# terms

id: MONDO:0017993
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare but serious cerebrovascular disorder involving thrombosis of the cerebral venous system. It affects children from the newborn period through childhood and adolescence. In childhood CSVT, acute infections of the head and neck such as mastoiditis are most common, followed by chronic underlying diseases such as nephrotic syndrome, cancer, and inflammatory bowel disease. Signs and symptoms are also age related. Seizures and altered mental status are the commonest manifestations in newborns. Headache, vomiting, and lethargy, sometimes with 6th nerve palsy, are the most common symptoms in children and adolescents.","definition_xrefs":["PMID:28798906"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebrovascular disorder","termid":"MONDO:0011057"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral sinovenous thrombosis","secondary_identifiers":["GARD:21485","Orphanet:329217"],"synonyms":[{"name":"CSVT","type":"exact"}],"termid":"MONDO:0017993","xrefs":{"Monarch":{"xref_id":"0017993"}}}


id: MONDO:0016460
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polyvalvular heart disease syndrome is a recently described syndrome characterized by the combination of polyvalvular heart disease, short stature, facial anomalies and intellectual deficit.","definition_xrefs":["Orphanet:228410"],"direct_ancestors":[{"relation_name":"is_a","term_name":"heart disorder","termid":"MONDO:0005267"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"polyvalvular heart disease syndrome","secondary_identifiers":["GARD:20594","MEDGEN:1376905","SCTID:723448007","UMLS:C4509918"],"synonyms":[{"name":"PHD syndrome","type":"exact"}],"termid":"MONDO:0016460","xrefs":{"Monarch":{"xref_id":"0016460"}}}


id: MOD:01878
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue and an L-threonine residue to L-threonine 5-hydroxyoxazole-4-carbothionic acid.","definition_xrefs":["RESID:AA0554","PubMed:20961038"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxazole/oxazoline ring crosslinked residues (Cys)","termid":"MOD:01856"},{"relation_name":"is_a","term_name":"crosslinked L-cysteine residue","termid":"MOD:02044"},{"relation_name":"is_a","term_name":"crosslinked L-threonine residue","termid":"MOD:02056"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-threonine 5-hydroxyoxazole-4-carbonthionic acid","synonyms":[{"name":"(4Z)-2-[(1S,2R)-1-amino-2-hydroxypropyl]-4-(sulfanylmethylidene)-1,3-oxazol-5(4H)-one [tautomer]","type":"exact"},{"name":"2-[(1S,2R)-1-amino-2-hydroxypropyl]-5-hydroxy-1,3-oxazole-4-carbothioic O-acid","type":"exact"},{"name":"CROSSLNK Threonine 5-hydroxy-oxazole-4-carbonthionic acid (Thr-Cys)","type":"exact"},{"name":"L-threonine 5-hydroxy-oxazole-4-carbonthionic acid","type":"exact"}],"termid":"MOD:01878"}


id: PBO:0072634
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ras suppressor protein 1","termid":"PBO:0072634"}


id: GO:0010061
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates trichoblast fate specification.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell fate specification","termid":"GO:0042659"},{"relation_name":"is_a","term_name":"regulation of plant epidermal cell differentiation","termid":"GO:1903888"},{"relation_name":"is_a","term_name":"regulation of root morphogenesis","termid":"GO:2000067"},{"relation_name":"regulates","term_name":"trichoblast fate specification","termid":"GO:0010057"}],"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 trichoblast fate specification","termid":"GO:0010061"}


id: GO:0002202
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The somatic process that results in the generation of sequence diversity of the variable lymphocyte receptors (VLR) of jawless fish.","definition_xrefs":["GOC:add","PMID:16373579"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic diversification of immune receptors","termid":"GO:0002200"}],"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":"somatic diversification of variable lymphocyte receptors of jawless fish","termid":"GO:0002202"}


id: GO:0071142
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex composed of a single type of SMAD family proteins. In the absence of Smad4, phosphorylation of R-SMADs results in their homotrimerization. However, these complexes do not appear to import into the nucleus and are assumed to be transcriptionally inactive.","definition_xrefs":["PMID:11779505","GOC:mah","PMID:16322555","GOC:bhm","PMID:9670020"],"direct_ancestors":[{"relation_name":"is_a","term_name":"SMAD protein complex","termid":"GO:0071141"},{"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":"homomeric SMAD protein complex","secondary_identifiers":["GO:0071143"],"synonyms":[{"name":"SMAD1 homotrimer complex","type":"narrow"},{"name":"SMAD1 protein complex","type":"narrow"},{"name":"SMAD2 homotrimer complex","type":"narrow"},{"name":"SMAD2 protein complex","type":"narrow"},{"name":"SMAD3 homotrimer complex","type":"narrow"},{"name":"SMAD3 protein complex","type":"narrow"}],"termid":"GO:0071142"}


id: GO:0005972
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete fibrinogen alpha chain (obsolete GO:0005972)","synonyms":[{"name":"fibrinogen alpha chain","type":"exact"}],"termid":"GO:0005972"}


id: GO:0003177
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the pulmonary valve over time, from its formation to the mature structure.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"semi-lunar valve development","termid":"GO:1905314"}],"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":"pulmonary valve development","termid":"GO:0003177"}


id: PBO:0079410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tubulin beta 8 class VIII pseudogene 4","termid":"PBO:0079410"}


id: PBO:0059204
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MAS related GPR family member X11, pseudogene","termid":"PBO:0059204"}


id: FYPO:0001911
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 glycosylation of one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal. Protein glycosylation is the addition of a carbohydrate or carbohydrate derivative unit to a protein amino acid.","definition_xrefs":["GO:0006486","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein glycosylation during vegetative growth","termid":"FYPO:0001910"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0002274","FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0002494"],"is_obsolete":false,"name":"decreased protein glycosylation during vegetative growth","synonyms":[{"name":"decreased protein glycosylation during mitotic cell cycle","type":"related"},{"name":"protein hypoglycosylation during vegetative growth","type":"exact"},{"name":"reduced protein glycosylation during vegetative growth","type":"exact"}],"termid":"FYPO:0001911"}


id: GO:0051583
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of dopamine into a presynaptic neuron or glial cell. In this context, dopamine is a catecholamine neurotransmitter and a metabolic precursor of noradrenaline and adrenaline.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catecholamine uptake involved in synaptic transmission","termid":"GO:0051934"},{"relation_name":"is_a","term_name":"dopamine uptake","termid":"GO:0090494"},{"relation_name":"part_of","term_name":"synaptic transmission, dopaminergic","termid":"GO:0001963"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0006810","GO:0023052","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"dopamine uptake involved in synaptic transmission","synonyms":[{"name":"dopamine import involved in synaptic transmission","type":"exact"},{"name":"dopamine reuptake involved in synaptic transmission","type":"exact"}],"termid":"GO:0051583"}


id: GO:0031361
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. The component of the thylakoid membrane consisting of the gene products having at least some part of their peptide sequence embedded in the hydrophobic region of the membrane.","definition_xrefs":["GOC:dos","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete integral component of thylakoid membrane (obsolete GO:0031361)","synonyms":[{"name":"integral to thylakoid membrane","type":"narrow"}],"termid":"GO:0031361"}


id: GO:0002865
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of an acute inflammatory response to an antigenic stimulus.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of acute inflammatory response","termid":"GO:0002674"},{"relation_name":"is_a","term_name":"negative regulation of inflammatory response to antigenic stimulus","termid":"GO:0002862"},{"relation_name":"is_a","term_name":"regulation of acute inflammatory response to antigenic stimulus","termid":"GO:0002864"},{"relation_name":"negatively_regulates","term_name":"acute inflammatory response to antigenic stimulus","termid":"GO:0002438"}],"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 acute inflammatory response to antigenic stimulus","synonyms":[{"name":"down regulation of acute inflammatory response to antigenic stimulus","type":"exact"},{"name":"down-regulation of acute inflammatory response to antigenic stimulus","type":"exact"},{"name":"downregulation of acute inflammatory response to antigenic stimulus","type":"exact"},{"name":"inhibition of acute inflammatory response to antigenic stimulus","type":"narrow"}],"termid":"GO:0002865"}


id: MONDO:0060782
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hematologic disorder which does not display the morphologic and/or clinical characteristics of an overt malignancy. Representative examples include atypical lymphoproliferative disorders and myelodysplastic syndromes.","definition_xrefs":["NCIT:C27274"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hematologic disorder","termid":"MONDO:0005570"},{"relation_name":"is_a","term_name":"precancerous condition","termid":"MONDO:0021074"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"premalignant hematological system disease","secondary_identifiers":["UMLS:C1335471","MEDGEN:233342"],"synonyms":[{"name":"premalignant hematologic condition","type":"exact"}],"termid":"MONDO:0060782","xrefs":{"Monarch":{"xref_id":"0060782"}}}


id: PBO:0034578
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-T-shaped_cell","termid":"PBO:0034578"}


id: PBO:0080302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 1 receptor 66 pseudogene","termid":"PBO:0080302"}


id: MONDO:0007501
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"preauricular fistulae, congenital","secondary_identifiers":["MESH:C563015","MEDGEN:154283","OMIM:128700","UMLS:C0546969"],"synonyms":[{"name":"Ear pits","type":"related"},{"name":"Pafc","type":"related"},{"name":"preauricular fistulae, congenital","type":"exact"}],"termid":"MONDO:0007501","xrefs":{"Monarch":{"xref_id":"0007501"}}}


id: PBO:0072490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein SA pseudogene 19","termid":"PBO:0072490"}


id: MONDO:0003417
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ophthalmoplegia","termid":"MONDO:0003425"},{"relation_name":"is_a","term_name":"strabismus","termid":"MONDO:0003432"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"internuclear ophthalmoplegia","secondary_identifiers":["ICD9:378.86","MEDGEN:101820","DOID:538","icd11.foundation:377040542","UMLS:C0152134","ICD10CM:H51.2","SCTID:49823009"],"termid":"MONDO:0003417","xrefs":{"Monarch":{"xref_id":"0003417"}}}


id: GO:0004511
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-tyrosine + tetrahydrobiopterin + O2 = 3,4-dihydroxy-L-phenylalanine + 4-alpha-hydroxytetrahydrobiopterin + H2O.","definition_xrefs":["EC:1.14.16.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen","termid":"GO:0016714"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"tyrosine 3-monooxygenase activity","secondary_identifiers":["RHEA:18201","MetaCyc:TYROSINE-3-MONOOXYGENASE-RXN","Reactome:R-HSA-209823"],"synonyms":[{"name":"L-tyrosine hydroxylase activity","type":"related"},{"name":"L-tyrosine,tetrahydrobiopterin:oxygen oxidoreductase (3-hydroxylating)","type":"related"},{"name":"tyrosine 3-hydroxylase activity","type":"exact"},{"name":"tyrosine hydroxylase activity","type":"exact"}],"termid":"GO:0004511"}


id: PBO:0031456
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_staurosporine","termid":"PBO:0031456"}


id: MONDO:0700299
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Cushing syndrome due to macronodular adrenal hyperplasia","termid":"MONDO:0009049"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ACTH-independent macronodular adrenal hyperplasia-3","secondary_identifiers":["OMIM:620990"],"termid":"MONDO:0700299","xrefs":{"Monarch":{"xref_id":"0700299"}}}


id: SO:0000221
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding leucyl tRNA (SO:0000264).","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA_primary_transcript","termid":"SO:0000210"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine_tRNA_primary_transcript","synonyms":[{"name":"leucine tRNA primary transcript","type":"exact"}],"termid":"SO:0000221"}


id: PBO:0002579
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"19S proteasome regulatory subunit Rpn10","termid":"PBO:0002579"}


id: GO:0044684
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 7,8-dihydromethanopterin + NADPH = 5,6,7,8-tetrahydromethanopterin + NADP.","definition_xrefs":["PMID:15028691","GOC:mengo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor","termid":"GO:0016646"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"dihydromethanopterin reductase activity","secondary_identifiers":["RHEA:42804","EC:1.5.99.15"],"termid":"GO:0044684"}


id: PBO:0002071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha,alpha-trehalose-phosphate synthase [UDP-forming]","termid":"PBO:0002071"}


id: PBO:0071119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 121","termid":"PBO:0071119"}


id: PBO:0014302
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ERMES complex GTPase sububit Gem1 (predicted)","termid":"PBO:0014302"}


id: PBO:0011440
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae OXA1","termid":"PBO:0011440"}


id: PBO:0031004
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_sodium_dodecyl_sulfate","termid":"PBO:0031004"}


id: GO:0008255
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The action characteristic of ecdysis-triggering hormone, a peptide hormone that, upon receptor binding, initiates pre-ecdysis and ecdysis (i.e. cuticle shedding) through direct action on the central nervous system.","definition_xrefs":["GOC:mah","PMID:9020043"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuropeptide hormone activity","termid":"GO:0005184"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0140677"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0098772","GO:0140677","GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"ecdysis-triggering hormone activity","termid":"GO:0008255"}


id: PBO:0006188
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_downstream_target","termid":"PBO:0006188"}


id: PBO:0040288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATPase Na+/K+ transporting subunit beta 3","termid":"PBO:0040288"}


id: FYPO:0003993
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell during a cellular response to menadione is lower than normal. Total RNA or a specific RNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0006551","FYPO:0000002"],"is_obsolete":false,"name":"decreased RNA level during cellular response to menadione","synonyms":[{"name":"decreased RNA accumulation during cellular response to menadione","type":"related"},{"name":"decreased RNA level during cellular response to menadione during mitotic cell cycle","type":"related"},{"name":"decreased RNA level during cellular response to menadione during vegetative growth","type":"exact"},{"name":"decreased transcript level during cellular response to menadione","type":"exact"},{"name":"reduced RNA level during cellular response to menadione","type":"exact"}],"termid":"FYPO:0003993"}


id: FYPO:0005938
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at late replication origins is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:24656819","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin at replication origin","termid":"FYPO:0004962"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0000002","FYPO:0001312","FYPO:0000138"],"is_obsolete":false,"name":"normal protein localization to chromatin at late replication origin","synonyms":[{"name":"normal protein localisation to chromatin at late replication origin","type":"exact"},{"name":"normal protein localization to chromatin at late origin","type":"exact"},{"name":"normal protein localization to chromatin at late replication origin during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromatin at late replication origin during vegetative growth","type":"exact"}],"termid":"FYPO:0005938"}


id: PBO:0053875
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 1151","termid":"PBO:0053875"}


id: MONDO:0004604
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A subtype of classical Hodgkin lymphoma with scattered Hodgkin and Reed-Sternberg cells and a nodular or less often diffuse cellular background consisting of small lymphocytes and with an absence of neutrophils and eosinophils. (WHO, 2008)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"classic Hodgkin lymphoma","termid":"MONDO:0009348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"Hodgkin's lymphoma, lymphocytic-histiocytic predominance","secondary_identifiers":["icd11.foundation:352299041","UMLS:C1266194","MEDGEN:224769","ONCOTREE:LRCHL","Orphanet:98845","NCIT:C6913","MedDRA:10020231","ICDO:9651/3","ICD9:201.4","GARD:19593","DOID:8543","SCTID:118607005"],"synonyms":[{"name":"Hodgkin lymphoma, lymphocyte-rich","type":"exact"},{"name":"Hodgkin lymphoma, lymphocytic-histiocytic predominance","type":"exact"},{"name":"Hodgkin's disease, lymphocyte predominance","type":"exact"},{"name":"Hodgkin's disease, lymphocyte predominance [obs]","type":"exact"},{"name":"LRCHL","type":"exact"},{"name":"classic Hodgkin lymphoma, lymphocyte-rich type","type":"exact"},{"name":"lymphocyte rich Hodgkin lymphoma","type":"exact"},{"name":"lymphocyte rich Hodgkin's disease","type":"exact"},{"name":"lymphocyte rich Hodgkin's lymphoma","type":"exact"},{"name":"lymphocyte rich classical Hodgkin lymphoma","type":"exact"},{"name":"lymphocyte rich classical Hodgkin's disease","type":"exact"},{"name":"lymphocyte rich classical Hodgkin's lymphoma","type":"exact"},{"name":"lymphocyte-rich Classic Hodgkin lymphoma","type":"exact"},{"name":"lymphocyte-rich classical Hodgkin lymphoma","type":"exact"},{"name":"lymphocyte-rich classical Hodgkin's lymphoma","type":"exact"}],"termid":"MONDO:0004604","xrefs":{"Monarch":{"xref_id":"0004604"}}}


id: PBO:0058267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4645","termid":"PBO:0058267"}


id: GO:0070324
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to thyroxine (T4) or triiodothyronine (T3), tyrosine-based hormones produced by the thyroid gland.","definition_xrefs":["GOC:rph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hormone binding","termid":"GO:0042562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"thyroid hormone binding","synonyms":[{"name":"thyroxine binding","type":"narrow"},{"name":"triiodothyronine binding","type":"narrow"}],"termid":"GO:0070324"}


id: MONDO:0013627
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any 3-M syndrome in which the cause of the disease is a mutation in the CCDC8 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3-M syndrome","termid":"MONDO:0007477"},{"relation_name":"is_a","term_name":"primordial dwarfism and slender bone disorder","termid":"MONDO:0800063"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"3M syndrome 3","secondary_identifiers":["GARD:15772","UMLS:C3280146","OMIM:614205","MEDGEN:481776"],"synonyms":[{"name":"3-M syndrome 3","type":"exact"},{"name":"3-M syndrome caused by mutation in CCDC8","type":"exact"},{"name":"3M syndrome 3","type":"exact"},{"name":"3M3","type":"related"},{"name":"CCDC8 3-M syndrome","type":"exact"},{"name":"three M syndrome 3","type":"exact"},{"name":"three M syndrome type 3","type":"exact"}],"termid":"MONDO:0013627","xrefs":{"Monarch":{"xref_id":"0013627"}}}


id: FYPO:0003988
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 a cell has actin cortical patches in one or more abnormal locations.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular physical quality phenotype during vegetative growth","termid":"FYPO:0001321"},{"relation_name":"is_a","term_name":"mislocalized actin cortical patches","termid":"FYPO:0006771"},{"relation_name":"output_of","term_name":"abnormal actin cortical patch localization during vegetative growth","termid":"FYPO:0000190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0004803","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0001320","FYPO:0000138"],"is_obsolete":false,"name":"mislocalized actin cortical patches during vegetative growth","synonyms":[{"name":"abnormal actin cortical patch location during vegetative growth","type":"exact"},{"name":"abnormal actin cortical patch position during vegetative growth","type":"exact"},{"name":"mislocalised actin cortical patches during vegetative growth","type":"exact"},{"name":"mislocalized F-actin patches during vegetative growth","type":"exact"},{"name":"mislocalized actin cortical patches during mitotic cell cycle","type":"related"},{"name":"mislocalized actin patches during vegetative growth","type":"exact"}],"termid":"FYPO:0003988"}


id: PBO:0042006
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 61","termid":"PBO:0042006"}


id: PBO:0058209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4501","termid":"PBO:0058209"}


id: GO:0004209
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete caspase-6 activity (obsolete GO:0004209)","synonyms":[{"name":"caspase-6 activity","type":"exact"}],"termid":"GO:0004209"}


id: GO:0141063
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The establishment of epigenetic modifications (imprints) in a plant central cell, leading to an asymmetry between the two maternal alleles and the paternal allele, and differential expression of the corresponding alleles in the developing endosperm. This can happen through heterochromatin formation or differential chromatin loop formation.","definition_xrefs":["PMID:28118754"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genomic imprinting","termid":"GO:0071514"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0006325"}],"interesting_parent_ids":["GO:0006325","GO:0008150","GO:0010467"],"is_obsolete":false,"name":"epigenetic programming in the central cell","termid":"GO:0141063"}


id: FYPO:0006434
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 medial cortical node of a cell is decreased, and the protein is instead detected distributed throughout the cell cortex. There may be little or no protein detected at the medial cortical node.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to medial cortical node","termid":"FYPO:0006326"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to medial cortical node, with protein distributed in cell cortex, during vegetative growth","synonyms":[{"name":"cortical drift","type":"related"},{"name":"decreased protein localisation to medial cortical node during vegetative growth, with protein distributed in cell cortex","type":"exact"},{"name":"decreased protein localisation to medial cortical node, with protein distributed in cell cortex, during vegetative growth","type":"exact"},{"name":"decreased protein localization to cytokinetic nodes, with protein distributed in cell cortex, during vegetative growth","type":"related"},{"name":"decreased protein localization to medial cortical node during vegetative growth, with protein distributed in cell cortex","type":"exact"},{"name":"decreased protein localization to medial cortical node during vegetative growth, with protein distributed in cortex","type":"exact"},{"name":"decreased protein localization to medial cortical node, with protein distributed in cell cortex, during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to medial cortical node, with protein distributed in cortex, during vegetative growth","type":"exact"},{"name":"decreased protein recruitment to medial cortical node, with protein distributed in cell cortex, during vegetative growth","type":"related"},{"name":"reduced protein localization to medial cortical node during vegetative growth, with protein distributed in cell cortex","type":"exact"},{"name":"reduced protein localization to medial cortical node, with protein distributed in cell cortex, during vegetative growth","type":"exact"}],"termid":"FYPO:0006434"}


id: PBO:0000403
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosome biogenesis protein (predicted)","termid":"PBO:0000403"}


id: MONDO:0009405
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cervical hypertrichosis peripheral neuropathy is a rare syndrome characterized by the association of congenital hypertrichosis in the anterior cervical region with peripheral sensory and motor neuropathy. It has been described in three members of the same family and in one unrelated boy. Associated features in the familial cases include retinal anomalies, spina bifida, kyphoscoliosis and hallux valgus, while that in the non-familial case includes developmental delay. An autosomal recessive mode of inheritance is suggested. There have been no further descriptions in the literature since 1993.","definition_xrefs":["Orphanet:2218"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hypertrichosis","termid":"MONDO:0019280"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"cervical hypertrichosis-peripheral neuropathy syndrome","secondary_identifiers":["GARD:1226","MEDGEN:341004","MESH:C565492","OMIM:239840","UMLS:C1855902"],"synonyms":[{"name":"cervical hypertrichosis peripheral neuropathy","type":"related"},{"name":"hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy","type":"related"}],"termid":"MONDO:0009405","xrefs":{"Monarch":{"xref_id":"0009405"}}}


id: MONDO:0013589
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any focal segmental glomerulosclerosis in which the cause of the disease is a mutation in the MYO1E gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited focal segmental glomerulosclerosis","termid":"MONDO:0005363"}],"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":"focal segmental glomerulosclerosis 6","secondary_identifiers":["GARD:15761","DOID:0111131","MEDGEN:481535","OMIM:614131","UMLS:C3279905"],"synonyms":[{"name":"FSGS6","type":"exact"},{"name":"MYO1E focal segmental glomerulosclerosis","type":"exact"},{"name":"focal segmental glomerulosclerosis 6","type":"exact"},{"name":"focal segmental glomerulosclerosis caused by mutation in MYO1E","type":"exact"},{"name":"focal segmental glomerulosclerosis type 6","type":"exact"},{"name":"glomerulosclerosis, focal segmental, 6","type":"related"}],"termid":"MONDO:0013589","xrefs":{"Monarch":{"xref_id":"0013589"}}}


id: PBO:0034333
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_developmental_contribution_from","termid":"PBO:0034333"}


id: PBO:0078774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 2-6","termid":"PBO:0078774"}


id: MONDO:0012287
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Stickler syndrome type 1","termid":"MONDO:0007160"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497","MONDO:0005328"],"is_obsolete":false,"name":"Stickler syndrome, type I, nonsyndromic ocular","secondary_identifiers":["UMLS:C1836080","MEDGEN:322820","GARD:15461","MESH:C563709","OMIM:609508"],"synonyms":[{"name":"Stickler syndrome, atypical","type":"related"},{"name":"Stickler syndrome, type I, predominantly ocular","type":"related"},{"name":"Stickler syndrome, type i, nonsyndromic ocular","type":"exact"},{"name":"rhegmatogenous retinal detachment, autosomal dominant","type":"related"}],"termid":"MONDO:0012287","xrefs":{"Monarch":{"xref_id":"0012287"}}}


id: PR:P22987
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- kin1 gene.","definition_xrefs":["UniProtKB:P22987","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 kinase kin1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC4F6.06","synonyms":[{"name":"Spom972h-kin1","type":"exact"}],"termid":"PR:P22987"}


id: FYPO:0000825
data:
  {"alleles_by_uniquename":{"SJAG_02621:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02621","name":"ago1delta","uniquename":"SJAG_02621:allele-1"},"SJAG_03118:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03118","name":"leo1delta","uniquename":"SJAG_03118:allele-1"},"SJAG_03689:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03689","name":"dcr1delta","uniquename":"SJAG_03689:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[119265,119263],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004982"},{"annotations":[119266,119264],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004573"}],"single_locus_phenotype":[{"annotations":[119251],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0004982"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA measured in a cell is higher than normal. Total RNA or a specific RNA, such as the mRNA transcribed from a gene of interest, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered RNA level during vegetative growth","termid":"FYPO:0001326"},{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"},{"relation_name":"is_a","term_name":"increased RNA level","termid":"FYPO:0001890"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02621":null,"SJAG_03118":null,"SJAG_03689":null},"genotype_count":3,"genotypes_by_uniquename":{"ago1delta__leo1delta":{"display_name":"ago1delta leo1delta","display_uniquename":"ago1delta__leo1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02621:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03118:allele-1","expression":"Null"}]}]},"dcr1delta":{"display_name":"dcr1delta","display_uniquename":"dcr1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]}]},"dcr1delta__leo1delta":{"display_name":"dcr1delta leo1delta","display_uniquename":"dcr1delta__leo1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03689:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03118:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0006551","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_02621","SJAG_03118","SJAG_03689"],"name":"increased RNA level during vegetative growth","references_by_uniquename":{"PMID:35226668":null},"secondary_identifiers":["FYPO:0002936","FYPO:0000910","FYPO:0001247"],"single_locus_annotated_genes":["SJAG_03689"],"single_locus_genotype_uniquenames":["dcr1delta"],"synonyms":[{"name":"RNA accumulation during vegetative growth","type":"related"},{"name":"RNA accumulation: increased during vegetative growth","type":"related"},{"name":"increased RNA accumulation during vegetative growth","type":"related"},{"name":"increased RNA level during mitotic cell cycle","type":"related"},{"name":"increased cellular RNA level during vegetative growth","type":"exact"},{"name":"increased cellular mRNA level during vegetative growth","type":"narrow"},{"name":"increased mRNA accumulation during vegetative growth","type":"related"},{"name":"increased mRNA level during mitotic cell cycle","type":"related"},{"name":"increased mRNA level during vegetative growth","type":"narrow"},{"name":"increased mRNA transcript level during vegetative growth","type":"narrow"},{"name":"increased messenger RNA level during vegetative growth","type":"narrow"},{"name":"increased transcript level during vegetative growth","type":"exact"}],"termid":"FYPO:0000825","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000162":null,"FYPO:0004573":null,"FYPO:0004982":null}}


id: PBO:0027074
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-multiseptate_vegetative_cell_with_binucleate_and_anucleate_compartments","termid":"PBO:0027074"}


id: SO:0000514
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"9 nucleotide recombination site (e.g. GGTTTTTGT), part of a J-gene recombination feature of an immunoglobulin/T-cell receptor gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"nonamer_of_recombination_feature_of_vertebrate_immune_system_gene","termid":"SO:0000562"},{"relation_name":"part_of","term_name":"J_gene_recombination_feature","termid":"SO:0000302"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"J_nonamer","synonyms":[{"name":"J nonamer","type":"exact"},{"name":"J-NONAMER","type":"exact"}],"termid":"SO:0000514"}


id: PBO:0067090
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 126, pseudogene","termid":"PBO:0067090"}


id: GO:0039022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the pronephric duct over time, from its formation to the mature structure. The pronephric duct collects the filtrate from the pronephric tubules and opens to the exterior of the pronephric kidney.","definition_xrefs":["PMID:15647339","GOC:mtg_kidney_jan10","XAO:0000063","ZFA:0000150"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephric duct development","termid":"GO:0072176"},{"relation_name":"part_of","term_name":"pronephros development","termid":"GO:0048793"}],"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":"pronephric duct development","termid":"GO:0039022"}


id: MONDO:0002390
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ossifying fibromyxoid tumor (obsolete MONDO:0002390)","termid":"MONDO:0002390","xrefs":{"Monarch":{"xref_id":"0002390"}}}


id: SO:0000842
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region of a gene that has a specific function.","direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"},{"relation_name":"part_of","term_name":"gene","termid":"SO:0000704"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gene_component_region","synonyms":[{"name":"gene component region","type":"exact"}],"termid":"SO:0000842"}


id: PBO:0062161
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily K member 2","termid":"PBO:0062161"}


id: PBO:0088304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"linear element protein Mug20","termid":"PBO:0088304"}


id: PBO:0043318
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CAP-Gly domain containing linker protein 1","termid":"PBO:0043318"}


id: PBO:0058906
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 12124","termid":"PBO:0058906"}


id: PBO:0050336
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A1pseudogene 38","termid":"PBO:0050336"}


id: PBO:0046602
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 4","termid":"PBO:0046602"}


id: PBO:0070843
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L13a pseudogene 22","termid":"PBO:0070843"}


id: MONDO:0012308
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare subtype of Joubert syndrome and related disorders (JSRD) characterized by the neurological features of JS associated with renal disease, in the absence of retinopathy.","definition_xrefs":["Orphanet:220497"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"familial cystic renal disease","termid":"MONDO:0019741"},{"relation_name":"excluded_subClassOf","term_name":"central nervous system malformation","termid":"MONDO:0020022"},{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Joubert syndrome with renal defect","secondary_identifiers":["MEDGEN:335526","SCTID:716999001","GARD:10169","UMLS:C1846790","OMIM:609583","icd11.foundation:1419767028","NCIT:C74997","MESH:C536296","DOID:0110999"],"synonyms":[{"name":"JBTS4","type":"exact"},{"name":"JS-R","type":"exact"},{"name":"Joubert syndrome 4","type":"related"},{"name":"Joubert syndrome type 4","type":"exact"},{"name":"Joubert syndrome with renal anomalies","type":"related"}],"termid":"MONDO:0012308","xrefs":{"Monarch":{"xref_id":"0012308"}}}


id: FYPO:0004281
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of xanthine DNA N-glycosylase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal DNA N-glycosylase activity","termid":"FYPO:0008216"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000654","FYPO:0000707","FYPO:0001985","FYPO:0000652","FYPO:0000661"],"is_obsolete":false,"name":"abnormal xanthine DNA N-glycosylase activity","termid":"FYPO:0004281"}


id: GO:0046479
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of glycosphingolipid, a compound with residues of sphingoid and at least one monosaccharide.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycosphingolipid metabolic process","termid":"GO:0006687"},{"relation_name":"is_a","term_name":"glycolipid catabolic process","termid":"GO:0019377"},{"relation_name":"is_a","term_name":"sphingolipid catabolic process","termid":"GO:0030149"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629"],"is_obsolete":false,"name":"glycosphingolipid catabolic process","secondary_identifiers":["Reactome:R-HSA-9840310"],"synonyms":[{"name":"glycosphingolipid breakdown","type":"exact"},{"name":"glycosphingolipid catabolism","type":"exact"},{"name":"glycosphingolipid degradation","type":"exact"}],"termid":"GO:0046479"}


id: MONDO:0002141
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An undifferentiated pleomorphic sarcoma arising from the skin. It is characterized by the presence of spindle cells in a storiform pattern and histiocytes with abundant cytoplasm.","definition_xrefs":["NCIT:C5576"],"direct_ancestors":[{"relation_name":"is_a","term_name":"undifferentiated pleomorphic sarcoma","termid":"MONDO:0002142"},{"relation_name":"is_a","term_name":"skin sarcoma","termid":"MONDO:0006414"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004992"],"is_obsolete":false,"name":"cutaneous undifferentiated pleomorphic sarcoma","secondary_identifiers":["DOID:1906","MEDGEN:224813","SCTID:404014008","UMLS:C1275254","ICD9:171.9"],"synonyms":[{"name":"cutaneous malignant fibrous histiocytoma","type":"exact"},{"name":"cutaneous unclassified pleomorphic sarcoma","type":"exact"},{"name":"cutaneous unclassified pleomorphic sarcoma (formerly cutaneous \"MFH\")","type":"exact"},{"name":"cutaneous unclassified pleomorphic sarcoma (formerly cutaneous \"malignant fibrous histiocytoma\")","type":"exact"},{"name":"cutaneous unclassified pleomorphic sarcoma (formerly cutaneous)","type":"exact"},{"name":"cutaneous undifferentiated pleomorphic sarcoma","type":"exact"},{"name":"malignant cutaneous fibrous histiocytoma","type":"exact"},{"name":"malignant fibrous histiocytoma of skin","type":"exact"},{"name":"malignant fibrous histiocytoma of the skin","type":"exact"},{"name":"malignant skin fibrous histiocytoma","type":"exact"},{"name":"undifferentiated pleomorphic sarcoma of zone of skin","type":"exact"},{"name":"zone of skin undifferentiated pleomorphic sarcoma","type":"exact"}],"termid":"MONDO:0002141","xrefs":{"Monarch":{"xref_id":"0002141"}}}


id: PBO:0004324
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zf-C3HC4 type (RING finger)/GCN5-related N acetyltransferase fusion protein","termid":"PBO:0004324"}


id: PBO:0060649
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear receptor coactivator 7","termid":"PBO:0060649"}


id: PBO:0043468
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CCR4-NOT transcription complex subunit 7","termid":"PBO:0043468"}


id: PBO:0091423
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"M-Factor precursor","termid":"PBO:0091423"}


id: GO:0072012
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The biological process whose specific outcome is the progression of a glomerulus vasculature from an initial condition to its mature state. This process begins with the formation of the glomerulus vasculature and ends with the mature structure. The glomerulus vasculature is composed of the tubule structures that carry blood or lymph in the glomerulus.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel development","termid":"GO:0001568"},{"relation_name":"is_a","term_name":"kidney vasculature development","termid":"GO:0061440"},{"relation_name":"part_of","term_name":"glomerulus development","termid":"GO:0032835"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"glomerulus vasculature development","synonyms":[{"name":"glomerulus capillary development","type":"related"}],"termid":"GO:0072012"}


id: GO:0160215
data:
  {"annotated_genes":["SJAG_00902","SJAG_04039","SJAG_00944","SJAG_02769","SJAG_04007","SJAG_03013","SJAG_04895","SJAG_01075","SJAG_01396","SJAG_04186","SJAG_03627","SJAG_01416","SJAG_00581","SJAG_03844","SJAG_02985","SJAG_01248"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[74847],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003860"},{"annotations":[77215,78560],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003986"},{"annotations":[91249],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004099"},{"annotations":[75344],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051500"},{"annotations":[107031,82170,96322,101168],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0047617"},{"annotations":[64757,109043],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031078"},{"annotations":[89518,79121],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032041"},{"annotations":[103726],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141222"},{"annotations":[89519],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140765"},{"annotations":[109044],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032129"},{"annotations":[114023,79122],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046969"},{"annotations":[109045],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140937"},{"annotations":[109046,96720],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034739"},{"annotations":[79123],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046970"},{"annotations":[109047],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180032"},{"annotations":[109048],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180033"},{"annotations":[72405],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000225"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: R-CO-X + H2O = R-COOH + HX, hydrolysis of an acyl group or groups from a substrate molecule.","definition_xrefs":["PMID:38355760","PMID:2760018","PMID:29637793"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity","termid":"GO:0003824"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00581":null,"SJAG_00902":null,"SJAG_00944":null,"SJAG_01075":null,"SJAG_01248":null,"SJAG_01396":null,"SJAG_01416":null,"SJAG_02769":null,"SJAG_02985":null,"SJAG_03013":null,"SJAG_03627":null,"SJAG_03844":null,"SJAG_04007":null,"SJAG_04039":null,"SJAG_04186":null,"SJAG_04895":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674"],"is_obsolete":false,"name":"deacylase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:0160215","terms_by_termid":{"GO:0000225":null,"GO:0003860":null,"GO:0003986":null,"GO:0004099":null,"GO:0031078":null,"GO:0032041":null,"GO:0032129":null,"GO:0034739":null,"GO:0046969":null,"GO:0046970":null,"GO:0047617":null,"GO:0051500":null,"GO:0140765":null,"GO:0140937":null,"GO:0141222":null,"GO:0180032":null,"GO:0180033":null}}


id: GO:0002303
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an antigenically naive gamma-delta T cell acquires the specialized features of an effector, regulatory, or memory T cell and contributes to an immune response. Effector T cells include cells which provide T cell help or exhibit cytotoxicity towards other cells.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gamma-delta T cell activation involved in immune response","termid":"GO:0002290"},{"relation_name":"is_a","term_name":"T cell differentiation involved in immune response","termid":"GO:0002292"},{"relation_name":"is_a","term_name":"gamma-delta T cell differentiation","termid":"GO:0042492"}],"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":"gamma-delta T cell differentiation involved in immune response","synonyms":[{"name":"gamma-delta T cell development involved in immune response","type":"related"},{"name":"gamma-delta T cell differentiation during immune response","type":"related"},{"name":"gamma-delta T lymphocyte differentiation during immune response","type":"related"},{"name":"gamma-delta T-cell differentiation during immune response","type":"related"},{"name":"gamma-delta T-lymphocyte differentiation during immune response","type":"related"}],"termid":"GO:0002303"}


id: PBO:0074380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SMG1 pseudogene 6","termid":"PBO:0074380"}


id: PR:O14177
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A charged multivesicular body protein 2a that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR10476:SF4","OMA:SCHPO01120"],"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":"ESCRT-III complex subunit did4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4F8.01","secondary_identifiers":["UniProtKB:O14177"],"synonyms":[{"name":"Spom972h-CHMP2A","type":"exact"},{"name":"vacuolar protein-sorting-associated protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14177"}


id: PBO:0036009
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_protein_tyrosine_phosphorylation_during_vegetative_growth","termid":"PBO:0036009"}


id: GO:1902463
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a location within a cell leading edge.","definition_xrefs":["GOC:lb","GOC:TermGenie","PMID:21543326"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization","termid":"GO:0008104"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to cell leading edge","synonyms":[{"name":"protein localisation in cell leading edge","type":"exact"},{"name":"protein localisation to cell leading edge","type":"exact"},{"name":"protein localization in cell leading edge","type":"exact"}],"termid":"GO:1902463"}


id: GO:0098908
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of action potential creation, propagation or termination in a neuron. This typically occurs via modulation of the activity or expression of voltage-gated ion channels.","definition_xrefs":["GOC:dph","GOC:tb","GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transmission of nerve impulse","termid":"GO:0051969"},{"relation_name":"is_a","term_name":"regulation of action potential","termid":"GO:0098900"},{"relation_name":"regulates","term_name":"neuronal action potential","termid":"GO:0019228"}],"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 neuronal action potential","synonyms":[{"name":"generation of action potential","type":"related"}],"termid":"GO:0098908"}


id: GO:0046534
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of photoreceptor cell differentiation. An example of this process is found in Drosophila melanogaster.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of neuron differentiation","termid":"GO:0045666"},{"relation_name":"is_a","term_name":"regulation of photoreceptor cell differentiation","termid":"GO:0046532"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"photoreceptor cell differentiation","termid":"GO:0046530"}],"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 photoreceptor cell differentiation","secondary_identifiers":["GO:0045675"],"synonyms":[{"name":"activation of photoreceptor cell differentiation","type":"narrow"},{"name":"activation of photoreceptor differentiation","type":"narrow"},{"name":"positive regulation of photoreceptor differentiation","type":"exact"},{"name":"stimulation of photoreceptor cell differentiation","type":"narrow"},{"name":"stimulation of photoreceptor differentiation","type":"narrow"},{"name":"up regulation of photoreceptor cell differentiation","type":"exact"},{"name":"up regulation of photoreceptor differentiation","type":"exact"},{"name":"up-regulation of photoreceptor cell differentiation","type":"exact"},{"name":"up-regulation of photoreceptor differentiation","type":"exact"},{"name":"upregulation of photoreceptor cell differentiation","type":"exact"},{"name":"upregulation of photoreceptor differentiation","type":"exact"}],"termid":"GO:0046534"}


id: MONDO:0007233
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital defect in the neck that occurs during early embryonic development. It is caused by developmental abnormalities of the pharyngeal arches and results in the development of a cyst or a fissure in the side of the neck.","definition_xrefs":["NCIT:C104813"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysts and fistulae of the face and oral cavity","termid":"MONDO:0015476"},{"relation_name":"is_a","term_name":"hereditary otorhinolaryngologic disease","termid":"MONDO:0018751"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"second branchial cleft anomaly","secondary_identifiers":["Orphanet:141022","UMLS:C3874315","SCTID:73381000119100","GARD:16968","MEDGEN:840602","OMIM:113600"],"synonyms":[{"name":"branchial cleft","type":"exact"},{"name":"branchial cleft anomalies","type":"related"},{"name":"branchial cleft remnant","type":"exact"},{"name":"branchial cysts","type":"related"},{"name":"second branchial cleft cyst","type":"exact"},{"name":"second branchial cleft fistula","type":"exact"}],"termid":"MONDO:0007233","xrefs":{"Monarch":{"xref_id":"0007233"}}}


id: GO:0004896
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a cytokine and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:add","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane signaling receptor activity","termid":"GO:0004888"},{"relation_name":"is_a","term_name":"immune receptor activity","termid":"GO:0140375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"cytokine receptor activity","secondary_identifiers":["GO:0004907"],"synonyms":[{"name":"IL receptor","type":"narrow"},{"name":"hematopoietin/interferon-class (D200-domain) cytokine receptor activity","type":"related"},{"name":"interleukin receptor activity","type":"narrow"}],"termid":"GO:0004896"}


id: PBO:0003554
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitotic spindle checkpoint protein Mad1","termid":"PBO:0003554"}


id: MONDO:0021659
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant epithelial neoplasm composed of a mixture of neuroendocrine cells with morphologic and immunohistochemical characteristics of carcinoid tumor and malignant glandular cells.","definition_xrefs":["NCIT:C4139"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carcinoma","termid":"MONDO:0004993"}],"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":"combined carcinoid and adenocarcinoma","secondary_identifiers":["ICDO:8244/3","UMLS:C0334302","ICDO:8245/3","MEDGEN:83124","MESH:C538230"],"synonyms":[{"name":"adenocarcinoid neoplasm","type":"exact"},{"name":"adenocarcinoid tumor","type":"exact"},{"name":"adenocarcinoid tumour","type":"exact"},{"name":"combined carcinoid and adenocarcinoma","type":"exact"},{"name":"combined carcinoid neoplasm and adenocarcinoma","type":"exact"},{"name":"combined carcinoid tumor and adenocarcinoma","type":"exact"},{"name":"combined carcinoid tumour and adenocarcinoma","type":"exact"},{"name":"composite carcinoid","type":"exact"},{"name":"composite carcinoid neoplasm","type":"exact"},{"name":"composite carcinoid tumor","type":"exact"},{"name":"composite carcinoid tumour","type":"exact"},{"name":"mixed carcinoid neoplasm","type":"exact"},{"name":"mixed carcinoid tumor","type":"exact"},{"name":"mixed carcinoid tumour","type":"exact"}],"termid":"MONDO:0021659","xrefs":{"Monarch":{"xref_id":"0021659"}}}


id: PBO:0042440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CDC42 binding protein kinase gamma","termid":"PBO:0042440"}


id: MONDO:0032737
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"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":"spastic paraplegia 80, autosomal dominant","secondary_identifiers":["UMLS:C5193084","OMIM:618418","Orphanet:631068","MEDGEN:1682111","DOID:0112341"],"synonyms":[{"name":"SPASTIC PARAPLEGIA 80, AUTOSOMAL DOMINANT","type":"exact"},{"name":"SPG80","type":"exact"},{"name":"autosomal dominant spastic paraplegia type 80","type":"exact"}],"termid":"MONDO:0032737","xrefs":{"Monarch":{"xref_id":"0032737"}}}


id: PBO:0073187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"selenoprotein P","termid":"PBO:0073187"}


id: PBO:0045449
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydropyrimidinase like 2","termid":"PBO:0045449"}


id: PBO:0063093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPARG activating RBM14 associated lncRNA 1","termid":"PBO:0063093"}


id: PBO:0041496
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 12 open reading frame 56","termid":"PBO:0041496"}


id: GO:1900575
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of emodin.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ketone biosynthetic process","termid":"GO:0042181"},{"relation_name":"is_a","term_name":"secondary metabolite biosynthetic process","termid":"GO:0044550"},{"relation_name":"is_a","term_name":"phenol-containing compound biosynthetic process","termid":"GO:0046189"},{"relation_name":"is_a","term_name":"emodin metabolic process","termid":"GO:1900573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"emodin biosynthetic process","synonyms":[{"name":"emodin anabolism","type":"exact"},{"name":"emodin biosynthesis","type":"exact"},{"name":"emodin formation","type":"exact"},{"name":"emodin synthesis","type":"exact"}],"termid":"GO:1900575"}


id: PBO:0079502
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thioredoxin like 4B","termid":"PBO:0079502"}


id: PBO:0065146
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protamine 2","termid":"PBO:0065146"}


id: PBO:0110498
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STAT1 regulated ILF2 complex interacting lncRNA","termid":"PBO:0110498"}


id: PBO:0052877
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin associated protein 8-2, pseudogene","termid":"PBO:0052877"}


id: MONDO:0005347
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A laboratory test result indicating elevated triglyceride concentration in the blood.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"hypertriglyceridemia","secondary_identifiers":["MEDGEN:167238","EFO:0004211","MESH:D015228","SCTID:302870006","UMLS:C0813230","HP:0002155"],"synonyms":[{"name":"hypertriglyceridemia","type":"exact"},{"name":"hypertriglyceridemia (disease)","type":"exact"}],"termid":"MONDO:0005347","xrefs":{"Monarch":{"xref_id":"0005347"}}}


id: GO:0002568
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The somatic process that results in the generation of sequence diversity of T cell receptor genes.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic diversification of immune receptors","termid":"GO:0002200"},{"relation_name":"part_of","term_name":"T cell differentiation","termid":"GO:0030217"}],"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":"somatic diversification of T cell receptor genes","synonyms":[{"name":"somatic diversification of TCR genes","type":"exact"}],"termid":"GO:0002568"}


id: GO:0045311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The growth of colonies in filamentous chains of cells as a result of a pheromone stimulus.","definition_xrefs":["GOC:ai","GOC:dph","GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"invasive filamentous growth","termid":"GO:0036267"},{"relation_name":"part_of","term_name":"response to pheromone","termid":"GO:0019236"}],"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":"invasive growth in response to pheromone","termid":"GO:0045311"}


id: GO:0051150
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of smooth muscle cell differentiation.","definition_xrefs":["GOC:ai","CL:0000192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle cell differentiation","termid":"GO:0051147"},{"relation_name":"regulates","term_name":"smooth muscle cell differentiation","termid":"GO:0051145"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of smooth muscle cell differentiation","termid":"GO:0051150"}


id: PBO:0018056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chorein homolog Vps13a (predicted)","termid":"PBO:0018056"}


id: PBO:0086859
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative S-adenosylmethionine-dependent lysine methyltransferase; responsible for modifying Lys-390 in translational elongation factor EF-1 alpha (eEF1A); has seven beta-strand methyltransferase motif; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm","termid":"PBO:0086859"}


id: PBO:0003711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycosyl hydrolase family 16 (predicted)","termid":"PBO:0003711"}


id: SO:0001791
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant that changes exon sequence.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_variant","termid":"SO:0001576"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exon_variant","secondary_identifiers":["http://snpeff.sourceforge.net/SnpEff_manual.html"],"synonyms":[{"name":"ANNOVAR:exonic","type":"exact"},{"name":"Jannovar:exon_variant","type":"exact"},{"name":"VAAST:exon_variant","type":"exact"},{"name":"exon variant","type":"exact"},{"name":"snpEff:EXON","type":"exact"}],"termid":"SO:0001791"}


id: MONDO:0013763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Joubert syndrome in which the cause of the disease is a mutation in the CEP41 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Joubert syndrome with ocular defect","termid":"MONDO:0016364"},{"relation_name":"is_a","term_name":"Joubert syndrome","termid":"MONDO:0018772"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005559","MONDO:0020022"],"is_obsolete":false,"name":"Joubert syndrome 15","secondary_identifiers":["DOID:0110984","OMIM:614464","GARD:15806","MEDGEN:482527","UMLS:C3280897"],"synonyms":[{"name":"CEP41 Joubert syndrome","type":"exact"},{"name":"JBTS15","type":"exact"},{"name":"Joubert syndrome 12/15, digenic","type":"related"},{"name":"Joubert syndrome 15","type":"exact"},{"name":"Joubert syndrome 9/15, digenic","type":"related"},{"name":"Joubert syndrome caused by mutation in CEP41","type":"exact"},{"name":"Joubert syndrome type 15","type":"exact"}],"termid":"MONDO:0013763","xrefs":{"Monarch":{"xref_id":"0013763"}}}


id: MONDO:0012058
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"myocardial infarction","termid":"MONDO:0005068"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myocardial infarction, susceptibility to, 2","secondary_identifiers":["MEDGEN:325275","OMIM:608557","UMLS:C1837871"],"synonyms":[{"name":"Mci2","type":"related"},{"name":"myocardial infarction, susceptibility to, 2","type":"exact"},{"name":"myocardial infarction, susceptibility to, type 2","type":"exact"}],"termid":"MONDO:0012058","xrefs":{"Monarch":{"xref_id":"0012058"}}}


id: PBO:0048132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fuzzy planar cell polarity protein","termid":"PBO:0048132"}


id: PBO:0011516
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unbinds SPAC11H11.04 with force 120 pN at probe speed 1.74 um/s","termid":"PBO:0011516"}


id: PBO:0113181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Largest subunit of the origin recognition complex; involved in directing DNA replication by binding to replication origins; also involved in transcriptional silencing; exhibits ATPase activity; role in chromatin organization at replication origins, along with chromatin remodellers; ORC1 has a paralog, SIR3, that arose from the whole genome duplication","termid":"PBO:0113181"}


id: PBO:0042386
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CD300c molecule","termid":"PBO:0042386"}


id: GO:0043424
data:
  {"annotated_genes":["SJAG_06592"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70241],"is_not":false,"summary":null,"term":"GO:0043424"}]},"cv_name":"molecular_function","definition":"Binding to a protein histidine kinase.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase binding","termid":"GO:0019901"}],"gene_count":1,"genes_by_uniquename":{"SJAG_06592":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0005488","GO:0003674","GO:0005515"],"is_obsolete":false,"name":"protein histidine kinase binding","references_by_uniquename":{"GO_REF:0000002":null},"synonyms":[{"name":"histidine kinase binding","type":"exact"},{"name":"histidine-protein kinase binding","type":"exact"},{"name":"protein-histidine kinase binding","type":"exact"}],"termid":"GO:0043424","terms_by_termid":{"GO:0043424":null}}


id: PBO:0031202
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-cell_cycle_arrest_phenotype","termid":"PBO:0031202"}


id: PBO:0120040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial tRNA (guanine-N2-)-methyltransferase Trm1.1 OR nuclear and mitochondrial tRNA (guanine-N2-)-methyltransferase Trm1.2","termid":"PBO:0120040"}


id: PR:Q9P7T6
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC694.04c gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P7T6"],"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":"UPF0160 protein C694.04c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC694.04c","synonyms":[{"name":"Spom972h-SPAC694.04c","type":"exact"}],"termid":"PR:Q9P7T6"}


id: PBO:0038492
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP binding cassette subfamily C member 3","termid":"PBO:0038492"}


id: GO:0018554
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,2-dihydroxynaphthalene + O2 = 2-hydroxychromene-2-carboxylate. C6 of the substrate molecular may have an NH2 group attached.","definition_xrefs":["UM-BBD_enzymeID:r0336"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on single donors with incorporation of molecular oxygen","termid":"GO:0016701"},{"relation_name":"is_a","term_name":"dioxygenase activity","termid":"GO:0051213"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"1,2-dihydroxynaphthalene dioxygenase activity","secondary_identifiers":["EC:1.13.11.56","RHEA:27310"],"termid":"GO:0018554"}


id: GO:0000216
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Progression from M phase to G1 phase of the mitotic cell cycle.","definition_xrefs":["GOC:mtg_cell_cycle","GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete M/G1 transition of mitotic cell cycle (obsolete GO:0000216)","synonyms":[{"name":"M/G1 transition of mitotic cell cycle","type":"exact"}],"termid":"GO:0000216"}


id: PBO:0074834
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 29","termid":"PBO:0074834"}


id: MONDO:0013739
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any chilblain lupus in which the cause of the disease is a mutation in the SAMHD1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial chilblain lupus","termid":"MONDO:0018827"},{"relation_name":"is_a","term_name":"SAMHD1-related type 1 interferonopathy","termid":"MONDO:0700260"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"chilblain lupus 2","secondary_identifiers":["GARD:18494","OMIM:614415","UMLS:C3280721","MEDGEN:482351"],"synonyms":[{"name":"CHBL2","type":"related"},{"name":"Chilblain lupus type 2","type":"exact"},{"name":"SAMHD1 chilblain lupus","type":"exact"},{"name":"chilblain lupus 2","type":"exact"},{"name":"chilblain lupus caused by mutation in SAMHD1","type":"exact"}],"termid":"MONDO:0013739","xrefs":{"Monarch":{"xref_id":"0013739"}}}


id: GO:0021737
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the emboliform nucleus over time, from its formation to the mature structure.","definition_xrefs":["GOC:dgh","GOC:dph","GOC:cls","GO_REF:0000021","GOC:curators","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural nucleus development","termid":"GO:0048857"},{"relation_name":"part_of","term_name":"cerebellum development","termid":"GO:0021549"}],"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":"emboliform nucleus development","termid":"GO:0021737"}


id: PBO:0083160
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; almost completely overlaps the verified gene CAF20","termid":"PBO:0083160"}


id: MONDO:0010666
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Miles-Carpenter syndrome (obsolete MONDO:0010666)","secondary_identifiers":["OMIM:309605"],"termid":"MONDO:0010666","xrefs":{"Monarch":{"xref_id":"0010666"}}}


id: PBO:0069187
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 441, pseudogene","termid":"PBO:0069187"}


id: GO:0035407
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histone H3 by the addition of an phosphate group to a threonine residue at position 11 of the histone.","definition_xrefs":["GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete histone H3-T11 phosphorylation (obsolete GO:0035407)","termid":"GO:0035407"}


id: MONDO:0012555
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Cornelia de Lange syndrome in which the cause of the disease is a mutation in the SMC3 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Cornelia de Lange syndrome","termid":"MONDO:0016033"},{"relation_name":"is_a","term_name":"non-syndromic limb reduction defect","termid":"MONDO:0019713"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cornelia de Lange syndrome 3","secondary_identifiers":["OMIM:610759","UMLS:C1853099","MEDGEN:339902","DOID:0080507","GARD:15499"],"synonyms":[{"name":"CDLS3","type":"related"},{"name":"Cornelia DE Lange syndrome 3","type":"related"},{"name":"Cornelia De Lange syndrome type 3","type":"exact"},{"name":"Cornelia de Lange syndrome 3","type":"exact"},{"name":"Cornelia de Lange syndrome caused by mutation in SMC3","type":"exact"},{"name":"Cornelia de Lange syndrome caused by mutation in Smc3","type":"exact"},{"name":"SMC3 Cornelia de Lange syndrome","type":"exact"},{"name":"Smc3 Cornelia de Lange syndrome","type":"exact"}],"termid":"MONDO:0012555","xrefs":{"Monarch":{"xref_id":"0012555"}}}


id: PBO:0068287
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribonuclease H2 subunit C pseudogene 1","termid":"PBO:0068287"}


id: PBO:0050317
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 19","termid":"PBO:0050317"}


id: GO:1900412
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. A regulation of transcription from RNA polymerase II promoter that results in regulation of histone methylation.","definition_xrefs":["PMID:15218150","GOC:mah","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of histone methylation by regulation of transcription from RNA polymerase II promoter (obsolete GO:1900412)","termid":"GO:1900412"}


id: PBO:0043955
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"crystallin beta-gamma domain containing 3","termid":"PBO:0043955"}


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


id: PBO:0050231
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group nucleosomal binding domain 2 pseudogene 9","termid":"PBO:0050231"}


id: GO:0071744
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An IgE immunoglobulin complex that is present in the plasma membrane of B cells and is composed of two identical immunoglobulin heavy chains of the IgE isotype and two identical immunoglobulin light chains and a signaling subunit, a heterodimer of the Ig-alpha and Ig-beta proteins.","definition_xrefs":["ISBN:0781765196","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"B cell receptor complex","termid":"GO:0019815"},{"relation_name":"is_a","term_name":"IgE immunoglobulin complex","termid":"GO:0071742"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"IgE B cell receptor complex","synonyms":[{"name":"membrane-bound IgE","type":"exact"},{"name":"surface IgE","type":"exact"}],"termid":"GO:0071744"}


id: RO:0002228
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"A sub-relations of parasite-of in which the parasite that can complete its life cycle independent of a host.","direct_ancestors":[{"relation_name":"is_a","term_name":"parasite_of","termid":"RO:0002444"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"facultative_parasite_of","termid":"RO:0002228"}


id: PBO:0091817
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae RAD23","termid":"PBO:0091817"}


id: GO:0042964
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the reduction of thioredoxin, a small disulfide-containing redox protein that serves as a general protein disulfide oxidoreductase.","definition_xrefs":["GOC:go_curators"],"gene_count":0,"genotype_count":0,"name":"obsolete thioredoxin reduction (obsolete GO:0042964)","synonyms":[{"name":"thioredoxin anabolism","type":"exact"},{"name":"thioredoxin biosynthesis","type":"exact"},{"name":"thioredoxin formation","type":"exact"},{"name":"thioredoxin synthesis","type":"exact"}],"termid":"GO:0042964"}


id: GO:0002132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the ribose of uridine at position 34 in the anticodon of a tRNA is post-transcriptionally methylated at the 2'-O position.","definition_xrefs":["ISBN:155581073X","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"wobble position ribose methylation","termid":"GO:0002130"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"part_of","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0006399","GO:0010467","GO:0008150"],"is_obsolete":false,"name":"wobble position uridine ribose methylation","termid":"GO:0002132"}


id: MONDO:0011425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dilated cardiomyopathy that has material basis in variation in the chromosome region 2q14-q22.","definition_xrefs":["DOID:0110429","PMID:10486326"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial isolated dilated cardiomyopathy","termid":"MONDO:0700335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"dilated cardiomyopathy 1H","secondary_identifiers":["GARD:15365","MESH:C536277","MEDGEN:348980","OMIM:604288","UMLS:C1858591"],"synonyms":[{"name":"CMD1H","type":"exact"},{"name":"cardiomyopathy, dilated, 1H","type":"related"},{"name":"cardiomyopathy, dilated, with conduction defect","type":"related"},{"name":"dilated cardiomyopathy type 1H","type":"exact"},{"name":"dilated cardiomyopathy with conduction defect","type":"exact"}],"termid":"MONDO:0011425","xrefs":{"Monarch":{"xref_id":"0011425"}}}


id: MONDO:0010254
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hematopoietic stem cell kinetics, control of (obsolete MONDO:0010254)","secondary_identifiers":["OMIM:300129"],"synonyms":[{"name":"hematopoietic stem cell kinetics, control of","type":"exact"}],"termid":"MONDO:0010254","xrefs":{"Monarch":{"xref_id":"0010254"}}}


id: GO:0097424
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Dense particles of heterochromatin, consisting of a loosely twisted strand about 600 Angstrom thick, found associated with the nucleolus.","definition_xrefs":["NIF_Subcellular:sao1210952635"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleolar chromatin","termid":"GO:0030874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"part_of","termid":"GO:0005730"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005694"}],"interesting_parent_ids":["GO:0005730","GO:0005634","GO:0005575","GO:0005694"],"is_obsolete":false,"name":"nucleolus-associated heterochromatin","termid":"GO:0097424"}


id: GO:0042621
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of poly(3-hydroxyalkanoates), polyesters of 3-hydroxyacids produced as intracellular granules by a large variety of bacteria.","definition_xrefs":["GOC:jl","PMID:9925580"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biosynthetic process","termid":"GO:0009058"},{"relation_name":"is_a","term_name":"poly(3-hydroxyalkanoate) metabolic process","termid":"GO:0042620"}],"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":"poly(3-hydroxyalkanoate) biosynthetic process","synonyms":[{"name":"PHA biosynthesis","type":"broad"},{"name":"PHA biosynthetic process","type":"broad"},{"name":"poly(3-hydroxyalkanoate) anabolism","type":"exact"},{"name":"poly(3-hydroxyalkanoate) biosynthesis","type":"exact"},{"name":"poly(3-hydroxyalkanoate) formation","type":"exact"},{"name":"poly(3-hydroxyalkanoate) synthesis","type":"exact"}],"termid":"GO:0042621"}


id: PBO:0083101
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA end-binding protein required for nonhomologous end joining (NHEJ); subunit of the DNA ligase IV complex involved in initial end binding, intermolecular ligation, and DNA ligase reactivation after completion of repair; phosphorylation by Tpk1p is required for DNA damage induced NHEJ and for nuclear targeting of Nej1p and Lif1p; human homolog NHEJ1 is phosphorylated by human Tpk1p homolog PRKACB, regulating NHEJ; transcriptionally repressed by MAT heterozygosity","termid":"PBO:0083101"}


id: GO:0043876
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-threonine (or D-allo-threonine) = glycine + acetaldehyde.","definition_xrefs":["PMID:9642221","MetaCyc:4.1.2.42-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"aldehyde-lyase activity","termid":"GO:0016832"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016829"],"is_obsolete":false,"name":"D-threonine aldolase activity","secondary_identifiers":["EC:4.1.2.42"],"synonyms":[{"name":"D-TA","type":"exact"},{"name":"D-allo-TA","type":"exact"},{"name":"D-allo-threonine aldolase activity","type":"exact"},{"name":"DtaAS","type":"related"},{"name":"low-specificity D-threonine aldolase","type":"narrow"}],"termid":"GO:0043876"}


id: PBO:0008883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mating-type M-specific polypeptide Mm/Mi","termid":"PBO:0008883"}


id: PBO:0000594
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-methyl-5-thioadenosine phosphorylase (predicted)","termid":"PBO:0000594"}


id: PBO:0077055
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombospondin type 1 domain containing 1","termid":"PBO:0077055"}


id: MONDO:0012565
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Fanconi anemia in which the cause of the disease is a mutation in the PALB2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Fanconi anemia","termid":"MONDO:0019391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046","MONDO:0021190","MONDO:0005066","MONDO:0002280"],"is_obsolete":false,"name":"Fanconi anemia complementation group N","secondary_identifiers":["OMIM:610832","UMLS:C1835817","GARD:15500","MEDGEN:372133","MESH:C563657","DOID:0111094"],"synonyms":[{"name":"FANCN","type":"exact"},{"name":"Fanconi Anemia, complementation group type N","type":"exact"},{"name":"Fanconi anaemia caused by mutation in PALB2","type":"exact"},{"name":"Fanconi anaemia complementation group type N","type":"exact"},{"name":"Fanconi anemia caused by mutation in PALB2","type":"exact"},{"name":"Fanconi anemia complementation group N","type":"exact"},{"name":"Fanconi anemia complementation group type N","type":"exact"},{"name":"Fanconi anemia, complementation group N","type":"related"},{"name":"PALB2 Fanconi anaemia","type":"exact"},{"name":"PALB2 Fanconi anemia","type":"exact"}],"termid":"MONDO:0012565","xrefs":{"Monarch":{"xref_id":"0012565"}}}


id: PBO:0065767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PZP alpha-2-macroglobulin like","termid":"PBO:0065767"}


id: PBO:0003843
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5.99.1.3","termid":"PBO:0003843"}


id: MONDO:0037938
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited metabolic disease that is has its basis in the disruption of aspartate family amino acid metabolic process.","definition_xrefs":["MONDO:patterns/inborn_metabolic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn disorder of amino acid metabolism","termid":"MONDO:0004736"},{"relation_name":"is_a","term_name":"inborn disorder of amino acid and other organic acid metabolism","termid":"MONDO:0019189"},{"relation_name":"is_a","term_name":"disorder of organic acid metabolism","termid":"MONDO:0045022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"inborn disorder of aspartate family metabolism","synonyms":[{"name":"inborn aspartate family amino acid metabolic process disorder","type":"exact"},{"name":"inborn error of aspartate family amino acid metabolic process","type":"exact"},{"name":"rare inborn error of aspartate family amino acid metabolic process","type":"exact"}],"termid":"MONDO:0037938","xrefs":{"Monarch":{"xref_id":"0037938"}}}


id: GO:0004415
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the random hydrolysis of (1->4) linkages between N-acetyl-beta-D-glucosamine and D-glucuronate residues in hyaluronate.","definition_xrefs":["EC:3.2.1.35"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosaminidase activity","termid":"GO:0015929"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016787","GO:0003824","GO:0003674","GO:0016798"],"is_obsolete":false,"name":"hyalurononglucosaminidase activity","secondary_identifiers":["Reactome:R-HSA-5693356","Reactome:R-HSA-9036077","Reactome:R-HSA-2160874","MetaCyc:3.2.1.35-RXN","Reactome:R-HSA-2160892","Reactome:R-HSA-2318585","Reactome:R-HSA-1793209"],"synonyms":[{"name":"chondroitinase I activity","type":"related"},{"name":"chondroitinase activity","type":"broad"},{"name":"hyaluronate 4-glycanohydrolase activity","type":"related"},{"name":"hyaluronidase activity","type":"broad"},{"name":"hyaluronoglucosaminidase activity","type":"exact"},{"name":"hyaluronoglucosidase activity","type":"related"}],"termid":"GO:0004415"}


id: PBO:0056382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitogen-activated protein kinase 12","termid":"PBO:0056382"}


id: PBO:0081734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 665","termid":"PBO:0081734"}


id: FYPO:0007916
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of  dihydrosphingosine-1-phosphate (DHS-1P) measured in a cell is higher than normal.","definition_xrefs":["PMID:35008733"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased phospholipid level","termid":"FYPO:0001288"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"increased cellular dihydrosphingosine-1-phosphate level","synonyms":[{"name":"increased cellular level of DHS-1P","type":"exact"}],"termid":"FYPO:0007916"}


id: GO:0045188
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of non-rapid eye movement sleep.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of circadian sleep/wake cycle, sleep","termid":"GO:0045187"},{"relation_name":"regulates","term_name":"circadian sleep/wake cycle, non-REM sleep","termid":"GO:0042748"}],"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 circadian sleep/wake cycle, non-REM sleep","synonyms":[{"name":"regulation of non-REM sleep","type":"exact"}],"termid":"GO:0045188"}


id: PBO:0086908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative vacuolar membrane transporter for cationic amino acids; likely contributes to amino acid homeostasis by exporting cationic amino acids from the vacuole; member of the PQ-loop family, with seven transmembrane domains; similar to mammalian PQLC2 vacuolar transporter; YPQ1 has a paralog, RTC2, that arose from the whole genome duplication","termid":"PBO:0086908"}


id: GO:1904434
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of ferrous iron binding.","definition_xrefs":["PMID:18353247","GOC:kom","GOC:TermGenie","GO_REF:0000059","GOC:BHF"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of ferrous iron binding (obsolete GO:1904434)","synonyms":[{"name":"activation of ferrous iron binding","type":"narrow"},{"name":"up regulation of ferrous iron binding","type":"exact"},{"name":"up-regulation of ferrous iron binding","type":"exact"},{"name":"upregulation of ferrous iron binding","type":"exact"}],"termid":"GO:1904434"}


id: GO:0047911
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: [(1->4)-alpha-D-galacturonide](n) + H2O = [(1->4)-alpha-D-galacturonide](n-1) + D-galacturonate.","definition_xrefs":["EC:3.2.1.67","MetaCyc:GALACTURAN-14-ALPHA-GALACTURONIDASE-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016798"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0016798","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"galacturan 1,4-alpha-galacturonidase activity","secondary_identifiers":["RHEA:14117"],"synonyms":[{"name":"exo-D-galacturonanase activity","type":"related"},{"name":"exo-D-galacturonase activity","type":"exact"},{"name":"exo-polygalacturonase activity","type":"exact"},{"name":"exopoly-D-galacturonase activity","type":"exact"},{"name":"exopolygalacturonase activity","type":"related"},{"name":"galacturan alpha-1,4-galacturonidase activity","type":"exact"},{"name":"poly(1,4-alpha-D-galacturonide) galacturonohydrolase activity","type":"related"},{"name":"poly(galacturonate) hydrolase activity","type":"related"}],"termid":"GO:0047911"}


id: GO:0010790
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which sister chromatids of a replicated chromosome are joined along the entire length of the chromosome during meiosis II.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"meiotic sister chromatid cohesion","termid":"GO:0051177"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007049"}],"interesting_parent_ids":["GO:0007049","GO:0008150"],"is_obsolete":false,"name":"meiotic sister chromatid cohesion involved in meiosis II","termid":"GO:0010790"}


id: MONDO:0000736
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution.","definition_xrefs":["PMID:12372090","DOID:0060304"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hyperpigmentation of the skin","termid":"MONDO:0019289"},{"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:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"dyschromatosis universalis hereditaria","secondary_identifiers":["SCTID:239082002","OMIMPS:127500","GARD:1996","Orphanet:241","MEDGEN:419691","NCIT:C173131","MESH:C535730","UMLS:C2930995"],"synonyms":[{"name":"DUH","type":"related"},{"name":"dyschromatosis universalis","type":"exact"}],"termid":"MONDO:0000736","xrefs":{"Monarch":{"xref_id":"0000736"}}}


id: PBO:0074238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 50 member 1","termid":"PBO:0074238"}


id: PBO:0043380
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"clustered mitochondria homolog pseudogene 10","termid":"PBO:0043380"}


id: GO:0022865
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables electron flow across a biological membrane, from donors localized on one side of the membrane to acceptors localized on the other side. These systems contribute to or subtract from the membrane potential, depending on the direction of electron flow. They are therefore important to cellular energetics.","definition_xrefs":["ISBN:0815340729","TC:5","GOC:mtg_transport"],"gene_count":0,"genotype_count":0,"name":"obsolete transmembrane electron transfer carrier (obsolete GO:0022865)","termid":"GO:0022865"}


id: MONDO:0003839
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm of the ovary with an invasive epithelial component and a fibrotic stroma. The epithelial component is characterized by the presence of malignant epithelial cells with intracytoplasmic mucin. Cystic spaces are also present which contain mucoid material.","definition_xrefs":["NCIT:C40034"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adenocarcinofibroma","termid":"MONDO:0002991"},{"relation_name":"is_a","term_name":"mucinous ovarian cancer","termid":"MONDO:0024282"}],"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":"ovarian mucinous adenocarcinofibroma","secondary_identifiers":["MEDGEN:384497","UMLS:C2212014","DOID:6278","ICDO:9015/3"],"synonyms":[{"name":"ovarian mucinous adenocarcinofibroma","type":"exact"},{"name":"ovarian mucinous malignant adenofibroma","type":"exact"}],"termid":"MONDO:0003839","xrefs":{"Monarch":{"xref_id":"0003839"}}}


id: MOD:01320
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Other","definition_xrefs":["PubMed:16078144","PubMed:9448752","Unimod:176#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Michael addition of BHT quinone methide to cysteine and lysine","termid":"MOD:00534"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Michael addition of BHT quinone methide to lysine","synonyms":[{"name":"BHT","type":"related"},{"name":"Michael addition of BHT quinone methide to Cysteine and Lysine","type":"related"}],"termid":"MOD:01320"}


id: GO:0046718
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process by which a symbiont breaches the plasma membrane or cell envelope and enters the host cell. The process ends when the symbiont or its genome is released into the host cell.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont entry into host","termid":"GO:0044409"},{"relation_name":"part_of","term_name":"viral life cycle","termid":"GO:0019058"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont entry into host cell","secondary_identifiers":["GO:0019063","VZ:936","Reactome:R-HSA-168270","Reactome:R-HSA-8876384"],"synonyms":[{"name":"entry of virus into host cell","type":"narrow"},{"name":"phage translocation","type":"narrow"},{"name":"viral entry into host cell","type":"narrow"},{"name":"viral penetration","type":"narrow"},{"name":"virion penetration","type":"narrow"},{"name":"virion penetration into host cell","type":"narrow"},{"name":"virus entry into host cell","type":"narrow"}],"termid":"GO:0046718"}


id: GO:0061090
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that increases the rate, frequency, or extent of sequestering of zinc ion. Sequestering of zinc ion is the process of binding or confining zinc ions such that they are separated from other components of a biological system.","definition_xrefs":["GOC:tb","GOC:BHF","GOC:dph"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of sequestering of zinc ion (obsolete GO:0061090)","termid":"GO:0061090"}


id: GO:0004442
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: D-myo-inositol 1,3-bisphosphate + H2O = D-myo-inositol 1-monophosphate + phosphate.","definition_xrefs":["GOC:go_curators","EC:3.1.3.65"],"gene_count":0,"genotype_count":0,"name":"obsolete inositol-1,4,-bisphosphate 3-phosphatase (obsolete GO:0004442)","synonyms":[{"name":"inositol-1,4,-bisphosphate 3-phosphatase","type":"exact"}],"termid":"GO:0004442"}


id: MONDO:0035689
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete syndrome of reduced sensitivity to thyroid hormone (obsolete MONDO:0035689)","secondary_identifiers":["Orphanet:596426"],"termid":"MONDO:0035689","xrefs":{"Monarch":{"xref_id":"0035689"}}}


id: PBO:0086517
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; conserved across S. cerevisiae strains; null mutant displays elevated sensitivity to expression of a mutant huntingtin fragment or of alpha-synuclein","termid":"PBO:0086517"}


id: PBO:0064420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partner of NOB1 homolog","termid":"PBO:0064420"}


id: PBO:0060443
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NACC family member 2","termid":"PBO:0060443"}


id: GO:0003940
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of alpha-L-iduronosidic linkages in dermatan sulfate. Can also hydrolyze alpha-L-iduronosidic linkages in heparan sulfate.","definition_xrefs":["EC:3.2.1.76","PMID:35011691"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016798","GO:0016787"],"is_obsolete":false,"name":"L-iduronidase activity","secondary_identifiers":["Reactome:R-HSA-9036037","Reactome:R-HSA-1678716","Reactome:R-HSA-9036041","Reactome:R-HSA-2206299","Reactome:R-HSA-1793186","MetaCyc:3.2.1.76-RXN","Reactome:R-HSA-2090037"],"synonyms":[{"name":"alpha-L-iduronidase activity","type":"related"},{"name":"glycosaminoglycan alpha-L-iduronohydrolase activity","type":"related"}],"termid":"GO:0003940"}


id: PBO:0011991
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ris Related Protein 1","termid":"PBO:0011991"}


id: MONDO:0008230
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":"peroxidase, salivary","secondary_identifiers":["OMIM:170990","UMLS:C1868425","MEDGEN:401440"],"synonyms":[{"name":"SAPX","type":"related"},{"name":"peroxidase, salivary","type":"exact"}],"termid":"MONDO:0008230","xrefs":{"Monarch":{"xref_id":"0008230"}}}


id: PBO:0110470
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cilia and flagella associated protein 263","termid":"PBO:0110470"}


id: PBO:0058285
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4661","termid":"PBO:0058285"}


id: MONDO:0012880
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the CHD7 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Kallmann syndrome","termid":"MONDO:0018800"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hypogonadotropic hypogonadism 5 with or without anosmia","secondary_identifiers":["OMIM:612370","UMLS:C3552553","GARD:10773","DOID:0090084","ICD10CM:E23.0","MEDGEN:765467","MESH:C567220"],"synonyms":[{"name":"CHD7 hypogonadotropic hypogonadism","type":"exact"},{"name":"HH5","type":"related"},{"name":"KAL5","type":"narrow"},{"name":"Kallmann syndrome 5","type":"related"},{"name":"hypogonadotropic hypogonadism 5 with or without anosmia","type":"exact"},{"name":"hypogonadotropic hypogonadism caused by mutation in CHD7","type":"exact"}],"termid":"MONDO:0012880","xrefs":{"Monarch":{"xref_id":"0012880"}}}


id: GO:0008807
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1-carboxyvinyl carboxyphosphonate = 3-(hydrohydroxyphosphoryl)pyruvate + CO2.","definition_xrefs":["EC:2.7.8.23"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, for other substituted phosphate groups","termid":"GO:0016780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016780"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016780","GO:0016740"],"is_obsolete":false,"name":"carboxyvinyl-carboxyphosphonate phosphorylmutase activity","secondary_identifiers":["MetaCyc:2.7.8.23-RXN","RHEA:14045"],"synonyms":[{"name":"1-carboxyvinyl carboxyphosphonate phosphorylmutase (decarboxylating)","type":"related"},{"name":"CPEP phosphonomutase activity","type":"related"},{"name":"carboxyphosphonoenolpyruvate phosphonomutase activity","type":"related"}],"termid":"GO:0008807"}


id: MONDO:0000801
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A allergic disease involving a green mud crab.","definition_xrefs":["MONDO:patterns/allergy"],"gene_count":0,"genotype_count":0,"name":"obsolete green mud crab allergy (obsolete MONDO:0000801)","secondary_identifiers":["DOID:0060526"],"synonyms":[{"name":"Scylla paramamosain allergy","type":"exact"},{"name":"allergy of green mud crab","type":"exact"},{"name":"crab allergy","type":"related"},{"name":"green mud crab allergic disease","type":"exact"}],"termid":"MONDO:0000801","xrefs":{"Monarch":{"xref_id":"0000801"}}}


id: PBO:0078681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (TTT) 14-1","termid":"PBO:0078681"}


id: FYPO:0007379
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 new growth zone forms along the lateral portion of the cell (often in the middle) before septation, such that a single cell grows in the form of the letter T.","definition_xrefs":["PomBase:mah","PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branched vegetative cell","termid":"FYPO:0000015"},{"relation_name":"is_a","term_name":"viable vegetative cell with abnormal cell shape","termid":"FYPO:0002197"},{"relation_name":"is_a","term_name":"T-shaped cell","termid":"FYPO:0005566"},{"relation_name":"output_of","term_name":"abnormal vegetative cell polarity","termid":"FYPO:0000026"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005568"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000004","FYPO:0000005","FYPO:0001985","FYPO:0005447","FYPO:0001320","FYPO:0005568","FYPO:0000002"],"is_obsolete":false,"name":"T-shaped vegetative cell","synonyms":[{"name":"T-shaped cell during vegetative growth","type":"exact"},{"name":"T-shaped vegetative cell during mitotic cell cycle","type":"related"}],"termid":"FYPO:0007379"}


id: GO:2000734
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of glial cell-derived neurotrophic factor receptor signaling pathway involved in ureteric bud formation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of signal transduction","termid":"GO:0009968"},{"relation_name":"is_a","term_name":"regulation of glial cell-derived neurotrophic factor receptor signaling pathway involved in ureteric bud formation","termid":"GO:2000733"},{"relation_name":"negatively_regulates","term_name":"glial cell-derived neurotrophic factor receptor signaling pathway involved in ureteric bud formation","termid":"GO:2000701"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of glial cell-derived neurotrophic factor receptor signaling pathway involved in ureteric bud formation","synonyms":[{"name":"negative regulation of GDNF receptor signaling pathway of ureteric bud formation","type":"exact"},{"name":"negative regulation of glial cell derived neurotrophic factor receptor signaling pathway of ureteric bud formation","type":"exact"},{"name":"negative regulation of glial cell line-derived neurotrophic factor receptor signalling pathway of ureteric bud formation","type":"exact"},{"name":"negative regulation of glial cell-derived neurotrophic factor receptor signaling pathway of ureteric bud formation","type":"exact"},{"name":"negative regulation of glial cell-derived neurotrophic factor receptor signalling pathway of ureteric bud formation","type":"exact"}],"termid":"GO:2000734"}


id: PR:O60173
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ATP-dependent RNA helicase DDX31 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO03199"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase dbp7 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC21H7.04","secondary_identifiers":["UniProtKB:O60173"],"synonyms":[{"name":"Spom972h-DDX31","type":"exact"}],"termid":"PR:O60173"}


id: GO:0030968
data:
  {"annotated_genes":["SJAG_01516","SJAG_04262","SJAG_00681","SJAG_03611","SJAG_04103","SJAG_03841","SJAG_04435","SJAG_03482","SJAG_04118","SJAG_01768","SJAG_00226","SJAG_04283","SJAG_02601","SJAG_04471","SJAG_00790","SJAG_00530"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[69709,72514,73066,78140,79038,98223,100758,106728,113400,113672,113808,115630,116384,116836],"is_not":false,"summary":null,"term":"GO:0030968"},{"annotations":[92572,68065],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036498"}]},"cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of the presence of unfolded proteins in the endoplasmic reticulum (ER) or other ER-related stress; results in changes in the regulation of transcription and translation.","definition_xrefs":["PMID:12042763","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to endoplasmic reticulum stress","termid":"GO:0034976"},{"relation_name":"is_a","term_name":"intracellular signal transduction","termid":"GO:0035556"},{"relation_name":"part_of","term_name":"cellular response to unfolded protein","termid":"GO:0034620"}],"gene_count":16,"genes_by_uniquename":{"SJAG_00226":null,"SJAG_00530":null,"SJAG_00681":null,"SJAG_00790":null,"SJAG_01516":null,"SJAG_01768":null,"SJAG_02601":null,"SJAG_03482":null,"SJAG_03611":null,"SJAG_03841":null,"SJAG_04103":null,"SJAG_04118":null,"SJAG_04262":null,"SJAG_04283":null,"SJAG_04435":null,"SJAG_04471":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"endoplasmic reticulum unfolded protein response","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-381119"],"synonyms":[{"name":"ER unfolded protein response","type":"exact"},{"name":"SREBP-mediated signalling pathway","type":"related"},{"name":"erUPR","type":"exact"}],"termid":"GO:0030968","terms_by_termid":{"GO:0030968":null,"GO:0036498":null}}


id: PBO:0084726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial inner membrane protein; role in mitophagy is disputed; implicated in cell wall biogenesis, the oxidative stress response, life span during starvation, and cell death; SUN family member; UTH1 has a paralog, NCA3, that arose from the whole genome duplication","termid":"PBO:0084726"}


id: MONDO:0007451
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nephrogenic diabetes insipidus","termid":"MONDO:0016383"}],"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":"diabetes insipidus, nephrogenic, autosomal","secondary_identifiers":["GARD:15058","UMLS:C1563706","DOID:0081061","MEDGEN:289643","OMIM:125800"],"synonyms":[{"name":"diabetes insipidus, nephrogenic, 2","type":"exact"},{"name":"diabetes insipidus, nephrogenic, autosomal","type":"exact"},{"name":"diabetes insipidus, nephrogenic, type 2","type":"related"}],"termid":"MONDO:0007451","xrefs":{"Monarch":{"xref_id":"0007451"}}}


id: PBO:0030653
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_methylamine","termid":"PBO:0030653"}


id: MONDO:0002979
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated squamous cell carcinoma characterized by a papillary, exophytic growth pattern and hyperkeratosis. The most commonly affected anatomic sites are the larynx, penis, cervix, vagina, and vulva.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"squamous cell carcinoma","termid":"MONDO:0005096"},{"relation_name":"is_a","term_name":"papillary carcinoma","termid":"MONDO:0006509"}],"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":"papillary squamous carcinoma","secondary_identifiers":["DOID:4385","NCIT:C4102","UMLS:C0334244","MEDGEN:83115","ICDO:8052/3"],"synonyms":[{"name":"papillary epidermoid carcinoma","type":"exact"},{"name":"papillary epidermoid cell carcinoma","type":"exact"},{"name":"papillary squamous carcinoma","type":"exact"},{"name":"papillary squamous cell carcinoma","type":"exact"}],"termid":"MONDO:0002979","xrefs":{"Monarch":{"xref_id":"0002979"}}}


id: MONDO:0859274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies","secondary_identifiers":["MEDGEN:1823969","UMLS:C5774196","OMIM:619995"],"termid":"MONDO:0859274","xrefs":{"Monarch":{"xref_id":"0859274"}}}


id: GO:0030034
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Assembly of the parallel bundle of actin filaments at the core of a microvillus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"parallel actin filament bundle assembly","termid":"GO:0030046"},{"relation_name":"part_of","term_name":"microvillus assembly","termid":"GO:0030033"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0030036"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0007010"}],"interesting_parent_ids":["GO:0007010","GO:0008150","GO:0030036","GO:0044085"],"is_obsolete":false,"name":"microvillar actin bundle assembly","termid":"GO:0030034"}


id: GO:0102346
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: (R)-3-hydroxycerotoyl-CoA(4-) = trans-2-hexacosenoyl-CoA(4-) + H2O.","definition_xrefs":["GOC:pz","EC:4.2.1.134"],"gene_count":0,"genotype_count":0,"name":"obsolete 3-hydroxy-cerotoyl-CoA dehydratase activity (obsolete GO:0102346)","termid":"GO:0102346"}


id: SO:0000478
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Genomic DNA of immunoglobulin/T-cell receptor gene including C-region (and introns if present) with 5' UTR (SO:0000204) and 3' UTR (SO:0000205).","direct_ancestors":[{"relation_name":"is_a","term_name":"vertebrate_immunoglobulin_T_cell_receptor_segment","termid":"SO:0000460"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C_gene_segment","synonyms":[{"name":"C gene","type":"exact"},{"name":"C_GENE","type":"exact"},{"name":"INSDC_feature:C_region","type":"exact"},{"name":"constant gene","type":"exact"}],"termid":"SO:0000478"}


id: MONDO:0023757
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Meralgia paresthetica is a condition characterized by tingling, numbness and burning pain in the outer thigh. These symptoms may become worse after walking or standing. The condition generally only affects one side of the body, although both sides may be involved in up to 20% of cases. Meralgia paresthetica is caused by compression of the lateral femoral cutaneous nerve (a sensory nerve to the skin on the outer thigh). This may be associated with a variety of causes such as tight clothing, obesity, and/or pregnancy. Treatment is based on the signs and symptoms present in each person and may include medications to manage pain. In most cases, conservative treatment by wearing looser clothing and/or losing weight generally resolves symptoms.","definition_xrefs":["GARD:0009417"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nerve compression syndrome","termid":"MONDO:0003615"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"}],"interesting_parent_ids":["MONDO:0005244"],"is_obsolete":false,"name":"meralgia paresthetica","secondary_identifiers":["MESH:C537458","GARD:9417","SCTID:85007004","MEDGEN:101817","UMLS:C0152110","ICD9:355.1"],"synonyms":[{"name":"Bernhardt-Roth syndrome","type":"related"},{"name":"bernhardt's paresthesia","type":"related"},{"name":"bernhardt-rot syndrome","type":"related"},{"name":"compression of lateral cutaneous femoral nerve of thigh","type":"related"},{"name":"entrapment of lateral cutaneous nerve of thigh","type":"related"},{"name":"lateral cutaneous femoral nerve of thigh syndrome","type":"related"},{"name":"lateral femoral cutaneous nerve entrapment","type":"related"},{"name":"meralgia paraesthetica familial (type)","type":"related"}],"termid":"MONDO:0023757","xrefs":{"Monarch":{"xref_id":"0023757"}}}


id: GO:0004290
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the cleavage of the Arg-Xaa bond in Lys-Arg-Xaa and Arg-Arg-Xaa to process Yeast alpha-factor pheromone and killer toxin precursors.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete kexin activity (obsolete GO:0004290)","synonyms":[{"name":"Kex 2p proteinase","type":"narrow"},{"name":"Kex2 endopeptidase","type":"narrow"},{"name":"Kex2 endoprotease","type":"narrow"},{"name":"Kex2 endoproteinase","type":"narrow"},{"name":"Kex2 protease","type":"narrow"},{"name":"Kex2 proteinase","type":"narrow"},{"name":"Kex2-like endoproteinase","type":"narrow"},{"name":"Kex2-like precursor protein processing endoprotease","type":"narrow"},{"name":"andrenorphin-Gly-generating enzyme","type":"related"},{"name":"endoproteinase Kex2p","type":"related"},{"name":"gene KEX2 dibasic proteinase","type":"narrow"},{"name":"kexin activity","type":"exact"},{"name":"paired-basic endopeptidase activity","type":"related"},{"name":"prohormone-processing KEX2 proteinase","type":"narrow"},{"name":"prohormone-processing endoprotease activity","type":"related"},{"name":"prohormone-processing proteinase activity","type":"related"},{"name":"protease KEX2","type":"related"},{"name":"proteinase Kex2p","type":"related"},{"name":"proteinase yscF activity","type":"narrow"},{"name":"yeast KEX2 protease activity","type":"narrow"},{"name":"yeast cysteine proteinase F","type":"related"}],"termid":"GO:0004290"}


id: PBO:0067618
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 790, pseudogene","termid":"PBO:0067618"}


id: GO:0070502
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of poly-gamma-glutamate, a polymer of D- and/or L-glutamic acid residues linked by gamma-peptidyl bonds, that forms all or part of a bacterial capsule.","definition_xrefs":["PMID:16689787","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"capsule organization","termid":"GO:0045230"},{"relation_name":"is_a","term_name":"poly-gamma-glutamate biosynthetic process","termid":"GO:0070501"}],"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":"capsule poly-gamma-glutamate biosynthetic process","synonyms":[{"name":"capsular poly-gamma-glutamate biosynthetic process","type":"exact"},{"name":"capsule poly-gamma-glutamate anabolism","type":"exact"},{"name":"capsule poly-gamma-glutamate biosynthesis","type":"exact"},{"name":"capsule poly-gamma-glutamate formation","type":"exact"},{"name":"capsule poly-gamma-glutamate synthesis","type":"exact"}],"termid":"GO:0070502"}


id: GO:0032619
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of interleukin-16 due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"interleukin-16 production","secondary_identifiers":["GO:0042234","GO:0072614"],"synonyms":[{"name":"IL-16 production","type":"exact"},{"name":"LCF production","type":"narrow"},{"name":"interleukin-16 biosynthetic process","type":"narrow"},{"name":"interleukin-16 secretion","type":"narrow"},{"name":"pro-interleukin-16 production","type":"exact"}],"termid":"GO:0032619"}


id: GO:1904928
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Any coreceptor activity that is involved in a canonical Wnt signaling pathway.","definition_xrefs":["GO_REF:0000061","GOC:PARL","GOC:bf","GOC:TermGenie","PMID:24431302"],"gene_count":0,"genotype_count":0,"name":"obsolete coreceptor activity involved in canonical Wnt signaling pathway (obsolete GO:1904928)","synonyms":[{"name":"Wnt co-receptor activity, canonical signaling","type":"exact"},{"name":"Wnt co-receptor, canonical pathway","type":"exact"},{"name":"coreceptor activity involved in Wnt receptor signaling pathway through beta-catenin","type":"exact"},{"name":"coreceptor activity involved in Wnt receptor signaling pathway via beta-catenin","type":"exact"},{"name":"coreceptor activity involved in Wnt receptor signalling pathway through beta-catenin","type":"exact"},{"name":"coreceptor activity involved in canonical Wnt receptor signaling pathway","type":"exact"},{"name":"coreceptor activity involved in canonical Wnt-activated signaling pathway","type":"exact"},{"name":"coreceptor activity involved in frizzled-1 receptor signaling pathway","type":"narrow"},{"name":"coreceptor, insoluble ligand activity involved in Wnt receptor signaling pathway through beta-catenin","type":"related"},{"name":"coreceptor, insoluble ligand activity involved in Wnt receptor signaling pathway via beta-catenin","type":"related"},{"name":"coreceptor, insoluble ligand activity involved in Wnt receptor signalling pathway through beta-catenin","type":"related"},{"name":"coreceptor, insoluble ligand activity involved in canonical Wnt receptor signaling pathway","type":"related"},{"name":"coreceptor, insoluble ligand activity involved in canonical Wnt signaling pathway","type":"related"},{"name":"coreceptor, insoluble ligand activity involved in canonical Wnt-activated signaling pathway","type":"related"},{"name":"coreceptor, insoluble ligand activity involved in frizzled-1 receptor signaling pathway","type":"related"},{"name":"coreceptor, soluble ligand activity involved in Wnt receptor signaling pathway through beta-catenin","type":"related"},{"name":"coreceptor, soluble ligand activity involved in Wnt receptor signaling pathway via beta-catenin","type":"related"},{"name":"coreceptor, soluble ligand activity involved in Wnt receptor signalling pathway through beta-catenin","type":"related"},{"name":"coreceptor, soluble ligand activity involved in canonical Wnt receptor signaling pathway","type":"related"},{"name":"coreceptor, soluble ligand activity involved in canonical Wnt signaling pathway","type":"related"},{"name":"coreceptor, soluble ligand activity involved in canonical Wnt-activated signaling pathway","type":"related"},{"name":"coreceptor, soluble ligand activity involved in frizzled-1 receptor signaling pathway","type":"related"}],"termid":"GO:1904928"}


id: FYPO:0000347
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a spore has a larger volume than normal. In a swollen cell, both length and diameter are greater than normal, although the cell is only considered elongated if the length:diameter ratio is also greater than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"swollen cell","termid":"FYPO:0000025"},{"relation_name":"is_a","term_name":"abnormal spore morphology","termid":"FYPO:0000348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"swollen spore","synonyms":[{"name":"enlarged spore","type":"related"},{"name":"increased spore size","type":"related"},{"name":"increased spore volume","type":"exact"},{"name":"large spore","type":"related"}],"termid":"FYPO:0000347"}


id: PBO:0089899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial serine-tRNA ligase","termid":"PBO:0089899"}


id: PBO:0058544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6090","termid":"PBO:0058544"}


id: MONDO:0015529
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Paroxysmal hemicrania (PH) is a primary headache disorder characterized by multiple attacks of unilateral pain that occur in association with cranial autonomic symptoms. The hallmarks of this syndrome are the relative shortness of the attacks and the complete response to indomethacin therapy.","definition_xrefs":["Orphanet:157835"],"direct_ancestors":[{"relation_name":"is_a","term_name":"trigeminal autonomic cephalalgia","termid":"MONDO:0015530"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paroxysmal Hemicrania","secondary_identifiers":["MESH:D051302","MEDGEN:235603","UMLS:C1399352","MedDRA:10019461","GARD:10794","EFO:1001822","SCTID:443094001","icd11.foundation:959737563","ICD9:339.03"],"termid":"MONDO:0015529","xrefs":{"Monarch":{"xref_id":"0015529"}}}


id: PBO:0086878
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative transcriptional repressor with Zn(2)-Cys(6) finger; negatively regulates transcription in response to oleate levels, based on mutant phenotype and localization to oleate-responsive promoters; the authentic, non-tagged protein is detected in highly purified mitochondria in high-throughput studies; forms nuclear foci upon DNA replication stress","termid":"PBO:0086878"}


id: PR:P09202
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A fructose-1,6-bisphosphatase class 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fructose-1,6-bisphosphatase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1198.14c","secondary_identifiers":["UniProtKB:P09202"],"synonyms":[{"name":"D-fructose-1,6-bisphosphate 1-phosphohydrolase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"FBPase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"SPBC1198.14c","type":"related"},{"name":"Spom972h-fbp","type":"exact"}],"termid":"PR:P09202"}


id: GO:0047966
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-glucose 6-sulfate + H2O = D-glucose + H+ + sulfate.","definition_xrefs":["EC:3.1.6.3","RHEA:19145"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfuric ester hydrolase activity","termid":"GO:0008484"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016788","GO:0016787"],"is_obsolete":false,"name":"glycosulfatase activity","secondary_identifiers":["KEGG_REACTION:R00534","MetaCyc:GLYCOSULFATASE-RXN"],"synonyms":[{"name":"glucosulfatase activity","type":"related"},{"name":"glycosulphatase activity","type":"exact"},{"name":"sugar-sulfate sulfohydrolase activity","type":"related"}],"termid":"GO:0047966"}


id: PBO:0089741
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA cleavage ubiquitin-protein ligase E3 Mpe1","termid":"PBO:0089741"}


id: PBO:0029942
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-mitotic_catastrophe_with_cut,_elongated_cell_during_cellular_response_to_hydroxyurea","termid":"PBO:0029942"}


id: GO:1990509
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"Protein complex involved in the disassembly of Mago-Y14 from the spliced mRNA during first round of translation, independently of the translational machinery. Conserved from fission yeast to humans.","definition_xrefs":["GOC:bhm","PMID:14968132"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex","termid":"GO:0032991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0032991","GO:0005575"],"is_obsolete":false,"name":"PYM-mago-Y14 complex","synonyms":[{"name":"PYM-mago-RNA-binding protein 8A complex","type":"exact"},{"name":"wibg-mago-tsu complex","type":"exact"}],"termid":"GO:1990509"}


id: GO:0016885
data:
  {"annotated_genes":["SJAG_03313","SJAG_00464"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79137],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0003989"},{"annotations":[74826],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0004736"}]},"cv_name":"molecular_function","definition":"Catalysis of the joining of two molecules via a carbon-carbon bond, with the concomitant hydrolysis of the diphosphate bond in ATP or a similar triphosphate.","definition_xrefs":["EC:6.4.-.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ligase activity","termid":"GO:0016874"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00464":null,"SJAG_03313":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016874"}],"interesting_parent_ids":["GO:0016874","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"ligase activity, forming carbon-carbon bonds","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0016885","terms_by_termid":{"GO:0003989":null,"GO:0004736":null}}


id: GO:0106072
data:
  {"annotated_genes":["SJAG_02311","SJAG_01245","SJAG_00266","SJAG_02426","SJAG_02481"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[115983,107527,91564,99956,92225],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110034"}]},"cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of an adenylate cyclase-activating G protein-coupled receptor signaling pathway.","definition_xrefs":["GOC:hjd","PMID:19246489"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of G protein-coupled receptor signaling pathway","termid":"GO:0045744"},{"relation_name":"is_a","term_name":"regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway","termid":"GO:0106070"},{"relation_name":"negatively_regulates","term_name":"adenylate cyclase-activating G protein-coupled receptor signaling pathway","termid":"GO:0007189"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00266":null,"SJAG_01245":null,"SJAG_02311":null,"SJAG_02426":null,"SJAG_02481":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"negative regulation of adenylate cyclase-activating G-protein coupled receptor signaling pathway","type":"exact"}],"termid":"GO:0106072","terms_by_termid":{"GO:0110034":null}}


id: FYPO:0006044
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells form mitotic spindle microtubules that are longer than normal, and the protruding kinetochore microtubules are surrounded by an extension of the nuclear envelope, with the kinetochore-attached end at the distal tip of the protrusion.","definition_xrefs":["PMID:27146110","PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"nuclear envelope protrusion present during mitosis","termid":"FYPO:0003788"},{"relation_name":"is_a","term_name":"long microtubules","termid":"FYPO:0000055"},{"relation_name":"is_a","term_name":"long mitotic spindle","termid":"FYPO:0000733"},{"relation_name":"is_a","term_name":"nuclear envelope protrusion present during mitosis","termid":"FYPO:0003788"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0002403"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0002403"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000054","FYPO:0002403","FYPO:0001320","FYPO:0000002","FYPO:0005447","FYPO:0000120","FYPO:0002399","FYPO:0001985"],"is_obsolete":false,"name":"long mitotic kinetochore microtubules with kinetochore at tip of nuclear envelope protrusion","synonyms":[{"name":"elongated mitotic kinetochore microtubules with kinetochore at tip of nuclear envelope protrusion","type":"exact"},{"name":"elongated mitotic kinetochore microtubules with kinetochore at tip of nuclear envelope protrusion during M-phase","type":"exact"},{"name":"long mitotic kinetochore microtubules with kinetochore at tip of nuclear envelope deformation","type":"related"},{"name":"long mitotic kinetochore microtubules with kinetochore at tip of nuclear envelope protrusion during mitotic cell cycle","type":"related"},{"name":"long mitotic kinetochore microtubules with kinetochore at tip of nuclear envelope protrusion during vegetative growth","type":"exact"},{"name":"long mitotic spindle microtubules with nuclear envelope protrusion from the kinetochore attached end of the microtubule","type":"exact"},{"name":"nuclear envelope protrusion with long mitotic kinetochore microtubules and kinetochore at tip of nuclear envelope protrusion","type":"exact"}],"termid":"FYPO:0006044"}


id: MOD:01634
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively removes or replaces an L-aspartic acid.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-aspartic acid residue","termid":"MOD:00904"},{"relation_name":"is_a","term_name":"natural, standard, encoded residue removal","termid":"MOD:01651"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-aspartic acid removal","termid":"MOD:01634"}


id: PR:Q9UT33
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DPH3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR21454:SF2","PRO:DNx","OMA:SCHPO01198"],"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":"diphthamide biosynthesis protein 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC8F11.02c","secondary_identifiers":["UniProtKB:Q9UT33"],"synonyms":[{"name":"Spom972h-DPH3","type":"exact"}],"termid":"PR:Q9UT33"}


id: MOD:00339
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to L-cysteinyl hydrogenase diiron subcluster.","definition_xrefs":["RESID:AA0334","PubMed:10694885","PubMed:9836629","Unimod:439#C"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron containing modified residue","termid":"MOD:00738"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-cysteine residue","termid":"MOD:02067"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-cysteinyl hydrogenase diiron subcluster","synonyms":[{"name":"1,7-biscarbonyl-1-(cystein-S-yl)-8-oxo-4-aza-2lambda(3),6 lambda(3)-dithia-1,7-diferratricyclo[4.2.0.0(2,7)]octane-1,7-dicarbonitrile","type":"exact"},{"name":"Diironsubcluster","type":"related"},{"name":"L-cysteinyl hydrogenase diiron subcluster","type":"exact"},{"name":"METAL Diiron subcluster","type":"exact"},{"name":"hydrogenase diiron subcluster","type":"related"},{"name":"mu-carbonyl-dicarbonyl-1kappaC,2kappaC-dicyanido-1kappaC,2kappaC-cysteinato-1kS-1,2-azadimethanthiol-1kS,2kS'-diiron","type":"exact"}],"termid":"MOD:00339"}


id: PBO:0090666
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial GIDA family tRNA uridine 5-carboxymethylaminomethyl modification enzyme Ips1","termid":"PBO:0090666"}


id: PBO:0070748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L10 pseudogene 4","termid":"PBO:0070748"}


id: PBO:0084699
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mitochondrial glutamyl-tRNA synthetase; predicted to be palmitoylated","termid":"PBO:0084699"}


id: GO:0140058
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of a neuron projection are generated and organized into branches. A neuron projection is any process extending from a neural cell, such as axons or dendrites.","definition_xrefs":["PMID:23270857","PMID:23764288","GOC:bc","GOC:aruk","PMID:17114044"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron projection morphogenesis","termid":"GO:0048812"}],"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":"neuron projection arborization","synonyms":[{"name":"branching morphogenesis of a neurite","type":"related"},{"name":"branching morphogenesis of a neuron projection","type":"related"},{"name":"neurite arborization","type":"exact"},{"name":"neurite branching","type":"exact"},{"name":"neuron projection branching","type":"exact"}],"termid":"GO:0140058"}


id: GO:0140700
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + GTP = 2 diphosphate + cyclic G-P(3'-5')A-P(2'-5') (cyclic 3',2' GAMP).","definition_xrefs":["PMID:34261127"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclic GMP-AMP synthase activity","termid":"GO:0140699"}],"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:0016779"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016740","GO:0016779"],"is_obsolete":false,"name":"3',2'-cyclic GMP-AMP synthase activity","synonyms":[{"name":"3',2' cyclic-GMP-AMP synthase activity","type":"exact"},{"name":"3',2'-cyclic GAMP synthase activity","type":"exact"}],"termid":"GO:0140700"}


id: GO:0071869
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 catecholamine stimulus. A catecholamine is any of a group of biogenic amines that includes 4-(2-aminoethyl)pyrocatechol [4-(2-aminoethyl)benzene-1,2-diol] and derivatives formed by substitution.","definition_xrefs":["GOC:mah","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to monoamine","termid":"GO:0071867"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to catecholamine","synonyms":[{"name":"response to catecholamine stimulus","type":"exact"}],"termid":"GO:0071869"}


id: SO:0000448
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An intron located in the 3' UTR.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"UTR_intron","termid":"SO:0000446"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_UTR_intron","synonyms":[{"name":"three prime UTR intron","type":"exact"}],"termid":"SO:0000448"}


id: SO:1000025
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transversion from adenine to thymine.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine_to_pyrimidine_transversion","termid":"SO:1000023"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"A_to_T_transversion","synonyms":[{"name":"A to T transversion","type":"exact"}],"termid":"SO:1000025"}


id: PBO:0076887
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis expressed 38","termid":"PBO:0076887"}


id: _global:causally_upstream_of_or_within,_negative_effect
data:
  {"annotation_feature_type":"gene","cv_name":"external","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_upstream_of_or_within","termid":"_global:causally_upstream_of_or_within"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"causally_upstream_of_or_within,_negative_effect","secondary_identifiers":["RO:0004046"],"termid":"_global:causally_upstream_of_or_within,_negative_effect"}


id: GO:0042369
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of vitamin D, any of a group of related, fat-soluble compounds that are derived from delta-5,7 steroids and play a central role in calcium metabolism. Specific forms of vitamin D include calciferol (ergocalciferol; vitamin D2) and cholecalciferol (calciol; vitamin D3).","definition_xrefs":["ISBN:0471331309","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid catabolic process","termid":"GO:0006706"},{"relation_name":"is_a","term_name":"vitamin D metabolic process","termid":"GO:0042359"},{"relation_name":"is_a","term_name":"fat-soluble vitamin catabolic process","termid":"GO:0042363"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0006766","GO:0006629","GO:0008150"],"is_obsolete":false,"name":"vitamin D catabolic process","synonyms":[{"name":"calciferol catabolic process","type":"narrow"},{"name":"calciferol catabolism","type":"narrow"},{"name":"cholecalciferol biosynthesis","type":"narrow"},{"name":"cholecalciferol biosynthetic process","type":"narrow"},{"name":"ergocalciferol biosynthesis","type":"narrow"},{"name":"ergocalciferol biosynthetic process","type":"narrow"},{"name":"vitamin D breakdown","type":"exact"},{"name":"vitamin D catabolism","type":"exact"},{"name":"vitamin D degradation","type":"exact"}],"termid":"GO:0042369"}


id: PBO:0030556
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_glutamate_import","termid":"PBO:0030556"}


id: MONDO:1011542
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ichthyosis that occurs in greater kudu.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ichthyosis, non-human animal","termid":"MONDO:1011427"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ichthyosis, greater kudu","secondary_identifiers":["OMIA:001993-9946"],"termid":"MONDO:1011542","xrefs":{"Monarch":{"xref_id":"1011542"}}}


id: MONDO:0005027
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A brain disorder characterized by episodes of abnormally increased neuronal discharge resulting in transient episodes of sensory or motor neurological dysfunction, or psychic dysfunction. These episodes may or may not be associated with loss of consciousness or convulsions.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"}],"gene_count":0,"genotype_count":0,"in_subsets":["pombe_mondo_slim"],"is_obsolete":false,"name":"epilepsy","secondary_identifiers":["EFO:0000474","ICD9:345.80","ICD9:345.90","MESH:D004827","NCIT:C3020","MEDGEN:4506","ICD9:345","DOID:1826","ICD10CM:G40","NIFSTD:birnlex_12718","SCTID:84757009","UMLS:C0014544","ICD10WHO:G40","ICD9:345.91","ICD9:345.9","ICD9:345.8"],"synonyms":[{"name":"epilepsy","type":"exact"},{"name":"seizure disorder","type":"exact"}],"termid":"MONDO:0005027","xrefs":{"Monarch":{"xref_id":"0005027"}}}


id: GO:0007042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that reduces the pH of the lysosomal lumen, measured by the concentration of the hydrogen ion.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vacuolar acidification","termid":"GO:0007035"},{"relation_name":"is_a","term_name":"regulation of lysosomal lumen pH","termid":"GO:0035751"}],"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":"lysosomal lumen acidification","synonyms":[{"name":"lysosome pH reduction","type":"exact"}],"termid":"GO:0007042"}


id: PBO:0117383
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"patatin like domain 1, omega-hydroxyceramide transacylase","termid":"PBO:0117383"}


id: GO:0005053
data:
  {"annotated_genes":["SJAG_00326"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72408],"is_not":false,"summary":null,"term":"GO:0005053"}]},"cv_name":"molecular_function","definition":"Binding to a type 2 peroxisome targeting signal, a nonapeptide with a broad consensus sequence of (R/K)-(L/V/I)-(XXXXX)-(H/Q)-(L/A/F).","definition_xrefs":["PMID:11687502","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peroxisome targeting sequence binding","termid":"GO:0000268"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00326":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005048"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005048","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"peroxisome matrix targeting signal-2 binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"PEX7","type":"narrow"},{"name":"PTS2 binding","type":"exact"},{"name":"PTS2 receptor","type":"exact"},{"name":"peroxisomal targeting signal 2 (PTS2) binding","type":"exact"},{"name":"peroxisome targeting signal-2 binding","type":"exact"},{"name":"peroxisome targeting signal-2 receptor","type":"narrow"}],"termid":"GO:0005053","terms_by_termid":{"GO:0005053":null}}


id: PBO:0082918
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytochrome c1 heme lyase; involved in maturation of cytochrome c1, which is a subunit of the mitochondrial ubiquinol-cytochrome-c reductase; links heme covalently to apocytochrome c1; human homolog HCCS can complement yeast cyt2 null mutant","termid":"PBO:0082918"}


id: MONDO:0800196
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cone dystrophy 4","termid":"MONDO:0013129"}],"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":"achromatopsia 5","secondary_identifiers":["UMLS:C2751309","MEDGEN:416519"],"synonyms":[{"name":"ACHM5","type":"exact"}],"termid":"MONDO:0800196","xrefs":{"Monarch":{"xref_id":"0800196"}}}


id: GO:0033780
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: taurochenodeoxycholate + O2 + reduced [NADPH--hemoprotein reductase] +  = taurohyocholate H+ + H2O + oxidized [NADPH--hemoprotein reductase]. Acts on taurochenodeoxycholate, taurodeoxycholate and less readily on lithocholate and chenodeoxycholate.","definition_xrefs":["EC:1.14.14.57"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen","termid":"GO:0016712"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"taurochenodeoxycholate 6alpha-hydroxylase activity","secondary_identifiers":["MetaCyc:RXN-7977"],"synonyms":[{"name":"CYP3A4","type":"related"},{"name":"CYP4A21","type":"related"},{"name":"taurochenodeoxycholate 6alpha-monooxygenase activity","type":"related"},{"name":"taurochenodeoxycholate,NADPH:oxygen oxidoreductase (6alpha-hydroxylating) activity","type":"related"}],"termid":"GO:0033780"}


id: PBO:0071874
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 12","termid":"PBO:0071874"}


id: GO:0060373
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the establishment or extent of a membrane potential in the depolarizing direction away from the resting potential in a ventricular cardiomyocyte.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of membrane depolarization","termid":"GO:0003254"}],"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 ventricular cardiac muscle cell membrane depolarization","synonyms":[{"name":"electrocardiogram QRS complex","type":"related"},{"name":"regulation of ventricular cardiomyocyte membrane depolarization","type":"exact"},{"name":"ventricular depolarization","type":"related"}],"termid":"GO:0060373"}


id: PBO:0081440
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ZNF295 antisense RNA 1","termid":"PBO:0081440"}


id: PBO:0004082
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding protein, involved in ribosome biogenesis (predicted)","termid":"PBO:0004082"}


id: PBO:0056557
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"minichromosome maintenance complex component 5","termid":"PBO:0056557"}


id: GO:0031680
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The heterodimer formed by the beta and gamma subunits of a heterotrimeric G protein, which dissociates from the alpha subunit upon guanine nuclotide exchange.","definition_xrefs":["GOC:mah"],"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:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005737","GO:0005575","GO:0032991"],"is_obsolete":false,"name":"G-protein beta/gamma-subunit complex","synonyms":[{"name":"G-beta/G-gamma complex","type":"exact"},{"name":"heterotrimeric G-protein GTPase, beta-subunit","type":"narrow"}],"termid":"GO:0031680"}


id: PBO:0059900
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND1 pseudogene 23","termid":"PBO:0059900"}


id: GO:0034465
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 carbon monoxide (CO) stimulus.","definition_xrefs":["GOC:ecd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to carbon monoxide","termid":"GO:0034465"}


id: MONDO:0006577
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, progressive, non-neoplastic pathologic process that arises from the maxillary sinus mucosal epithelium. It is characterized by the proliferation of keratinizing squamous epithelium and the formation of keratin sheets. It may lead to bone erosion and infections. Surgical removal is the appropriate treatment.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paranasal sinus disorder","termid":"MONDO:0001735"},{"relation_name":"is_a","term_name":"cholesteatoma","termid":"MONDO:0006530"},{"relation_name":"is_a","term_name":"mouth disorder","termid":"MONDO:0006858"},{"relation_name":"is_a","term_name":"disorder of facial skeleton","termid":"MONDO:0023369"}],"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":"maxillary sinus cholesteatoma","secondary_identifiers":["DOID:867","MEDGEN:277346","NCIT:C35868","UMLS:C1334644"],"synonyms":[{"name":"cholesteatoma (disease) of maxillary sinus","type":"exact"},{"name":"maxillary sinus cholesteatoma (disease)","type":"exact"}],"termid":"MONDO:0006577","xrefs":{"Monarch":{"xref_id":"0006577"}}}


id: GO:0030811
data:
  {"annotated_genes":["SJAG_02785","SJAG_00685","SJAG_05314"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[77912,74846],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045820"},{"annotations":[71770],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006110"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the breakdown of nucleotides.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nucleotide metabolic process","termid":"GO:0006140"},{"relation_name":"is_a","term_name":"regulation of catabolic process","termid":"GO:0009894"},{"relation_name":"regulates","term_name":"nucleotide catabolic process","termid":"GO:0009166"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00685":null,"SJAG_02785":null,"SJAG_05314":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"regulation of nucleotide catabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"regulation of nucleotide breakdown","type":"exact"},{"name":"regulation of nucleotide catabolism","type":"exact"},{"name":"regulation of nucleotide degradation","type":"exact"}],"termid":"GO:0030811","terms_by_termid":{"GO:0006110":null,"GO:0045820":null}}


id: PBO:0004061
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar membrane amino acid uptake transporter Fnx1","termid":"PBO:0004061"}


id: SO:0001202
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A ambisense_RNA_virus is a ss_RNA_viral_sequence that is the sequence of a single stranded RNA virus with both messenger and anti messenger polarity.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ss_RNA_viral_sequence","termid":"SO:0001199"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ambisense_ssRNA_viral_sequence","synonyms":[{"name":"ambisense single stranded RNA virus","type":"exact"},{"name":"ambisense ssRNA viral sequence","type":"exact"}],"termid":"SO:0001202"}


id: PBO:0086982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Regulatory subunit of the vacuolar transporter chaperone (VTC) complex; VTC complex is involved in membrane trafficking, vacuolar polyphosphate accumulation, microautophagy and non-autophagic vacuolar fusion; also has mRNA binding activity; protein abundance increases in response to DNA replication stress","termid":"PBO:0086982"}


id: PATO:0002083
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"Having extra or fewer parts.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"has number of","termid":"PATO:0001555"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"altered number of","termid":"PATO:0002083"}


id: GO:0051566
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: anthocyanidin 3-glucoside + UDP-rhamnose = anthocyanidin 3-rutinoside + UDP.","definition_xrefs":["PMID:8130800"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hexosyltransferase activity","termid":"GO:0016758"}],"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:0003824","GO:0016757","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"anthocyanidin 3-glucoside rhamnosyltransferase activity","synonyms":[{"name":"3RT activity","type":"broad"},{"name":"anthocyanidin 3-glucoside-rhamnosyltransferase activity","type":"exact"}],"termid":"GO:0051566"}


id: PBO:0083521
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified ORF PAC2/YER007W","termid":"PBO:0083521"}


id: GO:0030674
data:
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id: PBO:0000195
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mevalonicaciduria","termid":"PBO:0000195"}


id: PBO:0072834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sin3A associated protein 25","termid":"PBO:0072834"}


id: PBO:0041022
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"BPI fold containing family B member 5, pseudogene","termid":"PBO:0041022"}


id: GO:0060326
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a motile cell guided by a specific chemical concentration gradient. Movement may be towards a higher concentration (positive chemotaxis) or towards a lower concentration (negative chemotaxis).","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemotaxis","termid":"GO:0006935"},{"relation_name":"is_a","term_name":"cell migration","termid":"GO:0016477"},{"relation_name":"part_of","term_name":"cellular response to chemical stimulus","termid":"GO:0070887"}],"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","secondary_identifiers":["Reactome:R-HSA-9664424"],"termid":"GO:0060326"}


id: PBO:0001248
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.4.24.-","termid":"PBO:0001248"}


id: PBO:0038276
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase allele types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleotide_insertion","termid":"PBO:0038276"}


id: PBO:0059974
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND3 pseudogene 19","termid":"PBO:0059974"}


id: PATO:0000227
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  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000227 motor performance (obsolete PATO:0000227)","termid":"PATO:0000227"}


id: GO:0018782
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cis-3-chloroacrylic acid + H2O = H+ + HCl + malonate semialdehyde.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cis-chloroacrylic acid dehalogenase activity (obsolete GO:0018782)","termid":"GO:0018782"}


id: GO:0003222
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the trabecular cardiac ventricle muscle are generated and organized.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ventricular cardiac muscle tissue morphogenesis","termid":"GO:0055010"},{"relation_name":"is_a","term_name":"heart trabecula morphogenesis","termid":"GO:0061384"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"ventricular trabecula myocardium morphogenesis","synonyms":[{"name":"trabecula carnea morphogenesis","type":"related"}],"termid":"GO:0003222"}


id: PBO:0086828
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; YOR338W transcription is regulated by Azf1p and its transcript is a specific target of the G protein effector Scp160p; identified as being required for sporulation in a high-throughput mutant screen; YOR338W has a paralog, FUN19, that arose from the whole genome duplication","termid":"PBO:0086828"}


id: MONDO:0000889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Infections of the nervous system caused by bacteria of the genus haemophilus, and marked by prominent inflammation of the meninges. haemophilus influenzae type B is the most common causative organism. The condition primarily affects children under 6 years of age but may occur in adults.","definition_xrefs":["MESH:D008583"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bacterial meningitis","termid":"MONDO:0006670"},{"relation_name":"is_a","term_name":"haemophilus infectious disease","termid":"MONDO:0006926"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"haemophilus meningitis","secondary_identifiers":["UMLS:C0025292","EFO:1000955","DOID:0080179","MEDGEN:7535","SCTID:192643004","SCTID:5900006","MedDRA:10018953","ICD9:320.0"],"synonyms":[{"name":"Haemophilus influenzae bacterial meningitis","type":"exact"},{"name":"Haemophilus influenzae caused bacterial meningitis","type":"exact"}],"termid":"MONDO:0000889","xrefs":{"Monarch":{"xref_id":"0000889"}}}


id: PBO:0119640
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATR checkpoint kinase","termid":"PBO:0119640"}


id: PBO:0078951
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon TCT) 3-1","termid":"PBO:0078951"}


id: MONDO:0044879
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  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-invasive or invasive cystic epithelial neoplasm that affects almost exclusively females. It is characterized by the presence of columnar mucin-producing epithelial cells and ovarian-type stroma formation.","definition_xrefs":["NCIT:C41247"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucinous neoplasm","termid":"MONDO:0024338"},{"relation_name":"is_a","term_name":"cystic tumor of the pancreas","termid":"MONDO:0044880"}],"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":"pancreatic mucinous-cystic neoplasm","secondary_identifiers":["ONCOTREE:MCN","MEDGEN:274120","UMLS:C1518872"],"synonyms":[{"name":"Pancreatic mucinous cystic neoplasm","type":"exact"},{"name":"Pancreatic mucinous-cystic neoplasm","type":"exact"},{"name":"mucinous cystic neoplasm","type":"related"}],"termid":"MONDO:0044879","xrefs":{"Monarch":{"xref_id":"0044879"}}}


id: FYPO:0001701
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype observed in the vegetative growth phase of the life cycle in which cells show increased sensitivity to bortezomib. Cells stop growing (and may die) at a concentration of bortezomib that allows wild type cells to grow.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased sensitivity to chemical during vegetative growth","termid":"FYPO:0000127"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002683","FYPO:0000003","FYPO:0001985","FYPO:0005447","FYPO:0000139"],"is_obsolete":false,"name":"sensitive to bortezomib","synonyms":[{"name":"hypersensitive to bortezomib","type":"exact"},{"name":"sensitive to Velcade","type":"exact"},{"name":"sensitive to bortezomib during mitotic cell cycle","type":"related"},{"name":"sensitive to bortezomib during vegetative growth","type":"exact"}],"termid":"FYPO:0001701"}


id: PBO:0046577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endogenous retrovirus group K member 19, envelope","termid":"PBO:0046577"}


id: MONDO:0003816
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease involving the articular cartilage of joint.","direct_ancestors":[{"relation_name":"is_a","term_name":"arthropathy","termid":"MONDO:0006816"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"articular cartilage disorder","secondary_identifiers":["MEDGEN:510440","SCTID:53417006","ICD9:718.00","UMLS:C0158073","DOID:6227","ICD9:718.02","ICD9:718.0"],"synonyms":[{"name":"articular cartilage disorder","type":"exact"},{"name":"articular cartilage disorder involving ankle and foot","type":"narrow"},{"name":"articular cartilage disorder involving forearm","type":"narrow"},{"name":"articular cartilage disorder involving hand","type":"narrow"},{"name":"articular cartilage disorder involving multiple sites","type":"narrow"},{"name":"articular cartilage disorder involving pelvic region and thigh","type":"narrow"},{"name":"articular cartilage disorder involving shoulder region","type":"narrow"},{"name":"articular cartilage disorder involving upper arm","type":"narrow"},{"name":"articular cartilage disorder of ankle and/or foot","type":"narrow"},{"name":"articular cartilage disorder of forearm","type":"narrow"},{"name":"articular cartilage disorder of hand","type":"narrow"},{"name":"articular cartilage disorder of multiple sites","type":"narrow"},{"name":"articular cartilage disorder of shoulder region","type":"narrow"},{"name":"articular cartilage disorder of the pelvic region and thigh","type":"narrow"},{"name":"articular cartilage disorder of upper arm","type":"narrow"},{"name":"articular cartilage of joint disease","type":"exact"},{"name":"articular cartilage of joint disease or disorder","type":"exact"},{"name":"disease of articular cartilage of joint","type":"exact"},{"name":"disease or disorder of articular cartilage of joint","type":"exact"},{"name":"disorder of articular cartilage","type":"related"},{"name":"disorder of articular cartilage of joint","type":"exact"}],"termid":"MONDO:0003816","xrefs":{"Monarch":{"xref_id":"0003816"}}}


id: PBO:0028777
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  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-sensitive_to_caffeine_and_rapamycin","termid":"PBO:0028777"}


id: PBO:0080743
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X active specific transcript","termid":"PBO:0080743"}


id: MONDO:0008253
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":"platelet aggregation, spontaneous","secondary_identifiers":["MESH:C566800","MEDGEN:401406","OMIM:173400","UMLS:C1868263"],"synonyms":[{"name":"platelet aggregation, spontaneous","type":"exact"}],"termid":"MONDO:0008253","xrefs":{"Monarch":{"xref_id":"0008253"}}}


id: GO:0140348
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the movement of lysophosphatidylcholine from the exoplasmic to the cytosolic leaflet of a membrane, using energy from the hydrolysis of ATP.","definition_xrefs":["PMID:26945070"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycerophospholipid flippase activity","termid":"GO:0140333"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140303"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0140303","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"lysophosphatidylcholine flippase activity","synonyms":[{"name":"lysophosphatidylcholine flippase activity (exoplasmic to cytosolic leaflet)","type":"exact"}],"termid":"GO:0140348"}


id: GO:0017027
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  {"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 transmembrane receptor protein serine/threonine kinase receptor-associated protein activity (obsolete GO:0017027)","synonyms":[{"name":"transmembrane receptor protein serine/threonine kinase receptor-associated protein activity","type":"exact"}],"termid":"GO:0017027"}


id: PBO:0062136
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily F member 3","termid":"PBO:0062136"}


id: GO:0035127
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring after embryonic development, by which the anatomical structures of the limb are generated and organized. A limb is an appendage of an animal used for locomotion or grasping.","definition_xrefs":["ISBN:0395825172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"limb morphogenesis","termid":"GO:0035108"},{"relation_name":"is_a","term_name":"post-embryonic appendage morphogenesis","termid":"GO:0035120"}],"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 limb morphogenesis","termid":"GO:0035127"}


id: PBO:0068959
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 203, pseudogene","termid":"PBO:0068959"}


id: PR:O42894
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An exosome complex component RRP46 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02536"],"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":"exosome complex component rrp46 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC115.01c","secondary_identifiers":["UniProtKB:O42894"],"synonyms":[{"name":"Spom972h-EXOSC5","type":"exact"},{"name":"ribosomal RNA-processing protein 46 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O42894"}


id: MONDO:0008003
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant form of progressive external ophthalmoplegia.","definition_xrefs":["MONDO:patterns/autosomal_dominant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"progressive external ophthalmoplegia with mitochondrial DNA deletions","termid":"MONDO:0000090"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0005066","MONDO:0004069","MONDO:0000426","MONDO:0002320"],"is_obsolete":false,"name":"autosomal dominant progressive external ophthalmoplegia","secondary_identifiers":["Orphanet:254892","MESH:C563575","UMLS:C5231255","GARD:16486","MEDGEN:1686757"],"synonyms":[{"name":"PEOA1","type":"related"},{"name":"adPEO","type":"exact"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1","type":"related"},{"name":"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 1","type":"exact"},{"name":"progressive external ophthalmoplegia, autosomal dominant","type":"exact"}],"termid":"MONDO:0008003","xrefs":{"Monarch":{"xref_id":"0008003"}}}


id: PBO:0030933
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_sporulation_resulting_in_formation_of_ascus_containing_non-uniform_spores","termid":"PBO:0030933"}


id: PBO:0046429
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPH receptor B4","termid":"PBO:0046429"}


id: PBO:0043032
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"charged multivesicular body protein 4B","termid":"PBO:0043032"}


id: PBO:0003181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"horsetail movement protein Hrs1/Mcp6","termid":"PBO:0003181"}


id: GO:0004754
data:
  {"annotated_genes":["SJAG_02388"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57498],"is_not":false,"summary":null,"term":"GO:0004754"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-saccharopine + H2O + NAD+ = 2-oxoglutarate + L-lysine + H+ + NADH.","definition_xrefs":["RHEA:12440","EC:1.5.1.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"saccharopine dehydrogenase activity","termid":"GO:0004753"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02388":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"saccharopine dehydrogenase (NAD+, L-lysine-forming) activity","references_by_uniquename":{"GO_REF:0000003":null},"secondary_identifiers":["MetaCyc:1.5.1.7-RXN","KEGG_REACTION:R00715"],"synonyms":[{"name":"6-N-(L-1,3-dicarboxypropyl)-L-lysine:NAD+ oxidoreductase (L-lysine-forming)","type":"related"},{"name":"N6-(L-1,3-dicarboxypropyl)-L-lysine:NAD+ oxidoreductase (L-lysine-forming)","type":"related"},{"name":"N6-(glutar-2-yl)-L-lysine:NAD oxidoreductase (L-lysine-forming)","type":"related"},{"name":"dehydrogenase, saccharopine (nicotinamide adenine dinucleotide, lysine forming)","type":"related"},{"name":"epsilon-N-(L-glutaryl-2)-L-lysine:NAD oxidoreductase (L-lysine forming)","type":"related"}],"termid":"GO:0004754","terms_by_termid":{"GO:0004754":null}}


id: MONDO:0003261
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A papillary meningioma that affects the cerebellum.","definition_xrefs":["NCIT:C5270"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerebellar neoplasm","termid":"MONDO:0002913"},{"relation_name":"is_a","term_name":"papillary meningioma","termid":"MONDO:0021088"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"papillary meningioma of the cerebellum","secondary_identifiers":["UMLS:C1332902","DOID:5057","MEDGEN:234109"],"synonyms":[{"name":"cerebellar papillary meningioma","type":"related"},{"name":"cerebellum papillary meningioma","type":"exact"},{"name":"papillary meningioma of cerebellum","type":"exact"},{"name":"papillary meningioma of the cerebellum","type":"exact"}],"termid":"MONDO:0003261","xrefs":{"Monarch":{"xref_id":"0003261"}}}


id: MONDO:0030608
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited interstitial lung disease","termid":"MONDO:0031199"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interstitial lung disease 1","secondary_identifiers":["DOID:0060941","MEDGEN:1794231","UMLS:C5562021","OMIM:619611"],"synonyms":[{"name":"ILD1","type":"exact"},{"name":"interstitial lung disease 1","type":"exact"}],"termid":"MONDO:0030608","xrefs":{"Monarch":{"xref_id":"0030608"}}}


id: CHEBI:18420
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"A magnesium cation that has formula Mg.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"magnesium(2+)","secondary_identifiers":["CHEBI:49736","CHEBI:25112","CHEBI:13379","CHEBI:6635"],"termid":"CHEBI:18420"}


id: GO:0044028
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. An decrease in the epigenetic methylation of cytosine and adenosine residues in DNA.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA hypomethylation (obsolete GO:0044028)","termid":"GO:0044028"}


id: PBO:0027739
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_localization_to_cell_tip_during_cellular_response_to_salt_stress","termid":"PBO:0027739"}


id: PBO:0033757
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_spindle_pole_body_duplication","termid":"PBO:0033757"}


id: PBO:0113420
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA-binding ribosome assembly factor; constituent of early pre-60S particles; genetically and physically linked to most NOP8 60s ribosome pre-assembly complex members and to ribosomal protein Rpl3p; contains two independent RNA-interacting domains; associates with helix H95 in 3' region of 25S rRNA, in close proximity to binding sites of Npa1p and Rpl3p; interacts with several snoRNAs","termid":"PBO:0113420"}


id: GO:0160073
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a Casparian strip, a region of plant cell wall specialised to act as a seal to prevent back leakage of secreted material.","definition_xrefs":["PMID:28104889"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular component assembly","termid":"GO:0022607"},{"relation_name":"part_of","term_name":"plant-type cell wall assembly","termid":"GO:0071668"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0071554"],"is_obsolete":false,"name":"Casparian strip assembly","synonyms":[{"name":"Casparian strip formation","type":"exact"}],"termid":"GO:0160073"}


id: GO:0019438
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of aromatic compounds, any substance containing an aromatic carbon ring.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete aromatic compound biosynthetic process (obsolete GO:0019438)","termid":"GO:0019438"}


id: GO:0007498
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the mesoderm over time, from its formation to the mature structure. The mesoderm is the middle germ layer that develops into muscle, bone, cartilage, blood and connective tissue.","definition_xrefs":["GOC:tb","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tissue development","termid":"GO:0009888"}],"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":"mesoderm development","termid":"GO:0007498"}


id: GO:1903508
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of nucleic acid-templated transcription.","definition_xrefs":["GOC:txnOH","GOC:vw","GOC:pr","GO_REF:0000058","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of nucleic acid-templated transcription (obsolete GO:1903508)","synonyms":[{"name":"activation of nucleic acid-templated transcription","type":"narrow"},{"name":"up regulation of nucleic acid-templated transcription","type":"exact"},{"name":"up-regulation of nucleic acid-templated transcription","type":"exact"},{"name":"upregulation of nucleic acid-templated transcription","type":"exact"}],"termid":"GO:1903508"}


id: FYPO:0006162
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to chromatin is normal (i.e. indistinguishable from wild type) during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization during meiosis","termid":"FYPO:0003790"},{"relation_name":"is_a","term_name":"normal protein localization to chromatin","termid":"FYPO:0006163"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"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:0000257"],"is_obsolete":false,"name":"normal protein localization to chromatin during meiosis I","synonyms":[{"name":"normal protein localisation to chromatin during meiosis I","type":"exact"},{"name":"normal protein localization to chromatin during first meiotic nuclear division","type":"exact"}],"termid":"FYPO:0006162"}


id: GO:0052320
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates, maintains or increases the frequency, rate or extent of phytoalexin metabolism, the chemical reactions and pathways involving phytoalexins.","definition_xrefs":["GOC:mtg_pamgo_17jul06"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of phytoalexin metabolic process (obsolete GO:0052320)","synonyms":[{"name":"activation of phytoalexin metabolism","type":"narrow"},{"name":"positive regulation of phytoalexin metabolism","type":"related"},{"name":"stimulation of phytoalexin metabolism","type":"narrow"},{"name":"up regulation of phytoalexin metabolism","type":"exact"},{"name":"up-regulation of phytoalexin metabolism","type":"exact"},{"name":"upregulation of phytoalexin metabolism","type":"exact"}],"termid":"GO:0052320"}


id: MONDO:0003649
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the esophagus.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system neuroendocrine tumor, grade 1/2","termid":"MONDO:0000386"},{"relation_name":"is_a","term_name":"neoplasm of esophagus","termid":"MONDO:0021355"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0004335"],"is_obsolete":false,"name":"esophageal neuroendocrine tumor","secondary_identifiers":["UMLS:C2987260","NCIT:C95616","MEDGEN:459486","GARD:22058","Orphanet:506136","DOID:5784"],"synonyms":[{"name":"NEN of esophagus","type":"exact"},{"name":"NEN of oesophagus","type":"exact"},{"name":"esophageal NEN","type":"exact"},{"name":"esophageal NET","type":"exact"},{"name":"esophageal neuroendocrine neoplasm","type":"exact"},{"name":"esophageal neuroendocrine tumor","type":"exact"},{"name":"esophageal well differentiated endocrine tumor","type":"exact"},{"name":"esophageal well differentiated endocrine tumor/carcinoma","type":"exact"},{"name":"esophageal well differentiated endocrine tumour","type":"exact"},{"name":"esophagus NET","type":"exact"},{"name":"esophagus neuroendocrine neoplasm","type":"exact"},{"name":"esophagus neuroendocrine tumor","type":"exact"},{"name":"esophagus neuroendocrine tumor, well differentiated, low or intermediate grade","type":"exact"},{"name":"neuroendocrine neoplasm of esophagus","type":"exact"},{"name":"neuroendocrine neoplasm of oesophagus","type":"exact"},{"name":"neuroendocrine tumor of esophagus","type":"exact"},{"name":"neuroendocrine tumour of oesophagus","type":"exact"},{"name":"oesophagus NET","type":"exact"},{"name":"oesophagus neuroendocrine neoplasm","type":"exact"},{"name":"oesophagus neuroendocrine tumor, well differentiated, low or intermediate grade","type":"exact"},{"name":"oesophagus neuroendocrine tumour","type":"exact"}],"termid":"MONDO:0003649","xrefs":{"Monarch":{"xref_id":"0003649"}}}


id: GO:0042262
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which DNA is protected from damage by, for example, oxidative stress.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"DNA metabolic process","termid":"GO:0006259"},{"relation_name":"is_a","term_name":"cellular response to stress","termid":"GO:0033554"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006259","GO:0008150"],"is_obsolete":false,"name":"DNA protection","termid":"GO:0042262"}


id: PATO:0001620
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A structural quality inhering in a cell or blood vessel or capillary by virtue of the bearer's being in a rigid state of fullness resulting from pressure of the contents against the wall or membrane.","definition_xrefs":["WordNet:WordNet"],"direct_ancestors":[{"relation_name":"is_a","term_name":"structure","termid":"PATO:0000141"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"turgor","termid":"PATO:0001620"}


id: PBO:0087919
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transcription factor targeting filamentation genes and Ty1 expression; Ste12p activation of most filamentation gene promoters depends on Tec1p and Tec1p transcriptional activity is dependent on its association with Ste12p; binds to TCS elements upstream of filamentation genes, which are regulated by Tec1p/Ste12p/Dig1p complex; competes with Dig2p for binding to Ste12p/Dig1p; positive regulator of chronological life span; TEA/ATTS DNA-binding domain family member","termid":"PBO:0087919"}


id: PBO:0057246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 449c","termid":"PBO:0057246"}


id: FYPO:0007221
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 acetylation of lysine at position 18 of histone H3 in regions containing protein-coding genes is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:31260531","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal histone acetylation during vegetative growth","termid":"FYPO:0003221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000257","FYPO:0001312"],"is_obsolete":false,"name":"normal histone H3-K18 acetylation at protein coding gene during vegetative growth","synonyms":[{"name":"normal histone H3-K18 acetylation at protein coding gene during mitotic cell cycle","type":"related"},{"name":"normal histone H3-K18 acetylation at protein-coding gene during vegetative growth","type":"exact"},{"name":"normal histone H3K18 acetylation at protein coding gene during vegetative growth","type":"exact"}],"termid":"FYPO:0007221"}


id: MONDO:0015142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete ataxia syndrome (obsolete MONDO:0015142)","termid":"MONDO:0015142","xrefs":{"Monarch":{"xref_id":"0015142"}}}


id: GO:1905332
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of morphogenesis of an epithelium.","definition_xrefs":["GO_REF:0000058","PMID:25745997","GOC:bhm","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of morphogenesis of an epithelium","termid":"GO:1905330"},{"relation_name":"positively_regulates","term_name":"morphogenesis of an epithelium","termid":"GO:0002009"}],"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 morphogenesis of an epithelium","synonyms":[{"name":"activation of epithelium morphogenesis","type":"narrow"},{"name":"activation of morphogenesis of an epithelium","type":"narrow"},{"name":"positive regulation of epithelium morphogenesis","type":"exact"},{"name":"up regulation of epithelium morphogenesis","type":"exact"},{"name":"up regulation of morphogenesis of an epithelium","type":"exact"},{"name":"up-regulation of epithelium morphogenesis","type":"exact"},{"name":"up-regulation of morphogenesis of an epithelium","type":"exact"},{"name":"upregulation of epithelium morphogenesis","type":"exact"},{"name":"upregulation of morphogenesis of an epithelium","type":"exact"}],"termid":"GO:1905332"}


id: MOD:01651
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively removes or replaces a natural, standard, encoded residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"natural residue","termid":"MOD:00009"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"natural, standard, encoded residue removal","termid":"MOD:01651"}


id: PBO:0018067
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Threonine DeAminase","termid":"PBO:0018067"}


id: GO:0015417
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + H2O + polyamine(out) = ADP + phosphate + polyamine(in).","definition_xrefs":["RHEA:29999"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyamine transmembrane transporter activity","termid":"GO:0015203"},{"relation_name":"is_a","term_name":"ABC-type transporter activity","termid":"GO:0140359"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0003674","GO:0022857"],"is_obsolete":false,"name":"ABC-type polyamine transporter activity","secondary_identifiers":["GO:0015595","EC:7.6.2.11","MetaCyc:3.6.3.31-RXN"],"synonyms":[{"name":"ATP-dependent polyamine transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled polyamine transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled spermidine transmembrane transporter activity","type":"narrow"},{"name":"polyamine ABC transporter","type":"narrow"},{"name":"polyamine porter activity","type":"broad"},{"name":"polyamine-importing ATPase activity","type":"narrow"},{"name":"polyamine-transporting ATPase activity","type":"related"},{"name":"spermidine porter activity","type":"narrow"},{"name":"spermidine-importing ATPase activity","type":"narrow"}],"termid":"GO:0015417"}


id: MONDO:0001259
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ischemic necrosis of the pituitary gland.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"necrosis of pituitary","termid":"MONDO:0002721"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pituitary gland infarction","secondary_identifiers":["ICD9:253.8","MEDGEN:137969","NCIT:C27117","UMLS:C0342405","icd11.foundation:765046957","SCTID:95830009","DOID:1130"],"synonyms":[{"name":"pituitary gland infarction","type":"exact"},{"name":"pituitary infarct","type":"exact"},{"name":"pituitary infarction","type":"exact"}],"termid":"MONDO:0001259","xrefs":{"Monarch":{"xref_id":"0001259"}}}


id: PBO:0047893
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fragile site, aphidicolin type, common, fra(6)(q15)","termid":"PBO:0047893"}


id: GO:0050742
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The formation of a protein-FMN linkage via S-(4a-FMN)-L-cysteine.","definition_xrefs":["RESID:AA0351"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-FMN linkage via S-(4a-FMN)-L-cysteine (obsolete GO:0050742)","termid":"GO:0050742"}


id: SO:0001410
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A region which is the result of some arbitrary experimental procedure. The procedure may be carried out with biological material or inside a computer.","definition_xrefs":["SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"region","termid":"SO:0000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"experimental_feature","synonyms":[{"name":"analysis feature","type":"related"},{"name":"experimental output artefact","type":"exact"},{"name":"experimental_output_artefact","type":"exact"}],"termid":"SO:0001410"}


id: PBO:0077760
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TOMM20 pseudogene 2","termid":"PBO:0077760"}


id: PBO:0082178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADP-ribosylation factor GTPase activating protein (ARF GAP); involved in ER-Golgi transport; required for prospore membrane formation; regulates phospholipase Spo14p; shares functional similarity with Glo3p; GCS1 has a paralog, SPS18, that arose from the whole genome duplication","termid":"PBO:0082178"}


id: MOD:00101
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to L-lysine amide.","definition_xrefs":["RESID:AA0092","PubMed:6579533"],"direct_ancestors":[{"relation_name":"is_a","term_name":"C1-amidated residue","termid":"MOD:00883"},{"relation_name":"is_a","term_name":"modified L-lysine residue","termid":"MOD:00912"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-lysine amide","synonyms":[{"name":"(2S)-2,6-diaminohexanamide","type":"exact"},{"name":"L-lysine amide","type":"exact"},{"name":"LysN","type":"exact"},{"name":"MOD_RES Lysine amide","type":"exact"},{"name":"amidated L-lysine","type":"exact"},{"name":"lysinamide","type":"exact"}],"termid":"MOD:00101"}


id: PBO:0043983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colony stimulating factor 1","termid":"PBO:0043983"}


id: PBO:0080674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WHAMM pseudogene 1","termid":"PBO:0080674"}


id: PBO:0053259
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIF interleukin 6 family cytokine","termid":"PBO:0053259"}


id: MONDO:0006581
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Miliaria rubraor prickly heat occurs deeper in the epidermis (outside layer of skin) and results in very itchy red papules (bumps).","definition_xrefs":["EFO:1000735"],"direct_ancestors":[{"relation_name":"is_a","term_name":"miliaria","termid":"MONDO:0006580"}],"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":"miliaria rubra","secondary_identifiers":["MEDGEN:57902","DOID:11153","icd11.foundation:1245016385","ICD9:705.1","SCTID:44279002","UMLS:C0162423"],"synonyms":[{"name":"miliaria crystallina","type":"related"},{"name":"prickly heat - miliaria","type":"exact"},{"name":"sudamina","type":"exact"}],"termid":"MONDO:0006581","xrefs":{"Monarch":{"xref_id":"0006581"}}}


id: MONDO:0019795
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acalvaria is a rare malformation defined as missing scalp and flat bones over an area of the cranial vault. The size of the affected area is variable. In rare cases, acalvaria involves the whole of the dome-like superior portion of the cranium comprising the frontal, parietal, and occipital bones. Dura mater and associated muscles are absent in the affected area but the central nervous system is usually unaffected, although some neuropathological abnormality is often present (e.g. holoprosencephaly or gyration anomalies). Skull base and facial bones are normal.","definition_xrefs":["Orphanet:945"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disorder of development or morphogenesis","termid":"MONDO:0021147"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acalvaria","secondary_identifiers":["GARD:361","MEDGEN:418951","MESH:D009436","SCTID:203923004","icd11.foundation:1719021696","UMLS:C2930936","MESH:C535570"],"synonyms":[{"name":"Acrania","type":"exact"},{"name":"primary acalvaria","type":"related"}],"termid":"MONDO:0019795","xrefs":{"Monarch":{"xref_id":"0019795"}}}


id: GO:0050795
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of behavior, the internally coordinated responses (actions or inactions) of whole living organisms (individuals or groups) to internal or external stimuli.","definition_xrefs":["GOC:go_curators","GOC:pr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"regulates","term_name":"behavior","termid":"GO:0007610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of behavior","synonyms":[{"name":"regulation of behaviour","type":"exact"}],"termid":"GO:0050795"}


id: CHEBI:26710
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","definition":"An inorganic chloride salt having sodium(1+) as the counterion.","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sodium chloride","termid":"CHEBI:26710"}


id: MONDO:0004938
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The psychological or physiological need to take a substance in order to experience its effects or to avoid the effects of its absence.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"substance-related disorder","termid":"MONDO:0002494"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"substance dependence","secondary_identifiers":["ICD9:304.60","DOID:9973","SCTID:2403008","UMLS:C0038580","MEDGEN:20989","NCIT:C35458"],"synonyms":[{"name":"dependence","type":"exact"}],"termid":"MONDO:0004938","xrefs":{"Monarch":{"xref_id":"0004938"}}}


id: GO:0008212
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving mineralocorticoids, hormonal C21 corticosteroids synthesized from cholesterol. Mineralocorticoids act primarily on water and electrolyte balance.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"steroid metabolic process","termid":"GO:0008202"},{"relation_name":"is_a","term_name":"hormone metabolic process","termid":"GO:0042445"}],"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":"mineralocorticoid metabolic process","synonyms":[{"name":"mineralocorticoid metabolism","type":"exact"}],"termid":"GO:0008212"}


id: GO:0062125
data:
  {"annotated_genes":["SJAG_03550","SJAG_01517","SJAG_01249"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[112263,98212],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070131"},{"annotations":[99978],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070134"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mitochondrial gene expression. Gene expression is the process in which a gene's coding sequence is converted into a mature gene product (protein or RNA).","definition_xrefs":["PMID:28285835"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of gene expression","termid":"GO:0010468"},{"relation_name":"regulates","term_name":"mitochondrial gene expression","termid":"GO:0140053"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01249":null,"SJAG_01517":null,"SJAG_03550":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0140053"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150","GO:0140053"],"is_obsolete":false,"name":"regulation of mitochondrial gene expression","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0062125","terms_by_termid":{"GO:0070131":null,"GO:0070134":null}}


id: GO:0070791
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the cleistothecium over time, from its formation to the mature structure. The cleistothecium is a closed sexual fruiting body that contains ascospores in linear asci, characteristic of some filamentous Ascomycete fungi such as members of the genera Aspergillus and Emericella.","definition_xrefs":["ISBN:0471522295","PMID:17446882"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sporocarp development involved in sexual reproduction","termid":"GO:0000909"}],"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":"cleistothecium development","termid":"GO:0070791"}


id: MONDO:0003515
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A teratoma that arises from the fallopian tube. It is a rare tumor, often found incidentally.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teratoma","termid":"MONDO:0002601"},{"relation_name":"is_a","term_name":"fallopian tube germ cell tumor","termid":"MONDO:0003392"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fallopian tube teratoma","secondary_identifiers":["MEDGEN:309129","UMLS:C1517127","NCIT:C40131","DOID:5564"],"synonyms":[{"name":"fallopian tube teratoma","type":"exact"}],"termid":"MONDO:0003515","xrefs":{"Monarch":{"xref_id":"0003515"}}}


id: PBO:0044731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DEAD-box helicase 17","termid":"PBO:0044731"}


id: PBO:0057465
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR583 host gene","termid":"PBO:0057465"}


id: PBO:0083748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential component of the TIM23 complex; tethers the import motor and regulatory factors (PAM complex) to the translocation channel (Tim23p-Tim17p core complex); TIM23 complex is short for the translocase of the inner mitochondrial membrane","termid":"PBO:0083748"}


id: GO:1904551
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an arachidonic acid stimulus.","definition_xrefs":["GOC:TermGenie","GO_REF:0000071","PMID:16382163"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to fatty acid","termid":"GO:0071398"},{"relation_name":"is_a","term_name":"response to arachidonate","termid":"GO:1904550"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to arachidonate","synonyms":[{"name":"cellular response to arachidonic acid","type":"exact"}],"termid":"GO:1904551"}


id: GO:0140638
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A small heterodimeric protein complex that is required during early maturation of nascent 40S ribosomal subunits. The complex has endonuclease activity, it interacts with the small ribosomal subunit pre-rRNA and cleave it it to produce the mature 18S (or small ribosomal subunit) rRNA. In S. cerevisiae it is composed of Rcl1p and Bms1p.","definition_xrefs":["PMID:25064857","GOC:lnp","PMID:21849504"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoribonuclease complex","termid":"GO:1902555"}],"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":"small ribosomal subunit processing complex","synonyms":[{"name":"small ribosomal subunit maturation complex","type":"related"}],"termid":"GO:0140638"}


id: MOD:02022
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-lysine residue to N6-cervonoyl-L-lysine.","direct_ancestors":[{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"},{"relation_name":"is_a","term_name":"N-cervonoylated residue","termid":"MOD:02023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"},{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01875","MOD:01155"],"is_obsolete":false,"name":"N6-cervonoyl-L-lysine","termid":"MOD:02022"}


id: GO:0048512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The specific behavior of an organism that recurs with a regularity of approximately 24 hours.","definition_xrefs":["GOC:pr","GOC:bf","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"rhythmic behavior","termid":"GO:0007622"},{"relation_name":"is_a","term_name":"circadian rhythm","termid":"GO:0007623"}],"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":"circadian behavior","synonyms":[{"name":"circadian rhythm behavior","type":"exact"}],"termid":"GO:0048512"}


id: GO:0120550
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 5'-end (N(7)-methyl 5'-triphosphoguanosine)-(2'-O-methyl-ribonucleoside)-(ribonucleotide) in mRNA or snRNA + S-adenosyl-L-methionine = a 5'-end (N(7)-methyl 5'-triphosphoguanosine)-(2'-O-methyl-ribonucleoside)-(2'-O-methyl-ribonucleotide) in mRNA or snRNA + S-adenosyl-L-homocysteine + H+. This activity catalyzes the methylation of the ribose on the second transcribed nucleotide of mRNAs and snRNAs.","definition_xrefs":["EC:2.1.1.296"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-methyltransferase activity","termid":"GO:0008171"},{"relation_name":"is_a","term_name":"RNA methyltransferase activity","termid":"GO:0008173"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016741"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016741","GO:0140098","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"methyltransferase cap2 activity","secondary_identifiers":["MetaCyc:RXN-14928"],"synonyms":[{"name":"cap2-MTase activity","type":"exact"},{"name":"mRNA (nucleoside-2'-O-)-methyltransferase activity","type":"related"}],"termid":"GO:0120550"}


id: MONDO:0004073
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete dentin dysplasia (obsolete MONDO:0004073)","termid":"MONDO:0004073","xrefs":{"Monarch":{"xref_id":"0004073"}}}


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


id: MONDO:0016869
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal deletion","termid":"MONDO:0000761"},{"relation_name":"is_a","term_name":"chromosome 4 disorder","termid":"MONDO:0700011"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of chromosome 4","secondary_identifiers":["MEDGEN:1825958","GARD:20792","Orphanet:261781","UMLS:C5679648"],"synonyms":[{"name":"partial deletion of chromosome type 4","type":"exact"},{"name":"partial monosomy of chromosome 4","type":"exact"}],"termid":"MONDO:0016869","xrefs":{"Monarch":{"xref_id":"0016869"}}}


id: GO:1900863
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of cordyol C biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of small molecule metabolic process","termid":"GO:0062013"},{"relation_name":"is_a","term_name":"positive regulation of secondary metabolite biosynthetic process","termid":"GO:1900378"},{"relation_name":"is_a","term_name":"regulation of cordyol C biosynthetic process","termid":"GO:1900861"},{"relation_name":"positively_regulates","term_name":"cordyol C biosynthetic process","termid":"GO:1900799"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"positive regulation of cordyol C biosynthetic process","synonyms":[{"name":"activation of cordyol C biosynthetic process","type":"narrow"},{"name":"up regulation of cordyol C biosynthetic process","type":"exact"},{"name":"up-regulation of cordyol C biosynthetic process","type":"exact"},{"name":"upregulation of cordyol C biosynthetic process","type":"exact"}],"termid":"GO:1900863"}


id: PBO:0051661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"InaF motif containing 1","termid":"PBO:0051661"}


id: FYPO:0000214
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 mitotic chromosome condensation is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mitotic sister chromatid segregation","termid":"FYPO:0000141"},{"relation_name":"is_a","term_name":"abnormal chromosome condensation","termid":"FYPO:0000159"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"part_of","termid":"FYPO:0000337"},{"rel_name":"part_of","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"part_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"part_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000337"}],"interesting_parent_ids":["FYPO:0000337","FYPO:0000631","FYPO:0005447","FYPO:0000002","FYPO:0000641","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"abnormal mitotic chromosome condensation","synonyms":[{"name":"abnormal chromosome condensation during mitotic cell cycle","type":"related"},{"name":"abnormal mitotic chromosome condensation during vegetative growth","type":"exact"}],"termid":"FYPO:0000214"}


id: PBO:0071868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 6","termid":"PBO:0071868"}


id: PR:Q9USX8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- lea1 gene.","definition_xrefs":["UniProtKB:Q9USX8","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":"U2 small nuclear ribonucleoprotein A' (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1861.08c","synonyms":[{"name":"Spom972h-lea1","type":"exact"},{"name":"U2 snRNP A' (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9USX8"}


id: MONDO:0020764
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"carcinoma, non-human animal","termid":"MONDO:0700101"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Brown-Pearce carcinoma","secondary_identifiers":["MESH:D002284","EFO:1001278"],"synonyms":[{"name":"Brown-Pearce carcinoma","type":"exact"},{"name":"Brown-Pearce epithelioma","type":"exact"},{"name":"Brown-Pearce tumor","type":"exact"},{"name":"Brown-Pearce tumour","type":"exact"},{"name":"carcinoma, Brown Pearce","type":"exact"},{"name":"carcinoma, Brown-Pearce","type":"exact"},{"name":"epithelioma, Brown Pearce","type":"exact"},{"name":"epithelioma, Brown-Pearce","type":"exact"}],"termid":"MONDO:0020764","xrefs":{"Monarch":{"xref_id":"0020764"}}}


id: PBO:0113531
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Vacuolar membrane cation-chloride cotransporter (CCC); involved in potassium homeostasis and salt tolerance; localizes to sites of contact between vacuole and mitochondria (vCLAMPs); targeted to vacuole via AP-3 pathway; similar to mammalian electroneutral Na(+)-(K+)-C1- cotransporter family","termid":"PBO:0113531"}


id: GO:1905267
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any endonucleolytic RNA phosphodiester bond hydrolysis that is involved in tRNA processing.","definition_xrefs":["GO_REF:0000060","GOC:TermGenie","PMID:25401760"],"gene_count":0,"genotype_count":0,"name":"obsolete endonucleolytic cleavage involved in tRNA processing (obsolete GO:1905267)","synonyms":[{"name":"RNA phosphodiester bond hydrolysis, endonucleolytic involved in tRNA maturation","type":"exact"}],"termid":"GO:1905267"}


id: PBO:0111422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exocyst complex subunit Exo1","termid":"PBO:0111422"}


id: MONDO:0016377
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pitt-Hopkins-like syndrome is a rare, genetic, syndromic intellectual disability disorder characterized by severe intellectual disability, lack of speech with normal, or mildly delayed, motor development, episodic breathing abnormalities, early-onset seizures and facial dysmorphism which only includes a wide mouth. Abnormal sleep-wake cycles, autistic behavior and stereotypic movements are commonly associated.","definition_xrefs":["GARD:0011967"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"monogenic epilepsy","termid":"MONDO:0015653"},{"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":"Pitt-Hopkins-like syndrome","secondary_identifiers":["MEDGEN:1648432","GARD:11967","Orphanet:221150","UMLS:C4751168"],"synonyms":[{"name":"PTHSL","type":"exact"}],"termid":"MONDO:0016377","xrefs":{"Monarch":{"xref_id":"0016377"}}}


id: MONDO:0971142
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"malignant mesothelioma","termid":"MONDO:0006292"}],"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":"diffused pleural mesothelioma","secondary_identifiers":["UMLS:C5925095","MEDGEN:1863751","Orphanet:675837"],"termid":"MONDO:0971142","xrefs":{"Monarch":{"xref_id":"0971142"}}}


id: PBO:0073864
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 9 member B1","termid":"PBO:0073864"}


id: PBO:0078120
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor alpha variable 8-2","termid":"PBO:0078120"}


id: MONDO:0859176
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with motor and speech delay and behavioral abnormalities","secondary_identifiers":["MEDGEN:1794164","OMIM:619470","UMLS:C5561954"],"termid":"MONDO:0859176","xrefs":{"Monarch":{"xref_id":"0859176"}}}


id: PBO:0002696
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U2 snRNP-associated protein Sap145 (predicted)","termid":"PBO:0002696"}


id: GO:0000910
data:
  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id: GO:1901534
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id: MONDO:0013376
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  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"microphthalmia, isolated, with coloboma","termid":"MONDO:0000170"}],"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":"microphthalmia, isolated, with coloboma 6","secondary_identifiers":["MEDGEN:462318","OMIM:613703","UMLS:C3150968","GARD:15692"],"synonyms":[{"name":"MCOPCB6","type":"related"},{"name":"microphthalmia with coloboma 6","type":"exact"},{"name":"microphthalmia with coloboma 6, digenic","type":"exact"},{"name":"microphthalmia, isolated, with coloboma 6","type":"exact"},{"name":"microphthalmia, isolated, with coloboma type 6","type":"exact"}],"termid":"MONDO:0013376","xrefs":{"Monarch":{"xref_id":"0013376"}}}


id: PBO:0091990
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wtf antidote-like meiotic drive suppressor Wtf25","termid":"PBO:0091990"}


id: PBO:0058093
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4309","termid":"PBO:0058093"}


id: PBO:0032706
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id: PBO:0076690
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id: GO:0015056
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id: PBO:0045697
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id: PBO:0047404
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id: PBO:0113350
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id: GO:0039546
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways performed by a virus resulting in the hydrolysis of the host MAVS (mitochondrial inhibitor of viral signaling) protein by cleavage of peptide bonds, thereby inhibiting the host innate immune response. For example, MAVS harbors a C-terminal transmembrane domain that targets it to the mitochondrial outer membrane; cleavage within this domain removes MAVS from the membrane, thus preventing it from signaling.","definition_xrefs":["PMID:21436888","PMID:22238314"],"gene_count":0,"genotype_count":0,"name":"obsolete suppression by virus of host MAVS activity by MAVS proteolysis (obsolete GO:0039546)","synonyms":[{"name":"viral protease cleavage of MAVS","type":"exact"}],"termid":"GO:0039546"}


id: GO:0051304
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id: PBO:0088222
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id: PBO:0077355
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id: GO:0034773
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id: PBO:0029939
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id: PBO:0058808
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  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 7850","termid":"PBO:0058808"}


id: MONDO:0009479
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A multiple congenital anomaly characterized by exocrine pancreatic insufficiency, hypoplasia/aplasia of the nasal alae, hypodontia, sensorineural hearing loss, growth retardation, anal and urogenital malformations, and variable intellectual disability.","definition_xrefs":["Orphanet:2315"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic anorectal malformation (obsolete MONDO:0015246)","termid":"MONDO:0015246"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic hypothyroidism (obsolete MONDO:0015778)","termid":"MONDO:0015778"},{"relation_name":"excluded_subClassOf","term_name":"non-acquired combined pituitary hormone deficiency","termid":"MONDO:0018762"},{"relation_name":"excluded_subClassOf","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"},{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"hearing loss disorder","termid":"MONDO:0005365"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"inherited auditory system disease","termid":"MONDO:0037940"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0006025"],"is_obsolete":false,"name":"Johanson-Blizzard syndrome","secondary_identifiers":["GARD:80","MESH:C564907","NORD:1311","OMIM:243800","UMLS:C0175692","DOID:14694","SCTID:75979009","ICD9:759.89","OMIM:260450","MEDGEN:59798","icd11.foundation:1427330812","MESH:C535880"],"synonyms":[{"name":"JBS","type":"exact"},{"name":"Johanson-BLIZZARD syndrome","type":"related"},{"name":"Johanson-Blizzard syndrome","type":"exact"},{"name":"nasal alar hypoplasia, hypothyroidism, pancreatic achylia and congenital deafness","type":"related"},{"name":"nasal alar hypoplasia, hypothyroidism, pancreatic achylia, and congenital deafness","type":"related"},{"name":"pancreatic insufficiency, combined exocrine","type":"exact"}],"termid":"MONDO:0009479","xrefs":{"Monarch":{"xref_id":"0009479"}}}


id: MONDO:0005436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Postoperative ventricular dysfunction (VnD) occurs in 9-20% of coronary artery bypass graft (CABG) surgical patients and is associated with increased postoperative morbidity and mortality.","definition_xrefs":["EFO:0004889"],"direct_ancestors":[{"relation_name":"is_a","term_name":"coronary artery disorder","termid":"MONDO:0005010"},{"relation_name":"is_a","term_name":"cardiac ventricle disorder","termid":"MONDO:0045001"}],"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":"postoperative ventricular dysfunction","termid":"MONDO:0005436","xrefs":{"Monarch":{"xref_id":"0005436"}}}


id: PR:P21696
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gpd1 gene.","definition_xrefs":["UniProtKB:P21696","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":"glycerol-3-phosphate dehydrogenase [NAD(+)] 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC215.05","synonyms":[{"name":"GPD-C (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"GPDH-C (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gpd1","type":"exact"}],"termid":"PR:P21696"}


id: GO:1902637
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any neural crest cell differentiation that is involved in thymus development.","definition_xrefs":["GOC:TermGenie","GO_REF:0000060","GOC:nhn","PMID:15741317","PMID:18292542"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neural crest cell differentiation","termid":"GO:0014033"},{"relation_name":"part_of","term_name":"thymus development","termid":"GO:0048538"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"neural crest cell differentiation involved in thymus development","termid":"GO:1902637"}


id: PR:000059628
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A GTP-binding protein rhb1 (Schizosaccharomyces pombe) that is non-covalently bound to GDP.","definition_xrefs":["PomBase:VW","PRO:DAN"],"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":"Rhb1/GTP-","pombase_gene_id":"SPBC428.16c","synonyms":[{"name":"PomBase_original_PRO_term_name: GTP-binding protein rhb1, GDP-bound form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Rhb1/GTP-","type":"exact"},{"name":"Spom-rhb1/GDP+","type":"exact"}],"termid":"PR:000059628"}


id: GO:1904922
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of MAPK cascade involved in axon regeneration.","definition_xrefs":["GOC:kmv","GO_REF:0000058","GOC:TermGenie","PMID:20203177"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of MAPK cascade involved in axon regeneration (obsolete GO:1904922)","synonyms":[{"name":"activation of ERK/MAPK cascade involved in axon regeneration","type":"narrow"},{"name":"activation of MAP kinase cascade involved in axon regeneration","type":"narrow"},{"name":"activation of MAP kinase kinase kinase cascade involved in axon regeneration","type":"narrow"},{"name":"activation of MAPK cascade involved in axon regeneration","type":"narrow"},{"name":"activation of MAPK signal transduction involved in axon regeneration","type":"narrow"},{"name":"activation of MAPK signaling involved in axon regeneration","type":"related"},{"name":"activation of MAPK signalling involved in axon regeneration","type":"related"},{"name":"activation of MAPKKK cascade during sporulation involved in axon regeneration","type":"narrow"},{"name":"activation of MAPKKK cascade involved in axon regeneration","type":"narrow"},{"name":"activation of mitogen-activated protein kinase cascade involved in axon regeneration","type":"narrow"},{"name":"positive regulation of ERK/MAPK cascade involved in axon regeneration","type":"narrow"},{"name":"positive regulation of MAP kinase cascade involved in axon regeneration","type":"exact"},{"name":"positive regulation of MAP kinase kinase kinase cascade involved in axon regeneration","type":"exact"},{"name":"positive regulation of MAPK signal transduction involved in axon regeneration","type":"exact"},{"name":"positive regulation of MAPK signaling involved in axon regeneration","type":"related"},{"name":"positive regulation of MAPK signalling involved in axon regeneration","type":"related"},{"name":"positive regulation of MAPKKK cascade during sporulation involved in axon regeneration","type":"narrow"},{"name":"positive regulation of MAPKKK cascade involved in axon regeneration","type":"exact"},{"name":"positive regulation of mitogen-activated protein kinase cascade involved in axon regeneration","type":"exact"},{"name":"up regulation of ERK/MAPK cascade involved in axon regeneration","type":"narrow"},{"name":"up regulation of MAP kinase cascade involved in axon regeneration","type":"exact"},{"name":"up regulation of MAP kinase kinase kinase cascade involved in axon regeneration","type":"exact"},{"name":"up regulation of MAPK cascade involved in axon regeneration","type":"exact"},{"name":"up regulation of MAPK signal transduction involved in axon regeneration","type":"exact"},{"name":"up regulation of MAPK signaling involved in axon regeneration","type":"related"},{"name":"up regulation of MAPK signalling involved in axon regeneration","type":"related"},{"name":"up regulation of MAPKKK cascade during sporulation involved in axon regeneration","type":"narrow"},{"name":"up regulation of MAPKKK cascade involved in axon regeneration","type":"exact"},{"name":"up regulation of mitogen-activated protein kinase cascade involved in axon regeneration","type":"exact"},{"name":"up-regulation of ERK/MAPK cascade involved in axon regeneration","type":"narrow"},{"name":"up-regulation of MAP kinase cascade involved in axon regeneration","type":"exact"},{"name":"up-regulation of MAP kinase kinase kinase cascade involved in axon regeneration","type":"exact"},{"name":"up-regulation of MAPK cascade involved in axon regeneration","type":"exact"},{"name":"up-regulation of MAPK signal transduction involved in axon regeneration","type":"exact"},{"name":"up-regulation of MAPK signaling involved in axon regeneration","type":"related"},{"name":"up-regulation of MAPK signalling involved in axon regeneration","type":"related"},{"name":"up-regulation of MAPKKK cascade during sporulation involved in axon regeneration","type":"narrow"},{"name":"up-regulation of MAPKKK cascade involved in axon regeneration","type":"exact"},{"name":"up-regulation of mitogen-activated protein kinase cascade involved in axon regeneration","type":"exact"},{"name":"upregulation of ERK/MAPK cascade involved in axon regeneration","type":"narrow"},{"name":"upregulation of MAP kinase cascade involved in axon regeneration","type":"exact"},{"name":"upregulation of MAP kinase kinase kinase cascade involved in axon regeneration","type":"exact"},{"name":"upregulation of MAPK cascade involved in axon regeneration","type":"exact"},{"name":"upregulation of MAPK signal transduction involved in axon regeneration","type":"exact"},{"name":"upregulation of MAPK signaling involved in axon regeneration","type":"related"},{"name":"upregulation of MAPK signalling involved in axon regeneration","type":"related"},{"name":"upregulation of MAPKKK cascade during sporulation involved in axon regeneration","type":"narrow"},{"name":"upregulation of MAPKKK cascade involved in axon regeneration","type":"exact"},{"name":"upregulation of mitogen-activated protein kinase cascade involved in axon regeneration","type":"exact"}],"termid":"GO:1904922"}


id: PBO:0052742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 34","termid":"PBO:0052742"}


id: MONDO:0020494
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oculootodental syndrome is a contiguous gene syndrome comprising otodental syndrome (characterized by globodontia and sensorineural high-frequency hearing deficit) associated with eye abnormalities including, typically, iris and chorioretinal coloboma, as well as, on occasion, microcornea, microphtalmos, lenticular opacity, lens coloboma and iris pigment epithelial atrophy.","definition_xrefs":["Orphanet:99806"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 11","termid":"MONDO:0016910"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"oculootodental syndrome","secondary_identifiers":["MEDGEN:413814","UMLS:C2750325","GARD:16910"],"synonyms":[{"name":"OOD","type":"exact"}],"termid":"MONDO:0020494","xrefs":{"Monarch":{"xref_id":"0020494"}}}


id: GO:0032960
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways resulting in the formation of inositol trisphosphate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of inositol phosphate biosynthetic process","termid":"GO:0010919"},{"relation_name":"regulates","term_name":"inositol trisphosphate biosynthetic process","termid":"GO:0032959"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"regulation of inositol trisphosphate biosynthetic process","synonyms":[{"name":"regulation of IP3 biosynthesis","type":"exact"},{"name":"regulation of IP3 biosynthetic process","type":"exact"},{"name":"regulation of inositol trisphosphate anabolism","type":"exact"},{"name":"regulation of inositol trisphosphate biosynthesis","type":"exact"},{"name":"regulation of inositol trisphosphate formation","type":"exact"},{"name":"regulation of inositol trisphosphate synthesis","type":"exact"},{"name":"regulation of myo-inositol trisphosphate biosynthesis","type":"narrow"},{"name":"regulation of myo-inositol trisphosphate biosynthetic process","type":"narrow"}],"termid":"GO:0032960"}


id: PBO:0051409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 1-41 (pseudogene)","termid":"PBO:0051409"}


id: FYPO:0008251
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the amount of RNA transcribed from cenH measured in a cell is lower than normal. cenH is a region located between mat2-P and mat3-M that is homologous to centromeric repeats, and that produces non-coding RNAs and small interfering RNAs.","definition_xrefs":["PomBase:pc","PMID:25356590"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0006551","FYPO:0001320"],"is_obsolete":false,"name":"decreased cenH-derived RNA level","termid":"FYPO:0008251"}


id: MONDO:0100019
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A paroxysmal dyskinesia which manifest as dystonic movements brought on by sustained exercise, that is correlated with a deficiency in the gene ECHS1 (caused by a missence mutation). Onset is typically between age two and four years.","definition_xrefs":["PMID:28039521"],"direct_ancestors":[{"relation_name":"is_a","term_name":"paroxysmal dyskinesia","termid":"MONDO:0015427"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0003441"}],"interesting_parent_ids":["MONDO:0003441"],"is_obsolete":false,"name":"ECHS1-related paroxysmal dyskinesia","synonyms":[{"name":"ECHS1 deficiency-associated paroxysmal exercise-induced dyskinesia","type":"exact"}],"termid":"MONDO:0100019","xrefs":{"Monarch":{"xref_id":"0100019"}}}


id: MONDO:0011703
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"prion disease","termid":"MONDO:0005429"},{"relation_name":"is_a","term_name":"Mendelian encephalopathy","termid":"MONDO:0100198"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spongiform encephalopathy with neuropsychiatric features","secondary_identifiers":["UMLS:C1847650","OMIM:606688","MEDGEN:339812","MESH:C564678"],"synonyms":[{"name":"spongiform encephalopathy with neuropsychiatric features","type":"exact"}],"termid":"MONDO:0011703","xrefs":{"Monarch":{"xref_id":"0011703"}}}


id: PBO:0091908
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pil1 undergoes fast single-molecule exchange at eisosome ends","termid":"PBO:0091908"}


id: FYPO:0004057
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of intragenic meiotic recombination is increased. Intragenic meiotic recombination can result in gene conversion events.","definition_xrefs":["PMID:19436749","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased meiotic recombination","termid":"FYPO:0000487"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000293","FYPO:0000631","FYPO:0001985"],"is_obsolete":false,"name":"increased intragenic meiotic recombination","synonyms":[{"name":"increased meiotic intragenic recombination","type":"exact"}],"termid":"FYPO:0004057"}


id: GO:0019689
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways by which a pyrimidine nucleoside is synthesized from another pyrimidine nucleoside.","definition_xrefs":["ISBN:0306444747","GOC:mah","ISBN:0471394831"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleoside metabolic process","termid":"GO:0006213"},{"relation_name":"is_a","term_name":"nucleobase-containing small molecule interconversion","termid":"GO:0015949"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"pyrimidine nucleoside interconversion","termid":"GO:0019689"}


id: MONDO:0030472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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:0700092"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy 98","secondary_identifiers":["DOID:0070384","MEDGEN:1794227","OMIM:619605","UMLS:C5562017"],"synonyms":[{"name":"DEE98","type":"exact"}],"termid":"MONDO:0030472","xrefs":{"Monarch":{"xref_id":"0030472"}}}


id: PBO:0047669
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"flavin adenine dinucleotide synthetase 1","termid":"PBO:0047669"}


id: GO:0050009
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: NADP+ + propan-2-ol = acetone + H+ + NADPH.","definition_xrefs":["RHEA:21792","EC:1.1.1.80"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"isopropanol dehydrogenase (NADP+) activity","secondary_identifiers":["MetaCyc:ISOPROPANOL-DEHYDROGENASE-NADP+-RXN","KEGG_REACTION:R01550"],"synonyms":[{"name":"propan-2-ol:NADP+ oxidoreductase activity","type":"related"}],"termid":"GO:0050009"}


id: PBO:0066788
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 87","termid":"PBO:0066788"}


id: GO:1990676
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The lipid bilayer surrounding any of the thin, flattened compartments that form the trans portion of the Golgi complex.","definition_xrefs":["PMID:16038056","GOC:bhm","PMID:24119662"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Golgi cisterna membrane","termid":"GO:0032580"},{"relation_name":"part_of","term_name":"Golgi trans cisterna","termid":"GO:0000138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005794"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0005794"],"is_obsolete":false,"name":"Golgi trans cisterna membrane","synonyms":[{"name":"trans-Golgi cisterna membrane","type":"exact"}],"termid":"GO:1990676"}


id: PBO:0058504
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 5694","termid":"PBO:0058504"}


id: PBO:0063598
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisomal biogenesis factor 11 gamma","termid":"PBO:0063598"}


id: MONDO:1012738
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary chondrodysplaisa that occurs in dogs characterized by short limbs and radius curvus deformity.","definition_xrefs":["PMID:20018534"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrodysplasia, dog","termid":"MONDO:1011194"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hereditary chondrodysplasia, dog","secondary_identifiers":["OMIA:001790-9615"],"synonyms":[{"name":"Chondrodysplasia, Labrador retriever dog","type":"narrow"}],"termid":"MONDO:1012738","xrefs":{"Monarch":{"xref_id":"1012738"}}}


id: MONDO:0020219
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete corneogoniodysgenesis (obsolete MONDO:0020219)","secondary_identifiers":["Orphanet:98635"],"termid":"MONDO:0020219","xrefs":{"Monarch":{"xref_id":"0020219"}}}


id: PATO:0002110
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A cellular quality inhering in a bearer by virtue of its having most of the cellular characteristics of the tissue of origin.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"differentiated","termid":"PATO:0002099"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"well differentiated","termid":"PATO:0002110"}


id: MONDO:0013744
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cataract that has material basis in variation in the region 12q24.2-q24.3.","definition_xrefs":["DOID:0110252","PMID:21731060"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cerulean cataract","termid":"MONDO:0020374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"cataract 37","secondary_identifiers":["GARD:15800","OMIM:614422","MEDGEN:482388","UMLS:C3280758"],"synonyms":[{"name":"CCA5","type":"narrow"},{"name":"CTRCT37","type":"exact"},{"name":"cataract 37","type":"exact"},{"name":"cataract 37, autosomal dominant","type":"exact"},{"name":"cataract type 37","type":"exact"},{"name":"cataract, congenital, cerulean type, 5","type":"related"},{"name":"congenital cataract cerulean type 5","type":"narrow"}],"termid":"MONDO:0013744","xrefs":{"Monarch":{"xref_id":"0013744"}}}


id: MONDO:0013416
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any age-related macular degeneration in which the cause of the disease is a mutation in the ARMS2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"age-related macular degeneration","termid":"MONDO:0005150"}],"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":"age related macular degeneration 8","secondary_identifiers":["DOID:0110020","MEDGEN:462420","OMIM:613778","UMLS:C3151070"],"synonyms":[{"name":"ARMD8","type":"exact"},{"name":"ARMS2 age-related macular degeneration","type":"exact"},{"name":"age related macular degeneration type 8","type":"exact"},{"name":"age-related macular degeneration caused by mutation in ARMS2","type":"exact"},{"name":"macular Degeneration, age-related, type 8","type":"exact"},{"name":"macular degeneration, age-related, 8","type":"related"}],"termid":"MONDO:0013416","xrefs":{"Monarch":{"xref_id":"0013416"}}}


id: GO:1904352
data:
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id: FYPO:0009057
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process in which catastrophe rate (i.e. the frequency of transition from pause or growth to shrinkage) of microtubules is lower than normal as part of centromere clustering during meiotic prophase I.","definition_xrefs":["PMID:36435910"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased microtubule depolymerisation involved in meitotic centromere clustering during meiotic prophase I","termid":"FYPO:0009058"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000054","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased rate of microtubule catastrophe involved in meitotic centromere clustering during meiotic prophase I","termid":"FYPO:0009057"}


id: PBO:0052266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"lysine demethylase 4A","termid":"PBO:0052266"}


id: GO:0033211
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id: GO:0010608
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id: PBO:0000495
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates genes involved in vesicle mediated transport","termid":"PBO:0000495"}


id: PBO:0076501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 1","termid":"PBO:0076501"}


id: PBO:0040267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"atlastin GTPase 2","termid":"PBO:0040267"}


id: MONDO:0024555
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"megalencephalic leukoencephalopathy with subcortical cysts","termid":"MONDO:0011391"}],"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":"megalencephalic leukoencephalopathy with subcortical cysts 1","secondary_identifiers":["DOID:0080316","OMIM:604004","UMLS:C5779875","MEDGEN:1826136"],"synonyms":[{"name":"Lvm","type":"related"},{"name":"MLC1","type":"related"},{"name":"VL","type":"related"},{"name":"Vacuolating megalencephalic leukoencephalopathy with subcortical cysts","type":"related"},{"name":"Van Der Knaap disease","type":"related"},{"name":"leukoencephalopathy with swelling and cysts","type":"related"},{"name":"megalencephalic leukoencephalopathy with subcortical cysts","type":"broad"},{"name":"megalencephalic leukoencephalopathy with subcortical cysts 1","type":"exact"}],"termid":"MONDO:0024555","xrefs":{"Monarch":{"xref_id":"0024555"}}}


id: PBO:0044806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 105A","termid":"PBO:0044806"}


id: PBO:0061349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleophosmin 1 pseudogene 7","termid":"PBO:0061349"}


id: GO:0001408
data:
  {"annotated_genes":["SJAG_00760"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[64655],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903790"}]},"cv_name":"biological_process","definition":"The directed movement of guanine nucleotides, GTP, GDP, and/or GMP, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide transport","termid":"GO:0015865"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00760":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"guanine nucleotide transport","references_by_uniquename":{"GO_REF:0000108":null},"termid":"GO:0001408","terms_by_termid":{"GO:1903790":null}}


id: PBO:0003436
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Ppk27 (predicted)","termid":"PBO:0003436"}


id: PBO:0003215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual-specificity MAP kinase phosphatase Pmp1","termid":"PBO:0003215"}


id: PBO:0083648
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Elongin C, conserved among eukaryotes; forms a complex with Cul3p that polyubiquitylates monoubiquitylated RNA polymerase II to trigger its proteolysis; plays a role in global genomic repair","termid":"PBO:0083648"}


id: GO:0021898
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The initial commitment of cells whereby the developmental fate of a cell becomes restricted such that it will develop into some type of neuron in the forebrain.","definition_xrefs":["GOC:dgh","GO_REF:0000021","GOC:cls","GOC:dph","GOC:jid","PMID:12626695"],"direct_ancestors":[{"relation_name":"is_a","term_name":"forebrain neuron fate commitment","termid":"GO:0021877"}],"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":"commitment of multipotent stem cells to neuronal lineage in forebrain","termid":"GO:0021898"}


id: GO:0000943
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A complex of the retrotransposon RNA genome, reverse transcriptase, integrase, and associated molecules required for reproduction and integration of the retrotransposon into the host genome; the main structural molecule of the nucleocapsid is often a gag protein homolog.","definition_xrefs":["PMID:10861903","GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"nucleus","termid":"GO:0005634"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005634","GO:0005575"],"is_obsolete":false,"name":"retrotransposon nucleocapsid","secondary_identifiers":["Wikipedia:Virus-like_particle"],"synonyms":[{"name":"VLP","type":"exact"},{"name":"Virus-like particle","type":"exact"}],"termid":"GO:0000943"}


id: GO:0019930
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of peptidyl-aspartic acid to form peptidyl-cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid aspartate ester, typical of the barley lipid transfer protein 1.","definition_xrefs":["RESID:AA0316"],"gene_count":0,"genotype_count":0,"name":"obsolete cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid peptidyl-aspartate ester biosynthetic process from peptidyl-aspartic acid (obsolete GO:0019930)","synonyms":[{"name":"cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid peptidyl-aspartate ester anabolism from peptidyl-aspartic acid","type":"exact"},{"name":"cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid peptidyl-aspartate ester formation from peptidyl-aspartic acid","type":"exact"},{"name":"cis-14-hydroxy-10,13-dioxo-7-heptadecenoic acid peptidyl-aspartate ester synthesis from peptidyl-aspartic acid","type":"exact"}],"termid":"GO:0019930"}


id: GO:0047673
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: anthranilate + malonyl-CoA = N-malonylanthranilate + CoA.","definition_xrefs":["EC:2.3.1.113","RHEA:17557"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-malonyltransferase activity","termid":"GO:0050735"}],"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:0016746"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"anthranilate N-malonyltransferase activity","secondary_identifiers":["KEGG_REACTION:R00989","MetaCyc:ANTHRANILATE-N-MALONYLTRANSFERASE-RXN"],"synonyms":[{"name":"malonyl-CoA:anthranilate N-malonyltransferase activity","type":"related"}],"termid":"GO:0047673"}


id: GO:0035727
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  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to lysophosphatidic acid (LPA), a phospholipid derivative that acts as a potent mitogen due to its activation of high-affinity G protein-coupled receptors.","definition_xrefs":["GOC:curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phospholipid binding","termid":"GO:0005543"},{"relation_name":"is_a","term_name":"anion binding","termid":"GO:0043168"},{"relation_name":"is_a","term_name":"carbohydrate derivative binding","termid":"GO:0097367"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005488","GO:0008289","GO:0003674"],"is_obsolete":false,"name":"lysophosphatidic acid binding","synonyms":[{"name":"LPA binding","type":"exact"}],"termid":"GO:0035727"}


id: MONDO:0010424
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary pulmonary alveolar proteinosis","termid":"MONDO:0012580"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"surfactant metabolism dysfunction, pulmonary, 4","secondary_identifiers":["MEDGEN:393858","UMLS:C2677877","MESH:C567461","OMIM:300770","GARD:15263"],"synonyms":[{"name":"Csf2Ra deficiency","type":"related"},{"name":"Pap due to Csf2Ra deficiency","type":"related"},{"name":"SMDP4","type":"related"},{"name":"pulmonary alveolar proteinosis, congenital, 4","type":"related"},{"name":"surfactant metabolism dysfunction, pulmonary, 4","type":"exact"},{"name":"surfactant metabolism dysfunction, pulmonary, type 4","type":"exact"}],"termid":"MONDO:0010424","xrefs":{"Monarch":{"xref_id":"0010424"}}}


id: PBO:0064281
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pleckstrin homology and RUN domain containing M2","termid":"PBO:0064281"}


id: MONDO:0013221
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Miyoshi myopathy","termid":"MONDO:0009685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0005336"],"is_obsolete":false,"name":"Miyoshi muscular dystrophy 2","secondary_identifiers":["OMIM:613318","DOID:0070200","MEDGEN:413751","UMLS:C2750077","MESH:C567646","GARD:15648"],"synonyms":[{"name":"MIYOSHI muscular dystrophy 2","type":"related"},{"name":"MMD2","type":"exact"},{"name":"Miyoshi muscular dystrophy 2","type":"exact"},{"name":"Miyoshi myopathy 2","type":"related"}],"termid":"MONDO:0013221","xrefs":{"Monarch":{"xref_id":"0013221"}}}


id: PATO:0000926
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000926 intercross fertility (obsolete PATO:0000926)","termid":"PATO:0000926"}


id: PBO:0017853
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino acid transmembrane transporter Aat1","termid":"PBO:0017853"}


id: FYPO:0006814
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 acetylation of lysine at position 9 of histone H3 in centromere outer repeat regions occurs to a greater extent than normal.","definition_xrefs":["PMID:30652128","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H3-K9 acetylation during vegetative growth","termid":"FYPO:0000892"},{"relation_name":"is_a","term_name":"increased histone H3 acetylation during vegetative growth","termid":"FYPO:0002363"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0005447","FYPO:0000002","FYPO:0002494","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"increased histone H3-K9 acetylation at centromere outer repeat during vegetative growth","synonyms":[{"name":"abnormal histone H3-K9 acetylation at centromere otr during vegetative growth","type":"exact"},{"name":"abnormal histone H3-K9 acetylation at centromeric outer repeat region during vegetative growth","type":"exact"},{"name":"abnormal histone H3-K9 acetylation at pericentric region during vegetative growth","type":"related"},{"name":"abnormal histone H3-K9 acetylation at pericentromeric region during vegetative growth","type":"related"},{"name":"increased histone H3-K9 acetylation at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"increased histone H3K9 acetylation at centromere outer repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0006814"}


id: PBO:0048266
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polypeptide N-acetylgalactosaminyltransferase 4","termid":"PBO:0048266"}


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:0065485
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome activator subunit 2 pseudogene 4","termid":"PBO:0065485"}


id: PBO:0055105
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 2523","termid":"PBO:0055105"}


id: FYPO:0007468
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which dimethylation of lysine at position 9 of histone H3 occurs to a greater extent than normal during G0 phase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K9 methylation","termid":"FYPO:0007466"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0002274","FYPO:0002494","FYPO:0000002","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased histone H3-K9 dimethylation during G0","synonyms":[{"name":"increased histone H3 K9 dimethylation during G0","type":"exact"},{"name":"increased histone H3-K9 dimethylation during cell quiescence","type":"exact"},{"name":"increased histone H3-K9 dimethylation during quiescence","type":"exact"},{"name":"increased histone H3K9me2 during G0","type":"exact"},{"name":"increased histone lysine H3 K9 dimethylation during G0","type":"exact"}],"termid":"FYPO:0007468"}


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:tb","GOC:dph"],"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: PBO:0017568
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Walker-Warburg syndrome","termid":"PBO:0017568"}


id: GO:1905445
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of clathrin coat assembly.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","GOC:bf","PMID:15533940","GOC:PARL"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of protein-containing complex assembly","termid":"GO:0031334"},{"relation_name":"is_a","term_name":"regulation of clathrin coat assembly","termid":"GO:1905443"},{"relation_name":"positively_regulates","term_name":"clathrin coat assembly","termid":"GO:0048268"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0065003"},{"rel_name":"regulates","termid":"GO:0065003"},{"rel_name":"positively_regulates","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0065003","GO:0008150"],"is_obsolete":false,"name":"positive regulation of clathrin coat assembly","synonyms":[{"name":"activation of clathrin cage assembly","type":"narrow"},{"name":"activation of clathrin coat assembly","type":"narrow"},{"name":"positive regulation of clathrin cage assembly","type":"exact"},{"name":"up regulation of clathrin cage assembly","type":"exact"},{"name":"up regulation of clathrin coat assembly","type":"exact"},{"name":"up-regulation of clathrin cage assembly","type":"exact"},{"name":"up-regulation of clathrin coat assembly","type":"exact"},{"name":"upregulation of clathrin cage assembly","type":"exact"},{"name":"upregulation of clathrin coat assembly","type":"exact"}],"termid":"GO:1905445"}


id: PBO:0053059
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIM and SH3 protein 1","termid":"PBO:0053059"}


id: GO:1900501
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of butyryl-CoA catabolic process to butyrate.","definition_xrefs":["GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of amide metabolic process","termid":"GO:0034249"},{"relation_name":"is_a","term_name":"negative regulation of fatty acid biosynthetic process","termid":"GO:0045717"},{"relation_name":"is_a","term_name":"negative regulation of nucleobase-containing compound metabolic process","termid":"GO:0045934"},{"relation_name":"is_a","term_name":"negative regulation of phosphate metabolic process","termid":"GO:0045936"},{"relation_name":"is_a","term_name":"negative regulation of lipid catabolic process","termid":"GO:0050995"},{"relation_name":"is_a","term_name":"negative regulation of sulfur metabolic process","termid":"GO:0051175"},{"relation_name":"is_a","term_name":"regulation of butyryl-CoA catabolic process to butyrate","termid":"GO:1900500"},{"relation_name":"negatively_regulates","term_name":"butyryl-CoA catabolic process to butyrate","termid":"GO:0044581"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0055086"},{"rel_name":"regulates","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"negatively_regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0006790"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0044281","GO:0006790","GO:0055086","GO:0008150","GO:0006629"],"is_obsolete":false,"name":"negative regulation of butyryl-CoA catabolic process to butyrate","synonyms":[{"name":"down regulation of butyryl-CoA catabolic process to butyrate","type":"exact"},{"name":"down regulation of butyryl-CoA catabolism to butyrate","type":"exact"},{"name":"down-regulation of butyryl-CoA catabolic process to butyrate","type":"exact"},{"name":"down-regulation of butyryl-CoA catabolism to butyrate","type":"exact"},{"name":"downregulation of butyryl-CoA catabolic process to butyrate","type":"exact"},{"name":"downregulation of butyryl-CoA catabolism to butyrate","type":"exact"},{"name":"inhibition of butyryl-CoA catabolic process to butyrate","type":"narrow"},{"name":"inhibition of butyryl-CoA catabolism to butyrate","type":"exact"},{"name":"negative regulation of butyryl-CoA catabolism to butyrate","type":"exact"}],"termid":"GO:1900501"}


id: MONDO:0004713
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cancer involving a gingiva of lower jaw.","definition_xrefs":["MONDO:patterns/cancer"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gingival cancer","termid":"MONDO:0005507"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"lower gum cancer","secondary_identifiers":["DOID:9125","UMLS:C0432581","ICD9:143.1","MEDGEN:609602","SCTID:363384006"],"synonyms":[{"name":"cancer of gingiva of lower jaw","type":"exact"},{"name":"gingiva of lower jaw cancer","type":"exact"},{"name":"malignant gingiva of lower jaw neoplasm","type":"exact"},{"name":"malignant neoplasm of gingiva of lower jaw","type":"exact"},{"name":"malignant tumor of lower gingiva","type":"exact"},{"name":"malignant tumor of lower gum","type":"exact"},{"name":"malignant tumour of lower gingiva","type":"exact"},{"name":"malignant tumour of lower gum","type":"exact"}],"termid":"MONDO:0004713","xrefs":{"Monarch":{"xref_id":"0004713"}}}


id: PBO:0076911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor AP-2 alpha","termid":"PBO:0076911"}


id: GO:1904660
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of sensory perception of bitter taste.","definition_xrefs":["GOC:mr","GOC:TermGenie","PMID:1716172","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of sensory perception","termid":"GO:0051931"},{"relation_name":"regulates","term_name":"sensory perception of bitter taste","termid":"GO:0050913"}],"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 sensory perception of bitter taste","synonyms":[{"name":"regulation of bitter taste perception","type":"exact"}],"termid":"GO:1904660"}


id: MONDO:0016861
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Alagille syndrome","termid":"MONDO:0007318"},{"relation_name":"is_a","term_name":"partial monosomy of the short arm of chromosome 20","termid":"MONDO:0016898"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0004335","MONDO:0005267","MONDO:0002515"],"is_obsolete":false,"name":"Alagille syndrome due to 20p12 microdeletion","secondary_identifiers":["GARD:17250","Orphanet:261600","UMLS:C5679679","MEDGEN:1826025"],"synonyms":[{"name":"Alagille syndrome due to del(20)(p12)","type":"exact"},{"name":"Alagille syndrome due to monosomy 20p12","type":"exact"},{"name":"Alagille-Watson syndrome due to monosomy 20p12","type":"exact"},{"name":"Arteriohepatic dysplasia due to monosomy 20p12","type":"exact"},{"name":"syndromic bile duct paucity due to monosomy 20p12","type":"exact"}],"termid":"MONDO:0016861","xrefs":{"Monarch":{"xref_id":"0016861"}}}


id: PBO:0039413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase promoting complex subunit 16","termid":"PBO:0039413"}


id: PBO:0027446
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_antisense_RNA_transcription_at_stress_response_genes","termid":"PBO:0027446"}


id: PATO:0000766
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000766 relative consumption value (obsolete PATO:0000766)","termid":"PATO:0000766"}


id: MOD:00765
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue to S-(L-cysteinyl)-L-cysteine, forming a disulfide bond with free cysteine.","definition_xrefs":["RESID:AA0025#CYS1","Unimod:312","PubMed:1988019","PubMed:2076469","PubMed:366603","DeltaMass:260","PubMed:3083866","PubMed:7918467","PubMed:8344916","PubMed:2001356"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-cysteine residue","termid":"MOD:00905"},{"relation_name":"is_a","term_name":"disulfide conjugated residue","termid":"MOD:01862"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"cysteinylation (disulfide with free L-cysteine)","synonyms":[{"name":"(2R,2'R)-3,3'-disulfane-1,2-diylbis(2-aminopropanoic acid)","type":"exact"},{"name":"2-amino-3-(2-amino-2-carboxy-ethyl)disulfanyl-propanoic acid","type":"related"},{"name":"3,3'-disulfane-1,2-diylbis(2-azanylpropanoic acid)","type":"exact"},{"name":"3,3'-dithiobis(2-aminopropanoic acid)","type":"exact"},{"name":"3,3'-dithiobisalanine","type":"exact"},{"name":"3,3'-dithiodialanine","type":"exact"},{"name":"Cysteinylation","type":"exact"},{"name":"L-cystine","type":"exact"},{"name":"MOD_RES S-cysteinyl cysteine","type":"exact"},{"name":"S-cystenyl cystenyl","type":"exact"},{"name":"SCysCys","type":"exact"},{"name":"beta,beta'-diamino-beta,beta'-dicarboxydiethyldisulfide","type":"exact"},{"name":"beta,beta'-dithiodialanine","type":"exact"},{"name":"bis(alpha-aminopropionic acid)-beta-disulfide","type":"exact"},{"name":"bis(beta-amino-beta-carboxyethyl)disulfide","type":"exact"},{"name":"dicysteine","type":"exact"}],"termid":"MOD:00765"}


id: PBO:0078430
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Gly (anticodon TCC) 1-1","termid":"PBO:0078430"}


id: PBO:0045269
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynamin 1 pseudogene 9","termid":"PBO:0045269"}


id: PBO:0038899
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adhesion G protein-coupled receptor B1","termid":"PBO:0038899"}


id: PBO:0065819
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RAB5A, member RAS oncogene family","termid":"PBO:0065819"}


id: MONDO:0000891
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A fibrolamellar carcinoma that is characterized by the presence of both pure fibrolamellar hepatocellular carcinoma and and conventional hepatocellular carcinoma components.","definition_xrefs":["DOID:0080182"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibrolamellar hepatocellular carcinoma","termid":"MONDO:0006210"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"mixed fibrolamellar hepatocellular carcinoma","termid":"MONDO:0000891","xrefs":{"Monarch":{"xref_id":"0000891"}}}


id: GO:0048241
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of epinephrine into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"catecholamine transport","termid":"GO:0051937"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0051179","GO:0006810"],"is_obsolete":false,"name":"epinephrine transport","synonyms":[{"name":"adrenaline transport","type":"exact"}],"termid":"GO:0048241"}


id: GO:0102984
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: sulfonatoacetaldehyde + H2O + NAD = sulfonatoacetate + NADH + 2 H+.","definition_xrefs":["EC:1.2.1.73","GOC:pz"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"sulfoacetaldehyde dehydrogenase activity","secondary_identifiers":["MetaCyc:RXN-9592","RHEA:25637"],"termid":"GO:0102984"}


id: PBO:0116209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"armadillo-type fold protein, neurochondrin ortholog, implicated in calcium mediated signalling, and the regulation of cytoskeleton organization Asi1","termid":"PBO:0116209"}


id: PBO:0071909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 48","termid":"PBO:0071909"}


id: GO:0047102
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: H2O + NAD+ + 2-aminomuconate semialdehyde = NADH + 2-amino-muconate.","definition_xrefs":["EC:1.2.1.32","MetaCyc:1.2.1.32-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor","termid":"GO:0016620"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"aminomuconate-semialdehyde dehydrogenase activity","secondary_identifiers":["Reactome:R-HSA-71239","RHEA:14469","UM-BBD_reactionID:r1434"],"synonyms":[{"name":"2-aminomuconate semialdehyde dehydrogenase activity","type":"related"},{"name":"2-aminomuconate-6-semialdehyde:NAD+ 6-oxidoreductase activity","type":"related"},{"name":"2-hydroxymuconate semialdehyde dehydrogenase activity","type":"related"},{"name":"2-hydroxymuconic acid semialdehyde dehydrogenase activity","type":"related"},{"name":"2-hydroxymuconic semialdehyde dehydrogenase activity","type":"related"},{"name":"alpha-aminomuconic epsilon-semialdehyde dehydrogenase activity","type":"related"},{"name":"alpha-hydroxymuconic epsilon-semialdehyde dehydrogenase activity","type":"related"}],"termid":"GO:0047102"}


id: FYPO:0006050
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 rate, or speed, of mitotic sister chromatid separation is normal (i.e. indistinguishable from wild type). Mitotic sister chromatid separation is the process in which sister chromatids are physically detached from each other during mitosis.","definition_xrefs":["PomBase:mah","PMID:27146110"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal mitotic sister chromatid separation","termid":"FYPO:0004301"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0001320","FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal rate of mitotic sister chromatid separation","synonyms":[{"name":"normal mitotic sister chromatid separation rate","type":"exact"},{"name":"normal rate of mitotic sister chromatid separation during vegetative growth","type":"exact"},{"name":"normal rate of sister chromatid separation during mitosis","type":"exact"},{"name":"normal rate of sister chromatid separation during mitotic cell cycle","type":"related"}],"termid":"FYPO:0006050"}


id: MONDO:0000670
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An agnosia that is a loss of the ability to perceive any auditory information but whose hearing is intact.","definition_xrefs":["DOID:0060140"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auditory agnosia","termid":"MONDO:0000667"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cortical deafness","secondary_identifiers":["MEDGEN:98233","UMLS:C0392704"],"termid":"MONDO:0000670","xrefs":{"Monarch":{"xref_id":"0000670"}}}


id: PBO:0112989
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Actin filament binding protein; regulates actin filament capping by recruiting capping protein to endocytic sites and to the cytokinetic actin ring; interacts with the capping protein complex; adapter that links synaptojanins, Inp52p and Inp53p, to the cortical actin cytoskeleton; contains two WH2-like actin binding domains and a C-terminal capping protein interaction (CPI) motif","termid":"PBO:0112989"}


id: MONDO:0003514
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant form of teratoma.","definition_xrefs":["MONDO:patterns/malignant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teratoma","termid":"MONDO:0002601"},{"relation_name":"is_a","term_name":"malignant germ cell tumor","termid":"MONDO:0006290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"malignant teratoma","secondary_identifiers":["NCIT:C8884","UMLS:C4722083","DOID:5563","MEDGEN:1652407","NCIT:C4286","NCIT:C4287"],"synonyms":[{"name":"malignant extragonadal teratoma","type":"narrow"},{"name":"teratoma, malignant","type":"exact"}],"termid":"MONDO:0003514","xrefs":{"Monarch":{"xref_id":"0003514"}}}


id: PBO:0040258
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy related 12 pseudogene 1","termid":"PBO:0040258"}


id: GO:0047589
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-oxoglutarate + 5-aminopentanoate = 5-oxopentanoate + L-glutamate.","definition_xrefs":["RHEA:10212","EC:2.6.1.48"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transaminase activity","termid":"GO:0008483"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016769","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"5-aminovalerate transaminase activity","secondary_identifiers":["MetaCyc:VAGL-RXN","KEGG_REACTION:R02274"],"synonyms":[{"name":"5-aminopentanoate:2-oxoglutarate aminotransferase activity","type":"related"},{"name":"5-aminovalerate aminotransferase activity","type":"exact"},{"name":"delta-aminovalerate aminotransferase activity","type":"related"},{"name":"delta-aminovalerate transaminase activity","type":"related"}],"termid":"GO:0047589"}


id: PBO:0048273
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GALNT9 antisense RNA 1","termid":"PBO:0048273"}


id: PBO:0071761
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein lateral stalk subunit P1 pseudogene 8","termid":"PBO:0071761"}


id: PBO:0049353
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIi pseudogene 11","termid":"PBO:0049353"}


id: GO:0141107
data:
  {"annotated_genes":["SJAG_04890"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77165],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0141106"}]},"cv_name":"molecular_function","definition":"Binds to and modulates the activity of a methyltransferase.","definition_xrefs":["PMID:15899842","PMID:34669960"],"direct_ancestors":[{"relation_name":"is_a","term_name":"enzyme regulator activity","termid":"GO:0030234"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04890":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0098772"},{"rel_name":"is_a","termid":"GO:0030234"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0030234","GO:0098772","GO:0003674"],"is_obsolete":false,"name":"methyltransferase regulator activity","references_by_uniquename":{"GO_REF:0000033":null},"termid":"GO:0141107","terms_by_termid":{"GO:0141106":null}}


id: PBO:0031276
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_negative_regulation_of_G0_to_G1_transition","termid":"PBO:0031276"}


id: PBO:0028804
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_replication_fork_arrest_at_mating-type_locus","termid":"PBO:0028804"}


id: PBO:0076454
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transgelin 2","termid":"PBO:0076454"}


id: FYPO:0007630
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 acetylation of lysine at position 9 of histone H3 at ribosomal DNA occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased histone H3-K9 acetylation during vegetative growth","termid":"FYPO:0000892"}],"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:0002274"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0002274","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased histone H3-K9 acetylation at rDNA during vegetative growth","synonyms":[{"name":"increased histone H3-K9 acetylation at rDNA during mitotic cell cycle","type":"related"},{"name":"increased histone H3K9 acetylation at rDNA during vegetative growth","type":"exact"},{"name":"increased histone H3K9 acetylation at ribosomal DNA during vegetative growth","type":"exact"}],"termid":"FYPO:0007630"}


id: MONDO:0009328
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":"hemangiomatosis, cutaneous, with associated features","secondary_identifiers":["MESH:C562438","UMLS:C0220738","MEDGEN:67397","OMIM:234800"],"synonyms":[{"name":"hemangiomatosis, cutaneous, with associated features","type":"exact"}],"termid":"MONDO:0009328","xrefs":{"Monarch":{"xref_id":"0009328"}}}


id: MOD:01597
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"The protein modification reporter fragment produced by an Applied Biosystems iTRAQ8plex-116 reagent derivatized residue.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"derives_from","term_name":"iTRAQ8plex-116 reporter+balance reagent acylated residue","termid":"MOD:01549"},{"relation_name":"is_a","term_name":"iTRAQ8plex reporter fragment","termid":"MOD:01593"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iTRAQ8plex-116 reporter fragment","synonyms":[{"name":"4-methyl-1-methylidenepiperazin-1-ium","type":"exact"}],"termid":"MOD:01597"}


id: PBO:0088354
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"diphosphoinositol pentakisphosphate kinase/IP8 pyrophosphatase","termid":"PBO:0088354"}


id: PBO:0001288
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase Ras1","termid":"PBO:0001288"}


id: PBO:0085685
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in recovery from arrest in response to pheromone; acts in a cell cycle arrest recovery pathway independent from Far1p; interacts with Far3p, Far7p, Far8p, Far9p, and Far11p; potential Cdc28p substrate; FAR10 has a paralog, VPS64, that arose from the whole genome duplication","termid":"PBO:0085685"}


id: PBO:0064500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II subunit C pseudogene 1","termid":"PBO:0064500"}


id: MONDO:1010704
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any glycogen storage disease that occurs in sheep due to a mutation in the PYGM gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glycogen storage disease, non-human animal","termid":"MONDO:1011419"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycogen storage disease, PYGM-related, sheep","secondary_identifiers":["OMIA:001139-9940"],"synonyms":[{"name":"glycogen storage disease V, sheep","type":"related"},{"name":"ovine McArdle's disease","type":"exact"}],"termid":"MONDO:1010704","xrefs":{"Monarch":{"xref_id":"1010704"}}}


id: SO:0000328
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A DNA sequence used experimentally to detect the presence or absence of a complementary nucleic acid.","direct_ancestors":[{"relation_name":"is_a","term_name":"probe","termid":"SO:0000051"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microarray_oligo","synonyms":[{"name":"microarray oligo","type":"exact"},{"name":"microarray oligonucleotide","type":"exact"}],"termid":"SO:0000328"}


id: PBO:0067718
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal 16","termid":"PBO:0067718"}


id: PBO:0081207
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger with KRAB and SCAN domains 7 pseudogene 1","termid":"PBO:0081207"}


id: FYPO:0007692
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the activity of a DNA strand exchange activator is increased.","definition_xrefs":["PMID:33493431","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity regulator phenotype","termid":"FYPO:0007690"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"}],"interesting_parent_ids":["FYPO:0000652"],"is_obsolete":false,"name":"increased DNA strand exchange activator activity","synonyms":[{"name":"increased RecA-family recombinase activator activity","type":"exact"},{"name":"increased positive regulation of RecA-family recombinase activity","type":"related"}],"termid":"FYPO:0007692"}


id: FYPO:0009015
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A vegetative cell population phenotype in which a larger than normal proportion of cells is viable when grown with glycerol as carbon source. In High Throughput Phenotyping this is typically assessed using phloxine as a dye.","direct_ancestors":[{"relation_name":"is_a","term_name":"increased vegetative cell population viability","termid":"FYPO:0009008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002057"],"is_obsolete":false,"name":"increased cell population viability on glycerol carbon source","synonyms":[{"name":"increased cell population viability during vegetative growth on glycerol carbon source","type":"exact"}],"termid":"FYPO:0009015"}


id: PBO:0017035
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nus1 can form a catalytically active complex with human DHDS (hCIT)","termid":"PBO:0017035"}


id: PBO:0003871
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3.6.3.4","termid":"PBO:0003871"}


id: GO:0010660
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the rate or frequency of muscle cell apoptotic process, a form of programmed cell death induced by external or internal signals that trigger the activity of proteolytic caspases whose actions dismantle a muscle cell and result in its death.","definition_xrefs":["GOC:dph","GOC:tb","GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of apoptotic process","termid":"GO:0042981"},{"relation_name":"regulates","term_name":"muscle cell apoptotic process","termid":"GO:0010657"}],"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 muscle cell apoptotic process","synonyms":[{"name":"regulation of muscle cell apoptosis","type":"narrow"}],"termid":"GO:0010660"}


id: PBO:0083881
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ferric reductase; reduces siderophore-bound iron prior to uptake by transporters; expression induced by low iron levels","termid":"PBO:0083881"}


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


id: PBO:0088152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"V-ATPase assembly factor; functions with other V-ATPase assembly factors in the ER to efficiently assemble the V-ATPase membrane sector (V0); protein abundance increases in response to DNA replication stress","termid":"PBO:0088152"}


id: MONDO:0008881
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Kyphomelic dysplasia is a prenatal skeletal disease that causes dwarfism characterized bythe following: a disproportionately short stature with a short narrow chest,shortening and bending (bowing)of the limbs, flared irregular metaphyses of the bones, and characteristicfacial features.Bone changes are said to improve with age.Kyphomelic dysplasia is inherited in an autosomal recessive pattern. Recent studies indicate that Kyphomelic dysplasia is no longerconsidered it's ownentity and that individual cases should be further evaluated andre-classified as another existing chondrodysplasias, such as Schwartz-Jampel syndrome.","direct_ancestors":[{"relation_name":"is_a","term_name":"bent bone dysplasia","termid":"MONDO:0019698"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kyphomelic dysplasia","secondary_identifiers":["SCTID:254096001","UMLS:C0432239","OMIM:211350","MESH:C538128","GARD:10149","Orphanet:1801","ICD9:733.29","icd11.foundation:268821879","MEDGEN:140930"],"synonyms":[{"name":"bowing, congenital, with short bones","type":"related"},{"name":"congenital bowing with short bones","type":"related"},{"name":"kyphomelic dysplasia","type":"exact"}],"termid":"MONDO:0008881","xrefs":{"Monarch":{"xref_id":"0008881"}}}


id: MONDO:0007432
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete neuro-ophthalmological disease (obsolete MONDO:0015368)","termid":"MONDO:0015368"},{"relation_name":"excluded_subClassOf","term_name":"hereditary dementia","termid":"MONDO:0015547"},{"relation_name":"excluded_subClassOf","term_name":"leukodystrophy","termid":"MONDO:0019046"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral arteriopathy with subcortical infarcts and leukoencephalopathy","secondary_identifiers":["ICD9:447.8","NANDO:1200545","MEDGEN:199687","ICD9:323.9","OMIMPS:125310","DOID:13945","UMLS:C0751587"],"synonyms":[{"name":"CADASIL","type":"exact"},{"name":"Casil","type":"related"},{"name":"cerebral arteriopathy with subcortical infaracts and leukoencephalopathy","type":"exact"},{"name":"cerebral arteriopathy with subcortical infarcts and leukoencephalopathy","type":"exact"},{"name":"cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy","type":"related"},{"name":"dementia, hereditary multi-infarct type","type":"related"}],"termid":"MONDO:0007432","xrefs":{"Monarch":{"xref_id":"0007432"}}}


id: PBO:0086132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein required for localizing proteasomes to the nucleus; involved in cotranslational protein degradation; mediates interaction between nuclear import factor Srp1p and the proteasome; Sts1p and Srp1p couple proteasomes to nascent polypeptides emerging from the ribosome for cotranslational degradation; involved in ubiquitin-mediated protein degradation","termid":"PBO:0086132"}


id: PBO:0081271
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 35","termid":"PBO:0081271"}


id: FYPO:0002470
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the phosphorylation of one or more specific proteins, or of specific protein sites, occurs to a lower extent than normal during a cellular response to ionizing radiation.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein phosphorylation during vegetative growth","termid":"FYPO:0001838"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0002494"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320","FYPO:0002494","FYPO:0002274","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein phosphorylation during cellular response to ionizing radiation","synonyms":[{"name":"decreased protein phosphorylation during cellular response to IR","type":"exact"},{"name":"decreased protein phosphorylation during cellular response to ionizing radiation during mitotic cell cycle","type":"related"},{"name":"decreased protein phosphorylation during cellular response to ionizing radiation during vegetative growth","type":"exact"},{"name":"reduced protein phosphorylation during cellular response to IR","type":"exact"},{"name":"reduced protein phosphorylation during cellular response to ionizing radiation","type":"exact"}],"termid":"FYPO:0002470"}


id: PBO:0029217
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_heat","termid":"PBO:0029217"}


id: PBO:0072406
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S27 pseudogene 11","termid":"PBO:0072406"}


id: PR:O74359
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC28E12.02 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O74359"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"meiotically up-regulated gene 60 protein (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC28E12.02","synonyms":[{"name":"Spom972h-SPBC28E12.02","type":"exact"}],"termid":"PR:O74359"}


id: MONDO:0016486
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Beta-thalassemia (BT) major is a severe early-onset form of BT characterized by severe anemia requiring regular red blood cell transfusions.","definition_xrefs":["Orphanet:231214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-thalassemia HBB/LCRB","termid":"MONDO:0013517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0002280","MONDO:0005570"],"is_obsolete":false,"name":"beta-thalassemia major","secondary_identifiers":["NCIT:C129699","SCTID:26682008","UMLS:C0002875","ICD9:282.49","MEDGEN:283","DOID:0080771","GARD:17162"],"synonyms":[{"name":"Beta thalassemia Major","type":"exact"},{"name":"Cooley anaemia","type":"exact"},{"name":"Cooley anemia","type":"exact"},{"name":"Cooley's Anaemia","type":"exact"},{"name":"Cooley's Anemia","type":"exact"},{"name":"Mediterranean anaemia","type":"exact"},{"name":"Mediterranean anemia","type":"exact"}],"termid":"MONDO:0016486","xrefs":{"Monarch":{"xref_id":"0016486"}}}


id: PBO:0051152
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 3-32 (pseudogene)","termid":"PBO:0051152"}


id: PBO:0049358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIi pseudogene 16","termid":"PBO:0049358"}


id: PBO:0017867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA cleavage factor complex subunit Msi2","termid":"PBO:0017867"}


id: PBO:0026940
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_spore_germination_frequency","termid":"PBO:0026940"}


id: MONDO:0017860
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Methanol poisoning is a rare poisoning resulting in elevated anion gap metabolic acidosis, due to the alcohol dehydrogenase (ADH)-mediated production of formic acid (which is poisonous to the central nervous system), and characterized by dizziness, nausea, vomiting, confusion, metabolic acidosis, visual disturbances (which if left untreated can lead to blindness), coma, and death (due to respiratory failure).","definition_xrefs":["Orphanet:31825"],"direct_ancestors":[{"relation_name":"is_a","term_name":"poisoning","termid":"MONDO:0029000"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methanol poisoning","secondary_identifiers":["GARD:18804"],"termid":"MONDO:0017860","xrefs":{"Monarch":{"xref_id":"0017860"}}}


id: PBO:0057815
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 3135b","termid":"PBO:0057815"}


id: PBO:0074395
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 5","termid":"PBO:0074395"}


id: GO:0035532
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of production of chemokine (C-C motif) ligand 6 (CCL6).","definition_xrefs":["GOC:bf","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of chemokine production","termid":"GO:0032682"},{"relation_name":"is_a","term_name":"regulation of chemokine (C-C motif) ligand 6 production","termid":"GO:0035531"},{"relation_name":"negatively_regulates","term_name":"chemokine (C-C motif) ligand 6 production","termid":"GO:0035530"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of chemokine (C-C motif) ligand 6 production","secondary_identifiers":["GO:0035536"],"synonyms":[{"name":"negative regulation of CCL6 production","type":"exact"},{"name":"negative regulation of chemokine (C-C motif) ligand 6 secretion","type":"narrow"}],"termid":"GO:0035532"}


id: MONDO:0000591
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A cardiomyopathy that is due to abnormalities in heart muscle cells.","definition_xrefs":["Wikipedia:Cardiomyopathy"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiomyopathy","termid":"MONDO:0004994"}],"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":"intrinsic cardiomyopathy","secondary_identifiers":["DOID:0060036"],"synonyms":[{"name":"intrinsic cardiomyopathy","type":"exact"},{"name":"primary cardiomyopathy","type":"exact"}],"termid":"MONDO:0000591","xrefs":{"Monarch":{"xref_id":"0000591"}}}


id: MONDO:1010713
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pyruvate dehydrogenase deficiency that occurs in dog.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyruvate dehydrogenase deficiency, non-human animal","termid":"MONDO:1010105"},{"relation_name":"is_a","term_name":"peripheral neuropathy, dog","termid":"MONDO:1011007"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pyruvate dehydrogenase deficiency, dog","secondary_identifiers":["OMIA:001406-9615"],"termid":"MONDO:1010713","xrefs":{"Monarch":{"xref_id":"1010713"}}}


