# terms

id: FYPO:0009108
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which the spindle pole bodies (SPBs) of daughter nuclei are misoriented during mitotic telophase. Normally, SPBs face the cell tips at the end of anaphase when the spindle disassembles, but as microtubules are nucleated from SPBs and telophase nuclear positioning proceeds, the SPBs tend to face the cell equator.","definition_xrefs":["PMID:37099380"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular physical quality phenotype","termid":"FYPO:0000136"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002"],"is_obsolete":false,"name":"abnormal spindle pole body orientation during mitotic telophase","synonyms":[{"name":"abnormal spindle pole body angle during mitotic telophase","type":"exact"},{"name":"abnormal spindle pole body positioning within the nucleus during mitotic telophase","type":"exact"},{"name":"spindle pole body facing cell tips during mitotic telophase","type":"related"}],"termid":"FYPO:0009108"}


id: PBO:0083084
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA 3'-phosphatase; functions in repair of endogenous damage of double-stranded DNA, activity is specific for removal of 3' phosphates at strand breaks; similar to the l-2-haloacid dehalogenase superfamily; homolog of human polynucleotide kinase/3'-phosphatase","termid":"PBO:0083084"}


id: GO:0032113
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of carbohydrate phosphatase activity, the catalysis of the hydrolysis of phosphate from a carbohydrate phosphate.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of carbohydrate phosphatase activity (obsolete GO:0032113)","termid":"GO:0032113"}


id: MONDO:0009494
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Ketoadipicaciduria (obsolete MONDO:0009494)","termid":"MONDO:0009494","xrefs":{"Monarch":{"xref_id":"0009494"}}}


id: PBO:0051311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 1/OR2-3 (pseudogene)","termid":"PBO:0051311"}


id: PBO:0075079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 129","termid":"PBO:0075079"}


id: MONDO:0004923
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"lacrimal apparatus disorder","termid":"MONDO:0001854"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"chronic inflammation of lacrimal passage","secondary_identifiers":["DOID:9935","MEDGEN:509865","SCTID:267653001","UMLS:C0155239","ICD9:375.4"],"termid":"MONDO:0004923","xrefs":{"Monarch":{"xref_id":"0004923"}}}


id: PBO:0067871
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 173","termid":"PBO:0067871"}


id: PBO:0003709
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acetyl-CoA transporter (predicted)","termid":"PBO:0003709"}


id: PBO:0072307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S25 pseudogene 4","termid":"PBO:0072307"}


id: FYPO:0008086
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which autophagic degradation of the nucleus during nitrogen starvation is abolished .","definition_xrefs":["PMID:37191320"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal nucleophagy","termid":"FYPO:0008085"}],"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:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"abolished nucleophagy during nitrogen starvation","termid":"FYPO:0008086"}


id: PBO:0083126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Double-stranded DNA-dependent helicase of the DExH/D-box family; branch point-binding helicase that preferentially unwinds the nascent lagging strand with a 3' to 5' polarity at a replication fork; contains double-stranded DNA translocase activity; responsible for DNA branch migration; required for maintenance of the mitochondrial (mt) genome; localizes to the mitochondrial matrix; monomeric","termid":"PBO:0083126"}


id: PBO:0012592
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae YPT1","termid":"PBO:0012592"}


id: GO:0140907
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: R-CH + a halogen + FADH2 + O2 = R-C-halogen + FAD + H2O.","definition_xrefs":["PMID:34368824","PMID:28466644"],"direct_ancestors":[{"relation_name":"is_a","term_name":"halogenase activity","termid":"GO:0140906"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"flavin-dependent halogenase activity","termid":"GO:0140907"}


id: MONDO:0008310
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hutchinson-Gilford progeria syndrome is a rare, fatal, autosomal dominant and premature aging disease, beginning in childhood and characterized by growth reduction, failure to thrive, a typical facial appearance (prominent forehead, protuberant eyes, thin nose with a beaked tip, thin lips, micrognathia and protruding ears) and distinct dermatologic features (generalized alopecia, aged-looking skin, sclerotic and dimpled skin over the abdomen and extremities, prominent cutaneous vasculature, dyspigmentation, nail hypoplasia and loss of subcutaneous fat).","definition_xrefs":["Orphanet:740"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"primary osteolysis","termid":"MONDO:0019707"},{"relation_name":"is_a","term_name":"progeria","termid":"MONDO:0020732"},{"relation_name":"is_a","term_name":"laminopathy","termid":"MONDO:0021106"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019303"}],"interesting_parent_ids":["MONDO:0019303","MONDO:0006025"],"is_obsolete":false,"name":"Hutchinson-Gilford progeria syndrome","secondary_identifiers":["MEDGEN:46123","NANDO:2200833","GARD:7467","OMIM:176670","NANDO:1201007","UMLS:C0033300","MedDRA:10036794","NORD:1257","NCIT:C34951","ICD9:259.8","SCTID:238870004","DOID:3911"],"synonyms":[{"name":"HGPS","type":"exact"},{"name":"Hutchinson Gilford progeria syndrome","type":"related"},{"name":"Hutchinson Gilford syndrome","type":"exact"},{"name":"Hutchinson-Gilford disease","type":"exact"},{"name":"Hutchinson-Gilford progeria","type":"exact"},{"name":"Hutchinson-Gilford progeria syndrome","type":"exact"},{"name":"premature senility syndrome","type":"exact"},{"name":"progeria","type":"broad"},{"name":"progeria syndrome, childhood-onset","type":"related"}],"termid":"MONDO:0008310","xrefs":{"Monarch":{"xref_id":"0008310"}}}


id: PBO:0063999
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"piwi-interacting RNA cluster 33","termid":"PBO:0063999"}


id: PBO:0053886
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 1166","termid":"PBO:0053886"}


id: MONDO:0015140
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A progressive dementia with reduction of cognitive functions. It presents the same phenotype as sporadic Alzheimer disease (AD) but has an early age of onset, usually before 60 years old.","definition_xrefs":["Orphanet:1020"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"familial Alzheimer disease","termid":"MONDO:0100087"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0000426","MONDO:0005559"],"is_obsolete":false,"name":"early-onset autosomal dominant Alzheimer disease","secondary_identifiers":["GARD:12798"],"synonyms":[{"name":"EOFAD","type":"exact"},{"name":"early-onset familial autosomal dominant Alzheimer disease","type":"exact"},{"name":"early-onset, autosomal dominant Alzheimer disease","type":"related"}],"termid":"MONDO:0015140","xrefs":{"Monarch":{"xref_id":"0015140"}}}


id: PBO:0024876
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by Xenopus XMog1","termid":"PBO:0024876"}


id: GO:0042190
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of vanillin, an aromatic hydrocarbon which occurs naturally in black vanilla bean pods.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vanillin metabolic process","termid":"GO:0018982"},{"relation_name":"is_a","term_name":"phenol-containing compound catabolic process","termid":"GO:0019336"},{"relation_name":"is_a","term_name":"aldehyde catabolic process","termid":"GO:0046185"},{"relation_name":"is_a","term_name":"ether catabolic process","termid":"GO:1901502"}],"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":"vanillin catabolic process","synonyms":[{"name":"vanillic aldehyde catabolic process","type":"exact"},{"name":"vanillic aldehyde catabolism","type":"exact"},{"name":"vanillin breakdown","type":"exact"},{"name":"vanillin catabolism","type":"exact"},{"name":"vanillin degradation","type":"exact"}],"termid":"GO:0042190"}


id: MONDO:0008812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"AREDYLD stands for acral-renal-ectodermal-dysplasia-lipoatrophic-diabetes. This syndrome has been described in three individuals, one of whom was born to consanguineous parents. All patients had lipoatrophy, diabetes mellitus, generalized hypotrichosis, ectodermal dysplasia, renal alterations, dental abnormalities and other manifestations. It is probably transmitted as an autosomal recessive trait.","definition_xrefs":["Orphanet:1133"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"diabetes mellitus","termid":"MONDO:0005015"},{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"AREDYLD syndrome","secondary_identifiers":["MEDGEN:87435","MESH:C537427","SCTID:237610008","ICD9:753.3","UMLS:C0342280","GARD:8509","OMIM:207780","icd11.foundation:2007371732"],"synonyms":[{"name":"AREDYLD","type":"related"},{"name":"acral renal ectodermal dysplasia lipoatrophic diabetes","type":"related"},{"name":"acrorenal Field defect, ectodermal dysplasia, and lipoatrophic diabetes","type":"related"},{"name":"acrorenal defect-ectodermal dysplasia-diabetes syndrome","type":"exact"}],"termid":"MONDO:0008812","xrefs":{"Monarch":{"xref_id":"0008812"}}}


id: PBO:0083437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the uncharacterized ORF YOL036W","termid":"PBO:0083437"}


id: MONDO:0000264
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Pontiac fever (obsolete MONDO:0000264)","termid":"MONDO:0000264","xrefs":{"Monarch":{"xref_id":"0000264"}}}


id: PBO:0025442
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homocystinuria","termid":"PBO:0025442"}


id: PBO:0042437
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC42 intronic transcript 1","termid":"PBO:0042437"}


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


id: PBO:0038648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acyl-CoA oxidase 3, pristanoyl","termid":"PBO:0038648"}


id: GO:0002732
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of dendritic cell cytokine production.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of leukocyte mediated immunity","termid":"GO:0002705"},{"relation_name":"is_a","term_name":"positive regulation of cytokine production involved in immune response","termid":"GO:0002720"},{"relation_name":"is_a","term_name":"regulation of dendritic cell cytokine production","termid":"GO:0002730"},{"relation_name":"positively_regulates","term_name":"dendritic cell cytokine production","termid":"GO:0002371"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of dendritic cell cytokine production","synonyms":[{"name":"activation of dendritic cell cytokine production","type":"narrow"},{"name":"stimulation of dendritic cell cytokine production","type":"narrow"},{"name":"up regulation of dendritic cell cytokine production","type":"exact"},{"name":"up-regulation of dendritic cell cytokine production","type":"exact"},{"name":"upregulation of dendritic cell cytokine production","type":"exact"}],"termid":"GO:0002732"}


id: PBO:0046605
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K9, member 7","termid":"PBO:0046605"}


id: PBO:0114441
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane P-type proton ATPase, P3-type Pma2","termid":"PBO:0114441"}


id: MONDO:0035763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"kidney disorder","termid":"MONDO:0005240"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"idiopathic non-lupus full-house nephropathy","secondary_identifiers":["UMLS:C5680132","MEDGEN:1830099","Orphanet:567544","GARD:22285"],"synonyms":[{"name":"Idiopathic non-lupus FHN","type":"exact"}],"termid":"MONDO:0035763","xrefs":{"Monarch":{"xref_id":"0035763"}}}


id: PBO:0051000
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin binding protein 1","termid":"PBO:0051000"}


id: PBO:0047812
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box N1","termid":"PBO:0047812"}


id: MONDO:0009127
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":"dwarfism, low-birth-weight type, with unresponsiveness to growth hormone","secondary_identifiers":["OMIM:223500","MESH:C565615","UMLS:C1857197","MEDGEN:387764"],"synonyms":[{"name":"dwarfism, low-birth-weight type with unresponsiveness to growth hormone","type":"related"},{"name":"dwarfism, low-birth-weight type, with unresponsiveness to growth hormone","type":"exact"}],"termid":"MONDO:0009127","xrefs":{"Monarch":{"xref_id":"0009127"}}}


id: GO:0035946
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The set of processes involved in identifying and degrading messenger RNA (mRNA) within the mitochondrion.","definition_xrefs":["GOC:ans","PMID:19864255"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mitochondrial mRNA catabolic process","termid":"GO:0000958"},{"relation_name":"is_a","term_name":"mitochondrial RNA surveillance","termid":"GO:2000827"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016071"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0016071"],"is_obsolete":false,"name":"mitochondrial mRNA surveillance","synonyms":[{"name":"mitochondrial aberrant RNA catabolic process","type":"exact"},{"name":"mitochondrial mRNA quality control","type":"exact"},{"name":"mitochondrial messenger RNA surveillance","type":"exact"}],"termid":"GO:0035946"}


id: PBO:0064413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PNMA family member 6F","termid":"PBO:0064413"}


id: PBO:0091523
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"was previously incorrectly labelled as lcb3","termid":"PBO:0091523"}


id: MONDO:0001749
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A senile cataract that involves the lens cortex.","definition_xrefs":["MONDO:design_pattern"],"direct_ancestors":[{"relation_name":"is_a","term_name":"senile cataract","termid":"MONDO:0004847"},{"relation_name":"is_a","term_name":"cortical cataract","termid":"MONDO:0045051"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cortical senile cataract","secondary_identifiers":["ICD9:366.15","SCTID:78875003","MEDGEN:509748","DOID:13574","UMLS:C0154980"],"synonyms":[{"name":"cortical senile cataract","type":"exact"},{"name":"lens cortex senile cataract","type":"exact"},{"name":"senile cataract of lens cortex","type":"exact"}],"termid":"MONDO:0001749","xrefs":{"Monarch":{"xref_id":"0001749"}}}


id: GO:0061318
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a relatively unspecialized cell acquires specialized structural and/or functional features of a renal filtration cell. Renal filtration cells are specialized cells of the renal system that filter fluids by charge, size or both. Differentiation includes the processes involved in commitment of a cell to a specific fate and its subsequent development to the mature state.","definition_xrefs":["GOC:dph","GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"renal system development","termid":"GO:0072001"}],"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":"renal filtration cell differentiation","termid":"GO:0061318"}


id: GO:0061649
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"A histone reader that recognizes a histone bearing a ubiquinated lysine residue.","definition_xrefs":["PMID:24526689"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ubiquitin-modified protein reader activity","termid":"GO:0140036"},{"relation_name":"is_a","term_name":"histone reader activity","termid":"GO:0140566"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0060090"},{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140566"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0140566","GO:0003674","GO:0060090","GO:0030674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"ubiquitin-modified histone reader activity","synonyms":[{"name":"ubiquitin modification-dependent histone binding","type":"exact"},{"name":"ubiquitinated histone binding","type":"related"}],"termid":"GO:0061649"}


id: GO:0061497
data:
  {"annotated_genes":["SJAG_02332","SJAG_03835","SJAG_07018","SJAG_01215","SJAG_02609","SJAG_05196"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[100480,102306,108329,109094,110068,110919],"is_not":false,"summary":null,"term":"GO:0061497"}]},"cv_name":"cellular_component","definition":"One of three laminate structures that form the mitotic spindle pole body; the inner plaque is in the nucleus.","definition_xrefs":["GOC:dph","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inner plaque of spindle pole body","termid":"GO:0005822"},{"relation_name":"part_of","term_name":"mitotic spindle pole body","termid":"GO:0044732"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01215":null,"SJAG_02332":null,"SJAG_02609":null,"SJAG_03835":null,"SJAG_05196":null,"SJAG_07018":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005816"}],"interesting_parent_ids":["GO:0015630","GO:0005816","GO:0005575"],"is_obsolete":false,"name":"inner plaque of mitotic spindle pole body","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061497","terms_by_termid":{"GO:0061497":null}}


id: PBO:0066741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 38","termid":"PBO:0066741"}


id: MONDO:1012489
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hypotrichosis with short life expectancy, non-human animal","termid":"MONDO:1011759"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypotrichosis with short life expectancy, domestic cat","secondary_identifiers":["OMIA:001949-9685"],"termid":"MONDO:1012489","xrefs":{"Monarch":{"xref_id":"1012489"}}}


id: MONDO:0018176
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete polymicrogyria (obsolete MONDO:0018176)","termid":"MONDO:0018176","xrefs":{"Monarch":{"xref_id":"0018176"}}}


id: PomGeneEx:0000012
data:
  {"annotation_feature_type":"gene","cv_name":"PomGeneExRNA","definition":"A gene expression qualifier that indicates that an RNA is present at a lower level under one set of conditions or at one indicated time than otherwise.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased","termid":"PomGeneEx:0000003"},{"relation_name":"is_a","term_name":"RNA expression level","termid":"PomGeneEx:0000009"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA level decreased","synonyms":[{"name":"RNA expression decreased","type":"exact"},{"name":"decreased RNA level","type":"exact"}],"termid":"PomGeneEx:0000012"}


id: MONDO:0017880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Rift Valley fever (RVF), caused by the Rift Valley fever virus (RVFV), is an arbovirus characterized by a usually self-limiting febrile illness but that in some cases can also manifest with thrombosis, vision loss, hemorrhages and/or neurological symptoms.","definition_xrefs":["Orphanet:319251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral hemorrhagic fever","termid":"MONDO:0018087"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rift valley fever","secondary_identifiers":["SCTID:402917003","icd11.foundation:854137188","MESH:D012295","ICD10CM:A92.4","MEDGEN:20589","DOID:1328","GARD:21416","NCIT:C128419","MedDRA:10039143","UMLS:C0035613"],"synonyms":[{"name":"RVF","type":"exact"}],"termid":"MONDO:0017880","xrefs":{"Monarch":{"xref_id":"0017880"}}}


id: GO:0007612
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in an organism in which a relatively long-lasting adaptive behavioral change occurs as the result of experience.","definition_xrefs":["ISBN:0721662544","ISBN:0582227089"],"direct_ancestors":[{"relation_name":"is_a","term_name":"learning or memory","termid":"GO:0007611"}],"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":"learning","secondary_identifiers":["Wikipedia:Learning"],"termid":"GO:0007612"}


id: PBO:0039772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AQP5 and AQP2 antisense RNA 2","termid":"PBO:0039772"}


id: GO:0048528
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the post-embryonic root over time, from its formation to the mature structure.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"root development","termid":"GO:0048364"},{"relation_name":"is_a","term_name":"post-embryonic plant organ development","termid":"GO:0090696"}],"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":"post-embryonic root development","termid":"GO:0048528"}


id: PBO:0002700
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"possibly related to human/mouse periphilin","termid":"PBO:0002700"}


id: MONDO:0022263
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital hepatic fibrosis (obsolete MONDO:0022263)","termid":"MONDO:0022263","xrefs":{"Monarch":{"xref_id":"0022263"}}}


id: PBO:0044728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD/H-box helicase 11 like 17 (pseudogene)","termid":"PBO:0044728"}


id: PBO:0078485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ile (anticodon AAT) 5-5","termid":"PBO:0078485"}


id: MONDO:0002533
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adenoma characterized by the presence of papillary epithelial patterns.","definition_xrefs":["NCIT:C79951"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"papilloma","termid":"MONDO:0002363"},{"relation_name":"is_a","term_name":"adenoma","termid":"MONDO:0004972"},{"relation_name":"is_a","term_name":"papillary epithelial neoplasm","termid":"MONDO:0021096"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"papillary adenoma","secondary_identifiers":["DOID:3172","UMLS:C0205650","MEDGEN:59999"],"synonyms":[{"name":"adenoma, papillary, benign","type":"exact"},{"name":"glandular papilloma","type":"related"},{"name":"papillary adenoma","type":"exact"},{"name":"papillary adenoma NOS (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0002533","xrefs":{"Monarch":{"xref_id":"0002533"}}}


id: PBO:0027066
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_RNA_metabolic_process","termid":"PBO:0027066"}


id: PBO:0070362
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, Ro60-associated Y5","termid":"PBO:0070362"}


id: PBO:0080792
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"XPC complex subunit, DNA damage recognition and repair factor","termid":"PBO:0080792"}


id: MONDO:0021334
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Disorders characterized by abnormal proliferation of primary cells of the immune system or by excessive production of immunoglobulins.","definition_xrefs":["MESH:D007160"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder","termid":"MONDO:0005046"}],"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":"immunoproliferative disorder","secondary_identifiers":["UMLS:C0021070","SCTID:127071007","MEDGEN:7038","ICD9:203.80"],"synonyms":[{"name":"Disorder, Immunoproliferative","type":"related"},{"name":"Disorders, Immunoproliferative","type":"related"},{"name":"Immunoproliferative Disorder","type":"related"},{"name":"Immunoproliferative Disorders","type":"related"},{"name":"Immunoproliferative disease","type":"related"},{"name":"Immunoproliferative disorder","type":"related"},{"name":"immunoproliferative disorder","type":"exact"}],"termid":"MONDO:0021334","xrefs":{"Monarch":{"xref_id":"0021334"}}}


id: PBO:0050822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hyccin PI4KA lipid kinase complex subunit 2","termid":"PBO:0050822"}


id: GO:0050404
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: UDP-alpha-D-xylose + zeatin = O-beta-D-xylosylzeatin + H+ + UDP.","definition_xrefs":["EC:2.4.2.40","RHEA:14721"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-xylosyltransferase activity","termid":"GO:0035252"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016757"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0003824","GO:0016757"],"is_obsolete":false,"name":"zeatin O-beta-D-xylosyltransferase activity","secondary_identifiers":["MetaCyc:ZEATIN-O-BETA-D-XYLOSYLTRANSFERASE-RXN","KEGG_REACTION:R02119"],"synonyms":[{"name":"UDP-D-xylose:zeatin O-beta-D-xylosyltransferase activity","type":"related"},{"name":"uridine diphosphoxylose-zeatin xylosyltransferase activity","type":"related"},{"name":"zeatin O-b-D-xylosyltransferase activity","type":"exact"},{"name":"zeatin O-xylosyltransferase activity","type":"related"}],"termid":"GO:0050404"}


id: PBO:0049926
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HGH1 homolog","termid":"PBO:0049926"}


id: MONDO:1011767
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":"laminitis, non-human animal","secondary_identifiers":["OMIA:001225"],"termid":"MONDO:1011767","xrefs":{"Monarch":{"xref_id":"1011767"}}}


id: MONDO:0001797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chancroid is a bacterial infection that is spread through sexual contact. It is caused by a type of bacteria called Haemophilus ducreyi. Chancroid is characterized by a small bump on the genital which becomes a painful ulcer. Men may have just one ulcer, but women often develop four or more.About half of the people who are infected with a chancroid will develop enlarged inguinal lymph nodes, the nodes located in the fold between the leg and the lower abdomen. In some cases, the nodes will break through the skin and cause draining abscesses. The swollen lymph nodes and abscesses are often called buboes. Chancroid infections can be treated with antibiotics, including azithromycin, ceftriaxone, ciprofloxacin, and erythromycin. Large lymph node swellings need to be drained, either with a needle or local surgery.","direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"bacterial sexually transmitted disease","termid":"MONDO:0005323"},{"relation_name":"is_a","term_name":"haemophilus infectious disease","termid":"MONDO:0006926"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chancroid","secondary_identifiers":["UMLS:C0007947","ICD9:099.0","ICD10CM:A57","MESH:D002602","icd11.foundation:1357024926","GARD:9522","DOID:13778","SCTID:266143009","MEDGEN:872"],"synonyms":[{"name":"Chancroids","type":"related"},{"name":"Ulcus molle, skin","type":"exact"}],"termid":"MONDO:0001797","xrefs":{"Monarch":{"xref_id":"0001797"}}}


id: GO:0052338
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The perturbation by an organism of the symbiont cell wall, leading to damage or temporary subversion of the cell wall. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["ISBN:0198547684"],"gene_count":0,"genotype_count":0,"name":"obsolete perturbation by host of symbiont cell wall (obsolete GO:0052338)","synonyms":[{"name":"catabolism of symbiont cell wall by organism","type":"exact"},{"name":"degradation of symbiont cell wall by organism","type":"exact"},{"name":"disassembly by host of symbiont cell wall","type":"exact"},{"name":"disruption by host of symbiont cell wall","type":"related"}],"termid":"GO:0052338"}


id: PBO:0036343
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAK-related GC kinase Ppk11","termid":"PBO:0036343"}


id: PBO:0005415
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldehyde dehydrogenase Meu8 (predicted)","termid":"PBO:0005415"}


id: PBO:0090271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"60S ribosomal protein L6","termid":"PBO:0090271"}


id: PBO:0089623
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"signal recognition particle subunit Sec65","termid":"PBO:0089623"}


id: MONDO:0021370
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the minor salivary gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tumor of salivary gland","termid":"MONDO:0021357"},{"relation_name":"is_a","term_name":"mouth mucosa disorder","termid":"MONDO:0044992"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neoplasm of minor salivary gland","secondary_identifiers":["MEDGEN:138022","SCTID:126798006","UMLS:C0345613","NCIT:C4409"],"synonyms":[{"name":"minor salivary gland neoplasm","type":"exact"},{"name":"minor salivary gland neoplasm (disease)","type":"exact"},{"name":"minor salivary gland tumor","type":"exact"},{"name":"minor salivary gland tumour","type":"exact"},{"name":"neoplasm of minor salivary gland","type":"exact"},{"name":"neoplasm of the minor salivary gland","type":"exact"},{"name":"tumor of minor salivary gland","type":"exact"},{"name":"tumor of the minor salivary gland","type":"exact"},{"name":"tumour of minor salivary gland","type":"exact"},{"name":"tumour of the minor salivary gland","type":"exact"}],"termid":"MONDO:0021370","xrefs":{"Monarch":{"xref_id":"0021370"}}}


id: GO:0075086
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism stops, prevents, or reduces the frequency, rate or extent of transmembrane receptor-mediated cAMP signal transduction in the symbiont. 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 negative regulation by host of symbiont transmembrane receptor-mediated cAMP signal transduction (obsolete GO:0075086)","synonyms":[{"name":"downregulation by host of symbiont transmembrane receptor-mediated cAMP signal transduction","type":"exact"},{"name":"inhibition by host of symbiont transmembrane receptor-mediated cAMP signal transduction","type":"narrow"},{"name":"negative regulation by host of symbiont transmembrane receptor-mediated cAMP signaling","type":"exact"}],"termid":"GO:0075086"}


id: PBO:0086270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein tyrosine phosphatase; involved in cell cycle control and retrograde protein transport; regulates the phosphorylation state of Cdc28p; modulates phosphorylation of retromer component Vps26p; homolog of S. pombe cdc25","termid":"PBO:0086270"}


id: GO:1905153
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of membrane invagination.","definition_xrefs":["GOC:PARL","PMID:26589353","GO_REF:0000058","GOC:TermGenie","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"membrane invagination","termid":"GO:0010324"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0061024"}],"interesting_parent_ids":["GO:0008150","GO:0061024"],"is_obsolete":false,"name":"regulation of membrane invagination","termid":"GO:1905153"}


id: GO:0045179
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The region that lies just beneath the plasma membrane on the apical edge of a cell.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell cortex region","termid":"GO:0099738"},{"relation_name":"part_of","term_name":"apical part of cell","termid":"GO:0045177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005938"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0005938"],"is_obsolete":false,"name":"apical cortex","termid":"GO:0045179"}


id: GO:1901841
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of high voltage-gated calcium channel activity.","definition_xrefs":["GOC:BHF","GOC:TermGenie","PMID:12754254","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of voltage-gated calcium channel activity","termid":"GO:1901385"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"}],"interesting_parent_ids":["GO:0055085","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of high voltage-gated calcium channel activity","synonyms":[{"name":"regulation of high voltage gated calcium channel activity","type":"exact"},{"name":"regulation of high voltage-dependent calcium channel activity","type":"exact"}],"termid":"GO:1901841"}


id: MONDO:0800464
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A group of disorders including Paget disease of bone (PBD), inclusion body myopathy (IBM), and less frequently frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). Phenotypic presentation and severity are highly variable, and individuals within the same family may present with different associated conditions.","definition_xrefs":["PMID:33145792"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"proteostasis deficiencies","termid":"MONDO:0021179"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0021179"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0021179"],"is_obsolete":false,"name":"SQSTM1-related multisystem proteinopathy","synonyms":[{"name":"SQSTM1-related multisystem proteinopathy","type":"exact"}],"termid":"MONDO:0800464","xrefs":{"Monarch":{"xref_id":"0800464"}}}


id: PBO:0077116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIMM23B-AGAP6 readthrough (NMD candidate)","termid":"PBO:0077116"}


id: FYPO:0003723
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of bis(5'-adenosyl)-hexaphosphatase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal catalytic activity","termid":"FYPO:0000661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000654","FYPO:0000652","FYPO:0000661","FYPO:0001985"],"is_obsolete":false,"name":"abnormal bis(5'-adenosyl)-hexaphosphatase activity","termid":"FYPO:0003723"}


id: GO:1903339
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of cell wall organization or biogenesis.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cellular process","termid":"GO:0048523"},{"relation_name":"is_a","term_name":"regulation of cell wall organization or biogenesis","termid":"GO:1903338"},{"relation_name":"negatively_regulates","term_name":"cell wall organization or biogenesis","termid":"GO:0071554"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0071554"},{"rel_name":"regulates","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0071554"],"is_obsolete":false,"name":"negative regulation of cell wall organization or biogenesis","synonyms":[{"name":"down regulation of cell wall organisation or biogenesis","type":"exact"},{"name":"down regulation of cell wall organization or biogenesis","type":"exact"},{"name":"down regulation of cell wall organization or biogenesis at cellular level","type":"exact"},{"name":"down regulation of cellular cell wall organisation or biogenesis","type":"exact"},{"name":"down regulation of cellular cell wall organization or biogenesis","type":"exact"},{"name":"down-regulation of cell wall organisation or biogenesis","type":"exact"},{"name":"down-regulation of cell wall organization or biogenesis","type":"exact"},{"name":"down-regulation of cell wall organization or biogenesis at cellular level","type":"exact"},{"name":"down-regulation of cellular cell wall organisation or biogenesis","type":"exact"},{"name":"down-regulation of cellular cell wall organization or biogenesis","type":"exact"},{"name":"downregulation of cell wall organisation or biogenesis","type":"exact"},{"name":"downregulation of cell wall organization or biogenesis","type":"exact"},{"name":"downregulation of cell wall organization or biogenesis at cellular level","type":"exact"},{"name":"downregulation of cellular cell wall organisation or biogenesis","type":"exact"},{"name":"downregulation of cellular cell wall organization or biogenesis","type":"exact"},{"name":"inhibition of cell wall organisation or biogenesis","type":"narrow"},{"name":"inhibition of cell wall organization or biogenesis","type":"narrow"},{"name":"inhibition of cell wall organization or biogenesis at cellular level","type":"narrow"},{"name":"inhibition of cellular cell wall organisation or biogenesis","type":"narrow"},{"name":"inhibition of cellular cell wall organization or biogenesis","type":"narrow"},{"name":"negative regulation of cell wall organisation or biogenesis","type":"exact"},{"name":"negative regulation of cell wall organization or biogenesis at cellular level","type":"exact"},{"name":"negative regulation of cellular cell wall organisation or biogenesis","type":"exact"},{"name":"negative regulation of cellular cell wall organization or biogenesis","type":"exact"}],"termid":"GO:1903339"}


id: MONDO:0008798
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any isolated congenital anonychia in which the cause of the disease is a mutation in the RSPO4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isolated congenital anonychia","termid":"MONDO:0019211"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nonsyndromic congenital nail disorder 4","secondary_identifiers":["MEDGEN:120563","MESH:C536377","DOID:0080082","Orphanet:94150","DOID:0050643","UMLS:C0265998","OMIM:206800","GARD:16837"],"synonyms":[{"name":"HYPONYCHIA congenita","type":"exact"},{"name":"NDNC4","type":"related"},{"name":"RSPO4 isolated congenital anonychia","type":"exact"},{"name":"anonychia congenita","type":"related"},{"name":"anonychia congenita totalis","type":"related"},{"name":"anonychia totalis","type":"related"},{"name":"anonychia/hyponychia congenita","type":"related"},{"name":"isolated congenital anonychia caused by mutation in RSPO4","type":"exact"},{"name":"nail disorder, nonsyndromic congenital, 4","type":"related"},{"name":"nail disorder, nonsyndromic congenital, type 4","type":"exact"},{"name":"nonsyndromic congenital nail disorder 4","type":"exact"},{"name":"nonsyndromic congenital nail disorder type 4","type":"exact"}],"termid":"MONDO:0008798","xrefs":{"Monarch":{"xref_id":"0008798"}}}


id: GO:0002161
data:
  {"annotated_genes":["SJAG_03545","SJAG_01797","SJAG_00443","SJAG_04738","SJAG_01259","SJAG_01248","SJAG_04285","SJAG_02015","SJAG_02428"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[93205,94529,97161,97580,104165,112133,115543],"is_not":false,"summary":null,"term":"GO:0002161"},{"annotations":[105416],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043907"},{"annotations":[99947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051500"}]},"cv_name":"molecular_function","definition":"The hydrolysis of an incorrectly aminoacylated tRNA.","definition_xrefs":["GOC:hjd","PMID:14663147","PMID:16087889"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carboxylic ester hydrolase activity","termid":"GO:0052689"},{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00443":null,"SJAG_01248":null,"SJAG_01259":null,"SJAG_01797":null,"SJAG_02015":null,"SJAG_02428":null,"SJAG_03545":null,"SJAG_04285":null,"SJAG_04738":null},"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:0140101"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140101","GO:0003824","GO:0016787","GO:0003674","GO:0016788","GO:0140098"],"is_obsolete":false,"name":"aminoacyl-tRNA editing activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"amino acid proofreading activity","type":"related"},{"name":"aminoacyl-tRNA hydrolysis activity","type":"related"}],"termid":"GO:0002161","terms_by_termid":{"GO:0002161":null,"GO:0043907":null,"GO:0051500":null}}


id: PBO:0075160
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein polypeptide C pseudogene 16","termid":"PBO:0075160"}


id: GO:1904429
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of t-circle formation.","definition_xrefs":["GO_REF:0000058","PMID:22579284","GOC:BHF","GOC:BHF_telomere","GOC:nc","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of telomere maintenance","termid":"GO:0032204"},{"relation_name":"is_a","term_name":"regulation of cellular component biogenesis","termid":"GO:0044087"},{"relation_name":"regulates","term_name":"t-circle formation","termid":"GO:0090656"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0032200"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0044085","GO:0032200"],"is_obsolete":false,"name":"regulation of t-circle formation","synonyms":[{"name":"regulation of telomeric circle formation","type":"exact"}],"termid":"GO:1904429"}


id: PBO:0066132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ras association domain family member 10","termid":"PBO:0066132"}


id: PBO:0090696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"homocysteine methyltransferase","termid":"PBO:0090696"}


id: GO:0048508
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the embryonic meristem over time, from its formation to the mature structure.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"meristem development","termid":"GO:0048507"},{"relation_name":"part_of","term_name":"embryo development ending in seed dormancy","termid":"GO:0009793"}],"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 meristem development","termid":"GO:0048508"}


id: PBO:0070661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 32","termid":"PBO:0070661"}


id: GO:0071184
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that contains the cell adhesion molecules protocadherin-alpha-v4 and protocadherin-gamma-a1, and is involved in the regulation of protein localization to the plasma membrane.","definition_xrefs":["PMID:15347688"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protocadherin-alpha-protocadherin-gamma complex","termid":"GO:0071183"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0005886"],"is_obsolete":false,"name":"protocadherin-alpha-v4-protocadherin-gamma-a1 complex","synonyms":[{"name":"Pcdhga1-Pcdha4 complex","type":"narrow"}],"termid":"GO:0071184"}


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:dph","GOC:ebc"],"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: MONDO:0100076
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A scoliosis with no known cause arising in a juvenile.","direct_ancestors":[{"relation_name":"is_a","term_name":"idiopathic scoliosis","termid":"MONDO:0000726"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"juvenile idiopathic scoliosis","secondary_identifiers":["UMLS:C3495538","Orphanet:459696","MEDGEN:1843471"],"termid":"MONDO:0100076","xrefs":{"Monarch":{"xref_id":"0100076"}}}


id: PBO:0030950
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitochondrial_aggregation","termid":"PBO:0030950"}


id: MONDO:0010274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"testicular germ cell tumor","termid":"MONDO:0010108"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testicular germ cell tumor 1","secondary_identifiers":["MESH:C564559","MEDGEN:337402","UMLS:C1846164","OMIM:300228"],"synonyms":[{"name":"TGCT1","type":"exact"},{"name":"testicular germ cell tumor","type":"broad"},{"name":"testicular germ cell tumor 1","type":"exact"},{"name":"testicular germ cell tumour","type":"broad"}],"termid":"MONDO:0010274","xrefs":{"Monarch":{"xref_id":"0010274"}}}


id: PR:Q9US30
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- rsm19 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9US30"],"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":"ribosomal protein S19, mitochondrial (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1751.02c","synonyms":[{"name":"Spom972h-rsm19","type":"exact"}],"termid":"PR:Q9US30"}


id: PBO:0068043
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 348","termid":"PBO:0068043"}


id: PBO:0075135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nuclear ribonucleoprotein U5 subunit 200","termid":"PBO:0075135"}


id: PBO:0079093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Tyr (anticodon GTA) 6-1","termid":"PBO:0079093"}


id: PBO:0090507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, DDB1 and CUL4-associated factor Dca7","termid":"PBO:0090507"}


id: GO:0060756
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Behavior by which an organism locates food.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavior","termid":"GO:0007610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"foraging behavior","termid":"GO:0060756"}


id: PBO:0060083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 30","termid":"PBO:0060083"}


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


id: PBO:0045497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DSG1 antisense RNA 1","termid":"PBO:0045497"}


id: PBO:0083362
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; overlaps the verified gene SIK1/YLR197W","termid":"PBO:0083362"}


id: MONDO:0007747
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"hereditary epidermal appendage anomaly","termid":"MONDO:0021026"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005093"],"is_obsolete":false,"name":"isolated hyperchlorhidrosis","secondary_identifiers":["MEDGEN:333560","OMIM:143860","UMLS:C1840437","DOID:0111371","GARD:17984","Orphanet:542657","ICD9:276.9","SCTID:709413001"],"synonyms":[{"name":"hyperchlorhidrosis, isolated","type":"exact"},{"name":"isolated hyperchlorhidrosis","type":"exact"}],"termid":"MONDO:0007747","xrefs":{"Monarch":{"xref_id":"0007747"}}}


id: PATO:0000487
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A response quality inhering in a bearer by virtue of the bearer's disposition to react to a stimulus or an agent.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to","termid":"PATO:0000077"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"responsive to","synonyms":[{"name":"responsive","type":"exact"}],"termid":"PATO:0000487"}


id: PBO:0084555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Member of the seripauperin multigene family; encoded mainly in subtelomeric regions; SWAT-GFP fusion protein localizes to the endoplasmic reticulum and vacuole, while mCherry fusion localizes to just the vacuole; active during alcoholic fermentation; regulated by anaerobiosis; negatively regulated by oxygen; repressed by heme; identical to Pau18p","termid":"PBO:0084555"}


id: MONDO:0013505
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any azoospermia in which the cause of the disease is a mutation in the DPY19L2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"},{"relation_name":"is_a","term_name":"male infertility due to globozoospermia","termid":"MONDO:0015746"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 9","secondary_identifiers":["DOID:0111156","GARD:15735","UMLS:C3151407","DOID:0070175","MEDGEN:462757","OMIM:613958"],"synonyms":[{"name":"DPY19L2 azoospermia","type":"exact"},{"name":"SPGF9","type":"related"},{"name":"azoospermia caused by mutation in DPY19L2","type":"exact"},{"name":"globozoospermia, complete","type":"related"},{"name":"globozoospermia, total","type":"related"},{"name":"spermatogenic failure 9","type":"exact"},{"name":"spermatogenic failure type 9","type":"exact"}],"termid":"MONDO:0013505","xrefs":{"Monarch":{"xref_id":"0013505"}}}


id: PBO:0031817
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_autophagy","termid":"PBO:0031817"}


id: GO:0005816
data:
  {"annotated_genes":["SJAG_05207","SJAG_01050","SJAG_03835","SJAG_01242","SJAG_02514","SJAG_04943","SJAG_02248","SJAG_01422","SJAG_00773","SJAG_03708","SJAG_03540","SJAG_00856","SJAG_01760","SJAG_01790","SJAG_02266","SJAG_04980","SJAG_02556","SJAG_05290","SJAG_05309","SJAG_02624","SJAG_04901","SJAG_03615","SJAG_00333","SJAG_03491","SJAG_00910","SJAG_01546","SJAG_01563","SJAG_02186","SJAG_01777","SJAG_01805","SJAG_00666","SJAG_04931","SJAG_00646","SJAG_04558","SJAG_05266","SJAG_03592","SJAG_01745","SJAG_02921","SJAG_02736","SJAG_02045","SJAG_00356","SJAG_03810","SJAG_02724","SJAG_03891","SJAG_00907","SJAG_02886","SJAG_01370","SJAG_01662","SJAG_00100","SJAG_04239","SJAG_02923","SJAG_00082","SJAG_03936","SJAG_04498","SJAG_01785","SJAG_04597","SJAG_04140","SJAG_05205","SJAG_02737","SJAG_04595","SJAG_01224","SJAG_01483","SJAG_05196","SJAG_04884","SJAG_03342","SJAG_02058","SJAG_00794","SJAG_00807","SJAG_03351","SJAG_00317","SJAG_04551","SJAG_00724","SJAG_03216","SJAG_01371","SJAG_02368","SJAG_02609","SJAG_04010","SJAG_00719","SJAG_04455","SJAG_01620","SJAG_05185","SJAG_01799","SJAG_03264","SJAG_02795","SJAG_02444","SJAG_01538","SJAG_00229","SJAG_01188","SJAG_05260","SJAG_02529","SJAG_07018","SJAG_05315","SJAG_03501","SJAG_00800","SJAG_05264","SJAG_00142","SJAG_03116","SJAG_04745","SJAG_03259","SJAG_01297","SJAG_03508","SJAG_01146","SJAG_05978","SJAG_02232","SJAG_00113","SJAG_02550","SJAG_04609","SJAG_03048","SJAG_02246","SJAG_00104","SJAG_04841","SJAG_00472","SJAG_03695","SJAG_01401","SJAG_04457","SJAG_03052","SJAG_03843","SJAG_04653","SJAG_00526","SJAG_01386","SJAG_03915","SJAG_03026","SJAG_02336","SJAG_04143","SJAG_03681","SJAG_04468","SJAG_02104","SJAG_03892","SJAG_03287","SJAG_00405","SJAG_02561","SJAG_01232","SJAG_01464","SJAG_02332","SJAG_01756","SJAG_00982","SJAG_02098","SJAG_01082","SJAG_02616","SJAG_02169","SJAG_01330","SJAG_04280","SJAG_02761","SJAG_06270","SJAG_00918","SJAG_03200","SJAG_03612","SJAG_01215","SJAG_03376","SJAG_03544","SJAG_02286","SJAG_00140","SJAG_03092","SJAG_00430","SJAG_03602","SJAG_04461","SJAG_03062","SJAG_02542","SJAG_01775"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[87229,90203,93360,101823,109672,118813,118816,118821,118839],"is_not":false,"summary":null,"term":"GO:0005816"},{"annotations":[92315,99162],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990334"},{"annotations":[97773,96348,99350],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061493"},{"annotations":[112330,109093,112125,114616,116429,108328,110067],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061496"},{"annotations":[109094,110919,102306,110068,108329,100480],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061497"},{"annotations":[112126,102310,94686,100221,86875,114617,99352,96353,99417,91775,93270,102416,90770,96252,113421,110892,89234,103628,90470,93343,101850,107840,104591,110920,90199,97065,94788,113420,117633,87228,116418,100342,110713,99325,99324,109096,100341],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035974"},{"annotations":[106583,117071,95955,95443,96255,104526,110680,114618,102546,118722,92938,93357,93711,99576,108511,104669,109669,90817,99101,107820,114788,99630,111960,114181,109398,116682,100439,100014,93273,103390,118254,97292,110411,96770,98117,97521,110538,110009,86876,88431,100030,106990,117721,99695,89218,110069,102311,116695,95757,108226,116203,89120,96201,100767,113158,114444,99870,101822,90663,109660,116433,117639,99353,97775,91776,116009,101116,93419,92318,96354,101853,93739,92737,104974,93884,105933,113988,118734,95122,95863,101642,94252,110989,106331,96942,108241,112332,92004,95873,89603,90816,110922,89087,107735,109046,114406,100093,99164,118152,90201,115395,103216,114296,103319,107026,111171,97926,114964,108333,116769,93891,112495,116510,88716,109097,90461,104845,106118,90617,90471,89464,118724,112127,116790,91212,92403,100482,112255,90864,93216,95807,105805,104068,105871,105844,115499,117666,91235],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044732"},{"annotations":[90618,102312,104846,105872,110010,99354,100440,110681,106630,101854],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071958"},{"annotations":[101857,104528,99166,112334,108335,95124,110012,110687,113990,102315,110071,109099,105873,92319,107028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071957"},{"annotations":[114965,106584,108336,116434],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0061499"}]},"cv_name":"cellular_component","definition":"The microtubule organizing center in fungi; functionally homologous to the animal cell centrosome.","definition_xrefs":["ISBN:0879693568"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule organizing center","termid":"GO:0005815"}],"gene_count":159,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00100":null,"SJAG_00104":null,"SJAG_00113":null,"SJAG_00140":null,"SJAG_00142":null,"SJAG_00229":null,"SJAG_00317":null,"SJAG_00333":null,"SJAG_00356":null,"SJAG_00405":null,"SJAG_00430":null,"SJAG_00472":null,"SJAG_00526":null,"SJAG_00646":null,"SJAG_00666":null,"SJAG_00719":null,"SJAG_00724":null,"SJAG_00773":null,"SJAG_00794":null,"SJAG_00800":null,"SJAG_00807":null,"SJAG_00856":null,"SJAG_00907":null,"SJAG_00910":null,"SJAG_00918":null,"SJAG_00982":null,"SJAG_01050":null,"SJAG_01082":null,"SJAG_01146":null,"SJAG_01188":null,"SJAG_01215":null,"SJAG_01224":null,"SJAG_01232":null,"SJAG_01242":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01386":null,"SJAG_01401":null,"SJAG_01422":null,"SJAG_01464":null,"SJAG_01483":null,"SJAG_01538":null,"SJAG_01546":null,"SJAG_01563":null,"SJAG_01620":null,"SJAG_01662":null,"SJAG_01745":null,"SJAG_01756":null,"SJAG_01760":null,"SJAG_01775":null,"SJAG_01777":null,"SJAG_01785":null,"SJAG_01790":null,"SJAG_01799":null,"SJAG_01805":null,"SJAG_02045":null,"SJAG_02058":null,"SJAG_02098":null,"SJAG_02104":null,"SJAG_02169":null,"SJAG_02186":null,"SJAG_02232":null,"SJAG_02246":null,"SJAG_02248":null,"SJAG_02266":null,"SJAG_02286":null,"SJAG_02332":null,"SJAG_02336":null,"SJAG_02368":null,"SJAG_02444":null,"SJAG_02514":null,"SJAG_02529":null,"SJAG_02542":null,"SJAG_02550":null,"SJAG_02556":null,"SJAG_02561":null,"SJAG_02609":null,"SJAG_02616":null,"SJAG_02624":null,"SJAG_02724":null,"SJAG_02736":null,"SJAG_02737":null,"SJAG_02761":null,"SJAG_02795":null,"SJAG_02886":null,"SJAG_02921":null,"SJAG_02923":null,"SJAG_03026":null,"SJAG_03048":null,"SJAG_03052":null,"SJAG_03062":null,"SJAG_03092":null,"SJAG_03116":null,"SJAG_03200":null,"SJAG_03216":null,"SJAG_03259":null,"SJAG_03264":null,"SJAG_03287":null,"SJAG_03342":null,"SJAG_03351":null,"SJAG_03376":null,"SJAG_03491":null,"SJAG_03501":null,"SJAG_03508":null,"SJAG_03540":null,"SJAG_03544":null,"SJAG_03592":null,"SJAG_03602":null,"SJAG_03612":null,"SJAG_03615":null,"SJAG_03681":null,"SJAG_03695":null,"SJAG_03708":null,"SJAG_03810":null,"SJAG_03835":null,"SJAG_03843":null,"SJAG_03891":null,"SJAG_03892":null,"SJAG_03915":null,"SJAG_03936":null,"SJAG_04010":null,"SJAG_04140":null,"SJAG_04143":null,"SJAG_04239":null,"SJAG_04280":null,"SJAG_04455":null,"SJAG_04457":null,"SJAG_04461":null,"SJAG_04468":null,"SJAG_04498":null,"SJAG_04551":null,"SJAG_04558":null,"SJAG_04595":null,"SJAG_04597":null,"SJAG_04609":null,"SJAG_04653":null,"SJAG_04745":null,"SJAG_04841":null,"SJAG_04884":null,"SJAG_04901":null,"SJAG_04931":null,"SJAG_04943":null,"SJAG_04980":null,"SJAG_05185":null,"SJAG_05196":null,"SJAG_05205":null,"SJAG_05207":null,"SJAG_05260":null,"SJAG_05264":null,"SJAG_05266":null,"SJAG_05290":null,"SJAG_05309":null,"SJAG_05315":null,"SJAG_05978":null,"SJAG_06270":null,"SJAG_07018":null},"genotype_count":0,"in_subsets":["cc_goslim_japonicus"],"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0015630"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0015630","GO:0005575"],"is_obsolete":false,"name":"spindle pole body","references_by_uniquename":{"GO_REF:0000107":null,"PMID:21733045":null,"PMID:32109380":null,"PMID:32243490":null},"secondary_identifiers":["Wikipedia:Spindle_pole_body"],"synonyms":[{"name":"SPB","type":"exact"}],"termid":"GO:0005816","terms_by_termid":{"GO:0000093":null,"GO:0005816":null,"GO:0035974":null,"GO:0044732":null,"GO:0061493":null,"GO:0061496":null,"GO:0061497":null,"GO:0061499":null,"GO:0071957":null,"GO:0071958":null,"GO:1990334":null}}


id: PBO:0000920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase-promoting complex subunit Cut9","termid":"PBO:0000920"}


id: PBO:0055059
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 2475","termid":"PBO:0055059"}


id: MONDO:0004420
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare tumor characterized by malignant transformation of an eccrine spiradenoma of the breast.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant spiradenoma","termid":"MONDO:0004412"},{"relation_name":"is_a","term_name":"breast adenocarcinoma","termid":"MONDO:0004988"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"breast malignant eccrine spiradenoma","secondary_identifiers":["NCIT:C5180","UMLS:C1334565","DOID:7983","MEDGEN:277329"],"synonyms":[{"name":"breast malignant spiradenoma","type":"exact"},{"name":"malignant breast eccrine spiradenoma","type":"exact"},{"name":"malignant eccrine spiradenoma of breast","type":"exact"},{"name":"malignant eccrine spiradenoma of the breast","type":"exact"},{"name":"malignant spiradenoma of breast","type":"exact"}],"termid":"MONDO:0004420","xrefs":{"Monarch":{"xref_id":"0004420"}}}


id: PBO:0062890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovo like zinc finger 2","termid":"PBO:0062890"}


id: PBO:0004443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Smc5-6 complex non-SMC subunit Nse4","termid":"PBO:0004443"}


id: FYPO:0006308
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells form actin cables that are thicker than normal in the medial region of the cell.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thick actin cables","termid":"FYPO:0002437"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0004803"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320","FYPO:0004803","FYPO:0005447"],"is_obsolete":false,"name":"thick actin cables in medial region","synonyms":[{"name":"increased actin cable thickness in medial region","type":"exact"},{"name":"thick actin cables in medial region during mitotic cell cycle","type":"related"},{"name":"thick actin cables in medial region during vegetative growth","type":"exact"},{"name":"thick actin cables in medial region of cell","type":"exact"},{"name":"thick formin-nucleated actin cables in medial region","type":"exact"}],"termid":"FYPO:0006308"}


id: GO:0030739
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + O-demethylpuromycin = S-adenosyl-L-homocysteine + puromycin.","definition_xrefs":["EC:2.1.1.38"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016741","GO:0003824","GO:0003674","GO:0016740"],"is_obsolete":false,"name":"O-demethylpuromycin O-methyltransferase activity","secondary_identifiers":["MetaCyc:2.1.1.38-RXN","RHEA:22280"],"synonyms":[{"name":"O-demethylpuromycin methyltransferase activity","type":"related"},{"name":"S-adenosyl-L-methionine:O-demethylpuromycin O-methyltransferase activity","type":"related"}],"termid":"GO:0030739"}


id: GO:0035091
data:
  {"annotated_genes":["SJAG_02613","SJAG_01143","SJAG_04219","SJAG_02728","SJAG_00970","SJAG_04221","SJAG_00368","SJAG_02912","SJAG_01309","SJAG_02492","SJAG_04960","SJAG_02392","SJAG_01135","SJAG_00638","SJAG_01722","SJAG_01769","SJAG_03851","SJAG_02248","SJAG_02166","SJAG_04963","SJAG_01519","SJAG_00216","SJAG_04077","SJAG_03250","SJAG_00115","SJAG_01324","SJAG_04644","SJAG_00314","SJAG_00173","SJAG_00821","SJAG_02852","SJAG_05179","SJAG_01794","SJAG_02572","SJAG_01783","SJAG_02587","SJAG_00053","SJAG_01748","SJAG_02657","SJAG_01382","SJAG_04010","SJAG_03721","SJAG_00907","SJAG_00663","SJAG_03756","SJAG_03170","SJAG_02468","SJAG_00152","SJAG_03405","SJAG_05245","SJAG_00971","SJAG_02989","SJAG_04024","SJAG_01516","SJAG_01945","SJAG_00118","SJAG_00117","SJAG_01564","SJAG_04275"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[62463,89895,91774,92962,96949,98482,101217,103884,104468,106862,107118,108231,112357,114269,114701,115741,117054,117497,118517],"is_not":false,"summary":null,"term":"GO:0035091"},{"annotations":[105515,107693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005545"},{"annotations":[95346],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1901981"},{"annotations":[116962,87536,101928],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005547"},{"annotations":[97100,99783,98829,98108],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0080025"},{"annotations":[99784,104328,97101,101212,114722,90060,98109,99340,111948,109135,99203,108145,95420,99341,102933,90989,109287,109486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032266"},{"annotations":[105517,116534,101422,98791,106087,114380,90230,101259,87468,101268,117032,118475],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0005546"},{"annotations":[111989,98222,98792,93994,99618,101929],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070273"}]},"cv_name":"molecular_function","definition":"Binding to an inositol-containing glycerophospholipid, i.e. phosphatidylinositol (PtdIns) and its phosphorylated derivatives.","definition_xrefs":["GOC:bf","PMID:11395417","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid binding","termid":"GO:0005543"}],"gene_count":59,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00115":null,"SJAG_00117":null,"SJAG_00118":null,"SJAG_00152":null,"SJAG_00173":null,"SJAG_00216":null,"SJAG_00314":null,"SJAG_00368":null,"SJAG_00638":null,"SJAG_00663":null,"SJAG_00821":null,"SJAG_00907":null,"SJAG_00970":null,"SJAG_00971":null,"SJAG_01135":null,"SJAG_01143":null,"SJAG_01309":null,"SJAG_01324":null,"SJAG_01382":null,"SJAG_01516":null,"SJAG_01519":null,"SJAG_01564":null,"SJAG_01722":null,"SJAG_01748":null,"SJAG_01769":null,"SJAG_01783":null,"SJAG_01794":null,"SJAG_01945":null,"SJAG_02166":null,"SJAG_02248":null,"SJAG_02392":null,"SJAG_02468":null,"SJAG_02492":null,"SJAG_02572":null,"SJAG_02587":null,"SJAG_02613":null,"SJAG_02657":null,"SJAG_02728":null,"SJAG_02852":null,"SJAG_02912":null,"SJAG_02989":null,"SJAG_03170":null,"SJAG_03250":null,"SJAG_03405":null,"SJAG_03721":null,"SJAG_03756":null,"SJAG_03851":null,"SJAG_04010":null,"SJAG_04024":null,"SJAG_04077":null,"SJAG_04219":null,"SJAG_04221":null,"SJAG_04275":null,"SJAG_04644":null,"SJAG_04960":null,"SJAG_04963":null,"SJAG_05179":null,"SJAG_05245":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008289"}],"interesting_parent_ids":["GO:0008289","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"phosphatidylinositol binding","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"phosphoinositide binding","type":"exact"}],"termid":"GO:0035091","terms_by_termid":{"GO:0005545":null,"GO:0005546":null,"GO:0005547":null,"GO:0032266":null,"GO:0035091":null,"GO:0070273":null,"GO:0080025":null,"GO:1901981":null}}


id: PBO:0079992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP9Y pseudogene 30","termid":"PBO:0079992"}


id: MONDO:0024265
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Duane syndrome type 1 is the most common type of Duane syndrome, an eye movement disorder that is present at birth. People with Duane syndrome have restricted ability to move the affected eye(s) outward toward the ear (abduction) and/or inward toward the nose (adduction). The different types are distinguished by the eye movements that are most restricted. Duane syndrome type 1 is characterized by absent to very restricted abduction and normal to mildly restricted adduction. The eye opening (palpebral fissure) narrows and the eyeball retracts into the orbit with adduction. With abduction, the reverse occurs. One or both eyes may be affected. The majority of cases are sporadic (not inherited), while about 10% are familial. 70% of affected people do not have any other abnormalities at birth (isolated Duane syndrome). Treatment is mainly supportive and may include glasses or contact lenses for vision correction, eye patches, or surgery.","definition_xrefs":["GARD:0010763"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Duane retraction syndrome","termid":"MONDO:0007473"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Duane syndrome type 1","secondary_identifiers":["MEDGEN:201329","SCTID:128082002","UMLS:C0994516","OMIM:126800","GARD:10763"],"synonyms":[{"name":"DURS1","type":"exact"},{"name":"Drs","type":"related"},{"name":"Duane anomaly","type":"related"},{"name":"Duane retraction syndrome 1","type":"exact"},{"name":"Duane syndrome","type":"related"},{"name":"retraction syndrome","type":"related"}],"termid":"MONDO:0024265","xrefs":{"Monarch":{"xref_id":"0024265"}}}


id: PBO:0040890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BMP binding endothelial regulator","termid":"PBO:0040890"}


id: PBO:0063173
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polysaccharide biosynthesis domain containing 1","termid":"PBO:0063173"}


id: MONDO:0012291
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any selective IgA deficiency disease in which the cause of the disease is a mutation in the TNFRSF13B gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"selective IgA deficiency disease","termid":"MONDO:0001341"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"immunoglobulin A deficiency 2","secondary_identifiers":["MEDGEN:372182","GARD:10198","OMIM:609529","MESH:C536291","UMLS:C1836032"],"synonyms":[{"name":"IGAD2","type":"related"},{"name":"IMMUNOGLOBULIN A deficiency 2","type":"related"},{"name":"IgA, selective deficiency of, TACI related","type":"related"},{"name":"IgA, selective deficiency of, TACI-related","type":"related"},{"name":"Immunoglobulin A, selective deficiency of, TACI related","type":"related"},{"name":"Immunoglobulin A, selective deficiency of, TACI-related","type":"related"},{"name":"Immunoglobulin a deficiency type 2","type":"exact"},{"name":"TNFRSF13B selective IgA deficiency disease","type":"exact"},{"name":"immunoglobulin a deficiency 2","type":"exact"},{"name":"selective IgA deficiency disease caused by mutation in TNFRSF13B","type":"exact"}],"termid":"MONDO:0012291","xrefs":{"Monarch":{"xref_id":"0012291"}}}


id: PBO:0004165
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"siderophore-iron transporter Str1","termid":"PBO:0004165"}


id: PBO:0056687
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple EGF like domains 8","termid":"PBO:0056687"}


id: GO:0009242
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of colanic acid, a capsular bacterial polysaccharide.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule biosynthetic process","termid":"GO:0009059"},{"relation_name":"is_a","term_name":"colanic acid metabolic process","termid":"GO:0046377"},{"relation_name":"is_a","term_name":"carbohydrate derivative biosynthetic process","termid":"GO:1901137"}],"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":"colanic acid biosynthetic process","secondary_identifiers":["MetaCyc:COLANSYN-PWY"],"synonyms":[{"name":"M antigen biosynthesis","type":"exact"},{"name":"M antigen biosynthetic process","type":"exact"},{"name":"colanic acid anabolism","type":"exact"},{"name":"colanic acid biosynthesis","type":"exact"},{"name":"colanic acid formation","type":"exact"},{"name":"colanic acid synthesis","type":"exact"}],"termid":"GO:0009242"}


id: GO:0044080
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A process in which a symbiont alters or subverts a cGMP-mediated signal transduction pathway in its host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["MITRE:tk"],"gene_count":0,"genotype_count":0,"name":"obsolete symbiont-mediated perturbation of host cGMP-mediated signal transduction (obsolete GO:0044080)","synonyms":[{"name":"modulation by symbiont of host cGMP-mediated signal transduction","type":"exact"},{"name":"modulation by symbiont of host cGMP-mediated signal transduction pathway","type":"exact"},{"name":"modulation by symbiont of host cGMP-mediated signaling","type":"exact"},{"name":"modulation by symbiont of host cGMP-mediated signalling","type":"exact"},{"name":"modulation of host cGMP-mediated signal transduction by symbiont","type":"exact"},{"name":"perturbation of host cGMP-mediated signal transduction","type":"exact"},{"name":"regulation by symbiont of host cGMP-mediated signal transduction","type":"exact"}],"termid":"GO:0044080"}


id: GO:0050277
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + sedoheptulose = ADP + 2 H+ + sedoheptulose 7-phosphate.","definition_xrefs":["EC:2.7.1.14","RHEA:23844"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016301","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"sedoheptulokinase activity","secondary_identifiers":["MetaCyc:SEDOHEPTULOKINASE-RXN","Reactome:R-HSA-8959719","KEGG_REACTION:R01844"],"synonyms":[{"name":"ATP:sedoheptulose 7-phosphotransferase activity","type":"related"},{"name":"heptulokinase activity","type":"related"},{"name":"sedoheptulokinase (phosphorylating)","type":"related"}],"termid":"GO:0050277"}


id: GO:0090263
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency, or extent of the Wnt signaling pathway through beta-catenin, the series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of Wnt signaling pathway","termid":"GO:0030177"},{"relation_name":"is_a","term_name":"regulation of canonical Wnt signaling pathway","termid":"GO:0060828"},{"relation_name":"positively_regulates","term_name":"canonical Wnt signaling pathway","termid":"GO:0060070"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of canonical Wnt signaling pathway","secondary_identifiers":["GO:0035413","Reactome:R-HSA-4641257"],"synonyms":[{"name":"positive regulation of Wnt receptor signaling pathway through beta-catenin","type":"exact"},{"name":"positive regulation of canonical Wnt receptor signaling pathway","type":"exact"},{"name":"positive regulation of canonical Wnt receptor signalling pathway","type":"exact"},{"name":"positive regulation of canonical Wnt-activated signaling pathway","type":"exact"},{"name":"positive regulation of catenin import into nucleus","type":"narrow"},{"name":"positive regulation of catenin protein nuclear translocation","type":"narrow"}],"termid":"GO:0090263"}


id: MONDO:0001487
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer that involves the intrahepatic bile duct.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"gallbladder cancer","termid":"MONDO:0005411"},{"relation_name":"is_a","term_name":"bile duct cancer","termid":"MONDO:0003059"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0004992","MONDO:0002515"],"is_obsolete":false,"name":"intrahepatic bile duct cancer","secondary_identifiers":["DOID:12298","UMLS:C0546835","MEDGEN:639748","SCTID:187777008","ICD9:155.1"],"synonyms":[{"name":"Ca intrahepatic bile ducts","type":"exact"},{"name":"cancer of intrahepatic bile duct","type":"exact"},{"name":"malignant intrahepatic bile duct neoplasm","type":"exact"},{"name":"malignant neoplasm of intrahepatic bile duct","type":"exact"},{"name":"malignant neoplasm of intrahepatic bile ducts","type":"exact"},{"name":"malignant neoplasm of intrahepatic biliary passages","type":"exact"}],"termid":"MONDO:0001487","xrefs":{"Monarch":{"xref_id":"0001487"}}}


id: GO:0090577
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A transcription factor complex that acts at a regulatory region of a gene transcribed by RNA polymerase IV.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription regulator complex","termid":"GO:0005667"}],"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":"RNA polymerase IV transcription regulator complex","synonyms":[{"name":"RNA polymerase IV transcription factor complex","type":"narrow"}],"termid":"GO:0090577"}


id: PBO:0028086
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_nuclear_body","termid":"PBO:0028086"}


id: PBO:0078005
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNF receptor associated factor 5","termid":"PBO:0078005"}


id: MONDO:0021745
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A growth disorder that is observed between the ages of 2 and 15, caused by extreme emotional deprivation or stress.","definition_xrefs":["Wikipedia:Psychosocial_short_stature"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental disability","termid":"MONDO:0005287"},{"relation_name":"is_a","term_name":"pituitary dwarfism","termid":"MONDO:0006909"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psychosocial short stature","secondary_identifiers":["MEDGEN:264104","SCTID:39465007","icd11.foundation:2088216390","MESH:C535569","UMLS:C1455735"],"synonyms":[{"name":"Kaspar Hauser syndrome","type":"related"},{"name":"abuse dwarfism syndrome","type":"related"},{"name":"child abuse dwarfism","type":"related"},{"name":"psychosocial dwarfism","type":"related"}],"termid":"MONDO:0021745","xrefs":{"Monarch":{"xref_id":"0021745"}}}


id: PR:000045546
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A histone H2B-alpha (Schizosaccharomyces pombe) that has been monoubiquitinated on the most C-terminal Lys residue. Example: UniProtKB:P04913-1, Lys-120, PR:000044771.","definition_xrefs":["PRO:CNA","PMID:27098497","PomBase:MAH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone H2B-alpha (Schizosaccharomyces pombe)","termid":"PR:000045547"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"htb1/MonoUbiq(K119)","pombase_gene_id":"SPCC622.09","secondary_identifiers":["PR:000036916"],"synonyms":[{"name":"PomBase_original_PRO_term_name: histone H2B-alpha ubiquitinated 1 (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-htb1/Ubiq:1","type":"exact"},{"name":"htb1/MonoUbiq(K119)","type":"exact"},{"name":"htb1/MonoUbiq:(K120)","type":"exact"},{"name":"uH2B","type":"related"}],"termid":"PR:000045546"}


id: PBO:0113067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the TOM (translocase of outer membrane) complex; involved in the recognition and initial import steps for all mitochondrially-directed proteins, acting as a receptor for incoming precursor proteins; moonlighting role as a transcriptional regulator of mitochondrial proteins; age-dependent reduction in Tom70p results in mitochondrial dysfunction, a hallmark of aging; localizes to mitochondria–ER contact sites; TOM70 has a paralog, TOM71, that arose from the whole genome duplication","termid":"PBO:0113067"}


id: GO:0019128
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The racemization of peptidyl-tryptophan.","definition_xrefs":["RESID:AA0198"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-tryptophan racemization (obsolete GO:0019128)","termid":"GO:0019128"}


id: GO:0016817
data:
  {"annotated_genes":["SJAG_02679","SJAG_03406","SJAG_04150","SJAG_00884","SJAG_03471","SJAG_03502","SJAG_03892","SJAG_03497","SJAG_03570","SJAG_03927","SJAG_02619","SJAG_00768","SJAG_01435","SJAG_02991","SJAG_01240","SJAG_00378","SJAG_02366","SJAG_04064","SJAG_00645","SJAG_03886","SJAG_00604","SJAG_02516","SJAG_03676","SJAG_02431","SJAG_03708","SJAG_02295","SJAG_01449","SJAG_04470","SJAG_03832","SJAG_01615","SJAG_03682","SJAG_01154","SJAG_01816","SJAG_03950","SJAG_03036","SJAG_01500","SJAG_02738","SJAG_00650","SJAG_01344","SJAG_05032","SJAG_04477","SJAG_00330","SJAG_00226","SJAG_03982","SJAG_01929","SJAG_00500","SJAG_04169","SJAG_00659","SJAG_04355","SJAG_01831","SJAG_03371","SJAG_04210","SJAG_05030","SJAG_00332","SJAG_00712","SJAG_00995","SJAG_02339","SJAG_02336","SJAG_16455","SJAG_01489","SJAG_02132","SJAG_03137","SJAG_02233","SJAG_01913","SJAG_02267","SJAG_04487","SJAG_00766","SJAG_00136","SJAG_00424","SJAG_01653","SJAG_00599","SJAG_01625","SJAG_03896","SJAG_00414","SJAG_00906","SJAG_01180","SJAG_04114","SJAG_03703","SJAG_01024","SJAG_01400","SJAG_01944","SJAG_00669","SJAG_01131","SJAG_03567","SJAG_04955","SJAG_00853","SJAG_00447","SJAG_02558","SJAG_02399","SJAG_02708","SJAG_03161","SJAG_02180","SJAG_00773","SJAG_00457","SJAG_04599","SJAG_02247","SJAG_04531","SJAG_00587","SJAG_02114","SJAG_04511","SJAG_01644","SJAG_03797","SJAG_01339","SJAG_01010","SJAG_01405","SJAG_00930","SJAG_00541","SJAG_01874","SJAG_01002","SJAG_01471","SJAG_05332","SJAG_03320","SJAG_01410","SJAG_00373","SJAG_01655","SJAG_02400","SJAG_04118","SJAG_01179","SJAG_05010","SJAG_02605","SJAG_01696","SJAG_01762","SJAG_02994","SJAG_00923","SJAG_03684","SJAG_03613","SJAG_02061","SJAG_03362","SJAG_00729","SJAG_02084","SJAG_03850","SJAG_00806","SJAG_01945","SJAG_01669","SJAG_01379","SJAG_02457","SJAG_01499","SJAG_04242","SJAG_01875","SJAG_00390","SJAG_01419","SJAG_00705","SJAG_04157","SJAG_01851","SJAG_04154","SJAG_01774","SJAG_02824","SJAG_03461","SJAG_04745","SJAG_02331","SJAG_02895","SJAG_01129","SJAG_00878","SJAG_04375","SJAG_00984","SJAG_04055","SJAG_02302","SJAG_03964","SJAG_03866","SJAG_02848","SJAG_00790","SJAG_00938","SJAG_03453","SJAG_03363","SJAG_02353","SJAG_03345","SJAG_02563","SJAG_05294","SJAG_02444","SJAG_02704","SJAG_01095","SJAG_01662","SJAG_00663","SJAG_03688","SJAG_02382","SJAG_03495","SJAG_05209","SJAG_04692","SJAG_00863","SJAG_00851","SJAG_04003","SJAG_02598","SJAG_03977","SJAG_03534","SJAG_02242","SJAG_02684","SJAG_01277","SJAG_02561","SJAG_03798","SJAG_01402","SJAG_03415","SJAG_01530","SJAG_03072","SJAG_02373","SJAG_05313","SJAG_02602","SJAG_03091","SJAG_02394","SJAG_05295","SJAG_03515","SJAG_02292","SJAG_03358","SJAG_02074","SJAG_01391","SJAG_00564","SJAG_01438","SJAG_03658","SJAG_04679","SJAG_02521","SJAG_00871","SJAG_00898","SJAG_03948","SJAG_04566","SJAG_01613","SJAG_00466","SJAG_00111","SJAG_01354","SJAG_01397","SJAG_00475","SJAG_04001","SJAG_02581","SJAG_01651","SJAG_04509","SJAG_00516","SJAG_00018","SJAG_01620","SJAG_02606","SJAG_02077","SJAG_03732","SJAG_00570","SJAG_02825","SJAG_01807","SJAG_03785","SJAG_01664","SJAG_04167","SJAG_03923","SJAG_01817","SJAG_01510","SJAG_00430","SJAG_04862","SJAG_01558","SJAG_02374","SJAG_04038","SJAG_04755","SJAG_02897","SJAG_01447","SJAG_04874","SJAG_03560","SJAG_04488","SJAG_02182","SJAG_00947","SJAG_01456","SJAG_00065","SJAG_04939","SJAG_02997","SJAG_02656","SJAG_02265","SJAG_02604","SJAG_04277","SJAG_01731","SJAG_02571","SJAG_00589","SJAG_01544","SJAG_03237","SJAG_04343","SJAG_04004","SJAG_02798","SJAG_02226","SJAG_02023","SJAG_02384","SJAG_02082","SJAG_01677","SJAG_01152","SJAG_04187","SJAG_04666","SJAG_00983","SJAG_04596","SJAG_03496","SJAG_05213","SJAG_04015","SJAG_01879","SJAG_00272","SJAG_01597","SJAG_02943","SJAG_02926","SJAG_04258","SJAG_02545","SJAG_02748","SJAG_04147","SJAG_01595","SJAG_03909","SJAG_03897","SJAG_02199","SJAG_01546","SJAG_02957","SJAG_00132","SJAG_01769","SJAG_02575","SJAG_00757","SJAG_03443","SJAG_03011","SJAG_02782","SJAG_03374","SJAG_03915","SJAG_04757","SJAG_00212","SJAG_04940","SJAG_04121","SJAG_00244","SJAG_02286","SJAG_01186","SJAG_02356","SJAG_05019","SJAG_02460","SJAG_04410","SJAG_02610","SJAG_03342","SJAG_02171","SJAG_03451","SJAG_00857","SJAG_02856","SJAG_02187","SJAG_02906","SJAG_00609","SJAG_03846","SJAG_00344","SJAG_00031","SJAG_02056","SJAG_04351","SJAG_02872","SJAG_02595","SJAG_01297","SJAG_02378","SJAG_04203","SJAG_04870","SJAG_02640","SJAG_00231","SJAG_02601","SJAG_03780","SJAG_03050"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[88775,98457],"is_not":false,"summary":null,"term":"GO:0016817"},{"annotations":[91037,112972],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140932"},{"annotations":[96593,118100],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106379"},{"annotations":[99028],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044715"},{"annotations":[113452],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043262"},{"annotations":[112809],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047631"},{"annotations":[113453],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004050"},{"annotations":[94961,114552,87810,97421,101701,107231,75419,105561,92755,98438,98746,99442,107343,89682,110025,107754,93449,90010,112673,114607,102633,117383,96105,115804,107626,110556,95695,98512,115001,114584,112917,99815,112579,88745,95455,90007,107387,94942,89324,103979,112016,103574,89641,91450,102337,100134,88325,99389,112325,90011,90657,104960,99689,112880,93911,103786,97738,106566,88754,87238,103371,95962,114412,102003,90014,92337,117090,90009,99512,111736,117455,101191,95561,111291,110846,115683,101326,103260,100226,102174,89549,67055,106475,87389,92580,100517,106740,96439,112793,118226,87423,91197,111542,98738,104074,88072,98845,103412,95140,116192,103032,87176,94544,106829,98419,96545,107327,110485,114506,117686,91247,115430,89279,90378,99533,107080,100049,97249,103406,116727,98485,105921,95546,107284,102679,87513,106679,88110,115939,91393,96411,117706,101840,110044,112232,115000,110894,98977,87290,105090,88601,99119,100209,95480,112814,88225,98839,115410,88435,90012,102785,104575,90013,104009,95974,91537,89706,94756,114686,95936,89055,116025,94084,92161,116449,98065,107059,103049,117695,101595,118109,104183,113348,102763,113455,116923,91610,94262,114780,87459,90635,111188,113268,110736,110327,87636,97145,100379,102901,110879,112271,109738,104352,104681,103252,98570,108158,109367,115261,105716,118233,101093,96374,98535,90008,101137,88374,99043,94712,111838,96015,111768,96266,101130,111986,96578,102827,91986,116193,89769,95800,108713,87177,100082,118010,106440,103715,105687,96240,90280,88226,109248,88652,100636,90006,116807,118421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016887"},{"annotations":[88191],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034431"},{"annotations":[88192],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034432"},{"annotations":[110941],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047710"},{"annotations":[116585],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004081"},{"annotations":[88193],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008796"},{"annotations":[113456],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036384"},{"annotations":[99347,110479,88575],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010945"},{"annotations":[109888],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000810"},{"annotations":[111328],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004551"},{"annotations":[88194],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0008486"},{"annotations":[98493,118101],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035870"},{"annotations":[115182],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0120108"},{"annotations":[110398],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047874"},{"annotations":[96594],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036218"},{"annotations":[98494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004170"},{"annotations":[111280,115350,88195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000298"},{"annotations":[95278,104688,111281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004309"},{"annotations":[68862,90336],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003925"},{"annotations":[113457,99828],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004382"},{"annotations":[100463,104104,97391,92352,113458,111895,102996,110035,111896,87381,93088,99616,101702,115470,106929,97883,108223,117979,115433,116827,110036,118494,106690,92193,89213,92746,100351,102132,99217,100789,90783,100952,111897,116113,117866,106921,117980,116998,90339,102156,109763,88389,93087,105503,108195,100740,106629,117978,88720,93333,97321,104399,91508,102386,97802,91914,109250,93815,104913,95583,92281,106043,106668,96558,97241,97801,108759,93992,93086,110333,112364,111017,91473,103424,110936,93718,100160,103075,88918,108820,99141],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003924"},{"annotations":[104154],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061791"},{"annotations":[91665,96648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0016818"},{"annotations":[99554,93191,114100,96270,104689],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004427"},{"annotations":[104690],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052840"},{"annotations":[114555,88197,104691],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052846"},{"annotations":[88198,104692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052847"},{"annotations":[114556,88199,104693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052843"},{"annotations":[104694,88200],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0052845"},{"annotations":[118102],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036220"},{"annotations":[99462,102270],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990606"},{"annotations":[91185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034353"},{"annotations":[98486],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140818"},{"annotations":[104609],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000210"},{"annotations":[104610],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035529"},{"annotations":[113459,111329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047429"},{"annotations":[107352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004636"},{"annotations":[99829,111330],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017111"},{"annotations":[91187],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110152"},{"annotations":[104611],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110153"},{"annotations":[99830,113460],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045134"},{"annotations":[96595],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036221"},{"annotations":[118103],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036222"}]},"cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of any acid anhydride.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity","termid":"GO:0016787"}],"gene_count":340,"genes_by_uniquename":{"SJAG_00018":null,"SJAG_00031":null,"SJAG_00065":null,"SJAG_00111":null,"SJAG_00132":null,"SJAG_00136":null,"SJAG_00212":null,"SJAG_00226":null,"SJAG_00231":null,"SJAG_00244":null,"SJAG_00272":null,"SJAG_00330":null,"SJAG_00332":null,"SJAG_00344":null,"SJAG_00373":null,"SJAG_00378":null,"SJAG_00390":null,"SJAG_00414":null,"SJAG_00424":null,"SJAG_00430":null,"SJAG_00447":null,"SJAG_00457":null,"SJAG_00466":null,"SJAG_00475":null,"SJAG_00500":null,"SJAG_00516":null,"SJAG_00541":null,"SJAG_00564":null,"SJAG_00570":null,"SJAG_00587":null,"SJAG_00589":null,"SJAG_00599":null,"SJAG_00604":null,"SJAG_00609":null,"SJAG_00645":null,"SJAG_00650":null,"SJAG_00659":null,"SJAG_00663":null,"SJAG_00669":null,"SJAG_00705":null,"SJAG_00712":null,"SJAG_00729":null,"SJAG_00757":null,"SJAG_00766":null,"SJAG_00768":null,"SJAG_00773":null,"SJAG_00790":null,"SJAG_00806":null,"SJAG_00851":null,"SJAG_00853":null,"SJAG_00857":null,"SJAG_00863":null,"SJAG_00871":null,"SJAG_00878":null,"SJAG_00884":null,"SJAG_00898":null,"SJAG_00906":null,"SJAG_00923":null,"SJAG_00930":null,"SJAG_00938":null,"SJAG_00947":null,"SJAG_00983":null,"SJAG_00984":null,"SJAG_00995":null,"SJAG_01002":null,"SJAG_01010":null,"SJAG_01024":null,"SJAG_01095":null,"SJAG_01129":null,"SJAG_01131":null,"SJAG_01152":null,"SJAG_01154":null,"SJAG_01179":null,"SJAG_01180":null,"SJAG_01186":null,"SJAG_01240":null,"SJAG_01277":null,"SJAG_01297":null,"SJAG_01339":null,"SJAG_01344":null,"SJAG_01354":null,"SJAG_01379":null,"SJAG_01391":null,"SJAG_01397":null,"SJAG_01400":null,"SJAG_01402":null,"SJAG_01405":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01435":null,"SJAG_01438":null,"SJAG_01447":null,"SJAG_01449":null,"SJAG_01456":null,"SJAG_01471":null,"SJAG_01489":null,"SJAG_01499":null,"SJAG_01500":null,"SJAG_01510":null,"SJAG_01530":null,"SJAG_01544":null,"SJAG_01546":null,"SJAG_01558":null,"SJAG_01595":null,"SJAG_01597":null,"SJAG_01613":null,"SJAG_01615":null,"SJAG_01620":null,"SJAG_01625":null,"SJAG_01644":null,"SJAG_01651":null,"SJAG_01653":null,"SJAG_01655":null,"SJAG_01662":null,"SJAG_01664":null,"SJAG_01669":null,"SJAG_01677":null,"SJAG_01696":null,"SJAG_01731":null,"SJAG_01762":null,"SJAG_01769":null,"SJAG_01774":null,"SJAG_01807":null,"SJAG_01816":null,"SJAG_01817":null,"SJAG_01831":null,"SJAG_01851":null,"SJAG_01874":null,"SJAG_01875":null,"SJAG_01879":null,"SJAG_01913":null,"SJAG_01929":null,"SJAG_01944":null,"SJAG_01945":null,"SJAG_02023":null,"SJAG_02056":null,"SJAG_02061":null,"SJAG_02074":null,"SJAG_02077":null,"SJAG_02082":null,"SJAG_02084":null,"SJAG_02114":null,"SJAG_02132":null,"SJAG_02171":null,"SJAG_02180":null,"SJAG_02182":null,"SJAG_02187":null,"SJAG_02199":null,"SJAG_02226":null,"SJAG_02233":null,"SJAG_02242":null,"SJAG_02247":null,"SJAG_02265":null,"SJAG_02267":null,"SJAG_02286":null,"SJAG_02292":null,"SJAG_02295":null,"SJAG_02302":null,"SJAG_02331":null,"SJAG_02336":null,"SJAG_02339":null,"SJAG_02353":null,"SJAG_02356":null,"SJAG_02366":null,"SJAG_02373":null,"SJAG_02374":null,"SJAG_02378":null,"SJAG_02382":null,"SJAG_02384":null,"SJAG_02394":null,"SJAG_02399":null,"SJAG_02400":null,"SJAG_02431":null,"SJAG_02444":null,"SJAG_02457":null,"SJAG_02460":null,"SJAG_02516":null,"SJAG_02521":null,"SJAG_02545":null,"SJAG_02558":null,"SJAG_02561":null,"SJAG_02563":null,"SJAG_02571":null,"SJAG_02575":null,"SJAG_02581":null,"SJAG_02595":null,"SJAG_02598":null,"SJAG_02601":null,"SJAG_02602":null,"SJAG_02604":null,"SJAG_02605":null,"SJAG_02606":null,"SJAG_02610":null,"SJAG_02619":null,"SJAG_02640":null,"SJAG_02656":null,"SJAG_02679":null,"SJAG_02684":null,"SJAG_02704":null,"SJAG_02708":null,"SJAG_02738":null,"SJAG_02748":null,"SJAG_02782":null,"SJAG_02798":null,"SJAG_02824":null,"SJAG_02825":null,"SJAG_02848":null,"SJAG_02856":null,"SJAG_02872":null,"SJAG_02895":null,"SJAG_02897":null,"SJAG_02906":null,"SJAG_02926":null,"SJAG_02943":null,"SJAG_02957":null,"SJAG_02991":null,"SJAG_02994":null,"SJAG_02997":null,"SJAG_03011":null,"SJAG_03036":null,"SJAG_03050":null,"SJAG_03072":null,"SJAG_03091":null,"SJAG_03137":null,"SJAG_03161":null,"SJAG_03237":null,"SJAG_03320":null,"SJAG_03342":null,"SJAG_03345":null,"SJAG_03358":null,"SJAG_03362":null,"SJAG_03363":null,"SJAG_03371":null,"SJAG_03374":null,"SJAG_03406":null,"SJAG_03415":null,"SJAG_03443":null,"SJAG_03451":null,"SJAG_03453":null,"SJAG_03461":null,"SJAG_03471":null,"SJAG_03495":null,"SJAG_03496":null,"SJAG_03497":null,"SJAG_03502":null,"SJAG_03515":null,"SJAG_03534":null,"SJAG_03560":null,"SJAG_03567":null,"SJAG_03570":null,"SJAG_03613":null,"SJAG_03658":null,"SJAG_03676":null,"SJAG_03682":null,"SJAG_03684":null,"SJAG_03688":null,"SJAG_03703":null,"SJAG_03708":null,"SJAG_03732":null,"SJAG_03780":null,"SJAG_03785":null,"SJAG_03797":null,"SJAG_03798":null,"SJAG_03832":null,"SJAG_03846":null,"SJAG_03850":null,"SJAG_03866":null,"SJAG_03886":null,"SJAG_03892":null,"SJAG_03896":null,"SJAG_03897":null,"SJAG_03909":null,"SJAG_03915":null,"SJAG_03923":null,"SJAG_03927":null,"SJAG_03948":null,"SJAG_03950":null,"SJAG_03964":null,"SJAG_03977":null,"SJAG_03982":null,"SJAG_04001":null,"SJAG_04003":null,"SJAG_04004":null,"SJAG_04015":null,"SJAG_04038":null,"SJAG_04055":null,"SJAG_04064":null,"SJAG_04114":null,"SJAG_04118":null,"SJAG_04121":null,"SJAG_04147":null,"SJAG_04150":null,"SJAG_04154":null,"SJAG_04157":null,"SJAG_04167":null,"SJAG_04169":null,"SJAG_04187":null,"SJAG_04203":null,"SJAG_04210":null,"SJAG_04242":null,"SJAG_04258":null,"SJAG_04277":null,"SJAG_04343":null,"SJAG_04351":null,"SJAG_04355":null,"SJAG_04375":null,"SJAG_04410":null,"SJAG_04470":null,"SJAG_04477":null,"SJAG_04487":null,"SJAG_04488":null,"SJAG_04509":null,"SJAG_04511":null,"SJAG_04531":null,"SJAG_04566":null,"SJAG_04596":null,"SJAG_04599":null,"SJAG_04666":null,"SJAG_04679":null,"SJAG_04692":null,"SJAG_04745":null,"SJAG_04755":null,"SJAG_04757":null,"SJAG_04862":null,"SJAG_04870":null,"SJAG_04874":null,"SJAG_04939":null,"SJAG_04940":null,"SJAG_04955":null,"SJAG_05010":null,"SJAG_05019":null,"SJAG_05030":null,"SJAG_05032":null,"SJAG_05209":null,"SJAG_05213":null,"SJAG_05294":null,"SJAG_05295":null,"SJAG_05313":null,"SJAG_05332":null,"SJAG_16455":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"hydrolase activity, acting on acid anhydrides","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000003":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["EC:3.6.-.-"],"synonyms":[{"name":"hydrolase activity, acting on acid anhydrides, involved in cellular and subcellular movement","type":"narrow"}],"termid":"GO:0016817","terms_by_termid":{"GO:0000210":null,"GO:0000298":null,"GO:0000810":null,"GO:0003924":null,"GO:0003925":null,"GO:0004050":null,"GO:0004081":null,"GO:0004170":null,"GO:0004309":null,"GO:0004382":null,"GO:0004427":null,"GO:0004551":null,"GO:0004636":null,"GO:0008486":null,"GO:0008796":null,"GO:0010945":null,"GO:0016817":null,"GO:0016818":null,"GO:0016887":null,"GO:0017111":null,"GO:0034353":null,"GO:0034431":null,"GO:0034432":null,"GO:0035529":null,"GO:0035870":null,"GO:0036218":null,"GO:0036220":null,"GO:0036221":null,"GO:0036222":null,"GO:0036384":null,"GO:0043262":null,"GO:0044715":null,"GO:0045134":null,"GO:0047429":null,"GO:0047631":null,"GO:0047710":null,"GO:0047874":null,"GO:0052840":null,"GO:0052843":null,"GO:0052845":null,"GO:0052846":null,"GO:0052847":null,"GO:0061791":null,"GO:0106379":null,"GO:0110152":null,"GO:0110153":null,"GO:0120108":null,"GO:0140818":null,"GO:0140932":null,"GO:1990606":null}}


id: PBO:0065430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, ATPase 1 pseudogene 3","termid":"PBO:0065430"}


id: PBO:0090116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin binding WD repeat protein Aip1","termid":"PBO:0090116"}


id: GO:0048896
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The movement of a glial cell along the axons in a lateral line nerve.","definition_xrefs":["PMID:12062041"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell migration","termid":"GO:0008347"},{"relation_name":"part_of","term_name":"lateral line nerve development","termid":"GO:0048892"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lateral line nerve glial cell migration","synonyms":[{"name":"glial cell migration in lateral line nerve","type":"exact"}],"termid":"GO:0048896"}


id: PBO:0073749
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC2A4 regulator","termid":"PBO:0073749"}


id: GO:0043003
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of transport of Cystic Fibrosis Transmembrane conductance Regulator (CFTR) protein from the Golgi to the plasma membrane.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of Golgi to plasma membrane CFTR protein transport (obsolete GO:0043003)","synonyms":[{"name":"activation of Golgi to plasma membrane CFTR protein transport","type":"narrow"},{"name":"stimulation of Golgi to plasma membrane CFTR protein transport","type":"narrow"},{"name":"up regulation of Golgi to plasma membrane CFTR protein transport","type":"exact"},{"name":"up-regulation of Golgi to plasma membrane CFTR protein transport","type":"exact"},{"name":"upregulation of Golgi to plasma membrane CFTR protein transport","type":"exact"}],"termid":"GO:0043003"}


id: MONDO:0027652
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"chemotherapy-induced toxicity","termid":"MONDO:0800390"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-fluorouracil toxicity","secondary_identifiers":["Orphanet:240839"],"termid":"MONDO:0027652","xrefs":{"Monarch":{"xref_id":"0027652"}}}


id: GO:0032098
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process which modulates appetite, the desire or physical craving for food.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological quality","termid":"GO:0065008"},{"relation_name":"part_of","term_name":"response to nutrient levels","termid":"GO:0031667"}],"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 appetite","synonyms":[{"name":"regulation of hunger","type":"related"}],"termid":"GO:0032098"}


id: MONDO:0019694
data:
  {"annotated_genes":["SJAG_04528","SJAG_00339","SJAG_01216","SJAG_00373","SJAG_02463","SJAG_01941"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85421],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008701"},{"annotations":[84689,84688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010966"},{"annotations":[85786],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013223"},{"annotations":[86393],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010013"},{"annotations":[84640],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009593"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00339":null,"SJAG_00373":null,"SJAG_01216":null,"SJAG_01941":null,"SJAG_02463":null,"SJAG_04528":null},"genotype_count":0,"is_obsolete":false,"name":"spondylodysplastic dysplasia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1843363","Orphanet:93434","UMLS:C4736216","icd11.foundation:329165933","GARD:19193"],"termid":"MONDO:0019694","terms_by_termid":{"MONDO:0008701":null,"MONDO:0009593":null,"MONDO:0010013":null,"MONDO:0010966":null,"MONDO:0013223":null},"xrefs":{"Monarch":{"xref_id":"0019694"}}}


id: MONDO:0007744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial hyperlipidemia","termid":"MONDO:0001336"},{"relation_name":"is_a","term_name":"hyperalphalipoproteinemia","termid":"MONDO:0015903"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002525"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"cholesterol-ester transfer protein deficiency","secondary_identifiers":["UMLS:C3875011","DOID:0111369","OMIM:143470","SCTID:15771000119109","GARD:16724","MEDGEN:840020","Orphanet:79506"],"synonyms":[{"name":"CEPT deficiency","type":"exact"},{"name":"CETP deficiency","type":"related"},{"name":"HALP1","type":"related"},{"name":"Hdlcq10","type":"related"},{"name":"cholesterol ester transfer Protein deficiency","type":"related"},{"name":"familial hyperalphalipoproteinemia","type":"exact"},{"name":"high density lipoprotein cholesterol level QTL 10","type":"exact"},{"name":"high density lipoprotein cholesterol level quantitative trait locus 10","type":"related"},{"name":"hyperalphalipoproteinemia","type":"broad"},{"name":"hyperalphalipoproteinemia 1","type":"exact"},{"name":"hyperalphalipoproteinemia type 1","type":"exact"}],"termid":"MONDO:0007744","xrefs":{"Monarch":{"xref_id":"0007744"}}}


id: MONDO:0003594
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm characterized by the presence of a combination of liposarcomatous morphologic subtypes: myxoid/round cell and well differentiated/dedifferentiated liposarcoma or myxoid/round cell and pleomorphic liposarcoma.","definition_xrefs":["NCIT:C4253"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liposarcoma","termid":"MONDO:0005060"}],"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":"mixed liposarcoma","secondary_identifiers":["MEDGEN:87249","DOID:5703","UMLS:C0334472","ICDO:8855/3"],"synonyms":[{"name":"mixed liposarcoma","type":"exact"},{"name":"mixed liposarcoma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003594","xrefs":{"Monarch":{"xref_id":"0003594"}}}


id: MONDO:1012457
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"hemangiosarcoma, non-human animal","termid":"MONDO:1011823"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemangiosarcoma, cockatiel","secondary_identifiers":["OMIA:001813-13180"],"termid":"MONDO:1012457","xrefs":{"Monarch":{"xref_id":"1012457"}}}


id: GO:0005889
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that possesses hydrogen:potassium-exchanging ATPase activity; characterized in animal cells, where it maintains ionic gradients of K+ at the expense of ATP hydrolysis; The complex contains two obligatory subunits, the catalytic alpha subunit and a glycosylated beta subunit; two additional subunits, gamma and channel-inducing factor (CHIF), may also be present.","definition_xrefs":["PMID:11756431"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cation-transporting ATPase complex","termid":"GO:0090533"},{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"}],"interesting_parent_ids":["GO:0005575","GO:0005886","GO:0032991"],"is_obsolete":false,"name":"potassium:proton exchanging ATPase complex","synonyms":[{"name":"hydrogen/potassium-exchanging ATPase complex","type":"exact"},{"name":"hydrogen:potassium-exchanging ATPase complex","type":"exact"},{"name":"proton pump","type":"broad"}],"termid":"GO:0005889"}


id: GO:0102312
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 4-coumaryl-CoA + 2-oxoglutarate + O2 = 2,4-dihydroxycinnamoyl-CoA + succinate + carbon dioxide.","definition_xrefs":["PMID:22168819","PMID:22169019","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"2-oxoglutarate-dependent dioxygenase activity","termid":"GO:0016706"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"4-coumaroyl 2'-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-12963","EC:1.14.11.62","RHEA:57868"],"termid":"GO:0102312"}


id: PATO:0001923
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A positional quality inhering in a bearer by virtue of the bearer's being positioned towards the side of an organism.","definition_xrefs":["PATOC:mb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mislocalised","termid":"PATO:0000628"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mislocalised laterally","termid":"PATO:0001923"}


id: GO:2001176
data:
  {"annotated_genes":["SJAG_00973","SJAG_03421"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87690,105184],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001178"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mediator complex assembly.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein-containing complex assembly","termid":"GO:0043254"},{"relation_name":"regulates","term_name":"mediator complex assembly","termid":"GO:0036034"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00973":null,"SJAG_03421":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0065003"}],"interesting_parent_ids":["GO:0065003","GO:0044085","GO:0008150"],"is_obsolete":false,"name":"regulation of mediator complex assembly","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:2001176","terms_by_termid":{"GO:2001178":null}}


id: SO:0000338
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A highly repetitive and short (100-500 base pair) transposable element with terminal inverted repeats (TIR) and target site duplication (TSD). MITEs do not encode proteins.","direct_ancestors":[{"relation_name":"is_a","term_name":"terminal_inverted_repeat_element","termid":"SO:0000208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MITE","synonyms":[{"name":"miniature inverted repeat transposable element","type":"exact"}],"termid":"SO:0000338"}


id: MONDO:0013875
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any 3-methylglutaconic aciduria in which the cause of the disease is a mutation in the SERAC1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn mitochondrial metabolism disorder","termid":"MONDO:0004069"},{"relation_name":"is_a","term_name":"3-methylglutaconic aciduria","termid":"MONDO:0017359"},{"relation_name":"is_a","term_name":"disorder of phospholipids, sphingolipids and fatty acids biosynthesis","termid":"MONDO:0018117"},{"relation_name":"is_a","term_name":"SERAC1-related neurological disorder","termid":"MONDO:0100548"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0002525"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0004069","MONDO:0004736","MONDO:0005066","MONDO:0002525"],"is_obsolete":false,"name":"3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome","secondary_identifiers":["GARD:12963","DOID:0110001","MEDGEN:873604","SCTID:711409002","UMLS:C4040739","Orphanet:352328","OMIM:614739"],"synonyms":[{"name":"3-MGCA type IV (formerly)","type":"related"},{"name":"3-MGCA-4 (formerly)","type":"related"},{"name":"3-Methylglutaconic aciduria with dystonia-deafness, hepatopathy, encephalopathy, and Leigh-like syndrome","type":"related"},{"name":"3-Methylglutaconic aciduria, type 6","type":"related"},{"name":"3-methylglutaconic aciduria caused by mutation in SERAC1","type":"exact"},{"name":"3-methylglutaconic aciduria type 6","type":"exact"},{"name":"3-methylglutaconic aciduria type VI","type":"related"},{"name":"3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome","type":"exact"},{"name":"3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome","type":"exact"},{"name":"MEGDEL","type":"exact"},{"name":"MEGDEL syndrome","type":"exact"},{"name":"MGCA6","type":"exact"},{"name":"SERAC1 3-methylglutaconic aciduria","type":"exact"},{"name":"SERAC1 defect","type":"related"}],"termid":"MONDO:0013875","xrefs":{"Monarch":{"xref_id":"0013875"}}}


id: GO:0003418
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a chondroblast acquires specialized structural and/or functional features of a chondrocyte that will contribute to the growth of a bone. A chondrocyte is a polymorphic cell that forms cartilage.","definition_xrefs":["GOC:ascb_2009","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chondrocyte differentiation involved in endochondral bone morphogenesis","termid":"GO:0003413"},{"relation_name":"part_of","term_name":"growth plate cartilage development","termid":"GO:0003417"}],"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":"growth plate cartilage chondrocyte differentiation","termid":"GO:0003418"}


id: GO:0070083
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding a clathrin-sculpted monoamine transport vesicle.","definition_xrefs":["GOC:mg2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transport vesicle membrane","termid":"GO:0030658"},{"relation_name":"is_a","term_name":"clathrin-coated vesicle membrane","termid":"GO:0030665"},{"relation_name":"part_of","term_name":"clathrin-sculpted monoamine transport vesicle","termid":"GO:0070081"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0031410","GO:0005575","GO:0005737"],"is_obsolete":false,"name":"clathrin-sculpted monoamine transport vesicle membrane","synonyms":[{"name":"clathrin sculpted monoamine constitutive secretory pathway transport vesicle membrane","type":"exact"},{"name":"clathrin sculpted monoamine transport vesicle membrane","type":"exact"}],"termid":"GO:0070083"}


id: GO:0044094
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Any constituent part of a host cell's nucleus, a membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. The host is the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"host intracellular part","termid":"GO:0033646"},{"relation_name":"part_of","term_name":"host cell nucleus","termid":"GO:0042025"}],"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":"host cell nuclear part","termid":"GO:0044094"}


id: MONDO:0006538
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dermatitis herpetiformis (obsolete MONDO:0006538)","termid":"MONDO:0006538","xrefs":{"Monarch":{"xref_id":"0006538"}}}


id: MOD:01169
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts a source amino acid residue to L-oxoalanine.","definition_xrefs":["PubMed:8681943","RESID:AA0185","PubMed:9478923","DeltaMass:349","PubMed:14563551","PubMed:7628016"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified residue that can arise from different natural residues","termid":"MOD:00859"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-3-oxoalanine","synonyms":[{"name":"(S)-2-amino-3-oxopropanoic acid","type":"exact"},{"name":"2-amino-3-oxopropionic acid","type":"exact"},{"name":"C(alpha)-formylglycine","type":"related"},{"name":"L-3-oxoalanine","type":"exact"},{"name":"L-amino-malonic acid semialdehyde","type":"exact"},{"name":"L-aminomalonaldehydic acid","type":"exact"},{"name":"L-serinesemialdehyde","type":"related"},{"name":"MOD_RES 3-oxoalanine (Cys)","type":"exact"},{"name":"MOD_RES 3-oxoalanine (Ser)","type":"exact"}],"termid":"MOD:01169"}


id: GO:0018159
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The oxidation of peptidyl-L-methionine to peptidyl-L-methionine sulfone.","definition_xrefs":["RESID:AA0251"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-methionine oxidation (obsolete GO:0018159)","termid":"GO:0018159"}


id: GO:0009512
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Complex that transfers electrons from reduced plastoquinone to oxidized plastocyanin and translocates protons from the stroma to the lumen. The complex contains a core structure of three catalytic subunits: cytochrome b, the Rieske iron sulfur protein (ISP), and cytochrome f, which are arranged in an integral membrane-bound dimeric complex; additional subunits are present, and vary among different species.","definition_xrefs":["PMID:16228398","PMID:16352458","ISBN:0943088399"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytochrome complex","termid":"GO:0070069"},{"relation_name":"part_of","term_name":"thylakoid","termid":"GO:0009579"}],"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":"cytochrome b6f complex","secondary_identifiers":["Wikipedia:Cytochrome_b6f_complex"],"synonyms":[{"name":"cyt b(6)f complex","type":"exact"},{"name":"cyt b6-f complex","type":"exact"},{"name":"cyt b6/f complex","type":"exact"},{"name":"cyt b6f complex","type":"exact"},{"name":"cytochrome b(6)f complex","type":"exact"},{"name":"cytochrome b6-f complex","type":"exact"},{"name":"cytochrome b6/f complex","type":"exact"}],"termid":"GO:0009512"}


id: PBO:0000434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DYRK family protein kinase Pom1","termid":"PBO:0000434"}


id: FYPO:0000852
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 cells show decreased sensitivity to a salt stress.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"resistance to osmotic stress","termid":"FYPO:0000851"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000139","FYPO:0001985","FYPO:0000003"],"is_obsolete":false,"name":"resistance to salt stress","synonyms":[{"name":"increased growth during cellular response to salt stress","type":"exact"},{"name":"increased vegetative cell population growth during cellular response to salt stress","type":"exact"},{"name":"ionic stress resistance: increased","type":"related"},{"name":"resistance to salt stress during mitotic cell cycle","type":"related"},{"name":"resistant to salt stress","type":"exact"},{"name":"resistant to salt stress during vegetative growth","type":"exact"}],"termid":"FYPO:0000852"}


id: MONDO:0006485
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A usually aggressive malignant neoplasm arising from the uterine corpus and less often the cervix. It is characterized by the presence of two components: a malignant epithelial component and a sarcomatous component. In the uterine corpus the epithelial component is usually glandular whereas in the cervix is usually non-glandular. Carcinosarcoma of the cervix, although it is aggressive, it may have a better prognosis compared to the uterine corpus carcinosarcoma.","definition_xrefs":["NCIT:C42700"],"direct_ancestors":[{"relation_name":"is_a","term_name":"uterine cancer","termid":"MONDO:0002715"},{"relation_name":"is_a","term_name":"carcinosarcoma","termid":"MONDO:0002928"}],"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":"uterine carcinosarcoma","secondary_identifiers":["DOID:6171","UMLS:C0280630","MESH:D012192","EFO:1000613","MEDGEN:83678","ONCOTREE:UCS","SCTID:702369008"],"synonyms":[{"name":"carcinosarcoma of the uterus","type":"exact"},{"name":"malignant mixed mesodermal (Mullerian) tumor of the uterus","type":"exact"},{"name":"malignant mixed mesodermal (Mullerian) tumour of the uterus","type":"exact"},{"name":"malignant mixed mesodermal (Müllerian) tumor of the uterus","type":"exact"},{"name":"malignant mixed mesodermal (Müllerian) tumour of the uterus","type":"exact"},{"name":"mixed mullerian sarcoma of uterus","type":"exact"},{"name":"uterine carcinosarcoma","type":"exact"},{"name":"uterine carcinosarcoma/uterine malignant mixed mullerian tumor","type":"related"},{"name":"uterine carcinosarcoma/uterine malignant mixed mullerian tumour","type":"related"},{"name":"uterine malignant mixed mesodermal (Mullerian) tumor","type":"exact"},{"name":"uterine malignant mixed mesodermal (Mullerian) tumour","type":"exact"},{"name":"uterine malignant mixed mesodermal (Müllerian) tumor","type":"exact"},{"name":"uterine malignant mixed mesodermal (Müllerian) tumour","type":"exact"},{"name":"uterus carcinosarcoma","type":"exact"}],"termid":"MONDO:0006485","xrefs":{"Monarch":{"xref_id":"0006485"}}}


id: MONDO:0004175
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"endometrium adenocarcinoma","termid":"MONDO:0005461"},{"relation_name":"is_a","term_name":"endometrial endometrioid adenocarcinoma","termid":"MONDO:0006192"}],"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":"mucin-rich endometrial endometrioid adenocarcinoma","secondary_identifiers":["NCIT:C8717","DOID:7293","MEDGEN:269340","UMLS:C1513711"],"termid":"MONDO:0004175","xrefs":{"Monarch":{"xref_id":"0004175"}}}


id: GO:0097093
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of polyacyltrehalose, a pentaacylated, trehalose-based glycolipid.","definition_xrefs":["GOC:rs","PMID:19729090"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycolipid biosynthetic process","termid":"GO:0009247"},{"relation_name":"is_a","term_name":"polyacyltrehalose metabolic process","termid":"GO:0097092"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"polyacyltrehalose biosynthetic process","synonyms":[{"name":"polyacyltrehalose anabolism","type":"exact"},{"name":"polyacyltrehalose biosynthesis","type":"exact"},{"name":"polyacyltrehalose formation","type":"exact"},{"name":"polyacyltrehalose synthesis","type":"exact"}],"termid":"GO:0097093"}


id: GO:0060740
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of epithelia of the prostate gland are generated and organized. An epithelium consists of closely packed cells arranged in one or more layers, that covers the outer surfaces of the body or lines any internal cavity or tube.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"morphogenesis of an epithelium","termid":"GO:0002009"},{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"part_of","term_name":"prostate gland morphogenesis","termid":"GO:0060512"}],"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":"prostate gland epithelium morphogenesis","termid":"GO:0060740"}


id: MONDO:0019567
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Ehlers-Danlos syndrome in which the cause of the disease is a mutation in the COL5A1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome, classic type","termid":"MONDO:0007522"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Ehlers-Danlos syndrome, classic type, 1","secondary_identifiers":["Orphanet:90309","OMIM:130000","SCTID:83470009","DOID:14720","MEDGEN:78660","UMLS:C0268335","MESH:C536194","NCIT:C125696"],"synonyms":[{"name":"EDS I","type":"exact"},{"name":"EDSCL1","type":"exact"},{"name":"Ehlers-Danlos syndrome, classic type, 1","type":"exact"},{"name":"Ehlers-Danlos syndrome, type 1","type":"exact"},{"name":"Ehlers-Danlos syndrome, type I","type":"exact"},{"name":"type I Ehlers-Danlos syndrome","type":"exact"}],"termid":"MONDO:0019567","xrefs":{"Monarch":{"xref_id":"0019567"}}}


id: FYECO:0000142
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"An experimental condition in which adenine was added to the medium or assay buffer in excess compared to standard medium or assay buffers.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping excess","termid":"FYECO:0000109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"+ ade","synonyms":[{"name":"+ adenine","type":"related"}],"termid":"FYECO:0000142"}


id: GO:0060764
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that mediates the transfer of information from one cell to another and contributes to the progression of the mammary gland, from its initial state to the mature structure.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-cell signaling","termid":"GO:0007267"},{"relation_name":"part_of","term_name":"mammary gland development","termid":"GO:0030879"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"cell-cell signaling involved in mammary gland development","synonyms":[{"name":"cell-cell signalling involved in mammary gland development","type":"exact"}],"termid":"GO:0060764"}


id: MONDO:0004808
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"breast benign neoplasm","termid":"MONDO:0000620"},{"relation_name":"is_a","term_name":"integumentary system disorder","termid":"MONDO:0002051"},{"relation_name":"is_a","term_name":"breast disorder","termid":"MONDO:0002657"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign mammary dysplasia","secondary_identifiers":["MEDGEN:726820","SCTID:57993004","UMLS:C1305934","ICD9:610.8","DOID:9504","ICD9:610.9"],"synonyms":[{"name":"benign dysplasia of breast","type":"related"},{"name":"benign mammary dysplasia","type":"exact"}],"termid":"MONDO:0004808","xrefs":{"Monarch":{"xref_id":"0004808"}}}


id: MONDO:1011614
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Von Willebrand disease that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Von Willebrand disease, non-human animal","termid":"MONDO:1011411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Von Willebrand disease, horse","secondary_identifiers":["OMIA:001056-9796"],"termid":"MONDO:1011614","xrefs":{"Monarch":{"xref_id":"1011614"}}}


id: PBO:0080271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 34 pseudogene","termid":"PBO:0080271"}


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


id: PR:O74818
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A carboxypeptidase B that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02688"],"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 carboxypeptidase C337.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC337.07c","secondary_identifiers":["UniProtKB:O74818"],"synonyms":[{"name":"Spom972h-CPB1","type":"exact"}],"termid":"PR:O74818"}


id: PBO:0027407
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_nonsense-mediated_decay","termid":"PBO:0027407"}


id: GO:0030836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of actin depolymerization.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of actin filament depolymerization","termid":"GO:0030834"},{"relation_name":"is_a","term_name":"positive regulation of cytoskeleton organization","termid":"GO:0051495"},{"relation_name":"is_a","term_name":"positive regulation of protein depolymerization","termid":"GO:1901881"},{"relation_name":"is_a","term_name":"positive regulation of supramolecular fiber organization","termid":"GO:1902905"},{"relation_name":"positively_regulates","term_name":"actin filament depolymerization","termid":"GO:0030042"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0030036"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0030036"],"is_obsolete":false,"name":"positive regulation of actin filament depolymerization","secondary_identifiers":["GO:0030045"],"synonyms":[{"name":"actin filament destabilization","type":"exact"},{"name":"activation of actin filament depolymerization","type":"narrow"},{"name":"positive regulation of actin depolymerization","type":"exact"},{"name":"positive regulation of actin polymerization and/or depolymerization","type":"broad"},{"name":"stimulation of actin filament depolymerization","type":"narrow"},{"name":"up regulation of actin filament depolymerization","type":"exact"},{"name":"up-regulation of actin filament depolymerization","type":"exact"},{"name":"upregulation of actin filament depolymerization","type":"exact"}],"termid":"GO:0030836"}


id: GO:0030770
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine(1+) + demethylmacrocin = S-adenosyl-L-homocysteine + H+ + macrocin.","definition_xrefs":["EC:2.1.1.102","RHEA:17573"],"direct_ancestors":[{"relation_name":"is_a","term_name":"S-adenosylmethionine-dependent methyltransferase activity","termid":"GO:0008757"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016741","GO:0003824"],"is_obsolete":false,"name":"demethylmacrocin O-methyltransferase activity","secondary_identifiers":["KEGG_REACTION:R02859","MetaCyc:DEMETHYLMACROCIN-O-METHYLTRANSFERASE-RXN"],"synonyms":[{"name":"S-adenosyl-L-methionine:demethylmacrocin 2'''-O-methyltransferase activity","type":"related"},{"name":"demethylmacrocin methyltransferase activity","type":"related"}],"termid":"GO:0030770"}


id: GO:1900152
data:
  {"annotated_genes":["SJAG_02370"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060212"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay.","definition_xrefs":["GOC:TermGenie","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","termid":"GO:1900151"},{"relation_name":"is_a","term_name":"negative regulation of mRNA catabolic process","termid":"GO:1902373"},{"relation_name":"negatively_regulates","term_name":"nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","termid":"GO:0000288"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02370":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016071"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0016071"}],"interesting_parent_ids":["GO:0016071","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"down regulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"down regulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"down regulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"down regulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"down regulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"down regulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"down regulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"down regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"down-regulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"down-regulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"down-regulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"down-regulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"down-regulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"down-regulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"downregulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"downregulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"downregulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"downregulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"downregulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"downregulation of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"exact"},{"name":"inhibition of deadenylation-dependent mRNA decay","type":"narrow"},{"name":"inhibition of mRNA breakdown, deadenylation-dependent decay","type":"narrow"},{"name":"inhibition of mRNA catabolic process, deadenylation-dependent","type":"narrow"},{"name":"inhibition of mRNA catabolic process, deadenylylation-dependent","type":"narrow"},{"name":"inhibition of mRNA catabolism, deadenylation-dependent","type":"narrow"},{"name":"inhibition of mRNA catabolism, deadenylylation-dependent","type":"narrow"},{"name":"inhibition of mRNA degradation, deadenylation-dependent decay","type":"narrow"},{"name":"inhibition of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"narrow"},{"name":"inhibition of nuclear-transcribed mRNA catabolic process, deadenylation-dependent decay","type":"narrow"},{"name":"negative regulation of deadenylation-dependent mRNA decay","type":"exact"},{"name":"negative regulation of mRNA breakdown, deadenylation-dependent decay","type":"exact"},{"name":"negative regulation of mRNA catabolic process, deadenylation-dependent","type":"exact"},{"name":"negative regulation of mRNA catabolic process, deadenylylation-dependent","type":"exact"},{"name":"negative regulation of mRNA catabolism, deadenylation-dependent","type":"exact"},{"name":"negative regulation of mRNA catabolism, deadenylylation-dependent","type":"exact"},{"name":"negative regulation of mRNA degradation, deadenylation-dependent decay","type":"exact"},{"name":"negative regulation of nuclear mRNA catabolic process, deadenylation-dependent decay","type":"exact"}],"termid":"GO:1900152","terms_by_termid":{"GO:0060212":null}}


id: GO:0003268
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The series of molecular signals generated as a consequence of a fibroblast growth factor receptor binding to one of its physiological ligands contributing to the modulation of the frequency, rate or extent of cardioblast proliferation in the secondary heart field. A cardioblast is a cardiac precursor cell. It is a cell that has been committed to a cardiac fate, but will undergo more cell division rather than terminally differentiating.","definition_xrefs":["GOC:mtg_heart"],"gene_count":0,"genotype_count":0,"name":"obsolete fibroblast growth factor receptor signaling pathway involved in regulation of secondary heart field cardioblast proliferation (obsolete GO:0003268)","synonyms":[{"name":"fibroblast growth factor receptor signaling pathway involved in regulation of second heart field cardioblast cell proliferation","type":"exact"},{"name":"fibroblast growth factor receptor signaling pathway involved in regulation of secondary heart field cardioblast cell proliferation","type":"exact"},{"name":"fibroblast growth factor receptor signalling pathway involved in regulation of secondary heart field cardioblast cell proliferation","type":"exact"}],"termid":"GO:0003268"}


id: GO:0030107
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a MHC class I molecule of the HLA-A subclass to mediate signaling that inhibits activation of a lymphocyte.","definition_xrefs":["PMID:9368779","GOC:mah","PMID:11929129","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inhibitory MHC class I receptor activity","termid":"GO:0032396"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"HLA-A specific inhibitory MHC class I receptor activity","termid":"GO:0030107"}


id: MONDO:1012154
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Megaesophagus that occurs in domestic ferret.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"megaesophagus, non-human animal","termid":"MONDO:1011660"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"megaesophagus, domestic ferret","secondary_identifiers":["OMIA:000631-9669"],"termid":"MONDO:1012154","xrefs":{"Monarch":{"xref_id":"1012154"}}}


id: GO:0097444
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A specialization of the endomembrane system found in some classes of dendritic spines consisting of two or more closely apposed lamellae with interspersed electron dense material. The endomembrane component is continuous with the smooth endoplasmic reticulum.","definition_xrefs":["PMID:20400711","NIF_Subcellular:sao725931194","PMID:8987748"],"direct_ancestors":[{"relation_name":"is_a","term_name":"membrane-bounded organelle","termid":"GO:0043227"},{"relation_name":"part_of","term_name":"endomembrane system","termid":"GO:0012505"},{"relation_name":"part_of","term_name":"dendritic spine","termid":"GO:0043197"}],"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":"spine apparatus","synonyms":[{"name":"dense material","type":"narrow"}],"termid":"GO:0097444"}


id: GO:0033618
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form respiratory chain complex IV (also known as cytochrome c oxidase) in the plasma membrane.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory chain complex IV assembly","termid":"GO:0008535"},{"relation_name":"part_of","term_name":"plasma membrane organization","termid":"GO:0007009"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0065003","GO:0044085","GO:0061024"],"is_obsolete":false,"name":"plasma membrane respiratory chain complex IV assembly","synonyms":[{"name":"plasma membrane cytochrome c oxidase biogenesis","type":"broad"},{"name":"plasma membrane cytochrome c oxidase complex assembly","type":"exact"}],"termid":"GO:0033618"}


id: PBO:0078023
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 13","termid":"PBO:0078023"}


id: MONDO:0013077
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":"Santos syndrome","secondary_identifiers":["OMIM:613005","MEDGEN:414444","MESH:C567819","UMLS:C2751698"],"synonyms":[{"name":"Santos syndrome","type":"exact"},{"name":"fibular agenesis/hypoplasia, oligodactylous clubfeet, and anonychia/nail hypoplasia syndrome","type":"related"}],"termid":"MONDO:0013077","xrefs":{"Monarch":{"xref_id":"0013077"}}}


id: MONDO:0010643
data:
  {"annotated_genes":["SJAG_05979","SJAG_01349","SJAG_01748","SJAG_03453","SJAG_01013","SJAG_03905"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86847,86692,86848,86695,86694,86693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0018874"}]},"cv_name":"mondo","definition":"A clonal (malignant) hematopoietic disorder with an acute onset, affecting the bone marrow and the peripheral blood. The malignant cells show minimal differentiation and are called blasts, either myeloid blasts (myeloblasts) or lymphoid blasts (lymphoblasts).","definition_xrefs":["NCIT:C9300"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukemia","termid":"MONDO:0005059"},{"relation_name":"is_a","term_name":"acute disease","termid":"MONDO:0020683"}],"gene_count":6,"genes_by_uniquename":{"SJAG_01013":null,"SJAG_01349":null,"SJAG_01748":null,"SJAG_03453":null,"SJAG_03905":null,"SJAG_05979":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"acute leukemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:12603","ICDO:9801/3","SCTID:91855006","MEDGEN:43225","ICD9:208.00","UMLS:C0085669","NCIT:C9298","ICD9:208.0","MESH:C564112","EFO:1000068","HP:0002488"],"synonyms":[{"name":"acute leukaemia (disease)","type":"exact"},{"name":"acute leukemia","type":"exact"},{"name":"acute leukemia (disease)","type":"exact"},{"name":"leukemia, acute, X-linked","type":"related"},{"name":"stem cell leukaemia","type":"related"},{"name":"stem cell leukaemia (disease)","type":"related"},{"name":"stem cell leukemia","type":"related"},{"name":"stem cell leukemia (disease)","type":"related"}],"termid":"MONDO:0010643","terms_by_termid":{"MONDO:0018874":null},"xrefs":{"Monarch":{"xref_id":"0010643"}}}


id: PBO:0073304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SERPINE1 mRNA binding protein 1","termid":"PBO:0073304"}


id: MONDO:0014927
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Joubert syndrome in which the cause of the disease is a mutation in the B9D1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Joubert syndrome 27","secondary_identifiers":["GARD:16194","MEDGEN:934673","DOID:0110996","UMLS:C4310706","OMIM:617120"],"synonyms":[{"name":"B9D1 Joubert syndrome","type":"exact"},{"name":"JBTS27","type":"exact"},{"name":"Joubert syndrome 27","type":"exact"},{"name":"Joubert syndrome caused by mutation in B9D1","type":"exact"},{"name":"Joubert syndrome type 27","type":"exact"}],"termid":"MONDO:0014927","xrefs":{"Monarch":{"xref_id":"0014927"}}}


id: GO:1904178
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of adipose tissue development.","definition_xrefs":["GO_REF:0000058","PMID:23081848","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of developmental process","termid":"GO:0051093"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"is_a","term_name":"regulation of adipose tissue development","termid":"GO:1904177"},{"relation_name":"negatively_regulates","term_name":"adipose tissue development","termid":"GO:0060612"}],"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 adipose tissue development","synonyms":[{"name":"down regulation of adipogenesis","type":"related"},{"name":"down regulation of adipose tissue development","type":"exact"},{"name":"down-regulation of adipogenesis","type":"related"},{"name":"down-regulation of adipose tissue development","type":"exact"},{"name":"downregulation of adipogenesis","type":"related"},{"name":"downregulation of adipose tissue development","type":"exact"},{"name":"inhibition of adipogenesis","type":"related"},{"name":"inhibition of adipose tissue development","type":"narrow"},{"name":"negative regulation of adipogenesis","type":"related"}],"termid":"GO:1904178"}


id: PR:P40375
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An NAD-dependent malic enzyme that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04249","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":"NAD-dependent malic enzyme (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC794.12c","secondary_identifiers":["UniProtKB:P40375"],"synonyms":[{"name":"NAD-ME (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-maeA","type":"exact"}],"termid":"PR:P40375"}


id: PBO:0004477
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nem1-Spo7 phosphatase complex catalytic subunit Nem1 (predicted)","termid":"PBO:0004477"}


id: GO:0051059
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to NF-kappaB, a transcription factor for eukaryotic RNA polymerase II promoters.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II-specific DNA-binding transcription factor binding","termid":"GO:0061629"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"NF-kappaB binding","termid":"GO:0051059"}


id: PBO:0108921
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMX1 pseudogene 1","termid":"PBO:0108921"}


id: FYPO:0004077
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A sporulation phenotype that results in the formation of an ascus that contains a single spore that is larger than normal.","definition_xrefs":["PMID:15331764","PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal sporulation resulting in formation of ascus with fewer than four spores","termid":"FYPO:0003066"},{"relation_name":"output_of","term_name":"abolished meiosis I","termid":"FYPO:0003378"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000121"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000121","FYPO:0001985","FYPO:0005447","FYPO:0000631"],"is_obsolete":false,"name":"abnormal sporulation resulting in formation of ascus with single large spore","synonyms":[{"name":"abnormal ascospore formation resulting in formation of ascus with single large spore","type":"exact"},{"name":"abnormal sporulation resulting in formation of single-spored asci","type":"exact"}],"termid":"FYPO:0004077"}


id: MONDO:0001409
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acute or chronic inflammatory disease affecting the esophageal wall.","definition_xrefs":["NCIT:C9224"],"direct_ancestors":[{"relation_name":"is_a","term_name":"esophageal disorder","termid":"MONDO:0003749"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"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":"esophagitis","secondary_identifiers":["MEDGEN:4549","ICD9:530.1","SCTID:16761005","ICD9:530.10","MESH:D004941","UMLS:C0014868","DOID:11963","HP:0100633","ICD9:530.12"],"synonyms":[{"name":"acute esophagitis","type":"narrow"},{"name":"esophagitis","type":"exact"},{"name":"esophagitis (disease)","type":"exact"},{"name":"esophagus inflammation","type":"exact"},{"name":"inflammation of esophagus","type":"exact"},{"name":"inflammation of oesophagus","type":"exact"},{"name":"oesophagus inflammation","type":"exact"}],"termid":"MONDO:0001409","xrefs":{"Monarch":{"xref_id":"0001409"}}}


id: PBO:0059283
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein L40 pseudogene 1","termid":"PBO:0059283"}


id: PBO:0055262
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 2689","termid":"PBO:0055262"}


id: PBO:0044085
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cancer/testis antigen family 45 member A5","termid":"PBO:0044085"}


id: PBO:0034817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab geranylgeranyltransferase alpha subunit Bet4 (predicted)","termid":"PBO:0034817"}


id: GO:0010021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of amylopectin, the (1->4) linked alpha glucose units with alpha-(1->6) linkages.","definition_xrefs":["ISBN:0943088399"],"direct_ancestors":[{"relation_name":"is_a","term_name":"macromolecule biosynthetic process","termid":"GO:0009059"},{"relation_name":"is_a","term_name":"carbohydrate derivative biosynthetic process","termid":"GO:1901137"},{"relation_name":"is_a","term_name":"amylopectin metabolic process","termid":"GO:2000896"}],"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":"amylopectin biosynthetic process","synonyms":[{"name":"amylopectin anabolism","type":"exact"},{"name":"amylopectin biosynthesis","type":"exact"},{"name":"amylopectin formation","type":"exact"},{"name":"amylopectin synthesis","type":"exact"}],"termid":"GO:0010021"}


id: PBO:0068334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 41","termid":"PBO:0068334"}


id: MONDO:0009353
data:
  {"annotated_genes":["SJAG_01466","SJAG_03712"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84758,84759],"is_not":false,"summary":null,"term":"MONDO:0009353"}]},"cv_name":"mondo","definition":"Homocystinuria due to methylene tetrahydrofolate reductase (MTHFR) deficiency is a metabolic disorder characterized by neurological manifestations.","definition_xrefs":["Orphanet:395"],"direct_ancestors":[{"relation_name":"is_a","term_name":"homocystinuria","termid":"MONDO:0004737"},{"relation_name":"is_a","term_name":"disorder of folate metabolism and transport","termid":"MONDO:0017313"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01466":null,"SJAG_03712":null},"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:0005244"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"homocystinuria due to methylene tetrahydrofolate reductase deficiency","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C1856061","MEDGEN:343470","SCTID:41797007","NANDO:1201041","GARD:2734","MESH:C537357","OMIM:236250"],"synonyms":[{"name":"5,10 alpha methylenetetrahydro-folate reductase deficiency","type":"related"},{"name":"5,10-alpha-methylenetetrahydro-folate reductase deficiency","type":"related"},{"name":"Homocysteinemia due to methylenetetrahydro-folate reductase deficiency","type":"related"},{"name":"Homocysteinuria due to methylenetetrahydro-folate reductase deficiency","type":"related"},{"name":"MTHFR deficiency","type":"exact"},{"name":"MTHFR deficiency, thermolabile type","type":"related"},{"name":"Methylenetetrahydro-folate reductase deficiency","type":"related"},{"name":"homocystinuria due to MTHFR deficiency","type":"related"},{"name":"homocystinuria due to deficiency of N(5,10)-methylenetetrahydrofolate reductase activity","type":"related"},{"name":"homocystinuria due to methylene tetrahydrofolate reductase deficiency","type":"exact"},{"name":"methylene tetrahydrofolate reductase deficiency","type":"exact"},{"name":"methylenetetrahydrofolate reductase deficiency","type":"related"}],"termid":"MONDO:0009353","terms_by_termid":{"MONDO:0009353":null},"xrefs":{"Monarch":{"xref_id":"0009353"}}}


id: GO:0042160
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the covalent alteration of one or more amino acid or lipid residues occurring in a lipoprotein, any conjugated, water-soluble protein in which the nonprotein group consists of a lipid or lipids.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoprotein metabolic process","termid":"GO:0042157"}],"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":"lipoprotein modification","termid":"GO:0042160"}


id: GO:0140932
data:
  {"annotated_genes":["SJAG_05010","SJAG_01625"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91037,112972],"is_not":false,"summary":null,"term":"GO:0140932"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: a 5'-end (N2,N2,N7-trimethyl 5'-triphosphoguanosine)-ribonucleoside in mRNA + H2O = a 5'-end diphospho-ribonucleoside in mRNA + 2 H+ + N7-methyl-GMP. Can also use (N7-methyl 5'-triphosphoguanosine)-ribonucleoside in mRNA as a substrate.","definition_xrefs":["PMID:24742626","PMID:32723815"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrophosphatase activity","termid":"GO:0016462"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01625":null,"SJAG_05010":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"5'-(N(7)-methyl 5'-triphosphoguanosine)-[mRNA] diphosphatase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:3.6.1.59"],"synonyms":[{"name":"m(7)GpppN m(7)GMP phosphohydrolase activity","type":"exact"},{"name":"m(7)GpppX diphosphatase activity","type":"exact"},{"name":"m(7)GpppX pyrophosphatase activity","type":"exact"}],"termid":"GO:0140932","terms_by_termid":{"GO:0140932":null}}


id: PBO:0005885
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome b, Cob1 (predicted)","termid":"PBO:0005885"}


id: GO:0072588
data:
  {"annotated_genes":["SJAG_00566","SJAG_04754","SJAG_01234","SJAG_00083"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[105777,89485,94834,100659],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031429"}]},"cv_name":"cellular_component","definition":"A ribonucleoprotein complex that contains an RNA of the box H/ACA type and the four core proteins dyskerin, NOP10, NHP2, and GAR1 (human protein nomenclature). RNA pseudouridylation (isomerization of uridine to pseudouridine) is the major, and most likely the ancestral, function of H/ACA RNPs. Pseudouridylation targets include both large and small ribosomal RNAs (rRNAs), and small nuclear RNA (U2 snRNA). In addition to these catalytic H/ACA RNPs, a less abundant but more diverse class of structural H/ACA RNPs exists, which does not have pseudouridylation activity. These include the vertebrate telomerase RNP complex.","definition_xrefs":["PMID:17284456","GOC:BHF_telomerase","GOC:BHF","GOC:krc","GOC:mah","PMID:20227365","GOC:jbu","GOC:vw","PMID:25590339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sno(s)RNA-containing ribonucleoprotein complex","termid":"GO:0005732"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00083":null,"SJAG_00566":null,"SJAG_01234":null,"SJAG_04754":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":"box H/ACA RNP complex","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"box H/ACA snoRNP pseudouridylase complex","type":"related"},{"name":"sRNP complex","type":"narrow"}],"termid":"GO:0072588","terms_by_termid":{"GO:0031429":null}}


id: GO:0022408
data:
  {"annotated_genes":["SJAG_03473","SJAG_01778","SJAG_00926","SJAG_00156"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[98077,98794],"is_not":false,"summary":null,"term":"GO:0022408"},{"annotations":[103055,105743],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060257"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate or extent of cell adhesion to another cell.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell adhesion","termid":"GO:0007162"},{"relation_name":"is_a","term_name":"regulation of cell-cell adhesion","termid":"GO:0022407"},{"relation_name":"negatively_regulates","term_name":"cell-cell adhesion","termid":"GO:0098609"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00156":null,"SJAG_00926":null,"SJAG_01778":null,"SJAG_03473":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007155","GO:0008150"],"is_obsolete":false,"name":"negative regulation of cell-cell adhesion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of cell-cell adhesion","type":"exact"},{"name":"down-regulation of cell-cell adhesion","type":"exact"},{"name":"downregulation of cell-cell adhesion","type":"exact"},{"name":"inhibition of cell-cell adhesion","type":"narrow"}],"termid":"GO:0022408","terms_by_termid":{"GO:0022408":null,"GO:0060257":null}}


id: PBO:0080311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 75 pseudogene","termid":"PBO:0080311"}


id: PBO:0081589
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF516 antisense RNA 1","termid":"PBO:0081589"}


id: PBO:0043191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytoskeleton associated protein 2","termid":"PBO:0043191"}


id: GO:0070041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine + rRNA = S-adenosyl-L-homocysteine + rRNA containing C5-methyluridine.","definition_xrefs":["GOC:mah","GOC:imk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C-methyltransferase activity","termid":"GO:0008169"},{"relation_name":"is_a","term_name":"rRNA (uridine) methyltransferase activity","termid":"GO:0016436"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0140098","GO:0003674","GO:0016741"],"is_obsolete":false,"name":"rRNA (uridine-C5-)-methyltransferase activity","termid":"GO:0070041"}


id: PBO:0074419
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 18","termid":"PBO:0074419"}


id: GO:0075102
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which the host organism stops, prevents, or reduces the frequency, rate or extent of the symbiont MAP kinase-mediated signal transduction. 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 negative regulation by host of symbiont MAP kinase-mediated signal transduction (obsolete GO:0075102)","termid":"GO:0075102"}


id: GO:0003217
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process pertaining to the initial formation of a cardiac right atrium from unspecified parts.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac atrium formation","termid":"GO:0003210"},{"relation_name":"part_of","term_name":"cardiac right atrium morphogenesis","termid":"GO:0003213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cardiac right atrium formation","termid":"GO:0003217"}


id: GO:0019039
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 viral-cell fusion molecule activity (obsolete GO:0019039)","synonyms":[{"name":"viral-cell fusion molecule activity","type":"exact"}],"termid":"GO:0019039"}


id: PBO:0059763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO3 pseudogene 37","termid":"PBO:0059763"}


id: MONDO:0003130
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A solid, unencapsulated tumor of the kidney composed of spindle mesenchymal cells that resemble fibroblasts or muscle cells. The homogeneous mass typically extends into the renal parenchyma and replaces most of the kidney. In most cases, mesoblastic nephroma is benign and occurs in the fetus or newborn, and rarely in the older child or the adult.","definition_xrefs":["MESH:D018201"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney cancer","termid":"MONDO:0002367"}],"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":"mesoblastic nephroma","secondary_identifiers":["SCTID:307604008","EFO:0007365","ICD9:236.99","UMLS:C0206628","MEDGEN:64620","DOID:4772"],"synonyms":[{"name":"mesoblastic nephroma","type":"exact"},{"name":"mesoblastic nephroma (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0003130","xrefs":{"Monarch":{"xref_id":"0003130"}}}


id: PBO:0045192
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJB6 pseudogene 5","termid":"PBO:0045192"}


id: PBO:0084464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAP kinase kinase of the HOG signaling pathway; activated under severe osmotic stress; mitophagy-specific regulator; plays a role in regulating Ty1 transposition","termid":"PBO:0084464"}


id: PBO:0031561
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_DNA_binding","termid":"PBO:0031561"}


id: GO:0140987
data:
  {"annotated_genes":["SJAG_00612"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[102357],"is_not":false,"summary":null,"term":"GO:0140987"}]},"cv_name":"molecular_function","definition":"Enables the transfer of ATP from one side of a membrane to the other according to the reaction: ATP(out) + phosphate(in) = ATP(in) + phosphate(out).","definition_xrefs":["PMID:15123600"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ATP transmembrane transporter activity","termid":"GO:0005347"},{"relation_name":"is_a","term_name":"organophosphate:phosphate antiporter activity","termid":"GO:0015315"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00612":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"ATP:phosphate antiporter activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["RHEA:65840"],"synonyms":[{"name":"ATP:inorganic phosphate antiporter activity","type":"exact"},{"name":"inorganic phosphate:ATP antiporter activity","type":"exact"}],"termid":"GO:0140987","terms_by_termid":{"GO:0140987":null}}


id: GO:0072306
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the occurrence or rate of mesenchymal stem cell death by apoptotic process that contributes to the shaping of the nephron in the metanephros.","definition_xrefs":["GOC:mtg_kidney_jan10","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of mesenchymal cell apoptotic process involved in nephron morphogenesis","termid":"GO:0072041"},{"relation_name":"is_a","term_name":"regulation of mesenchymal cell apoptotic process involved in metanephric nephron morphogenesis","termid":"GO:0072304"},{"relation_name":"is_a","term_name":"positive regulation of mesenchymal cell apoptotic process involved in metanephros development","termid":"GO:1900213"},{"relation_name":"positively_regulates","term_name":"mesenchymal stem cell maintenance involved in metanephric nephron morphogenesis","termid":"GO:0072309"},{"relation_name":"positively_regulates","term_name":"mesenchymal cell apoptotic process involved in metanephric nephron morphogenesis","termid":"GO:1901147"}],"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 mesenchymal cell apoptotic process involved in metanephric nephron morphogenesis","synonyms":[{"name":"positive regulation of mesenchymal stem cell apoptosis involved in metanephric nephron morphogenesis","type":"narrow"},{"name":"positive regulation of mesenchymal stem cell apoptotic process involved in metanephric nephron morphogenesis","type":"exact"}],"termid":"GO:0072306"}


id: FYPO:0001936
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of proton-transporting ATP synthase activity by a rotational mechanism is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased catalytic activity","termid":"FYPO:0000663"},{"relation_name":"is_a","term_name":"abnormal proton-transporting ATP synthase activity, rotational mechanism","termid":"FYPO:0001935"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0002114"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0002114","FYPO:0000661","FYPO:0000707","FYPO:0000654","FYPO:0000002","FYPO:0000652","FYPO:0001985","FYPO:0000138","FYPO:0005447"],"is_obsolete":false,"name":"decreased proton-transporting ATP synthase activity, rotational mechanism","synonyms":[{"name":"decreased hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"},{"name":"decreased mitochondrial proton-transporting ATP synthase activity","type":"narrow"},{"name":"decreased proton-transporting ATP synthase activity","type":"related"},{"name":"reduced mitochondrial proton-transporting ATP synthase activity","type":"narrow"},{"name":"reduced proton-transporting ATP synthase activity, rotational mechanism","type":"exact"}],"termid":"FYPO:0001936"}


id: PBO:0040563
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"beta-1,4-N-acetyl-galactosaminyltransferase 3","termid":"PBO:0040563"}


id: PBO:0004142
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing factor Prp17","termid":"PBO:0004142"}


id: GO:0071985
data:
  {"annotated_genes":["SJAG_05303","SJAG_04643","SJAG_02117","SJAG_01586","SJAG_07012","SJAG_04349","SJAG_01981","SJAG_00416","SJAG_01242","SJAG_03756","SJAG_04912","SJAG_02912","SJAG_04489","SJAG_03511","SJAG_02349","SJAG_03783","SJAG_02234","SJAG_02584","SJAG_01281","SJAG_00900","SJAG_04822","SJAG_05207","SJAG_04047","SJAG_01686","SJAG_03250","SJAG_04936","SJAG_04070","SJAG_04024","SJAG_00821","SJAG_03892"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[117023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032509"},{"annotations":[88087,109702,106617,114371,91122,98188,112060,102645,103231,98367,103625],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032511"},{"annotations":[109286,106052,91486,97452,104467,95452,114205,90037,110126,106861,87601,87432,115886,100390,108864,110958,91123,90988,91772],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043328"}]},"cv_name":"biological_process","definition":"A vesicle-mediated transport process in which transmembrane proteins are ubiquitylated to facilitate their entry into luminal vesicles of multivesicular bodies (MVBs); upon subsequent fusion of MVBs with lysosomes or vacuoles, the cargo proteins are degraded.","definition_xrefs":["PMID:17603537","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vesicle-mediated transport","termid":"GO:0016192"}],"gene_count":30,"genes_by_uniquename":{"SJAG_00416":null,"SJAG_00821":null,"SJAG_00900":null,"SJAG_01242":null,"SJAG_01281":null,"SJAG_01586":null,"SJAG_01686":null,"SJAG_01981":null,"SJAG_02117":null,"SJAG_02234":null,"SJAG_02349":null,"SJAG_02584":null,"SJAG_02912":null,"SJAG_03250":null,"SJAG_03511":null,"SJAG_03756":null,"SJAG_03783":null,"SJAG_03892":null,"SJAG_04024":null,"SJAG_04047":null,"SJAG_04070":null,"SJAG_04349":null,"SJAG_04489":null,"SJAG_04643":null,"SJAG_04822":null,"SJAG_04912":null,"SJAG_04936":null,"SJAG_05207":null,"SJAG_05303":null,"SJAG_07012":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192","GO:0051179"],"is_obsolete":false,"name":"multivesicular body sorting pathway","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0071985","terms_by_termid":{"GO:0032509":null,"GO:0032511":null,"GO:0043328":null}}


id: PBO:0079482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taxilin gamma pseudogene, Y-linked","termid":"PBO:0079482"}


id: FYPO:0002574
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 normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization during vegetative growth","termid":"FYPO:0000644"},{"relation_name":"is_a","term_name":"normal protein localization to centromere","termid":"FYPO:0007853"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001312","FYPO:0001320","FYPO:0000257"],"is_obsolete":false,"name":"normal protein localization to centromere during vegetative growth","synonyms":[{"name":"normal protein localisation to centromere during vegetative growth","type":"exact"},{"name":"normal protein localisation to chromosome, centromeric region during vegetative growth","type":"exact"},{"name":"normal protein localization to centromere during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromosome, centric region during vegetative growth","type":"exact"},{"name":"normal protein localization to chromosome, centromeric region during vegetative growth","type":"exact"}],"termid":"FYPO:0002574"}


id: GO:0072147
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a glomerular parietal epithelial cell. Glomerular parietal epithelial cells are specialized epithelial cells that form tight junctions as a barrier to protein transport. These cells may also give rise to podocytes.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epithelial cell fate commitment","termid":"GO:0072148"},{"relation_name":"is_a","term_name":"glomerular epithelial cell fate commitment","termid":"GO:0072314"},{"relation_name":"part_of","term_name":"glomerular parietal epithelial cell differentiation","termid":"GO:0072139"}],"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":"glomerular parietal epithelial cell fate commitment","synonyms":[{"name":"Bowman's capsule cell fate commitment","type":"exact"}],"termid":"GO:0072147"}


id: GO:0141052
data:
  {"annotated_genes":["SJAG_03041","SJAG_03664","SJAG_03997","SJAG_03286","SJAG_03635","SJAG_02401"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[111724,86870],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051864"},{"annotations":[117258],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140680"},{"annotations":[86871],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032453"},{"annotations":[112554,86872],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034647"},{"annotations":[111725,117259],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032454"},{"annotations":[102732,93569],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140683"}]},"cv_name":"molecular_function","definition":"Catalysis of the removal of a methyl group from a modified lysine residue of the histone H3 protein. This is a dioxygenase reaction that is dependent on Fe(II) and 2-oxoglutarate.","definition_xrefs":["PMID:17947579"],"direct_ancestors":[{"relation_name":"is_a","term_name":"histone demethylase activity","termid":"GO:0032452"}],"gene_count":6,"genes_by_uniquename":{"SJAG_02401":null,"SJAG_03041":null,"SJAG_03286":null,"SJAG_03635":null,"SJAG_03664":null,"SJAG_03997":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032452"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140096"}],"interesting_parent_ids":["GO:0032452","GO:0003674","GO:0003824","GO:0140096"],"is_obsolete":false,"name":"histone H3 demethylase activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0141052","terms_by_termid":{"GO:0032453":null,"GO:0032454":null,"GO:0034647":null,"GO:0051864":null,"GO:0140680":null,"GO:0140683":null}}


id: PBO:0085396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane permease; mediates uptake of glycerophosphoinositol and glycerophosphocholine as sources of the nutrients inositol and phosphate; expression and transport rate are regulated by phosphate and inositol availability","termid":"PBO:0085396"}


id: PBO:0072532
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 62","termid":"PBO:0072532"}


id: MONDO:8000001
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Discitis caused by infection with Staphylococcus.","definition_xrefs":["PMID:27070599"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial arthritis","termid":"MONDO:0004471"},{"relation_name":"is_a","term_name":"staphylococcus aureus infection","termid":"MONDO:0005545"},{"relation_name":"is_a","term_name":"infectious discitis","termid":"MONDO:8000000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"staphylococcus discitis","termid":"MONDO:8000001","xrefs":{"Monarch":{"xref_id":"8000001"}}}


id: PBO:0062644
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 11 subfamily N member 1 pseudogene","termid":"PBO:0062644"}


id: GO:0102081
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: homotaurine + 2-oxoglutarate(2-) = 3-sulfopropanal + L-glutamate(1-).","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete homotaurine:2-oxoglutarate aminotransferase activity (obsolete GO:0102081)","termid":"GO:0102081"}


id: GO:0021530
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a cell becomes capable of differentiating autonomously into an oligodendrocyte in an environment that is neutral with respect to the developmental pathway.","definition_xrefs":["GOC:dph","GOC:jid","GOC:dgh","GO_REF:0000021","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oligodendrocyte cell fate specification","termid":"GO:0021778"},{"relation_name":"part_of","term_name":"spinal cord oligodendrocyte cell differentiation","termid":"GO:0021529"}],"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":"spinal cord oligodendrocyte cell fate specification","termid":"GO:0021530"}


id: PBO:0083622
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"E3-binding protein of the mitochondrial pyruvate dehydrogenase complex; plays a structural role in the complex by binding and positioning dihydrolipoamide dehydrogenase (E3) to the dihydrolipoamide acetyltransferase (E2) core","termid":"PBO:0083622"}


id: PBO:0017449
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-parasite_of","termid":"PBO:0017449"}


id: PBO:0031890
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial iron-sulfur cluster assembly protein Iba57 (predicted)","termid":"PBO:0031890"}


id: PBO:0029377
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-lipid_particles_present_in_decreased_numbers","termid":"PBO:0029377"}


id: MONDO:0041093
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"central retinal vein occlusion","termid":"MONDO:0002303"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"central retinal vein occlusion with macular edema","secondary_identifiers":["SCTID:232039004","UMLS:C0339498","MEDGEN:573198"],"synonyms":[{"name":"central retinal vein occlusion with macular edema","type":"exact"}],"termid":"MONDO:0041093","xrefs":{"Monarch":{"xref_id":"0041093"}}}


id: PBO:0048117
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fucose mutarotase","termid":"PBO:0048117"}


id: PBO:0036532
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human COQ3 with an S. pombe MTS","termid":"PBO:0036532"}


id: GO:0015013
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The polymerization of one or more heparan sulfate chains via a xylose link onto serine residues in the core protein of a proteoglycan.","definition_xrefs":["ISBN:0815316194"],"gene_count":0,"genotype_count":0,"name":"obsolete heparan sulfate proteoglycan biosynthetic process, linkage to polypeptide (obsolete GO:0015013)","synonyms":[{"name":"heparan sulfate proteoglycan anabolism, linkage to polypeptide","type":"exact"},{"name":"heparan sulfate proteoglycan formation, linkage to polypeptide","type":"exact"},{"name":"heparan sulfate proteoglycan synthesis, linkage to polypeptide","type":"exact"},{"name":"heparan sulphate proteoglycan biosynthesis, linkage to polypeptide","type":"exact"},{"name":"heparan sulphate proteoglycan biosynthetic process, linkage to polypeptide","type":"exact"},{"name":"heparin proteoglycan biosynthetic process, linkage to polypeptide","type":"related"}],"termid":"GO:0015013"}


id: PBO:0058081
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4299","termid":"PBO:0058081"}


id: SO:0002174
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A deletion that is the result of base-calling or assembly error.","direct_ancestors":[{"relation_name":"is_a","term_name":"sequence_alteration_artifact","termid":"SO:0002172"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deletion_artifact","synonyms":[{"name":"deletion artifact","type":"exact"}],"termid":"SO:0002174"}


id: PBO:0000832
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO E1-like activator enzyme Rad31","termid":"PBO:0000832"}


id: FYPO:0001164
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population growth phenotype in which cells grow normally (i.e. indistinguishably from wild type) in a medium containing glucose as the carbon source.","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:0002058"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0002057","FYPO:0000003","FYPO:0002060","FYPO:0002058","FYPO:0000257"],"is_obsolete":false,"name":"normal growth on glucose carbon source","synonyms":[{"name":"normal cell population growth on glucose carbon source","type":"exact"},{"name":"normal vegetative cell population growth on dextrose carbon source","type":"exact"},{"name":"normal vegetative cell population growth on glucose carbon source","type":"exact"}],"termid":"FYPO:0001164"}


id: PBO:0046232
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongin C pseudogene 26","termid":"PBO:0046232"}


id: MONDO:0009241
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fountain syndrome is an extremely rare multi-systemic genetic disorder characterized by intellectual disability, deafness, skeletal abnormalities and coarse facial features.","definition_xrefs":["Orphanet:3219"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"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":"fountain syndrome","secondary_identifiers":["GARD:64","MESH:C537270","OMIM:229120","SCTID:720957007","UMLS:C0795944","MEDGEN:208650"],"synonyms":[{"name":"deafness, skeletal dysplasia, lip granuloma","type":"related"},{"name":"deafness-skeletal dysplasia-coarse face with full lips syndrome","type":"exact"},{"name":"deafness-skeletal dysplasia-lip granuloma syndrome","type":"exact"},{"name":"fountain syndrome","type":"exact"},{"name":"intellectual disability, deafness, skeletal abnormalities, coarse face with full lips","type":"related"},{"name":"intellectual disability, sensorineural deafness, skeletal abnormalities, and coarse face with full lips","type":"related"},{"name":"mental retardation, sensorineural deafness, skeletal abnormalities, and coarse face with full lips","type":"related"}],"termid":"MONDO:0009241","xrefs":{"Monarch":{"xref_id":"0009241"}}}


id: MONDO:0018942
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acquired skeletal muscle disease","termid":"MONDO:0016105"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"macrophagic myofasciitis","secondary_identifiers":["SCTID:718175009","Orphanet:592","MESH:C537829","MEDGEN:419858","UMLS:C2931639","GARD:176"],"synonyms":[{"name":"MMF","type":"exact"},{"name":"Macrophagic myofasciitis, childhood","type":"related"}],"termid":"MONDO:0018942","xrefs":{"Monarch":{"xref_id":"0018942"}}}


id: PR:O94519
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- spf30 gene.","definition_xrefs":["UniProtKB:O94519","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":"splicing factor spf30 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1281.02c","synonyms":[{"name":"Spom972h-spf30","type":"exact"},{"name":"survival of motor neuron-related-splicing factor 30 homolog (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94519"}


id: MONDO:0043775
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Complete or severe weakness of the muscles of respiration. This condition may be associated with motor neuron diseases; peripheral nerve diseases; neuromuscular junction diseases; spinal cord diseases; injury to the phrenic nerve; and other disorders.","definition_xrefs":["MESH:D012133"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diaphragm disorder","termid":"MONDO:0005728"},{"relation_name":"is_a","term_name":"palsy","termid":"MONDO:0006496"},{"relation_name":"is_a","term_name":"respiratory failure","termid":"MONDO:0021113"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"respiratory paralysis","secondary_identifiers":["UMLS:C0035232","MEDGEN:19748","SCTID:64228003"],"synonyms":[{"name":"diaphragmatic paralysis","type":"related"},{"name":"muscle paralysis, respiratory","type":"related"},{"name":"muscle paralyzes, respiratory","type":"related"},{"name":"paralysis of diaphragm","type":"exact"},{"name":"paralysis, diaphragmatic","type":"related"},{"name":"paralysis, respiratory","type":"related"},{"name":"paralysis, respiratory muscle","type":"related"},{"name":"respiratory muscle paralysis","type":"related"}],"termid":"MONDO:0043775","xrefs":{"Monarch":{"xref_id":"0043775"}}}


id: PR:O60110
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ER membrane protein complex subunit 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03191"],"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":"TPR repeat protein oca3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC15C4.01c","secondary_identifiers":["UniProtKB:O60110"],"synonyms":[{"name":"Spom972h-EMC2","type":"exact"},{"name":"overexpression-mediated cell cycle arrest protein 3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O60110"}


id: PR:Q9P374
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC19B12.07c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P374"],"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":"zinc finger protein C19B12.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC19B12.07c","synonyms":[{"name":"Spom972h-SPAC19B12.07c","type":"exact"}],"termid":"PR:Q9P374"}


id: MONDO:0013694
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive non-syndromic intellectual disability","termid":"MONDO:0019502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0037792"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0037792","MONDO:0006025"],"is_obsolete":false,"name":"intellectual disability, autosomal recessive 31","secondary_identifiers":["MEDGEN:482153","DOID:0081191","UMLS:C3280523","OMIM:614329","GARD:22553"],"synonyms":[{"name":"MRT31","type":"exact"},{"name":"intellectual disability, autosomal recessive 31","type":"exact"},{"name":"mental retardation, autosomal recessive 31","type":"related"}],"termid":"MONDO:0013694","xrefs":{"Monarch":{"xref_id":"0013694"}}}


id: GO:0019146
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-arabinose 5-phosphate = D-ribulose 5-phosphate + 2 H+.","definition_xrefs":["EC:5.3.1.13","RHEA:23104"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, interconverting aldoses and ketoses","termid":"GO:0016861"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"arabinose-5-phosphate isomerase activity","secondary_identifiers":["KEGG_REACTION:R01530","MetaCyc:DARAB5PISOM-RXN"],"synonyms":[{"name":"D-arabinose-5-phosphate aldose-ketose-isomerase activity","type":"related"},{"name":"D-arabinose-5-phosphate ketol-isomerase activity","type":"related"},{"name":"arabinose phosphate isomerase activity","type":"related"},{"name":"phosphoarabinoisomerase activity","type":"related"}],"termid":"GO:0019146"}


id: GO:1902754
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of renal amino acid absorption.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:1526373","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of renal amino acid absorption","termid":"GO:1902752"},{"relation_name":"positively_regulates","term_name":"renal amino acid absorption","termid":"GO:1990297"}],"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 renal amino acid absorption","synonyms":[{"name":"activation of renal amino acid absorption","type":"narrow"},{"name":"up regulation of renal amino acid absorption","type":"exact"},{"name":"up-regulation of renal amino acid absorption","type":"exact"},{"name":"upregulation of renal amino acid absorption","type":"exact"}],"termid":"GO:1902754"}


id: FYPO:0006493
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of chitin synthase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal chitin synthase activity","termid":"FYPO:0006491"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000707","FYPO:0000652","FYPO:0000661","FYPO:0000654"],"is_obsolete":false,"name":"increased chitin synthase activity","termid":"FYPO:0006493"}


id: GO:0035336
data:
  {"annotated_genes":["SJAG_03909","SJAG_04007","SJAG_03471"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[105088,112915],"is_not":false,"summary":null,"term":"GO:0035336"},{"annotations":[106963],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0035338"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving long-chain fatty-acyl-CoAs, any derivative of coenzyme A in which the sulfhydryl group is in a thioester linkage with a long-chain fatty-acyl group. A long-chain fatty acid has an aliphatic tail containing 13 to 22 carbons.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty-acyl-CoA metabolic process","termid":"GO:0035337"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03471":null,"SJAG_03909":null,"SJAG_04007":null},"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:0006790"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0055086","GO:0044281","GO:0008150","GO:0006629","GO:0006790"],"is_obsolete":false,"name":"long-chain fatty-acyl-CoA metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"long-chain fatty acyl CoA metabolic process","type":"exact"},{"name":"long-chain fatty acyl-CoA metabolism","type":"exact"}],"termid":"GO:0035336","terms_by_termid":{"GO:0035336":null,"GO:0035338":null}}


id: GO:1900484
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of protein targeting to vacuolar membrane.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of protein targeting to membrane","termid":"GO:0090315"},{"relation_name":"is_a","term_name":"negative regulation of intracellular protein transport","termid":"GO:0090317"},{"relation_name":"is_a","term_name":"regulation of protein targeting to vacuolar membrane","termid":"GO:1900483"},{"relation_name":"is_a","term_name":"negative regulation of vacuolar transport","termid":"GO:1903336"},{"relation_name":"negatively_regulates","term_name":"protein targeting to vacuolar membrane","termid":"GO:0044395"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0006605"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006605"}],"interesting_parent_ids":["GO:0006810","GO:0006605","GO:0008150"],"is_obsolete":false,"name":"negative regulation of protein targeting to vacuolar membrane","synonyms":[{"name":"down regulation of protein targeting to vacuolar membrane","type":"exact"},{"name":"down-regulation of protein targeting to vacuolar membrane","type":"exact"},{"name":"downregulation of protein targeting to vacuolar membrane","type":"exact"},{"name":"inhibition of protein targeting to vacuolar membrane","type":"narrow"}],"termid":"GO:1900484"}


id: GO:0045150
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of acetoin, 3-hydroxy-2-butanone.","definition_xrefs":["GOC:mlg"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ketone catabolic process","termid":"GO:0042182"},{"relation_name":"is_a","term_name":"acetoin metabolic process","termid":"GO:0045149"},{"relation_name":"is_a","term_name":"alcohol catabolic process","termid":"GO:0046164"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"acetoin catabolic process","synonyms":[{"name":"acetoin breakdown","type":"exact"},{"name":"acetoin catabolism","type":"exact"},{"name":"acetoin degradation","type":"exact"}],"termid":"GO:0045150"}


id: MONDO:0000628
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the central nervous system.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system benign neoplasm","termid":"MONDO:0000648"},{"relation_name":"is_a","term_name":"central nervous system neoplasm","termid":"MONDO:0006130"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"central nervous system organ benign neoplasm","secondary_identifiers":["UMLS:C0347509","MEDGEN:488882","DOID:0060090"],"synonyms":[{"name":"central nervous system benign neoplasm","type":"exact"}],"termid":"MONDO:0000628","xrefs":{"Monarch":{"xref_id":"0000628"}}}


id: PBO:0087756
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the tRNA splicing endonuclease; tRNA splicing endonuclease (Sen complex) is composed of Sen2p, Sen15p, Sen34p, and Sen54p; Sen complex also cleaves the CBP1 mRNA at the mitochondrial surface","termid":"PBO:0087756"}


id: GO:0032915
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of production of transforming growth factor-beta2.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transforming growth factor beta2 production","termid":"GO:0032909"},{"relation_name":"is_a","term_name":"positive regulation of transforming growth factor beta production","termid":"GO:0071636"},{"relation_name":"positively_regulates","term_name":"transforming growth factor beta2 production","termid":"GO:0032906"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of transforming growth factor beta2 production","synonyms":[{"name":"activation of transforming growth factor-beta2 production","type":"narrow"},{"name":"positive regulation of TGF-B2 production","type":"exact"},{"name":"positive regulation of TGFB2 production","type":"exact"},{"name":"positive regulation of transforming growth factor-beta2 production","type":"exact"},{"name":"stimulation of transforming growth factor-beta2 production","type":"narrow"},{"name":"up regulation of transforming growth factor-beta2 production","type":"exact"},{"name":"up-regulation of transforming growth factor-beta2 production","type":"exact"},{"name":"upregulation of transforming growth factor-beta2 production","type":"exact"}],"termid":"GO:0032915"}


id: GO:0004187
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the preferential release of a C-terminal arginine or lysine residue. Function is inhibited by diisopropyl fluorophosphate and sensitive to thiol-blocking reagents.","definition_xrefs":["EC:3.4.16.6"],"gene_count":0,"genotype_count":0,"name":"obsolete carboxypeptidase D activity (obsolete GO:0004187)","synonyms":[{"name":"CPDW-II","type":"related"},{"name":"KEX1 carboxypeptidase activity","type":"related"},{"name":"KEX1 proteinase activity","type":"related"},{"name":"KEX1DELTAp","type":"related"},{"name":"carboxypeptidase D activity","type":"exact"},{"name":"carboxypeptidase KEX1 activity","type":"narrow"},{"name":"carboxypeptidase Kex1","type":"related"},{"name":"carboxypeptidase S1 activity","type":"related"},{"name":"cereal serine carboxypeptidase II","type":"related"},{"name":"gene KEX1 serine carboxypeptidase","type":"narrow"},{"name":"saccharomyces cerevisiae KEX1 gene product","type":"related"}],"termid":"GO:0004187"}


id: GO:1990071
data:
  {"annotated_genes":["SJAG_02525","SJAG_01415","SJAG_02655","SJAG_03663","SJAG_04837","SJAG_03467","SJAG_02750","SJAG_04021","SJAG_04618","SJAG_04358"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[88138,88822,96799,98606,99261,102028,102874,104384,109317,115922],"is_not":false,"summary":null,"term":"GO:1990071"}]},"cv_name":"cellular_component","definition":"A complex that mediates intra-Golgi traffic, Golgi exit, endosome-to-Golgi traffic, and the trafficking of autophagy proteins from Golgi to the phagophore assembly site. Binds to a component of the COPI coat. In yeast it includes the following subunits: Bet3 (as homodimer), Bet5, Tca17, Trs20, Trs23, Trs31, Trs33, Trs65, Trs120, Trs130. The whole complex is thought to dimerize with itself.","definition_xrefs":["PMID:22669257","GOC:bhm","PMID:20375281"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TRAPP complex","termid":"GO:0030008"},{"relation_name":"part_of","term_name":"endosome","termid":"GO:0005768"},{"relation_name":"part_of","term_name":"Golgi apparatus","termid":"GO:0005794"}],"gene_count":10,"genes_by_uniquename":{"SJAG_01415":null,"SJAG_02525":null,"SJAG_02655":null,"SJAG_02750":null,"SJAG_03467":null,"SJAG_03663":null,"SJAG_04021":null,"SJAG_04358":null,"SJAG_04618":null,"SJAG_04837":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005768"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005794"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0031410","GO:0005794","GO:0005575","GO:0005737","GO:0032991","GO:0005768"],"is_obsolete":false,"name":"TRAPPII protein complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990071","terms_by_termid":{"GO:1990071":null}}


id: SO:0000517
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"12 or 23 nucleotide spacer between the J-nonamer and the J-heptamer of a J-gene recombination feature of an immunoglobulin/T-cell receptor gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"vertebrate_immune_system_gene_recombination_spacer","termid":"SO:0000563"},{"relation_name":"part_of","term_name":"J_gene_recombination_feature","termid":"SO:0000302"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"J_spacer","synonyms":[{"name":"J spacer","type":"exact"},{"name":"J-SPACER","type":"exact"}],"termid":"SO:0000517"}


id: MOD:00703
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a hydrogen atom with a group derived from an isoprene polymer, such as a geranyl (C10), farnesyl (C15) or geranylgeranyl (C20) group.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alkylated residue","termid":"MOD:00001"},{"relation_name":"is_a","term_name":"lipoconjugated residue","termid":"MOD:01155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"isoprenylated residue","synonyms":[{"name":"IpRes","type":"exact"}],"termid":"MOD:00703"}


id: GO:0010952
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of peptidase activity, the hydrolysis of peptide bonds within proteins.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of proteolysis","termid":"GO:0045862"},{"relation_name":"is_a","term_name":"positive regulation of hydrolase activity","termid":"GO:0051345"},{"relation_name":"is_a","term_name":"regulation of peptidase activity","termid":"GO:0052547"}],"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 peptidase activity","termid":"GO:0010952"}


id: MOD:02046
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that contains an L-glutamine residue crosslinked to one or more amino acid residues.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-glutamine residue","termid":"MOD:00907"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crosslinked L-glutamine residue","synonyms":[{"name":"XlnkGln","type":"exact"}],"termid":"MOD:02046"}


id: MONDO:0013784
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare genetic neurological disorder characterized by neonatal onset of rigidity and intractable seizures, with episodic jerking already beginning in utero. Affected infants have small heads, remain visually inattentive, do not feed independently, and make no developmental progress. Frequent spontaneous apnea and bradycardia usually culminate in cardiopulmonary arrest and death in infancy, although some cases were described with a milder clinical course and survival into childhood.","definition_xrefs":["Orphanet:435845"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monogenic epilepsy","termid":"MONDO:0015653"},{"relation_name":"is_a","term_name":"developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"neonatal-onset encephalopathy with rigidity and seizures","secondary_identifiers":["UMLS:C3281029","GARD:17718","MEDGEN:482659","OMIM:614498"],"synonyms":[{"name":"RMFSL","type":"related"},{"name":"lethal neonatal rigidity-multifocal seizure syndrome","type":"exact"},{"name":"lethal neonatal spasticity-epileptic encephalopathy syndrome","type":"exact"},{"name":"neonatal-onset encephalopathy with rigidity and seizures","type":"exact"},{"name":"rigidity and multifocal seizure syndrome, lethal neonatal","type":"related"}],"termid":"MONDO:0013784","xrefs":{"Monarch":{"xref_id":"0013784"}}}


id: PBO:0091167
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, Reiske ISP-associated subunit Qcr10","termid":"PBO:0091167"}


id: MONDO:0100363
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any herpes simplex type 2 infectious disease that involves the genitals.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genital herpes","termid":"MONDO:0005770"},{"relation_name":"is_a","term_name":"herpes simplex type 2 infectious disease","termid":"MONDO:0100360"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"genital herpes simplex type 2 infectious disorder","termid":"MONDO:0100363","xrefs":{"Monarch":{"xref_id":"0100363"}}}


id: GO:0047245
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-acetyl-D-glucosaminyldiphosphoundecaprenol + UDP-D-glucose = beta-D-glucosyl-1,4-N-acetyl-D-glucosaminyldiphosphoundecaprenol + UDP.","definition_xrefs":["MetaCyc:2.4.1.188-RXN","EC:2.4.1.188"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UDP-glucosyltransferase activity","termid":"GO:0035251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016757","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"N-acetylglucosaminyldiphosphoundecaprenol glucosyltransferase activity","secondary_identifiers":["RHEA:20952"],"synonyms":[{"name":"UDP-D-glucose:N-acetylglucosaminyl pyrophosphorylundecaprenol glucosyltransferase activity","type":"related"},{"name":"UDP-glucose:N-acetyl-D-glucosaminyldiphosphoundecaprenol 4-beta-D-glucosyltransferase activity","type":"related"},{"name":"UDPglucose:N-acetyl-D-glucosaminyldiphosphoundecaprenol 4-beta-D-glucosyltransferase activity","type":"related"},{"name":"uridine diphosphoglucose-acetylglucosaminylpyrophosphorylundecaprenol glucosyltransferase activity","type":"related"}],"termid":"GO:0047245"}


id: MONDO:0013463
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any dextro-looped transposition of the great arteries in which the cause of the disease is a mutation in the GDF1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"dextro-looped transposition of the great arteries","termid":"MONDO:0019443"},{"relation_name":"is_a","term_name":"congenital heart defects, multiple types","termid":"MONDO:0000119"},{"relation_name":"is_a","term_name":"dextro-looped transposition of the great arteries","termid":"MONDO:0019443"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"congenital heart defects, multiple types, 6","secondary_identifiers":["MEDGEN:462571","OMIM:613854","UMLS:C3151221","DOID:0060772"],"synonyms":[{"name":"CHTD6","type":"related"},{"name":"DTGA3","type":"exact"},{"name":"GDF1 dextro-looped transposition of the great arteries","type":"exact"},{"name":"congenital heart defects, multiple types, 6","type":"exact"},{"name":"dextro-looped transposition of the great arteries 3","type":"exact"},{"name":"dextro-looped transposition of the great arteries caused by mutation in GDF1","type":"exact"},{"name":"dextro-looped transposition of the great arteries type 3","type":"exact"},{"name":"transposition of the great arteries, dextro-looped 3","type":"related"},{"name":"transposition of the great arteries, dextro-looped 3, formerly","type":"related"},{"name":"transposition of the great arteries, dextro-looped type 3","type":"exact"}],"termid":"MONDO:0013463","xrefs":{"Monarch":{"xref_id":"0013463"}}}


id: PBO:0031659
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_pseudohyphal_growth","termid":"PBO:0031659"}


id: PBO:0030559
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_glutamate_import","termid":"PBO:0030559"}


id: PBO:0075942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STAG1 divergent transcript","termid":"PBO:0075942"}


id: PBO:0005016
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"P-TEFb-cap methyltransferase Pcm1","termid":"PBO:0005016"}


id: MONDO:0011351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the TECTA gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 21","secondary_identifiers":["MESH:C566353","MEDGEN:355030","DOID:0110479","GARD:22595","OMIM:603629","UMLS:C1863655"],"synonyms":[{"name":"DFNB21","type":"narrow"},{"name":"TECTA autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 21","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 21","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in TECTA","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in tecta","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 21","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 21","type":"exact"},{"name":"deafness, autosomal recessive 21","type":"narrow"},{"name":"deafness, autosomal recessive type 21","type":"narrow"},{"name":"tecta autosomal recessive nonsyndromic deafness","type":"narrow"}],"termid":"MONDO:0011351","xrefs":{"Monarch":{"xref_id":"0011351"}}}


id: PBO:0085873
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; identical to the C-terminal 119 amino acid residues of the MATalpha2 protein; a2 sequence is not present in SGD because the sequenced S288C strain is MATalpha, not MATa","termid":"PBO:0085873"}


id: GO:0102936
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + gypsogenate = gypsogenate-28-beta-D-glucoside + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete gypsogenate-UDP-glucosyltransferase activity (obsolete GO:0102936)","termid":"GO:0102936"}


id: PBO:0073063
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syndecan 1","termid":"PBO:0073063"}


id: PBO:0068484
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 65, pseudogene","termid":"PBO:0068484"}


id: MONDO:0002467
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic or neoplastic disorder affecting the inner ear. Causes are inner ear infections, head injuries, and neoplasms (e.g., acoustic schwannoma). Symptoms include dizziness, imbalance, nausea, and vision problems.","definition_xrefs":["NCIT:C27166"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auditory system disorder","termid":"MONDO:0002409"},{"relation_name":"is_a","term_name":"disorder of ear","termid":"MONDO:0021205"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inner ear disorder","secondary_identifiers":["SCTID:232297009","MEDGEN:141671","EFO:0009672","ICD10CM:H80-H83","DOID:2952","UMLS:C0494559","MESH:D007759"],"synonyms":[{"name":"disease of internal ear","type":"exact"},{"name":"disease or disorder of internal ear","type":"exact"},{"name":"disorder of internal ear","type":"exact"},{"name":"inner Ear disorder","type":"exact"},{"name":"internal Ear disorder","type":"exact"},{"name":"internal ear disease","type":"exact"},{"name":"internal ear disease or disorder","type":"exact"},{"name":"labyrinthine disease","type":"exact"},{"name":"vestibular disorder","type":"narrow"}],"termid":"MONDO:0002467","xrefs":{"Monarch":{"xref_id":"0002467"}}}


id: PBO:0085290
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pex3p interacting protein, required for pexophagy; interacts with Atg8p and Atg11p; mRNA is weakly cell cycle regulated, peaking in G2 phase; YJL185C is a non-essential gene","termid":"PBO:0085290"}


id: MONDO:0032572
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":"cardiac, facial, and digital anomalies with developmental delay","secondary_identifiers":["NCIT:C179868","OMIM:618164","MEDGEN:1648330","UMLS:C4748484"],"synonyms":[{"name":"CAFDADD","type":"related"},{"name":"CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY","type":"related"}],"termid":"MONDO:0032572","xrefs":{"Monarch":{"xref_id":"0032572"}}}


id: PBO:0068590
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 41, pseudogene","termid":"PBO:0068590"}


id: PBO:0060903
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal differentiation 2","termid":"PBO:0060903"}


id: FYPO:0000088
data:
  {"alleles_by_uniquename":{"SJAG_00364:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00364","name":"rad3delta","uniquename":"SJAG_00364:allele-1"},"SJAG_01205:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01205","name":"crb2delta","uniquename":"SJAG_01205:allele-1"},"SJAG_01680:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01680","name":"chk1delta","uniquename":"SJAG_01680:allele-1"},"SJAG_04287:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04287","name":"cds1delta","uniquename":"SJAG_04287:allele-1"},"SJAG_04671:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04671","name":"mrc1delta","uniquename":"SJAG_04671:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119017],"is_not":false,"summary":null,"term":"FYPO:0000088"}],"single_locus_phenotype":[{"annotations":[119015,119016,119021,119022,119023],"is_not":false,"summary":null,"term":"FYPO:0000088"}]},"cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to hydroxyurea. Cells stop growing (and may die) at a concentration of hydroxyurea that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sensitive to DNA damaging agents","termid":"FYPO:0000266"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00364":null,"SJAG_01205":null,"SJAG_01680":null,"SJAG_04287":null,"SJAG_04671":null},"genotype_count":6,"genotypes_by_uniquename":{"cds1delta":{"display_name":"cds1delta","display_uniquename":"cds1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04287:allele-1","expression":"Null"}]}]},"chk1delta":{"display_name":"chk1delta","display_uniquename":"chk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01680:allele-1","expression":"Null"}]}]},"chk1delta__crb2delta":{"display_name":"chk1delta crb2delta","display_uniquename":"chk1delta__crb2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01680:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_01205:allele-1","expression":"Null"}]}]},"crb2delta":{"display_name":"crb2delta","display_uniquename":"crb2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01205:allele-1","expression":"Null"}]}]},"mrc1delta":{"display_name":"mrc1delta","display_uniquename":"mrc1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04671:allele-1","expression":"Null"}]}]},"rad3delta":{"display_name":"rad3delta","display_uniquename":"rad3delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00364:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0001985","FYPO:0000139","FYPO:0005447","FYPO:0000003"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_01680","SJAG_01205"],"name":"sensitive to hydroxyurea","references_by_uniquename":{"PMID:23090706":null},"single_locus_annotated_genes":["SJAG_00364","SJAG_01205","SJAG_01680","SJAG_04671","SJAG_04287"],"single_locus_genotype_uniquenames":["cds1delta","rad3delta","chk1delta","crb2delta","mrc1delta"],"synonyms":[{"name":"hypersensitive to hydroxyurea","type":"exact"},{"name":"sensitive to HU","type":"exact"},{"name":"sensitive to hydroxyurea during mitotic cell cycle","type":"related"},{"name":"sensitive to hydroxyurea during vegetative growth","type":"exact"}],"termid":"FYPO:0000088","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0000088":null,"FYPO_EXT:0000001":null,"FYPO_EXT:0000002":null}}


id: PATO:0000280
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000280 backcross fertility (obsolete PATO:0000280)","termid":"PATO:0000280"}


id: RO:0002334
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"inverse of regulates","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_downstream_of_or_within","termid":"RO:0002427"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulated_by","termid":"RO:0002334"}


id: PBO:0045177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNAJA4 divergent transcript","termid":"PBO:0045177"}


id: MONDO:0014407
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome in which the cause of the disease is a mutation in the AKT3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome","termid":"MONDO:0019375"},{"relation_name":"is_a","term_name":"AKT3-related overgrowth spectrum","termid":"MONDO:0800485"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2","secondary_identifiers":["GARD:18078","OMIM:615937","UMLS:C4014738","MEDGEN:863175"],"synonyms":[{"name":"AKT3 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome","type":"exact"},{"name":"MPPH2","type":"related"},{"name":"megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2","type":"exact"},{"name":"megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 2","type":"exact"},{"name":"megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in AKT3","type":"exact"}],"termid":"MONDO:0014407","xrefs":{"Monarch":{"xref_id":"0014407"}}}


id: PBO:0036539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chorismate synthase Aro2 (predicted)","termid":"PBO:0036539"}


id: PBO:0004592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MADS-box transcription factor Pvg4 (predicted)","termid":"PBO:0004592"}


id: PATO:0001914
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A physiological state which is characterized by normal electrical activity in neuronal tissue.","definition_xrefs":["PATOC:mb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"physiological state","termid":"PATO:0001912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-ictal","termid":"PATO:0001914"}


id: PBO:0079035
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Val (anticodon AAC) 4-1","termid":"PBO:0079035"}


id: MONDO:0957919
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lui-Jee-Baron syndrome","secondary_identifiers":["UMLS:C5882664","MEDGEN:1849943","OMIM:301114"],"termid":"MONDO:0957919","xrefs":{"Monarch":{"xref_id":"0957919"}}}


id: GO:0046680
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 DDT stimulus. DDT, dichlorodiphenyltrichloroethane, is a chlorinated hydrocarbon pesticide moderately toxic to humans and other animals.","definition_xrefs":["ISBN:0721662544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to insecticide","termid":"GO:0017085"}],"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 DDT","synonyms":[{"name":"DDT resistance","type":"related"},{"name":"DDT susceptibility/resistance","type":"related"}],"termid":"GO:0046680"}


id: FYPO:0005220
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 protein oligomerization is abnormal.","definition_xrefs":["GO:0051259","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein-containing complex assembly","termid":"FYPO:0000447"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"abnormal protein oligomerization","synonyms":[{"name":"abnormal protein oligomerisation","type":"exact"},{"name":"abnormal protein oligomerization during mitotic cell cycle","type":"related"},{"name":"abnormal protein oligomerization during vegetative growth","type":"exact"}],"termid":"FYPO:0005220"}


id: GO:0035037
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An endocytosis process that results in penetration of the egg shell through the micropyle (a specialized anterior opening in the vitelline envelope) and entry of the entire sperm, including the surrounding plasma membrane and the sperm tail, into the egg cytoplasm. This step in fertilization is seen in Drosophila, where a plasma membrane fusion event between the sperm and the egg does not occur.","definition_xrefs":["PMID:9630751","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocytosis","termid":"GO:0006897"},{"relation_name":"part_of","term_name":"single fertilization","termid":"GO:0007338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179","GO:0016192"],"is_obsolete":false,"name":"sperm entry","termid":"GO:0035037"}


id: PBO:0060106
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND6 pseudogene 7","termid":"PBO:0060106"}


id: PBO:0069055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 301, pseudogene","termid":"PBO:0069055"}


id: PBO:0027589
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_duration_of_protein_tyrosine_phosphorylation_during_cellular_response_to_salt_stress","termid":"PBO:0027589"}


id: PBO:0078030
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha joining 20","termid":"PBO:0078030"}


id: PBO:0036185
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_threonine_phosphorylation_during_mitosis","termid":"PBO:0036185"}


id: PBO:0068653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4 small nuclear 34, pseudogene","termid":"PBO:0068653"}


id: GO:0046705
data:
  {"annotated_genes":["SJAG_00779"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115074],"is_not":false,"summary":null,"term":"GO:0046705"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of CDP, cytidine (5'-)diphosphate.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine ribonucleoside diphosphate biosynthetic process","termid":"GO:0009194"},{"relation_name":"is_a","term_name":"pyrimidine ribonucleotide biosynthetic process","termid":"GO:0009220"},{"relation_name":"is_a","term_name":"CDP metabolic process","termid":"GO:0046704"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00779":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"CDP biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"CDP anabolism","type":"exact"},{"name":"CDP biosynthesis","type":"exact"},{"name":"CDP formation","type":"exact"},{"name":"CDP synthesis","type":"exact"}],"termid":"GO:0046705","terms_by_termid":{"GO:0046705":null}}


id: PBO:0074554
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 7","termid":"PBO:0074554"}


id: PBO:0029089
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_without_cell_division,_spheroid_cell","termid":"PBO:0029089"}


id: PBO:0043221
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Charcot-Leyden crystal galectin","termid":"PBO:0043221"}


id: FYPO:0000129
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 formed in the shape of a sphere.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spheroid vegetative cell","termid":"FYPO:0000021"},{"relation_name":"is_a","term_name":"spherical cell","termid":"FYPO:0001956"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000005","FYPO:0001320"],"is_obsolete":false,"name":"spherical vegetative cell","synonyms":[{"name":"orb during vegetative growth","type":"exact"},{"name":"spherical cells during vegetative growth","type":"exact"},{"name":"spherical vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0000129"}


id: SO:0001759
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A pseudogene, deactivated from original state by mutation, fixed in a population,where the ortholog in a reference species such as mouse remains functional.","definition_xrefs":["SO:ke","GENCODE:http://www.gencodegenes.org/gencode_biotypes.html"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non_processed_pseudogene","termid":"SO:0001760"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unitary_pseudogene","synonyms":[{"name":"INSDC_feature:gene","type":"broad"},{"name":"INSDC_qualifier:unitary","type":"exact"},{"name":"disabled gene","type":"related"},{"name":"unitary pseudogene","type":"related"}],"termid":"SO:0001759"}


id: PBO:0065494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome assembly chaperone 3","termid":"PBO:0065494"}


id: PBO:0073795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 6 member 2","termid":"PBO:0073795"}


id: PBO:0063519
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyridoxal kinase","termid":"PBO:0063519"}


id: GO:0021698
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the cerebellar cortex. This process pertains to the physical shaping of a rudimentary structure. The cerebellar cortex is a thin mantle of gray matter that covers the surface of each cerebral hemisphere. It has a characteristic morphology with convolutions (gyri) and crevices (sulci) that have specific functions. Six layers of nerve cells and the nerve pathways that connect them comprise the cerebellar cortex. Together, these regions are responsible for the processes of conscious thought, perception, emotion and memory as well as advanced motor function.","definition_xrefs":["ISBN:0838580343","GOC:cls","GOC:dgh","GO_REF:0000021","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure arrangement","termid":"GO:0048532"},{"relation_name":"part_of","term_name":"cerebellar cortex morphogenesis","termid":"GO:0021696"}],"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":"cerebellar cortex structural organization","synonyms":[{"name":"cerebellar cortex structural organisation","type":"exact"}],"termid":"GO:0021698"}


id: GO:0098690
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A synapse that uses glycine as a neurotransmitter.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synapse","termid":"GO:0045202"}],"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":"glycinergic synapse","termid":"GO:0098690"}


id: GO:0019630
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving quinate, the anion of quinic acid. The acid occurs commonly in plants, either free or as esters, and is used as a medicine.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"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:0044281","GO:0008150"],"is_obsolete":false,"name":"quinate metabolic process","synonyms":[{"name":"quinate metabolism","type":"exact"},{"name":"quinic acid metabolic process","type":"exact"},{"name":"quinic acid metabolism","type":"exact"}],"termid":"GO:0019630"}


id: PBO:0075364
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SRY-box transcription factor 4","termid":"PBO:0075364"}


id: PBO:0082130
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Actin assembly factor; C-terminal WCA domain activates Arp2/3 complex-mediated nucleation of branched actin filaments, polyproline domain nucleates actin filaments independent of Arp2/3; mutants are defective in endocytosis, bud site selection, cytokinesis; human homolog WAS (Wiskott-Aldrich Syndrome) implicated in severe immunodeficiency; human WAS complements yeast null mutant, but only in presence of WIPF1, which mediates localization of WAS to cortical patches","termid":"PBO:0082130"}


id: GO:0051032
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of nucleic acids from one side of a membrane to the other. Nucleic acids are single or double-stranded polynucleotides involved in the storage, transmission and transfer of genetic information.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleobase-containing compound transmembrane transporter activity","termid":"GO:0015932"},{"relation_name":"is_a","term_name":"macromolecule transmembrane transporter activity","termid":"GO:0022884"}],"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:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"nucleic acid transmembrane transporter activity","termid":"GO:0051032"}


id: MONDO:0018472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial isolated trichomegaly is a rare genetic hair anomaly characterized by a prolonged anagen phase of the eyelash hairs, leading to extreme eyelash growth that may result in corneal irritation. Increased growth of hair on other parts of the face (eyebrows, cheeks, forehead) and/or the body (chest, arms, legs) may be associated.","definition_xrefs":["Orphanet:411788"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trichomegaly","termid":"MONDO:0008593"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"familial isolated trichomegaly","secondary_identifiers":["GARD:13167","icd11.foundation:1611595637","SCTID:764523004","MEDGEN:1639703","UMLS:C4706941","DOID:0111566"],"termid":"MONDO:0018472","xrefs":{"Monarch":{"xref_id":"0018472"}}}


id: PBO:0039702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"APAF1 interacting protein","termid":"PBO:0039702"}


id: PBO:0086344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pseudouridine synthase; catalyzes pseudouridylation at positions 35 and 56 in U2 snRNA, position 50 in 5S rRNA, position 13 in cytoplasmic tRNAs, and position 35 in pre-tRNA(Tyr); also pseudouridylates some mRNAs; relocates from nucleus to cytoplasm during heat shock and differentially modifies some mRNAs during heat shock; conserved in archaea, vertebrates, and some bacteria","termid":"PBO:0086344"}


id: PBO:0083742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential component of the MIND kinetochore complex; joins kinetochore subunits contacting DNA to those contacting microtubules; required for accurate chromosome segregation; complex consists of Mtw1p Including Nnf1p-Nsl1p-Dsn1p (MIND)","termid":"PBO:0083742"}


id: GO:0034792
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: hypophosphite + 2-oxoglutarate + O2 = succinate + phosphite + CO2.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete hypophosphite dioxygenase activity (obsolete GO:0034792)","termid":"GO:0034792"}


id: PBO:0070920
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L17 pseudogene 28","termid":"PBO:0070920"}


id: MONDO:0002095
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm arising from the blood vessels.","definition_xrefs":["NCIT:C8538"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"arterial disorder","termid":"MONDO:0000473"},{"relation_name":"is_a","term_name":"cardiovascular cancer","termid":"MONDO:0002100"},{"relation_name":"is_a","term_name":"blood vessel neoplasm","termid":"MONDO:0021080"}],"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":"vascular cancer","secondary_identifiers":["Orphanet:673466","UMLS:C1458139","DOID:175","MESH:D009383","MEDGEN:264315"],"synonyms":[{"name":"Haemangiomatous tumor","type":"broad"},{"name":"Haemangiomatous tumour","type":"broad"},{"name":"blood vessel neoplasm","type":"broad"},{"name":"blood vessel tumor","type":"broad"},{"name":"blood vessel tumor (morphologic abnormality)","type":"broad"},{"name":"blood vessel tumor disorder","type":"broad"},{"name":"blood vessel tumors","type":"broad"},{"name":"blood vessel tumors (morphologic abnormality)","type":"broad"},{"name":"blood vessel tumour","type":"broad"},{"name":"blood vessel tumour (morphologic abnormality)","type":"broad"},{"name":"blood vessel tumour disorder","type":"broad"},{"name":"blood vessel tumours","type":"broad"},{"name":"blood vessel tumours (morphologic abnormality)","type":"broad"},{"name":"cancer of vasculature","type":"exact"},{"name":"leiomyosarcoma of the renal vein","type":"narrow"},{"name":"malignant blood vessel neoplasm","type":"exact"},{"name":"malignant blood vessel tumor","type":"exact"},{"name":"malignant blood vessel tumour","type":"exact"},{"name":"malignant great vessel tumour","type":"related"},{"name":"malignant neoplasm of vasculature","type":"exact"},{"name":"malignant tumor of pulmonary artery","type":"narrow"},{"name":"malignant tumor of pulmonary vein","type":"narrow"},{"name":"malignant tumour of pulmonary artery","type":"narrow"},{"name":"malignant tumour of pulmonary vein","type":"narrow"},{"name":"malignant vascular neoplasm","type":"exact"},{"name":"malignant vascular tumor","type":"exact"},{"name":"malignant vascular tumour","type":"exact"},{"name":"malignant vasculature neoplasm","type":"exact"},{"name":"neoplasm of great vessel","type":"broad"},{"name":"pulmonary artery cancer","type":"exact"},{"name":"pulmonary artery malignant neoplasm","type":"exact"},{"name":"pulmonary vein malignant neoplasm","type":"exact"},{"name":"renal vein leiomyosarcoma","type":"related"},{"name":"vascular tissue neoplasm","type":"related"},{"name":"vascular tumors","type":"broad"},{"name":"vascular tumours","type":"broad"},{"name":"vasculature cancer","type":"exact"}],"termid":"MONDO:0002095","xrefs":{"Monarch":{"xref_id":"0002095"}}}


id: MONDO:0003943
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare benign slow growing adipose tumor, characterized by the presence of polygonal brown fat cells with abundant cytoplasm, that arises within the nervous system.","definition_xrefs":["NCIT:C6997"],"direct_ancestors":[{"relation_name":"is_a","term_name":"central nervous system lipoma","termid":"MONDO:0003844"},{"relation_name":"is_a","term_name":"hibernoma","termid":"MONDO:0021168"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"central nervous system hibernoma","secondary_identifiers":["MEDGEN:317749","UMLS:C1708362","DOID:6607"],"synonyms":[{"name":"central nervous system hibernoma","type":"exact"},{"name":"hibernoma of central nervous system","type":"exact"},{"name":"hibernoma of nervous system","type":"exact"},{"name":"hibernoma of the central nervous system","type":"exact"},{"name":"nervous system hibernoma","type":"related"}],"termid":"MONDO:0003943","xrefs":{"Monarch":{"xref_id":"0003943"}}}


id: GO:2000459
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of astrocyte chemotaxis.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of chemotaxis","termid":"GO:0050922"},{"relation_name":"is_a","term_name":"negative regulation of glial cell migration","termid":"GO:1903976"},{"relation_name":"is_a","term_name":"regulation of astrocyte chemotaxis","termid":"GO:2000458"},{"relation_name":"negatively_regulates","term_name":"astrocyte chemotaxis","termid":"GO:0035700"}],"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 chemotaxis","termid":"GO:2000459"}


id: GO:0007632
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The behavior of an organism in response to a visual stimulus.","definition_xrefs":["GOC:jid","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"behavior","termid":"GO:0007610"},{"relation_name":"is_a","term_name":"response to light stimulus","termid":"GO:0009416"}],"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":"visual behavior","synonyms":[{"name":"behavioral response to visual stimulus","type":"exact"},{"name":"behavioural response to visual stimulus","type":"exact"},{"name":"visual behaviour","type":"exact"}],"termid":"GO:0007632"}


id: PATO:0000654
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000654 alcochol value (obsolete PATO:0000654)","termid":"PATO:0000654"}


id: PBO:0110502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TNFRSF10B antisense RNA 1","termid":"PBO:0110502"}


id: PR:Q10156
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- lkh1 gene.","definition_xrefs":["UniProtKB:Q10156","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":"dual specificity protein kinase lkh1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1D4.11c","synonyms":[{"name":"Spom972h-lkh1","type":"exact"}],"termid":"PR:Q10156"}


id: PBO:0064488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase I subunit A","termid":"PBO:0064488"}


id: FYPO:0006498
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a greater extent than normal during a cellular response to ultraviolet light.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein phosphorylation during vegetative growth","termid":"FYPO:0001038"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0002494","FYPO:0002274"],"is_obsolete":false,"name":"increased protein phosphorylation during cellular response to UV","synonyms":[{"name":"increased protein phosphorylation during cellular response to UV during mitotic cell cycle","type":"related"},{"name":"increased protein phosphorylation during cellular response to UV during vegetative growth","type":"exact"},{"name":"increased protein phosphorylation during cellular response to ultraviolet light","type":"exact"}],"termid":"FYPO:0006498"}


id: PR:O13990
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- bgl2 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O13990"],"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":"glucan 1,3-beta-glucosidase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC26H5.08c","synonyms":[{"name":"Exo-1,3-beta-glucanase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-bgl2","type":"exact"}],"termid":"PR:O13990"}


id: PBO:0044240
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cupin superfamily member 1, pseudogene","termid":"PBO:0044240"}


id: PBO:0070862
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L14","termid":"PBO:0070862"}


id: PATO:0001328
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A symmetry quality inhering in a bearer by virtue of the bearer's being capable of division into symmetrical halves by any longitudinal plane passing through the axis.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"radial symmetry","termid":"PATO:0001325"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actinomorphic","termid":"PATO:0001328"}


id: MOD:01699
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively adds a hydrogen cation, a proton, forming a cationic residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification categorized by chemical process","termid":"MOD:01156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protonated residue","synonyms":[{"name":"H+NRes","type":"exact"}],"termid":"MOD:01699"}


id: PBO:0085635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in histone H4 acetylation at ribosomal protein genes; interacts with and modulates NuA4 histone acetyltransferase complex; required for growth on glycerol as a carbon source; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies; contains a segment predicted to resemble the winged-helix/forkhead domain located in DNA-binding proteins","termid":"PBO:0085635"}


id: MONDO:0009350
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome characterized by Potter sequence, heart defect, cleft palate, polydactyly, and skeletal defects.","definition_xrefs":["DOID:0060566","PMID:3232694"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Holzgreve-Wagner-Rehder syndrome","secondary_identifiers":["MEDGEN:344650","MESH:C535327","OMIM:236110","GARD:2728","Orphanet:2167","UMLS:C1856095"],"synonyms":[{"name":"Complex congenital heart defect, renal agenesis and cleft lip and palate","type":"related"},{"name":"Holzgreve Wagner Rehder syndrome","type":"exact"},{"name":"Holzgreve syndrome","type":"exact"},{"name":"cleft palate-Potter sequence-congenital heart anomalies-mesoaxial polydactyly-multiple malformations syndrome","type":"exact"}],"termid":"MONDO:0009350","xrefs":{"Monarch":{"xref_id":"0009350"}}}


id: GO:1904332
data:
  {"annotated_genes":["SJAG_00573"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[111251],"is_not":false,"summary":null,"term":"GO:1904332"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of error-prone translesion synthesis.","definition_xrefs":["GOC:TermGenie","PMID:22761594","GOC:kmv","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of DNA repair","termid":"GO:0045738"},{"relation_name":"is_a","term_name":"regulation of error-prone translesion synthesis","termid":"GO:1904331"},{"relation_name":"is_a","term_name":"negative regulation of DNA biosynthetic process","termid":"GO:2000279"},{"relation_name":"negatively_regulates","term_name":"error-prone translesion synthesis","termid":"GO:0042276"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00573":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"negatively_regulates","termid":"GO:0006281"},{"rel_name":"regulates","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0006281","GO:0008150"],"is_obsolete":false,"name":"negative regulation of error-prone translesion synthesis","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"down regulation of error-prone postreplication DNA repair","type":"related"},{"name":"down regulation of error-prone translesion synthesis","type":"exact"},{"name":"down regulation of mutagenic PRR","type":"exact"},{"name":"down regulation of mutagenic postreplication DNA repair","type":"related"},{"name":"down-regulation of error-prone postreplication DNA repair","type":"related"},{"name":"down-regulation of error-prone translesion synthesis","type":"exact"},{"name":"down-regulation of mutagenic PRR","type":"exact"},{"name":"down-regulation of mutagenic postreplication DNA repair","type":"related"},{"name":"downregulation of error-prone postreplication DNA repair","type":"related"},{"name":"downregulation of error-prone translesion synthesis","type":"exact"},{"name":"downregulation of mutagenic PRR","type":"exact"},{"name":"downregulation of mutagenic postreplication DNA repair","type":"related"},{"name":"inhibition of error-prone postreplication DNA repair","type":"related"},{"name":"inhibition of error-prone translesion synthesis","type":"narrow"},{"name":"inhibition of mutagenic PRR","type":"narrow"},{"name":"inhibition of mutagenic postreplication DNA repair","type":"related"},{"name":"negative regulation of error-prone postreplication DNA repair","type":"related"},{"name":"negative regulation of mutagenic PRR","type":"exact"},{"name":"negative regulation of mutagenic postreplication DNA repair","type":"related"}],"termid":"GO:1904332","terms_by_termid":{"GO:1904332":null}}


id: GO:0070833
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The phosphatidylcholine biosynthetic process that begins with an initial N-methylation with phospho-base phosphoethanolamine, followed by two downstream N-methylations on phosphatidyl-bases, phosphatidyl-N-methylethanolamine and phosphatidyl-N-dimethylethanolamine. The process ends with the conversion of a phosphatidyl-N-dimethylethanolamine to a phosphatidylcholine.","definition_xrefs":["MetaCyc:PWY4FS-3"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatidylcholine biosynthetic process","termid":"GO:0006656"},{"relation_name":"is_a","term_name":"primary amino compound metabolic process","termid":"GO:1901160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"phosphatidylcholine biosynthesis from phosphoryl-ethanolamine via CDP-N-methylethanolamine","termid":"GO:0070833"}


id: PATO:0000484
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000484 tactile hyporesponsive (obsolete PATO:0000484)","termid":"PATO:0000484"}


id: PBO:0042718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cell cycle exit and neuronal differentiation 1","termid":"PBO:0042718"}


id: GO:0000260
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: ATP + H2O + H+(in) = ADP + phosphate + H+(out). Found in vacuoles of eukaryotes and in bacteria.","definition_xrefs":["TC:3.A.2.2.3","TC:3.A.2.2.1"],"gene_count":0,"genotype_count":0,"name":"obsolete hydrogen-translocating V-type ATPase activity (obsolete GO:0000260)","synonyms":[{"name":"hydrogen-translocating V-type ATPase activity","type":"exact"}],"termid":"GO:0000260"}


id: PBO:0043753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COX7C pseudogene 1","termid":"PBO:0043753"}


id: MONDO:0016148
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete qualitative or quantitative defects of collagen 6 (obsolete MONDO:0016148)","termid":"MONDO:0016148","xrefs":{"Monarch":{"xref_id":"0016148"}}}


id: GO:0106094
data:
  {"annotated_genes":["SJAG_01538","SJAG_04558","SJAG_05196"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[96200,102308,112331],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034993"},{"annotations":[96203,102316],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990612"}]},"cv_name":"cellular_component","definition":"A nuclear membrane protein complex which connects the nuclear outer and inner membranes together, and links thereby links the nuclear lumen to cytoplasmic microtubules.","definition_xrefs":["GOC:vw","PMID:19225124"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear membrane protein complex","termid":"GO:0106083"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01538":null,"SJAG_04558":null,"SJAG_05196":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"nuclear membrane microtubule tethering complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0106094","terms_by_termid":{"GO:0034993":null,"GO:1990612":null}}


id: PBO:0052116
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"potassium voltage-gated channel subfamily C member 4","termid":"PBO:0052116"}


id: GO:0001072
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binds to RNA, typically within the nascent RNA transcript, to promote readthrough of a transcription termination site and thus extending the length of the RNA transcript produced. Examples of antitermination factors which bind the nascent RNA include the lambda N protein and the HIV-1 tat protein.","definition_xrefs":["GOC:txnOH","PMID:8332211"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcription regulator activity","termid":"GO:0140110"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140110"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0140110"],"is_obsolete":false,"name":"transcription antitermination factor activity, RNA binding","synonyms":[{"name":"RNA binding transcription antitermination factor activity","type":"exact"}],"termid":"GO:0001072"}


id: GO:0070695
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that is composed of AKTIP/FTS, FAM160A2/p107FHIP, and one or more members of the Hook family of proteins, HOOK1, HOOK2, and HOOK3. The complex is thought to promote vesicle trafficking and/or fusion, and associates with the homotypic vesicular sorting complex (the HOPS complex).","definition_xrefs":["GOC:mah","GOC:ab","PMID:18799622"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"},{"relation_name":"part_of","term_name":"cytoplasm","termid":"GO:0005737"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005737","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"FHF complex","termid":"GO:0070695"}


id: PBO:0076434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 11 like 10","termid":"PBO:0076434"}


id: MONDO:0006669
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Endocarditis that is caused by an infection with a bacterial agent.","definition_xrefs":["NCIT:C128359"],"direct_ancestors":[{"relation_name":"is_a","term_name":"infective endocarditis","termid":"MONDO:0000565"},{"relation_name":"is_a","term_name":"bacterial infectious disease","termid":"MONDO:0005113"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"bacterial endocarditis","secondary_identifiers":["EFO:1000830","UMLS:C0014121","MEDGEN:41779","MESH:D004697","icd11.foundation:1924438986","HP:0006689","MedDRA:10004019","SCTID:301183007"],"synonyms":[{"name":"Bacteria caused endocarditis (disease)","type":"exact"},{"name":"Bacteria endocarditis (disease)","type":"exact"},{"name":"bacterial endocarditis","type":"exact"},{"name":"bacterial endocarditis (disease)","type":"exact"}],"termid":"MONDO:0006669","xrefs":{"Monarch":{"xref_id":"0006669"}}}


id: MONDO:0015483
data:
  {"annotated_genes":["SJAG_03578","SJAG_00731","SJAG_01444"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86512],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013385"},{"annotations":[85169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009558"},{"annotations":[84844],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030067"}]},"cv_name":"mondo","definition":"A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)","definition_xrefs":["MESH:D008342"],"direct_ancestors":[{"relation_name":"is_a","term_name":"otorhinolaryngologic disease","termid":"MONDO:0024623"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00731":null,"SJAG_01444":null,"SJAG_03578":null},"genotype_count":0,"is_obsolete":false,"name":"mandibulofacial dysostosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MedDRA:10051456","GARD:19980","icd11.foundation:470731247","Orphanet:155899"],"synonyms":[{"name":"bilateral and symmetric oto-mandibular dysplasia","type":"exact"}],"termid":"MONDO:0015483","terms_by_termid":{"MONDO:0009558":null,"MONDO:0013385":null,"MONDO:0030067":null},"xrefs":{"Monarch":{"xref_id":"0015483"}}}


id: GO:1904016
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 Thyroglobulin triiodothyronine stimulus.","definition_xrefs":["GO_REF:0000071","PMID:7531505","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to Thyroglobulin triiodothyronine","termid":"GO:1904016"}


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


id: PBO:0060401
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"N-6 adenine-specific DNA methyltransferase 1","termid":"PBO:0060401"}


id: PBO:0068335
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 43","termid":"PBO:0068335"}


id: SO:0002008
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant whereby at least one base of a codon encoding a rare amino acid is changed, resulting in a different encoded amino acid.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"non_conservative_missense_variant","termid":"SO:0001586"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"rare_amino_acid_variant","secondary_identifiers":["http://snpeff.sourceforge.net/SnpEff_manual.html"],"synonyms":[{"name":"Jannovar:rare_amino_acid_variant","type":"exact"},{"name":"rare amino acid variant","type":"exact"},{"name":"snpEff:RARE_AMINO_ACID","type":"exact"}],"termid":"SO:0002008"}


id: PBO:0068714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4atac small nuclear 3, pseudogene","termid":"PBO:0068714"}


id: FYPO:0006561
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the binding of one protein to a CDK-cyclin complex is normal (i.e. indistinguishable from wild type) during the G1 phase of the mitotic cell cycle. The protein whose binding to the CDK-cyclin complex is assayed may be encoded by the mutated gene, or may be encoded by a different gene.","definition_xrefs":["PMID:8521500","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein complex binding","termid":"FYPO:0005232"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000702"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000652","FYPO:0000702","FYPO:0000257"],"is_obsolete":false,"name":"normal CDK-cyclin complex binding during mitotic G1 phase","synonyms":[{"name":"normal CDK-cyclin complex binding during G1 phase during vegetative growth","type":"exact"},{"name":"normal CDK-cyclin complex binding during G1 phase of mitotic cell cycle","type":"exact"},{"name":"normal cyclin-CDK complex binding during mitotic G1 phase","type":"exact"}],"termid":"FYPO:0006561"}


id: GO:0018748
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: iprodione + OH- = 3,5-dichlorophenylcarboximide + N-isopropylcarbamate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete iprodione amidohydrolase activity (obsolete GO:0018748)","termid":"GO:0018748"}


id: PBO:0004897
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ku domain protein Pku80","termid":"PBO:0004897"}


id: PBO:0017592
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial F1-ATPase chaperone Atp12 (predicted)","termid":"PBO:0017592"}


id: PBO:0028207
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_punctate_nuclear_protein_localization_during_cellular_response_to_ionizing_radiation","termid":"PBO:0028207"}


id: PBO:0090526
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c oxidase assembly protein Coa4","termid":"PBO:0090526"}


id: GO:0140511
data:
  {"annotated_genes":["SJAG_00680"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[93317],"is_not":false,"summary":null,"term":"GO:0140511"}]},"cv_name":"cellular_component","definition":"Either of the regions of a mitotic nuclear bridge proximal to the main portion of each daughter nucleus. The nuclear envelope in the stalk regions is depleted of nuclear pore complexes.","definition_xrefs":["PMID:32848252"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"mitotic nuclear bridge","termid":"GO:0140510"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00680":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005634"}],"interesting_parent_ids":["GO:0005634","GO:0005575"],"is_obsolete":false,"name":"mitotic nuclear bridge stalk","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140511","terms_by_termid":{"GO:0140511":null}}


id: MONDO:0013053
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type is a rare syndrome with cardiac malformations, characterized by prenatal-onset growth retardation (low birth weight and short stature), hypotonia, developmental delay and intellectual disability associated with microcephaly and craniofacial (low anterior hairline, hypotelorism, thick lips with carp-shaped mouth, high-arched palate, low-set ears), cardiac (conotruncal heart malformations such as tetralogy of Fallot) and skeletal (hypoplastic thumbs and first metacarpals) abnormalities.","definition_xrefs":["Orphanet:217026"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type","secondary_identifiers":["OMIM:612946","MEDGEN:414129","SCTID:719395001","UMLS:C2751878","MESH:C567850","GARD:17116"],"synonyms":[{"name":"Hadziselimovic syndrome","type":"exact"},{"name":"microcephaly-faciocardioskeletal syndrome","type":"exact"}],"termid":"MONDO:0013053","xrefs":{"Monarch":{"xref_id":"0013053"}}}


id: PBO:0052642
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 8 pseudogene 10","termid":"PBO:0052642"}


id: GO:1904077
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of estrogen biosynthetic process.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:24530842"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of steroid biosynthetic process","termid":"GO:0010894"},{"relation_name":"is_a","term_name":"negative regulation of hormone biosynthetic process","termid":"GO:0032353"},{"relation_name":"is_a","term_name":"regulation of estrogen biosynthetic process","termid":"GO:1904076"},{"relation_name":"negatively_regulates","term_name":"estrogen biosynthetic process","termid":"GO:0006703"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"negative regulation of estrogen biosynthetic process","synonyms":[{"name":"down regulation of estrogen anabolism","type":"exact"},{"name":"down regulation of estrogen biosynthesis","type":"exact"},{"name":"down regulation of estrogen biosynthetic process","type":"exact"},{"name":"down regulation of estrogen formation","type":"exact"},{"name":"down regulation of estrogen synthesis","type":"exact"},{"name":"down regulation of oestrogen biosynthesis","type":"exact"},{"name":"down regulation of oestrogen biosynthetic process","type":"exact"},{"name":"down-regulation of estrogen anabolism","type":"exact"},{"name":"down-regulation of estrogen biosynthesis","type":"exact"},{"name":"down-regulation of estrogen biosynthetic process","type":"exact"},{"name":"down-regulation of estrogen formation","type":"exact"},{"name":"down-regulation of estrogen synthesis","type":"exact"},{"name":"down-regulation of oestrogen biosynthesis","type":"exact"},{"name":"down-regulation of oestrogen biosynthetic process","type":"exact"},{"name":"downregulation of estrogen anabolism","type":"exact"},{"name":"downregulation of estrogen biosynthesis","type":"exact"},{"name":"downregulation of estrogen biosynthetic process","type":"exact"},{"name":"downregulation of estrogen formation","type":"exact"},{"name":"downregulation of estrogen synthesis","type":"exact"},{"name":"downregulation of oestrogen biosynthesis","type":"exact"},{"name":"downregulation of oestrogen biosynthetic process","type":"exact"},{"name":"inhibition of estrogen anabolism","type":"narrow"},{"name":"inhibition of estrogen biosynthesis","type":"narrow"},{"name":"inhibition of estrogen biosynthetic process","type":"narrow"},{"name":"inhibition of estrogen formation","type":"narrow"},{"name":"inhibition of estrogen synthesis","type":"narrow"},{"name":"inhibition of oestrogen biosynthesis","type":"narrow"},{"name":"inhibition of oestrogen biosynthetic process","type":"narrow"},{"name":"negative regulation of estrogen anabolism","type":"exact"},{"name":"negative regulation of estrogen biosynthesis","type":"exact"},{"name":"negative regulation of estrogen formation","type":"exact"},{"name":"negative regulation of estrogen synthesis","type":"exact"},{"name":"negative regulation of oestrogen biosynthesis","type":"exact"},{"name":"negative regulation of oestrogen biosynthetic process","type":"exact"}],"termid":"GO:1904077"}


id: PBO:0077127
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TINAG antisense RNA 1","termid":"PBO:0077127"}


id: FYPO:0007646
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a vegetatively growing cell has one or more septa, and one nucleus that is not in the normal location. The cell also has one or more compartments with no nucleus.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"septated vegetative cell","termid":"FYPO:0002342"},{"relation_name":"is_a","term_name":"mononucleate vegetative cell with mislocalized nucleus","termid":"FYPO:0006339"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"septated mononucleate vegetative cell with mislocalized nucleus and anucleate compartment","synonyms":[{"name":"cytokinesis in the absence of nuclear division","type":"related"},{"name":"cytokinesis without nuclear division","type":"related"},{"name":"mononucleate septated vegetative cell with mislocalized nucleus","type":"exact"},{"name":"septated mononucleate cell","type":"exact"},{"name":"septated mononucleate cell with abnormal nucleus location","type":"exact"},{"name":"septated mononucleate cell with abnormal nucleus position","type":"exact"},{"name":"septated mononucleate cell with asymmetrically localized nucleus","type":"exact"},{"name":"septated mononucleate cell with displaced nucleus","type":"exact"},{"name":"septated mononucleate cell with mislocalised nucleus","type":"exact"},{"name":"septated mononucleate cell with mislocalized nucleus during vegetative growth","type":"exact"},{"name":"septated mononucleate cell with misplaced nucleus","type":"exact"},{"name":"septated mononucleate vegetative cell with mislocalized nucleus","type":"exact"},{"name":"septated mononucleate vegetative cell with mislocalized nucleus during mitotic cell cycle","type":"related"},{"name":"septated vegetative cell with mislocalized mononucleus","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:0007646"}


id: GO:0050809
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to diazepam, one of the most widely used benzodiazepine drugs. It is used as an anti-anxiety-hypnotic agent and has the proprietary name Valium.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"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":"diazepam binding","synonyms":[{"name":"Valium binding","type":"exact"},{"name":"diazepam binding inhibitor activity","type":"related"}],"termid":"GO:0050809"}


id: GO:0030317
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed, self-propelled movement of a cilium (aka flagellum) that contributes to the movement of a flagellated sperm.","definition_xrefs":["GO_REF:0000060","GOC:TermGenie","PMID:26680031","GOC:cilia","GOC:krc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cilium-dependent cell motility","termid":"GO:0060285"},{"relation_name":"is_a","term_name":"cilium movement involved in cell motility","termid":"GO:0060294"},{"relation_name":"is_a","term_name":"sperm motility","termid":"GO:0097722"}],"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":"flagellated sperm motility","secondary_identifiers":["Wikipedia:Sperm_motility","GO:0097724","GO:1905419"],"synonyms":[{"name":"flagellated sperm movement","type":"exact"},{"name":"sperm flagellum movement","type":"exact"},{"name":"sperm flagellum movement involved in flagellated sperm motility","type":"exact"},{"name":"sperm flagellum movement involved in flagellated sperm movement","type":"exact"},{"name":"sperm motility","type":"broad"},{"name":"sperm movement","type":"broad"}],"termid":"GO:0030317"}


id: PBO:0113156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HMG-CoA reductase; catalyzes conversion of HMG-CoA to mevalonate, which is a rate-limiting step in sterol biosynthesis; one of two isozymes; localizes to nuclear envelope; overproduction induces formation of karmellae; forms foci at nuclear periphery upon DNA replication stress; expressed almost exclusively on the peri-nuclear side of the ER; human homolog HMGCR can complement yeast hmg1 mutant","termid":"PBO:0113156"}


id: PBO:0069404
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 664, pseudogene","termid":"PBO:0069404"}


id: GO:0008146
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of a sulfate group from 3'-phosphoadenosine 5'-phosphosulfate to the hydroxyl group of an acceptor, producing the sulfated derivative and 3'-phosphoadenosine 5'-phosphate.","definition_xrefs":["EC:2.8.2.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transferase activity, transferring sulphur-containing groups","termid":"GO:0016782"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016782","GO:0003824"],"is_obsolete":false,"name":"sulfotransferase activity","secondary_identifiers":["Reactome:R-HSA-2022061","Reactome:R-HSA-176588","Reactome:R-HSA-176669","Reactome:R-HSA-9753277","Reactome:R-HSA-176604"],"synonyms":[{"name":"sulphotransferase activity","type":"exact"}],"termid":"GO:0008146"}


id: MONDO:0019578
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Nodular lichen myxedematosus is a rare form of localized lichen myxedematosus characterized by the development of skin-coloured mucinous nodules on the limbs and trunk, with mild or absent papular eruption.","definition_xrefs":["Orphanet:90393"],"direct_ancestors":[{"relation_name":"is_a","term_name":"localized lichen myxedematosus","termid":"MONDO:0019446"}],"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":"nodular lichen myxedematosus","secondary_identifiers":["MEDGEN:894327","GARD:19137","UMLS:C4273968","SCTID:717257000"],"synonyms":[{"name":"atypical tuberous myxedema of Jadassohn-Dosseker","type":"exact"}],"termid":"MONDO:0019578","xrefs":{"Monarch":{"xref_id":"0019578"}}}


id: GO:1904802
data:
  {"annotated_genes":["SJAG_00087"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[113799],"is_not":false,"summary":null,"term":"GO:1904802"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a RITS complex.","definition_xrefs":["GO_REF:0000079","GOC:TermGenie","PMID:26443059"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-RNA complex assembly","termid":"GO:0022618"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00087":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0065003"],"is_obsolete":false,"name":"RITS complex assembly","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"RITS complex formation","type":"exact"}],"termid":"GO:1904802","terms_by_termid":{"GO:1904802":null}}


id: PBO:0067879
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 181","termid":"PBO:0067879"}


id: FYPO:0002686
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of trehalose measured in a spore is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased cellular trehalose level","termid":"FYPO:0002685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular trehalose level in spore","synonyms":[{"name":"increased trehalose accumulation in spore","type":"related"}],"termid":"FYPO:0002686"}


id: PBO:0034720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIIH complex DNA helicase (ERCC-3) subunit Ptr8","termid":"PBO:0034720"}


id: GO:0160041
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The receptor ligand activity of any polypeptide expressed in, and secreted from a neuron.","definition_xrefs":["PMID:21922398","PMID:18806786"],"direct_ancestors":[{"relation_name":"is_a","term_name":"receptor ligand activity","termid":"GO:0048018"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0098772"}],"interesting_parent_ids":["GO:0003674","GO:0098772","GO:0005515","GO:0005488","GO:0140677"],"is_obsolete":false,"name":"neuropeptide activity","termid":"GO:0160041"}


id: FYPO:0006358
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which chromatin remodeling, i.e. any dynamic structural change to chromatin, does not occur when the cell is subject to glucose starvation.","definition_xrefs":["PMID:28674280","GO:0006338","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished cellular process","termid":"FYPO:0005449"},{"relation_name":"is_a","term_name":"abnormal chromatin remodeling","termid":"FYPO:0006356"}],"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:0000641"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000641","FYPO:0001985","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"abolished chromatin remodeling during glucose starvation","synonyms":[{"name":"abolished chromatin modeling during glucose starvation","type":"exact"},{"name":"abolished chromatin remodeling during glucose depletion","type":"exact"},{"name":"abolished chromatin remodeling during glucose deprivation","type":"related"},{"name":"abolished chromatin remodeling during glucose limitation","type":"related"},{"name":"abolished chromatin remodelling during glucose starvation","type":"exact"},{"name":"chromatin remodeling during glucose starvation abolished","type":"exact"}],"termid":"FYPO:0006358"}


id: GO:0018878
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving beta-1,2,3,4,5,6-hexachlorocyclohexane that occur in presence of oxygen.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-1,2,3,4,5,6-hexachlorocyclohexane metabolic process","termid":"GO:0018877"}],"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":"aerobic beta-1,2,3,4,5,6-hexachlorocyclohexane metabolic process","synonyms":[{"name":"aerobic beta-1,2,3,4,5,6-hexachlorocyclohexane metabolism","type":"exact"}],"termid":"GO:0018878"}


id: MOD:01509
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces the O4'-hydrogen atom of a tyrosine residue with the Applied Biosystems iTRAQ4plex-117 reporter+balance group.","definition_xrefs":["OMSSA:178","Unimod:214#Y","OMSSA:213","Unimod:889#Y"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"},{"relation_name":"is_a","term_name":"iTRAQ4plex-117, mTRAQ heavy, reporter+balance reagent acylated residue","termid":"MOD:01506"},{"relation_name":"is_a","term_name":"iTRAQ4plex reporter+balance reagent O-acylated residue","termid":"MOD:01713"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ4plex-117, mTRAQ heavy, reporter+balance reagent O4'-acylated tyrosine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"Applied Biosystems mTRAQ(TM) reagent","type":"related"},{"name":"Representative mass and accurate mass for 116 & 117","type":"related"},{"name":"iTRAQ","type":"related"},{"name":"iTRAQ117Y","type":"exact"},{"name":"iTRAQ4plex","type":"related"},{"name":"mTRAQ heavy","type":"related"},{"name":"mTRAQ heavy on Y","type":"exact"}],"termid":"MOD:01509"}


id: PBO:0011973
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by S. cerevisiae COQ2","termid":"PBO:0011973"}


id: PBO:0003977
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA snR5","termid":"PBO:0003977"}


id: FYPO:0003064
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which the size, shape, or structure of the microtubule cytoskeleton is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal microtubule cytoskeleton","termid":"FYPO:0002399"},{"relation_name":"is_a","term_name":"abnormal cytoskeleton morphology","termid":"FYPO:0003063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002399"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0002399"],"is_obsolete":false,"name":"abnormal microtubule cytoskeleton morphology","termid":"FYPO:0003064"}


id: MONDO:0026170
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete genetic central nervous system malformation (obsolete MONDO:0026170)","secondary_identifiers":["Orphanet:183506"],"termid":"MONDO:0026170","xrefs":{"Monarch":{"xref_id":"0026170"}}}


id: SO:0002235
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A polypeptide region that mediates binding to SUMO. The motif contains a hydrophobic core sequence consisting of three or four Ile, Leu, or Val residues plus one acidic or polar residue at position 2 or 3.","definition_xrefs":["PMID:15388847,PMID:16524884"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein_protein_contact","termid":"SO:0001093"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"SO:0000839"}],"interesting_parent_ids":["SO:0000839"],"is_obsolete":false,"name":"SUMO_interaction_motif","synonyms":[{"name":"SBM","type":"exact"},{"name":"SIM","type":"exact"},{"name":"SUMO binding motif","type":"exact"},{"name":"SUMO interaction motif","type":"exact"}],"termid":"SO:0002235"}


id: PBO:0068742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U5B small nuclear 5, pseudogene","termid":"PBO:0068742"}


id: PBO:0003851
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ACN9 family protein (predicted)","termid":"PBO:0003851"}


id: PBO:0000727
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial anion transporter (predicted)","termid":"PBO:0000727"}


id: PBO:0083961
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"General transcriptional co-repressor; acts together with Tup1p; also acts as part of a transcriptional co-activator complex that recruits the SWI/SNF and SAGA complexes to promoters; can form the prion [OCT+]","termid":"PBO:0083961"}


id: MONDO:0019551
data:
  {"annotated_genes":["SJAG_00252","SJAG_01383","SJAG_00031"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85985],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011002"},{"annotations":[86444,86445],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032792"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete autosomal dominant hereditary axonal motor and sensory neuropathy (obsolete MONDO:0015360)","termid":"MONDO:0015360"},{"relation_name":"is_a","term_name":"hereditary motor and sensory neuropathy","termid":"MONDO:0015358"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00031":null,"SJAG_00252":null,"SJAG_01383":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"hereditary motor and sensory neuropathy type 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0080068","GARD:16787","icd11.foundation:467894833","Orphanet:90120","UMLS:C0393807","MEDGEN:140747"],"synonyms":[{"name":"CMT6","type":"exact"},{"name":"Charcot-Marie-Tooth disease type 6","type":"exact"},{"name":"hereditary motor and sensory neuropathy type 6","type":"exact"},{"name":"peripheral neuropathy and optic atrophy","type":"exact"}],"termid":"MONDO:0019551","terms_by_termid":{"MONDO:0011002":null,"MONDO:0032792":null},"xrefs":{"Monarch":{"xref_id":"0019551"}}}


id: GO:0000080
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle 'gap' phase which is the interval between the completion of DNA segregation by mitosis and the beginning of DNA synthesis.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G1 phase","termid":"GO:0051318"},{"relation_name":"part_of","term_name":"mitotic interphase","termid":"GO:0051329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0051329"}],"interesting_parent_ids":["GO:0051329","GO:0008150"],"is_obsolete":false,"name":"mitotic G1 phase","secondary_identifiers":["Reactome:R-HSA-69236"],"synonyms":[{"name":"G1 phase of mitotic cell cycle","type":"exact"}],"termid":"GO:0000080"}


id: PBO:0051375
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 3/OR2-268 (non-functional)","termid":"PBO:0051375"}


id: GO:2000063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of ureter smooth muscle cell differentiation.","definition_xrefs":["GOC:mtg_kidney_jan10","GOC:obol","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of smooth muscle cell differentiation","termid":"GO:0051152"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of ureter smooth muscle cell differentiation","termid":"GO:2000061"},{"relation_name":"positively_regulates","term_name":"ureter smooth muscle cell differentiation","termid":"GO:0072193"}],"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 ureter smooth muscle cell differentiation","termid":"GO:2000063"}


id: PBO:0084312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Isopentenyl diphosphate:dimethylallyl diphosphate isomerase; catalyzes an essential activation step in the isoprenoid biosynthetic pathway; required for viability; isopentenyl diphosphate:dimethylallyl diphosphate isomerase is also known as IPP isomerase","termid":"PBO:0084312"}


id: FYPO:0004475
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 initiation of nuclear DNA replication is decreased. Initiation may be affected at one or more origins.","definition_xrefs":["PomBase:mah","PMID:22970243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic DNA replication initiation","termid":"FYPO:0001344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0005447","FYPO:0000002","FYPO:0000293","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"decreased mitotic DNA replication initiation","synonyms":[{"name":"decreased DNA replication initiation during mitotic cell cycle","type":"exact"},{"name":"decreased DNA replication initiation during vegetative growth","type":"exact"},{"name":"reduced mitotic DNA replication initiation","type":"exact"}],"termid":"FYPO:0004475"}


id: PBO:0090760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rab GAP Gyp1","termid":"PBO:0090760"}


id: GO:0006927
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any apoptotic process in a transformed cell, a cell that has undergone changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm.","definition_xrefs":["GOC:jl","GOC:mtg_apoptosis"],"gene_count":0,"genotype_count":0,"name":"obsolete transformed cell apoptotic process (obsolete GO:0006927)","synonyms":[{"name":"apoptosis of transformed cells","type":"exact"},{"name":"killing transformed cells","type":"exact"},{"name":"programmed cell death of transformed cells by apoptosis","type":"exact"},{"name":"programmed cell death, transformed cells","type":"exact"},{"name":"transformed cell apoptosis","type":"narrow"},{"name":"transformed cell programmed cell death by apoptosis","type":"exact"}],"termid":"GO:0006927"}


id: MONDO:0011137
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinitis pigmentosa in which the cause of the disease is a mutation in the ABCA4 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"},{"relation_name":"is_a","term_name":"ABCA4-related retinopathy","termid":"MONDO:0800406"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004736","MONDO:0005066"],"is_obsolete":false,"name":"retinitis pigmentosa 19","secondary_identifiers":["ICD10CM:H35.5","UMLS:C1866422","GARD:10398","MEDGEN:400996","DOID:0110354","MESH:C566637","OMIM:601718"],"synonyms":[{"name":"ABCA4 retinitis pigmentosa","type":"exact"},{"name":"RP 19","type":"related"},{"name":"RP19","type":"exact"},{"name":"retinitis pigmentosa 19","type":"exact"},{"name":"retinitis pigmentosa caused by mutation in ABCA4","type":"exact"},{"name":"retinitis pigmentosa type 19","type":"exact"}],"termid":"MONDO:0011137","xrefs":{"Monarch":{"xref_id":"0011137"}}}


id: PATO:0001179
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0001179 immune (obsolete PATO:0001179)","termid":"PATO:0001179"}


id: GO:0035157
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that restricts, stops or prevents a cell from adopting a fusion cell fate. Once the terminal and fusion fates have been correctly induced, inhibitory feedback loops prevent the remaining branch cells from assuming similar fates.","definition_xrefs":["PMID:10684581"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell fate specification","termid":"GO:0009996"},{"relation_name":"is_a","term_name":"negative regulation of multicellular organismal process","termid":"GO:0051241"},{"relation_name":"negatively_regulates","term_name":"fusion cell fate specification","termid":"GO:0035156"}],"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 fusion cell fate specification","synonyms":[{"name":"down regulation of fusion cell fate specification","type":"exact"},{"name":"down-regulation of fusion cell fate specification","type":"exact"},{"name":"downregulation of fusion cell fate specification","type":"exact"},{"name":"inhibition of fusion cell fate specification","type":"narrow"}],"termid":"GO:0035157"}


id: PBO:0079507
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin pseudogene 5","termid":"PBO:0079507"}


id: GO:0002861
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of an inflammatory response to an antigenic stimulus.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of inflammatory response","termid":"GO:0050727"},{"relation_name":"is_a","term_name":"regulation of immune response","termid":"GO:0050776"},{"relation_name":"regulates","term_name":"inflammatory response to antigenic stimulus","termid":"GO:0002437"}],"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 inflammatory response to antigenic stimulus","termid":"GO:0002861"}


id: MONDO:0007872
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A multiple congenital anomaly syndrome characterized by hypoplasia, aplasia or atresia of the lacrimal system; anomalies of the ears and hearing loss; hypoplasias, apalsias or atresias of the salivary glands; dental anomalies and digital malformations.","definition_xrefs":["Orphanet:2363"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete nose and cavum anomaly (obsolete MONDO:0015503)","termid":"MONDO:0015503"},{"relation_name":"excluded_subClassOf","term_name":"obsolete hereditary otorhinolaryngological malformation (obsolete MONDO:0018562)","termid":"MONDO:0018562"},{"relation_name":"excluded_subClassOf","term_name":"obsolete EEC syndrome and related syndrome (obsolete MONDO:0020197)","termid":"MONDO:0020197"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"polydactyly-syndactyly-triphalangism","termid":"MONDO:0800066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"LADD syndrome","secondary_identifiers":["SCTID:23817003","DOID:0081370","MEDGEN:78545","MESH:C538132","NORD:1345","OMIMPS:149730","DOID:0050331","UMLS:C0265269","ICD9:759.89","GARD:6848"],"synonyms":[{"name":"LACRIMOAURICULODENTODIGITAL syndrome","type":"exact"},{"name":"LADD","type":"related"},{"name":"LADD syndrome","type":"exact"},{"name":"Lacrimo-auriculo-dento-digital syndrome","type":"exact"},{"name":"Lacrimoauriculodento-digital syndrome","type":"exact"},{"name":"Lacrimoauriculoradiodental syndrome","type":"exact"},{"name":"Levy Hollister syndrome","type":"exact"},{"name":"Levy-Hollister syndrome","type":"exact"},{"name":"lacrimoauriculodentodigital syndrome","type":"exact"},{"name":"lard syndrome","type":"exact"}],"termid":"MONDO:0007872","xrefs":{"Monarch":{"xref_id":"0007872"}}}


id: GO:1901891
data:
  {"annotated_genes":["SJAG_01188","SJAG_00526","SJAG_02645","SJAG_01386","SJAG_00514","SJAG_04468","SJAG_04666","SJAG_01805","SJAG_04776","SJAG_03508","SJAG_03342","SJAG_00082","SJAG_03704","SJAG_03936","SJAG_02514","SJAG_04943","SJAG_03048","SJAG_04455","SJAG_04597","SJAG_04509","SJAG_05290","SJAG_01464","SJAG_03353","SJAG_03631","SJAG_03581","SJAG_02169","SJAG_06270","SJAG_01114","SJAG_01790","SJAG_03681","SJAG_00229","SJAG_00883","SJAG_03592"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99167],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010974"},{"annotations":[101874],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905757"},{"annotations":[90208,92940,109662,106725,115400,95126,91216,106586,107030,92407,100773,104530,99169,92323,99091],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031030"},{"annotations":[117392,91902,88717,105874,112856,114967,89345,104673,106535,93286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140281"},{"annotations":[87013,93900,91903],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905758"},{"annotations":[101888,93290,87014,89478,110015],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031031"},{"annotations":[77728,87372,89347,94067,91907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032955"},{"annotations":[117394],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140279"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cell septum assembly.","definition_xrefs":["GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokinetic process","termid":"GO:0032954"},{"relation_name":"is_a","term_name":"regulation of cellular component biogenesis","termid":"GO:0044087"},{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"cell septum assembly","termid":"GO:0090529"}],"gene_count":33,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00229":null,"SJAG_00514":null,"SJAG_00526":null,"SJAG_00883":null,"SJAG_01114":null,"SJAG_01188":null,"SJAG_01386":null,"SJAG_01464":null,"SJAG_01790":null,"SJAG_01805":null,"SJAG_02169":null,"SJAG_02514":null,"SJAG_02645":null,"SJAG_03048":null,"SJAG_03342":null,"SJAG_03353":null,"SJAG_03508":null,"SJAG_03581":null,"SJAG_03592":null,"SJAG_03631":null,"SJAG_03681":null,"SJAG_03704":null,"SJAG_03936":null,"SJAG_04455":null,"SJAG_04468":null,"SJAG_04509":null,"SJAG_04597":null,"SJAG_04666":null,"SJAG_04776":null,"SJAG_04943":null,"SJAG_05290":null,"SJAG_06270":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"regulates","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0044085","GO:0007049","GO:0008150"],"is_obsolete":false,"name":"regulation of cell septum assembly","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:1901891","terms_by_termid":{"GO:0010974":null,"GO:0031030":null,"GO:0031031":null,"GO:0032955":null,"GO:0140279":null,"GO:0140281":null,"GO:1905757":null,"GO:1905758":null}}


id: PBO:0002192
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ShuGOshin","termid":"PBO:0002192"}


id: PBO:0068716
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U4atac small nuclear 5, pseudogene","termid":"PBO:0068716"}


id: MONDO:0000560
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete spinocerebellar ataxia type 4 (obsolete MONDO:0000560)","termid":"MONDO:0000560","xrefs":{"Monarch":{"xref_id":"0000560"}}}


id: GO:0030129
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A clathrin coat found on a synaptic vesicle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"clathrin vesicle coat","termid":"GO:0030125"},{"relation_name":"part_of","term_name":"synaptic vesicle membrane","termid":"GO:0030672"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0031410"},{"rel_name":"part_of","termid":"GO:0005737"}],"interesting_parent_ids":["GO:0032991","GO:0005575","GO:0031410","GO:0005737"],"is_obsolete":false,"name":"clathrin coat of synaptic vesicle","termid":"GO:0030129"}


id: MONDO:0014302
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive spastic paraplegia type 62 is a pure or complex form of hereditary spastic paraplegia characterized by an onset in the first decade of life of spastic paraperesis (more prominent in lower than upper extremities) and unsteady gait, as well as increased deep tendon reflexes, amyotrophy, cerebellar ataxia, and flexion contractures of the knees, in some.","definition_xrefs":["Orphanet:401785"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pure hereditary spastic paraplegia","termid":"MONDO:0015149"}],"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":"hereditary spastic paraplegia 62","secondary_identifiers":["MEDGEN:924879","GARD:17657","OMIM:615681","SCTID:765045003","UMLS:C4284588","DOID:0110813"],"synonyms":[{"name":"ERLIN1 autosomal recessive pure spastic paraplegia","type":"exact"},{"name":"SPG62","type":"exact"},{"name":"autosomal recessive pure spastic paraplegia caused by mutation in ERLIN1","type":"exact"},{"name":"autosomal recessive spastic paraplegia 62","type":"exact"},{"name":"autosomal recessive spastic paraplegia type 62","type":"exact"},{"name":"hereditary spastic paraplegia type 62","type":"exact"},{"name":"spastic paraplegia 62, autosomal recessive","type":"exact"}],"termid":"MONDO:0014302","xrefs":{"Monarch":{"xref_id":"0014302"}}}


id: GO:0032674
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-5 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-5 production","termid":"GO:0032634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of interleukin-5 production","secondary_identifiers":["GO:0045405","GO:2000662"],"synonyms":[{"name":"regulation of IL-5 production","type":"exact"},{"name":"regulation of interleukin-5 biosynthetic process","type":"narrow"},{"name":"regulation of interleukin-5 secretion","type":"narrow"}],"termid":"GO:0032674"}


id: MONDO:0018208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"neurofibromatosis type 1","termid":"MONDO:0018975"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"neurofibromatosis type 1 due to NF1 mutation or intragenic deletion","secondary_identifiers":["Orphanet:363700","GARD:17570","MEDGEN:1842855","UMLS:C5779636"],"synonyms":[{"name":"Von Recklinghausen disease due to NF1 mutation or intragenic deletion","type":"exact"}],"termid":"MONDO:0018208","xrefs":{"Monarch":{"xref_id":"0018208"}}}


id: MONDO:0004605
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"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":"chronic ulcer of skin","secondary_identifiers":["ICD9:707.9","ICD9:707.8","DOID:8549","MEDGEN:510410","SCTID:19429009","ICD9:707","UMLS:C0157738"],"synonyms":[{"name":"callous ulcer","type":"exact"},{"name":"callous ulcer (morphologic abnormality)","type":"exact"},{"name":"indolent ulcer","type":"exact"},{"name":"indolent ulcer (morphologic abnormality)","type":"exact"}],"termid":"MONDO:0004605","xrefs":{"Monarch":{"xref_id":"0004605"}}}


id: GO:0071541
data:
  {"annotated_genes":["SJAG_04891","SJAG_04744","SJAG_02164","SJAG_04900","SJAG_02995","SJAG_03472","SJAG_03147","SJAG_02628","SJAG_04981"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[89417,94273,96341,97221,97280,98429,104812,105099,110187],"is_not":false,"summary":null,"term":"GO:0071541"}]},"cv_name":"cellular_component","definition":"An eukaryotic translation initiation factor 3 complex that contains the PCI-domain protein eIF3m.","definition_xrefs":["PMID:19061185","PMID:15904532"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eukaryotic translation initiation factor 3 complex","termid":"GO:0005852"}],"gene_count":9,"genes_by_uniquename":{"SJAG_02164":null,"SJAG_02628":null,"SJAG_02995":null,"SJAG_03147":null,"SJAG_03472":null,"SJAG_04744":null,"SJAG_04891":null,"SJAG_04900":null,"SJAG_04981":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"eukaryotic translation initiation factor 3 complex, eIF3m","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"eIF3m-containing eukaryotic translation initiation factor 3 complex","type":"exact"}],"termid":"GO:0071541","terms_by_termid":{"GO:0071541":null}}


id: PBO:0082798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of transport protein particle (TRAPP) complex II; TRAPPII is a multimeric guanine nucleotide-exchange factor for the GTPase Ypt1p, regulating intra-Golgi and endosome-Golgi traffic","termid":"PBO:0082798"}


id: PBO:0087080
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ribosomal 60S subunit protein L41B; comprises only 25 amino acids; rpl41a rpl41b double null mutant is viable; homologous to mammalian ribosomal protein L41, no bacterial homolog; RPL41B has a paralog, RPL41A, that arose from the whole genome duplication","termid":"PBO:0087080"}


id: FYPO:0003306
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population phenotype in which the mitotic index is lower than normal. The mitotic index is the proportion of the population undergoing mitosis at any given time.","definition_xrefs":["PomBase:mah","PMID:22684255","PMID:11683392"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell population phenotype","termid":"FYPO:0000003"},{"relation_name":"is_a","term_name":"abnormal phenotype","termid":"FYPO:0001985"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"decreased mitotic index","synonyms":[{"name":"reduced mitotic index","type":"exact"}],"termid":"FYPO:0003306"}


id: FYPO:0002367
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which dimethylation of lysine at position 4 of histone H3 occurs to a lower extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased histone H3-K4 methylation during vegetative growth","termid":"FYPO:0002366"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0002274","FYPO:0002494","FYPO:0005447","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"decreased histone H3-K4 dimethylation during vegetative growth","synonyms":[{"name":"decreased histone H3 K4 dimethylation during vegetative growth","type":"exact"},{"name":"decreased histone H3-K4 dimethylation during mitotic cell cycle","type":"related"},{"name":"decreased histone H3K4 dimethylation during vegetative growth","type":"exact"},{"name":"decreased histone H3K4me2 during vegetative growth","type":"exact"},{"name":"decreased histone lysine H3 K4 dimethylation during vegetative growth","type":"exact"},{"name":"reduced histone H3-K4 dimethylation during vegetative growth","type":"exact"}],"termid":"FYPO:0002367"}


id: FYPO:0003803
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 telomere of a chromosome is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to chromosome during vegetative growth","termid":"FYPO:0002839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein localization to telomere","synonyms":[{"name":"decreased protein localisation to telomere","type":"exact"},{"name":"decreased protein localization to chromosome, telomeric region","type":"exact"},{"name":"decreased protein localization to telomere during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to telomere during vegetative growth","type":"exact"},{"name":"decreased protein localization to telomeric region","type":"exact"},{"name":"reduced protein localization to telomere","type":"exact"}],"termid":"FYPO:0003803"}


id: PBO:0050158
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 14","termid":"PBO:0050158"}


id: PBO:0060759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase subunit B4 pseudogene 3","termid":"PBO:0060759"}


id: SO:0001928
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A duplication of the distal region of a chromosome.","definition_xrefs":["SO:bm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"duplication","termid":"SO:1000035"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal_duplication","synonyms":[{"name":"distal duplication","type":"exact"}],"termid":"SO:0001928"}


id: MONDO:0009911
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":"prolactin deficiency, isolated","secondary_identifiers":["MESH:C562708","MEDGEN:75758","OMIM:264110","SCTID:67873006","UMLS:C0271586","ICD9:253.4"],"synonyms":[{"name":"prolactin deficiency, isolated","type":"exact"}],"termid":"MONDO:0009911","xrefs":{"Monarch":{"xref_id":"0009911"}}}


id: PBO:0061638
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nudix hydrolase 16 like 2, pseudogene","termid":"PBO:0061638"}


id: RO:HOM0000048
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Orthology that involves two genes that experienced duplications more recent than the species split that created them.","direct_ancestors":[{"relation_name":"is_a","term_name":"in_orthology_relationship_with","termid":"RO:HOM0000017"},{"relation_name":"is_a","term_name":"in_many_to_many_homology_relationship_with","termid":"RO:HOM0000036"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_many_to_many_orthology_relationship_with","synonyms":[{"name":"co-orthology","type":"related"},{"name":"many to many orthologous to","type":"exact"},{"name":"many-to-many orthology","type":"exact"},{"name":"many:many orthology","type":"exact"},{"name":"trans-homology","type":"related"},{"name":"trans-orthology","type":"exact"}],"termid":"RO:HOM0000048"}


id: PR:O94250
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC13B11.03c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94250"],"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":"hydroxyacylglutathione hydrolase C13B11.03c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC13B11.03c","synonyms":[{"name":"Glx II (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPCC13B11.03c","type":"exact"},{"name":"glyoxalase II (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94250"}


id: MONDO:0003329
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Blockage in any part of the ureter causing obstruction of urine flow from the kidney to the urinary bladder. The obstruction may be congenital, acquired, unilateral, bilateral, complete, partial, acute, or chronic. Depending on the degree and duration of the obstruction, clinical features vary greatly such as hydronephrosis and obstructive nephropathy.","definition_xrefs":["MESH:D014517"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ureteral disorder","termid":"MONDO:0001926"},{"relation_name":"is_a","term_name":"urinary tract obstruction","termid":"MONDO:0003330"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ureteral obstruction","secondary_identifiers":["ICD9:593.4","SCTID:20018005","DOID:5199","MEDGEN:12012","HP:0006000","UMLS:C0041956"],"synonyms":[{"name":"ureteral obstruction","type":"exact"},{"name":"ureteral obstruction (disease)","type":"exact"}],"termid":"MONDO:0003329","xrefs":{"Monarch":{"xref_id":"0003329"}}}


id: MONDO:0016773
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Atrophic lichen planus (LP) is a rare variant of cutaneous lichen planus characterized by the development of pale papules or plaques with an atrophic center.","definition_xrefs":["Orphanet:254449"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lichen planus","termid":"MONDO:0006572"}],"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":"atrophic lichen planus","secondary_identifiers":["UMLS:C0023647","GARD:12675","icd11.foundation:1633911307","MedDRA:10056959","MEDGEN:9754","NCIT:C34777","SCTID:25858008"],"synonyms":[{"name":"atrophic LP","type":"exact"}],"termid":"MONDO:0016773","xrefs":{"Monarch":{"xref_id":"0016773"}}}


id: PBO:0064339
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDX1 associated lncRNA, upregulator of transcription","termid":"PBO:0064339"}


id: PR:O13880
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- vht1 gene.","definition_xrefs":["UniProtKB:O13880","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":"vitamin H transporter 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1B3.16c","synonyms":[{"name":"H(+)/biotin symporter vht1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-vht1","type":"exact"}],"termid":"PR:O13880"}


id: PBO:0065329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine protease 53","termid":"PBO:0065329"}


id: PBO:0048522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycerophosphodiester phosphodiesterase domain containing 5","termid":"PBO:0048522"}


id: GO:1904378
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Maintaining an endoplasmic reticulum (ER) protein in an unfolded, soluble state that contributes to its degradation by the cytoplasmic proteasome. Maintaining ER-resident proteins in an unfolded yet soluble state condition after their retro-translocation favors their turnover by the cytosolic proteasome.","definition_xrefs":["GO_REF:0000060","GOC:nc","GOC:TermGenie","GOC:PARL","GOC:BHF","GOC:bf","PMID:21636303"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maintenance of unfolded protein","termid":"GO:0036506"},{"relation_name":"part_of","term_name":"ERAD pathway","termid":"GO:0036503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0030163"}],"interesting_parent_ids":["GO:0008150","GO:0030163"],"is_obsolete":false,"name":"maintenance of unfolded protein involved in ERAD pathway","synonyms":[{"name":"ERAD chaperone-like activity","type":"related"},{"name":"chaperone holdase activity","type":"related"},{"name":"holdase activity","type":"related"},{"name":"maintenance of unfolded protein during ERAD","type":"related"},{"name":"maintenance of unfolded protein involved in ER-associated degradation pathway","type":"related"},{"name":"maintenance of unfolded protein involved in endoplasmic reticulum-associated degradation","type":"exact"},{"name":"maintenance of unfolded protein involved in endoplasmic reticulum-associated protein degradation pathway","type":"related"}],"termid":"GO:1904378"}


id: MONDO:0018600
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"nuclear oculomotor paralysis","termid":"MONDO:0015083"}],"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":"congenital abducens nerve palsy","secondary_identifiers":["MEDGEN:724505","Orphanet:440233","GARD:21837","UMLS:C1302994"],"synonyms":[{"name":"benign congenital sixth cranial nerve palsy","type":"exact"},{"name":"congenital CNVI palsy","type":"exact"}],"termid":"MONDO:0018600","xrefs":{"Monarch":{"xref_id":"0018600"}}}


id: GO:0009374
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to biotin (cis-tetrahydro-2-oxothieno(3,4-d)imidazoline-4-valeric acid), the (+) enantiomer of which is very widely distributed in cells and serves as a carrier in a number of enzymatic beta-carboxylation reactions.","definition_xrefs":["GOC:jl","ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitamin binding","termid":"GO:0019842"},{"relation_name":"is_a","term_name":"amide binding","termid":"GO:0033218"},{"relation_name":"is_a","term_name":"monocarboxylic acid binding","termid":"GO:0033293"},{"relation_name":"is_a","term_name":"heterocyclic compound binding","termid":"GO:1901363"},{"relation_name":"is_a","term_name":"sulfur compound binding","termid":"GO:1901681"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"biotin binding","synonyms":[{"name":"vitamin B7 binding","type":"exact"},{"name":"vitamin H binding","type":"exact"}],"termid":"GO:0009374"}


id: PBO:0069604
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 881, pseudogene","termid":"PBO:0069604"}


id: FYPO:0003712
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells contain more Skb1-containing lateral cortical nodes than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"lateral cortical nodes present in increased numbers","synonyms":[{"name":"Skb1-containing cortical nodes present in increased numbers","type":"exact"},{"name":"additional lateral cortical nodes present during vegetative growth","type":"exact"},{"name":"extra lateral cortical nodes during vegetative growth","type":"exact"},{"name":"lateral cortical nodes present in greater numbers","type":"exact"},{"name":"lateral cortical nodes present in increased numbers during mitotic cell cycle","type":"related"},{"name":"lateral cortical nodes present in increased numbers during vegetative growth","type":"exact"}],"termid":"FYPO:0003712"}


id: PBO:0058471
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5579","termid":"PBO:0058471"}


id: PBO:0050358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1 pseudogene 61","termid":"PBO:0050358"}


id: PBO:0031408
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-pear-shaped_cell","termid":"PBO:0031408"}


id: PBO:0026818
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_punctate_nuclear_protein_localization","termid":"PBO:0026818"}


id: PBO:0070868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPL14 pseudogene 6","termid":"PBO:0070868"}


id: GO:0047937
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 D-glucose 1-phosphate = D-glucose + D-glucose 1,6-bisphosphate.","definition_xrefs":["EC:2.7.1.41","MetaCyc:GLUCOSE-1-PHOSPHATE-PHOSPHODISMUTASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"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:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016301","GO:0003674","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"glucose-1-phosphate phosphodismutase activity","secondary_identifiers":["RHEA:16397"],"synonyms":[{"name":"D-glucose-1-phosphate:D-glucose-1-phosphate 6-phosphotransferase activity","type":"related"},{"name":"glucose 1-phosphate transphosphorylase activity","type":"related"},{"name":"phosphodismutase activity","type":"related"}],"termid":"GO:0047937"}


id: PBO:0045303
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNM3 opposite strand/antisense RNA","termid":"PBO:0045303"}


id: PBO:0077177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"toll like receptor 1","termid":"PBO:0077177"}


id: GO:0005105
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 1 fibroblast growth factor receptor (FGFR1).","definition_xrefs":["GOC:fb_curators","GOC:ceb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroblast growth factor receptor binding","termid":"GO:0005104"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"type 1 fibroblast growth factor receptor binding","synonyms":[{"name":"FGFR1 binding","type":"broad"},{"name":"FGFR1 ligand","type":"narrow"},{"name":"breathless binding","type":"narrow"},{"name":"breathless ligand","type":"narrow"},{"name":"type 1 fibroblast growth factor receptor ligand","type":"narrow"}],"termid":"GO:0005105"}


id: PBO:0031409
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-elongated_cell","termid":"PBO:0031409"}


id: MONDO:0002320
data:
  {"annotated_genes":["SJAG_02509","SJAG_04825","SJAG_02160","SJAG_02163","SJAG_01465","SJAG_04887","SJAG_03025","SJAG_01360","SJAG_03418","SJAG_03672","SJAG_02623","SJAG_02774","SJAG_03712","SJAG_02289","SJAG_04425","SJAG_04881","SJAG_04728","SJAG_03698","SJAG_05327","SJAG_04074","SJAG_03703","SJAG_05313","SJAG_00742","SJAG_02791","SJAG_04156","SJAG_04042","SJAG_01507","SJAG_04821","SJAG_01825","SJAG_03970","SJAG_02523","SJAG_03106","SJAG_03635","SJAG_03286","SJAG_03664","SJAG_03067","SJAG_00853","SJAG_00312","SJAG_00185","SJAG_03145","SJAG_03311","SJAG_00112","SJAG_00924","SJAG_00804","SJAG_04003","SJAG_01712","SJAG_01872","SJAG_06022","SJAG_04600","SJAG_04938","SJAG_00992","SJAG_01410","SJAG_02658","SJAG_02824","SJAG_00321","SJAG_04387","SJAG_04183","SJAG_04816","SJAG_00826","SJAG_04537","SJAG_04119","SJAG_02470","SJAG_00831","SJAG_02431","SJAG_01491","SJAG_02362","SJAG_02103","SJAG_02317","SJAG_03353","SJAG_03188","SJAG_01466","SJAG_03056","SJAG_00156","SJAG_02313","SJAG_00379","SJAG_04822","SJAG_01025","SJAG_04665","SJAG_01286","SJAG_04980","SJAG_03681","SJAG_01253","SJAG_04316","SJAG_04459","SJAG_02096","SJAG_02165","SJAG_00964","SJAG_00106","SJAG_00885","SJAG_04681","SJAG_03066","SJAG_01298","SJAG_05219","SJAG_05229","SJAG_02050","SJAG_03379","SJAG_04053","SJAG_03597","SJAG_04755","SJAG_02723","SJAG_00773","SJAG_02194","SJAG_03120","SJAG_05245","SJAG_01540","SJAG_02889","SJAG_01918","SJAG_01926","SJAG_04619","SJAG_02913"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86089],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012099"},{"annotations":[84504],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014700"},{"annotations":[84922],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014558"},{"annotations":[84685],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012248"},{"annotations":[86154,86153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013162"},{"annotations":[85435],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014142"},{"annotations":[84766],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014601"},{"annotations":[85945],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013812"},{"annotations":[84970],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012986"},{"annotations":[86410],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010477"},{"annotations":[84884],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014529"},{"annotations":[86353],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0015026"},{"annotations":[86048],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957264"},{"annotations":[84753],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044701"},{"annotations":[84971],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012399"},{"annotations":[86272],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011402"},{"annotations":[84777],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014023"},{"annotations":[85619],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014896"},{"annotations":[85464],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012518"},{"annotations":[85656],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013883"},{"annotations":[84899],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014543"},{"annotations":[84896],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014542"},{"annotations":[84738],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014590"},{"annotations":[85524],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012157"},{"annotations":[84776],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008070"},{"annotations":[84825],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0800341"},{"annotations":[84650],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012239"},{"annotations":[85371,85370],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008409"},{"annotations":[86369],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010472"},{"annotations":[84604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014647"},{"annotations":[84921],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033364"},{"annotations":[85603],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0034106"},{"annotations":[86468],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032808"},{"annotations":[86491],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032822"},{"annotations":[84649],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013049"},{"annotations":[85411],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013578"},{"annotations":[86679],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044646"},{"annotations":[86660,86661],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008675"},{"annotations":[86744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030669"},{"annotations":[84572],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0040500"},{"annotations":[84762,84763],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014602"},{"annotations":[86438],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032787"},{"annotations":[85382,85381],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0026763"},{"annotations":[86479],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030886"},{"annotations":[85404],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024567"},{"annotations":[86505],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010532"},{"annotations":[86195],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044319"},{"annotations":[84870,84869],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030912"},{"annotations":[85093],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014832"},{"annotations":[85720,85721],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011053"},{"annotations":[86688],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008939"},{"annotations":[85326,85327],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009479"},{"annotations":[86395],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013454"},{"annotations":[84937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012990"},{"annotations":[86448],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032794"},{"annotations":[85115],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012056"},{"annotations":[84593],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060650"},{"annotations":[84913],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014552"},{"annotations":[84751],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014596"},{"annotations":[84647,84648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012703"},{"annotations":[85500,85499],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014716"},{"annotations":[85836],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011246"},{"annotations":[85011],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0054593"},{"annotations":[85915],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013790"},{"annotations":[84618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014062"},{"annotations":[86382],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010466"},{"annotations":[85246,85247],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009682"},{"annotations":[85340,85341,85342],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009364"},{"annotations":[85428],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014140"},{"annotations":[86147,86148],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013154"},{"annotations":[84737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0033556"},{"annotations":[86152],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013159"},{"annotations":[85433],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014141"},{"annotations":[86150,86151],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013160"},{"annotations":[85765],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032596"},{"annotations":[84747,84748],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008050"},{"annotations":[84964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009709"},{"annotations":[86210],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009725"},{"annotations":[85355],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012538"},{"annotations":[84968],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009736"},{"annotations":[86365],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014466"},{"annotations":[86841,86843,86839,86840,86837,86838,86842],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011120"},{"annotations":[84892],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030037"},{"annotations":[85013],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0060502"},{"annotations":[84529,84530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011966"},{"annotations":[86458,86457,86459],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014966"},{"annotations":[85760],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032588"},{"annotations":[85030],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011213"},{"annotations":[84586],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014679"},{"annotations":[86020],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024528"},{"annotations":[84651],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012238"},{"annotations":[85022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013117"},{"annotations":[85835],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009783"},{"annotations":[84613],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014656"},{"annotations":[85906],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020845"},{"annotations":[85548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0957993"},{"annotations":[85286],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014800"},{"annotations":[86244],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013468"},{"annotations":[85920],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011835"},{"annotations":[85530],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030482"},{"annotations":[85297],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014806"},{"annotations":[85296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014807"},{"annotations":[85067],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0031007"},{"annotations":[86366],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010574"},{"annotations":[86542,86543,86544],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010355"},{"annotations":[86159],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010286"},{"annotations":[85117],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014848"},{"annotations":[86618],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008644"},{"annotations":[85128],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014296"},{"annotations":[84540],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010655"},{"annotations":[85632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010306"},{"annotations":[84794],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010496"}]},"cv_name":"mondo","definition":"An abnormality of the nervous system that is present at birth or detected in the neonatal period.","definition_xrefs":["NCIT:C97172"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete congenital abnormality (obsolete MONDO:0000839)","termid":"MONDO:0000839"},{"relation_name":"is_a","term_name":"nervous system disorder","termid":"MONDO:0005071"}],"gene_count":110,"genes_by_uniquename":{"SJAG_00106":null,"SJAG_00112":null,"SJAG_00156":null,"SJAG_00185":null,"SJAG_00312":null,"SJAG_00321":null,"SJAG_00379":null,"SJAG_00742":null,"SJAG_00773":null,"SJAG_00804":null,"SJAG_00826":null,"SJAG_00831":null,"SJAG_00853":null,"SJAG_00885":null,"SJAG_00924":null,"SJAG_00964":null,"SJAG_00992":null,"SJAG_01025":null,"SJAG_01253":null,"SJAG_01286":null,"SJAG_01298":null,"SJAG_01360":null,"SJAG_01410":null,"SJAG_01465":null,"SJAG_01466":null,"SJAG_01491":null,"SJAG_01507":null,"SJAG_01540":null,"SJAG_01712":null,"SJAG_01825":null,"SJAG_01872":null,"SJAG_01918":null,"SJAG_01926":null,"SJAG_02050":null,"SJAG_02096":null,"SJAG_02103":null,"SJAG_02160":null,"SJAG_02163":null,"SJAG_02165":null,"SJAG_02194":null,"SJAG_02289":null,"SJAG_02313":null,"SJAG_02317":null,"SJAG_02362":null,"SJAG_02431":null,"SJAG_02470":null,"SJAG_02509":null,"SJAG_02523":null,"SJAG_02623":null,"SJAG_02658":null,"SJAG_02723":null,"SJAG_02774":null,"SJAG_02791":null,"SJAG_02824":null,"SJAG_02889":null,"SJAG_02913":null,"SJAG_03025":null,"SJAG_03056":null,"SJAG_03066":null,"SJAG_03067":null,"SJAG_03106":null,"SJAG_03120":null,"SJAG_03145":null,"SJAG_03188":null,"SJAG_03286":null,"SJAG_03311":null,"SJAG_03353":null,"SJAG_03379":null,"SJAG_03418":null,"SJAG_03597":null,"SJAG_03635":null,"SJAG_03664":null,"SJAG_03672":null,"SJAG_03681":null,"SJAG_03698":null,"SJAG_03703":null,"SJAG_03712":null,"SJAG_03970":null,"SJAG_04003":null,"SJAG_04042":null,"SJAG_04053":null,"SJAG_04074":null,"SJAG_04119":null,"SJAG_04156":null,"SJAG_04183":null,"SJAG_04316":null,"SJAG_04387":null,"SJAG_04425":null,"SJAG_04459":null,"SJAG_04537":null,"SJAG_04600":null,"SJAG_04619":null,"SJAG_04665":null,"SJAG_04681":null,"SJAG_04728":null,"SJAG_04755":null,"SJAG_04816":null,"SJAG_04821":null,"SJAG_04822":null,"SJAG_04825":null,"SJAG_04881":null,"SJAG_04887":null,"SJAG_04938":null,"SJAG_04980":null,"SJAG_05219":null,"SJAG_05229":null,"SJAG_05245":null,"SJAG_05313":null,"SJAG_05327":null,"SJAG_06022":null},"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"is_obsolete":false,"name":"congenital nervous system disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:105425","UMLS:C0497552","ICD9:742","DOID:2490"],"synonyms":[{"name":"congenital abnormality of the nervous system","type":"exact"},{"name":"congenital nervous system disorder","type":"exact"},{"name":"congenital neurologic anomaly","type":"exact"}],"termid":"MONDO:0002320","terms_by_termid":{"MONDO:0008050":null,"MONDO:0008070":null,"MONDO:0008409":null,"MONDO:0008644":null,"MONDO:0008675":null,"MONDO:0008939":null,"MONDO:0009364":null,"MONDO:0009479":null,"MONDO:0009682":null,"MONDO:0009709":null,"MONDO:0009725":null,"MONDO:0009736":null,"MONDO:0009783":null,"MONDO:0010286":null,"MONDO:0010306":null,"MONDO:0010355":null,"MONDO:0010466":null,"MONDO:0010472":null,"MONDO:0010477":null,"MONDO:0010496":null,"MONDO:0010532":null,"MONDO:0010574":null,"MONDO:0010655":null,"MONDO:0011053":null,"MONDO:0011120":null,"MONDO:0011213":null,"MONDO:0011246":null,"MONDO:0011402":null,"MONDO:0011835":null,"MONDO:0011966":null,"MONDO:0012056":null,"MONDO:0012099":null,"MONDO:0012157":null,"MONDO:0012238":null,"MONDO:0012239":null,"MONDO:0012248":null,"MONDO:0012399":null,"MONDO:0012518":null,"MONDO:0012538":null,"MONDO:0012703":null,"MONDO:0012986":null,"MONDO:0012990":null,"MONDO:0013049":null,"MONDO:0013117":null,"MONDO:0013154":null,"MONDO:0013159":null,"MONDO:0013160":null,"MONDO:0013162":null,"MONDO:0013454":null,"MONDO:0013468":null,"MONDO:0013578":null,"MONDO:0013790":null,"MONDO:0013812":null,"MONDO:0013883":null,"MONDO:0014023":null,"MONDO:0014062":null,"MONDO:0014140":null,"MONDO:0014141":null,"MONDO:0014142":null,"MONDO:0014296":null,"MONDO:0014466":null,"MONDO:0014529":null,"MONDO:0014542":null,"MONDO:0014543":null,"MONDO:0014552":null,"MONDO:0014558":null,"MONDO:0014590":null,"MONDO:0014596":null,"MONDO:0014601":null,"MONDO:0014602":null,"MONDO:0014647":null,"MONDO:0014656":null,"MONDO:0014679":null,"MONDO:0014700":null,"MONDO:0014716":null,"MONDO:0014800":null,"MONDO:0014806":null,"MONDO:0014807":null,"MONDO:0014832":null,"MONDO:0014848":null,"MONDO:0014896":null,"MONDO:0014966":null,"MONDO:0015026":null,"MONDO:0020845":null,"MONDO:0024528":null,"MONDO:0024567":null,"MONDO:0026763":null,"MONDO:0030037":null,"MONDO:0030482":null,"MONDO:0030669":null,"MONDO:0030886":null,"MONDO:0030912":null,"MONDO:0031007":null,"MONDO:0032588":null,"MONDO:0032596":null,"MONDO:0032787":null,"MONDO:0032794":null,"MONDO:0032808":null,"MONDO:0032822":null,"MONDO:0033364":null,"MONDO:0033556":null,"MONDO:0034106":null,"MONDO:0040500":null,"MONDO:0044319":null,"MONDO:0044646":null,"MONDO:0044701":null,"MONDO:0054593":null,"MONDO:0060502":null,"MONDO:0060650":null,"MONDO:0800341":null,"MONDO:0957264":null,"MONDO:0957993":null},"xrefs":{"Monarch":{"xref_id":"0002320"}}}


id: GO:0021535
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The orderly movement of a cell that will reside in the hindbrain.","definition_xrefs":["GOC:cls","GO_REF:0000021","GOC:dph","GOC:jid","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"},{"relation_name":"part_of","term_name":"hindbrain development","termid":"GO:0030902"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell migration in hindbrain","termid":"GO:0021535"}


id: PBO:0029569
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_small_vegetative_cell_population_(obsolete_FYPO:0002152)","termid":"PBO:0029569"}


id: PBO:0040344
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit f pseudogene 1","termid":"PBO:0040344"}


id: MONDO:0015705
data:
  {"annotated_genes":["SJAG_00185"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84964],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009709"}]},"cv_name":"mondo","definition":"Autosomal recessive centronuclear myopathy (AR-CNM) is an inherited neuromuscular disorder defined by numerous centrally placed nuclei on muscle biopsy and clinical features of a congenital myopathy.","definition_xrefs":["Orphanet:169186"],"direct_ancestors":[{"relation_name":"is_a","term_name":"centronuclear myopathy","termid":"MONDO:0018947"},{"relation_name":"is_a","term_name":"autosomal recessive titinopathy","termid":"MONDO:0100493"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00185":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0006025","MONDO:0002320"],"is_obsolete":false,"name":"autosomal recessive centronuclear myopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["icd11.foundation:1844602815","MEDGEN:771131","SCTID:240081004","GARD:12718","DOID:0111216","UMLS:C3645536"],"synonyms":[{"name":"AR-CNM","type":"exact"},{"name":"centronuclear myopathy, autosomal recessive","type":"exact"}],"termid":"MONDO:0015705","terms_by_termid":{"MONDO:0009709":null},"xrefs":{"Monarch":{"xref_id":"0015705"}}}


id: MONDO:0002812
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of the anatomical structures of the inner ear secondary to an infectious process. Symptoms include severe vertigo, nausea, vomiting, anxiety, and pain. Viral etiology is most common, and recent history of an upper respiratory infection is common. In rare cases an infection of the middle ear can spread to the inner ear, resulting in a bacterial or fungal etiology.","definition_xrefs":["NCIT:C27339"],"direct_ancestors":[{"relation_name":"is_a","term_name":"labyrinthitis","termid":"MONDO:0002008"},{"relation_name":"is_a","term_name":"ear infection","termid":"MONDO:0021666"},{"relation_name":"is_a","term_name":"post-infectious disorder","termid":"MONDO:0021669"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"infectious otitis interna","secondary_identifiers":["MEDGEN:217000","UMLS:C1168225"],"synonyms":[{"name":"infectious labyrinthitis","type":"exact"},{"name":"infectious otitis interna","type":"exact"},{"name":"inner Ear infection","type":"exact"},{"name":"inner ear infection","type":"exact"},{"name":"internal Ear infection","type":"exact"}],"termid":"MONDO:0002812","xrefs":{"Monarch":{"xref_id":"0002812"}}}


id: PBO:0031730
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-premature_meiosis","termid":"PBO:0031730"}


id: PBO:0090533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-AN1 type zinc finger protein, involved in ER membrane translocation","termid":"PBO:0090533"}


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


id: PBO:0035872
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-long_cytoplasmic_microtubules_curved_around_cell_end_during_mitotic_interphase","termid":"PBO:0035872"}


id: GO:0051310
data:
  {"annotated_genes":["SJAG_01775","SJAG_03989","SJAG_00418","SJAG_02731","SJAG_04745","SJAG_01837","SJAG_05295","SJAG_02761","SJAG_02346","SJAG_04140","SJAG_02451","SJAG_01224","SJAG_04412","SJAG_00678","SJAG_05266","SJAG_01211","SJAG_00930","SJAG_00918","SJAG_05319","SJAG_04623","SJAG_04280","SJAG_02286","SJAG_03437","SJAG_04040","SJAG_01297","SJAG_01370","SJAG_02336","SJAG_03540","SJAG_01278","SJAG_01601","SJAG_00207","SJAG_03698","SJAG_03126","SJAG_00082","SJAG_03217","SJAG_01613","SJAG_03683","SJAG_04884","SJAG_00768","SJAG_07002","SJAG_03048","SJAG_02624","SJAG_03543","SJAG_05019","SJAG_01371","SJAG_02045","SJAG_01805","SJAG_01082","SJAG_05220","SJAG_03327","SJAG_00794","SJAG_04076","SJAG_04259","SJAG_05290","SJAG_02814","SJAG_00646","SJAG_00302","SJAG_00335","SJAG_04508","SJAG_03220","SJAG_03926"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[116162],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051316"},{"annotations":[87343,93312],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051456"},{"annotations":[117642,94791,90868,111175,118157,98120,89516,109806,87478,104968,90475,99876,109401,95045,113274,109851,87230,97396,116023,100830,101938],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051315"},{"annotations":[111448],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0008608"},{"annotations":[98121,113276,87286,115033,107309,89764,116556,100831,93276],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031619"},{"annotations":[107740],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099607"},{"annotations":[109402,94257],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0099606"},{"annotations":[98123,107744,98729,93683,103397],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990942"},{"annotations":[93684,98124,116411,116165,107745,103398,101515,101940,98628,113591,118189,113278,100017,88838,89222,109386,98125,103045,112110,112109,112723,93314,108371,90463,101514,106993,88618,113995,101513,112111],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990758"},{"annotations":[101864],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902424"},{"annotations":[115506,111452,104672],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:1902425"},{"annotations":[93288,101884,110693,116174,89476],"is_not":false,"rel_names":["part_of","regulates"],"summary":null,"term":"GO:0140429"},{"annotations":[116177],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904967"},{"annotations":[116178],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0140273"},{"annotations":[108633],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031134"},{"annotations":[113593,100835,112724,100019,97397,109388,89224,98129,104971,109809,90465,93293,95046,108634,88620,106995,109852,101941,115423,107313,116413,94796,108373],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0051455"}]},"cv_name":"biological_process","definition":"A chromosome localization process whereby chromosomes are positioned in a specific order and orientation at the metaphase plate (spindle equator), during chromosome segregation. This alignment ensures that each daughter cell will receive the correct number of chromosomes during cell division.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of chromosome localization","termid":"GO:0051303"},{"relation_name":"part_of","term_name":"nuclear chromosome segregation","termid":"GO:0098813"}],"gene_count":61,"genes_by_uniquename":{"SJAG_00082":null,"SJAG_00207":null,"SJAG_00302":null,"SJAG_00335":null,"SJAG_00418":null,"SJAG_00646":null,"SJAG_00678":null,"SJAG_00768":null,"SJAG_00794":null,"SJAG_00918":null,"SJAG_00930":null,"SJAG_01082":null,"SJAG_01211":null,"SJAG_01224":null,"SJAG_01278":null,"SJAG_01297":null,"SJAG_01370":null,"SJAG_01371":null,"SJAG_01601":null,"SJAG_01613":null,"SJAG_01775":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_02045":null,"SJAG_02286":null,"SJAG_02336":null,"SJAG_02346":null,"SJAG_02451":null,"SJAG_02624":null,"SJAG_02731":null,"SJAG_02761":null,"SJAG_02814":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03217":null,"SJAG_03220":null,"SJAG_03327":null,"SJAG_03437":null,"SJAG_03540":null,"SJAG_03543":null,"SJAG_03683":null,"SJAG_03698":null,"SJAG_03926":null,"SJAG_03989":null,"SJAG_04040":null,"SJAG_04076":null,"SJAG_04140":null,"SJAG_04259":null,"SJAG_04280":null,"SJAG_04412":null,"SJAG_04508":null,"SJAG_04623":null,"SJAG_04745":null,"SJAG_04884":null,"SJAG_05019":null,"SJAG_05220":null,"SJAG_05266":null,"SJAG_05290":null,"SJAG_05295":null,"SJAG_05319":null,"SJAG_07002":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007049","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"metaphase chromosome alignment","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"chromosome congression","type":"narrow"}],"termid":"GO:0051310","terms_by_termid":{"GO:0008608":null,"GO:0031134":null,"GO:0031619":null,"GO:0051315":null,"GO:0051316":null,"GO:0051455":null,"GO:0051456":null,"GO:0099606":null,"GO:0099607":null,"GO:0140273":null,"GO:0140429":null,"GO:1902424":null,"GO:1902425":null,"GO:1904967":null,"GO:1990758":null,"GO:1990942":null}}


id: GO:0071434
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a motile cell in response to the presence of angiotensin.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell chemotaxis","termid":"GO:0060326"}],"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 chemotaxis to angiotensin","synonyms":[{"name":"angiotensin mediated chemotaxis","type":"broad"},{"name":"angiotensin-mediated cell chemotaxis","type":"exact"}],"termid":"GO:0071434"}


id: PR:O94472
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC1919.02 gene.","definition_xrefs":["UniProtKB:O94472","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":"protein pbn1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1919.02","synonyms":[{"name":"Spom972h-SPCC1919.02","type":"exact"}],"termid":"PR:O94472"}


id: PBO:0074497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SNAP25 antisense RNA 1","termid":"PBO:0074497"}


id: PBO:0064406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PNMA family member 1","termid":"PBO:0064406"}


id: MONDO:0850306
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A type 1 diabetes mellitus that is characterized by a less intensive autoimmune process, highly variable β-cell destruction, different degrees of insulin resistance and heterogeneous titre and pattern of islet autoantibody, sharing features with both type 1 and type 2 diabetes mellitus.","definition_xrefs":["DOID:0080846"],"direct_ancestors":[{"relation_name":"is_a","term_name":"type 1 diabetes mellitus","termid":"MONDO:0005147"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005015"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005046","MONDO:0005066","MONDO:0005015"],"is_obsolete":false,"name":"latent autoimmune diabetes in adults","secondary_identifiers":["MEDGEN:895261","UMLS:C1739108","icd11.foundation:1918279014"],"termid":"MONDO:0850306","xrefs":{"Monarch":{"xref_id":"0850306"}}}


id: MONDO:0020369
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chandler syndrome, the most frequent clinical variant of iridocorneal endothelial (ICE) syndrome, is characterized by very few iris abnormalities but more severe corneal edema and less severe secondary glaucoma than seen in the other two ICE syndrome variants: Cogan-Reese syndrome and essential iris atrophy.","definition_xrefs":["Orphanet:98979"],"direct_ancestors":[{"relation_name":"is_a","term_name":"corneal dystrophy","termid":"MONDO:0018102"},{"relation_name":"is_a","term_name":"iridocorneal endothelial syndrome","termid":"MONDO:0018988"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"Chandler syndrome","secondary_identifiers":["DOID:11554","GARD:6033","NORD:918","SCTID:416960004","UMLS:C0544008","ICD9:371.57","MedDRA:10057487","MEDGEN:107777","icd11.foundation:806443940"],"synonyms":[{"name":"Chandler's Syndrome","type":"exact"},{"name":"Chandler's syndrome","type":"exact"},{"name":"dystrophy of corneal endothelium","type":"exact"},{"name":"endothelial corneal dystrophy","type":"exact"},{"name":"posterior membrane corneal dystrophy","type":"exact"}],"termid":"MONDO:0020369","xrefs":{"Monarch":{"xref_id":"0020369"}}}


id: PBO:0086295
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein with a role in regulating Swe1p-dependent polarized growth; involved in maintaining Cdc55p in the cytoplasm where it promotes mitotic entry; involved in mitotic exit through Cdc14p regulation; interacts with silencing proteins at telomeres; has a role in Bcy1p localization; implicated in mRNA nuclear export; ZDS1 has a paralog, ZDS2, that arose from the whole genome duplication","termid":"PBO:0086295"}


id: GO:0070629
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving (1->4)-alpha-glucans, compounds composed of glucose residues linked by (1->4)-alpha-D-glucosidic bonds.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"alpha-glucan metabolic process","termid":"GO:0030978"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0008150","GO:0005975"],"is_obsolete":false,"name":"(1->4)-alpha-glucan metabolic process","synonyms":[{"name":"(1->4)-alpha-D-glucan metabolism","type":"exact"},{"name":"1,4-alpha-D-glucan metabolism","type":"exact"},{"name":"1,4-alpha-glucan metabolism","type":"exact"},{"name":"alpha-1,4 glucan metabolic process","type":"exact"},{"name":"alpha-1,4 glucan metabolism","type":"exact"}],"termid":"GO:0070629"}


id: FYPO:0006574
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of RNA measured in a cell during a cellular response to a pheromone is normal (i.e. indistinguishable from wild type). Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level","termid":"FYPO:0000840"}],"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 RNA level during cellular response to pheromone","synonyms":[{"name":"normal RNA accumulation during cellular response to pheromone","type":"related"},{"name":"normal mRNA level during cellular response to pheromone","type":"narrow"},{"name":"normal transcript level during cellular response to pheromone","type":"exact"}],"termid":"FYPO:0006574"}


id: MONDO:1011269
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hereditary progressive, bilateral lens opacity affecting dogs within the first few months of life due to a mutation in the HSF4 gene.","definition_xrefs":["PMID:17611257"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"vision disorder, non-human animal","termid":"MONDO:1011367"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"early onset cataract HSF4-related, dog","secondary_identifiers":["OMIA:001758-9615"],"termid":"MONDO:1011269","xrefs":{"Monarch":{"xref_id":"1011269"}}}


id: PATO:0000193
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000193 mating (obsolete PATO:0000193)","termid":"PATO:0000193"}


