"name":"up regulation of G-protein-enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"up-regulation of G protein activated inward rectifier potassium channel activity","type":"exact"},{"name":"up-regulation of G protein enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"up-regulation of G-protein activated inward rectifier potassium channel activity","type":"exact"},{"name":"up-regulation of G-protein enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"up-regulation of G-protein-activated inward rectifier potassium channel activity","type":"exact"},{"name":"up-regulation of G-protein-enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"upregulation of G protein activated inward rectifier potassium channel activity","type":"exact"},{"name":"upregulation of G protein enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"upregulation of G-protein activated inward rectifier potassium channel activity","type":"exact"},{"name":"upregulation of G-protein enhanced inward rectifier potassium channel activity","type":"exact"},{"name":"upregulation of G-protein-activated inward rectifier potassium channel activity","type":"exact"},{"name":"upregulation of G-protein-enhanced inward rectifier potassium channel activity","type":"exact"}],"termid":"GO:1900129"}


id: GO:0071368
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cytokinin stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cytokinin","termid":"GO:0009735"},{"relation_name":"is_a","term_name":"cellular response to hormone stimulus","termid":"GO:0032870"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to cytokinin stimulus","termid":"GO:0071368"}


id: PBO:0052969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trans-L-3-hydroxyproline dehydratase","termid":"PBO:0052969"}


id: MONDO:0011648
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"meningioma","termid":"MONDO:0016642"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"radiation-induced meningioma","secondary_identifiers":["MESH:C536266","UMLS:C1853554","MEDGEN:381204","OMIM:606190","GARD:8491"],"synonyms":[{"name":"Mnri","type":"related"},{"name":"meningioma, radiation-induced","type":"related"},{"name":"radiation induced meningioma","type":"related"}],"termid":"MONDO:0011648","xrefs":{"Monarch":{"xref_id":"0011648"}}}


id: PBO:0064419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PNN antisense RNA 1","termid":"PBO:0064419"}


id: MONDO:0003660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A lymphoma that occurs in an adult.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lymphoma","termid":"MONDO:0005062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"adult lymphoma","secondary_identifiers":["DOID:5825","MEDGEN:233965","NANDO:2100004","NCIT:C7587","UMLS:C1332206"],"synonyms":[{"name":"adult lymphoma","type":"exact"},{"name":"lymphoma","type":"broad"},{"name":"lymphoma of adults","type":"exact"}],"termid":"MONDO:0003660","xrefs":{"Monarch":{"xref_id":"0003660"}}}


id: PBO:0085298
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pheromone-regulated protein; proposed to be involved in mating; predicted to have 5 transmembrane segments; induced by treatment with 8-methoxypsoralen and UVA irradiation","termid":"PBO:0085298"}


id: GO:0018979
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving trichloroethylene, a toxic, colorless, photoreactive, chlorinated hydrocarbon liquid, commonly used as a metal degreaser and solvent.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chlorinated hydrocarbon metabolic process","termid":"GO:0042196"}],"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":"trichloroethylene metabolic process","secondary_identifiers":["UM-BBD_pathwayID:tce"],"synonyms":[{"name":"TCE metabolic process","type":"exact"},{"name":"TCE metabolism","type":"exact"},{"name":"trichloroethene metabolic process","type":"exact"},{"name":"trichloroethene metabolism","type":"exact"},{"name":"trichloroethylene metabolism","type":"exact"}],"termid":"GO:0018979"}


id: GO:0060068
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reproductive developmental process whose specific outcome is the progression of the vagina over time, from its formation to the mature structure.","definition_xrefs":["GOC:ebc","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"female genitalia development","termid":"GO:0030540"}],"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":"vagina development","termid":"GO:0060068"}


id: MONDO:0008154
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"osteoma","termid":"MONDO:0005166"},{"relation_name":"is_a","term_name":"benign neoplasm of lower jaw bone","termid":"MONDO:0021522"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteomas of mandible","secondary_identifiers":["MEDGEN:318953","OMIM:166400","UMLS:C1833733","MESH:C563485"],"synonyms":[{"name":"osteomas of mandible","type":"exact"}],"termid":"MONDO:0008154","xrefs":{"Monarch":{"xref_id":"0008154"}}}


id: PBO:0117076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PEA15 antisense RNA 1","termid":"PBO:0117076"}


id: PBO:0004136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U4/U6 x U5 tri-snRNP complex subunit Prp1","termid":"PBO:0004136"}


id: PBO:0003761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin cortical patch component End3 (predicted)","termid":"PBO:0003761"}


id: GO:0051355
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events contributing to equilibrioception by which an organism senses the position, location, orientation, and movement of the body and its parts. Proprioception plays an important role in the ability of an organism to perceive its orientation with respect to gravity.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proprioception","termid":"GO:0019230"},{"relation_name":"part_of","term_name":"equilibrioception","termid":"GO:0050957"}],"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":"proprioception involved in equilibrioception","synonyms":[{"name":"equilibrioception by proprioception","type":"exact"},{"name":"perception of orientation with respect to gravity by proprioception","type":"exact"},{"name":"proprioception during equilibrioception","type":"related"}],"termid":"GO:0051355"}


id: PBO:0061781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"OCIA domain containing 2","termid":"PBO:0061781"}


id: PBO:0062406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 31 pseudogene","termid":"PBO:0062406"}


id: GO:1900655
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of diorcinol biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of small molecule metabolic process","termid":"GO:0062012"},{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"regulates","term_name":"diorcinol biosynthetic process","termid":"GO:1900572"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"regulation of diorcinol biosynthetic process","synonyms":[{"name":"regulation of diorcinol anabolism","type":"exact"},{"name":"regulation of diorcinol biosynthesis","type":"exact"},{"name":"regulation of diorcinol formation","type":"exact"},{"name":"regulation of diorcinol synthesis","type":"exact"}],"termid":"GO:1900655"}


id: PBO:0091467
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial Ppr10-Associated protein","termid":"PBO:0091467"}


id: MONDO:0018935
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hairy cell leukemia (HCL) is a rare type of leukemia in which abnormal B-lymphocytes are present in the bone marrow, spleen and peripheral blood. It is a slowly progressive chronic lymphocytic leukemia (CLL). The name comes from the abnormally shaped lymphocytes with hair-like projections.","definition_xrefs":["Orphanet:58017"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B-cell chronic lymphocytic leukemia","termid":"MONDO:0004948"}],"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:0005570","MONDO:0005046"],"is_obsolete":false,"name":"hairy cell leukemia","secondary_identifiers":["EFO:1000956","ICD10CM:C91.4","ICDO:9940/3","NORD:1213","ICD9:202.4","UMLS:C0023443","NCIT:C7402","icd11.foundation:82152208","MedDRA:10019055","MEDGEN:9727","GARD:6560","MESH:D007943","DOID:285","SCTID:118613001","ONCOTREE:HCL","MedDRA:10019053"],"synonyms":[{"name":"HCL","type":"exact"},{"name":"HCL-C","type":"exact"},{"name":"classic hairy cell leukaemia","type":"related"},{"name":"classic hairy cell leukemia","type":"related"},{"name":"hairy cell leukemia","type":"exact"},{"name":"leukemic reticuloendotheliosis","type":"exact"}],"termid":"MONDO:0018935","xrefs":{"Monarch":{"xref_id":"0018935"}}}


id: GO:0033487
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of pelargonidin 3-O-glucoside, a basic anthocyanin responsible for red to magenta coloration of flowers and fruits.","definition_xrefs":["GOC:mah","MetaCyc:PWY-5125"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flavonoid biosynthetic process","termid":"GO:0009813"},{"relation_name":"is_a","term_name":"beta-glucoside biosynthetic process","termid":"GO:1901806"}],"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":"pelargonidin 3-O-glucoside biosynthetic process","synonyms":[{"name":"pelargonidin 3-O-glucoside anabolism","type":"exact"},{"name":"pelargonidin 3-O-glucoside biosynthesis","type":"exact"},{"name":"pelargonidin 3-O-glucoside formation","type":"exact"},{"name":"pelargonidin 3-O-glucoside synthesis","type":"exact"}],"termid":"GO:0033487"}


id: GO:1901412
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of tetrapyrrole biosynthetic process from glutamate.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of tetrapyrrole biosynthetic process from glutamate","termid":"GO:1901410"},{"relation_name":"is_a","term_name":"positive regulation of tetrapyrrole biosynthetic process","termid":"GO:1901465"},{"relation_name":"is_a","term_name":"positive regulation of glutamate metabolic process","termid":"GO:2000213"},{"relation_name":"positively_regulates","term_name":"tetrapyrrole biosynthetic process from glutamate","termid":"GO:0033526"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0033013"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"positively_regulates","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0033013"}],"interesting_parent_ids":["GO:0006520","GO:0008150","GO:0033013","GO:0044281"],"is_obsolete":false,"name":"positive regulation of tetrapyrrole biosynthetic process from glutamate","synonyms":[{"name":"activation of tetrapyrrole anabolism from glutamate","type":"exact"},{"name":"activation of tetrapyrrole biosynthesis from glutamate","type":"exact"},{"name":"activation of tetrapyrrole biosynthetic process from glutamate","type":"narrow"},{"name":"activation of tetrapyrrole formation from glutamate","type":"exact"},{"name":"activation of tetrapyrrole synthesis from glutamate","type":"exact"},{"name":"positive regulation of tetrapyrrole anabolism from glutamate","type":"exact"},{"name":"positive regulation of tetrapyrrole biosynthesis from glutamate","type":"exact"},{"name":"positive regulation of tetrapyrrole formation from glutamate","type":"exact"},{"name":"positive regulation of tetrapyrrole synthesis from glutamate","type":"exact"},{"name":"up regulation of tetrapyrrole anabolism from glutamate","type":"exact"},{"name":"up regulation of tetrapyrrole biosynthesis from glutamate","type":"exact"},{"name":"up regulation of tetrapyrrole biosynthetic process from glutamate","type":"exact"},{"name":"up regulation of tetrapyrrole formation from glutamate","type":"exact"},{"name":"up regulation of tetrapyrrole synthesis from glutamate","type":"exact"},{"name":"up-regulation of tetrapyrrole anabolism from glutamate","type":"exact"},{"name":"up-regulation of tetrapyrrole biosynthesis from glutamate","type":"exact"},{"name":"up-regulation of tetrapyrrole biosynthetic process from glutamate","type":"exact"},{"name":"up-regulation of tetrapyrrole formation from glutamate","type":"exact"},{"name":"up-regulation of tetrapyrrole synthesis from glutamate","type":"exact"},{"name":"upregulation of tetrapyrrole anabolism from glutamate","type":"exact"},{"name":"upregulation of tetrapyrrole biosynthesis from glutamate","type":"exact"},{"name":"upregulation of tetrapyrrole biosynthetic process from glutamate","type":"exact"},{"name":"upregulation of tetrapyrrole formation from glutamate","type":"exact"},{"name":"upregulation of tetrapyrrole synthesis from glutamate","type":"exact"}],"termid":"GO:1901412"}


id: PBO:0014614
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"antisense RNA complementary to adh1, major transcript","termid":"PBO:0014614"}


id: MONDO:0060765
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A polypoid lesion composed of fibrous tissue and epithelium. Representative examples include skin tag, anal fibroepithelial polyp, and gingival fibroepithelial polyp.","definition_xrefs":["NCIT:C3337"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyp","termid":"MONDO:0005079"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fibroepithelial polyp","secondary_identifiers":["MEDGEN:1849971","UMLS:C5848070"],"synonyms":[{"name":"fibroepithelial polyp","type":"exact"},{"name":"fibropapilloma, benign","type":"exact"}],"termid":"MONDO:0060765","xrefs":{"Monarch":{"xref_id":"0060765"}}}


id: MONDO:0003441
data:
  {"annotated_genes":["SJAG_04840","SJAG_01236","SJAG_03900","SJAG_01598","SJAG_04966","SJAG_02007","SJAG_03098","SJAG_02210","SJAG_04003","SJAG_00690","SJAG_02680","SJAG_03551","SJAG_03275","SJAG_01772","SJAG_03244","SJAG_01942"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014557"},{"annotations":[87233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012994"},{"annotations":[88374],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0025691"},{"annotations":[87836,87835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030486"},{"annotations":[87876,87877],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030513"},{"annotations":[88743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030958"},{"annotations":[88131],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957385"},{"annotations":[86828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007495"},{"annotations":[88824],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015003"},{"annotations":[88918],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030676"},{"annotations":[88058],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010334"},{"annotations":[87910],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014889"},{"annotations":[86993],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007493"},{"annotations":[87631],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010747"}]},"cv_name":"mondo","definition":"A movement disorder characterized by sustained or intermittent muscle contractions, resulting in abnormal movements and/or postures.","definition_xrefs":["NCIT:C34563"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extrapyramidal and movement disease","termid":"MONDO:0001815"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00690":null,"SJAG_01236":null,"SJAG_01598":null,"SJAG_01772":null,"SJAG_01942":null,"SJAG_02007":null,"SJAG_02210":null,"SJAG_02680":null,"SJAG_03098":null,"SJAG_03244":null,"SJAG_03275":null,"SJAG_03551":null,"SJAG_03900":null,"SJAG_04003":null,"SJAG_04840":null,"SJAG_04966":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"is_obsolete":false,"name":"dystonic disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:3940","SCTID:15802004","ICD9:333.90","DOID:543","HP:0001332","UMLS:C0013421","MESH:D020821","ICD10CM:G24"],"synonyms":[{"name":"dystonia","type":"exact"},{"name":"dystonia disorder","type":"related"},{"name":"dystonia disorders","type":"related"},{"name":"dystonic disease","type":"exact"},{"name":"dystonic disorder","type":"exact"}],"termid":"MONDO:0003441","terms_by_termid":{"MONDO:0007493":null,"MONDO:0007495":null,"MONDO:0010334":null,"MONDO:0010747":null,"MONDO:0012994":null,"MONDO:0014557":null,"MONDO:0014889":null,"MONDO:0015003":null,"MONDO:0025691":null,"MONDO:0030486":null,"MONDO:0030513":null,"MONDO:0030676":null,"MONDO:0030958":null,"MONDO:0957385":null},"xrefs":{"Monarch":{"xref_id":"0003441"}}}


id: PBO:0055543
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 2979","termid":"PBO:0055543"}


id: FYPO:0002180
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A mixed population phenotype in which cells in the population are viable, some cells are longer than normal, and the rest of the cells are of normal morphology (i.e. size, shape, and structure).","definition_xrefs":["PomBase:mah","PomBase:jh"],"gene_count":0,"genotype_count":0,"name":"obsolete viable mixed vegetative cell population including cell with normal morphology and long cells (obsolete FYPO:0002180)","synonyms":[{"name":"long low penetrance","type":"related"}],"termid":"FYPO:0002180"}


id: GO:0061365
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the activity of triglyceride lipase.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of lipase activity","termid":"GO:0060193"}],"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 triglyceride lipase activity","synonyms":[{"name":"positive regulation of TAG activity","type":"exact"}],"termid":"GO:0061365"}


id: PBO:0074107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 28 member 3","termid":"PBO:0074107"}


id: MONDO:0001643
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine exophthalmos","termid":"MONDO:0001509"},{"relation_name":"is_a","term_name":"facial paralysis","termid":"MONDO:0001835"},{"relation_name":"is_a","term_name":"ophthalmoplegia","termid":"MONDO:0003425"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exophthalmic ophthalmoplegia","secondary_identifiers":["MEDGEN:508900","UMLS:C0152135","ICD9:376.22","DOID:13135","SCTID:69763009"],"termid":"MONDO:0001643","xrefs":{"Monarch":{"xref_id":"0001643"}}}


id: PBO:0086230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein that interacts with Arp2/3 complex; interacts with Arp2/3 complex to stimulate actin filament debranching and inhibit actin nucleation; has similarity to Cof1p and also to human glia maturation factor (GMF); null mutant displays elevated mitochondrial genome loss","termid":"PBO:0086230"}


id: PBO:0029272
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_chromatin_during_cellular_response_to_methyl_methanesulfonate","termid":"PBO:0029272"}


id: MONDO:0013361
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital factor II deficiency is an inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms.","definition_xrefs":["Orphanet:325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"congenital vitamin K-dependent coagulation factors deficiency","termid":"MONDO:0015722"},{"relation_name":"is_a","term_name":"prothrombin deficiency","termid":"MONDO:0024307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005570"],"is_obsolete":false,"name":"congenital prothrombin deficiency","secondary_identifiers":["MEDGEN:124425","SCTID:73975000","UMLS:C0272317","NCIT:C131737","GARD:2926","NANDO:2200673","MESH:D007020","OMIM:613679","ICD9:286.3","DOID:2235"],"synonyms":[{"name":"Dysprothrombinemia","type":"exact"},{"name":"congenital factor II deficiency","type":"related"},{"name":"congenital prothrombin deficiency","type":"exact"},{"name":"factor 2 deficiency","type":"broad"},{"name":"factor II deficiency","type":"broad"},{"name":"hereditary prothrombin deficiency","type":"exact"},{"name":"hypoprothrombinemia","type":"broad"},{"name":"prothrombin deficiency","type":"broad"},{"name":"prothrombin deficiency, congenital","type":"related"}],"termid":"MONDO:0013361","xrefs":{"Monarch":{"xref_id":"0013361"}}}


id: MONDO:0005309
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Traumatic or pathological injury to the spine in which the continuity of a vertebral bone is broken. Symptoms include back pain and difficulty bending and twisting.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone fracture","termid":"MONDO:0005315"},{"relation_name":"is_a","term_name":"spinal injury","termid":"MONDO:0037747"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinal fracture","secondary_identifiers":["EFO:0003902","SCTID:50448004","MESH:D016103"],"synonyms":[{"name":"bone fracture of vertebral column","type":"exact"},{"name":"vertebral column bone fracture","type":"exact"}],"termid":"MONDO:0005309","xrefs":{"Monarch":{"xref_id":"0005309"}}}


id: PBO:0085642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in lipid droplet (LD) assembly; forms a complex with Sei1p at ER-LD contact sites, stabilizing contact sites; ensures that LDs bud from the ER towards the cytosolic side of the membrane; null mutants have decreased net negative cell surface charge and localized accumulation of phosphatidic acid (PA) marker proteins; GFP-fusion protein expression is induced in response to MMS; null mutant can be complemented by the human seipin, BSCL2","termid":"PBO:0085642"}


id: PBO:0087223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Scaffold-type E3 ligase; required for cullin neddylation and ubiquitin ligase activation; contains a ubiquitin-binding domain (UBA) for ubiquitin and Nedd8 (Rub1p) interaction and a PONY domain involved in cullin binding and neddylation","termid":"PBO:0087223"}


id: PBO:0027976
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_histone_H3-K4_dimethylation_at_protein_coding_gene","termid":"PBO:0027976"}


id: FYECO:0000432
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in rich medium containing galactose as the carbon source, yeast extract and other components. The concentration of galactose 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":"galactose YE","synonyms":[{"name":"galactose rich medium","type":"broad"}],"termid":"FYECO:0000432"}


id: PBO:0070278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, variant U1 small nuclear 19","termid":"PBO:0070278"}


id: PBO:0085371
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphotyrosine-specific protein phosphatase; major role in the pheromone adaptive response through dephosphorylation of the Fus3p MAPK with a minor role by Ptp2p and Msg5p; minor role in the inactivation of Hog1p MAPK during osmolarity sensing with major role by Ptp2p; dephosphorylates and regulates the localization of Hog1p; minor role in the cell wall integrity pathway through tyrosine dephosphorylation of the MAPK Slt2p while Ptp2p plays a major role; localizes to the cytoplasm","termid":"PBO:0085371"}


id: GO:0034815
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cis-4-(8-hydroxypyren-7-yl)-2-oxobut-3-enoate = 10-oxabenzo(def)chrysen-9-one + formate + H+.","definition_xrefs":["UM-BBD_reactionID:r1135"],"gene_count":0,"genotype_count":0,"name":"obsolete cis-4-(8-hydroxypyren-7-yl)-2-oxobut-3-enoate lyase activity (obsolete GO:0034815)","termid":"GO:0034815"}


id: GO:1903952
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of voltage-gated potassium channel activity involved in atrial cardiac muscle cell action potential repolarization.","definition_xrefs":["PMID:25281747","GOC:mtg_cardiac_conduct_nov11","GOC:BHF","GOC:nc","GO_REF:0000059","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of voltage-gated potassium channel activity involved in atrial cardiac muscle cell action potential repolarization (obsolete GO:1903952)","synonyms":[{"name":"regulation of voltage-gated potassium channel activity involved in atrial cardiomyocyte action potential repolarization","type":"exact"}],"termid":"GO:1903952"}


id: GO:0048931
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a glial cell in the posterior lateral line nerve.","definition_xrefs":["PMID:15832385"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lateral line nerve glial cell differentiation","termid":"GO:0048895"},{"relation_name":"part_of","term_name":"posterior lateral line nerve development","termid":"GO:0048918"}],"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":"posterior lateral line nerve glial cell differentiation","termid":"GO:0048931"}


id: MONDO:0016100
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"},{"relation_name":"is_a","term_name":"acquired rippling muscle disease","termid":"MONDO:0021142"}],"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":"rippling muscle disease with myasthenia gravis","secondary_identifiers":["MEDGEN:1657345","Orphanet:206575","UMLS:C4749335","GARD:20353","icd11.foundation:327350590"],"synonyms":[{"name":"Rmd-MG","type":"exact"},{"name":"acquired rippling muscle disease","type":"broad"},{"name":"immune-mediated rippling muscle disease","type":"exact"}],"termid":"MONDO:0016100","xrefs":{"Monarch":{"xref_id":"0016100"}}}


id: PBO:0059543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded tRNA-Lys (AAA/G)","termid":"PBO:0059543"}


id: MONDO:0012875
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory bowel disease that has material basis in variation in the chromosome region 18p11.","definition_xrefs":["PMID:17554261","DOID:0110906"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory bowel disease","termid":"MONDO:0005265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005046"],"is_obsolete":false,"name":"inflammatory bowel disease 21","secondary_identifiers":["MEDGEN:436705","OMIM:612354","UMLS:C2676507","MESH:C567338"],"synonyms":[{"name":"IBD21","type":"exact"},{"name":"inflammatory bowel disease 21","type":"exact"},{"name":"inflammatory bowel disease type 21","type":"exact"}],"termid":"MONDO:0012875","xrefs":{"Monarch":{"xref_id":"0012875"}}}


id: MONDO:0010686
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"N syndrome is characterized by intellectual deficit, deafness, ocular anomalies, T-cell leukemia, cryptorchidism, hypospadias and spasticity.","definition_xrefs":["Orphanet:2608"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"hereditary neoplastic syndrome","termid":"MONDO:0015356"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N syndrome","secondary_identifiers":["UMLS:C2936859","icd11.foundation:2040480507","DOID:0050769","MEDGEN:424834","OMIM:310465","GARD:3902","SCTID:723410002","MESH:C536108"],"synonyms":[{"name":"N syndrome","type":"exact"},{"name":"NSX","type":"exact"},{"name":"intellectual disability, malformations, chromosome breakage, and development of T-cell leukaemia","type":"related"},{"name":"intellectual disability, malformations, chromosome breakage, and development of T-cell leukemia","type":"related"},{"name":"mental retardation, malformations, chromosome breakage, and development of T-cell leukaemia","type":"related"},{"name":"mental retardation, malformations, chromosome breakage, and development of T-cell leukemia","type":"related"}],"termid":"MONDO:0010686","xrefs":{"Monarch":{"xref_id":"0010686"}}}


id: MONDO:0009818
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Osteopetrosis with renal tubular acidosis is a rare disorder characterized by osteopetrosis, renal tubular acidosis (RTA), and neurological disorders related to cerebral calcifications.","definition_xrefs":["Orphanet:2785"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive osteopetrosis","termid":"MONDO:0019026"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005328"],"is_obsolete":false,"name":"autosomal recessive osteopetrosis 3","secondary_identifiers":["GARD:4154","OMIM:259730","DOID:0110941","ICD9:588.89","SCTID:254122007","NCIT:C118438","MEDGEN:91042","MESH:C536058","UMLS:C0345407"],"synonyms":[{"name":"Autosomal Recessive osteopetrosis, type 3","type":"exact"},{"name":"CA2 osteopetrosis (disease)","type":"exact"},{"name":"Guibaud Vainsel syndrome","type":"related"},{"name":"Guibaud-Vainsel syndrome","type":"exact"},{"name":"OPTB3","type":"exact"},{"name":"autosomal recessive osteopetrosis 3 with renal tubular acidosis","type":"exact"},{"name":"autosomal recessive osteopetrosis type 3","type":"exact"},{"name":"carbonic anhydrase 2 deficiency","type":"exact"},{"name":"carbonic anhydrase II deficiency","type":"exact"},{"name":"marble brain disease","type":"exact"},{"name":"mixed RTA","type":"exact"},{"name":"mixed renal tubular acidosis","type":"exact"},{"name":"osteopetrosis (disease) caused by mutation in CA2","type":"exact"},{"name":"osteopetrosis autosomal recessive 3","type":"related"},{"name":"osteopetrosis with renal tubular acidosis","type":"exact"},{"name":"osteopetrosis, autosomal recessive 3","type":"related"},{"name":"osteopetrosis, autosomal recessive 3, with renal tubular acidosis","type":"exact"},{"name":"osteopetrosis, autosomal recessive type 3","type":"exact"},{"name":"renal tubular acidosis type 3","type":"exact"}],"termid":"MONDO:0009818","xrefs":{"Monarch":{"xref_id":"0009818"}}}


id: GO:0062231
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of larval somatic muscle development.","definition_xrefs":["PMID:25758712","PMID:16643882"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of somatic muscle development","termid":"GO:0062224"},{"relation_name":"is_a","term_name":"regulation of larval somatic muscle development","termid":"GO:0062229"},{"relation_name":"positively_regulates","term_name":"larval somatic muscle development","termid":"GO:0007526"}],"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 larval somatic muscle development","termid":"GO:0062231"}


id: GO:0015098
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of molybdate (MoO4 2-) ions from one side of a membrane to the other. Molybdate is the bivalent anion derived from molybdic acid.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inorganic anion transmembrane transporter activity","termid":"GO:0015103"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"molybdate ion transmembrane transporter activity","synonyms":[{"name":"molybdate transporter activity","type":"exact"}],"termid":"GO:0015098"}


id: PBO:0086791
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; transcriptionally regulated by Upc2p via an upstream sterol response element; SWAT-GFP fusion protein localizes to the cell periphery, while mCherry fusion localizes to both the cell periphery and vacuole; YHL026C is not an essential gene; in 2005 the start site was moved 141 nt upstream (see Locus History)","termid":"PBO:0086791"}


id: MONDO:0005781
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hantavirus pulmonary syndrome (obsolete MONDO:0005781)","termid":"MONDO:0005781","xrefs":{"Monarch":{"xref_id":"0005781"}}}


id: MONDO:0004654
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pyomyositis (obsolete MONDO:0004654)","termid":"MONDO:0004654","xrefs":{"Monarch":{"xref_id":"0004654"}}}


id: PBO:0045255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deoxyribonuclease 1 like 1","termid":"PBO:0045255"}


id: PBO:0039285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALG1 like 14, pseudogene","termid":"PBO:0039285"}


id: PBO:0030435
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_tRNA_methyltransferase_activity","termid":"PBO:0030435"}


id: MOD:01975
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-(poly-3-hydroxybutyrate)-L-cysteine.","definition_xrefs":["PubMed:19711985","PubMed:9888824","RESID:AA0617"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-acylated residue","termid":"MOD:00672"},{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"S-poly(3-hydroxybutyrate)-L-cysteine","synonyms":[{"name":"(alpha)-([(2R)-2-amino-2-carboxyethyl]sulfanyl)-(omega)-[(3R)-3-hydroxybutanoyl]-poly([(3R)-3-methyl-1-oxopropane-1,3-diyl]oxy)","type":"exact"},{"name":"MOD_RES S-poly(beta-hydroxybutyryl)lysine","type":"exact"},{"name":"S-poly(3-hydroxybutanoate)cysteine","type":"exact"},{"name":"S-poly(3-hydroxybutanoic acid)cysteine","type":"exact"},{"name":"S-poly(3-hydroxybutyrate)-L-cysteine","type":"exact"},{"name":"S-poly(3-hydroxybutyrate)cysteine","type":"exact"},{"name":"S-poly(3-hydroxybutyric acid)cysteine","type":"exact"},{"name":"S-poly(beta-hydroxybutyrate)cysteine","type":"exact"},{"name":"S-poly[(R)-3-hydroxybutyrate]cysteine","type":"exact"}],"termid":"MOD:01975"}


id: MONDO:0033375
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"orofaciodigital syndrome","termid":"MONDO:0015375"}],"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":"orofaciodigital syndrome 17","secondary_identifiers":["UMLS:C4693640","DOID:0080289","MEDGEN:1644516","OMIM:617926"],"synonyms":[{"name":"OFD17","type":"related"},{"name":"Ofds 17","type":"related"},{"name":"oral-Facial-digital syndrome, type 17","type":"related"},{"name":"orofaciodigital syndrome XVII","type":"related"}],"termid":"MONDO:0033375","xrefs":{"Monarch":{"xref_id":"0033375"}}}


id: MONDO:0014957
data:
  {"annotated_genes":["SJAG_03081"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89000],"is_not":false,"summary":null,"term":"MONDO:0014957"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03081":null},"genotype_count":0,"is_obsolete":false,"name":"language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4310678","MEDGEN:934645","OMIM:617182"],"synonyms":[{"name":"LADCI","type":"exact"},{"name":"language delay and ADHD/cognitive impairment with or without cardiac arrhythmia","type":"exact"},{"name":"language delay and attention Deficit-hyperactivity disorder/cognitive impairment with or without Cardiac arrhythmia","type":"exact"},{"name":"language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia; LADCI","type":"exact"}],"termid":"MONDO:0014957","terms_by_termid":{"MONDO:0014957":null},"xrefs":{"Monarch":{"xref_id":"0014957"}}}


id: PBO:0040903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMS1 pseudogene 7","termid":"PBO:0040903"}


id: PBO:0027321
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitochondrial_electron_transport,_NADH_to_ubiquinone","termid":"PBO:0027321"}


id: PBO:0112003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquinol-cytochrome-c reductase complex subunit 8, hinge protein Qcr6","termid":"PBO:0112003"}


id: GO:0103010
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: gibberellin A53 + 2-oxoglutarate + O2 = gibberellin A97 + succinate + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gibberellin A53,2-oxoglutarate:oxygen oxidoreductase activity (GA97-forming) (obsolete GO:0103010)","termid":"GO:0103010"}


id: PBO:0046444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epsin 3","termid":"PBO:0046444"}


id: PBO:0063060
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pantothenate kinase 1","termid":"PBO:0063060"}


id: PBO:0069454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 719, pseudogene","termid":"PBO:0069454"}


id: MONDO:0017595
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"B-cell non-Hodgkin lymphoma","termid":"MONDO:0015759"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"aggressive B-cell non-Hodgkin lymphoma","secondary_identifiers":["GARD:21245","MEDGEN:1791561","NCIT:C178541","Orphanet:300846","UMLS:C5555120"],"synonyms":[{"name":"aggressive B-cell NHL","type":"exact"}],"termid":"MONDO:0017595","xrefs":{"Monarch":{"xref_id":"0017595"}}}


id: PBO:0053893
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 1177","termid":"PBO:0053893"}


id: GO:0032198
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process involved in the transposition of miniature inverted-repeat transposable elements (MITEs).","definition_xrefs":["ISBN:1555812090","GOC:jp"],"gene_count":0,"genotype_count":0,"name":"obsolete MITE transposition (obsolete GO:0032198)","termid":"GO:0032198"}


id: PBO:0113010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase subunit of imitation-switch (ISWI) class chromatin remodelers; with Ioc3p forms Isw1a complex involved in repression of transcription initiation; with Ioc2p and Ioc4p forms Isw1b complex involved in regulation of transcription elongation; Isw1b recruited to ORFs by H3K36 methylation and acts with Chd1p to prevent trans-histone exchange over coding regions; binds to 3'UTR of HAC1 mRNA and limits its nuclear export attenuating the UPR","termid":"PBO:0113010"}


id: GO:0045643
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of eosinophil differentiation.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of granulocyte differentiation","termid":"GO:0030852"},{"relation_name":"regulates","term_name":"eosinophil differentiation","termid":"GO:0030222"}],"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 eosinophil differentiation","termid":"GO:0045643"}


id: PBO:0069608
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 885, pseudogene","termid":"PBO:0069608"}


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


id: GO:0061570
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process of introducing a phosphate group into dCDP to produce a dCTP.","definition_xrefs":["GOC:dph","PMID:23416111"],"gene_count":0,"genotype_count":0,"name":"obsolete dCDP phosphorylation (obsolete GO:0061570)","termid":"GO:0061570"}


id: PBO:0027843
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_duration_of_protein_localization_to_double-strand_break_site","termid":"PBO:0027843"}


id: PBO:0040606
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BAGE family member 4","termid":"PBO:0040606"}


id: MONDO:0019409
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Idiopathic juvenile osteoporosis (IJO) is a primary condition of bone demineralization childhood or adolescence that presents with pain in the back and extremities, walking difficulties, multiple fractures, and radiological evidence of osteoporosis. Onset usually occurs in the prepubertal period, between 8 and 12 years of age.","definition_xrefs":["Orphanet:85193"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"osteoporosis","termid":"MONDO:0005298"},{"relation_name":"is_a","term_name":"rheumatic disorder","termid":"MONDO:0005554"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"idiopathic disease","termid":"MONDO:0700007"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"idiopathic juvenile osteoporosis","secondary_identifiers":["SCTID:3345002","NCIT:C119996","UMLS:C0264080","DOID:12559","MEDGEN:120494","GARD:6760","icd11.foundation:183642011","ICD9:733.02","MESH:C537700","OMIM:259750"],"synonyms":[{"name":"IJO","type":"exact"},{"name":"Ijo","type":"exact"},{"name":"Paediatric osteoporosis","type":"exact"},{"name":"Pediatric osteoporosis","type":"exact"},{"name":"idiopathic juvenile osteoporosis","type":"exact"},{"name":"idiopathic osteoporosis","type":"exact"},{"name":"juvenile osteoporosis","type":"exact"},{"name":"osteoporosis, juvenile","type":"related"}],"termid":"MONDO:0019409","xrefs":{"Monarch":{"xref_id":"0019409"}}}


id: PBO:0072435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S28 pseudogene 9","termid":"PBO:0072435"}


id: PBO:0028277
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_branched,_elongated,_multiseptate_vegetative_cell","termid":"PBO:0028277"}


id: MONDO:0014814
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any advanced sleep phase syndrome in which the cause of the disease is a mutation in the PER3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"advanced sleep phase syndrome","termid":"MONDO:0015609"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"advanced sleep phase syndrome 3","secondary_identifiers":["DOID:0110013","GARD:16165","OMIM:616882","UMLS:C4225169","MEDGEN:909447"],"synonyms":[{"name":"FASPS3","type":"exact"},{"name":"PER3 advanced sleep phase syndrome","type":"exact"},{"name":"advanced sleep phase syndrome caused by mutation in PER3","type":"exact"},{"name":"advanced sleep phase syndrome type 3","type":"exact"},{"name":"advanced sleep phase syndrome, familial, 3","type":"exact"},{"name":"advanced sleep phase syndrome, familial, type 3","type":"exact"},{"name":"familial advanced sleep phase syndrome 3","type":"exact"}],"termid":"MONDO:0014814","xrefs":{"Monarch":{"xref_id":"0014814"}}}


id: MONDO:1011119
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hypogonadism that occurs in deer.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypogonadism, non-human animal","termid":"MONDO:1010276"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadism, deer","secondary_identifiers":["OMIA:000522-9850"],"termid":"MONDO:1011119","xrefs":{"Monarch":{"xref_id":"1011119"}}}


id: PBO:0041146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BTF3 pseudogene 1","termid":"PBO:0041146"}


id: PBO:0043939
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CREB regulated transcription coactivator 3","termid":"PBO:0043939"}


id: PBO:0083496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene YJL194W/CDC6","termid":"PBO:0083496"}


id: FYPO:0002409
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an elongated germ tube, and undergoes a single round of cell division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination with elongated germ tube","termid":"FYPO:0000314"},{"relation_name":"is_a","term_name":"inviable after spore germination, single cell division, abnormal cell shape","termid":"FYPO:0002420"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000004","FYPO:0000005","FYPO:0001320"],"is_obsolete":false,"name":"inviable after spore germination, single cell division, with elongated germ tube","synonyms":[{"name":"inviable after spore germination, single cell division, elongated cell","type":"exact"},{"name":"inviable following spore germination, single cell division, with elongated, germ tube","type":"exact"},{"name":"inviable germinated spore, single cell division, with elongated germ tube","type":"exact"},{"name":"lethal after spore germination, single cell division, with elongated germ tube","type":"exact"}],"termid":"FYPO:0002409"}


id: GO:1904524
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of DNA amplification.","definition_xrefs":["PMID:26195783","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA amplification","termid":"GO:1904523"},{"relation_name":"is_a","term_name":"negative regulation of DNA biosynthetic process","termid":"GO:2000279"},{"relation_name":"negatively_regulates","term_name":"DNA amplification","termid":"GO:0006277"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"negatively_regulates","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"negative regulation of DNA amplification","synonyms":[{"name":"down regulation of DNA amplification","type":"exact"},{"name":"down-regulation of DNA amplification","type":"exact"},{"name":"downregulation of DNA amplification","type":"exact"},{"name":"inhibition of DNA amplification","type":"narrow"}],"termid":"GO:1904524"}


