# terms

id: PBO:0067355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 453, pseudogene","termid":"PBO:0067355"}


id: FYPO:0004035
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of thioredoxin-disulfide reductase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal cellular process","termid":"FYPO:0000628"},{"relation_name":"is_a","term_name":"abnormal oxidoreductase activity","termid":"FYPO:0000689"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"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:0005447"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0000652","FYPO:0000654","FYPO:0000707"],"is_obsolete":false,"name":"abnormal thioredoxin-disulfide reductase activity","termid":"FYPO:0004035"}


id: PBO:0091531
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cruciform-Cutting Endonuclease","termid":"PBO:0091531"}


id: PBO:0016537
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae YPR081C","termid":"PBO:0016537"}


id: PBO:0029804
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_vegetative_cell_population_with_abnormal_cell_shape_(obsolete_FYPO:0002433)","termid":"PBO:0029804"}


id: PBO:0047767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FOS like 2, AP-1 transcription factor subunit","termid":"PBO:0047767"}


id: PBO:0116698
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFKB1 antisense RNA 1","termid":"PBO:0116698"}


id: PBO:0047394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 34","termid":"PBO:0047394"}


id: CHEBI:28304
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":"heparin","termid":"CHEBI:28304"}


id: GO:0140127
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A histone reader that recognizes a histone H3 dimethylate at arginine 8. The methylation can be symmetrical or asymmetrical.","definition_xrefs":["PMID:24589551"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H3 reader activity","termid":"GO:0140006"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140566"},{"rel_name":"is_a","termid":"GO:0030674"}],"interesting_parent_ids":["GO:0060090","GO:0003674","GO:0140566","GO:0030674"],"is_obsolete":false,"name":"histone H3R8me2 reader activity","termid":"GO:0140127"}


id: PBO:0072031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S10 pseudogene 1","termid":"PBO:0072031"}


id: PBO:0070226
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 160 pseudogene","termid":"PBO:0070226"}


id: PBO:0090963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol-4 kinase plasma membrane scaffold Efr3","termid":"PBO:0090963"}


id: MONDO:0022647
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cardiomelic syndrome stratton Koehler type","termid":"MONDO:0022647","xrefs":{"Monarch":{"xref_id":"0022647"}}}


id: GO:1905715
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cornification.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:26014679"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of programmed cell death","termid":"GO:0043067"},{"relation_name":"regulates","term_name":"cornification","termid":"GO:0070268"}],"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 cornification","termid":"GO:1905715"}


id: MONDO:1011088
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Renal dysplasia that occurs in domestic cat.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"renal dysplasia, non-human animal","termid":"MONDO:1010268"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"renal dysplasia, domestic cat","secondary_identifiers":["OMIA:001135-9685"],"termid":"MONDO:1011088","xrefs":{"Monarch":{"xref_id":"1011088"}}}


id: MONDO:0021158
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"gonorrhea","termid":"MONDO:0004277"},{"relation_name":"is_a","term_name":"epididymo-orchitis","termid":"MONDO:0004778"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gonococcal epididymo-orchitis","secondary_identifiers":["MEDGEN:574637","SCTID:236772009","UMLS:C0341782"],"termid":"MONDO:0021158","xrefs":{"Monarch":{"xref_id":"0021158"}}}


id: GO:0034706
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An ion channel complex through which sodium ions pass.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cation channel complex","termid":"GO:0034703"}],"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":"sodium channel complex","termid":"GO:0034706"}


id: MONDO:0009011
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete constriction rings syndrome (obsolete MONDO:0009011)","termid":"MONDO:0009011","xrefs":{"Monarch":{"xref_id":"0009011"}}}


id: PBO:0042350
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD84 molecule","termid":"PBO:0042350"}


id: SO:0000977
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_region","termid":"SO:0000833"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anchor_binding_site","synonyms":[{"name":"anchor binding site","type":"exact"}],"termid":"SO:0000977"}


id: FYPO:0000955
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing lead ions.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0002058","FYPO:0002057","FYPO:0002060","FYPO:0000003","FYPO:0000139"],"is_obsolete":false,"name":"normal growth on lead ion","synonyms":[{"name":"normal cell population growth in presence of lead ion","type":"exact"},{"name":"normal cell population growth on lead ion","type":"exact"},{"name":"normal cellular response to lead ion","type":"related"},{"name":"normal vegetative cell population growth on lead ion","type":"exact"}],"termid":"FYPO:0000955"}


id: GO:0034978
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the homeodomain proteins PDX1, PBX1b and MRG1 (MEIS2) and is involved in the transcriptional regulation of pancreatic acinar cell-specific genes.","definition_xrefs":["PMID:11279116","PMID:9710595"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear protein-containing complex","termid":"GO:0140513"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"PDX1-PBX1b-MRG1 complex","synonyms":[{"name":"acinar cell-specific C complex","type":"exact"}],"termid":"GO:0034978"}


id: PBO:0043317
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"clathrin interactor 1","termid":"PBO:0043317"}


id: PBO:0074564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA host gene 18","termid":"PBO:0074564"}


id: PBO:0087272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ser/Thr protein kinase involved in salt tolerance, nutrient response; functions in regulation of Trk1p-Trk2p potassium transporter; overexpression affects the Fe-S and lipoamide containing proteins in the mitochondrion; required for lipoylation of Lat1p, Kgd2p and Gcv3p; partially redundant with Hal5p; has similarity to Npr1p; localizes to the cytoplasm and mitochondrion","termid":"PBO:0087272"}


id: PBO:0072964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCG5 antisense RNA 1","termid":"PBO:0072964"}


id: MONDO:0012190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolysis bullosa simplex","termid":"MONDO:0017610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"epidermolysis bullosa simplex 7, with nephropathy and deafness","secondary_identifiers":["MEDGEN:323004","Orphanet:300333","MESH:C563798","GARD:17367","UMLS:C1836823","OMIM:609057"],"synonyms":[{"name":"epidermolysis bullosa simplex 7, with nephropathy and deafness","type":"exact"},{"name":"nephropathy with pretibial epidermolysis bullosa and deafness","type":"related"},{"name":"nephrotic syndrome - deafness - pretibial epidermolysis bullosa syndrome","type":"exact"},{"name":"nephrotic syndrome-hearing loss-pretibial epidermolysis bullosa syndrome","type":"exact"}],"termid":"MONDO:0012190","xrefs":{"Monarch":{"xref_id":"0012190"}}}


id: MONDO:0010470
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Baratela-Scott syndrome (obsolete MONDO:0010470)","secondary_identifiers":["OMIM:300881"],"termid":"MONDO:0010470","xrefs":{"Monarch":{"xref_id":"0010470"}}}


id: PBO:0031793
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-delayed_cell_cycle_phase_transition","termid":"PBO:0031793"}


id: MONDO:0024632
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"phagocytic cell dysfunction","termid":"MONDO:0024627"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"defective phagocytic cell opsonization","secondary_identifiers":["SCTID:234578009","MEDGEN:585045","UMLS:C0398733"],"synonyms":[{"name":"defective phagocytic cell opsonization","type":"exact"}],"termid":"MONDO:0024632","xrefs":{"Monarch":{"xref_id":"0024632"}}}


id: GO:0052590
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: sn-glycerol 3-phosphate + a ubiquinone = glycerone phosphate + a ubiquinol.","definition_xrefs":["MetaCyc:RXN0-5260"],"gene_count":0,"genotype_count":0,"name":"obsolete sn-glycerol-3-phosphate:ubiquinone oxidoreductase activity (obsolete GO:0052590)","termid":"GO:0052590"}


id: FYPO:0001725
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of L-aspartate measured in the cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell during vegetative growth","termid":"FYPO:0001316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal cellular aspartate level","synonyms":[{"name":"normal cellular L-aspartate level","type":"exact"},{"name":"normal cellular aspartate level during mitotic cell cycle","type":"related"},{"name":"normal cellular aspartate level during vegetative growth","type":"exact"},{"name":"normal cellular aspartic acid level","type":"related"},{"name":"normal level of aspartate in cell","type":"exact"}],"termid":"FYPO:0001725"}


id: PBO:0073871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 9 member C1","termid":"PBO:0073871"}


id: PR:Q1RKN3
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tlh2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q1RKN3"],"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":"ATP-dependent DNA helicase tlh2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBCPT2R1.08c","synonyms":[{"name":"Spom972h-tlh2","type":"exact"},{"name":"Sub-telomeric helicase RecQ homolog 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q1RKN3"}


id: PBO:0083746
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential component of the TIM23 complex; acts as receptor for the translocase of the inner mitochondrial membrane (TIM23) complex guiding incoming precursors from the TOM complex; may control the gating of the Tim23p-Tim17p channel","termid":"PBO:0083746"}


id: GO:0140743
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the synthesis of a lncRNA.","definition_xrefs":["PMID:33767452","PMID:33913806"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA-templated transcription","termid":"GO:0006355"},{"relation_name":"regulates","term_name":"lncRNA transcription","termid":"GO:0140742"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006355","GO:0010467","GO:0006351","GO:0008150"],"is_obsolete":false,"name":"regulation of lncRNA transcription","termid":"GO:0140743"}


id: PBO:0070396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAR related orphan receptor B","termid":"PBO:0070396"}


id: GO:1905829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of prostaglandin catabolic process.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:12432938"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of lipid catabolic process","termid":"GO:0050995"},{"relation_name":"is_a","term_name":"regulation of prostaglandin catabolic process","termid":"GO:1905828"},{"relation_name":"negatively_regulates","term_name":"prostaglandin catabolic process","termid":"GO:1905344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"negative regulation of prostaglandin catabolic process","synonyms":[{"name":"down regulation of prostaglandin breakdown","type":"exact"},{"name":"down regulation of prostaglandin catabolic process","type":"exact"},{"name":"down regulation of prostaglandin catabolism","type":"exact"},{"name":"down regulation of prostaglandin degradation","type":"exact"},{"name":"down-regulation of prostaglandin breakdown","type":"exact"},{"name":"down-regulation of prostaglandin catabolic process","type":"exact"},{"name":"down-regulation of prostaglandin catabolism","type":"exact"},{"name":"down-regulation of prostaglandin degradation","type":"exact"},{"name":"downregulation of prostaglandin breakdown","type":"exact"},{"name":"downregulation of prostaglandin catabolic process","type":"exact"},{"name":"downregulation of prostaglandin catabolism","type":"exact"},{"name":"downregulation of prostaglandin degradation","type":"exact"},{"name":"inhibition of prostaglandin breakdown","type":"narrow"},{"name":"inhibition of prostaglandin catabolic process","type":"narrow"},{"name":"inhibition of prostaglandin catabolism","type":"narrow"},{"name":"inhibition of prostaglandin degradation","type":"narrow"},{"name":"negative regulation of prostaglandin breakdown","type":"exact"},{"name":"negative regulation of prostaglandin catabolism","type":"exact"},{"name":"negative regulation of prostaglandin degradation","type":"exact"}],"termid":"GO:1905829"}


id: GO:1905600
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of receptor-mediated endocytosis involved in cholesterol transport.","definition_xrefs":["GOC:nc","GOC:TermGenie","GOC:BHF","PMID:22848640","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular transport","termid":"GO:0032386"},{"relation_name":"is_a","term_name":"regulation of receptor-mediated endocytosis","termid":"GO:0048259"},{"relation_name":"regulates","term_name":"receptor-mediated endocytosis involved in cholesterol transport","termid":"GO:0090118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"regulation of receptor-mediated endocytosis involved in cholesterol transport","synonyms":[{"name":"regulation of receptor-mediated endocytosis involved in intracellular cholesterol transport","type":"related"},{"name":"regulation of receptor-mediated endocytosis of LDL","type":"related"},{"name":"regulation of receptor-mediated endocytosis of low-density lipoprotein involved in cholesterol transport","type":"related"},{"name":"regulation of receptor-mediated endocytosis of low-density lipoprotein particle involved in cholesterol transport","type":"related"}],"termid":"GO:1905600"}


id: MONDO:0100393
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly t(8;16). (A cytogenetic abnormality that involves a translocation between chromosomes 8 and 16.)","definition_xrefs":["NCIT:C175583"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"acute myeloid leukemia, t(8;16)","synonyms":[{"name":"AML, t(8;16)","type":"exact"}],"termid":"MONDO:0100393","xrefs":{"Monarch":{"xref_id":"0100393"}}}


id: PBO:0003513
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetraspan protein Dni2 (predicted)","termid":"PBO:0003513"}


id: PBO:0036020
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-premature_protein_localization_to_nucleus_during_vegetative_growth","termid":"PBO:0036020"}


id: PBO:0085432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Polyamine transporter of the major facilitator superfamily; member of the 12-spanner drug:H(+) antiporter DHA1 family; recognizes spermine, putrescine, and spermidine; localizes to the plasma membrane","termid":"PBO:0085432"}


id: MONDO:0006329
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An olfactory neuroblastoma arising in the paranasal sinus.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant cranial nerve neoplasm","termid":"MONDO:0002433"},{"relation_name":"is_a","term_name":"olfactory nerve neoplasm","termid":"MONDO:0002722"},{"relation_name":"is_a","term_name":"extracranial neuroblastoma","termid":"MONDO:0002749"},{"relation_name":"is_a","term_name":"intracranial primitive neuroectodermal tumor","termid":"MONDO:0003142"}],"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":"olfactory neuroblastoma","secondary_identifiers":["icd11.foundation:2007774165","ICDO:9522/3","ICDO:9523/3","DOID:369","NCIT:C3789","ONCOTREE:ONBL","SCTID:422886007","EFO:1000407"],"synonyms":[{"name":"Asthesioneuroblastoma","type":"exact"},{"name":"Asthesioneuroblastoma (morphologic abnormality)","type":"exact"},{"name":"Esthesioneuroepithelioma","type":"related"},{"name":"Esthesioneuroepithelioma (morphologic abnormality)","type":"related"},{"name":"Esthesioneuroepithelioma [dup] (morphologic abnormality)","type":"related"},{"name":"esthesioneuroblastoma","type":"related"},{"name":"esthesioneuroblastoma (morphologic abnormality)","type":"related"},{"name":"olfactory esthesioneuroblastoma","type":"exact"},{"name":"olfactory neuroblastoma","type":"exact"},{"name":"olfactory neuroepithelioma","type":"exact"},{"name":"paranasal sinus olfactory neuroblastoma","type":"exact"}],"termid":"MONDO:0006329","xrefs":{"Monarch":{"xref_id":"0006329"}}}


id: PBO:0088724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial [2Fe-2S] cluster assembly protein, LYR family Isd11","termid":"PBO:0088724"}


id: GO:0051448
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to gonadotropin-releasing hormone (GnRH), a peptide hormone responsible for the release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) from the anterior pituitary. GnRH is synthesized and released by the hypothalamus.","definition_xrefs":["GOC:pr","PMID:1984190"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide hormone binding","termid":"GO:0017046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"gonadotropin-releasing hormone binding","synonyms":[{"name":"GnRH binding","type":"exact"},{"name":"gonadotrophin releasing hormone binding","type":"exact"}],"termid":"GO:0051448"}


id: GO:0050109
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: morphine + NAD(P)+ = morphinone + NAD(P)H + H+.","definition_xrefs":["MetaCyc:MORPHINE-6-DEHYDROGENASE-RXN","EC:1.1.1.218"],"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:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"morphine 6-dehydrogenase activity","synonyms":[{"name":"morphine:NAD(P)+ 6-oxidoreductase activity","type":"related"},{"name":"naloxone reductase activity","type":"related"},{"name":"reductase, naloxone","type":"related"}],"termid":"GO:0050109"}


id: PR:Q9P3W1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A general transcription factor IIE subunit 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR13097:SF3","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":"transcription initiation factor IIE subunit alpha (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC458.07","secondary_identifiers":["UniProtKB:Q9P3W1"],"synonyms":[{"name":"SPAC458.07","type":"related"},{"name":"Spom972h-GTF2E1","type":"exact"},{"name":"TFIIE-alpha (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9P3W1"}


id: PBO:0082039
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-deoxyglucose-6-phosphate phosphatase; member of a family of low molecular weight phosphatases, induced by oxidative and osmotic stress, confers 2-deoxyglucose resistance when overexpressed; DOG2 has a paralog, DOG1, that arose from a single-locus duplication; the last half of DOG1 and DOG2 are subject to gene conversions among S. cerevisiae, S. paradoxus, and S. mikatae","termid":"PBO:0082039"}


id: GO:0002777
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of an antimicrobial peptide. Such peptides may have protective properties against bacteria, fungi, viruses, or protozoa.","definition_xrefs":["ISBN:0781735149","PMID:11807545","GOC:add","PMID:15638771"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptide biosynthetic process","termid":"GO:0043043"},{"relation_name":"part_of","term_name":"antimicrobial peptide production","termid":"GO:0002775"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"antimicrobial peptide biosynthetic process","termid":"GO:0002777"}


id: PR:O13701
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ptr6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13701"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription initiation factor TFIID subunit 7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC13F5.02c","synonyms":[{"name":"Spom972h-ptr6","type":"exact"},{"name":"TAFII-55 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"transcription initiation factor TFIID 55 kDa subunit (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13701"}


id: FYPO:0004029
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which 5' deoxyribonuclease (pyrimidine dimer) activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal 5' deoxyribonuclease (pyrimidine dimer) activity","termid":"FYPO:0004028"},{"relation_name":"is_a","term_name":"abolished endodeoxyribonuclease activity","termid":"FYPO:0007141"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000002","FYPO:0001985","FYPO:0000707","FYPO:0000652","FYPO:0005447","FYPO:0000661"],"is_obsolete":false,"name":"abolished 5' deoxyribonuclease (pyrimidine dimer) activity","synonyms":[{"name":"5' deoxyribonuclease (pyrimidine dimer) activity abolished","type":"exact"}],"termid":"FYPO:0004029"}


id: GO:0090194
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of glomerulus development, the progression of the glomerulus over time from its initial formation until its mature state. The glomerulus is a capillary tuft surrounded by Bowman's capsule in nephrons of the vertebrate kidney.","definition_xrefs":["GOC:dph","GOC:tb","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of kidney development","termid":"GO:0090185"},{"relation_name":"is_a","term_name":"regulation of glomerulus development","termid":"GO:0090192"},{"relation_name":"negatively_regulates","term_name":"glomerulus development","termid":"GO:0032835"}],"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 glomerulus development","termid":"GO:0090194"}


id: GO:0099185
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is carried out at the cellular level which results in the assembly, arrangement of constituent parts, or disassembly of cytoskeletal structures comprised of intermediate filament and their associated proteins in the postsynaptic cytoskeleton.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intermediate filament cytoskeleton organization","termid":"GO:0045104"},{"relation_name":"is_a","term_name":"postsynaptic cytoskeleton organization","termid":"GO:0099188"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0008150","GO:0007010"],"is_obsolete":false,"name":"postsynaptic intermediate filament cytoskeleton organization","termid":"GO:0099185"}


id: PBO:0013071
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ataxia-Two Homolog","termid":"PBO:0013071"}


id: PBO:0053055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucyl-tRNA synthetase 1","termid":"PBO:0053055"}


id: MONDO:0007466
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":"DNA, satellite, 3","secondary_identifiers":["OMIM:126370"],"synonyms":[{"name":"D1Z1","type":"related"},{"name":"DNA, satellite, III","type":"related"},{"name":"DNA, satellite, type 3","type":"exact"},{"name":"HS3","type":"related"}],"termid":"MONDO:0007466","xrefs":{"Monarch":{"xref_id":"0007466"}}}


id: PBO:0069771
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1054, pseudogene","termid":"PBO:0069771"}


id: PBO:0003122
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1.11.1.-","termid":"PBO:0003122"}


id: SO:0001042
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The nucleotide sequence of a virus that infects bacteria.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral_sequence","termid":"SO:0001041"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phage_sequence","secondary_identifiers":["http://en.wikipedia.org/wiki/Bacteriophage"],"synonyms":[{"name":"bacteriophage","type":"exact"},{"name":"phage","type":"exact"},{"name":"phage sequence","type":"exact"}],"termid":"SO:0001042"}


id: MONDO:0005936
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections with nontuberculous mycobacteria (atypical mycobacteria): M. kansasii, M. marinum, M. scrofulaceum, M. flavescens, M. gordonae, M. obuense, M. gilvum, M. duvali, M. szulgai, M. intracellulare (see mycobacterium avium complex;), M. xenopi (littorale), M. ulcerans, M. buruli, M. terrae, M. fortuitum (minetti, giae), M. chelonae.","definition_xrefs":["MESH:D009165"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pneumonia","termid":"MONDO:0005249"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"recurrent pneumonia","secondary_identifiers":["SCTID:699014000","MEDGEN:195802","EFO:0007461","HP:0006532","UMLS:C0694550"],"synonyms":[{"name":"recurrent pneumonia","type":"exact"},{"name":"recurrent pneumonia (disease)","type":"exact"}],"termid":"MONDO:0005936","xrefs":{"Monarch":{"xref_id":"0005936"}}}


id: PBO:0084443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Maltose permease; high-affinity maltose transporter (alpha-glucoside transporter); encoded in the MAL3 complex locus; member of the 12 transmembrane domain superfamily of sugar transporters; functional in genomic reference strain S288C","termid":"PBO:0084443"}


id: PBO:0078695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Leu (anticodon AAG) 6-1","termid":"PBO:0078695"}


id: GO:1902038
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 differentiation.","definition_xrefs":["PMID:23403623","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of hematopoietic progenitor cell differentiation","termid":"GO:1901534"},{"relation_name":"is_a","term_name":"regulation of hematopoietic stem cell differentiation","termid":"GO:1902036"},{"relation_name":"is_a","term_name":"positive regulation of stem cell differentiation","termid":"GO:2000738"},{"relation_name":"positively_regulates","term_name":"hematopoietic stem cell differentiation","termid":"GO:0060218"}],"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 differentiation","synonyms":[{"name":"activation of haematopoietic stem cell differentiation","type":"narrow"},{"name":"activation of haemopoietic stem cell differentiation","type":"narrow"},{"name":"activation of hematopoietic stem cell differentiation","type":"narrow"},{"name":"activation of hemopoietic stem cell differentiation","type":"narrow"},{"name":"positive regulation of haematopoietic stem cell differentiation","type":"exact"},{"name":"positive regulation of haemopoietic stem cell differentiation","type":"exact"},{"name":"positive regulation of hemopoietic stem cell differentiation","type":"exact"},{"name":"up regulation of haematopoietic stem cell differentiation","type":"exact"},{"name":"up regulation of haemopoietic stem cell differentiation","type":"exact"},{"name":"up regulation of hematopoietic stem cell differentiation","type":"exact"},{"name":"up regulation of hemopoietic stem cell differentiation","type":"exact"},{"name":"up-regulation of haematopoietic stem cell differentiation","type":"exact"},{"name":"up-regulation of haemopoietic stem cell differentiation","type":"exact"},{"name":"up-regulation of hematopoietic stem cell differentiation","type":"exact"},{"name":"up-regulation of hemopoietic stem cell differentiation","type":"exact"},{"name":"upregulation of haematopoietic stem cell differentiation","type":"exact"},{"name":"upregulation of haemopoietic stem cell differentiation","type":"exact"},{"name":"upregulation of hematopoietic stem cell differentiation","type":"exact"},{"name":"upregulation of hemopoietic stem cell differentiation","type":"exact"}],"termid":"GO:1902038"}


id: PBO:0052645
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 13","termid":"PBO:0052645"}


id: PBO:0083250
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; identified by gene-trapping, microarray-based expression analysis, and genome-wide homology searching","termid":"PBO:0083250"}


id: GO:0102956
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + sinapoyl aldehyde = H+ + sinapaldehyde glucoside + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete UDP-glucose:sinapaldehyde 4-beta-D-glucosyltransferase activity (obsolete GO:0102956)","termid":"GO:0102956"}


id: PBO:0085249
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Perilipin, involved in formation and stability of lipid droplets; expression pattern suggests a role in respiratory growth; computational analysis of large-scale protein-protein interaction data suggests a role in ATP/ADP exchange","termid":"PBO:0085249"}


id: PBO:0035863
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_secretion_during_vegetative_growth","termid":"PBO:0035863"}


id: MONDO:0006802
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by abnormal secretion of antidiuretic hormone in conjunction with neoplastic growth occurring anywhere in the body.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pituitary gland disorder","termid":"MONDO:0003381"},{"relation_name":"is_a","term_name":"ectopic hormone secretion syndrome associated with neoplasia","termid":"MONDO:0045072"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inappropriate ADH syndrome","secondary_identifiers":["MESH:D007177","NCIT:C3988","Orphanet:83449","NANDO:2200323","NANDO:1200376","UMLS:C0021141","EFO:1000982","SCTID:55004003","MEDGEN:5772","DOID:3401","NANDO:2100116","ICD9:253.6","MedDRA:10042818"],"synonyms":[{"name":"SIADH","type":"exact"},{"name":"ectopic ADH secretion","type":"exact"},{"name":"ectopic antidiuretic hormone secretion","type":"exact"},{"name":"inappropriate ADH secretion","type":"exact"},{"name":"inappropriate Arginine vasopressin secretion","type":"exact"},{"name":"inappropriate antidiuretic hormone secretion syndrome","type":"exact"},{"name":"syndrome of inappropriate antidiuretic hormone","type":"exact"},{"name":"syndrome of inappropriate antidiuretic hormone secretion","type":"exact"},{"name":"syndrome of inappropriate secretion of ADH","type":"exact"},{"name":"syndrome of inappropriate secretion of antidiuretic hormone","type":"exact"},{"name":"syndrome of inappropriate vasopressin secretion","type":"exact"}],"termid":"MONDO:0006802","xrefs":{"Monarch":{"xref_id":"0006802"}}}


id: GO:0051767
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a nitric-oxide synthase, an enzyme which catalyzes the reaction L-arginine + n NADPH + n H+ + m O2 = citrulline + nitric oxide + n NADP+.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete nitric-oxide synthase biosynthetic process (obsolete GO:0051767)","synonyms":[{"name":"NO synthase biosynthesis","type":"exact"},{"name":"NO synthase biosynthetic process","type":"exact"},{"name":"NOS biosynthesis","type":"exact"},{"name":"NOS biosynthetic process","type":"exact"},{"name":"NOS1 biosynthesis","type":"narrow"},{"name":"NOS2 biosynthesis","type":"narrow"},{"name":"NOS2 synthase biosynthesis","type":"narrow"},{"name":"NOS2 synthase biosynthetic process","type":"narrow"},{"name":"NOS3 biosynthesis","type":"narrow"},{"name":"brain nitric-oxide synthase biosynthetic process","type":"narrow"},{"name":"endothelial nitric-oxide synthase biosynthetic process","type":"narrow"},{"name":"inducible nitric-oxide synthase biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase (type 2) biosynthesis","type":"narrow"},{"name":"nitric-oxide synthase (type 2) biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase (type II) biosynthesis","type":"narrow"},{"name":"nitric-oxide synthase (type II) biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase 2 biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase-1 biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase-2 biosynthetic process","type":"narrow"},{"name":"nitric-oxide synthase-3 biosynthetic process","type":"narrow"}],"termid":"GO:0051767"}


id: SO:1001286
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A recoding stimulatory signal, downstream sequence important for recoding that contains repetitive elements.","definition_xrefs":["SO:ke","PMID:12519954"],"direct_ancestors":[{"relation_name":"is_a","term_name":"three_prime_recoding_site","termid":"SO:1001277"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_repeat_recoding_signal","synonyms":[{"name":"three prime repeat recoding signal","type":"exact"}],"termid":"SO:1001286"}


id: MONDO:0004422
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A meningioma that affects the falx cerebri.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterior cranial fossa meningioma","termid":"MONDO:0002997"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral falx meningioma","secondary_identifiers":["MEDGEN:272627","NCIT:C5267","UMLS:C1333597","DOID:7986"],"synonyms":[{"name":"Falcine meningioma","type":"exact"},{"name":"falx cerebri meningioma","type":"exact"},{"name":"falx cerebri meningioma (disease)","type":"exact"},{"name":"meningioma (disease) of falx cerebri","type":"exact"},{"name":"meningioma of cerebral falx","type":"exact"},{"name":"meningioma of falx cerebri","type":"exact"},{"name":"meningioma of falx of cerebrum","type":"exact"},{"name":"meningioma of the cerebral falx","type":"exact"},{"name":"meningioma of the falx cerebri","type":"exact"},{"name":"meningioma of the falx of the cerebrum","type":"exact"}],"termid":"MONDO:0004422","xrefs":{"Monarch":{"xref_id":"0004422"}}}


id: PR:G2TRM7
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- tam5 gene.","definition_xrefs":["PRO:DNx","UniProtKB:G2TRM7"],"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 tam5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC16E8.18c","synonyms":[{"name":"Spom972h-tam5","type":"exact"},{"name":"transcripts altered in meiosis protein 5 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:G2TRM7"}


id: PBO:0085070
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nonfunctional protein with homology to IMP dehydrogenase; blocked reading frame, located close to the telomere; not expressed at detectable levels; YAR073W and YAR075W comprise a continuous reading frame in most strains of S. cerevisiae; YAR073W/YAR075W together have a paralog, IMD2, that arose from a segmental duplication","termid":"PBO:0085070"}


id: MONDO:0010018
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":"second metatarsal-metacarpal syndrome","secondary_identifiers":["MESH:C564824","OMIM:269630","MEDGEN:341415","UMLS:C1849259"],"synonyms":[{"name":"second metatarsal-metacarpal syndrome","type":"exact"}],"termid":"MONDO:0010018","xrefs":{"Monarch":{"xref_id":"0010018"}}}


id: PBO:0085246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Peptidyl-prolyl cis-trans isomerase (PPIase); nuclear proline isomerase; affects expression of multiple genes via its role in nucleosome assembly; catalyzes isomerization of proline residues in histones H3 and H4, which affects lysine methylation of those histones; PPIase domain acts as a transcriptional repressor when tethered to DNA by lexA, and repressor activity is dependent on PPIase activity; contains a nucleoplasmin-like fold and can form pentamers","termid":"PBO:0085246"}


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


id: PBO:0110483
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LSM2 pseudogene 1","termid":"PBO:0110483"}


id: MONDO:0008018
data:
  {"annotated_genes":["SJAG_02226","SJAG_01620"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86006,86007],"is_not":false,"summary":null,"term":"MONDO:0008018"}]},"cv_name":"mondo","definition":"Muir-Torre syndrome (MTS) is a form of hereditary nonpolyposis colon cancer (HNPCC) characterized by cutaneous sebaceous tumors, keratoacanthomas and at least one visceral malignancy, most frequently gastrointestinal carcinoma.","definition_xrefs":["Orphanet:587"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"Lynch syndrome","termid":"MONDO:0005835"},{"relation_name":"excluded_subClassOf","term_name":"obsolete inherited skin tumor (obsolete MONDO:0015950)","termid":"MONDO:0015950"},{"relation_name":"excluded_subClassOf","term_name":"obsolete rare skin tumor or hamartoma (obsolete MONDO:0019300)","termid":"MONDO:0019300"},{"relation_name":"excluded_subClassOf","term_name":"benign tumor of palpebral epidermis","termid":"MONDO:0020173"},{"relation_name":"excluded_subClassOf","term_name":"obsolete palpebral sebaceous gland tumor (obsolete MONDO:0020176)","termid":"MONDO:0020176"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"hereditary nonpolyposis colon cancer","termid":"MONDO:0018630"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01620":null,"SJAG_02226":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0000426","MONDO:0004335"],"is_obsolete":false,"name":"Muir-Torre syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D055653","DOID:0050465","SCTID:403824007","UMLS:C1321489","MedDRA:10063042","GARD:6821","MEDGEN:231157","NCIT:C84905","icd11.foundation:229304403","OMIM:158320"],"synonyms":[{"name":"MRTES","type":"related"},{"name":"MUIR-Torre syndrome","type":"related"},{"name":"Muir-Torre syndrome","type":"exact"},{"name":"cutaneous sebaceous neoplasms and keratoacanthomas multiple with gastrointestinal and other carcinomas","type":"related"},{"name":"cutaneous sebaceous neoplasms and keratoacanthomas, multiple, with gastrointestinal and Other carcinomas","type":"related"},{"name":"multiple keratoacanthoma, Muir-Torre type","type":"exact"}],"termid":"MONDO:0008018","terms_by_termid":{"MONDO:0008018":null},"xrefs":{"Monarch":{"xref_id":"0008018"}}}


id: MONDO:0016916
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete partial deletion of the long arm of chromosome 18 (obsolete MONDO:0016916)","termid":"MONDO:0016916","xrefs":{"Monarch":{"xref_id":"0016916"}}}


id: MONDO:0004568
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An ileus caused by abdominal or pelvic surgery, infections, disorders that affect the muscles and nerves, and medications. Signs and symptoms include those of intestinal obstruction.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ileus","termid":"MONDO:0004567"}],"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":"paralytic ileus","secondary_identifiers":["MESH:D007418","icd11.foundation:1868011045","DOID:8442","ICD9:560.1","SCTID:55525008","HP:0002590","NCIT:C93045","MEDGEN:18293","UMLS:C0030446"],"synonyms":[{"name":"paralytic ileus","type":"exact"},{"name":"paralytic ileus (disease)","type":"exact"}],"termid":"MONDO:0004568","xrefs":{"Monarch":{"xref_id":"0004568"}}}


id: GO:1904677
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of somatic stem cell division.","definition_xrefs":["GOC:BHF","GOC:BHF_miRNA","GOC:rph","PMID:19409607","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell division","termid":"GO:0051781"},{"relation_name":"is_a","term_name":"regulation of somatic stem cell division","termid":"GO:1904675"},{"relation_name":"positively_regulates","term_name":"somatic stem cell division","termid":"GO:0048103"}],"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 somatic stem cell division","synonyms":[{"name":"activation of somatic stem cell division","type":"narrow"},{"name":"activation of somatic stem cell renewal","type":"narrow"},{"name":"positive regulation of somatic stem cell renewal","type":"exact"},{"name":"up regulation of somatic stem cell division","type":"exact"},{"name":"up regulation of somatic stem cell renewal","type":"exact"},{"name":"up-regulation of somatic stem cell division","type":"exact"},{"name":"up-regulation of somatic stem cell renewal","type":"exact"},{"name":"upregulation of somatic stem cell division","type":"exact"},{"name":"upregulation of somatic stem cell renewal","type":"exact"}],"termid":"GO:1904677"}


id: MONDO:0002176
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A malignant neoplasm involving the connective tissue","gene_count":0,"genotype_count":0,"name":"obsolete connective tissue cancer (obsolete MONDO:0002176)","secondary_identifiers":["DOID:201","MESH:D009372","SCTID:126598008"],"synonyms":[{"name":"cancer of connective tissue","type":"exact"},{"name":"connective tissue cancer","type":"exact"},{"name":"connective tissue neoplasm","type":"broad"},{"name":"malignant connective tissue neoplasm","type":"exact"},{"name":"malignant neoplasm of connective tissue","type":"exact"},{"name":"neoplasm of connective tissues","type":"broad"}],"termid":"MONDO:0002176","xrefs":{"Monarch":{"xref_id":"0002176"}}}


id: MONDO:0000746
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. The protrusion of a sac-like structure containing fibroadipose tissue through an abnormal opening in the inguinal region.","definition_xrefs":["NCIT:C34690"],"gene_count":0,"genotype_count":0,"name":"obsolete inguinal hernia (obsolete MONDO:0000746)","secondary_identifiers":["MESH:D006552","ICD9:550.90","SCTID:396232000","ICD9:550","DOID:0060320","HP:0000023"],"termid":"MONDO:0000746","xrefs":{"Monarch":{"xref_id":"0000746"}}}


id: GO:0100056
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any transcription from RNA polymerase II promoter process that negatively regulates phosphatidylserine biosynthetic process.","definition_xrefs":["GOC:cjm","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of phosphatidylserine biosynthetic process by transcription from RNA polymerase II promoter (obsolete GO:0100056)","termid":"GO:0100056"}


id: MOD:00928
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative","definition_xrefs":["PubMed:16771548","Unimod:513"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reagent derivatized residue","termid":"MOD:00848"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"[3-(2,5)-dioxopyrrolidin-1-yloxycarbonyl)-propyl]dimethyloctylammonium","synonyms":[{"name":"C8-QAT","type":"related"},{"name":"[3-(2,5)-Dioxopyrrolidin-1-yloxycarbonyl)-propyl]dimethyloctylammonium","type":"related"}],"termid":"MOD:00928"}


id: PATO:0001688
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An elevation 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 position","termid":"PATO:0001475"},{"relation_name":"is_a","term_name":"elevation","termid":"PATO:0001687"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased elevation","synonyms":[{"name":"elevated","type":"related"},{"name":"high elevation","type":"exact"}],"termid":"PATO:0001688"}


id: PBO:0072283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S24 pseudogene 1","termid":"PBO:0072283"}


id: PBO:0055368
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 2797","termid":"PBO:0055368"}


id: FYPO:0005355
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 site-specific DNA replication termination at RTS1 barrier in the mating type region is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA replication","termid":"FYPO:0000217"},{"relation_name":"is_a","term_name":"abnormal genetic imprinting at mating-type locus","termid":"FYPO:0003079"}],"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":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000293","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abnormal site-specific DNA replication termination at RTS1 barrier","synonyms":[{"name":"abnormal site-specific DNA replication termination at RTS1 barrier during mitotic cell cycle","type":"related"},{"name":"abnormal site-specific DNA replication termination at RTS1 barrier during vegetative growth","type":"exact"}],"termid":"FYPO:0005355"}


id: MONDO:0009861
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Phenylketonuria (PKU) is the most common inborn error of amino acid metabolism and is characterized by mild to severe mental disability in untreated patients.","definition_xrefs":["Orphanet:716"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"disorder of phenylalanine metabolism","termid":"MONDO:0017306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0006025","MONDO:0005066"],"is_obsolete":false,"name":"phenylketonuria","secondary_identifiers":["DOID:9281","MESH:D010661","NANDO:1200785","MEDGEN:19244","UMLS:C0031485","SCTID:7573000","NORD:1574","OMIM:261600","MedDRA:10034872","NANDO:2200467","NANDO:1200784","GARD:7383","NCIT:C81315","icd11.foundation:444122923","ICD9:270.1","NANDO:2201075"],"synonyms":[{"name":"HPA, non-PKU mild","type":"related"},{"name":"PAH deficiency","type":"exact"},{"name":"PKU","type":"exact"},{"name":"hyperphenylalaninemia, non-PKU mild","type":"exact"},{"name":"imbecilitus phenylpyruvica","type":"related"},{"name":"oligophrenia Phenylpyruvica","type":"related"},{"name":"oligophrenia phenylpyruvica","type":"related"},{"name":"phenylalanine hydroxylase deficiency","type":"exact"},{"name":"phenylalaninemia","type":"exact"},{"name":"phenylketonuria","type":"exact"},{"name":"phenylketonuria, maternal","type":"related"},{"name":"phenylpyruvic oligophrenia","type":"related"}],"termid":"MONDO:0009861","xrefs":{"Monarch":{"xref_id":"0009861"}}}


id: PBO:0002308
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HECT-type ubiquitin-protein ligase E3 Pub1","termid":"PBO:0002308"}


id: PBO:0049404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"guanylate cyclase activator 1C","termid":"PBO:0049404"}


id: PBO:0066248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RBMS3 antisense RNA 1","termid":"PBO:0066248"}


id: PBO:0061954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 2 subfamily A member 7","termid":"PBO:0061954"}


id: PBO:0053651
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 703","termid":"PBO:0053651"}


id: PR:000049980
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA repair protein rad9 (Schizosaccharomyces pombe) that has been phosphorylated on a residue equivalent to Ser-423 of the amino acid sequence represented by UniProtKB:P26306. Example: UniProtKB:P26306, Ser-423, MOD:00046.","definition_xrefs":["PomBase:MAH","PRO:CNA","PMID:21561865"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA repair protein rad9 (Schizosaccharomyces pombe)","termid":"PR:000044575"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rad9/Phos(S423)","pombase_gene_id":"SPAC664.07c","synonyms":[{"name":"PomBase_original_PRO_term_name: DNA repair protein rad9 phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"rad9/Phos(S423)","type":"exact"}],"termid":"PR:000049980"}


id: GO:0042777
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ATP driven by transport of protons across a plasma membrane to generate an electrochemical gradient (proton-motive force).","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton motive force-driven ATP synthesis","termid":"GO:0015986"}],"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":"proton motive force-driven plasma membrane ATP synthesis","synonyms":[{"name":"ATP synthesis coupled proton transport","type":"related"},{"name":"plasma membrane ATP synthesis coupled proton transport","type":"related"}],"termid":"GO:0042777"}


id: PBO:0039190
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"akirin 1 pseudogene 1","termid":"PBO:0039190"}


id: PATO:0000481
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000481 negative regulation (obsolete PATO:0000481)","termid":"PATO:0000481"}


id: PBO:0072344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S26 pseudogene 30","termid":"PBO:0072344"}


id: PBO:0063634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"profilin 1 pseudogene 12","termid":"PBO:0063634"}


id: PBO:0108763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"4-phosphoerythronate phosphatase/2-phosphoglycolate phophatase, involved in detoxification of glycolytic by-products","termid":"PBO:0108763"}


id: PBO:0076686
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription elongation factor A like 4","termid":"PBO:0076686"}


id: RO:0002092
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","direct_ancestors":[{"relation_name":"is_a","term_name":"ends_during","termid":"RO:0002093"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"happens_during","termid":"RO:0002092"}


id: GO:0070904
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The directed movement of L-ascorbic acid from one side of an epithelium to the other.","definition_xrefs":["GOC:mah","GOC:yaf"],"gene_count":0,"genotype_count":0,"name":"obsolete transepithelial L-ascorbic acid transport (obsolete GO:0070904)","synonyms":[{"name":"transepithelial L-ascorbate transport","type":"exact"},{"name":"transepithelial vitamin C transport","type":"exact"}],"termid":"GO:0070904"}


id: PR:000059631
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A kinetochore protein spc7 (Schizosaccharomyces pombe) that has been phosphorylated on residues at positions equivalent to Thr-257, Thr-338, Thr-366, Thr-395, Thr-422, Thr-453, Thr-507, Thr-529, and Thr-552 of the amino acid sequence represented by UniProtKB:O59757. Example: UniProtKB:O59757, Thr-257/Thr-338/Thr-366/Thr-395/Thr-422/Thr-453/Thr-507/Thr-529/Thr-552, MOD:00047.","definition_xrefs":["PRO:DAN","PomBase:VW","PMID:22521786"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein","termid":"PR:000000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Spc7/Phos-MELT","pombase_gene_id":"SPCC1020.02","synonyms":[{"name":"PomBase_original_PRO_term_name: kinetochore protein spc7 phosphorylated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spc7/Phos-MELT","type":"exact"},{"name":"Spom-spc7/Phos:1","type":"exact"},{"name":"UniProtKB:O59757, Thr-257/Thr-338/Thr-366/Thr-395/Thr-422/Thr-453/Thr-507/Thr-529/Thr-552, MOD:00047","type":"narrow"}],"termid":"PR:000059631"}


id: GO:0052507
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of symbiont jasmonic acid-mediated signal transduction pathways during the symbiont defense response. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of defense-related symbiont jasmonic acid-mediated signal transduction pathway (obsolete GO:0052507)","synonyms":[{"name":"activation by organism of defense-related symbiont SA-mediated signal transduction pathway","type":"narrow"},{"name":"activation by organism of defense-related symbiont jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"induction by organism of defense-related symbiont SA-mediated signal transduction pathway","type":"narrow"},{"name":"induction by organism of defense-related symbiont jasmonic acid-mediated signal transduction pathway","type":"narrow"},{"name":"positive regulation by organism of defense-related symbiont SA-mediated signal transduction pathway","type":"exact"},{"name":"positive regulation by organism of defense-related symbiont jasmonic acid-mediated signal transduction pathway","type":"exact"},{"name":"upregulation by organism of defense-related symbiont SA-mediated signal transduction pathway","type":"narrow"},{"name":"upregulation by organism of defense-related symbiont jasmonic acid-mediated signal transduction pathway","type":"narrow"}],"termid":"GO:0052507"}


id: PBO:0055288
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 2715","termid":"PBO:0055288"}


id: MONDO:0017979
data:
  {"annotated_genes":["SJAG_00610","SJAG_03453","SJAG_01787"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87002],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013767"},{"annotations":[86172,86173],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:8000024"}]},"cv_name":"mondo","definition":"Autoimmune lymphoproliferative syndrome (ALPS) is a rare, inherited disorder characterized by non-malignant lymphoproliferation, multilineage cytopenias, and a lifelong increased risk of Hodgkin's and non-Hodgkin's lymphoma.","definition_xrefs":["Orphanet:3261"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"lymphoid hemopathy","termid":"MONDO:0015757"},{"relation_name":"is_a","term_name":"type IV hypersensitivity disease","termid":"MONDO:0002459"},{"relation_name":"is_a","term_name":"autoimmune disease","termid":"MONDO:0007179"},{"relation_name":"is_a","term_name":"lymphoproliferative syndrome","termid":"MONDO:0016537"},{"relation_name":"is_a","term_name":"neoplastic syndrome","termid":"MONDO:0021058"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01787":null,"SJAG_03453":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"autoimmune lymphoproliferative syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MedDRA:10069521","GARD:8686","MESH:D056735","DOID:6688","NANDO:1200352","NCIT:C37864","icd11.foundation:1072688797","CSP:1560-5548","ICD9:279.41","NANDO:2200726"],"synonyms":[{"name":"ALPS","type":"exact"},{"name":"ALPS (autoimmune lymphoproliferative syndrome)","type":"exact"},{"name":"Canale-Smith syndrome","type":"exact"},{"name":"FAS deficiency","type":"exact"},{"name":"autoimmune lymphoproliferative syndrome type 1, autosomal dominant","type":"related"}],"termid":"MONDO:0017979","terms_by_termid":{"MONDO:0013767":null,"MONDO:8000024":null},"xrefs":{"Monarch":{"xref_id":"0017979"}}}


id: MONDO:0100051
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mast cell activation syndrome where neither an allergy or other underlying disease is association, nor KIT-mutated mast cells are detectable.","definition_xrefs":["PMID:23409940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mast cell activation syndrome","termid":"MONDO:0100004"},{"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:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"idiopathic mast cell activation syndrome","secondary_identifiers":["MEDGEN:1786072","UMLS:C4267894"],"synonyms":[{"name":"idiopathic MACS","type":"exact"}],"termid":"MONDO:0100051","xrefs":{"Monarch":{"xref_id":"0100051"}}}


id: CHEBI:52717
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"L-Phenylalaninamide substituted at the amide nitrogen by a 1-(dihydroxyboranyl)-3-methylbutyl group and at N(alpha) by a pyrazin-2-ylcarbonyl group. It is a dipeptidyl boronic acid that reversibly inhibits the 26S proteasome.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bortezomib","termid":"CHEBI:52717"}


id: MONDO:0100156
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal recessive disorder characterized by onset of megaloblastic anemia associated with decreased serum vitamin B12 (cobalamin, Cbl) in infancy or early childhood. Low molecular weight (LMW) proteinuria is frequently present, but sometimes occurs later and is usually mild or subclinical. Patients often present with vague symptoms, including failure to thrive, loss of appetite, fatigue, lethargy, and/or recurrent infections. Some patients may present later in childhood with neurologic abnormalities related to B12 deficiency, such as sensorimotor neuropathy and/or cognitive disturbances.","definition_xrefs":["OMIM:261100"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"Imerslund-Grasbeck syndrome","termid":"MONDO:0009853"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0006025","MONDO:0005570","MONDO:0005066"],"is_obsolete":false,"name":"Imerslund-Grasbeck syndrome type 1","secondary_identifiers":["UMLS:C4016819","MEDGEN:865256","NCIT:C131677"],"synonyms":[{"name":"Imerslund-Grasbeck syndrome 1","type":"exact"},{"name":"Imerslund-Grasbeck syndrome type 1","type":"exact"},{"name":"MGA-1","type":"exact"},{"name":"MGA1","type":"exact"},{"name":"Mga1","type":"exact"},{"name":"enterocyte cobalamin malabsorption","type":"exact"},{"name":"enterocyte intrinsic factor receptor, defect of","type":"exact"},{"name":"megaloblastic Anaemia type 1","type":"exact"},{"name":"megaloblastic Anemia type 1","type":"exact"},{"name":"megaloblastic anemia, 1","type":"exact"},{"name":"megaloblastic anemia, Finnish type","type":"exact"},{"name":"pernicious anemia, juvenile, due to selective intestinal malabsorption of vitamin b12, with proteinuria","type":"exact"}],"termid":"MONDO:0100156","xrefs":{"Monarch":{"xref_id":"0100156"}}}


id: MONDO:0014723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome 17","termid":"MONDO:0016967"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PMP22-RAI1 contiguous gene duplication syndrome","secondary_identifiers":["UMLS:C4225255","GARD:17859","OMIM:616652","Orphanet:477817","MEDGEN:894862"],"synonyms":[{"name":"17p11.2p12 microduplication syndrome","type":"exact"},{"name":"YUAN-Harel-Lupski syndrome","type":"related"},{"name":"YUHAL","type":"exact"},{"name":"Yuan-Harel-Lupski syndrome","type":"exact"},{"name":"dup(17)(p11.2p12)","type":"exact"},{"name":"trisomy 17p11.2-p12","type":"exact"},{"name":"trisomy 17p11.2p12","type":"exact"}],"termid":"MONDO:0014723","xrefs":{"Monarch":{"xref_id":"0014723"}}}


id: MONDO:0016571
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Macrocephaly-short stature-paraplegia syndrome is characterized by macrocephaly and midface hypoplasia, intellectual deficit, short stature, spastic paraplegia and severe central nervous system anomalies (hydrocephalus and Dandy-Walker malformation). It has been described in two unrelated adults.","definition_xrefs":["Orphanet:2427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0020022","MONDO:0002320"],"is_obsolete":false,"name":"macrocephaly-short stature-paraplegia syndrome","secondary_identifiers":["SCTID:722033000","MESH:C537718","UMLS:C2931595","MEDGEN:419845","GARD:172"],"synonyms":[{"name":"Volcke Soekarman syndrome","type":"exact"},{"name":"Volcke-Soekarman syndrome","type":"exact"},{"name":"macrocephaly, intellectual disability, short stature, spastic paraplegia and cns malformations","type":"exact"}],"termid":"MONDO:0016571","xrefs":{"Monarch":{"xref_id":"0016571"}}}


id: GO:0045236
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a chemokine receptor in the CXCR family.","definition_xrefs":["PMID:11910892","GOC:ceb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemokine receptor binding","termid":"GO:0042379"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"CXCR chemokine receptor binding","synonyms":[{"name":"C-X-C chemokine receptor ligand","type":"narrow"},{"name":"CXC chemokine receptor ligand","type":"narrow"},{"name":"alpha chemokine receptor binding","type":"exact"},{"name":"alpha chemokine receptor ligand","type":"narrow"}],"termid":"GO:0045236"}


id: PBO:0050166
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 3 pseudogene 22","termid":"PBO:0050166"}


id: PBO:0049575
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2B.W histone 3, pseudogene","termid":"PBO:0049575"}


id: GO:0007268
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The vesicular release of classical neurotransmitter molecules from a presynapse, across a chemical synapse, the subsequent activation of neurotransmitter receptors at the postsynapse of a target cell (neuron, muscle, or secretory cell) and the effects of this activation on the postsynaptic membrane potential and ionic composition of the postsynaptic cytosol. This process encompasses both spontaneous and evoked release of neurotransmitter and all parts of synaptic vesicle exocytosis. Evoked transmission starts with the arrival of an action potential at the presynapse.","definition_xrefs":["GOC:jl","MeSH:D009435"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anterograde trans-synaptic signaling","termid":"GO:0098916"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"chemical synaptic transmission","secondary_identifiers":["Reactome:R-HSA-451307","Wikipedia:Neurotransmission","Reactome:R-HSA-442742","Reactome:R-HSA-9620244","Reactome:R-HSA-442720","Reactome:R-HSA-451308","Reactome:R-HSA-442729","Reactome:R-HSA-9619483","Reactome:R-HSA-9619229","Reactome:R-HSA-112316"],"synonyms":[{"name":"neurotransmission","type":"related"},{"name":"signal transmission across a synapse","type":"broad"},{"name":"synaptic transmission","type":"broad"}],"termid":"GO:0007268"}


id: GO:0004690
data:
  {"annotated_genes":["SJAG_04312","SJAG_01245"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[73747],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004691"},{"annotations":[71328],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0004862"}]},"cv_name":"molecular_function","definition":"cNMP-dependent catalysis of the reaction: ATP + a protein = ADP + a phosphoprotein.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein serine/threonine kinase activity","termid":"GO:0004674"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01245":null,"SJAG_04312":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0003674","GO:0016301","GO:0004672","GO:0140096","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"cyclic nucleotide-dependent protein kinase activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0004690","terms_by_termid":{"GO:0004691":null,"GO:0004862":null}}


id: MONDO:1010652
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pelger-Huet anomaly that occurs in rabbit.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Pelger-Huet anomaly, non-human animal","termid":"MONDO:1010077"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pelger-Huet anomaly, rabbit","secondary_identifiers":["OMIA:000783-9986"],"termid":"MONDO:1010652","xrefs":{"Monarch":{"xref_id":"1010652"}}}


id: GO:0090254
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell elongates and contributes to imaginal disc-derived wing morphogenesis.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unidimensional cell growth","termid":"GO:0009826"},{"relation_name":"is_a","term_name":"post-embryonic animal morphogenesis","termid":"GO:0009886"},{"relation_name":"part_of","term_name":"imaginal disc-derived wing morphogenesis","termid":"GO:0007476"}],"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 elongation involved in imaginal disc-derived wing morphogenesis","termid":"GO:0090254"}


id: GO:0015331
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the stereospecific transfer of asparagine or glutamine across a biological membrane.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete asparagine/glutamine permease activity (obsolete GO:0015331)","synonyms":[{"name":"asparagine/glutamine permease activity","type":"exact"}],"termid":"GO:0015331"}


id: GO:1905693
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of phosphatidic acid biosynthetic process.","definition_xrefs":["GOC:TermGenie","PMID:23767959","GO_REF:0000058","GOC:bc","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of phospholipid biosynthetic process","termid":"GO:0071071"},{"relation_name":"regulates","term_name":"phosphatidic acid biosynthetic process","termid":"GO:0006654"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"regulation of phosphatidic acid biosynthetic process","synonyms":[{"name":"regulation of phosphatidic acid anabolism","type":"exact"},{"name":"regulation of phosphatidic acid biosynthesis","type":"exact"},{"name":"regulation of phosphatidic acid formation","type":"exact"},{"name":"regulation of phosphatidic acid synthesis","type":"exact"}],"termid":"GO:1905693"}


id: PBO:0084184
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Histone deacetylase, component of both the Rpd3S and Rpd3L complexes; regulates transcription, silencing, autophagy and other processes by influencing chromatin remodeling; forms at least two different complexes which have distinct functions and members; Rpd3(L) recruitment to the subtelomeric region is regulated by interaction with the arginine methyltransferase, Hmt1p","termid":"PBO:0084184"}


id: MONDO:0015808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Folliculotropic mycosis fungoides is a rare variant of mycosis fungoides (MF), a form of cutaneous T-cell lymphoma, and is characterized by the presence of folliculotropic infiltrates in patch-plaque lesions usually involving the head and neck area.","definition_xrefs":["Orphanet:178512"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"mycosis fungoides","termid":"MONDO:0009691"},{"relation_name":"is_a","term_name":"secondary catabolic mucinosis of skin","termid":"MONDO:0021655"},{"relation_name":"is_a","term_name":"mycosis fungoides variant","termid":"MONDO:0045071"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"folliculotropic mycosis fungoides","secondary_identifiers":["icd11.foundation:1335995469","GARD:20154","SCTID:404109006","ICD9:701.8","NCIT:C35685","UMLS:C1627767","MEDGEN:302080"],"synonyms":[{"name":"alopecia mucinosa (t cell lymphoma)","type":"related"},{"name":"follicular mucinosis type mycosis fungoides","type":"exact"},{"name":"follicular mycosis fungoides","type":"exact"},{"name":"folliculotropic mycosis fungoides","type":"exact"},{"name":"mycosis fungoides-associated follicular mucinosis","type":"exact"}],"termid":"MONDO:0015808","xrefs":{"Monarch":{"xref_id":"0015808"}}}


id: PBO:0030672
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_heterochromatin_during_vegetative_growth","termid":"PBO:0030672"}


id: PBO:0090946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ER membrane protein disulfide isomerase Pdi4","termid":"PBO:0090946"}


id: MONDO:0012269
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"3q29 microdeletion syndrome is a recurrent subtelomeric deletion syndrome with variable clinical manifestations including intellectual deficit and dysmorphic features.","definition_xrefs":["Orphanet:65286"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 3","termid":"MONDO:0016902"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 3q29 microdeletion syndrome","secondary_identifiers":["OMIM:609425","MESH:C567184","UMLS:C2674949","SCTID:716456000","GARD:11974","DOID:0060419","MEDGEN:393265","DECIPHER:37"],"synonyms":[{"name":"3q subtelomere deletion syndrome","type":"exact"},{"name":"3q29 deletion","type":"related"},{"name":"3q29 deletion syndrome","type":"related"},{"name":"3q29 microdeletion syndrome","type":"exact"},{"name":"3qter deletion","type":"exact"},{"name":"Del(3)(q29)","type":"exact"},{"name":"chromosome 3q29 deletion syndrome","type":"related"},{"name":"chromosome 3q29 microdeletion syndrome, isolated cases","type":"exact"},{"name":"microdeletion 3Q29 syndrome","type":"related"},{"name":"monosomy 3q29","type":"exact"},{"name":"monosomy 3qter","type":"exact"}],"termid":"MONDO:0012269","xrefs":{"Monarch":{"xref_id":"0012269"}}}


id: MONDO:0003942
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chromophobe renal cell carcinoma","termid":"MONDO:0017885"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240","MONDO:0004992"],"is_obsolete":false,"name":"eosinophilic variant of chromophobe renal cell carcinoma","secondary_identifiers":["DOID:6606","MEDGEN:232458","UMLS:C1333405","NCIT:C27889"],"synonyms":[{"name":"eosinophilic variant of chromophobe renal cell carcinoma","type":"exact"}],"termid":"MONDO:0003942","xrefs":{"Monarch":{"xref_id":"0003942"}}}


id: GO:1903994
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of protein stabilization.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:18573880"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of protein stabilization (obsolete GO:1903994)","synonyms":[{"name":"activation of lysosomal protein stabilization","type":"narrow"},{"name":"activation of positive regulation of protein stability","type":"narrow"},{"name":"activation of protein sequestering","type":"related"},{"name":"activation of protein stabilization","type":"narrow"},{"name":"activation of protein stabilization activity","type":"related"},{"name":"positive regulation of lysosomal protein stabilization","type":"narrow"},{"name":"positive regulation of positive regulation of protein stability","type":"exact"},{"name":"positive regulation of protein sequestering","type":"related"},{"name":"positive regulation of protein stabilization","type":"exact"},{"name":"positive regulation of protein stabilization activity","type":"related"},{"name":"up regulation of lysosomal protein stabilization","type":"narrow"},{"name":"up regulation of positive regulation of protein stability","type":"exact"},{"name":"up regulation of protein sequestering","type":"related"},{"name":"up regulation of protein stabilization","type":"exact"},{"name":"up regulation of protein stabilization activity","type":"related"},{"name":"up-regulation of lysosomal protein stabilization","type":"narrow"},{"name":"up-regulation of positive regulation of protein stability","type":"exact"},{"name":"up-regulation of protein sequestering","type":"related"},{"name":"up-regulation of protein stabilization","type":"exact"},{"name":"up-regulation of protein stabilization activity","type":"related"},{"name":"upregulation of lysosomal protein stabilization","type":"narrow"},{"name":"upregulation of positive regulation of protein stability","type":"exact"},{"name":"upregulation of protein sequestering","type":"related"},{"name":"upregulation of protein stabilization","type":"exact"},{"name":"upregulation of protein stabilization activity","type":"related"}],"termid":"GO:1903994"}


id: GO:0061521
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires the specialized structural and/or functional features of a hepatic stellate cell.","definition_xrefs":["GOC:dph","PMID:9407545"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"hepatic stellate cell differentiation","termid":"GO:0061521"}


id: PBO:0066537
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulator of G protein signaling 3","termid":"PBO:0066537"}


id: GO:1990882
data:
  {"annotated_genes":["SJAG_01877"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[72700],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904812"}]},"cv_name":"biological_process","definition":"The modification of rRNA structure by addition of an acetyl group to rRNA. An acetyl group is CH3CO-, derived from acetic [ethanoic] acid.","definition_xrefs":["PMID:25402480"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rRNA modification","termid":"GO:0000154"},{"relation_name":"is_a","term_name":"RNA acetylation","termid":"GO:1990884"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01877":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0042254"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0042254","GO:0044085"],"is_obsolete":false,"name":"rRNA acetylation","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:1990882","terms_by_termid":{"GO:1904812":null}}


id: GO:0075338
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the increase in size or mass of an organism, or the progression of an organism from an initial condition to a later condition, occurring in, on or near the exterior of its host organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation of growth or development of symbiont during interaction with host (obsolete GO:0075338)","synonyms":[{"name":"modulation of growth or development of symbiont during interaction with host","type":"exact"}],"termid":"GO:0075338"}


id: MONDO:0004935
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acquired carotenemia (obsolete MONDO:0004935)","termid":"MONDO:0004935","xrefs":{"Monarch":{"xref_id":"0004935"}}}


id: MONDO:1011792
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"musculoskeletal system disorder, non-human animal","termid":"MONDO:1011335"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subacute progressive myopathy, non-human animal","secondary_identifiers":["OMIA:000696"],"termid":"MONDO:1011792","xrefs":{"Monarch":{"xref_id":"1011792"}}}


id: GO:1901519
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving aspyridone B.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyketide metabolic process","termid":"GO:0030638"},{"relation_name":"is_a","term_name":"pyridine-containing compound metabolic process","termid":"GO:0072524"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0019748"],"is_obsolete":false,"name":"aspyridone B metabolic process","synonyms":[{"name":"aspyridone B metabolism","type":"exact"}],"termid":"GO:1901519"}


id: PBO:0053217
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galectin 14","termid":"PBO:0053217"}


id: PBO:0044146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chitobiase","termid":"PBO:0044146"}


id: GO:0006382
data:
  {"annotated_genes":["SJAG_00352","SJAG_04380","SJAG_04189"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[101432,59301,74059],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0002100"}]},"cv_name":"biological_process","definition":"The conversion of an adenosine residue to inosine in an RNA molecule by deamination.","definition_xrefs":["PMID:11092837"],"direct_ancestors":[{"relation_name":"is_a","term_name":"base conversion or substitution editing","termid":"GO:0016553"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00352":null,"SJAG_04189":null,"SJAG_04380":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"adenosine to inosine editing","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-75064"],"termid":"GO:0006382","terms_by_termid":{"GO:0002100":null}}


id: GO:0034464
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A ciliary protein complex involved in cilium biogenesis. It consists of at least seven Bardet-Biedl syndrome (BBS) proteins and BBIP10. It moves in association with IFT trains through cilia (likely as an IFT-A/B adaptor or cargo), and is required for the integrity of IFT-A and IFT-B.","definition_xrefs":["PMID:15231740","PMID:17574030","GOC:cilia","GOC:BHF","PMID:26498262"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cilium","termid":"GO:0005929"}],"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":"BBSome","synonyms":[{"name":"Bardet-Biedl syndrome complex","type":"exact"}],"termid":"GO:0034464"}


id: PBO:0063300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PC-esterase domain containing 1A","termid":"PBO:0063300"}


id: GO:1990861
data:
  {"annotated_genes":["SJAG_02663"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[79297],"is_not":false,"summary":null,"term":"GO:1990861"}]},"cv_name":"cellular_component","definition":"A protein complex that cleaves ubiquitin from specific substrates. In the budding yeast Saccharomyces cerevisiae, this complex consists of Ubp3p and Bre5p.","definition_xrefs":["GOC:rb","PMID:12778054","PMID:18391941"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peptidase complex","termid":"GO:1905368"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02663":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"Ubp3-Bre5 deubiquitination complex","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"Ubp3-Bre5 ubiquitin protease complex","type":"exact"}],"termid":"GO:1990861","terms_by_termid":{"GO:1990861":null}}


id: PBO:0090130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-FYVE type zinc finger protein and glutamine sensor Pib2","termid":"PBO:0090130"}


id: PBO:0058501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5692c-1","termid":"PBO:0058501"}


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


id: PATO:0001790
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A density which is lower relative to the normal or average.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"dense","termid":"PATO:0001164"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased mass density","synonyms":[{"name":"low density","type":"exact"}],"termid":"PATO:0001790"}


id: GO:0140341
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the movement of phosphatidylethanolamine from the cytosolic to the exoplasmic leaflet of a membrane, using energy from the hydrolysis of ATP.","definition_xrefs":["PMID:10029989"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid transporter activity","termid":"GO:0005548"},{"relation_name":"is_a","term_name":"floppase activity","termid":"GO:0140328"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140303"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0140303","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"phosphatidylethanolamine floppase activity","synonyms":[{"name":"phosphatidylethanolamine floppase activity (cytosolic to exoplasmic leaflet)","type":"exact"}],"termid":"GO:0140341"}


id: GO:0000269
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the energy independent passage of toxins, sized less than 1000 Da, across a membrane towards the outside of the cell. The transmembrane portions of porins consist exclusively of beta-strands which form a beta-barrel. They are found in the outer membranes of Gram-negative bacteria, mitochondria, plastids and possibly acid-fast Gram-positive bacteria.","definition_xrefs":["GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porin activity","termid":"GO:0015288"},{"relation_name":"is_a","term_name":"toxin transmembrane transporter activity","termid":"GO:0019534"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"toxin export channel activity","termid":"GO:0000269"}


id: PBO:0011137
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor Pho7","termid":"PBO:0011137"}


id: PBO:0031496
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_methyl_methanesulfonate","termid":"PBO:0031496"}


id: PBO:0052993
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LAMA4 antisense RNA 1","termid":"PBO:0052993"}


id: FYPO:0002695
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of methylenetetrahydrofolate reductase (NADPH) activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal oxidoreductase activity","termid":"FYPO:0000689"}],"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:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000661","FYPO:0001985","FYPO:0000707","FYPO:0000654"],"is_obsolete":false,"name":"abnormal methylenetetrahydrofolate reductase (NADPH) activity","termid":"FYPO:0002695"}


id: MONDO:0002056
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign tumor of the breast characterized by the presence of stromal and epithelial elements. It presents as a painless, solitary, slow growing, firm, and mobile mass. It is the most common benign breast lesion. It usually occurs in women of childbearing age. The majority of fibroadenomas do not recur after complete excision. A slightly increased risk of developing cancer within fibroadenomas or in the breast tissue of patients previously treated for fibroadenomas has been reported.","definition_xrefs":["NCIT:C3744"],"direct_ancestors":[{"relation_name":"is_a","term_name":"breast benign neoplasm","termid":"MONDO:0000620"},{"relation_name":"is_a","term_name":"breast fibroepithelial neoplasm","termid":"MONDO:0021046"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast fibroadenoma","secondary_identifiers":["SCTID:254847007","ICDO:9010/0","ONCOTREE:FA","MEDGEN:64231","DOID:1618","UMLS:C0178421","MESH:D018226"],"synonyms":[{"name":"Complex fibroadenoma of breast","type":"exact"},{"name":"FA","type":"related"},{"name":"breast fibroadenoma","type":"exact"},{"name":"cellular fibroadenoma","type":"exact"},{"name":"fibroadenoma","type":"exact"},{"name":"fibroadenoma of breast","type":"exact"},{"name":"fibroadenoma of the breast","type":"exact"},{"name":"fibroadenoma, benign","type":"exact"},{"name":"juvenile fibroadenoma","type":"exact"},{"name":"juvenile fibroadenoma (morphologic abnormality)","type":"exact"},{"name":"juvenile fibroadenoma of breast","type":"exact"}],"termid":"MONDO:0002056","xrefs":{"Monarch":{"xref_id":"0002056"}}}


id: GO:0004299
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the cleavage at peptide bonds with very broad specificity.","definition_xrefs":["EC:3.4.25.1"],"gene_count":0,"genotype_count":0,"name":"obsolete proteasome endopeptidase activity (obsolete GO:0004299)","synonyms":[{"name":"multicatalytic endopeptidase","type":"related"},{"name":"proteasome","type":"related"},{"name":"proteasome endopeptidase activity","type":"exact"},{"name":"proteasome endopeptidase complex","type":"related"}],"termid":"GO:0004299"}


id: GO:1990578
data:
  {"annotated_genes":["SJAG_01329","SJAG_04583","SJAG_00784","SJAG_03281","SJAG_01785","SJAG_01227","SJAG_01422"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[87715,95054,98130,98982,100923,106646,115903],"is_not":false,"summary":null,"term":"GO:1990578"}]},"cv_name":"cellular_component","definition":"The membrane of the perinuclear endoplasmic reticulum, which is the portion of endoplasmic reticulum, the intracellular network of tubules and cisternae, that occurs near the nucleus.","definition_xrefs":["PMID:25454947"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle membrane","termid":"GO:0031090"},{"relation_name":"part_of","term_name":"endoplasmic reticulum membrane","termid":"GO:0005789"},{"relation_name":"part_of","term_name":"perinuclear endoplasmic reticulum","termid":"GO:0097038"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00784":null,"SJAG_01227":null,"SJAG_01329":null,"SJAG_01422":null,"SJAG_01785":null,"SJAG_03281":null,"SJAG_04583":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005789"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005783"}],"interesting_parent_ids":["GO:0005789","GO:0005737","GO:0005783","GO:0005575"],"is_obsolete":false,"name":"perinuclear endoplasmic reticulum membrane","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"perinuclear ER membrane","type":"exact"}],"termid":"GO:1990578","terms_by_termid":{"GO:1990578":null}}


id: PBO:0005043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DUF1751 family protein","termid":"PBO:0005043"}


id: PBO:0079646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2R2 antisense RNA 1","termid":"PBO:0079646"}


id: PBO:0051795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQCJ-SCHIP1 readthrough antisense RNA 1","termid":"PBO:0051795"}


id: PBO:0071326
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L27 pseudogene 2","termid":"PBO:0071326"}


id: PBO:0041784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CAPS2 antisense RNA 1","termid":"PBO:0041784"}


id: GO:0015187
data:
  {"annotated_genes":["SJAG_00626","SJAG_04984"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70288,78201],"is_not":false,"summary":null,"term":"GO:0015187"}]},"cv_name":"molecular_function","definition":"Enables the transfer of glycine from one side of a membrane to the other. Glycine is aminoethanoic acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"neutral L-amino acid transmembrane transporter activity","termid":"GO:0015175"},{"relation_name":"is_a","term_name":"carboxylic acid transmembrane transporter activity","termid":"GO:0046943"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00626":null,"SJAG_04984":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"glycine transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"glycine betaine/proline porter activity","type":"narrow"},{"name":"glycine transporter activity","type":"broad"},{"name":"proline/glycine/betaine:hydrogen/sodium symporter activity","type":"narrow"}],"termid":"GO:0015187","terms_by_termid":{"GO:0015187":null}}


id: GO:0102326
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-hydroxy-6-oxo-6-(2,3-dihydroxyphenyl)-hexa-2,4-dienoate + H2O = 2,3-dihydroxybenzoate + 2-oxopent-4-enoate + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-hydroxy-6-oxo-6-(2,3-dihydroxyphenyl)-hexa-2,4-dienoate hydrolase activity (obsolete GO:0102326)","termid":"GO:0102326"}


id: GO:1901679
data:
  {"annotated_genes":["SJAG_04328","SJAG_00760","SJAG_00612","SJAG_02050","SJAG_03503","SJAG_00154","SJAG_03334"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63931],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903790"},{"annotations":[101678],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990554"},{"annotations":[101679],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990553"},{"annotations":[58912],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140021"},{"annotations":[103171,58911],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990544"},{"annotations":[107875],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990548"},{"annotations":[93246],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990549"},{"annotations":[79564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990519"}]},"cv_name":"biological_process","definition":"The directed movement of nucleotide across a membrane.","definition_xrefs":["GOC:TermGenie","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide transport","termid":"GO:0006862"},{"relation_name":"is_a","term_name":"transmembrane transport","termid":"GO:0055085"}],"gene_count":7,"genes_by_uniquename":{"SJAG_00154":null,"SJAG_00612":null,"SJAG_00760":null,"SJAG_02050":null,"SJAG_03334":null,"SJAG_03503":null,"SJAG_04328":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179","GO:0055085"],"is_obsolete":false,"name":"nucleotide transmembrane transport","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"nucleotide membrane transport","type":"exact"}],"termid":"GO:1901679","terms_by_termid":{"GO:0140021":null,"GO:1903790":null,"GO:1990519":null,"GO:1990544":null,"GO:1990548":null,"GO:1990549":null,"GO:1990553":null,"GO:1990554":null}}


id: PBO:0057714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1301","termid":"PBO:0057714"}


id: PBO:0004073
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diacylglycerol binding protein Bzz1 (predicted)","termid":"PBO:0004073"}


id: PBO:0038945
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acireductone dioxygenase 1","termid":"PBO:0038945"}


id: MONDO:0018539
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare epithelial tumor of small intestine (obsolete MONDO:0018539)","secondary_identifiers":["Orphanet:425368"],"synonyms":[{"name":"rare epithelial tumor of small bowel","type":"exact"}],"termid":"MONDO:0018539","xrefs":{"Monarch":{"xref_id":"0018539"}}}


id: GO:0140856
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a ubiquitin molecule to histone 2A at the lysine-13 residue.","definition_xrefs":["PMID:22980979","PMID:28624371"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H2A ubiquitin ligase activity","termid":"GO:0141053"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0004842"},{"rel_name":"is_a","termid":"GO:0019787"},{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0140096","GO:0003824","GO:0004842","GO:0016746","GO:0019787"],"is_obsolete":false,"name":"histone H2AK13 ubiquitin ligase activity","synonyms":[{"name":"histone ubiquitin ligase activity (H2A-K13 specific)","type":"exact"}],"termid":"GO:0140856"}


id: PBO:0113411
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L24B; forms two bridges within ribosome, stimulates translation initiation and elongation; homologous to mammalian ribosomal protein L24, no bacterial homolog; RPL24B has a paralog, RPL24A, that arose from the whole genome duplication","termid":"PBO:0113411"}


id: FYPO:0007114
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the amount, distribution, and morphology of microtubule bundles are normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal subcellular component","termid":"FYPO:0001233"}],"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:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal microtubule bundle","synonyms":[{"name":"normal MT bundle","type":"exact"},{"name":"normal microtubule array","type":"related"},{"name":"normal microtubule bundle physical object quality","type":"exact"}],"termid":"FYPO:0007114"}


id: PBO:0042103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 175","termid":"PBO:0042103"}


id: MONDO:0015248
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by cerebellar-like ataxia, photosensitivity (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, single palmar transverse crease, high-arched palate, pseudohypertrophy of the calves and aortic valve lesions. There have been no further descriptions in the literature since 1983.","definition_xrefs":["Orphanet:1184"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary ataxia","termid":"MONDO:0100309"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ataxia-photosensitivity-short stature syndrome","secondary_identifiers":["MEDGEN:1655873","UMLS:C4751230","GARD:2287"],"synonyms":[{"name":"Fenton Wilkinson Toselano syndrome","type":"exact"},{"name":"Fenton-Wilkinson-Toselano syndrome","type":"exact"}],"termid":"MONDO:0015248","xrefs":{"Monarch":{"xref_id":"0015248"}}}


id: MOD:01292
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"OBSOLETE because redundant and identical to MOD:00075. Map to MOD:00075.","definition_xrefs":["Unimod:529"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE MOD:01292 dimethylation of proline residue (obsolete MOD:01292)","synonyms":[{"name":"Delta:H(5)C(2)","type":"related"},{"name":"Dimethylation of proline residue","type":"related"}],"termid":"MOD:01292"}


id: FYPO:0005115
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is elongated and has an abnormal shape featuring a constriction at the center of the cell, corresponding to the cell division site. In some such cells, the diameter at the ends is much greater than in wild-type cells.","definition_xrefs":["PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"elongated vegetative cell","termid":"FYPO:0001122"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"elongated vegetative cell with central constriction","synonyms":[{"name":"cell morphology, elongated dumbbell","type":"related"},{"name":"cell morphology, long dumbbell","type":"related"},{"name":"elongated cell with central constriction during mitotic cell cycle","type":"related"},{"name":"elongated cell with central constriction during vegetative growth","type":"exact"},{"name":"elongated dumbbell morphology","type":"related"},{"name":"elongated dumbbell-shaped vegetative cell","type":"related"},{"name":"elongated swollen vegetative cell with constricted region at cell division site","type":"exact"}],"termid":"FYPO:0005115"}


id: PBO:0108836
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GATOR1-SEACIT GTPase activating complex subunit Iml1","termid":"PBO:0108836"}


id: PBO:0079661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBE2V1 pseudogene 9","termid":"PBO:0079661"}


id: GO:0033390
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of putrescine, 1,4-diaminobutane, from other compounds, including arginine, via the intermediate N-carbamoylputrescine; in this pathway, arginine is converted to agmatine, and agmatine is converted to putrescine in two single enzymatic steps.","definition_xrefs":["GOC:mah","MetaCyc:PWY-43"],"direct_ancestors":[{"relation_name":"is_a","term_name":"putrescine biosynthetic process from arginine","termid":"GO:0033388"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006520"}],"interesting_parent_ids":["GO:0006520","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"putrescine biosynthetic process from arginine via N-carbamoylputrescine","synonyms":[{"name":"putrescine anabolism from arginine via N-carbamoylputrescine","type":"exact"},{"name":"putrescine biosynthesis from arginine via N-carbamoylputrescine","type":"exact"},{"name":"putrescine formation from arginine via N-carbamoylputrescine","type":"exact"},{"name":"putrescine synthesis from arginine via N-carbamoylputrescine","type":"exact"}],"termid":"GO:0033390"}


id: GO:0007144
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which the first meiotic division occurs in the female germline.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiosis I","termid":"GO:0007127"},{"relation_name":"is_a","term_name":"female meiotic nuclear division","termid":"GO:0007143"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0140013"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0140013","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"female meiosis I","synonyms":[{"name":"female meiosis I nuclear division","type":"exact"}],"termid":"GO:0007144"}


id: MONDO:1010016
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Mitral valve stenosis that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder, non-human animal","termid":"MONDO:1012982"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitral valve stenosis, non-human animal","secondary_identifiers":["OMIA:000655"],"termid":"MONDO:1010016","xrefs":{"Monarch":{"xref_id":"1010016"}}}


id: GO:0046922
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of an alpha-L-fucosyl residue from GDP- beta-L-fucose to the serine hydroxy group of a protein acceptor.","definition_xrefs":["EC:2.4.1.221"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fucosyltransferase activity","termid":"GO:0008417"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a protein","termid":"GO:0140096"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016757","GO:0016740","GO:0003824","GO:0003674","GO:0140096"],"is_obsolete":false,"name":"peptide-O-fucosyltransferase activity","secondary_identifiers":["Reactome:R-HSA-1912349","Reactome:R-HSA-5173192","MetaCyc:2.4.1.221-RXN"],"synonyms":[{"name":"GDP-L-fucose:polypeptide fucosyltransferase activity","type":"related"},{"name":"GDP-beta-L-fucose:polypeptide O-alpha-L-fucosyltransferase activity","type":"related"},{"name":"GDP-fucose protein O-fucosyltransferase activity","type":"related"},{"name":"GDP-fucose:polypeptide fucosyltransferase activity","type":"related"}],"termid":"GO:0046922"}


id: GO:0021852
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The migration of a pyramidal neuron precursor from the ventricular zone to the correct layer of the cerebral cortex.","definition_xrefs":["GOC:jid","PMID:12626695","PMID:22192824","GO_REF:0000021","GOC:cls","GOC:dgh","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebral cortex radial glia-guided migration","termid":"GO:0021801"},{"relation_name":"is_a","term_name":"radial glia-guided pyramidal neuron migration","termid":"GO:0140650"},{"relation_name":"part_of","term_name":"pyramidal neuron development","termid":"GO:0021860"}],"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":"pyramidal neuron migration to cerebral cortex","synonyms":[{"name":"projection neuron migration","type":"related"},{"name":"pyramidal neuron migration","type":"broad"}],"termid":"GO:0021852"}


id: PBO:0083107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DnaJ-like chaperone required for nuclear membrane fusion during mating; localizes to the ER membrane; exhibits genetic interactions with KAR2","termid":"PBO:0083107"}


id: MONDO:0859218
data:
  {"annotated_genes":["SJAG_03265"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86461],"is_not":false,"summary":null,"term":"MONDO:0859218"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03265":null},"genotype_count":0,"is_obsolete":false,"name":"developmental delay with variable neurologic and brain abnormalities","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:619694","MEDGEN:1794270","UMLS:C5562060"],"termid":"MONDO:0859218","terms_by_termid":{"MONDO:0859218":null},"xrefs":{"Monarch":{"xref_id":"0859218"}}}


id: MONDO:0000501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Jensen syndrome (obsolete MONDO:0000501)","secondary_identifiers":["MESH:C537568","DOID:0050867"],"synonyms":[{"name":"Jensen syndrome","type":"related"},{"name":"Opticoacustic nerve atrophy with dementia","type":"related"},{"name":"deafness-opticoacoustic nerve atrophy-dementia syndrome","type":"related"},{"name":"nerve deafness optic nerve atrophy, and dementia","type":"related"},{"name":"opticoacoustic nerve atrophy with dementia","type":"exact"},{"name":"syndrome of opticoacoustic nerve atrophy with dementia","type":"related"}],"termid":"MONDO:0000501","xrefs":{"Monarch":{"xref_id":"0000501"}}}


id: GO:0036075
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Ossification that requires the replacement of a preexisting tissue prior to bone tissue formation.","definition_xrefs":["GO_REF:0000034"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ossification","termid":"GO:0001503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"replacement ossification","synonyms":[{"name":"indirect ossification","type":"exact"}],"termid":"GO:0036075"}


id: GO:0034718
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the survival motor neuron (SMN) protein and Gemin2; may form the stable core of the larger SMN complex.","definition_xrefs":["GOC:mah","PMID:17640873"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription regulator complex","termid":"GO:0090575"},{"relation_name":"is_a","term_name":"Sm-like protein family complex","termid":"GO:0120114"}],"gene_count":0,"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"}],"interesting_parent_ids":["GO:0005575","GO:0032991","GO:0005634"],"is_obsolete":false,"name":"SMN-Gemin2 complex","termid":"GO:0034718"}


id: GO:1902515
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of thioredoxin-disulfide reductase activity.","definition_xrefs":["GOC:bhm","PMID:10947986","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase complex","termid":"GO:1990204"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"thioredoxin-disulfide reductase complex","termid":"GO:1902515"}


id: PBO:0076919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor AP-4","termid":"PBO:0076919"}


id: GO:1902366
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of Notch signaling pathway involved in somitogenesis.","definition_xrefs":["PMID:21795391","GOC:dph","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of Notch signaling pathway","termid":"GO:0008593"},{"relation_name":"regulates","term_name":"Notch signaling pathway involved in somitogenesis","termid":"GO:1902359"}],"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:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of Notch signaling pathway involved in somitogenesis","synonyms":[{"name":"regulation of N signaling pathway involved in formation of mesodermal clusters","type":"exact"},{"name":"regulation of N signaling pathway involved in somitogenesis","type":"exact"},{"name":"regulation of N signalling pathway involved in formation of mesodermal clusters","type":"exact"},{"name":"regulation of N signalling pathway involved in somitogenesis","type":"exact"},{"name":"regulation of Notch receptor signaling pathway involved in formation of mesodermal clusters","type":"exact"},{"name":"regulation of Notch receptor signaling pathway involved in somitogenesis","type":"exact"},{"name":"regulation of Notch receptor signalling pathway involved in formation of mesodermal clusters","type":"exact"},{"name":"regulation of Notch receptor signalling pathway involved in somitogenesis","type":"exact"},{"name":"regulation of Notch signaling pathway involved in formation of mesodermal clusters","type":"exact"},{"name":"regulation of Notch signalling pathway involved in formation of mesodermal clusters","type":"exact"},{"name":"regulation of Notch signalling pathway involved in somitogenesis","type":"exact"},{"name":"regulation of Notch-receptor signaling pathway involved in formation of mesodermal clusters","type":"exact"},{"name":"regulation of Notch-receptor signaling pathway involved in somitogenesis","type":"exact"},{"name":"regulation of Notch-receptor signalling pathway involved in formation of mesodermal clusters","type":"exact"},{"name":"regulation of Notch-receptor signalling pathway involved in somitogenesis","type":"exact"}],"termid":"GO:1902366"}


id: FYECO:0000319
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which brefeldin A (BFA) was added to the medium or assay buffer.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ BFA","synonyms":[{"name":"+ brefeldin A","type":"exact"}],"termid":"FYECO:0000319"}


id: PBO:0001176
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.1.11.-","termid":"PBO:0001176"}


id: PBO:0117112
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SCFD2 antisense RNA 1","termid":"PBO:0117112"}


id: GO:0048577
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces short-day photoperiodism, where the response associated with the photoperiodism is flowering. Flowering is defined by the switch from the vegetative to the reproductive phase.","definition_xrefs":["ISBN:0709408862","ISBN:0697037754","GOC:pj","ISBN:0582015952","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of post-embryonic development","termid":"GO:0048581"},{"relation_name":"is_a","term_name":"negative regulation of response to stimulus","termid":"GO:0048585"},{"relation_name":"is_a","term_name":"regulation of short-day photoperiodism, flowering","termid":"GO:0048587"},{"relation_name":"negatively_regulates","term_name":"short-day photoperiodism, flowering","termid":"GO:0048575"}],"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 short-day photoperiodism, flowering","synonyms":[{"name":"down regulation of short-day photoperiodism, flowering","type":"exact"},{"name":"down-regulation of short-day photoperiodism, flowering","type":"exact"},{"name":"downregulation of short-day photoperiodism, flowering","type":"exact"},{"name":"inhibition of short-day photoperiodism, flowering","type":"narrow"}],"termid":"GO:0048577"}


id: PBO:0001296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PUA domain","termid":"PBO:0001296"}


id: MOD:00889
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-prolinium (charged L-proline) residue to N,N-dimethyl-L-proline.","definition_xrefs":["Unimod:36#P"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"protonated L-proline (L-prolinium) residue","termid":"MOD:00888"},{"relation_name":"is_a","term_name":"N,N-dimethyl-L-proline","termid":"MOD:00075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"N,N-dimethyl-L-proline (from L-prolinium)","termid":"MOD:00889"}


id: PBO:0004246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"condensin complex subunit Cut14","termid":"PBO:0004246"}


id: GO:1903153
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any ferrous iron transmembrane transporter activity that is involved in ferrous iron import into cell.","definition_xrefs":["GO_REF:0000061","GOC:TermGenie","ISBN:0-8249-3695-6","GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete ferrous iron transmembrane transporter activity involved in ferrous iron import into cell (obsolete GO:1903153)","synonyms":[{"name":"ferrous iron transmembrane transporter activity involved in ferrous ion import into cell","type":"exact"},{"name":"ferrous iron transmembrane transporter activity involved in ferrous iron import into cell","type":"exact"}],"termid":"GO:1903153"}


id: GO:0034303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which differentiated, resting cells are formed, usually within a fruiting body by Myxobacteria. The myxospore is more resistant to high temperature, desiccation, and UV than vegetative myxobacteria.","definition_xrefs":["ISBN:0122268008","GOC:ds"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asexual sporulation resulting in formation of a cellular spore","termid":"GO:0043936"}],"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":"myxospore formation","termid":"GO:0034303"}


id: MONDO:1011021
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary late onset progressive symmetric ataxia, truncal sway, pelvic limb hypermetria, and impaired balance in dogs due to a variation in the CAPN1 gene.","definition_xrefs":["PMID:37341581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder, non-human animal","termid":"MONDO:1011308"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spinocerebellar ataxia, CAPN1-related, dog","secondary_identifiers":["OMIA:001820-9615"],"termid":"MONDO:1011021","xrefs":{"Monarch":{"xref_id":"1011021"}}}


id: FYPO:0000372
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of RNA modification is decreased. All RNA modification may be decreased, or one or more specific RNA modifications may be selectively affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal RNA modification","termid":"FYPO:0000370"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000294"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000294","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased RNA modification","synonyms":[{"name":"RNA modification: decreased","type":"related"},{"name":"decreased RNA modification during mitotic cell cycle","type":"related"},{"name":"decreased RNA modification during vegetative growth","type":"exact"},{"name":"reduced RNA modification","type":"exact"}],"termid":"FYPO:0000372"}


id: PBO:0079505
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin pseudogene 3","termid":"PBO:0079505"}


id: PBO:0086367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative alternate subunit of succinate dehydrogenase (SDH); mitochondrial inner membrane protein; genetic interaction with SDH4 suggests that Shh4p can function as a functional SDH subunit; a fraction copurifies with SDH subunit Sdh3p; expression induced by nitrogen limitation in a GLN3, GAT1-dependent manner; Shh4p has greater similarity to human SDHD (subunit D of SDH, implicated in paraganglioma) than does its paralog Sdh4p","termid":"PBO:0086367"}


id: PBO:0110380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IL9R pseudogene 6","termid":"PBO:0110380"}


id: PBO:0042886
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 299","termid":"PBO:0042886"}


id: MONDO:0044319
data:
  {"annotated_genes":["SJAG_02774"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87059],"is_not":false,"summary":null,"term":"MONDO:0044319"}]},"cv_name":"mondo","definition":"IDDFSDA is an autosomal recessive severe multisystem disorder characterized by poor overall growth, developmental delay, early-onset seizures, intellectual disability, and dysmorphic features. There is phenotypic variability. The most severely affected patients have a neurodevelopmental disorder with microcephaly, absent speech, and inability to walk, and they require feeding tubes. Some patients have congenital heart defects or nonspecific abnormalities on brain imaging. Less severely affected individuals have mild to moderate intellectual disability with normal speech and motor development (summary by {1:Santiago-Sim et al., 2017}).","definition_xrefs":["OMIM:617452"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"monogenic epilepsy","termid":"MONDO:0015653"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02774":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005027"],"is_obsolete":false,"name":"intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4479520","GARD:17942","Orphanet:505237","MEDGEN:1375601"],"synonyms":[{"name":"IDDFSDA","type":"related"},{"name":"intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies","type":"exact"}],"termid":"MONDO:0044319","terms_by_termid":{"MONDO:0044319":null},"xrefs":{"Monarch":{"xref_id":"0044319"}}}


id: PBO:0048282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GALNT16 and EXD2 antisense RNA 1","termid":"PBO:0048282"}


id: MONDO:1012130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"immunoglobulin A deficiency, non-human animal","termid":"MONDO:1011726"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin A deficiency, dog","secondary_identifiers":["OMIA:000552-9615"],"termid":"MONDO:1012130","xrefs":{"Monarch":{"xref_id":"1012130"}}}


id: MONDO:0008841
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ataxia telangiectasia","termid":"MONDO:0008840"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005047","MONDO:0005559"],"is_obsolete":false,"name":"ataxia-telangiectasia with generalized skin pigmentation and early death","secondary_identifiers":["OMIM:208910","UMLS:C1859615","GARD:15141","MEDGEN:395306","MESH:C565930"],"synonyms":[{"name":"ataxia-telangiectasia with generalized skin pigmentation and early death","type":"exact"}],"termid":"MONDO:0008841","xrefs":{"Monarch":{"xref_id":"0008841"}}}


id: PBO:0068246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 28S ribosomal 3","termid":"PBO:0068246"}


id: GO:0031458
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2O + a betaine(out) = ADP + phosphate + a betaine(in).","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"ABC-type betaine transporter activity","synonyms":[{"name":"ABC-type betaine transmembrane transporter activity","type":"exact"},{"name":"ATP-dependent betaine transporter activity","type":"exact"},{"name":"ATPase-coupled betaine transporter activity","type":"related"},{"name":"betaine ABC transporter","type":"narrow"},{"name":"betaine-transporting ATPase activity","type":"exact"}],"termid":"GO:0031458"}


id: MOD:00742
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes a copper atom or a cluster containing copper for hydrogen atoms, or that coordinates a copper ion.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metal or metal cluster containing modified residue","termid":"MOD:00698"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"copper containing modified residue","synonyms":[{"name":"CuRes","type":"exact"}],"termid":"MOD:00742"}


id: MONDO:0010191
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Type 3 von Willebrand disease (type 3 VWD) is the most severe form of VWD characterized by a bleeding disorder associated with a total or near-total absence of Willebrand factor (von Willebrand factor; VWF) in the plasma and cellular compartments, also leading to a profound deficiency of plasmatic factor VIII (FVIII).","definition_xrefs":["Orphanet:166096"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary von Willebrand disease","termid":"MONDO:0019565"}],"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":"von Willebrand disease 3","secondary_identifiers":["GARD:17025","OMIM:277480","DOID:0111054","UMLS:C1264041","SCTID:128108002","MEDGEN:266075","MESH:D056729","NCIT:C85213"],"synonyms":[{"name":"VON WILLEBRAND disease, type 3","type":"related"},{"name":"VWD type 3","type":"exact"},{"name":"VWD, type 3","type":"related"},{"name":"VWD3","type":"exact"},{"name":"Von Willebrand disease, type 3","type":"related"},{"name":"von Willebrand disease 3","type":"exact"},{"name":"von Willebrand disease type 3","type":"exact"},{"name":"von Willebrand disease type III","type":"exact"},{"name":"von Willebrand's disease 3","type":"exact"},{"name":"von Willebrand's disease type 3","type":"exact"}],"termid":"MONDO:0010191","xrefs":{"Monarch":{"xref_id":"0010191"}}}


id: PBO:0082681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the ESCRT-II complex; contains the GLUE (GRAM Like Ubiquitin binding in EAP45) domain which is involved in interactions with ESCRT-I and ubiquitin-dependent sorting of proteins into the endosome; plays a role in the formation of mutant huntingtin (Htt) aggregates in yeast","termid":"PBO:0082681"}


id: MONDO:0700262
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any type 1 interferonopathies in which the cause of the disease is a variation in the IFIH1 gene. Individuals with variants in IFIH1 can present with a variety of phenotypes, including Aicardi-Goutieres syndrome and singleton-Merten syndrome.","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"type 1 interferonopathy","termid":"MONDO:0700264"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IFIH1-related type 1 interferonopathy","termid":"MONDO:0700262","xrefs":{"Monarch":{"xref_id":"0700262"}}}


id: PBO:0066677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RLF pseudogene 1","termid":"PBO:0066677"}


id: PBO:0038278
data:
  {"annotation_feature_type":"gene","cv_name":"feature_relationshipprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eco_evidence","termid":"PBO:0038278"}


id: PBO:0038622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alkaline ceramidase 3","termid":"PBO:0038622"}


id: FYPO:0007663
data:
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id: PBO:0060997
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id: PBO:0076779
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TEA domain transcription factor 2","termid":"PBO:0076779"}


id: GO:0002043
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id: GO:0048766
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id: GO:0048583
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id: PBO:0056714
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id: MONDO:0003599
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare malignant adipose tissue neoplasm of the vulva.","definition_xrefs":["NCIT:C40321"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"},{"relation_name":"is_a","term_name":"vulva sarcoma","termid":"MONDO:0005214"}],"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":"vulvar liposarcoma","secondary_identifiers":["DOID:5711","UMLS:C2184082","MEDGEN:412161"],"synonyms":[{"name":"liposarcoma of mammalian vulva","type":"exact"},{"name":"mammalian vulva liposarcoma","type":"exact"},{"name":"vulvar liposarcoma","type":"exact"}],"termid":"MONDO:0003599","xrefs":{"Monarch":{"xref_id":"0003599"}}}


id: PBO:0067825
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 127","termid":"PBO:0067825"}


id: PBO:0082976
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic thioredoxin isoenzyme; part of the thioredoxin system that protects cells from oxidative and reductive stress; subunit of the LMA1 complex, with Pbi2p, that promotes vacuole inheritance; cofactor for Tsa1p; required for ER-Golgi transport; facilitates mitochondrial import of small Tims (Tim9p, Tim10p, Tim13p) by maintaining them in reduced form along with Trx2p; component of a signal transduction redox relay in a light sensing pathway; abundance increases under DNA replication stress","termid":"PBO:0082976"}


id: GO:0031391
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id: PBO:0003455
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id: FYECO:0000350
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id: GO:0005014
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id: MONDO:0009934
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id: PBO:0054400
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  {"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 1796","termid":"PBO:0054400"}


id: PBO:0065164
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proline rich basic protein 1","termid":"PBO:0065164"}


id: GO:0050013
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-dehydropantoate = 3-methyl-2-oxobutanoate + formaldehyde.","definition_xrefs":["MetaCyc:KETOPANTOALDOLASE-RXN","EC:4.1.2.12"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016829"],"is_obsolete":false,"name":"2-dehydropantoate aldolase activity","secondary_identifiers":["RHEA:23276"],"synonyms":[{"name":"2-dehydropantoate formaldehyde-lyase (3-methyl-2-oxobutanoate-forming)","type":"related"},{"name":"2-dehydropantoate formaldehyde-lyase activity","type":"related"},{"name":"ketopantoaldolase activity","type":"exact"}],"termid":"GO:0050013"}


id: PBO:0052763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 55","termid":"PBO:0052763"}


id: SO:0001751
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A SL2_acceptor_site which appends the SL6 RNA leader sequence to the 5' end of an mRNA. SL6 acceptor sites occur in genes in internal segments of polycistronic transcripts.","definition_xrefs":["SO:nlw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SL2_acceptor_site","termid":"SO:0000709"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SL6_acceptor_site","synonyms":[{"name":"SL6 acceptor site","type":"exact"}],"termid":"SO:0001751"}


id: PBO:0058486
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5681a","termid":"PBO:0058486"}


id: MONDO:0008283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cronkhite-Canada syndrome (CCS) is a rare gastrointestinal (GI) polyposis syndrome characterized by the association of non-hereditary GI polyposis with the cutaneous triad of alopecia, nail changes and hyperpigmentation.","definition_xrefs":["Orphanet:2930"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"gastric hamartomatous polyp","termid":"MONDO:0006224"},{"relation_name":"is_a","term_name":"digestive system disorder","termid":"MONDO:0004335"},{"relation_name":"is_a","term_name":"intestinal polyposis syndrome","termid":"MONDO:0015185"},{"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:0004335"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005093"],"is_obsolete":false,"name":"Cronkhite-Canada syndrome","secondary_identifiers":["icd11.foundation:79007466","UMLS:C0282207","MedDRA:10062907","GARD:4427","DOID:6225","MESH:D044483","NCIT:C7035","MEDGEN:129128","OMIM:175500","SCTID:76304001","NANDO:1200901","NORD:1017"],"synonyms":[{"name":"Cronkhite-Canada disease","type":"related"},{"name":"Cronkhite-Canada syndrome","type":"exact"},{"name":"gastric Cronkhite Canada polyposis","type":"exact"},{"name":"gastrointestinal polyposis-ectodermal changes syndrome","type":"exact"},{"name":"gastrointestinal polyposis-skin pigmentation-alopecia-fingernail changes syndrome","type":"exact"},{"name":"polyposis skin pigmentation alopecia fingernail changes","type":"related"},{"name":"polyposis, skin pigmentation, alopecia, and fingernail changes","type":"related"}],"termid":"MONDO:0008283","xrefs":{"Monarch":{"xref_id":"0008283"}}}


id: GO:0046847
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The assembly of a filopodium, a thin, stiff protrusion extended by the leading edge of a motile cell such as a crawling fibroblast or amoeba, or an axonal growth cone.","definition_xrefs":["GOC:mah","GOC:tb","GOC:dph","PMID:18464790","PMID:16337369"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane bounded cell projection assembly","termid":"GO:0120031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"filopodium assembly","synonyms":[{"name":"filopodia biosynthesis","type":"related"},{"name":"filopodia formation","type":"related"},{"name":"filopodium formation","type":"related"}],"termid":"GO:0046847"}


id: GO:0022607
data:
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level","type":"exact"}],"termid":"GO:0022607","terms_by_termid":{"GO:0000027":null,"GO:0000028":null,"GO:0000045":null,"GO:0000073":null,"GO:0000147":null,"GO:0000244":null,"GO:0000245":null,"GO:0000348":null,"GO:0000349":null,"GO:0000350":null,"GO:0000354":null,"GO:0000387":null,"GO:0000388":null,"GO:0000389":null,"GO:0000393":null,"GO:0000395":null,"GO:0000492":null,"GO:0000493":null,"GO:0000707":null,"GO:0000730":null,"GO:0000915":null,"GO:0000917":null,"GO:0000921":null,"GO:0001188":null,"GO:0001731":null,"GO:0001732":null,"GO:0003400":null,"GO:0006294":null,"GO:0006334":null,"GO:0006376":null,"GO:0006617":null,"GO:0007020":null,"GO:0007021":null,"GO:0007084":null,"GO:0010257":null,"GO:0010265":null,"GO:0010772":null,"GO:0016226":null,"GO:0017004":null,"GO:0022618":null,"GO:0030041":null,"GO:0030476":null,"GO:0030833":null,"GO:0030954":null,"GO:0030999":null,"GO:0031024":null,"GO:0031030":null,"GO:0031031":null,"GO:0031321":null,"GO:0031322":null,"GO:0031468":null,"GO:0031671":null,"GO:0032120":null,"GO:0032231":null,"GO:0032955":null,"GO:0033615":null,"GO:0033617":null,"GO:0033962":null,"GO:0034063":null,"GO:0034080":null,"GO:0034462":null,"GO:0034551":null,"GO:0034553":null,"GO:0035493":null,"GO:0042255":null,"GO:0042256":null,"GO:0043248":null,"GO:0044571":null,"GO:0044572":null,"GO:0045899":null,"GO:0046785":null,"GO:0048268":null,"GO:0051016":null,"GO:0051017":null,"GO:0051123":null,"GO:0051131":null,"GO:0051225":null,"GO:0051256":null,"GO:0051292":null,"GO:0051382":null,"GO:0051415":null,"GO:0051417":null,"GO:0061753":null,"GO:0061804":null,"GO:0062123":null,"GO:0070072":null,"GO:0070096":null,"GO:0070196":null,"GO:0070583":null,"GO:0070649":null,"GO:0070682":null,"GO:0070898":null,"GO:0070941":null,"GO:0071520":null,"GO:0071562":null,"GO:0090006":null,"GO:0090306":null,"GO:0090307":null,"GO:0097250":null,"GO:0110161":null,"GO:0120306":null,"GO:0140042":null,"GO:0140278":null,"GO:0140281":null,"GO:0140454":null,"GO:0140529":null,"GO:0140530":null,"GO:0140641":null,"GO:0140642":null,"GO:0180023":null,"GO:1901673":null,"GO:1902626":null,"GO:1902775":null,"GO:1902917":null,"GO:1902977":null,"GO:1902985":null,"GO:1903023":null,"GO:1903024":null,"GO:1903087":null,"GO:1903241":null,"GO:1903359":null,"GO:1903475":null,"GO:1903479":null,"GO:1903499":null,"GO:1903500":null,"GO:1903501":null,"GO:1904600":null,"GO:1904802":null,"GO:1904868":null,"GO:1905143":null,"GO:1905323":null,"GO:1905324":null,"GO:1905560":null,"GO:1905561":null,"GO:1905757":null,"GO:1905758":null,"GO:1990113":null,"GO:1990114":null,"GO:1990115":null,"GO:1990344":null,"GO:1990810":null,"GO:2000432":null,"GO:2000786":null,"GO:2001178":null}}


id: PBO:0027090
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_vegetative_cell_with_cell_death_during_mitosis","termid":"PBO:0027090"}


id: PBO:0059116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mov10 like RISC complex RNA helicase 1","termid":"PBO:0059116"}


id: MOD:00310
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-arginine residue to N5-methyl-L-arginine.","definition_xrefs":["PubMed:9792625","RESID:AA0305","PubMed:9873020","PubMed:11875433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monomethylated L-arginine","termid":"MOD:00414"},{"relation_name":"is_a","term_name":"N-methylated residue","termid":"MOD:00602"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00427"}],"interesting_parent_ids":["MOD:00427"],"is_obsolete":false,"name":"N5-methyl-L-arginine","synonyms":[{"name":"(2S)-2-amino-5-(N-methylcarbamimidamido)pentanoic acid","type":"exact"},{"name":"MOD_RES N5-methylarginine","type":"exact"},{"name":"Methyl","type":"related"},{"name":"Methylation","type":"related"},{"name":"N5-carbamimidoyl-N5-methyl-L-ornithine","type":"exact"},{"name":"N5-methyl-L-arginine","type":"exact"},{"name":"N5-methylated L-arginine","type":"exact"},{"name":"N5Me1Arg","type":"exact"},{"name":"delta-N-methylarginine","type":"exact"}],"termid":"MOD:00310"}


id: GO:0060067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The reproductive developmental process whose specific outcome is the progression of the cervix over time, from its formation to the mature structure.","definition_xrefs":["GOC:ebc","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive structure development","termid":"GO:0048608"}],"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":"cervix development","synonyms":[{"name":"Mullerian tract development","type":"related"}],"termid":"GO:0060067"}


id: PBO:0092007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA Asparagine (guu), mitochondrial","termid":"PBO:0092007"}


id: MONDO:0010372
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Clark-Baraitser syndrome (obsolete MONDO:0010372)","termid":"MONDO:0010372","xrefs":{"Monarch":{"xref_id":"0010372"}}}


id: MONDO:1012875
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Parkinson disease that occurs in crab-eating macaques due to a mutation in the PINK1 gene created by genetic engineering or gene editing.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Parkinson disease, non-human animal","termid":"MONDO:1012984"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Parkinson disease, PINK1-related, crab-eating macaque","secondary_identifiers":["OMIA:002361-9541"],"termid":"MONDO:1012875","xrefs":{"Monarch":{"xref_id":"1012875"}}}


id: MONDO:0009443
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Harlequin ichthyosis (HI) is the most severe variant of autosomal recessive congenital ichthyosis (ARCI). It is characterized at birth by the presence of large, thick, plate-like scales over the whole body associated with severe ectropion, eclabium, and flattened ears, that later develops into a severe scaling erythroderma.","definition_xrefs":["Orphanet:457"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive congenital ichthyosis 4A","termid":"MONDO:0011026"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005328"],"is_obsolete":false,"name":"autosomal recessive congenital ichthyosis 4B","secondary_identifiers":["MEDGEN:108615","OMIM:242500","NCIT:C98934","NORD:1287","MedDRA:10019163","NANDO:1200614","UMLS:C0598226","NANDO:2200992","GARD:6568","SCTID:205548006","DOID:0060713"],"synonyms":[{"name":"'Harlequin fetus'","type":"related"},{"name":"ARCI4B","type":"exact"},{"name":"HI","type":"exact"},{"name":"Harlequin Ichthyosis","type":"exact"},{"name":"Harlequin fetus","type":"related"},{"name":"Harlequin foetus","type":"related"},{"name":"autosomal recessive congenital ichthyosis type 4B","type":"exact"},{"name":"harlequin ichthyosis","type":"exact"},{"name":"harlequin type ichthyosis congenita","type":"exact"},{"name":"harlequin type ichthyosis fetalis","type":"exact"},{"name":"hi","type":"exact"},{"name":"ichthyosis , congenital, autosomal recessive 4b (harlequin)","type":"exact"},{"name":"ichthyosis congenita, Harlequin fetus type","type":"related"},{"name":"ichthyosis congenita, Harlequin foetus type","type":"related"},{"name":"ichthyosis congenita, Harlequin type","type":"exact"},{"name":"ichthyosis fetalis, Harlequin type","type":"exact"},{"name":"ichthyosis, congenital, autosomal recessive 4B","type":"related"},{"name":"ichthyosis, congenital, autosomal recessive type 4B","type":"exact"}],"termid":"MONDO:0009443","xrefs":{"Monarch":{"xref_id":"0009443"}}}


id: FYECO:0000164
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","gene_count":0,"genotype_count":0,"name":"OBSOLETE FYECO:0000164 anti-tubulin antibodies added (obsolete FYECO:0000164)","synonyms":[{"name":"anti-tubulin antibody added","type":"exact"}],"termid":"FYECO:0000164"}


id: MONDO:0018295
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital disorder of glycosylation with deafness as a major feature (obsolete MONDO:0018295)","secondary_identifiers":["Orphanet:371212"],"synonyms":[{"name":"CDG with deafness as a major feature","type":"exact"}],"termid":"MONDO:0018295","xrefs":{"Monarch":{"xref_id":"0018295"}}}


id: MONDO:1011348
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Post-Infectious disorder that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non-human animal disease","termid":"MONDO:0005583"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"post-infectious disorder, non-human animal","termid":"MONDO:1011348","xrefs":{"Monarch":{"xref_id":"1011348"}}}


id: PATO:0002004
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape that inheres in a part of a surface. An object can have different surface shapes on different parts of its surface.","definition_xrefs":["PATOC:CJM"],"gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0002004 surface shape (obsolete PATO:0002004)","termid":"PATO:0002004"}


id: PBO:0075223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin 2","termid":"PBO:0075223"}


id: GO:0009474
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete nonaheme cytochrome c (obsolete GO:0009474)","synonyms":[{"name":"nonaheme cytochrome c","type":"exact"}],"termid":"GO:0009474"}


id: PBO:0056543
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MCF.2 cell line derived transforming sequence-like 2","termid":"PBO:0056543"}


id: MONDO:0012290
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"CEDNIK syndrome is a neurocutaneaous syndrome characterized by severe developmental abnormalities of the nervous system and aberrant differentiation of the epidermis.","definition_xrefs":["Orphanet:66631"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"diffuse palmoplantar keratoderma","termid":"MONDO:0017666"}],"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":"CEDNIK syndrome","secondary_identifiers":["MESH:C537943","UMLS:C1836033","GARD:9940","OMIM:609528","SCTID:722385008","MEDGEN:332113","DOID:0060337"],"synonyms":[{"name":"CEDNIK syndrome","type":"exact"},{"name":"cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome","type":"exact"},{"name":"cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome","type":"related"},{"name":"cerebral dysgenesis-neuropathy-ichthyosis-palmoplantar keratoderma syndrome","type":"exact"}],"termid":"MONDO:0012290","xrefs":{"Monarch":{"xref_id":"0012290"}}}


id: PBO:0091637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sub-telomeric 5Tm protein family Ftm6","termid":"PBO:0091637"}


id: MONDO:0800438
data:
  {"annotated_genes":["SJAG_01058"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85950],"is_not":false,"summary":null,"term":"MONDO:0800438"}]},"cv_name":"mondo","definition":"Any developmental delay with short stature, dysmorphic facial features, and sparse hair in which the cause of the disease is a mutation in the DPH1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"excluded_subClassOf","term_name":"obsolete dysostosis of genetic origin (obsolete MONDO:0018454)","termid":"MONDO:0018454"},{"relation_name":"is_a","term_name":"developmental delay with short stature, dysmorphic facial features, and sparse hair","termid":"MONDO:0031632"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01058":null},"genotype_count":0,"is_obsolete":false,"name":"developmental delay with short stature, dysmorphic facial features, and sparse hair 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0070477","OMIM:616901","Orphanet:459061","GARD:17814"],"synonyms":[{"name":"DEDSSH1","type":"exact"},{"name":"Loucks-Innes syndrome","type":"related"},{"name":"developmental delay with short stature, dysmorphic facial features, and sparse hair","type":"broad"},{"name":"developmental delay with short stature, dysmorphic features, and sparse hair 1","type":"exact"},{"name":"developmental delay-short stature-dysmorphic features-sparse hair syndrome","type":"broad"},{"name":"diphtamide deficiency syndrome","type":"exact"}],"termid":"MONDO:0800438","terms_by_termid":{"MONDO:0800438":null},"xrefs":{"Monarch":{"xref_id":"0800438"}}}


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


id: GO:0140738
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An inflammasome complex that consists of NLRP6, PYCARD/ASC and caspase-1 or caspase-4/caspase-11.","definition_xrefs":["PMID:34678144","PMID:30674671"],"direct_ancestors":[{"relation_name":"is_a","term_name":"canonical inflammasome complex","termid":"GO:0061702"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005829"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005737","GO:0005829","GO:0005575"],"is_obsolete":false,"name":"NLRP6 inflammasome complex","termid":"GO:0140738"}


id: GO:1902689
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of NAD metabolic process.","definition_xrefs":["GOC:di","GOC:TermGenie","PMID:19846558","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of purine nucleotide metabolic process","termid":"GO:1900543"},{"relation_name":"is_a","term_name":"regulation of NAD metabolic process","termid":"GO:1902688"},{"relation_name":"negatively_regulates","term_name":"NAD metabolic process","termid":"GO:0019674"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0055086","GO:0008150"],"is_obsolete":false,"name":"negative regulation of NAD metabolic process","synonyms":[{"name":"down regulation of NAD (oxidized) metabolic process","type":"exact"},{"name":"down regulation of NAD (oxidized) metabolism","type":"exact"},{"name":"down regulation of NAD metabolic process","type":"exact"},{"name":"down regulation of NAD metabolism","type":"exact"},{"name":"down regulation of NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"down regulation of nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"down regulation of nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"down regulation of oxidized NAD metabolic process","type":"exact"},{"name":"down regulation of oxidized NAD metabolism","type":"exact"},{"name":"down regulation of oxidized nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"down regulation of oxidized nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"down-regulation of NAD (oxidized) metabolic process","type":"exact"},{"name":"down-regulation of NAD (oxidized) metabolism","type":"exact"},{"name":"down-regulation of NAD metabolic process","type":"exact"},{"name":"down-regulation of NAD metabolism","type":"exact"},{"name":"down-regulation of NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"down-regulation of nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"down-regulation of nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"down-regulation of oxidized NAD metabolic process","type":"exact"},{"name":"down-regulation of oxidized NAD metabolism","type":"exact"},{"name":"down-regulation of oxidized nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"down-regulation of oxidized nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"downregulation of NAD (oxidized) metabolic process","type":"exact"},{"name":"downregulation of NAD (oxidized) metabolism","type":"exact"},{"name":"downregulation of NAD metabolic process","type":"exact"},{"name":"downregulation of NAD metabolism","type":"exact"},{"name":"downregulation of NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"downregulation of nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"downregulation of nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"downregulation of oxidized NAD metabolic process","type":"exact"},{"name":"downregulation of oxidized NAD metabolism","type":"exact"},{"name":"downregulation of oxidized nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"downregulation of oxidized nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"inhibition of NAD (oxidized) metabolic process","type":"narrow"},{"name":"inhibition of NAD (oxidized) metabolism","type":"narrow"},{"name":"inhibition of NAD metabolic process","type":"narrow"},{"name":"inhibition of NAD metabolism","type":"narrow"},{"name":"inhibition of NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"inhibition of nicotinamide adenine dinucleotide metabolic process","type":"narrow"},{"name":"inhibition of nicotinamide adenine dinucleotide metabolism","type":"narrow"},{"name":"inhibition of oxidized NAD metabolic process","type":"narrow"},{"name":"inhibition of oxidized NAD metabolism","type":"narrow"},{"name":"inhibition of oxidized nicotinamide adenine dinucleotide metabolic process","type":"narrow"},{"name":"inhibition of oxidized nicotinamide adenine dinucleotide metabolism","type":"narrow"},{"name":"negative regulation of NAD (oxidized) metabolic process","type":"exact"},{"name":"negative regulation of NAD (oxidized) metabolism","type":"exact"},{"name":"negative regulation of NAD metabolism","type":"exact"},{"name":"negative regulation of NAD phosphorylation and dephosphorylation","type":"narrow"},{"name":"negative regulation of nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"negative regulation of nicotinamide adenine dinucleotide metabolism","type":"exact"},{"name":"negative regulation of oxidized NAD metabolic process","type":"exact"},{"name":"negative regulation of oxidized NAD metabolism","type":"exact"},{"name":"negative regulation of oxidized nicotinamide adenine dinucleotide metabolic process","type":"exact"},{"name":"negative regulation of oxidized nicotinamide adenine dinucleotide metabolism","type":"exact"}],"termid":"GO:1902689"}


id: FYPO:0002769
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the spindle pole body is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to microtubule cytoskeleton","termid":"FYPO:0004090"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abnormal protein localization to spindle pole body","synonyms":[{"name":"abnormal protein localisation to spindle pole body","type":"exact"},{"name":"abnormal protein localization to SPB","type":"exact"}],"termid":"FYPO:0002769"}


id: PBO:0082739
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the RSC chromatin remodeling complex; essential for mitotic growth; RSC6 has a paralog, SNF12, that arose from the whole genome duplication","termid":"PBO:0082739"}


id: PBO:0005031
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulphate transporter (predicted)","termid":"PBO:0005031"}


id: MONDO:0007704
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"osteoarthritis susceptibility 2","secondary_identifiers":["MEDGEN:854385","OMIM:140600","UMLS:C3887526"],"synonyms":[{"name":"Dipoa","type":"related"},{"name":"Heberden nodes","type":"related"},{"name":"MATN3 osteoarthritis","type":"exact"},{"name":"OADIP","type":"related"},{"name":"OS2","type":"related"},{"name":"hand osteoarthritis","type":"related"},{"name":"osteoarthritis caused by mutation in MATN3","type":"exact"},{"name":"osteoarthritis of distal interphalangeal joints","type":"related"},{"name":"osteoarthritis susceptibility 2","type":"exact"},{"name":"osteoarthritis susceptibility type 2","type":"exact"}],"termid":"MONDO:0007704","xrefs":{"Monarch":{"xref_id":"0007704"}}}


id: GO:0044527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of a peptidyl-cystine residue in a protein by the direct addition of H2S, followed by the removal of 2 protons to form peptidyl-cysteine persulfide.","definition_xrefs":["GOC:jl","GOC:jsg"],"gene_count":0,"genotype_count":0,"name":"obsolete formation of peptidyl-cystine persulfide by sulphur transfer from H2S (obsolete GO:0044527)","termid":"GO:0044527"}


id: PATO:0002059
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"The specific wavelength of light emitted by a fluorescent molecule, such as a labelled probe, upon absorption of light at the (higher) excitation wavelength.","definition_xrefs":["web:http://www.expertglossary.com/"],"direct_ancestors":[{"relation_name":"is_a","term_name":"radiation emitting quality","termid":"PATO:0001299"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"emmision wavelength","termid":"PATO:0002059"}


id: PBO:0085860
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 vacuole; not an essential gene; induced by treatment with 8-methoxypsoralen and UVA irradiation; relocalizes from nucleus to vacuole upon DNA replication stress; YLR297W has a paralog, YOR186W, that arose from the whole genome duplication","termid":"PBO:0085860"}


id: GO:1905769
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of double-stranded telomeric DNA binding.","definition_xrefs":["GOC:BHF","GOC:nc","GOC:BHF_telomere","PMID:18812185","GO_REF:0000059","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of double-stranded telomeric DNA binding (obsolete GO:1905769)","synonyms":[{"name":"activation of double-stranded telomeric DNA binding","type":"narrow"},{"name":"up regulation of double-stranded telomeric DNA binding","type":"exact"},{"name":"up-regulation of double-stranded telomeric DNA binding","type":"exact"},{"name":"upregulation of double-stranded telomeric DNA binding","type":"exact"}],"termid":"GO:1905769"}


id: FYPO:0005058
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which meiotic DNA double-strand break clipping is decreased. Meiotic DNA double-strand break clipping is the process by which SPO11/Rec12-oligonucleotide complexes are removed from 5' DNA double-strand breaks induced during meiosis.","definition_xrefs":["PMID:26130711","PomBase:mah","GO:1990898"],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000293","FYPO:0000002","FYPO:0000631","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased meiotic DNA double-strand break clipping","synonyms":[{"name":"reduced meiotic DNA double-strand break clipping","type":"exact"}],"termid":"FYPO:0005058"}


id: PBO:0060353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MYO18B antisense RNA 1","termid":"PBO:0060353"}


id: FYPO:0005027
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an inviable cell that does not divide, has a larger diameter and volume than normal, contains two nuclei and more than one septum, and has an abnormal shape featuring a constriction at the center of the cell, corresponding to the cell division site. In some such cells, the diameter at the ends is much greater than in wild-type cells.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multinucleate multiseptate vegetative cell","termid":"FYPO:0001252"},{"relation_name":"is_a","term_name":"inviable septated vegetative cell with abnormal cell morphology","termid":"FYPO:0002452"},{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division, swollen binucleate cell with central constriction","termid":"FYPO:0002987"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0000004","FYPO:0000032","FYPO:0001985","FYPO:0000631","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"inviable after spore germination, without cell division, swollen binucleate multiseptate cell with central constriction","synonyms":[{"name":"inviable after spore germination, binucleate without cell division, swollen with multiple septa","type":"exact"},{"name":"inviable after spore germination, undivided swollen binucleate multiseptate cell with central constriction","type":"exact"},{"name":"inviable after spore germination, without cell division, swollen binucleate multiseptate cell with central constriction, with nuclear division without cytokinesis","type":"exact"},{"name":"inviable after spore germination, without cell division, swollen binucleate multiseptate cell with constricted region at cell division site","type":"exact"},{"name":"inviable after spore germination, without cell division, swollen dumbbell-shaped binucleate multiseptate cell","type":"related"},{"name":"inviable following spore germination, without cell division, swollen binucleate multiseptate cell with central constriction","type":"exact"},{"name":"inviable germinated spore, without cell division, swollen binucleate multiseptate cell with central constriction","type":"exact"},{"name":"lethal after spore germination, without cell division, swollen binucleate multiseptate cell with central constriction","type":"exact"}],"termid":"FYPO:0005027"}


id: FYPO:0001407
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cell growth is decreased relative to normal in a medium containing glucose as the carbon source.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased vegetative cell population growth","termid":"FYPO:0001355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002060"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0002058","FYPO:0000003","FYPO:0000139","FYPO:0002060","FYPO:0002057","FYPO:0001985"],"is_obsolete":false,"name":"decreased cell population growth on glucose carbon source","secondary_identifiers":["FYPO:0001163","FYPO:0001161"],"synonyms":[{"name":"decreased aerobic cell population growth on glucose carbon source","type":"narrow"},{"name":"decreased growth on glucose carbon source","type":"broad"},{"name":"decreased hypoxic cell population growth on glucose carbon source","type":"narrow"},{"name":"decreased vegetative cell growth on glucose carbon source","type":"exact"},{"name":"reduced cell growth on glucose carbon source","type":"exact"},{"name":"slow cell growth on glucose carbon source","type":"narrow"}],"termid":"FYPO:0001407"}


id: PBO:0012234
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chalcone related protein family","termid":"PBO:0012234"}


id: PBO:0013835
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferrochelatase Hem15 (predicted)","termid":"PBO:0013835"}


id: GO:0009702
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-arabinose + ATP = beta-L-arabinose 1-phosphate + ADP + 2 H+.","definition_xrefs":["EC:2.7.1.46","RHEA:20153"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"},{"relation_name":"is_a","term_name":"carbohydrate kinase activity","termid":"GO:0019200"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016301"],"is_obsolete":false,"name":"L-arabinokinase activity","secondary_identifiers":["KEGG_REACTION:R01754","MetaCyc:L-ARABINOKINASE-RXN"],"synonyms":[{"name":"ATP:L-arabinose 1-phosphotransferase activity","type":"exact"},{"name":"L-arabinokinase (phosphorylating)","type":"related"}],"termid":"GO:0009702"}


id: MONDO:0016555
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"transient congenital hypothyroidism","termid":"MONDO:0015792"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transient congenital hypothyroidism due to maternal factor","secondary_identifiers":["UMLS:C5680929","MEDGEN:1842783","GARD:20645","Orphanet:238696"],"termid":"MONDO:0016555","xrefs":{"Monarch":{"xref_id":"0016555"}}}


id: PBO:0051580
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 17 receptor D","termid":"PBO:0051580"}


id: GO:1905118
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ribonucleoside-diphosphate reductase activity.","definition_xrefs":["GO_REF:0000059","GOC:TermGenie","GOC:bhm","PMID:24733891"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of oxidoreductase activity","termid":"GO:0051353"}],"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 ribonucleoside-diphosphate reductase activity","synonyms":[{"name":"activation of RNR","type":"related"},{"name":"activation of adenosylcobalamin-dependent ribonucleotide reductase activity","type":"related"},{"name":"activation of aerobic non-heme iron-dependent ribonucleotide reductase activity","type":"related"},{"name":"activation of anaerobic iron-sulfur-dependent ribonucleotide reductase activity","type":"related"},{"name":"activation of class I ribonucleotide reductase activity","type":"related"},{"name":"activation of class II ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"activation of class II ribonucleotide reductase activity","type":"related"},{"name":"activation of class III ribonucleotide reductase activity","type":"related"},{"name":"activation of nucleoside diphosphate reductase activity","type":"related"},{"name":"activation of purine/pyrimidine nucleoside diphosphate reduction","type":"related"},{"name":"activation of ribonucleoside 5'-diphosphate reductase activity","type":"related"},{"name":"activation of ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"activation of ribonucleotide diphosphate reductase activity","type":"related"},{"name":"positive regulation of RNR","type":"related"},{"name":"positive regulation of adenosylcobalamin-dependent ribonucleotide reductase activity","type":"related"},{"name":"positive regulation of aerobic non-heme iron-dependent ribonucleotide reductase activity","type":"related"},{"name":"positive regulation of anaerobic iron-sulfur-dependent ribonucleotide reductase activity","type":"related"},{"name":"positive regulation of class I ribonucleotide reductase activity","type":"related"},{"name":"positive regulation of class II ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"positive regulation of class II ribonucleotide reductase activity","type":"related"},{"name":"positive regulation of class III ribonucleotide reductase activity","type":"related"},{"name":"positive regulation of nucleoside diphosphate reductase activity","type":"related"},{"name":"positive regulation of purine/pyrimidine nucleoside diphosphate reduction","type":"related"},{"name":"positive regulation of ribonucleoside 5'-diphosphate reductase activity","type":"related"},{"name":"positive regulation of ribonucleotide diphosphate reductase activity","type":"related"},{"name":"up regulation of RNR","type":"related"},{"name":"up regulation of adenosylcobalamin-dependent ribonucleotide reductase activity","type":"related"},{"name":"up regulation of aerobic non-heme iron-dependent ribonucleotide reductase activity","type":"related"},{"name":"up regulation of anaerobic iron-sulfur-dependent ribonucleotide reductase activity","type":"related"},{"name":"up regulation of class I ribonucleotide reductase activity","type":"related"},{"name":"up regulation of class II ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"up regulation of class II ribonucleotide reductase activity","type":"related"},{"name":"up regulation of class III ribonucleotide reductase activity","type":"related"},{"name":"up regulation of nucleoside diphosphate reductase activity","type":"related"},{"name":"up regulation of purine/pyrimidine nucleoside diphosphate reduction","type":"related"},{"name":"up regulation of ribonucleoside 5'-diphosphate reductase activity","type":"related"},{"name":"up regulation of ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"up regulation of ribonucleotide diphosphate reductase activity","type":"related"},{"name":"up-regulation of RNR","type":"related"},{"name":"up-regulation of adenosylcobalamin-dependent ribonucleotide reductase activity","type":"related"},{"name":"up-regulation of aerobic non-heme iron-dependent ribonucleotide reductase activity","type":"related"},{"name":"up-regulation of anaerobic iron-sulfur-dependent ribonucleotide reductase activity","type":"related"},{"name":"up-regulation of class I ribonucleotide reductase activity","type":"related"},{"name":"up-regulation of class II ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"up-regulation of class II ribonucleotide reductase activity","type":"related"},{"name":"up-regulation of class III ribonucleotide reductase activity","type":"related"},{"name":"up-regulation of nucleoside diphosphate reductase activity","type":"related"},{"name":"up-regulation of purine/pyrimidine nucleoside diphosphate reduction","type":"related"},{"name":"up-regulation of ribonucleoside 5'-diphosphate reductase activity","type":"related"},{"name":"up-regulation of ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"up-regulation of ribonucleotide diphosphate reductase activity","type":"related"},{"name":"upregulation of RNR","type":"related"},{"name":"upregulation of adenosylcobalamin-dependent ribonucleotide reductase activity","type":"related"},{"name":"upregulation of aerobic non-heme iron-dependent ribonucleotide reductase activity","type":"related"},{"name":"upregulation of anaerobic iron-sulfur-dependent ribonucleotide reductase activity","type":"related"},{"name":"upregulation of class I ribonucleotide reductase activity","type":"related"},{"name":"upregulation of class II ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"upregulation of class II ribonucleotide reductase activity","type":"related"},{"name":"upregulation of class III ribonucleotide reductase activity","type":"related"},{"name":"upregulation of nucleoside diphosphate reductase activity","type":"related"},{"name":"upregulation of purine/pyrimidine nucleoside diphosphate reduction","type":"related"},{"name":"upregulation of ribonucleoside 5'-diphosphate reductase activity","type":"related"},{"name":"upregulation of ribonucleoside-diphosphate reductase activity","type":"related"},{"name":"upregulation of ribonucleotide diphosphate reductase activity","type":"related"}],"termid":"GO:1905118"}


id: MOD:01569
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces an O3-hydrogen atom of a threonine residue with the Applied Biosystems iTRAQ8plex-118 reporter+balance group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ8plex-118 reporter+balance reagent acylated residue","termid":"MOD:01563"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter+balance reagent O-acylated residue","termid":"MOD:01714"},{"relation_name":"is_a","term_name":"O3-acylated L-threonine","termid":"MOD:02004"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-118 reporter+balance reagent O3-acylated threonine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"}],"termid":"MOD:01569"}


id: PBO:0082881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cyanamide hydratase that detoxifies cyanamide; member of the HD domain metalloprotein superfamily; expression is induced over 100-fold by cyanamide and by SN2-type DNA alkylating agents such as MMS and DMA; induction decreased in rad6 and rad18 mutants; gene and protein are identical to DDI2 and Ddi2p","termid":"PBO:0082881"}


id: GO:0003702
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Functions to initiate or regulate RNA polymerase II transcription.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete RNA polymerase II transcription factor activity (obsolete GO:0003702)","synonyms":[{"name":"RNA polymerase II transcription factor activity","type":"exact"}],"termid":"GO:0003702"}


id: GO:0045283
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A membrane-bound flavoenzyme complex consisting of four subunits, A, B, C, and D. A and B comprise the membrane-extrinsic catalytic domain and C (InterPro:IPR003510; InterPro:IPR004224) and D (InterPro:IPR003418) link the catalytic centers to the electron-transport chain. This family consists of the 13 kDa hydrophobic subunit D. This component may be required to anchor the catalytic components of the fumarate reductase complex to the cytoplasmic membrane. Fumarate reductase couples the reduction of fumarate to succinate to the oxidation of quinol to quinone, in a reaction opposite to that catalyzed by the related complex II of the respiratory chain (succinate dehydrogenase-(ubiquinone)).","definition_xrefs":["InterPro:IPR003418","InterPro:IPR004224"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane protein complex","termid":"GO:0098796"},{"relation_name":"is_a","term_name":"respiratory chain complex","termid":"GO:0098803"},{"relation_name":"is_a","term_name":"catalytic complex","termid":"GO:1902494"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"fumarate reductase complex","termid":"GO:0045283"}


id: PR:Q10211
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC4H3.03c gene.","definition_xrefs":["UniProtKB:Q10211","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C4H3.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4H3.03c","synonyms":[{"name":"Spom972h-SPAC4H3.03c","type":"exact"}],"termid":"PR:Q10211"}


id: GO:0180038
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex consisting of cyclin L and cyclin-dependent kinase 11 (CDK11). Cyclins are characterized by periodicity in protein abundance throughout the cell cycle. Cyclin-dependent kinases represent a family of serine/threonine protein kinases that become active upon binding to a cyclin regulatory partner.","definition_xrefs":["PMID:23122962","PMID:32446654"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclin-dependent protein kinase holoenzyme complex","termid":"GO:0000307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"cyclin L-CDK11 complex","synonyms":[{"name":"Cdk11-Cyclin L complex","type":"exact"}],"termid":"GO:0180038"}


id: FYECO:0000172
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which zinc ions were added to the assay buffer in excess compared to standard assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"+ ions","termid":"FYECO:0000030"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ Zn ions","synonyms":[{"name":"zinc ions added","type":"exact"}],"termid":"FYECO:0000172"}


id: MONDO:0003255
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An exceptionally rare, generally benign, granular cell tumor that arises from the mediastinum. All the reported cases were located in the posterior mediastinum.","definition_xrefs":["NCIT:C6601"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"mediastinal neural neoplasm","termid":"MONDO:0003098"},{"relation_name":"is_a","term_name":"granular cell tumor","termid":"MONDO:0006235"},{"relation_name":"is_a","term_name":"neoplasm of mediastinum","termid":"MONDO:0021386"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediastinal granular cell myoblastoma","secondary_identifiers":["MEDGEN:235309","DOID:5046","UMLS:C1334656"],"synonyms":[{"name":"granular cell myoblastoma of mediastinum","type":"exact"},{"name":"granular cell myoblastoma of the mediastinum","type":"exact"},{"name":"granular cell neoplasm of mediastinum","type":"exact"},{"name":"granular cell neoplasm of the mediastinum","type":"exact"},{"name":"granular cell tumor of mediastinum","type":"exact"},{"name":"granular cell tumor of the mediastinum","type":"exact"},{"name":"granular cell tumour of mediastinum","type":"exact"},{"name":"granular cell tumour of the mediastinum","type":"exact"},{"name":"mediastinal granular cell myoblastoma","type":"exact"},{"name":"mediastinal granular cell neoplasm","type":"exact"},{"name":"mediastinal granular cell tumor","type":"exact"},{"name":"mediastinal granular cell tumour","type":"exact"},{"name":"mediastinum granular cell tumor","type":"exact"},{"name":"mediastinum granular cell tumour","type":"exact"}],"termid":"MONDO:0003255","xrefs":{"Monarch":{"xref_id":"0003255"}}}


id: PBO:0005364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Ucp12 (predicted)","termid":"PBO:0005364"}


id: PBO:0061661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin 35 pseudogene 1","termid":"PBO:0061661"}


id: MONDO:0017122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature (obsolete MONDO:0017122)","secondary_identifiers":["Orphanet:269573"],"termid":"MONDO:0017122","xrefs":{"Monarch":{"xref_id":"0017122"}}}


id: MONDO:0015505
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete tracheal anomaly (obsolete MONDO:0015505)","secondary_identifiers":["icd11.foundation:679333287","Orphanet:156252"],"termid":"MONDO:0015505","xrefs":{"Monarch":{"xref_id":"0015505"}}}


id: PBO:0004179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-Pro dipeptidase (predicted)","termid":"PBO:0004179"}


id: GO:1905526
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of Golgi lumen acidification.","definition_xrefs":["GO_REF:0000058","GOC:dph","GOC:TermGenie","PMID:23447592"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular pH reduction","termid":"GO:0032847"},{"relation_name":"regulates","term_name":"Golgi lumen acidification","termid":"GO:0061795"}],"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 Golgi lumen acidification","termid":"GO:1905526"}


id: FYPO:0005446
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a specific molecular function is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal molecular function","termid":"FYPO:0000707"}],"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"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000707","FYPO:0001985"],"is_obsolete":false,"name":"abolished molecular function","synonyms":[{"name":"molecular function abolished","type":"exact"}],"termid":"FYPO:0005446"}


id: MONDO:0024996
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Usher syndrome, type 2b (obsolete MONDO:0024996)","secondary_identifiers":["OMIM:276905"],"synonyms":[{"name":"US2B","type":"related"},{"name":"USH2B","type":"related"}],"termid":"MONDO:0024996","xrefs":{"Monarch":{"xref_id":"0024996"}}}


id: GO:0019297
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving coenzyme B (7-mercaptoheptanoylthreonine phosphate), a coenzyme involved in the utilization of methane by methanogenic prokaryotes.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified amino acid metabolic process","termid":"GO:0006575"},{"relation_name":"is_a","term_name":"phosphorus metabolic process","termid":"GO:0006793"},{"relation_name":"is_a","term_name":"monocarboxylic acid metabolic process","termid":"GO:0032787"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"coenzyme B metabolic process","synonyms":[{"name":"coenzyme B metabolism","type":"exact"}],"termid":"GO:0019297"}


id: PBO:0111646
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"negative cofactor 2 complex subunit Bur6","termid":"PBO:0111646"}


id: PBO:0046693
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ETNK1 divergent transcript","termid":"PBO:0046693"}


id: PBO:0080161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"variable charge X-linked 3A","termid":"PBO:0080161"}


id: MONDO:0700082
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chromosomal disorder in which (part or full) chromosome 21 is attached to another chromosome, resulting in the presence of a third copy of part of full chromosome 21 genetic material. A Robertsonian translocation is a structural chromosomal anomaly in which two acrocentric chromosomes break, resulting in the fusion of the nonhomologous chromosomes’ long arms to form a single, large chromosome.","definition_xrefs":["PMID:1831959","PMID:23097978","PMID:29956287"],"direct_ancestors":[{"relation_name":"is_a","term_name":"translocation Down syndrome","termid":"MONDO:0700128"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Robertsonian translocation Down syndrome","secondary_identifiers":["UMLS:C5707615","MEDGEN:1816520","NCIT:C188150"],"termid":"MONDO:0700082","xrefs":{"Monarch":{"xref_id":"0700082"}}}


id: MONDO:0004272
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A tuberculosis that involves the urinary bladder.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial urinary tract infection","termid":"MONDO:0005247"},{"relation_name":"is_a","term_name":"urogenital tuberculosis","termid":"MONDO:0006002"},{"relation_name":"is_a","term_name":"urinary bladder disorder","termid":"MONDO:0006026"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"urinary bladder tuberculosis","secondary_identifiers":["ICD9:016.10","ICD9:016.14","MEDGEN:509075","SCTID:32268008","UMLS:C0152793","DOID:754","ICD9:016.1"],"synonyms":[{"name":"bladder tuberculosis","type":"related"},{"name":"bladder tuberculous","type":"exact"},{"name":"tuberculosis of bladder","type":"exact"},{"name":"tuberculosis of bladder, unspecified examination","type":"exact"},{"name":"tuberculous cystitis","type":"exact"},{"name":"urinary bladder tuberculosis","type":"exact"}],"termid":"MONDO:0004272","xrefs":{"Monarch":{"xref_id":"0004272"}}}


id: MONDO:0016043
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Isolated cleft lip is a fissure type embryopathy extending from the upper lip to the nasal base.","definition_xrefs":["Orphanet:199302"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cleft lip","termid":"MONDO:0004747"},{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"isolated cleft lip","secondary_identifiers":["MEDGEN:40327","UMLS:C0008924","GARD:17091","MedDRA:10009259","icd11.foundation:172183323"],"synonyms":[{"name":"isolated cleft lip (disease)","type":"exact"},{"name":"nonsyndromic cleft lip (disease)","type":"exact"}],"termid":"MONDO:0016043","xrefs":{"Monarch":{"xref_id":"0016043"}}}


id: GO:0035323
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An intercellular bridge that connects the germline cells of a male cyst.","definition_xrefs":["PMID:9635420"],"direct_ancestors":[{"relation_name":"is_a","term_name":"germline ring canal","termid":"GO:0045172"}],"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":"male germline ring canal","synonyms":[{"name":"spermatocyte ring canal","type":"narrow"},{"name":"testicular ring canal","type":"narrow"}],"termid":"GO:0035323"}


id: PBO:0054858
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 2272","termid":"PBO:0054858"}


id: PR:O60183
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sat1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O60183"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein sat1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC23E6.08","synonyms":[{"name":"Spom972h-sat1","type":"exact"}],"termid":"PR:O60183"}


id: MONDO:0008995
data:
  {"annotated_genes":["SJAG_02289"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86583],"is_not":false,"summary":null,"term":"MONDO:0008995"}]},"cv_name":"mondo","definition":"Yunis-Varon syndrome is a rare condition that affects many different parts of the body. Signs and symptoms are generally present from birth and may include underdeveloped or absent collarbones (clavicles); large fontanelles; characteristic facial features; hypotonia (reduced muscle tone) and/or abnormalities of the fingers and toes. Affected people may also experience feeding difficulties, breathing problems, brain malformations, heart defects, skeletal abnormalities, developmental delay, and/or intellectual disability. Yunis-Varon syndrome is caused by changes (mutations) in the FIG4 gene and isinherited in an autosomal recessive manner. Treatment is based on the signs and symptoms present in each person.","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02289":null},"genotype_count":0,"is_obsolete":false,"name":"Yunis-Varon syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NORD:1875","MESH:C536719","icd11.foundation:1696991249","DOID:0060589","Orphanet:3472","OMIM:216340","UMLS:C1857663","GARD:331","MEDGEN:341818"],"synonyms":[{"name":"YVS","type":"related"},{"name":"Yunis Varon Syndrome","type":"exact"},{"name":"Yunis Varon syndrome","type":"exact"},{"name":"Yunis-Varon syndrome","type":"exact"},{"name":"Yunis-Varón syndrome","type":"exact"},{"name":"cleidocranial dysplasia with micrognathia, absent thumbs, and distal Aphalangia","type":"related"},{"name":"cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia","type":"exact"},{"name":"cleidocranial dysplasia-micrognathia-absent thumbs syndrome","type":"exact"}],"termid":"MONDO:0008995","terms_by_termid":{"MONDO:0008995":null},"xrefs":{"Monarch":{"xref_id":"0008995"}}}


id: GO:0098545
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which a protein complex is maintained in a specific location within the cytoplasm and is prevented from moving elsewhere.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of location in cell","termid":"GO:0051651"},{"relation_name":"is_a","term_name":"maintenance of protein complex location","termid":"GO:0098544"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"maintenance of protein complex location in cytoplasm","termid":"GO:0098545"}


id: PBO:0000003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene characterisation status","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved unknown","termid":"PBO:0000003"}


id: MONDO:0009995
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rheumatic fever-related antigen (obsolete MONDO:0009995)","secondary_identifiers":["OMIM:268240"],"synonyms":[{"name":"rheumatic fever, acute, susceptibility to","type":"related"},{"name":"rheumatic fever-related antigen","type":"exact"}],"termid":"MONDO:0009995","xrefs":{"Monarch":{"xref_id":"0009995"}}}


id: MONDO:0014710
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency in which the cause of the disease is a mutation in the RORC gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited susceptibility to mycobacterial diseases","termid":"MONDO:0019146"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency","secondary_identifiers":["OMIM:616622","Orphanet:477857","MEDGEN:1799070","UMLS:C5567647","DOID:0111940"],"synonyms":[{"name":"IMD42","type":"exact"},{"name":"RORC autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency","type":"exact"},{"name":"autosomal recessive MSMD due to complete RORgamma receptor defiency","type":"exact"},{"name":"autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in RORC","type":"exact"},{"name":"autosomal recessive primary immunodeficiency due to RORC mutation","type":"exact"},{"name":"immunodeficiency 42","type":"exact"},{"name":"immunodeficiency type 42","type":"exact"}],"termid":"MONDO:0014710","xrefs":{"Monarch":{"xref_id":"0014710"}}}


id: PBO:0041489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 12 open reading frame 4","termid":"PBO:0041489"}


id: GO:0060085
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which the extent of smooth muscle contraction is reduced in the bladder outlet that contributes to the expulsion of urine from the body.","definition_xrefs":["GOC:dph","PMID:15827347"],"direct_ancestors":[{"relation_name":"is_a","term_name":"relaxation of smooth muscle","termid":"GO:0044557"},{"relation_name":"is_a","term_name":"negative regulation of smooth muscle contraction","termid":"GO:0045986"},{"relation_name":"part_of","term_name":"micturition","termid":"GO:0060073"}],"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":"smooth muscle relaxation of the bladder outlet","synonyms":[{"name":"synaptic transmission involved in urination","type":"exact"}],"termid":"GO:0060085"}


id: PBO:0089341
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMARCAD1 family ATPase Fft2","termid":"PBO:0089341"}


id: GO:0005614
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A type of extracellular matrix found in interstitial connective tissue, characterized by the presence of fibronectins, proteoglycans, and types I, III, V, VI, VII and XII collagens.","definition_xrefs":["PMID:33605520","PMID:8450001","PMID:39223427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"collagen-containing extracellular matrix","termid":"GO:0062023"}],"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":"interstitial matrix","termid":"GO:0005614"}


id: GO:0007156
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of a plasma membrane adhesion molecule in one cell to an identical molecule in an adjacent cell.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell adhesion via plasma-membrane adhesion molecules","termid":"GO:0098742"}],"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":"homophilic cell adhesion via plasma membrane adhesion molecules","termid":"GO:0007156"}


id: PBO:0064257
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleckstrin homology domain containing A5","termid":"PBO:0064257"}


id: GO:1990326
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen homotrimer of alpha1(XXVIII) chains.","definition_xrefs":["PMID:17876790","GOC:bhm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"collagen trimer","termid":"GO:0005581"},{"relation_name":"part_of","term_name":"collagen-containing extracellular matrix","termid":"GO:0062023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"collagen type XXVIII trimer","termid":"GO:1990326"}


id: PBO:0047048
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 110 member C","termid":"PBO:0047048"}


id: PBO:0005309
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 Dim1","termid":"PBO:0005309"}


id: PBO:0071205
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L23a pseudogene 46","termid":"PBO:0071205"}


id: MONDO:0009943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A bone dysplasia characterized by genu valgum, metaphyseal anomalies with broadening of the long bones extending into the diaphyses and giving the femora and tibiae an 'Erlenmeyer flask'' appearance, widening of the ribs and clavicles, platyspondyly and cortical thinning.","definition_xrefs":["Orphanet:3005"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with increased bone density (obsolete MONDO:0019703)","termid":"MONDO:0019703"},{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"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":"Pyle disease","secondary_identifiers":["MESH:C536252","UMLS:C0265294","SCTID:27837003","OMIM:265900","GARD:4612","icd11.foundation:651364947","NANDO:2201367","ICD10CM:Q78.5","MEDGEN:82704","ICD9:758.5","DOID:0080019"],"synonyms":[{"name":"Bakwin-Krida syndrome","type":"exact"},{"name":"Pyl","type":"related"},{"name":"Pyle disease","type":"exact"},{"name":"Pyle's disease","type":"exact"},{"name":"Pyle's syndrome","type":"exact"},{"name":"Pyle-Cohn syndrome","type":"exact"},{"name":"chondrodysplasia calcificans metaphysealis","type":"exact"},{"name":"metaphyseal dysplasia","type":"broad"},{"name":"metaphyseal dysplasia Pyle type","type":"related"},{"name":"metaphyseal dysplasia, Pyle type","type":"exact"}],"termid":"MONDO:0009943","xrefs":{"Monarch":{"xref_id":"0009943"}}}


id: MONDO:0000761
data:
  {"annotated_genes":["SJAG_03424","SJAG_02035","SJAG_00786","SJAG_03286","SJAG_03635","SJAG_00112","SJAG_04324","SJAG_01806","SJAG_01548","SJAG_00441","SJAG_01465","SJAG_02317","SJAG_02846","SJAG_04663","SJAG_01804","SJAG_03244"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86509,86510,86508],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013256"},{"annotations":[86074,86075],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007925"},{"annotations":[86622],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010334"},{"annotations":[86337,86339,86336,86338,86340,86341,86335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010767"},{"annotations":[85982],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014848"},{"annotations":[87482],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008644"},{"annotations":[85959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008684"}]},"cv_name":"mondo","definition":"A chromosomal disorder consisting of the absence of a part of a chromosome.","direct_ancestors":[{"relation_name":"is_a","term_name":"chromosomal disorder","termid":"MONDO:0019040"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00112":null,"SJAG_00441":null,"SJAG_00786":null,"SJAG_01465":null,"SJAG_01548":null,"SJAG_01804":null,"SJAG_01806":null,"SJAG_02035":null,"SJAG_02317":null,"SJAG_02846":null,"SJAG_03244":null,"SJAG_03286":null,"SJAG_03424":null,"SJAG_03635":null,"SJAG_04324":null,"SJAG_04663":null},"genotype_count":0,"is_obsolete":false,"name":"syndrome caused by partial chromosomal deletion","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0060388"],"synonyms":[{"name":"chromosomal deletion syndrome","type":"related"},{"name":"microdeletion syndrome","type":"exact"}],"termid":"MONDO:0000761","terms_by_termid":{"MONDO:0007925":null,"MONDO:0008644":null,"MONDO:0008684":null,"MONDO:0010334":null,"MONDO:0010767":null,"MONDO:0013256":null,"MONDO:0014848":null},"xrefs":{"Monarch":{"xref_id":"0000761"}}}


id: MONDO:0007780
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hypertelorism, Teebi type (obsolete MONDO:0007780)","termid":"MONDO:0007780","xrefs":{"Monarch":{"xref_id":"0007780"}}}


id: PBO:0070092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 6 pseudogene","termid":"PBO:0070092"}


id: PBO:0027583
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_autophagy_during_nitrogen_starvation","termid":"PBO:0027583"}


id: GO:0048712
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of astrocyte differentiation.","definition_xrefs":["GOC:vp","PMID:15139015"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of glial cell differentiation","termid":"GO:0045686"},{"relation_name":"is_a","term_name":"regulation of astrocyte differentiation","termid":"GO:0048710"},{"relation_name":"negatively_regulates","term_name":"astrocyte differentiation","termid":"GO:0048708"}],"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 astrocyte differentiation","synonyms":[{"name":"down regulation of astrocyte differentiation","type":"exact"},{"name":"down-regulation of astrocyte differentiation","type":"exact"},{"name":"downregulation of astrocyte differentiation","type":"exact"},{"name":"inhibition of astrocyte differentiation","type":"narrow"}],"termid":"GO:0048712"}


id: FYPO:0002983
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of serine residues in one or more specific proteins, or of specific protein sites, does not occur during a cellular response to DNA damage.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete abolished protein serine phosphorylation during cellular response to DNA damage (obsolete FYPO:0002983)","synonyms":[{"name":"abolished protein serine phosphorylation during cellular response to DNA damage during mitotic cell cycle","type":"related"},{"name":"abolished protein serine phosphorylation during cellular response to DNA damage during vegetative growth","type":"exact"},{"name":"protein serine phosphorylation abolished during cellular response to DNA damage","type":"exact"}],"termid":"FYPO:0002983"}


id: PBO:0049595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 clustered histone 13","termid":"PBO:0049595"}


id: MONDO:0008816
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Arnold-Chiari malformation type II is a rare, central nervous system malformation characterized by caudal displacement of the cerebellum, pons, medulla and fourth ventricle through the foramen magnum into the spinal canal, and is typically associated with myelomeningocele. Variable other central nervous system abnormalities might be present (partial or complete agenesis of the corpus callosum, a small fourth ventricle, obstructive hydrocephalus, falx and tentorium defects, and polygyria). Symptoms include hypotonia, apnea with cyanosis, dysphagia, opisthotonus, nystagmus, spasticity, ataxia, and occipital headache.","definition_xrefs":["Orphanet:1136"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Chiari malformation","termid":"MONDO:0000115"},{"relation_name":"is_a","term_name":"spina bifida cystica","termid":"MONDO:0017069"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"Chiari malformation type II","secondary_identifiers":["OMIM:207950","MEDGEN:108222","SCTID:373587001","UMLS:C0555206","GARD:9232","MedDRA:10056945"],"synonyms":[{"name":"Arnold Chiari malformation type II","type":"related"},{"name":"Arnold-Chiari malformation","type":"related"},{"name":"Arnold-Chiari malformation type 2","type":"exact"},{"name":"Arnold-Chiari malformation type II","type":"exact"},{"name":"Chiari malformation type 2","type":"exact"},{"name":"Chiari malformation type II","type":"exact"},{"name":"Chiari type II malformation","type":"related"},{"name":"Cm2","type":"related"}],"termid":"MONDO:0008816","xrefs":{"Monarch":{"xref_id":"0008816"}}}


id: GO:0098874
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A series of sequential, propagated action potentials occurring in a single cell.","definition_xrefs":["ISBN:978-0071390118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of membrane potential","termid":"GO:0042391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"spike train","secondary_identifiers":["GO:0099603"],"synonyms":[{"name":"burst of action potentials","type":"exact"},{"name":"spike-train","type":"exact"}],"termid":"GO:0098874"}


id: MONDO:0007501
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":"preauricular fistulae, congenital","secondary_identifiers":["MEDGEN:154283","MESH:C563015","OMIM:128700","UMLS:C0546969"],"synonyms":[{"name":"Ear pits","type":"related"},{"name":"Pafc","type":"related"},{"name":"preauricular fistulae, congenital","type":"exact"}],"termid":"MONDO:0007501","xrefs":{"Monarch":{"xref_id":"0007501"}}}


id: PBO:0116678
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARF like GTPase 9","termid":"PBO:0116678"}


id: PBO:0048118
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"furin, paired basic amino acid cleaving enzyme","termid":"PBO:0048118"}


id: PBO:0075209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide N","termid":"PBO:0075209"}


id: GO:1903627
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of dUTP diphosphatase activity.","definition_xrefs":["GOC:TermGenie","PMID:1315924","GO_REF:0000059"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of dUTP diphosphatase activity (obsolete GO:1903627)","synonyms":[{"name":"regulation of dUTP nucleotidohydrolase activity","type":"exact"},{"name":"regulation of dUTP pyrophosphatase activity","type":"exact"},{"name":"regulation of dUTPase activity","type":"exact"},{"name":"regulation of deoxyuridine-triphosphatase activity","type":"exact"},{"name":"regulation of desoxyuridine 5'-triphosphatase activity","type":"exact"},{"name":"regulation of desoxyuridine 5'-triphosphate nucleotidohydrolase activity","type":"exact"}],"termid":"GO:1903627"}


id: GO:0008634
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of survival gene product expression; survival gene products are those that antagonize the apoptotic program. Regulation can be at the transcriptional, translational, or posttranslational level.","definition_xrefs":["GOC:tb","GOC:go_curators","GOC:mtg_apoptosis","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of survival gene product expression (obsolete GO:0008634)","synonyms":[{"name":"down regulation of survival gene product activity","type":"broad"},{"name":"down-regulation of survival gene product activity","type":"broad"},{"name":"downregulation of survival gene product activity","type":"broad"},{"name":"inhibition of survival gene product activity","type":"narrow"},{"name":"negative regulation of survival gene product activity","type":"broad"},{"name":"negative regulation of survival gene product expression","type":"exact"},{"name":"negative regulation of survival gene products","type":"broad"}],"termid":"GO:0008634"}


id: SO:0001457
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region defined by a set of transcribed sequences from the same gene or expressed pseudogene.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"has_part","term_name":"reagent","termid":"SO:0000695"},{"relation_name":"is_a","term_name":"experimental_feature","termid":"SO:0001410"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcribed_cluster","synonyms":[{"name":"transcribed cluster","type":"exact"},{"name":"unigene cluster","type":"related"}],"termid":"SO:0001457"}


id: PATO:0001654
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An alignment quality inhering in a bearer by virtue of the bearer's being in a improper spatial positioning with respect to an additional entity.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alignment","termid":"PATO:0001652"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"misaligned with","synonyms":[{"name":"misaligned ","type":"exact"},{"name":"unaligned with","type":"exact"}],"termid":"PATO:0001654"}


id: GO:0075147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the symbiont organism modulates the frequency, rate or extent of its signal transduction as a result of detecting molecules of its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of signal transduction in response to host (obsolete GO:0075147)","synonyms":[{"name":"regulation of symbiont signal transduction in response to host","type":"exact"}],"termid":"GO:0075147"}


id: MONDO:0030293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary angioedema","termid":"MONDO:0019623"}],"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":"angioedema, hereditary, 5","secondary_identifiers":["MEDGEN:1780904","OMIM:619361","UMLS:C5543508"],"synonyms":[{"name":"HAE5","type":"exact"},{"name":"angioedema, hereditary, 5","type":"exact"}],"termid":"MONDO:0030293","xrefs":{"Monarch":{"xref_id":"0030293"}}}


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


id: PBO:0003012
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldo/keto reductase family protein","termid":"PBO:0003012"}


id: PBO:0012575
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S phase delayed","termid":"PBO:0012575"}


id: PBO:0017920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"R3H and G-patch domain Sqs1(predicted)","termid":"PBO:0017920"}


id: MONDO:0009542
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"malabsorption syndrome","termid":"MONDO:0020598"}],"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":"lysine malabsorption syndrome","secondary_identifiers":["UMLS:C0796023","MEDGEN:167097","OMIM:247950","MESH:C563080"],"synonyms":[{"name":"lysine malabsorption syndrome","type":"exact"}],"termid":"MONDO:0009542","xrefs":{"Monarch":{"xref_id":"0009542"}}}


id: PBO:0046988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 86 member M, pseudogene","termid":"PBO:0046988"}


id: GO:0061726
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The disaggregation of a mitochondrion into its constituent components.","definition_xrefs":["PMID:25009776","GOC:autophagy"],"gene_count":0,"genotype_count":0,"name":"obsolete mitochondrion disassembly (obsolete GO:0061726)","synonyms":[{"name":"mitochondrion degradation","type":"exact"}],"termid":"GO:0061726"}


id: GO:1990591
data:
  {"annotated_genes":["SJAG_02029","SJAG_04725"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[103115,110335],"is_not":false,"summary":null,"term":"GO:1990591"}]},"cv_name":"biological_process","definition":"The directed movement of asparagine into the vacuole across the vacuolar membrane.","definition_xrefs":["PMID:20388511"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amino acid transmembrane import into vacuole","termid":"GO:0032975"},{"relation_name":"is_a","term_name":"asparagine transmembrane transport","termid":"GO:1903713"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02029":null,"SJAG_04725":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0055085","GO:0008150"],"is_obsolete":false,"name":"asparagine transmembrane import into vacuole","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990591","terms_by_termid":{"GO:1990591":null}}


id: GO:0018132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a peptidyl serine-peptidyl cysteine cross-link by the condensation of a serine hydroxyl with the carbonyl of the preceding residue and alpha-beta dehydrogenation.","definition_xrefs":["PMID:8895467","RESID:AA0238"],"gene_count":0,"genotype_count":0,"name":"obsolete peptide cross-linking via L-cysteine oxazolecarboxylic acid (obsolete GO:0018132)","termid":"GO:0018132"}


id: RO:0002531
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of immediately downstream of","direct_ancestors":[{"relation_name":"is_a","term_name":"sequentially_adjacent_to","termid":"RO:0002515"},{"relation_name":"is_a","term_name":"is_upstream_of_sequence_of","termid":"RO:0002528"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"is_immediately_upstream_of_sequence_of","termid":"RO:0002531"}


id: PBO:0000192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell wall protein Asl1, predicted O-glucosyl hydrolase","termid":"PBO:0000192"}


id: PBO:0091918
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FrataXiN","termid":"PBO:0091918"}


id: GO:1903537
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any meiotic cell cycle process that is involved in oocyte maturation.","definition_xrefs":["GOC:jz","PMID:25212395","GO_REF:0000060","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"},{"relation_name":"part_of","term_name":"oocyte maturation","termid":"GO:0001556"}],"gene_count":0,"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":"meiotic cell cycle process involved in oocyte maturation","synonyms":[{"name":"meiosis involved in oocyte maturation","type":"broad"}],"termid":"GO:1903537"}


id: FYPO:0003851
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002058","FYPO:0002060","FYPO:0000257","FYPO:0002057","FYPO:0000003"],"is_obsolete":false,"name":"normal growth on MTT","synonyms":[{"name":"normal cell population growth in presence of MTT","type":"exact"},{"name":"normal cell population growth on MTT","type":"exact"},{"name":"normal cellular response to MTT","type":"related"},{"name":"normal growth on 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide","type":"exact"},{"name":"normal vegetative cell population growth on MTT","type":"exact"}],"termid":"FYPO:0003851"}


id: PBO:0086026
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; undergoes sumoylation; transcription induced under cell wall stress; protein levels are reduced under anaerobic conditions; protein abundance increases in response to DNA replication stress; originally thought to be a mitochondrial ribosomal protein based on sequence analysis","termid":"PBO:0086026"}


id: GO:0051516
data:
  {"annotated_genes":["SJAG_00244","SJAG_02169","SJAG_02392","SJAG_00514","SJAG_03581"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115350],"is_not":false,"summary":null,"term":"GO:0051516"},{"annotations":[96180,90204,94914],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051519"},{"annotations":[91065],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051517"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of bipolar cell growth, polarized growth from both ends of a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of unidimensional cell growth","termid":"GO:0051510"},{"relation_name":"regulates","term_name":"bipolar cell growth","termid":"GO:0042815"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00244":null,"SJAG_00514":null,"SJAG_02169":null,"SJAG_02392":null,"SJAG_03581":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of bipolar cell growth","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0051516","terms_by_termid":{"GO:0051516":null,"GO:0051517":null,"GO:0051519":null}}


id: PBO:0081007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger and BTB domain containing 44","termid":"PBO:0081007"}


id: MONDO:0009383
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hyperbilirubinemia","termid":"MONDO:0002408"},{"relation_name":"is_a","term_name":"liver disorder","termid":"MONDO:0005154"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515","MONDO:0005066"],"is_obsolete":false,"name":"transient familial neonatal hyperbilirubinemia","secondary_identifiers":["MESH:C562692","UMLS:C0270210","GARD:2791","OMIM:237900","Orphanet:2312","MEDGEN:75718"],"synonyms":[{"name":"HBLRTFN","type":"related"},{"name":"Lucey-Driscoll syndrome","type":"exact"},{"name":"breast milk jaundice","type":"related"},{"name":"hyperbilirubinemia transient familial neonatal","type":"related"},{"name":"hyperbilirubinemia, familial transient neonatal","type":"exact"},{"name":"hyperbilirubinemia, transient familial neonatal","type":"related"},{"name":"transient familial hyperbilirubinemia","type":"related"}],"termid":"MONDO:0009383","xrefs":{"Monarch":{"xref_id":"0009383"}}}


id: GO:0044359
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The process in which an organism effects a change in the function of proteins in a second organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete modulation of molecular function in another organism (obsolete GO:0044359)","synonyms":[{"name":"modulation of molecular function in other organism","type":"exact"}],"termid":"GO:0044359"}


id: MONDO:0019397
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"unknown leukodystrophy","secondary_identifiers":["Orphanet:84096"],"termid":"MONDO:0019397","xrefs":{"Monarch":{"xref_id":"0019397"}}}


id: SO:0002062
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A contiguous cluster of translocations, usually the result of a single catastrophic event such as chromothripsis or chromoanasynthesis.","definition_xrefs":["NCBI:th"],"direct_ancestors":[{"relation_name":"is_a","term_name":"complex_structural_alteration","termid":"SO:0001784"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complex_chromosomal_rearrangement","synonyms":[{"name":"complex chromosomal rearrangement","type":"exact"}],"termid":"SO:0002062"}


id: SO:0002072
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A position or feature where two sequences have been compared.","direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_feature","termid":"SO:0000110"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sequence_comparison","synonyms":[{"name":"INSDC_feature:misc_feature","type":"broad"},{"name":"INSDC_note:sequence_comparison","type":"exact"},{"name":"sequence comparison","type":"exact"}],"termid":"SO:0002072"}


id: GO:1900850
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of pseurotin A biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of biosynthetic process","termid":"GO:0009890"},{"relation_name":"is_a","term_name":"negative regulation of amide metabolic process","termid":"GO:0034249"},{"relation_name":"is_a","term_name":"negative regulation of small molecule metabolic process","termid":"GO:0062014"},{"relation_name":"is_a","term_name":"regulation of pseurotin A biosynthetic process","termid":"GO:1900849"},{"relation_name":"negatively_regulates","term_name":"pseurotin A biosynthetic process","termid":"GO:1900790"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"negative regulation of pseurotin A biosynthetic process","synonyms":[{"name":"down regulation of pseurotin A biosynthetic process","type":"exact"},{"name":"down-regulation of pseurotin A biosynthetic process","type":"exact"},{"name":"downregulation of pseurotin A biosynthetic process","type":"exact"}],"termid":"GO:1900850"}


id: MONDO:0016893
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of chromosome 11","termid":"MONDO:0016876"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of the short arm of chromosome 11","secondary_identifiers":["GARD:20815","icd11.foundation:127054483","MEDGEN:419498","UMLS:C2931801","Orphanet:261947"],"synonyms":[{"name":"partial deletion of chromosome 11p","type":"exact"},{"name":"partial deletion of the short arm of chromosome type 11","type":"exact"},{"name":"partial monosomy of chromosome 11p","type":"exact"},{"name":"partial monosomy of the short arm of chromosome 11","type":"exact"}],"termid":"MONDO:0016893","xrefs":{"Monarch":{"xref_id":"0016893"}}}


id: PBO:0083695
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Epoxide hydrolase; member of the alpha/beta hydrolase fold family; may have a role in detoxification of epoxides","termid":"PBO:0083695"}


id: GO:0051711
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the killing by an organism of cells in another organism.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell killing","termid":"GO:0031342"},{"relation_name":"is_a","term_name":"regulation of killing of cells of another organism","termid":"GO:0051709"},{"relation_name":"negatively_regulates","term_name":"killing of cells of another organism","termid":"GO:0031640"}],"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 killing of cells of another organism","secondary_identifiers":["GO:0052490","Reactome:R-HSA-9662851"],"synonyms":[{"name":"down regulation of killing of cells of another organism","type":"exact"},{"name":"down-regulation of killing of cells of another organism","type":"exact"},{"name":"downregulation of killing of cells of another organism","type":"exact"},{"name":"inhibition of killing of cells of another organism","type":"narrow"},{"name":"negative regulation of killing of cells of other organism","type":"exact"}],"termid":"GO:0051711"}


id: MONDO:0018996
data:
  {"annotated_genes":["SJAG_03923","SJAG_02242"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86966,86967],"is_not":false,"summary":null,"term":"MONDO:0018996"}]},"cv_name":"mondo","definition":"A rare autosomal recessive cerebellar ataxia (ARCA), characterized by progressive cerebellar ataxia associated with frequent oculomotor apraxia, severe neuropathy and an elevated serum alpha-fetoprotein (AFP) level.","definition_xrefs":["Orphanet:64753"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"},{"relation_name":"is_a","term_name":"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy","termid":"MONDO:0020771"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02242":null,"SJAG_03923":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0021190"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0006025","MONDO:0005559","MONDO:0021190","MONDO:0005066"],"is_obsolete":false,"name":"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:606002","MESH:C537308","UMLS:C1853761","NCIT:C165500","GARD:12860","DOID:0050755","SCTID:725408001","MEDGEN:340052"],"synonyms":[{"name":"AOA2","type":"exact"},{"name":"SCAN 2","type":"exact"},{"name":"SCAN2","type":"exact"},{"name":"SCAR1","type":"related"},{"name":"ataxia with oculomotor apraxia type 2","type":"exact"},{"name":"ataxia-ocular apraxia 2","type":"exact"},{"name":"ataxia-oculomotor apraxia 2","type":"exact"},{"name":"ataxia-oculomotor apraxia type 2","type":"exact"},{"name":"autosomal recessive spinocerebellar ataxia-1","type":"related"},{"name":"spinocerebellar ataxia with axonal neuropathy type 2","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive 1","type":"exact"},{"name":"spinocerebellar ataxia, autosomal recessive type 1","type":"exact"}],"termid":"MONDO:0018996","terms_by_termid":{"MONDO:0018996":null},"xrefs":{"Monarch":{"xref_id":"0018996"}}}


id: GO:0035829
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A renal system process in which rubidium ions are taken up from the collecting ducts and proximal and distal loops of the nephron. In non-mammalian species, absorption may occur in related structures.","definition_xrefs":["GOC:yaf"],"gene_count":0,"genotype_count":0,"name":"obsolete renal rubidium ion absorption (obsolete GO:0035829)","synonyms":[{"name":"renal Rb+ absorption","type":"exact"},{"name":"renal rubidium cation absorption","type":"exact"}],"termid":"GO:0035829"}


id: GO:0097135
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex consisting of cyclin E2 and cyclin-dependent kinase 2 (CDK2). Cyclins are characterized by periodicity in protein abundance throughout the cell cycle. Cyclin-dependent kinases represent a family of serine/threonine protein kinases that become active upon binding to a cyclin regulatory partner.","definition_xrefs":["PMID:15935619","GOC:so"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclin-dependent protein kinase holoenzyme complex","termid":"GO:0000307"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"cyclin E2-CDK2 complex","termid":"GO:0097135"}


id: FYPO:0006825
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the mitotic spindle pole body does not occur during mitosis.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to mitotic spindle pole body","termid":"FYPO:0000941"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0005447","FYPO:0000138","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"abolished protein localization to mitotic spindle pole body during mitosis","synonyms":[{"name":"abolished protein localisation to mitotic spindle pole body during mitosis","type":"exact"},{"name":"abolished protein localization to mitotic SPB during mitosis","type":"exact"},{"name":"abolished protein localization to mitotic spindle pole body during mitotic M phase","type":"related"},{"name":"abolished protein localization to mitotic spindle pole body during mitotic M-phase","type":"related"},{"name":"abolished protein localization to mitotic spindle pole body during mitotic nuclear division","type":"exact"},{"name":"protein absent from mitotic spindle pole body during mitosis","type":"related"},{"name":"protein localisation to mitotic spindle pole body abolished during mitosis","type":"exact"},{"name":"protein localization to mitotic spindle pole body abolished during mitosis","type":"exact"},{"name":"protein localization to spindle pole body abolished during mitosis during vegetative growth","type":"exact"}],"termid":"FYPO:0006825"}


id: PR:O94347
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP-dependent (S)-NAD(P)H-hydrate dehydratase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent (S)-NAD(P)H-hydrate dehydratase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC61.03","secondary_identifiers":["UniProtKB:O94347"],"synonyms":[{"name":"ATP-dependent NAD(P)HX dehydratase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-CARKD","type":"exact"}],"termid":"PR:O94347"}


id: PBO:0038425
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"A2ML1 antisense RNA 1","termid":"PBO:0038425"}


id: GO:0010595
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of the orderly movement of an endothelial cell into the extracellular matrix to form an endothelium.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of endothelial cell migration","termid":"GO:0010594"},{"relation_name":"is_a","term_name":"positive regulation of cell migration","termid":"GO:0030335"},{"relation_name":"positively_regulates","term_name":"endothelial cell migration","termid":"GO:0043542"}],"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 endothelial cell migration","termid":"GO:0010595"}


id: MONDO:1011284
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary marked delay in recovery of dark adaptation and degeneration of the area centralis (equivalent to the human macula) in cats due to a variation in the RDH5 gene.","definition_xrefs":["PMID:34726233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"central retinal degeneration, domestic cat","termid":"MONDO:1012240"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinopathy, RDH5-related, domestic cat","secondary_identifiers":["OMIA:002469-9685"],"termid":"MONDO:1011284","xrefs":{"Monarch":{"xref_id":"1011284"}}}


id: MONDO:0015880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndromic diaphragmatic or thoracic malformation (obsolete MONDO:0015880)","secondary_identifiers":["Orphanet:180779"],"termid":"MONDO:0015880","xrefs":{"Monarch":{"xref_id":"0015880"}}}


id: FYPO:0003068
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 at replication forks is decreased during a cellular response to hydroxyurea.","definition_xrefs":["PMID:22682245","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to chromatin during vegetative growth","termid":"FYPO:0002909"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to chromatin at replication forks during cellular response to hydroxyurea","synonyms":[{"name":"decreased protein localisation to chromatin at replication forks during cellular response to hydroxyurea","type":"exact"},{"name":"decreased protein localization to chromatin at replication forks during cellular response to HU","type":"exact"},{"name":"decreased protein localization to chromatin at replication forks during cellular response to hydroxyurea during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to chromatin at replication forks during cellular response to hydroxyurea during vegetative growth","type":"exact"},{"name":"reduced protein localization to chromatin at replication forks during cellular response to hydroxyurea","type":"exact"}],"termid":"FYPO:0003068"}


id: GO:1900472
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of phosphatidylcholine biosynthetic process by activating or increasing the frequency, rate or extent of transcription from an RNA polymerase II promoter.","definition_xrefs":["GOC:TermGenie","PMID:8056324","PMID:8614637","GOC:dgf"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of phosphatidylcholine biosynthetic process by positive regulation of transcription from RNA polymerase II promoter (obsolete GO:1900472)","synonyms":[{"name":"positive regulation of phosphatidylcholine anabolism by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of phosphatidylcholine biosynthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of phosphatidylcholine formation by positive regulation of transcription from RNA polymerase II promoter","type":"exact"},{"name":"positive regulation of phosphatidylcholine synthesis by positive regulation of transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:1900472"}


id: PBO:0018009
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aconitate hydratase/mitochondrial ribosomal protein subunit L21, fusion protein","termid":"PBO:0018009"}


id: PBO:0063522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prodynorphin","termid":"PBO:0063522"}


id: PBO:0002100
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"6.2.1.-","termid":"PBO:0002100"}


id: PBO:0005417
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hsk1-Dfp1 kinase complex regulatory subunit Dfp1","termid":"PBO:0005417"}


id: GO:0036278
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the frequency, rate or extent of transcription from an RNA polymerase II promoter as a result of a deprivation of nitrogen.","definition_xrefs":["PMID:21118960","GOC:al"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of transcription from RNA polymerase II promoter in response to nitrogen starvation (obsolete GO:0036278)","termid":"GO:0036278"}


id: PBO:0080947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger BED-type containing 2","termid":"PBO:0080947"}


id: GO:0060185
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The opening and spreading out of the outer ear.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure arrangement","termid":"GO:0048532"},{"relation_name":"part_of","term_name":"outer ear morphogenesis","termid":"GO:0042473"}],"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":"outer ear unfolding","termid":"GO:0060185"}


id: PBO:0030270
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_negative_regulation_of_mitotic_DNA_replication_initiation","termid":"PBO:0030270"}


id: PBO:0077616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMSB4X pseudogene 7","termid":"PBO:0077616"}


id: PBO:0070904
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 12","termid":"PBO:0070904"}


id: PBO:0041870
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calsequestrin 2","termid":"PBO:0041870"}


id: MONDO:0006957
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Dental caries involving the tooth root, cementum, or cervical area of the tooth.","definition_xrefs":["MESH:D017213"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enamel caries","termid":"MONDO:0002233"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"root caries","secondary_identifiers":["ICD9:521.08","SCTID:30512007","EFO:1001163","DOID:14089","MEDGEN:57954","UMLS:C0162644"],"synonyms":[{"name":"cementum caries","type":"exact"},{"name":"cementum dental caries","type":"exact"},{"name":"dental caries of cementum","type":"exact"},{"name":"dental caries of root surface","type":"exact"},{"name":"root caries","type":"exact"}],"termid":"MONDO:0006957","xrefs":{"Monarch":{"xref_id":"0006957"}}}


id: MONDO:0020759
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"childhood absence epilepsy","termid":"MONDO:0010826"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epilepsy, childhood absence, susceptibility to, 1","secondary_identifiers":["OMIM:600131","MEDGEN:325057","UMLS:C1838604"],"synonyms":[{"name":"ECA1","type":"exact"},{"name":"epilepsy, childhood absence, 1","type":"exact"},{"name":"epilepsy, childhood absence, susceptibility to, 1","type":"exact"}],"termid":"MONDO:0020759","xrefs":{"Monarch":{"xref_id":"0020759"}}}


id: FYPO:0008298
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 ergosta-5,7-dienol measured in a cell is higher than normal.","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:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"ergosta-5,7-dienol level","termid":"FYPO:0008298"}


id: PBO:0079900
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 III subunit XI","termid":"PBO:0079900"}


id: PBO:0029006
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-intron-specific_abnormal_mRNA_splicing,_via_spliceosome","termid":"PBO:0029006"}


id: PBO:0060414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAA50 pseudogene 1","termid":"PBO:0060414"}


id: PBO:0031043
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_actin_cytoskeleton_organization_during_vegetative_growth","termid":"PBO:0031043"}


id: PBO:0036544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uroporphyrin methyltransferase Met1","termid":"PBO:0036544"}


id: PBO:0054785
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 2198","termid":"PBO:0054785"}


id: GO:0038193
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A G protein-coupled receptor signaling pathway initiated by thromboxane A2 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":["GOC:nhn","PMID:15893915"],"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":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"thromboxane A2 signaling pathway","synonyms":[{"name":"TXA(2) receptor signaling","type":"exact"},{"name":"TXA2 signaling","type":"exact"}],"termid":"GO:0038193"}


id: GO:0018338
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of a protein amino acid by cinnamylation.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete protein amino acid cinnamylation (obsolete GO:0018338)","synonyms":[{"name":"protein amino acid cinnamylation","type":"exact"}],"termid":"GO:0018338"}


id: PBO:0042660
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEA cell adhesion molecule 16, tectorial membrane component","termid":"PBO:0042660"}


id: SOFP:mol_type
data:
  {"annotation_feature_type":"gene","cv_name":"feature_property","definition":"The type of molecule","definition_xrefs":["so:sjc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feature_property","termid":"SOFP:feature_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mol_type","termid":"SOFP:mol_type"}


id: PBO:0032732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor eIF2B beta subunit","termid":"PBO:0032732"}


id: PBO:0043158
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"capicua transcriptional repressor pseudogene 26","termid":"PBO:0043158"}


id: PBO:0001839
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycine decarboxylase T subunit (predicted)","termid":"PBO:0001839"}


id: PBO:0064782
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPM1B divergent transcript","termid":"PBO:0064782"}


id: PBO:0089028
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome export GTPase Nog2","termid":"PBO:0089028"}


id: PBO:0039246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldehyde dehydrogenase 1 family member L1","termid":"PBO:0039246"}


id: GO:0036465
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The trafficking of synaptic vesicles from the pre-synaptic membrane so the vesicle can dock and prime for another round of exocytosis and neurotransmitter release. Recycling occurs after synaptic vesicle exocytosis, and is necessary to replenish presynaptic vesicle pools, sustain transmitter release and preserve the structural integrity of the presynaptic membrane. Recycling can occur following transient fusion with the presynaptic membrane (kiss and run), or via endocytosis of presynaptic membrane.","definition_xrefs":["PMID:23245563","GOC:PARL","PMID:15217342","PMID:22026965","GOC:bf","GOC:pad"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport","termid":"GO:0006810"},{"relation_name":"is_a","term_name":"establishment of localization in cell","termid":"GO:0051649"},{"relation_name":"part_of","term_name":"synaptic vesicle cycle","termid":"GO:0099504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"synaptic vesicle recycling","synonyms":[{"name":"kiss-and-run synaptic vesicle recycling","type":"narrow"},{"name":"kiss-and-stay synaptic vesicle recycling","type":"narrow"}],"termid":"GO:0036465"}


id: MONDO:0014456
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive severe congenital neutropenia","termid":"MONDO:0028226"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive severe congenital neutropenia due to JAGN1 deficiency","secondary_identifiers":["MEDGEN:863391","DOID:0112134","OMIM:616022","GARD:17702","Orphanet:423384","UMLS:C4014954"],"synonyms":[{"name":"SCN6","type":"related"},{"name":"neutropenia, severe congenital, 6, autosomal recessive","type":"related"}],"termid":"MONDO:0014456","xrefs":{"Monarch":{"xref_id":"0014456"}}}


id: PBO:0024875
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae MOG1","termid":"PBO:0024875"}


id: PBO:0077548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transmembrane protein 256 pseudogene 1","termid":"PBO:0077548"}


id: PBO:0062320
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 6 subfamily C member 2","termid":"PBO:0062320"}


id: FYPO:0007325
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which an interaction between a protein and a transfer RNA (tRNA) is increased. 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":"increased protein-RNA interaction","termid":"FYPO:0002135"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0002131"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000652","FYPO:0001985","FYPO:0002131"],"is_obsolete":false,"name":"increased tRNA binding","synonyms":[{"name":"increased protein-tRNA interaction","type":"exact"},{"name":"increased protein-transfer RNA interaction","type":"exact"},{"name":"increased transfer RNA binding","type":"exact"}],"termid":"FYPO:0007325"}


id: PBO:0039624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annexin A7","termid":"PBO:0039624"}


id: PBO:0048991
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glypican 3","termid":"PBO:0048991"}


id: MONDO:0009605
data:
  {"annotated_genes":["SJAG_03929","SJAG_04217"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85891,85892],"is_not":false,"summary":null,"term":"MONDO:0009605"}]},"cv_name":"mondo","definition":"Any methemoglobinemia in which the cause of the disease is a mutation in the CYB5A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary methemoglobinemia","termid":"MONDO:0018963"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03929":null,"SJAG_04217":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"methemoglobinemia type 4","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4285231","DOID:0112316","OMIM:250790","MEDGEN:925090","MESH:C567102","GARD:15196"],"synonyms":[{"name":"CYB5A methemoglobinemia","type":"exact"},{"name":"METAG","type":"related"},{"name":"isolated 17,20-lyase deficiency, Pure","type":"related"},{"name":"methemoglobinemia and ambiguous genitalia","type":"related"},{"name":"methemoglobinemia caused by mutation in CYB5A","type":"exact"},{"name":"methemoglobinemia due to deficiency of cytochrome B5","type":"related"},{"name":"methemoglobinemia due to deficiency of cytochrome B5, formerly","type":"related"},{"name":"methemoglobinemia type 4","type":"exact"},{"name":"methemoglobinemia type IV","type":"related"},{"name":"methemoglobinemia type IV, formerly","type":"related"}],"termid":"MONDO:0009605","terms_by_termid":{"MONDO:0009605":null},"xrefs":{"Monarch":{"xref_id":"0009605"}}}


id: GO:0048762
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized features of a mesenchymal cell. A mesenchymal cell is a loosely associated cell that is part of the connective tissue in an organism. Mesenchymal cells give rise to more mature connective tissue cell types.","definition_xrefs":["GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"mesenchyme development","termid":"GO:0060485"}],"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":"mesenchymal cell differentiation","termid":"GO:0048762"}


id: MONDO:0018260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"}],"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":"scalp syndrome","secondary_identifiers":["Orphanet:370052","UMLS:C4751599","GARD:21592","MEDGEN:1665599"],"synonyms":[{"name":"sebaceous nevus-CNS malformations-aplasia cutis congenital-limbal dermoid-pigmented nevus syndrome","type":"exact"},{"name":"sebaceous nevus-central nervous system malformations-aplasia cutis congenital-limbal dermoid-pigmented nevus syndrome","type":"exact"}],"termid":"MONDO:0018260","xrefs":{"Monarch":{"xref_id":"0018260"}}}


id: GO:0048706
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring during the embryonic phase, whose specific outcome is the progression of the skeleton over time, from its formation to the mature structure.","definition_xrefs":["GOC:dsf","GOC:dph","GOC:jid","GOC:tb","PMID:16049113"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal system development","termid":"GO:0001501"},{"relation_name":"part_of","term_name":"chordate embryonic development","termid":"GO:0043009"}],"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":"embryonic skeletal system development","synonyms":[{"name":"embryonic skeletal development","type":"exact"}],"termid":"GO:0048706"}


id: PBO:0086775
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; SWAT-GFP and mCherry fusion proteins localize to the cell periphery; predicted to be palmitoylated","termid":"PBO:0086775"}


id: PBO:0040181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aspartate beta-hydroxylase domain containing 2","termid":"PBO:0040181"}


id: PBO:0005432
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically upregulated gene Mug117","termid":"PBO:0005432"}


id: PBO:0040778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bestrophin 4","termid":"PBO:0040778"}


id: GO:1905358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of snRNA pseudouridine synthesis.","definition_xrefs":["GO_REF:0000058","PMID:27268497","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of RNA metabolic process","termid":"GO:0051254"},{"relation_name":"is_a","term_name":"regulation of snRNA pseudouridine synthesis","termid":"GO:1905356"},{"relation_name":"positively_regulates","term_name":"snRNA pseudouridine synthesis","termid":"GO:0031120"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016073"},{"rel_name":"positively_regulates","termid":"GO:0016073"}],"interesting_parent_ids":["GO:0008150","GO:0016073"],"is_obsolete":false,"name":"positive regulation of snRNA pseudouridine synthesis","synonyms":[{"name":"activation of snRNA pseudouridine synthesis","type":"narrow"},{"name":"up regulation of snRNA pseudouridine synthesis","type":"exact"},{"name":"up-regulation of snRNA pseudouridine synthesis","type":"exact"},{"name":"upregulation of snRNA pseudouridine synthesis","type":"exact"}],"termid":"GO:1905358"}


id: MONDO:0850130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinoma","termid":"MONDO:0004970"}],"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":"gastroesophageal adenocarcinoma","secondary_identifiers":["DOID:0080375"],"termid":"MONDO:0850130","xrefs":{"Monarch":{"xref_id":"0850130"}}}


id: MONDO:0003986
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete MONDO:0003986 (obsolete MONDO:0003986)","termid":"MONDO:0003986","xrefs":{"Monarch":{"xref_id":"0003986"}}}


id: PBO:0063146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PATJ divergent transcript","termid":"PBO:0063146"}


id: PBO:0076650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T-box transcription factor 5","termid":"PBO:0076650"}


id: PBO:0030813
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_isocitrate_dehydrogenase_(NAD+)_activity","termid":"PBO:0030813"}


id: PBO:0065788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"queuine tRNA-ribosyltransferase catalytic subunit 1 pseudogene 1","termid":"PBO:0065788"}


id: PR:Q09823
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rec10 gene.","definition_xrefs":["UniProtKB:Q09823","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":"meiotic recombination protein rec10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC25G10.04c","synonyms":[{"name":"Spom972h-rec10","type":"exact"}],"termid":"PR:Q09823"}


id: MONDO:0007156
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":"arthritis, sacroiliac","secondary_identifiers":["OMIM:108100","UMLS:C0748473","MEDGEN:148186","MESH:C563037"],"synonyms":[{"name":"arthritis, sacroiliac","type":"exact"}],"termid":"MONDO:0007156","xrefs":{"Monarch":{"xref_id":"0007156"}}}


id: PBO:0043278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C-type lectin domain family 4 member A","termid":"PBO:0043278"}


id: PBO:0043767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase copper chaperone COX17","termid":"PBO:0043767"}


id: MONDO:0003692
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant mesenchymoma occurring in adults.","definition_xrefs":["NCIT:C7947"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant mesenchymoma","termid":"MONDO:0003633"}],"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":"adult malignant mesenchymoma","secondary_identifiers":["UMLS:C0279548","DOID:5894","MEDGEN:83523"],"synonyms":[{"name":"adult malignant mesenchymoma","type":"exact"},{"name":"malignant mesenchymoma","type":"broad"},{"name":"malignant mesenchymoma of adults","type":"exact"}],"termid":"MONDO:0003692","xrefs":{"Monarch":{"xref_id":"0003692"}}}


id: GO:2001220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of G2 phase of mitotic cell cycle.","definition_xrefs":["GOC:mtg_cell_cycle","GOC:obol"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of G2 phase of mitotic cell cycle (obsolete GO:2001220)","synonyms":[{"name":"negative regulation of G2 phase of mitotic cell cycle","type":"exact"}],"termid":"GO:2001220"}


id: PBO:0061247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nitric oxide synthase 1 adaptor protein","termid":"PBO:0061247"}


id: GO:0033034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of myeloid cell apoptotic process.","definition_xrefs":["GOC:add","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of myeloid cell apoptotic process","termid":"GO:0033032"},{"relation_name":"is_a","term_name":"positive regulation of apoptotic process","termid":"GO:0043065"},{"relation_name":"positively_regulates","term_name":"myeloid cell apoptotic process","termid":"GO:0033028"}],"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 myeloid cell apoptotic process","synonyms":[{"name":"activation of myeloid cell apoptosis","type":"narrow"},{"name":"positive regulation of myeloid cell apoptosis","type":"narrow"},{"name":"stimulation of myeloid cell apoptosis","type":"narrow"},{"name":"up regulation of myeloid cell apoptosis","type":"exact"},{"name":"up-regulation of myeloid cell apoptosis","type":"exact"},{"name":"upregulation of myeloid cell apoptosis","type":"exact"}],"termid":"GO:0033034"}


id: PBO:0113477
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO-like domain protein; binds Holliday junctions and replication fork structures; stimulates the Mms4-Mus81 endonuclease in the resolution of sister chromatid junctions; role in recombination-mediated DNA damage tolerance by recruiting Rad51p; facilitate Elg1p binding to stalled replication forks; prevents toxic intermediate accumulation during replication-associated recombinational repair; role in silencing, chromatid cohesion and the intra-S-phase DNA damage checkpoint; RENi family member","termid":"PBO:0113477"}


id: PBO:0071969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 kinase B2","termid":"PBO:0071969"}


id: PBO:0061894
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"opsin 1, medium wave sensitive 2","termid":"PBO:0061894"}


id: PBO:0000720
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulated by Pap1","termid":"PBO:0000720"}


id: PBO:0039700
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"apoptosis inhibitor 5 pseudogene 1","termid":"PBO:0039700"}


id: PBO:0067600
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 763, pseudogene","termid":"PBO:0067600"}


id: GO:0006783
data:
  {"annotated_genes":["SJAG_04515","SJAG_03961","SJAG_01192","SJAG_04397","SJAG_02876","SJAG_03173","SJAG_03862","SJAG_04944","SJAG_01786","SJAG_05283","SJAG_02896","SJAG_01841","SJAG_01155","SJAG_00097","SJAG_00699","SJAG_01372","SJAG_04109"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[74700,101412,105514,112182,114178],"is_not":false,"summary":null,"term":"GO:0006783"},{"annotations":[80403,78714],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006784"},{"annotations":[63148,60268,80273,57224,67756,63010,64832,59191],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0006782"},{"annotations":[71735,77145],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019354"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of heme, any compound of iron complexed in a porphyrin (tetrapyrrole) ring, from less complex precursors.","definition_xrefs":["GOC:jl","PMID:11788607"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porphyrin-containing compound biosynthetic process","termid":"GO:0006779"},{"relation_name":"is_a","term_name":"heme metabolic process","termid":"GO:0042168"},{"relation_name":"is_a","term_name":"pigment biosynthetic process","termid":"GO:0046148"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00097":null,"SJAG_00699":null,"SJAG_01155":null,"SJAG_01192":null,"SJAG_01372":null,"SJAG_01786":null,"SJAG_01841":null,"SJAG_02876":null,"SJAG_02896":null,"SJAG_03173":null,"SJAG_03862":null,"SJAG_03961":null,"SJAG_04109":null,"SJAG_04397":null,"SJAG_04515":null,"SJAG_04944":null,"SJAG_05283":null},"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":"heme biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:HEMESYN2-PWY","Reactome:R-HSA-189451"],"synonyms":[{"name":"haem biosynthesis","type":"exact"},{"name":"haem biosynthetic process","type":"exact"},{"name":"heme anabolism","type":"exact"},{"name":"heme biosynthesis","type":"exact"},{"name":"heme formation","type":"exact"},{"name":"heme synthesis","type":"exact"}],"termid":"GO:0006783","terms_by_termid":{"GO:0006782":null,"GO:0006783":null,"GO:0006784":null,"GO:0019354":null}}


id: MONDO:0003096
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma arising from the deep soft tissues.","definition_xrefs":["NCIT:C6555"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hemangioma","termid":"MONDO:0006500"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deep hemangioma","secondary_identifiers":["DOID:469","MEDGEN:232421","UMLS:C1333265"],"synonyms":[{"name":"deep angioma","type":"exact"},{"name":"deep hemangioma","type":"exact"}],"termid":"MONDO:0003096","xrefs":{"Monarch":{"xref_id":"0003096"}}}


id: PBO:0004193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial inner membrane peptidase complex catalytic subunit 2 (predicted)","termid":"PBO:0004193"}


id: PBO:0001849
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spindle pole body docking protein Cut11","termid":"PBO:0001849"}


id: PBO:0058751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6875","termid":"PBO:0058751"}


id: PBO:0061834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2-oxoglutarate and iron dependent oxygenase domain containing 2","termid":"PBO:0061834"}


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


id: MONDO:0021969
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Banti syndrome (obsolete MONDO:0021969)","secondary_identifiers":["NANDO:1200438"],"termid":"MONDO:0021969","xrefs":{"Monarch":{"xref_id":"0021969"}}}


id: GO:0009575
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The space enclosed by the double membrane of a chromoplast but excluding the photosynthetic material.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plastid stroma","termid":"GO:0009532"},{"relation_name":"part_of","term_name":"chromoplast","termid":"GO:0009509"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0005575"],"is_obsolete":false,"name":"chromoplast stroma","termid":"GO:0009575"}


id: PBO:0039147
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AK3 pseudogene 2","termid":"PBO:0039147"}


id: MONDO:1012658
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinal degeneration that occurs in cats due to a mutation in the CEP290 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinal degeneration, domestic cat","termid":"MONDO:1011245"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinal degeneration, CEP290-related, domestic cat","secondary_identifiers":["OMIA:001244-9685"],"synonyms":[{"name":"late-onset hereditary retinal degeneration, domestic cat","type":"related"},{"name":"retinal degeneration II, domestic cat","type":"related"}],"termid":"MONDO:1012658","xrefs":{"Monarch":{"xref_id":"1012658"}}}


id: PBO:0083206
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps the verified gene YJL065C/DLS1","termid":"PBO:0083206"}


id: FYPO:0005417
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mitotic spindle elongation begins earlier than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic spindle elongation","termid":"FYPO:0000131"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000337"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000337","FYPO:0000631","FYPO:0000641","FYPO:0001985","FYPO:0000054","FYPO:0005447"],"is_obsolete":false,"name":"premature mitotic spindle elongation","synonyms":[{"name":"advanced mitotic spindle elongation","type":"exact"},{"name":"premature mitotic sister chromatid separation during vegetative growth","type":"related"},{"name":"premature spindle elongation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0005417"}


id: PBO:0113221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA-binding protein; interacts with the UBA domain of mRNA export factor Mex67p; participates in the export of Msn2/4 stress-dependent mRNAs; partially redundant function with paralog PES4 in the steady-state expression, translational timing and localization of a subset of Ndt80-dependent mRNAs that are protected until translated near the end of meiosis II; redundant role with PES4 in sporulation; shuttles between the nucleus and cytoplasm, localizes to stress granules and the prospore membrane","termid":"PBO:0113221"}


id: GO:0106210
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of culmorin, a sesquiterpenoid fungal metabolite and mycotoxin produced by some ascomycete species such as Fusarium culmorum, F. graminearum, F. venenatum and Leptosphaeria oraemaris.","definition_xrefs":["PMID:26673640","PMID:19880637","GOC:ach"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sesquiterpenoid biosynthetic process","termid":"GO:0016106"},{"relation_name":"is_a","term_name":"diol biosynthetic process","termid":"GO:0034312"},{"relation_name":"is_a","term_name":"mycotoxin biosynthetic process","termid":"GO:0043386"},{"relation_name":"is_a","term_name":"sesquiterpene biosynthetic process","termid":"GO:0051762"},{"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:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"culmorin biosynthetic process","synonyms":[{"name":"culmorin anabolism","type":"exact"},{"name":"culmorin biosynthesis","type":"exact"},{"name":"culmorin formation","type":"exact"},{"name":"culmorin synthesis","type":"exact"}],"termid":"GO:0106210"}


id: MONDO:0021233
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the ear.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"head and neck neoplasm","termid":"MONDO:0005586"},{"relation_name":"is_a","term_name":"disorder of ear","termid":"MONDO:0021205"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ear neoplasm","secondary_identifiers":["UMLS:C0013449","NCIT:C3000","MEDGEN:4431"],"synonyms":[{"name":"Ear neoplasms","type":"exact"},{"name":"Ear tumor","type":"exact"},{"name":"Ear tumour","type":"exact"},{"name":"ear neoplasm (disease)","type":"exact"},{"name":"ear tumor","type":"exact"},{"name":"ear tumour","type":"exact"},{"name":"neoplasm of Ear","type":"exact"},{"name":"neoplasm of ear","type":"exact"},{"name":"neoplasm of the Ear","type":"exact"},{"name":"tumor of Ear","type":"exact"},{"name":"tumor of ear","type":"exact"},{"name":"tumor of the Ear","type":"exact"},{"name":"tumour of Ear","type":"exact"},{"name":"tumour of ear","type":"exact"},{"name":"tumour of the Ear","type":"exact"}],"termid":"MONDO:0021233","xrefs":{"Monarch":{"xref_id":"0021233"}}}


id: PBO:0061487
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurogranin","termid":"PBO:0061487"}


id: PBO:0049629
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 32","termid":"PBO:0049629"}


id: PBO:0070592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7a pseudogene 58","termid":"PBO:0070592"}


id: FYPO:0000451
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the centromere of a chromosome is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to centromere during vegetative growth","termid":"FYPO:0000449"},{"relation_name":"is_a","term_name":"increased protein localization to chromosome during vegetative growth","termid":"FYPO:0002840"},{"relation_name":"is_a","term_name":"increased protein localization to centromere","termid":"FYPO:0006239"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"increased protein localization to centromere during vegetative growth","synonyms":[{"name":"increased protein localisation to centromere during vegetative growth","type":"exact"},{"name":"increased protein localisation to chromosome, centromeric region during vegetative growth","type":"exact"},{"name":"increased protein localization to centromere during mitotic cell cycle","type":"related"},{"name":"increased protein localization to chromosome, centric region during vegetative growth","type":"exact"},{"name":"increased protein localization to chromosome, centromeric region during vegetative growth","type":"exact"}],"termid":"FYPO:0000451"}


id: PBO:0000558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iron responsive transcriptional regulator, peptidase family (predicted)","termid":"PBO:0000558"}


id: MONDO:0003214
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma with apocrine differentiation arising from the sweat glands. It presents as single or multiple nodular lesions which may be ulcerated or hemorrhagic and is usually in the axilla and less often in the anogenital region. It grows in the dermis and infiltrates subcutaneous tissues. It is characterized by the presence of large cells with abundant eosinophilic cytoplasm and large often vesicular nuclei. Most cases are slow growing tumors and have a prolonged course.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"apocrine sweat gland cancer","termid":"MONDO:0003215"},{"relation_name":"is_a","term_name":"sweat gland carcinoma","termid":"MONDO:0005524"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"apocrine adenocarcinoma","secondary_identifiers":["ICDO:8401/3","NCIT:C4169","UMLS:C0334346","DOID:4933","MEDGEN:569650"],"synonyms":[{"name":"apocrine adenocarcinoma (morphologic abnormality)","type":"exact"},{"name":"apocrine carcinoma","type":"exact"},{"name":"apocrine gland adenocarcinoma","type":"exact"},{"name":"apocrine gland carcinoma","type":"exact"},{"name":"carcinoma of apocrine gland","type":"exact"},{"name":"carcinoma of the apocrine gland","type":"exact"}],"termid":"MONDO:0003214","xrefs":{"Monarch":{"xref_id":"0003214"}}}


id: FYPO:0007509
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the trimethylation of lysine at position 9 of histone H3 in silent mating-type cassettes occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah","PMID:17434129"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H3-K9 trimethylation during vegetative growth","termid":"FYPO:0000879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0002494","FYPO:0005447","FYPO:0000002","FYPO:0002274"],"is_obsolete":false,"name":"increased histone H3-K9 trimethylation at silent mating-type cassette during vegetative growth","synonyms":[{"name":"increased histone H3 K9 trimethylation at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 trimethylation at mating-type region heterochromatin during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 trimethylation at silent mating-type cassette during mitotic cell cycle","type":"related"},{"name":"increased histone H3K9 trimethylation at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"increased histone H3K9me3 at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"increased histone lysine H3 K9 trimethylation at silent mating-type cassette during vegetative growth","type":"exact"}],"termid":"FYPO:0007509"}


id: FYPO:0007099
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the lengthening of the distance between poles of the meiotic spindle that occurs as part of the first meiotic nuclear division is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton organization","termid":"FYPO:0000054"},{"relation_name":"is_a","term_name":"abnormal meiotic chromosome segregation","termid":"FYPO:0000151"},{"relation_name":"is_a","term_name":"normal meiotic cell cycle process","termid":"FYPO:0007078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000631","FYPO:0000002","FYPO:0000257","FYPO:0000054"],"is_obsolete":false,"name":"normal spindle elongation in meiosis I","synonyms":[{"name":"normal meiotic spindle elongation in first meiotic nuclear division","type":"exact"},{"name":"normal meiotic spindle elongation in meiosis I","type":"exact"}],"termid":"FYPO:0007099"}


id: PBO:0082019
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZXD family zinc finger C","termid":"PBO:0082019"}


id: PBO:0004770
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA cleavage and polyadenylation specificity factor complex subunit Ctf1","termid":"PBO:0004770"}


id: FYPO:0002000
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a cell is inviable, and contains one nucleus and one or more septa. The nucleus is not in the normal location.","definition_xrefs":["PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"septated vegetative cell","termid":"FYPO:0002342"},{"relation_name":"is_a","term_name":"inviable mononucleate vegetative cell","termid":"FYPO:0006430"},{"relation_name":"is_a","term_name":"septated mononucleate vegetative cell with mislocalized nucleus and anucleate compartment","termid":"FYPO:0007646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000004","FYPO:0001985","FYPO:0005447","FYPO:0000002","FYPO:0000138"],"is_obsolete":false,"name":"inviable septated mononucleate vegetative cell","secondary_identifiers":["FYPO:0005276"],"synonyms":[{"name":"cytokinesis in the absence of nuclear division","type":"related"},{"name":"cytokinesis without nuclear division","type":"related"},{"name":"inviable cell with cytokinesis in the absence of nuclear division","type":"related"},{"name":"inviable cell with cytokinesis without nuclear division","type":"related"},{"name":"inviable cell with premature septation","type":"related"},{"name":"inviable cell with septation in the absence of nuclear division","type":"related"},{"name":"inviable cell with septation independent of mitosis","type":"related"},{"name":"inviable cell with septation without nuclear division","type":"related"},{"name":"inviable septated mononucleate cell","type":"exact"},{"name":"inviable septated mononucleate cell during vegetative growth","type":"exact"},{"name":"inviable septated mononucleate vegetative cell during mitotic cell cycle","type":"related"},{"name":"inviable septated mononucleate vegetative cell with mislocalized nucleus","type":"exact"},{"name":"lethal; septated mononucleate vegetative cell","type":"exact"},{"name":"septation in the absence of nuclear division","type":"related"},{"name":"septation independent of mitosis","type":"related"},{"name":"septation without nuclear division","type":"related"}],"termid":"FYPO:0002000"}


id: internal:broad
data:
  {"annotation_feature_type":"gene","cv_name":"synonym_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"broad","termid":"internal:broad"}


id: GO:0097337
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 ziprasidone stimulus. Ziprasidone is a piperazine compound having 1,2-benzothiazol-3-yl- and 2-(6-chloro-1,3-dihydro-2-oxindol-5-yl)ethyl substituents attached to the nitrogen atoms.","definition_xrefs":["GOC:pr"],"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 ziprasidone","termid":"GO:0097337"}


id: PBO:0084384
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Low-affinity glucose transporter of the major facilitator superfamily; expression is induced by Hxk2p in the presence of glucose and repressed by Rgt1p when glucose is limiting; HXT1 has a paralog, HXT6, what arose from the whole genome duplication","termid":"PBO:0084384"}


id: PBO:0062910
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"purinergic receptor P2X 3","termid":"PBO:0062910"}


id: SO:0001290
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"N4-methylcytidine is a modified cytidine.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_cytidine","termid":"SO:0001275"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N4_methylcytidine","secondary_identifiers":["RNAMOD:082"],"synonyms":[{"name":"N4 methylcytidine","type":"exact"},{"name":"N4-methylcytidine","type":"exact"},{"name":"m4C","type":"exact"}],"termid":"SO:0001290"}


id: GO:0061312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals initiated by the binding of a member of the BMP (bone morphogenetic protein) family to its receptor on the surface of a target cell, which contributes to the progression of the heart over time.","definition_xrefs":["GOC:dph","GOC:mtg_heart"],"gene_count":0,"genotype_count":0,"name":"obsolete BMP signaling pathway involved in heart development (obsolete GO:0061312)","synonyms":[{"name":"BMP signalling pathway involved in heart development","type":"exact"}],"termid":"GO:0061312"}


id: PATO:0000009
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000009 absolute speed (obsolete PATO:0000009)","termid":"PATO:0000009"}


id: MONDO:0021026
data:
  {"annotated_genes":["SJAG_00104","SJAG_00566","SJAG_04110","SJAG_03206","SJAG_04627","SJAG_01207","SJAG_01235","SJAG_01797","SJAG_00612","SJAG_01416","SJAG_00993","SJAG_01159","SJAG_00995","SJAG_01378","SJAG_04754","SJAG_01836","SJAG_04454","SJAG_05979","SJAG_01181","SJAG_00083","SJAG_03453","SJAG_04565","SJAG_03112","SJAG_00159","SJAG_04266","SJAG_03249","SJAG_02342"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85798],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009185"},{"annotations":[85379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014112"},{"annotations":[85382,85381,85380],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014113"},{"annotations":[85385,85386,85387],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014114"},{"annotations":[85528],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010221"},{"annotations":[86258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007485"},{"annotations":[85826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013521"},{"annotations":[85460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014690"},{"annotations":[85662,85663],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009136"},{"annotations":[85823],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013519"},{"annotations":[85825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013520"},{"annotations":[85633],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014600"},{"annotations":[86091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031057"},{"annotations":[86839],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010584"},{"annotations":[87392],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013997"},{"annotations":[87603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012853"},{"annotations":[86084,86085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009440"},{"annotations":[87490],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010854"},{"annotations":[87314],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010152"},{"annotations":[87366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011125"},{"annotations":[85647],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014615"},{"annotations":[85648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014619"},{"annotations":[85661],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010495"},{"annotations":[85979],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014841"},{"annotations":[87329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032806"},{"annotations":[86452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030517"},{"annotations":[86457],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030518"}]},"cv_name":"mondo","definition":"An instance of epidermal appendage anomaly that is caused by a modification of the individual's genome.","definition_xrefs":["MONDO:patterns/genetic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"gene_count":27,"genes_by_uniquename":{"SJAG_00083":null,"SJAG_00104":null,"SJAG_00159":null,"SJAG_00566":null,"SJAG_00612":null,"SJAG_00993":null,"SJAG_00995":null,"SJAG_01159":null,"SJAG_01181":null,"SJAG_01207":null,"SJAG_01235":null,"SJAG_01378":null,"SJAG_01416":null,"SJAG_01797":null,"SJAG_01836":null,"SJAG_02342":null,"SJAG_03112":null,"SJAG_03206":null,"SJAG_03249":null,"SJAG_03453":null,"SJAG_04110":null,"SJAG_04266":null,"SJAG_04454":null,"SJAG_04565":null,"SJAG_04627":null,"SJAG_04754":null,"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"hereditary epidermal appendage anomaly","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:183447","GARD:20265","MEDGEN:1843118","UMLS:C5680583"],"synonyms":[{"name":"genetic epidermal appendage anomaly","type":"exact"}],"termid":"MONDO:0021026","terms_by_termid":{"MONDO:0007485":null,"MONDO:0009136":null,"MONDO:0009185":null,"MONDO:0009440":null,"MONDO:0010152":null,"MONDO:0010221":null,"MONDO:0010495":null,"MONDO:0010584":null,"MONDO:0010854":null,"MONDO:0011125":null,"MONDO:0012853":null,"MONDO:0013519":null,"MONDO:0013520":null,"MONDO:0013521":null,"MONDO:0013997":null,"MONDO:0014112":null,"MONDO:0014113":null,"MONDO:0014114":null,"MONDO:0014600":null,"MONDO:0014615":null,"MONDO:0014619":null,"MONDO:0014690":null,"MONDO:0014841":null,"MONDO:0030517":null,"MONDO:0030518":null,"MONDO:0031057":null,"MONDO:0032806":null},"xrefs":{"Monarch":{"xref_id":"0021026"}}}


id: PBO:0002750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Niemann-Pick disease type C2 protein hE1 homolog (predicted)","termid":"PBO:0002750"}


id: GO:0047125
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADP+ + L-pipecolate = NADPH + delta1-piperideine-2-carboxylate.","definition_xrefs":["EC:1.5.1.21"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor","termid":"GO:0016646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"delta1-piperideine-2-carboxylate reductase activity","secondary_identifiers":["MetaCyc:RXN-8166","RHEA:12524"],"synonyms":[{"name":"1,2-didehydropipecolate reductase activity","type":"related"},{"name":"1,2-didehydropipecolic reductase activity","type":"related"},{"name":"D1-piperideine-2-carboxylate reductase activity","type":"exact"},{"name":"L-pipecolate:NADP+ 2-oxidoreductase activity","type":"related"},{"name":"P2C reductase activity","type":"related"},{"name":"delta 1-piperideine-2-carboxylate reductase activity","type":"exact"}],"termid":"GO:0047125"}


id: PBO:0079220
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tau tubulin kinase 2","termid":"PBO:0079220"}


id: PBO:0078788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 11-2","termid":"PBO:0078788"}


id: GO:0072759
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a topoisomerase inhibitor stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to chemical stimulus","termid":"GO:0070887"},{"relation_name":"is_a","term_name":"response to topoisomerase inhibitor","termid":"GO:0072758"}],"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 topoisomerase inhibitor","termid":"GO:0072759"}


id: PBO:0054701
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 2110","termid":"PBO:0054701"}


id: MONDO:1012611
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A liver disorder characterized by chronic conjugated hyperbilirubinemia and gross dark brown to black discoloration of the liver that occurs in sheep.","definition_xrefs":["OMIA:000497-9940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver disorder, non-human animal","termid":"MONDO:1012967"},{"relation_name":"is_a","term_name":"hyperbilirubinemia, non-human animal","termid":"MONDO:1012974"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conjugated hyperbilirubinemia, sheep","synonyms":[{"name":"hyperbilirubinaemia II, sheep","type":"related"}],"termid":"MONDO:1012611","xrefs":{"Monarch":{"xref_id":"1012611"}}}


id: PBO:0005754
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S20 (predicted)","termid":"PBO:0005754"}


id: MONDO:0007041
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Apert syndrome (AS) is a frequent form of acrocephalosyndactyly, a group of inherited congenital malformation disorders, characterized by craniosynostosis, midface hypoplasia, and finger and toe anomalies and/or syndactyly.","definition_xrefs":["Orphanet:87"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"is_a","term_name":"acrocephalosyndactyly","termid":"MONDO:0019796"}],"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":"Apert syndrome","secondary_identifiers":["NORD:793","OMIM:101200","MEDGEN:7858","UMLS:C0001193","NANDO:1200667","MESH:D000168","NANDO:2200844","GARD:5833","SCTID:205258009","icd11.foundation:1962779847","MedDRA:10002943","NCIT:C99099"],"synonyms":[{"name":"ACS 1","type":"related"},{"name":"ACS 2","type":"related"},{"name":"ACS1","type":"exact"},{"name":"Apert syndrome","type":"exact"},{"name":"Apert-Crouzon disease","type":"related"},{"name":"Vogt Cephalodactyly","type":"related"},{"name":"acrocephalo-syndactyly type 1","type":"related"},{"name":"acrocephalosyndactyly type 1","type":"exact"},{"name":"acrocephalosyndactyly type I","type":"exact"},{"name":"acrocephalosyndactyly, type 1","type":"related"},{"name":"acrocephalosyndactyly, type 2","type":"related"},{"name":"syndactylic oxycephaly","type":"related"},{"name":"type I Acrocephalosyndactyly","type":"exact"}],"termid":"MONDO:0007041","xrefs":{"Monarch":{"xref_id":"0007041"}}}


id: PBO:0048732
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glutamate dehydrogenase 1 pseudogene 3","termid":"PBO:0048732"}


id: PBO:0046304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ENAH actin regulator","termid":"PBO:0046304"}


id: PBO:0042548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 12","termid":"PBO:0042548"}


id: PBO:0049462
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycogenin 2 pseudogene 2","termid":"PBO:0049462"}


id: GO:0043892
data:
  {"annotated_genes":["SJAG_02960"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[105372],"is_not":false,"summary":null,"term":"GO:0043892"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: lactaldehyde + NADP+ = methylglyoxal + NADPH + H+.","definition_xrefs":["EC:1.1.1.283"],"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":1,"genes_by_uniquename":{"SJAG_02960":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"methylglyoxal reductase (NADPH) activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:21748","MetaCyc:1.1.1.283-RXN"],"synonyms":[{"name":"Gre2","type":"related"},{"name":"lactaldehyde dehydrogenase (NADP+)","type":"exact"},{"name":"lactaldehyde:NADP+ oxidoreductase activity","type":"related"},{"name":"methylglyoxal reductase (NADPH-dependent) activity","type":"exact"}],"termid":"GO:0043892","terms_by_termid":{"GO:0043892":null}}


id: PBO:0074386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMG7 antisense RNA 1","termid":"PBO:0074386"}


id: PBO:0087640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the GET complex; involved in insertion of proteins into the ER membrane; required for the retrieval of HDEL proteins from the Golgi to the ER in an ERD2 dependent fashion and for meiotic nuclear division","termid":"PBO:0087640"}


id: PBO:0028684
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_establishment_of_mitotic_spindle_pole_body_localization_to_nuclear_envelope","termid":"PBO:0028684"}


id: PBO:0061736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoredoxin pseudogene 1","termid":"PBO:0061736"}


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


id: PBO:0075651
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPRY domain containing 7 pseudogene 1","termid":"PBO:0075651"}


id: GO:0042098
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The expansion of a T cell population by cell division. Follows T cell activation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell activation","termid":"GO:0042110"},{"relation_name":"is_a","term_name":"lymphocyte proliferation","termid":"GO:0046651"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"T cell proliferation","secondary_identifiers":["GO:0042111"],"synonyms":[{"name":"T lymphocyte proliferation","type":"exact"},{"name":"T-cell proliferation","type":"exact"},{"name":"T-lymphocyte proliferation","type":"exact"}],"termid":"GO:0042098"}


id: FYPO:0004549
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell cycle checkpoint phenotype in which the S-phase DNA damage checkpoint (also known as the intra-S phase DNA damage checkpoint) is normal (i.e. indistinguishable from wild type) when the cell is exposed to ultraviolet light. The S phase DNA damage checkpoint slows progression through S phase in response to DNA damage.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic DNA damage checkpoint during cellular response to UV","termid":"FYPO:0002102"},{"relation_name":"is_a","term_name":"normal S-phase DNA damage checkpoint","termid":"FYPO:0003530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000631"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000631","FYPO:0001320","FYPO:0000257","FYPO:0000298","FYPO:0001312"],"is_obsolete":false,"name":"normal S-phase DNA damage checkpoint during cellular response to UV","synonyms":[{"name":"normal S-phase DNA damage checkpoint activation during cellular response to UV","type":"exact"},{"name":"normal S-phase DNA damage checkpoint during cellular response to UV during mitotic cell cycle","type":"exact"},{"name":"normal S-phase DNA damage checkpoint during cellular response to UV during vegetative growth","type":"exact"},{"name":"normal S-phase DNA damage checkpoint during cellular response to ultraviolet light","type":"exact"},{"name":"normal intra-S phase DNA damage checkpoint during cellular response to UV","type":"exact"},{"name":"normal mitotic S-phase DNA damage checkpoint during cellular response to UV","type":"exact"}],"termid":"FYPO:0004549"}


id: PBO:0005533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cu metalloregulatory transcription factor Cuf2 (predicted)","termid":"PBO:0005533"}


id: MOD:00293
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts three L-cysteine residues, an L-serine residue and a four-iron four-sulfur cluster to tris-L-cysteinyl L-serinyl tetrairon tetrasulfide.","definition_xrefs":["RESID:AA0288"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron-sulfur cluster containing modification","termid":"MOD:00739"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-cysteine residue","termid":"MOD:02067"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-serine residue","termid":"MOD:02072"}],"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":"tris-L-cysteinyl L-serinyl tetrairon tetrasulfide","synonyms":[{"name":"tetra-mu3-sulfidotris(S-cysteinyliron)(O3-serinyliron)","type":"exact"},{"name":"tris-L-cysteinyl L-serinyl tetrairon tetrasulfide","type":"exact"}],"termid":"MOD:00293"}


