# terms

id: GO:0075509
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any endocytosis that is involved in the uptake of a virus into a host cell.","definition_xrefs":["GOC:jl","VZ:977","GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont entry into host cell","termid":"GO:0046718"}],"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":"endocytosis involved in viral entry into host cell","synonyms":[{"name":"viral entry into host cell via endocytosis","type":"related"},{"name":"viral penetration via endocytosis followed by endosome disruption","type":"exact"},{"name":"virus endocytosis by host","type":"exact"}],"termid":"GO:0075509"}


id: GO:0034940
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 5-oxo-4,5-dihydropyrrole-2-carboxylate + 2 H2O = 2-oxoglutarate + NH3.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 5-oxo-4,5-dihydropyrrole-2-carboxylate amidase activity (obsolete GO:0034940)","termid":"GO:0034940"}


id: PBO:0072912
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SREBF chaperone","termid":"PBO:0072912"}


id: MONDO:0017134
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Odonto-onycho dysplasia-alopecia syndrome is a rare, genetic ectodermal dysplasia syndrome characterized by almost total alopecia with only sparse, thin, brittle, slow-growing scalp hair, fair and sparse eyebrows and eyelashes, absent axillary and pubic hair, fragile and brittle fingernails, thick and brittle toenails (both with a subungual corneal layer), hypodontia, microdontia, widely spaced teeth with hypoplastic enamel, mild palmoplantar keratosis, cafe-au-lait spots and areolae anomalies. There have been no further descriptions in the literature since 1985.","definition_xrefs":["Orphanet:2722"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectodermal dysplasia syndrome","termid":"MONDO:0019287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"odonto-onycho dysplasia-alopecia syndrome","secondary_identifiers":["UMLS:C4706599","GARD:4051","MEDGEN:1648007"],"synonyms":[{"name":"odonto onycho dysplasia with alopecia","type":"related"}],"termid":"MONDO:0017134","xrefs":{"Monarch":{"xref_id":"0017134"}}}


id: GO:0099577
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates synaptic transmission by regulating translation occurring at the presynapse.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"presynaptic modulation of chemical synaptic transmission","termid":"GO:0099171"},{"relation_name":"is_a","term_name":"regulation of translation at synapse, modulating synaptic transmission","termid":"GO:0099547"},{"relation_name":"is_a","term_name":"regulation of translation at presynapse","termid":"GO:0140244"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0023052","GO:0008150"],"is_obsolete":false,"name":"regulation of translation at presynapse, modulating synaptic transmission","termid":"GO:0099577"}


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


id: MONDO:0003156
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete adenosquamous carcinoma (obsolete MONDO:0003156)","termid":"MONDO:0003156","xrefs":{"Monarch":{"xref_id":"0003156"}}}


id: MONDO:0019352
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete sporotrichosis (obsolete MONDO:0019352)","termid":"MONDO:0019352","xrefs":{"Monarch":{"xref_id":"0019352"}}}


id: PBO:0078489
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Ile (anticodon AAT) 8-1","termid":"PBO:0078489"}


id: MOD:00669
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces a residue hydroxyl group with a octanoyloxy group.","definition_xrefs":["Unimod:426"],"direct_ancestors":[{"relation_name":"is_a","term_name":"octanoylated residue","termid":"MOD:00666"},{"relation_name":"is_a","term_name":"O-acylated residue","termid":"MOD:00671"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"O-octanoylated residue","synonyms":[{"name":"OOctRes","type":"exact"},{"name":"Octanoyl","type":"related"},{"name":"octanoyl","type":"related"}],"termid":"MOD:00669"}


id: GO:1905104
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an ouabain stimulus.","definition_xrefs":["PMID:23643758","GO_REF:0000071","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete response to ouabain (obsolete GO:1905104)","termid":"GO:1905104"}


id: GO:0043676
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The layer of sexine which forms a roof over the columella, granules or other infratectal elements.","definition_xrefs":["PMID:33706055"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"sexine","termid":"GO:0043673"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"tectum","synonyms":[{"name":"sexine 2","type":"exact"}],"termid":"GO:0043676"}


id: MONDO:0003814
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete gastric diffuse adenocarcinoma (obsolete MONDO:0003814)","termid":"MONDO:0003814","xrefs":{"Monarch":{"xref_id":"0003814"}}}


id: MONDO:0020034
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Any of the forms of respiratory tract neoplasm that have a rare incidence.","definition_xrefs":["MONDO:patterns/rare"],"gene_count":0,"genotype_count":0,"name":"obsolete rare respiratory tract neoplasm (obsolete MONDO:0020034)","secondary_identifiers":["Orphanet:98060"],"synonyms":[{"name":"rare respiratory cancer","type":"narrow"},{"name":"rare respiratory neoplasm","type":"exact"},{"name":"rare respiratory tract neoplasm","type":"exact"},{"name":"rare respiratory tumor","type":"exact"}],"termid":"MONDO:0020034","xrefs":{"Monarch":{"xref_id":"0020034"}}}


id: PBO:0045982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EHHADH antisense RNA 1","termid":"PBO:0045982"}


id: PBO:0064842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein phosphatase 1 regulatory subunit 12B pseudogene 2","termid":"PBO:0064842"}


id: PBO:0088539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial carrier, inorganic phosphate/copper","termid":"PBO:0088539"}


id: FYPO:0005286
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 heterochromatin is assembled over a larger region near the centromere than normal, such that it extends beyond the IRC1L boundary element.","definition_xrefs":["PMID:25972440","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased spatial extent of centromeric heterochromatin assembly","termid":"FYPO:0004948"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000641","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"heterochromatin assembly beyond boundary element IRC1L","synonyms":[{"name":"heterochromatin assembly beyond boundary element IRC1L during mitotic cell cycle","type":"related"},{"name":"heterochromatin assembly beyond boundary element IRC1L during vegetative growth","type":"exact"},{"name":"heterochromatin formation beyond boundary element IRC1L","type":"exact"}],"termid":"FYPO:0005286"}


id: MONDO:0011597
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inherited susceptibility or predisposition to developing atopic dermatitis that is associated with variation in the region 20p.","definition_xrefs":["DOID:0110099","PMID:11279517","MONDO:patterns/inherited_susceptibility"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"atopic eczema","termid":"MONDO:0004980"},{"relation_name":"is_a","term_name":"dermatitis, atopic, susceptibility to","termid":"MONDO:0100178"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dermatitis, atopic, 3","secondary_identifiers":["UMLS:C1853964","MESH:C565292","MEDGEN:344173","OMIM:605804"],"synonyms":[{"name":"ATOD3","type":"exact"},{"name":"atopic dermatitis 3","type":"exact"},{"name":"atopic dermatitis type 3","type":"exact"},{"name":"atopic dermatitis with asthma","type":"exact"},{"name":"dermatitis, ATOPIC, 3","type":"related"},{"name":"dermatitis, Atopic, with asthma","type":"related"},{"name":"dermatitis, atopic, susceptibility to, 3","type":"exact"}],"termid":"MONDO:0011597","xrefs":{"Monarch":{"xref_id":"0011597"}}}


id: PBO:0041963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 6","termid":"PBO:0041963"}


id: PBO:0038798
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 3B (pseudogene)","termid":"PBO:0038798"}


id: MONDO:0005675
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Congenital disorder of lambs caused by a virus closely related to or identical with certain strains of bovine viral diarrhea virus.","definition_xrefs":["MESH:D001882"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sheep disease","termid":"MONDO:0024985"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"border disease","secondary_identifiers":["EFO:0007177"],"termid":"MONDO:0005675","xrefs":{"Monarch":{"xref_id":"0005675"}}}


id: PBO:0110473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CPSF6 pseudogene 1","termid":"PBO:0110473"}


id: PBO:0059100
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mortality factor 4 like 1 pseudogene 6","termid":"PBO:0059100"}


id: GO:0032282
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An acetyl-CoA carboxylase complex located in the stroma of a plastid.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetyl-CoA carboxylase complex","termid":"GO:0009317"},{"relation_name":"part_of","term_name":"plastid stroma","termid":"GO:0009532"}],"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":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0005737","GO:0032991"],"is_obsolete":false,"name":"plastid acetyl-CoA carboxylase complex","synonyms":[{"name":"plastid ACCase complex","type":"exact"}],"termid":"GO:0032282"}


id: MONDO:0016197
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"qualitative or quantitative protein defects in neuromuscular diseases","termid":"MONDO:0016139"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"qualitative or quantitative defects of selenoprotein N1","secondary_identifiers":["UMLS:C5680834","GARD:20436","Orphanet:209193","MEDGEN:1842545"],"termid":"MONDO:0016197","xrefs":{"Monarch":{"xref_id":"0016197"}}}


id: FYPO:0001451
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which cells show decreased sensitivity to freezing.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"resistance to cold","termid":"FYPO:0001450"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000003"}],"interesting_parent_ids":["FYPO:0000139","FYPO:0005447","FYPO:0000003","FYPO:0001985"],"is_obsolete":false,"name":"resistance to freezing","synonyms":[{"name":"increased growth during cellular response to freezing","type":"exact"},{"name":"increased vegetative cell population growth during cellular response to freezing","type":"exact"},{"name":"resistance to freezing during mitotic cell cycle","type":"related"},{"name":"resistance to freezing during vegetative growth","type":"exact"},{"name":"resistant to freeze-thawing","type":"related"},{"name":"resistant to freezing","type":"exact"}],"termid":"FYPO:0001451"}


id: PBO:0055943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"leucine rich repeat containing 52","termid":"PBO:0055943"}


id: GO:0018078
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The iodination of peptidyl-thyronine, formed from tyrosine.","definition_xrefs":["RESID:AA0178","RESID:AA0177"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-thyronine iodination (obsolete GO:0018078)","termid":"GO:0018078"}


id: PBO:0051010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"insulin like growth factor 1","termid":"PBO:0051010"}


id: PBO:0005093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PAZ domain","termid":"PBO:0005093"}


id: PBO:0044821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defensin beta 109D (pseudogene)","termid":"PBO:0044821"}


id: GO:1901208
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of heart looping.","definition_xrefs":["GOC:BHF","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of heart looping","termid":"GO:1901207"},{"relation_name":"is_a","term_name":"negative regulation of morphogenesis of an epithelium","termid":"GO:1905331"},{"relation_name":"negatively_regulates","term_name":"heart looping","termid":"GO:0001947"}],"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 heart looping","synonyms":[{"name":"down regulation of cardiac looping","type":"exact"},{"name":"down regulation of heart looping","type":"exact"},{"name":"down-regulation of cardiac looping","type":"exact"},{"name":"down-regulation of heart looping","type":"exact"},{"name":"downregulation of cardiac looping","type":"exact"},{"name":"downregulation of heart looping","type":"exact"},{"name":"inhibition of cardiac looping","type":"exact"},{"name":"inhibition of heart looping","type":"narrow"},{"name":"negative regulation of cardiac looping","type":"exact"}],"termid":"GO:1901208"}


id: MONDO:0017760
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete disorder of other vitamins and cofactors metabolism and transport (obsolete MONDO:0017760)","secondary_identifiers":["Orphanet:309833"],"termid":"MONDO:0017760","xrefs":{"Monarch":{"xref_id":"0017760"}}}


id: GO:0004237
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of dipeptides.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete membrane dipeptidase activity (obsolete GO:0004237)","synonyms":[{"name":"membrane dipeptidase activity","type":"exact"}],"termid":"GO:0004237"}


id: PBO:0034445
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_protein_localization_to_spindle_during_meiosis_I","termid":"PBO:0034445"}


id: GO:0035879
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of lactate across a plasma membrane.","definition_xrefs":["GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lactate transmembrane transport","termid":"GO:0035873"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085","GO:0051179"],"is_obsolete":false,"name":"plasma membrane lactate transport","synonyms":[{"name":"lactate plasma membrane transport","type":"exact"}],"termid":"GO:0035879"}


id: PBO:0081490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 385B","termid":"PBO:0081490"}


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


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: PBO:0060677
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NDNF antisense RNA 1","termid":"PBO:0060677"}


id: PBO:0030960
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_histone_H3-K9_trimethylation_at_centromere_outer_repeat","termid":"PBO:0030960"}


id: PBO:0089587
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TIM22 inner membrane protein import complex and succinate dehydrogenase (SDH) anchor subunit Tim18","termid":"PBO:0089587"}


id: PBO:0045962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"egl-9 family hypoxia inducible factor 1 pseudogene 1","termid":"PBO:0045962"}


id: GO:0048654
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the anther are generated and organized.","definition_xrefs":["GOC:sm","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"floral organ morphogenesis","termid":"GO:0048444"},{"relation_name":"part_of","term_name":"stamen morphogenesis","termid":"GO:0048448"},{"relation_name":"part_of","term_name":"anther development","termid":"GO:0048653"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"anther morphogenesis","termid":"GO:0048654"}


id: PBO:0048842
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glyceronephosphate O-acyltransferase pseudogene","termid":"PBO:0048842"}


id: PBO:0041550
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 18 open reading frame 63","termid":"PBO:0041550"}


id: FYPO:0003777
data:
  {"alleles_by_uniquename":{"SJAG_01745:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01745","name":"lem2delta","uniquename":"SJAG_01745:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118692],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0003657"}]},"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 endoplasmic reticulum is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization during vegetative growth","termid":"FYPO:0000443"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"},{"relation_name":"is_a","term_name":"abnormal protein localization to endoplasmic reticulum","termid":"FYPO:0006377"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01050":null,"SJAG_01745":null},"genotype_count":1,"genotypes_by_uniquename":{"lem2delta":{"display_name":"lem2delta","display_uniquename":"lem2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01745:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0005447","FYPO:0001985","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"abnormal protein localization to endoplasmic reticulum during vegetative growth","references_by_uniquename":{"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_01745"],"single_locus_genotype_uniquenames":["lem2delta"],"synonyms":[{"name":"abnormal protein localisation to endoplasmic reticulum during vegetative growth","type":"exact"},{"name":"abnormal protein localization to ER during vegetative growth","type":"exact"},{"name":"abnormal protein localization to endoplasmic reticulum during mitotic cell cycle","type":"related"}],"termid":"FYPO:0003777","terms_by_termid":{"FYECO:0000137":null,"FYPO:0003657":null,"FYPO_EXT:0000001":null}}


id: FYPO:0004574
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","gene_count":0,"genotype_count":0,"name":"OBSOLETE FYPO:0004574 DEPRECATED increased subtelomere-derived RNA level (obsolete FYPO:0004574)","termid":"FYPO:0004574"}


id: PBO:0031342
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_hydroxyurea","termid":"PBO:0031342"}


id: PBO:0079172
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis specific protein Y-linked 1","termid":"PBO:0079172"}


id: GO:0009212
data:
  {"annotated_genes":["SJAG_04657","SJAG_00885","SJAG_04665","SJAG_04627"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[106730],"is_not":false,"summary":null,"term":"GO:0009212"},{"annotations":[117462,88890,91947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006235"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of pyrimidine deoxyribonucleoside triphosphate, a compound consisting of a pyrimidine base linked to a deoxyribose sugar esterified with triphosphate on the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleoside triphosphate biosynthetic process","termid":"GO:0009148"},{"relation_name":"is_a","term_name":"pyrimidine deoxyribonucleoside triphosphate metabolic process","termid":"GO:0009211"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00885":null,"SJAG_04627":null,"SJAG_04657":null,"SJAG_04665":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"pyrimidine deoxyribonucleoside triphosphate biosynthetic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"pyrimidine deoxyribonucleoside triphosphate anabolism","type":"exact"},{"name":"pyrimidine deoxyribonucleoside triphosphate biosynthesis","type":"exact"},{"name":"pyrimidine deoxyribonucleoside triphosphate formation","type":"exact"},{"name":"pyrimidine deoxyribonucleoside triphosphate synthesis","type":"exact"}],"termid":"GO:0009212","terms_by_termid":{"GO:0006235":null,"GO:0009212":null}}


id: GO:0002707
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of lymphocyte mediated immunity.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of leukocyte mediated immunity","termid":"GO:0002704"},{"relation_name":"is_a","term_name":"regulation of lymphocyte mediated immunity","termid":"GO:0002706"},{"relation_name":"negatively_regulates","term_name":"lymphocyte mediated immunity","termid":"GO:0002449"}],"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 lymphocyte mediated immunity","synonyms":[{"name":"down regulation of lymphocyte mediated immunity","type":"exact"},{"name":"down-regulation of lymphocyte mediated immunity","type":"exact"},{"name":"downregulation of lymphocyte mediated immunity","type":"exact"},{"name":"inhibition of lymphocyte mediated immunity","type":"narrow"}],"termid":"GO:0002707"}


id: PBO:0079908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquinol-cytochrome c reductase core protein 2 pseudogene 1","termid":"PBO:0079908"}


id: GO:1990385
data:
  {"annotated_genes":["SJAG_01837","SJAG_04412","SJAG_03073","SJAG_00930"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[100911,103023,116106,118122],"is_not":false,"summary":null,"term":"GO:1990385"}]},"cv_name":"cellular_component","definition":"The area in the center of the meiotic spindle where the spindle microtubules from opposite poles overlap.","definition_xrefs":["PMID:12707312","GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spindle midzone","termid":"GO:0051233"},{"relation_name":"part_of","term_name":"meiotic spindle","termid":"GO:0072687"}],"gene_count":4,"genes_by_uniquename":{"SJAG_00930":null,"SJAG_01837":null,"SJAG_03073":null,"SJAG_04412":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015630"}],"interesting_parent_ids":["GO:0005575","GO:0015630"],"is_obsolete":false,"name":"meiotic spindle midzone","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:1990385","terms_by_termid":{"GO:1990385":null}}


id: MOD:01367
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative -","definition_xrefs":["Unimod:478#P"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fluorescein-5-thiosemicarbazide","termid":"MOD:00626"},{"relation_name":"is_a","term_name":"modified L-proline residue","termid":"MOD:00915"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fluorescein-5-thiosemicarbazide - site P","synonyms":[{"name":"FTC","type":"related"},{"name":"fluorescein-5-thiosemicarbazide","type":"related"}],"termid":"MOD:01367"}


id: GO:1990217
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts the production of phytoalexins in the host organism. Phytoalexins are produced by plants to fight against pathogens. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:21402357"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host phytoalexin production","termid":"GO:0052165"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host phytoalexin production","synonyms":[{"name":"negative regulation by symbiont of host phytoalexin production","type":"exact"},{"name":"suppression by symbiont of host phytoalexin production","type":"exact"}],"termid":"GO:1990217"}


id: MONDO:0010394
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete leukoencephalopathy-metaphyseal chondrodysplasia syndrome (obsolete MONDO:0010394)","secondary_identifiers":["OMIM:300660"],"termid":"MONDO:0010394","xrefs":{"Monarch":{"xref_id":"0010394"}}}


id: MONDO:0021121
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A vascular proliferation characterized by the presence of prominent endothelial cells and the formation of vascular channels. Hemangioendotheliomas may display borderline or low grade characteristics.","definition_xrefs":["NCIT:C3084"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel neoplasm","termid":"MONDO:0021080"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"hemangioendothelioma","secondary_identifiers":["ICDO:9130/1","SCTID:403980002","MESH:D006390","UMLS:C0018915","MEDGEN:42384"],"synonyms":[{"name":"angioendothelioma","type":"exact"},{"name":"hemangioendothelioma","type":"exact"}],"termid":"MONDO:0021121","xrefs":{"Monarch":{"xref_id":"0021121"}}}


id: SO:0002055
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A variant whereby the gene product is not functional or the gene product is not produced.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functionally_abnormal","termid":"SO:0002218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"null_mutation","synonyms":[{"name":"null mutation","type":"exact"}],"termid":"SO:0002055"}


id: GO:0034644
data:
  {"annotated_genes":["SJAG_04190","SJAG_00272","SJAG_00208","SJAG_01010","SJAG_02199","SJAG_02828","SJAG_02182","SJAG_01648","SJAG_04877","SJAG_02334","SJAG_02200","SJAG_01262","SJAG_03898","SJAG_00729","SJAG_00863","SJAG_02818","SJAG_00814","SJAG_05197","SJAG_04150"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[104402,94737,108568,102314],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1904161"},{"annotations":[111721,87527,93468,89089,96628,94561,103714,110274,110874,105412,93164,95521,106451,94772,112274],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070914"}]},"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 ultraviolet radiation (UV light) stimulus. Ultraviolet radiation is electromagnetic radiation with a wavelength in the range of 10 to 380 nanometers.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to UV","termid":"GO:0009411"},{"relation_name":"is_a","term_name":"cellular response to light stimulus","termid":"GO:0071482"}],"gene_count":19,"genes_by_uniquename":{"SJAG_00208":null,"SJAG_00272":null,"SJAG_00729":null,"SJAG_00814":null,"SJAG_00863":null,"SJAG_01010":null,"SJAG_01262":null,"SJAG_01648":null,"SJAG_02182":null,"SJAG_02199":null,"SJAG_02200":null,"SJAG_02334":null,"SJAG_02818":null,"SJAG_02828":null,"SJAG_03898":null,"SJAG_04150":null,"SJAG_04190":null,"SJAG_04877":null,"SJAG_05197":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to UV","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"cellular response to UV light stimulus","type":"exact"},{"name":"cellular response to UV radiation stimulus","type":"exact"},{"name":"cellular response to ultraviolet light stimulus","type":"exact"},{"name":"cellular response to ultraviolet radiation stimulus","type":"exact"}],"termid":"GO:0034644","terms_by_termid":{"GO:0070914":null,"GO:1904161":null}}


id: MONDO:0027767
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Loss and redistribution of subcutaneous and/or visceral adipose tissue from specific regions of the body.","definition_xrefs":["NCIT:C131296"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipodystrophy","termid":"MONDO:0006573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005093"],"is_obsolete":false,"name":"partial lipodystrophy","secondary_identifiers":["UMLS:C4316789","MEDGEN:1386287","DOID:0080299"],"termid":"MONDO:0027767","xrefs":{"Monarch":{"xref_id":"0027767"}}}


id: PBO:0060191
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mucin 12, cell surface associated","termid":"PBO:0060191"}


id: PBO:0017726
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit S7, Rsm7(predicted)","termid":"PBO:0017726"}


id: PBO:0035836
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_ubiquitination_during_vegetative_growth","termid":"PBO:0035836"}


id: MONDO:0011426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An adult-onset disorder of neurodegeneration with brain iron accumulation (NBIA) characterized by anemia, retinal degeneration, diabetes and various neurological symptoms.","definition_xrefs":["Orphanet:48818"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye degenerative disorder","termid":"MONDO:0004884"},{"relation_name":"is_a","term_name":"inherited deficiency anemia","termid":"MONDO:0016624"},{"relation_name":"is_a","term_name":"disorder of iron metabolism and transport","termid":"MONDO:0017763"},{"relation_name":"is_a","term_name":"neurodegeneration with brain iron accumulation","termid":"MONDO:0018307"},{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328","MONDO:0005570","MONDO:0002280","MONDO:0002039","MONDO:0005559","MONDO:0005066"],"is_obsolete":false,"name":"aceruloplasminemia","secondary_identifiers":["NORD:707","UMLS:C0878682","OMIM:604290","SCTID:124224004","MEDGEN:168057","DOID:0050711","ICD9:277.6","NANDO:1200540","NANDO:2200582","GARD:9499"],"synonyms":[{"name":"aceruloplasminemia","type":"exact"},{"name":"cerebellar ataxia","type":"broad"},{"name":"ceruloplasmin deficiency","type":"related"},{"name":"familial apoceruloplasmin deficiency","type":"related"},{"name":"hemosiderosis, systemic, due to aceruloplasminemia","type":"related"},{"name":"hereditary ceruloplasmin deficiency","type":"exact"},{"name":"hypoceruloplasminemia","type":"related"},{"name":"hypoceruloplasminemia, hereditary","type":"exact"},{"name":"systemic hemosiderosis due to aceruloplasminemia","type":"related"}],"termid":"MONDO:0011426","xrefs":{"Monarch":{"xref_id":"0011426"}}}


id: MONDO:0958226
data:
  {"annotated_genes":["SJAG_02896"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86630],"is_not":false,"summary":null,"term":"MONDO:0958226"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"leukodystrophy","termid":"MONDO:0019046"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02896":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"leukoencephalopathy, porphyria-related","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620711"],"termid":"MONDO:0958226","terms_by_termid":{"MONDO:0958226":null},"xrefs":{"Monarch":{"xref_id":"0958226"}}}


id: GO:1904850
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of establishment of protein localization to telomere.","definition_xrefs":["GO_REF:0000058","GOC:BHF","GOC:BHF_telomere","GOC:nc","GOC:TermGenie","PMID:25467444"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of establishment of protein localization to telomere","termid":"GO:0070203"},{"relation_name":"is_a","term_name":"negative regulation of protein localization to chromosome, telomeric region","termid":"GO:1904815"},{"relation_name":"is_a","term_name":"negative regulation of establishment of protein localization","termid":"GO:1904950"},{"relation_name":"negatively_regulates","term_name":"establishment of protein localization to telomere","termid":"GO:0070200"}],"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 establishment of protein localization to telomere","synonyms":[{"name":"down regulation of establishment of protein localisation to telomere","type":"exact"},{"name":"down regulation of establishment of protein localization to chromosome, telomeric region","type":"exact"},{"name":"down regulation of establishment of protein localization to telomere","type":"exact"},{"name":"down-regulation of establishment of protein localisation to telomere","type":"exact"},{"name":"down-regulation of establishment of protein localization to chromosome, telomeric region","type":"exact"},{"name":"down-regulation of establishment of protein localization to telomere","type":"exact"},{"name":"downregulation of establishment of protein localisation to telomere","type":"exact"},{"name":"downregulation of establishment of protein localization to chromosome, telomeric region","type":"exact"},{"name":"downregulation of establishment of protein localization to telomere","type":"exact"},{"name":"inhibition of establishment of protein localisation to telomere","type":"narrow"},{"name":"inhibition of establishment of protein localization to chromosome, telomeric region","type":"narrow"},{"name":"inhibition of establishment of protein localization to telomere","type":"narrow"},{"name":"negative regulation of establishment of protein localisation to telomere","type":"exact"},{"name":"negative regulation of establishment of protein localization to chromosome, telomeric region","type":"exact"}],"termid":"GO:1904850"}


id: MONDO:0009379
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Rotor syndrome (RT) is a benign, inherited liver disorder characterized by chronic, predominantly conjugated, nonhemolytic hyperbilirubinemia with normal liver histology.","definition_xrefs":["Orphanet:3111"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary hyperbilirubinemia","termid":"MONDO:0002408"}],"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":"Rotor syndrome","secondary_identifiers":["MEDGEN:67435","OMIM:237450","SCTID:32891000","icd11.foundation:1965776012","GARD:218","UMLS:C0220991","MedDRA:10039234"],"synonyms":[{"name":"HBLRR","type":"related"},{"name":"Rotor syndrome","type":"exact"},{"name":"Rotor-type hyperbilirubinemia","type":"related"},{"name":"hyperbilirubinemia, ROTOR type","type":"related"},{"name":"hyperbilirubinemia, Rotor type","type":"exact"},{"name":"hyperbilirubinemia, rotor type, digenic","type":"exact"}],"termid":"MONDO:0009379","xrefs":{"Monarch":{"xref_id":"0009379"}}}


id: MONDO:0008864
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Biemond syndrome type 2 (BS2) is a rare genetic neurological and developmental disorder reported in a very small number of patients with a poorly defined phenotype which includes iris coloboma, short stature, obesity, hypogonadism, postaxial polydactyly, and intellectual disability. Hydrocephalus and facial dysostosis were also reported. BS2 shares features with Bardet-Biedl syndrome. There have been no further descriptions in the literature since 1997.","definition_xrefs":["Orphanet:141333"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Biemond syndrome type 2","secondary_identifiers":["UMLS:C1859487","GARD:882","MEDGEN:347159","MESH:C565902","SCTID:717887003","OMIM:210350"],"synonyms":[{"name":"BIEMOND syndrome II","type":"related"},{"name":"BS2","type":"related"},{"name":"Biemond syndrome 2","type":"related"},{"name":"Biemond syndrome type 2","type":"exact"},{"name":"hypogonadism-short stature-coloboma-preaxial polydactyly syndrome","type":"exact"},{"name":"iris coloboma, intellectual disability, obesity, hypogenitalism, and postaxial polydactyly","type":"related"},{"name":"iris coloboma, mental retardation, obesity, hypogenitalism, and postaxial polydactyly","type":"related"}],"termid":"MONDO:0008864","xrefs":{"Monarch":{"xref_id":"0008864"}}}


id: MONDO:0022293
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-neoplastic or neoplastic disorder that affects the blood vessels of the penis. Representative examples include atherosclerosis, venous leak, and hemangioma.","definition_xrefs":["NCIT:C35218"],"direct_ancestors":[{"relation_name":"is_a","term_name":"penile disorder","termid":"MONDO:0002036"},{"relation_name":"is_a","term_name":"vascular disorder","termid":"MONDO:0005385"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vascular disorder of penis","secondary_identifiers":["ICD9:607.82","SCTID:198029003","MEDGEN:102349","UMLS:C0156307"],"synonyms":[{"name":"Penile Vascular Disorder","type":"related"},{"name":"Penile vascular disorder","type":"related"},{"name":"Penis vascular disorder","type":"related"},{"name":"Vascular disorder of penis","type":"related"},{"name":"penile vascular disorder","type":"exact"}],"termid":"MONDO:0022293","xrefs":{"Monarch":{"xref_id":"0022293"}}}


id: PBO:0085889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; involved in nuclear processes of the Ran-GTPase cycle; involved in nuclear protein export; contains Ran Binding Domain and FxFG repeats; interacts with Srm1p, GTP-Gsp1p, Rna1p and Crm1p; relocalizes to the cytosol in response to hypoxia; not essential for viability","termid":"PBO:0085889"}


id: GO:1905151
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of voltage-gated sodium channel activity.","definition_xrefs":["PMID:24198377","GO_REF:0000059","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of voltage-gated sodium channel activity","termid":"GO:1905150"},{"relation_name":"is_a","term_name":"negative regulation of sodium ion transmembrane transporter activity","termid":"GO:2000650"},{"relation_name":"is_a","term_name":"negative regulation of cation channel activity","termid":"GO:2001258"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"negatively_regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0055085"},{"rel_name":"negatively_regulates","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0055085"],"is_obsolete":false,"name":"negative regulation of voltage-gated sodium channel activity","synonyms":[{"name":"down regulation of voltage gated sodium channel activity","type":"exact"},{"name":"down regulation of voltage-dependent sodium channel activity","type":"exact"},{"name":"down regulation of voltage-gated sodium channel activity","type":"exact"},{"name":"down regulation of voltage-gated sodium ion channel activity","type":"exact"},{"name":"down regulation of voltage-sensitive sodium channel","type":"exact"},{"name":"down-regulation of voltage gated sodium channel activity","type":"exact"},{"name":"down-regulation of voltage-dependent sodium channel activity","type":"exact"},{"name":"down-regulation of voltage-gated sodium channel activity","type":"exact"},{"name":"down-regulation of voltage-gated sodium ion channel activity","type":"exact"},{"name":"down-regulation of voltage-sensitive sodium channel","type":"exact"},{"name":"downregulation of voltage gated sodium channel activity","type":"exact"},{"name":"downregulation of voltage-dependent sodium channel activity","type":"exact"},{"name":"downregulation of voltage-gated sodium channel activity","type":"exact"},{"name":"downregulation of voltage-gated sodium ion channel activity","type":"exact"},{"name":"downregulation of voltage-sensitive sodium channel","type":"exact"},{"name":"inhibition of voltage gated sodium channel activity","type":"narrow"},{"name":"inhibition of voltage-dependent sodium channel activity","type":"narrow"},{"name":"inhibition of voltage-gated sodium channel activity","type":"narrow"},{"name":"inhibition of voltage-gated sodium ion channel activity","type":"narrow"},{"name":"inhibition of voltage-sensitive sodium channel","type":"narrow"},{"name":"negative regulation of voltage gated sodium channel activity","type":"exact"},{"name":"negative regulation of voltage-dependent sodium channel activity","type":"exact"},{"name":"negative regulation of voltage-gated sodium ion channel activity","type":"exact"},{"name":"negative regulation of voltage-sensitive sodium channel","type":"exact"}],"termid":"GO:1905151"}


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


id: GO:0043736
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of alkylated DNA; recognizes and removes both N-3- and N-7-methyl purines by cleaving the N-C1' glycosidic bond between the target damaged DNA base and the deoxyribose sugar. The reaction releases a free base and leaves an apurinic (AP) site.","definition_xrefs":["PMID:10375529"],"gene_count":0,"genotype_count":0,"name":"obsolete DNA-3-methyladenine glycosylase IV activity (obsolete GO:0043736)","synonyms":[{"name":"DNA-3-methyladenine glycosylase IV activity","type":"exact"},{"name":"Mpg II","type":"narrow"},{"name":"MpgII","type":"narrow"}],"termid":"GO:0043736"}


id: PBO:0003182
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"horsetail movement protein Hrs1","termid":"PBO:0003182"}


id: MONDO:0015518
data:
  {"annotated_genes":["SJAG_02274"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84737],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010080"}]},"cv_name":"mondo","definition":"Several syndromes of bilateral symmetric spongy degeneration of the caudate nucleaus, putamen and globus pallidus characterized by developmental regression, choreoathetosis and dystonia progressing to spastic quadriparesis. IBSN can be familial or sporadic.","definition_xrefs":["Orphanet:1576"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare genetic syndromic intellectual disability (obsolete MONDO:0015983)","termid":"MONDO:0015983"},{"relation_name":"excluded_subClassOf","term_name":"obsolete miscellaneous movement disorder due to neurodegenerative disease (obsolete MONDO:0017641)","termid":"MONDO:0017641"},{"relation_name":"excluded_subClassOf","term_name":"obsolete miscellaneous movement disorder due to genetic neurodegenerative disease (obsolete MONDO:0017662)","termid":"MONDO:0017662"},{"relation_name":"is_a","term_name":"neurodegenerative disease","termid":"MONDO:0005559"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02274":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"infantile bilateral striatal necrosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0795996","ICD10CM:G23.2","GARD:5040","SCTID:718174008","icd11.foundation:1947032348","MEDGEN:167090","NANDO:2100242","NANDO:2200888"],"synonyms":[{"name":"IBSN","type":"exact"},{"name":"SNDI","type":"related"},{"name":"infantile bilateral striatal necrosis","type":"exact"},{"name":"infantile striatonigral degeneration","type":"exact"},{"name":"infantile striatonigral necrosis","type":"exact"},{"name":"striatal degeneration familial","type":"related"},{"name":"striatonigral degeneration infantile","type":"related"}],"termid":"MONDO:0015518","terms_by_termid":{"MONDO:0010080":null},"xrefs":{"Monarch":{"xref_id":"0015518"}}}


id: PBO:0114751
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cohesin unloading factor (WAPL) Wpl1","termid":"PBO:0114751"}


id: PBO:0003997
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DNA polymerase zeta Rev7 (predicted)","termid":"PBO:0003997"}


id: GO:2000825
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of androgen receptor activity.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of transcription by RNA polymerase II","termid":"GO:0006357"},{"relation_name":"is_a","term_name":"positive regulation of DNA-binding transcription factor activity","termid":"GO:0051091"},{"relation_name":"is_a","term_name":"positive regulation of signaling receptor activity","termid":"GO:2000273"}],"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:0006355"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0006351","GO:0008150","GO:0010467","GO:0006355","GO:0023052"],"is_obsolete":false,"name":"positive regulation of androgen receptor activity","termid":"GO:2000825"}


id: FYPO:0008078
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which meiotic sister kinetochore association in meiotic metaphase I, is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:34851403"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal meiotic cell cycle process","termid":"FYPO:0007078"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal meiotic sister kinetochore association in meiotic metaphase I","termid":"FYPO:0008078"}


id: MONDO:0003482
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A infectious disease involving the Pediculus humanus corporis.","definition_xrefs":["MONDO:patterns/infectious_disease_by_agent"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lice infestation","termid":"MONDO:0003472"}],"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":"Pediculus humanus corporis infestation","secondary_identifiers":["UMLS:C0030758","DOID:5513","ICD9:132.1","SCTID:25188002","MEDGEN:508023"],"synonyms":[{"name":"Pediculus corporis","type":"exact"},{"name":"Pediculus corporis [body louse]","type":"exact"},{"name":"Pediculus humanus corporis infection","type":"exact"},{"name":"Pediculus humanus infestation","type":"exact"},{"name":"body louse infestation","type":"exact"},{"name":"infections, Pediculus humanus corporis","type":"related"}],"termid":"MONDO:0003482","xrefs":{"Monarch":{"xref_id":"0003482"}}}


id: PBO:0074473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"smoothelin like 2","termid":"PBO:0074473"}


id: PBO:0034656
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_DNA_recombination_frequency_at_subtelomere","termid":"PBO:0034656"}


id: MONDO:0003606
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant neoplasm involving the adrenal medulla","direct_ancestors":[{"relation_name":"is_a","term_name":"adrenal gland cancer","termid":"MONDO:0002817"},{"relation_name":"is_a","term_name":"adrenal medulla neoplasm","termid":"MONDO:0021237"}],"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":"adrenal medulla cancer","secondary_identifiers":["NCIT:C4396","MEDGEN:87485","SCTID:371965009","UMLS:C0344456","GARD:5755","DOID:5719"],"synonyms":[{"name":"adrenal medulla cancer","type":"exact"},{"name":"adrenal medulla neoplasm","type":"broad"},{"name":"adrenal medulla tumor","type":"broad"},{"name":"adrenal medulla tumour","type":"broad"},{"name":"cancer of adrenal medulla","type":"exact"},{"name":"malignant adrenal medulla neoplasm","type":"exact"},{"name":"malignant adrenal medulla tumor","type":"exact"},{"name":"malignant adrenal medulla tumour","type":"exact"},{"name":"malignant neoplasm of adrenal medulla","type":"exact"},{"name":"malignant neoplasm of the adrenal medulla","type":"exact"},{"name":"malignant tumor of adrenal medulla","type":"exact"},{"name":"malignant tumor of the adrenal medulla","type":"exact"},{"name":"malignant tumour of adrenal medulla","type":"exact"},{"name":"malignant tumour of the adrenal medulla","type":"exact"}],"termid":"MONDO:0003606","xrefs":{"Monarch":{"xref_id":"0003606"}}}


id: GO:0106371
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: O2 + primary fluorescent chlorophyll catabolite + reduced [NADPH--hemoprotein reductase] = formate + 2 H+ + oxidized [NADPH--hemoprotein reductase] + primary fluorescent dioxobilin-type chlorophyll catabolite.","definition_xrefs":["RHEA:67172","PMID:23723324"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"fluorescent chlorophyll catabolite monooxygenase (deformylase) activity","termid":"GO:0106371"}


id: PBO:0082956
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytoplasmic protein involved in halotolerance; decreases intracellular Na+ (via Ena1p) and increases intracellular K+ by decreasing efflux; expression repressed by Ssn6p-Tup1p and Sko1p and induced by NaCl, KCl, and sorbitol through Gcn4p","termid":"PBO:0082956"}


id: PBO:0088056
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin protease cofactor; forms deubiquitination complex with Ubp3p that coregulates anterograde and retrograde transport between the ER and Golgi compartments, deubiquitinating COPII and COPI vesicle coat constituents, Sec23p and Sec27p; involved along with Ubp3p in the steady-state retention of Golgi membrane proteins, such as glycosyltransferases; null is sensitive to brefeldin A","termid":"PBO:0088056"}


id: PBO:0030359
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_RNA_level_during_cellular_response_to_hypoxia","termid":"PBO:0030359"}


id: MONDO:0002370
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign, borderline, or malignant transitional cell neoplasm arising from the ovary. It constitutes between 1% and 2% of all ovarian neoplasms. The average age at presentation is about 50 years. Grossly it is usually unilateral, firm and white or yellowish. Microscopically it consists of solid and cystic nests of epithelial cells resembling transitional epithelium surrounded by an abundant stromal component of dense, fibroblastic nature.","definition_xrefs":["NCIT:C3872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian epithelial tumor","termid":"MONDO:0002229"},{"relation_name":"is_a","term_name":"Brenner tumor","termid":"MONDO:0024235"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ovarian Brenner tumor","secondary_identifiers":["DOID:2636","UMLS:C5234884","SCTID:254859006","MEDGEN:1716777"],"synonyms":[{"name":"Brenner neoplasm of ovary","type":"exact"},{"name":"Brenner neoplasm of the ovary","type":"exact"},{"name":"Brenner tumor","type":"broad"},{"name":"Brenner tumor of ovary","type":"exact"},{"name":"Brenner tumor of the ovary","type":"exact"},{"name":"Brenner tumour","type":"broad"},{"name":"Brenner tumour of ovary","type":"exact"},{"name":"Brenner tumour of the ovary","type":"exact"},{"name":"benign ovarian Brenner tumor","type":"narrow"},{"name":"benign ovarian Brenner tumour","type":"narrow"},{"name":"ovarian Brenner neoplasm","type":"exact"},{"name":"ovarian Brenner tumor","type":"exact"},{"name":"ovary Brenner tumor","type":"exact"},{"name":"ovary Brenner tumour","type":"exact"}],"termid":"MONDO:0002370","xrefs":{"Monarch":{"xref_id":"0002370"}}}


id: PBO:0085988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; required for normal microtubule organization","termid":"PBO:0085988"}


id: PBO:0089860
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"plasma membrane stretch-activated calcium ion channel Yam8","termid":"PBO:0089860"}


id: MONDO:0006326
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A melanoma arising from and extending beyond the structures of the eye.","definition_xrefs":["NCIT:C7913"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ocular melanoma","termid":"MONDO:0006325"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005328"],"is_obsolete":false,"name":"ocular melanoma with extraocular extension","secondary_identifiers":["UMLS:C0278869","MEDGEN:75884"],"synonyms":[{"name":"extraocular extension melanoma","type":"exact"},{"name":"extraocular extension of melanoma","type":"exact"},{"name":"ocular melanoma with extraocular extension","type":"exact"}],"termid":"MONDO:0006326","xrefs":{"Monarch":{"xref_id":"0006326"}}}


id: GO:1900707
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of tensidol A biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone biosynthetic process","termid":"GO:0010566"},{"relation_name":"is_a","term_name":"regulation of amide metabolic process","termid":"GO:0034248"},{"relation_name":"is_a","term_name":"regulation of secondary metabolite biosynthetic process","termid":"GO:1900376"},{"relation_name":"regulates","term_name":"tensidol A biosynthetic process","termid":"GO:1900605"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0019748","GO:0044281"],"is_obsolete":false,"name":"regulation of tensidol A biosynthetic process","synonyms":[{"name":"regulation of tensidol A anabolism","type":"exact"},{"name":"regulation of tensidol A biosynthesis","type":"exact"},{"name":"regulation of tensidol A formation","type":"exact"},{"name":"regulation of tensidol A synthesis","type":"exact"}],"termid":"GO:1900707"}


id: GO:0060713
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the labyrinthine layer of the placenta is generated and organized.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic morphogenesis","termid":"GO:0048598"},{"relation_name":"part_of","term_name":"embryonic placenta morphogenesis","termid":"GO:0060669"},{"relation_name":"part_of","term_name":"labyrinthine layer development","termid":"GO:0060711"}],"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":"labyrinthine layer morphogenesis","termid":"GO:0060713"}


id: PBO:0029539
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_mixed_population_including_spores,_germinated_spores_and_cells_with_normal_morphology_(obsolete_FYPO:0002183)","termid":"PBO:0029539"}


id: PBO:0026932
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_HMW_ubiquitin_conjugate_level","termid":"PBO:0026932"}


id: PBO:0061530
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NSMCE1 divergent transcript","termid":"PBO:0061530"}


id: GO:0047816
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-arabinose + NAD+ = D-arabinono-1,4-lactone + NADH.","definition_xrefs":["RHEA:20457"],"direct_ancestors":[{"relation_name":"is_a","term_name":"D-arabinose 1-dehydrogenase [NAD(P)+] activity","termid":"GO:0045290"}],"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:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"D-arabinose 1-dehydrogenase (NAD+) activity","secondary_identifiers":["MetaCyc:D-ARABINOSE-1-DEHYDROGENASE-RXN","EC:1.1.1.116"],"synonyms":[{"name":"D-arabinose:NAD+ 1-oxidoreductase activity","type":"related"},{"name":"NAD-pentose-dehydrogenase activity","type":"related"},{"name":"arabinose(fucose)dehydrogenase activity","type":"related"}],"termid":"GO:0047816"}


id: FYPO:0004346
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 non-coding RNA genes is decreased.","definition_xrefs":["PomBase:mah","PMID:25002536"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to chromatin during vegetative growth","termid":"FYPO:0002909"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0000138","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein localization to chromatin at ncRNA genes","synonyms":[{"name":"decreased protein localisation to chromatin at ncRNA genes","type":"exact"},{"name":"decreased protein localization to chromatin at ncRNA genes during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to chromatin at ncRNA genes during vegetative growth","type":"exact"},{"name":"decreased protein localization to chromatin at non-coding RNA genes","type":"exact"},{"name":"reduced protein localization to chromatin at ncRNA genes","type":"exact"}],"termid":"FYPO:0004346"}


id: MONDO:0030515
data:
  {"annotated_genes":["SJAG_04176"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85623],"is_not":false,"summary":null,"term":"MONDO:0030515"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04176":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 63","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0112356","MEDGEN:1794265","OMIM:619689","UMLS:C5562055"],"synonyms":[{"name":"SPGF63","type":"exact"}],"termid":"MONDO:0030515","terms_by_termid":{"MONDO:0030515":null},"xrefs":{"Monarch":{"xref_id":"0030515"}}}


id: PBO:0067535
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 679, pseudogene","termid":"PBO:0067535"}


id: GO:0018244
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The glycosylation of protein via peptidyl-tryptophan, 1'-glycosyl-L-tryptophan; results in the formation of an (S)-2-amino-3-(1-D-mannopyranosyloxy-1H-indol-3-yl)propanoic acid residue.","definition_xrefs":["RESID:AA0156"],"gene_count":0,"genotype_count":0,"name":"obsolete protein N-linked glycosylation via tryptophan (obsolete GO:0018244)","termid":"GO:0018244"}


id: GO:0019163
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: pyridoxamine 5'-phosphate + 2-oxoglutarate = pyridoxal 5'-phosphate + D-glutamate.","definition_xrefs":["EC:2.6.1.54"],"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:0016769"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0016769","GO:0016740","GO:0003824"],"is_obsolete":false,"name":"pyridoxamine-phosphate transaminase activity","secondary_identifiers":["MetaCyc:PYRDAMPTRANS-RXN","RHEA:15877"],"synonyms":[{"name":"pyridoxamine 5'-phosphate transaminase activity","type":"related"},{"name":"pyridoxamine 5'-phosphate-alpha-ketoglutarate transaminase activity","type":"related"},{"name":"pyridoxamine phosphate aminotransferase activity","type":"related"},{"name":"pyridoxamine-5'-phosphate:2-oxoglutarate aminotransferase (D-glutamate-forming)","type":"related"},{"name":"pyridoxamine-phosphate aminotransferase activity","type":"exact"}],"termid":"GO:0019163"}


id: GO:0141030
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which an organism effects a change that impairs the structure or function of the host actin cytoskeleton by depolymerizing the host filamentous actin. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["PMID:11889090","PMID:28800062"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host actin cytoskeleton","termid":"GO:0141027"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated perturbation of host actin cytoskeleton via filamentous actin depolymerization","termid":"GO:0141030"}


id: SO:0002157
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene cassette array containing H+ mating type specific information.","definition_xrefs":["PMID:18354497"],"direct_ancestors":[{"relation_name":"is_a","term_name":"silent_mating_type_cassette_array","termid":"SO:0001984"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mat2P","termid":"SO:0002157"}


id: PBO:0084338
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Kinetochore localized protein of unknown function; interacts with Cnn1p (CENP-T); orthologous to human centromere constitutive-associated network (CCAN) subunit CENP-W and fission yeast new1","termid":"PBO:0084338"}


id: GO:1905344
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of prostaglandin.","definition_xrefs":["GOC:rl","PMID:25290914","GO_REF:0000068","GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"prostanoid catabolic process","termid":"GO:0062232"}],"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":"prostaglandin catabolic process","synonyms":[{"name":"prostaglandin breakdown","type":"exact"},{"name":"prostaglandin catabolism","type":"exact"},{"name":"prostaglandin degradation","type":"exact"}],"termid":"GO:1905344"}


id: GO:0015462
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: ATP + H2O + protein(out) = ADP + phosphate + protein(in).","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-transporting ATPase activity","termid":"GO:0015450"},{"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:0022857"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0140318"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0140318","GO:0005215"],"is_obsolete":false,"name":"ABC-type protein transporter activity","synonyms":[{"name":"ABC-type protein transmembrane transporter activity","type":"exact"},{"name":"ATPase-coupled protein transmembrane transporter activity","type":"related"},{"name":"pilin/fimbrilin exporter activity","type":"narrow"},{"name":"protein ABC transporter","type":"exact"},{"name":"protein-transmembrane transporting ATPase activity","type":"related"},{"name":"protein-transporting ATPase activity","type":"broad"}],"termid":"GO:0015462"}


id: GO:0039673
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont inhibits or disrupts the dendritic cell mediated immune response of the host organism. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:jl","GOC:bf","UniProtKB-KW:KW-1118"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host innate immune response","termid":"GO:0052167"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated suppression of host dendritic cell mediated immune response","secondary_identifiers":["VZ:869"],"synonyms":[{"name":"evasion by virus of host dendritic cell activity","type":"related"},{"name":"evasion by virus of host dendritic cell response","type":"exact"},{"name":"impairing dendritic cell function by virus","type":"exact"},{"name":"modulation of host dendritic cell activity by virus","type":"broad"}],"termid":"GO:0039673"}


id: PBO:0027236
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cenH-derived_RNA_level","termid":"PBO:0027236"}


id: PBO:0058626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6758","termid":"PBO:0058626"}


id: PBO:0065163
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prion locus lncRNA, testis expressed","termid":"PBO:0065163"}


id: MONDO:0020452
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital anomaly of the inferior vena cava","termid":"MONDO:0019830"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inferior vena cava interruption","secondary_identifiers":["SCTID:93031005","GARD:19664","UMLS:C5680291","MEDGEN:1806633","ICD9:747.49","Orphanet:99123"],"synonyms":[{"name":"IVC interruption","type":"exact"},{"name":"Inferior caval vein interruption","type":"exact"}],"termid":"MONDO:0020452","xrefs":{"Monarch":{"xref_id":"0020452"}}}


id: GO:0018312
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The transfer, from NAD, of ADP-ribose to peptidyl-serine to form peptidyl-O-(ADP-ribosyl)-L-serine.","definition_xrefs":["RESID:AA0237"],"gene_count":0,"genotype_count":0,"name":"obsolete peptidyl-serine ADP-ribosylation (obsolete GO:0018312)","termid":"GO:0018312"}


id: PBO:0036268
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dystonia 8","termid":"PBO:0036268"}


id: MONDO:0008080
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"schwannomatosis","termid":"MONDO:0008075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005093"],"is_obsolete":false,"name":"neurofibromatosis, type III, mixed central and peripheral","secondary_identifiers":["GARD:15094","MEDGEN:419422","OMIM:162260","SCTID:254240003","UMLS:C2931480","MESH:C537389"],"synonyms":[{"name":"NF3A","type":"related"},{"name":"Nf 3","type":"related"},{"name":"neurofibromas, palmar cutaneous","type":"related"},{"name":"neurofibromatosis, type III, Riccardi type","type":"related"},{"name":"neurofibromatosis, type III, mixed central and peripheral","type":"exact"},{"name":"neurofibromatosis, type III, of Riccardi","type":"related"}],"termid":"MONDO:0008080","xrefs":{"Monarch":{"xref_id":"0008080"}}}


id: PBO:0085227
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Part of a Vps34p phosphatidylinositol 3-kinase complex; functions in carboxypeptidase Y (CPY) sorting; binds Vps30p and Vps34p to promote production of phosphatidylinositol 3-phosphate (PtdIns3P) which stimulates kinase activity; required for overflow degradation of misfolded proteins when ERAD is saturated","termid":"PBO:0085227"}


id: MOD:00977
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from DeltaMass","definition_xrefs":["DeltaMass:0"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sodium containing modified residue","termid":"MOD:00747"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"disodium salt","termid":"MOD:00977"}


id: MONDO:0012644
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Jeune syndrome in which the cause of the disease is a mutation in the IFT80 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Jeune syndrome","termid":"MONDO:0018770"}],"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":"asphyxiating thoracic dystrophy 2","secondary_identifiers":["MESH:C566982","DOID:0110086","UMLS:C1970005","OMIM:611263","MEDGEN:370804","GARD:15511"],"synonyms":[{"name":"ATD2","type":"exact"},{"name":"IFT80 Jeune syndrome","type":"exact"},{"name":"Jeune syndrome caused by mutation in IFT80","type":"exact"},{"name":"SRTD2","type":"exact"},{"name":"asphyxiating thoracic dystrophy 2","type":"exact"},{"name":"asphyxiating thoracic dystrophy type 2","type":"exact"},{"name":"short-rib thoracic dysplasia 2 with or without polydactyly","type":"exact"}],"termid":"MONDO:0012644","xrefs":{"Monarch":{"xref_id":"0012644"}}}


id: GO:0140663
data:
  {"annotated_genes":["SJAG_02895","SJAG_02994"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[98440,99530],"is_not":false,"summary":null,"term":"GO:0140663"}]},"cv_name":"molecular_function","definition":"Binding to and delivering metal ions to a target protein, driven by ATP hydrolysis.","definition_xrefs":["PMID:16843540"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metallochaperone activity","termid":"GO:0016530"},{"relation_name":"is_a","term_name":"ATP-dependent activity","termid":"GO:0140657"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02895":null,"SJAG_02994":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140104"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0140104","GO:0003674"],"is_obsolete":false,"name":"ATP-dependent FeS chaperone activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0140663","terms_by_termid":{"GO:0140663":null}}


id: FYPO:0006211
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates but dies before forming a germ tube or dividing. Such spores exit dormancy and undergo isotropic swelling but the spore wall does not rupture and no germ tube emerges.","definition_xrefs":["PMID:28572514","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination, without cell division","termid":"FYPO:0001991"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000004"],"is_obsolete":false,"name":"inviable after spore germination, before germ tube formation","synonyms":[{"name":"inviable following spore germination, before germ tube formation","type":"exact"},{"name":"inviable germinated spore, without germ tube formation","type":"exact"},{"name":"lethal after spore germination, before germ tube formation","type":"exact"}],"termid":"FYPO:0006211"}


id: PBO:0051329
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin kappa variable 2-23 (pseudogene)","termid":"PBO:0051329"}


id: MONDO:0044309
data:
  {"annotated_genes":["SJAG_01588","SJAG_02802"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86345,86346],"is_not":false,"summary":null,"term":"MONDO:0044309"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Diamond-Blackfan anemia","termid":"MONDO:0015253"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01588":null,"SJAG_02802":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0002280"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0002280"],"is_obsolete":false,"name":"Diamond-Blackfan anemia 16","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1385861","DOID:0111893","GARD:16227","OMIM:617408","UMLS:C4479424"],"synonyms":[{"name":"DBA16","type":"related"},{"name":"Diamond-Blackfan anemia 16","type":"exact"}],"termid":"MONDO:0044309","terms_by_termid":{"MONDO:0044309":null},"xrefs":{"Monarch":{"xref_id":"0044309"}}}


id: GO:0072256
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the developmental fate of a cell becomes restricted such that it will develop into a metanephric glomerular mesangial cell.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerular mesangial cell fate commitment","termid":"GO:0072152"},{"relation_name":"part_of","term_name":"metanephric glomerular mesangial cell differentiation","termid":"GO:0072254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric glomerular mesangial cell fate commitment","termid":"GO:0072256"}


id: PBO:0078804
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Asn (anticodon GTT) 21-1","termid":"PBO:0078804"}


id: PR:O13824
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A regulator of nonsense transcripts 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR12839:SF7","PRO:DNx","OMA:SCHPO01031"],"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":"nonsense-mediated mRNA decay protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC19A8.08","secondary_identifiers":["UniProtKB:O13824"],"synonyms":[{"name":"Spom972h-UPF2","type":"exact"},{"name":"up-frameshift suppressor 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13824"}


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


id: PBO:0069001
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 245, pseudogene","termid":"PBO:0069001"}


id: PBO:0089549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WD repeat protein, Vid27 family, conserved in fungi and plants","termid":"PBO:0089549"}


id: PBO:0041652
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel auxiliary subunit beta 2","termid":"PBO:0041652"}


id: GO:0050094
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-methionine + glyoxylate = 4-methylthio-2-oxobutanoate + glycine.","definition_xrefs":["RHEA:22884","EC:2.6.1.73"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016769"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016769","GO:0003824","GO:0016740"],"is_obsolete":false,"name":"methionine-glyoxylate transaminase activity","secondary_identifiers":["MetaCyc:METHIONINE--GLYOXYLATE-TRANSAMINASE-RXN","KEGG_REACTION:R00652"],"synonyms":[{"name":"L-methionine:glyoxylate aminotransferase activity","type":"related"},{"name":"MGAT activity","type":"related"},{"name":"methionine-glyoxylate aminotransferase activity","type":"related"}],"termid":"GO:0050094"}


id: GO:0033757
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: sucrose + acceptor = 3-dehydro-alpha-D-glucosyl-beta-D-fructofuranoside + reduced acceptor.","definition_xrefs":["EC:1.1.99.13"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on CH-OH group of donors","termid":"GO:0016614"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"glucoside 3-dehydrogenase activity","secondary_identifiers":["RHEA:16589","MetaCyc:GLUCOSIDE-3-DEHYDROGENASE-RXN","Wikipedia:Glucoside_3-dehydrogenase"],"synonyms":[{"name":"D-aldohexopyranoside dehydrogenase","type":"related"},{"name":"D-aldohexoside:(acceptor) 3-oxidoreductase","type":"related"},{"name":"D-aldohexoside:acceptor 3-oxidoreductase","type":"related"},{"name":"D-aldohexoside:cytochrome c oxidoreductase","type":"related"},{"name":"hexopyranoside-cytochrome c oxidoreductase","type":"related"}],"termid":"GO:0033757"}


id: PBO:0066624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RIC8 guanine nucleotide exchange factor A","termid":"PBO:0066624"}


id: PBO:0029452
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_after_spore_germination,_without_cell_division,_cell_cycle_arrest,_elongated_cell","termid":"PBO:0029452"}


id: GO:0022856
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the PEP-dependent, phosphoryl transfer-driven transport of substances across a membrane. The transport happens by catalysis of the reaction: protein N-phosphohistidine + sorbitol(out) = protein histidine + sorbitol phosphate(in). This differs from primary and secondary active transport in that the solute is modified during transport.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-N(PI)-phosphohistidine-sugar phosphotransferase activity","termid":"GO:0008982"},{"relation_name":"is_a","term_name":"sorbitol transmembrane transporter activity","termid":"GO:0015576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0016740","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"protein-N(PI)-phosphohistidine-sorbitol phosphotransferase system transporter activity","synonyms":[{"name":"sorbitol PTS transporter activity","type":"exact"}],"termid":"GO:0022856"}


id: MONDO:0005386
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder of the arteries supplying the upper and lower extremity and the visceral organs. This includes the mesenteric arteries, the renal arteries and the aorta and excludes cerebrovascular arterial disease. Patients experience cramping and pain usually in the calves and thighs while walking. The symptoms subside with rest.","definition_xrefs":["NCIT:C84496"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arterial disorder","termid":"MONDO:0000473"},{"relation_name":"is_a","term_name":"peripheral vascular disease","termid":"MONDO:0005294"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peripheral arterial disease","secondary_identifiers":["ICD9:443.81","MESH:D058729","MEDGEN:352846","DOID:0050830","EFO:0004265","SCTID:399957001","UMLS:C1704436"],"synonyms":[{"name":"PAD","type":"exact"},{"name":"pad","type":"exact"},{"name":"peripheral arterial disorder","type":"exact"},{"name":"peripheral artery disease","type":"related"}],"termid":"MONDO:0005386","xrefs":{"Monarch":{"xref_id":"0005386"}}}


id: PBO:0076306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"synaptogyrin 2 pseudogene 2","termid":"PBO:0076306"}


id: MOD:00181
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tyrosine residue to O4'-sulfo-L-tyrosine.","definition_xrefs":["PubMed:14752058","PubMed:2303439","RESID:AA0172","OMSSA:114","PubMed:3801003","DeltaMass:88","PubMed:3778455","Unimod:40#Y","PubMed:10226369"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sulfated residue","termid":"MOD:00695"},{"relation_name":"is_a","term_name":"residues isobaric at 243.02-243.03 Da","termid":"MOD:00774"},{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O4'-sulfo-L-tyrosine","synonyms":[{"name":"(S)-2-amino-3-(4-sulfooxyphenyl)propanoic acid","type":"exact"},{"name":"2-amino-3-(4-hydroxyphenyl)propanoic acid 4'-sulfate","type":"exact"},{"name":"MOD_RES Sulfotyrosine","type":"exact"},{"name":"O-Sulfonation","type":"related"},{"name":"O4'-sulfo-L-tyrosine","type":"exact"},{"name":"O4-sulfotyrosine","type":"exact"},{"name":"OSulfTyr","type":"exact"},{"name":"Sulfo","type":"related"},{"name":"Sulphation (of O of Tyrosine)","type":"exact"},{"name":"Tyrosinyl Sulphate","type":"exact"},{"name":"sulfationy","type":"exact"},{"name":"tyrosine sulfate","type":"exact"},{"name":"tyrosine-O-sulfonic acid","type":"exact"},{"name":"tyrosine-O-sulphonic acid","type":"exact"}],"termid":"MOD:00181"}


id: GO:0070376
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of signal transduction mediated by the ERK5 cascade.","definition_xrefs":["ISBN:0121245462","GOC:add","ISBN:0896039986"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of MAPK cascade","termid":"GO:0043408"},{"relation_name":"regulates","term_name":"ERK5 cascade","termid":"GO:0070375"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of ERK5 cascade","synonyms":[{"name":"regulation of BMK cascade","type":"exact"},{"name":"regulation of BMK signaling pathway","type":"exact"},{"name":"regulation of BMK signalling pathway","type":"exact"},{"name":"regulation of BMK1 cascade","type":"exact"},{"name":"regulation of ERK5 signaling pathway","type":"exact"},{"name":"regulation of MAPK7 cascade","type":"exact"}],"termid":"GO:0070376"}


id: MONDO:1012351
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"progressive neuronopathy, non-human animal","termid":"MONDO:1011871"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"progressive neuronopathy, dog","secondary_identifiers":["OMIA:001282-9615"],"termid":"MONDO:1012351","xrefs":{"Monarch":{"xref_id":"1012351"}}}


id: PBO:0050795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"5-hydroxytryptamine receptor 5A","termid":"PBO:0050795"}


id: MONDO:0021571
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple sclerosis, susceptibility to","termid":"MONDO:0007462"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple sclerosis, susceptibility to 1","secondary_identifiers":["OMIM:126200","MEDGEN:854774","UMLS:C3888106"],"synonyms":[{"name":"MS","type":"related"},{"name":"MS1","type":"exact"},{"name":"disseminated sclerosis","type":"related"},{"name":"multiple sclerosis, disease progression, modifier of","type":"exact"},{"name":"multiple sclerosis, susceptibility to","type":"related"},{"name":"multiple sclerosis, susceptibility to, 1","type":"exact"},{"name":"susceptibility to multiple sclerosis","type":"related"}],"termid":"MONDO:0021571","xrefs":{"Monarch":{"xref_id":"0021571"}}}


id: GO:0050451
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 CoA + NADP+ = CoA-disulfide + NADPH + H+.","definition_xrefs":["RHEA:14705"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disulfide oxidoreductase activity","termid":"GO:0015036"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor","termid":"GO:0016668"}],"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:0015036"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0016491","GO:0015036","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"CoA-disulfide reductase (NADPH) activity","secondary_identifiers":["EC:1.8.1.14","MetaCyc:COA-DISULFIDE-REDUCTASE-NADH-RXN"],"synonyms":[{"name":"CoA-disulfide reductase (NADH) activity","type":"related"},{"name":"CoA-disulfide reductase (NADP) activity","type":"exact"},{"name":"CoA-disulfide reductase activity","type":"broad"},{"name":"CoA-disulphide reductase activity","type":"broad"},{"name":"CoADR activity","type":"related"},{"name":"NADH:CoA-disulfide oxidoreductase activity","type":"related"},{"name":"coenzyme A disulfide reductase activity","type":"related"}],"termid":"GO:0050451"}


id: GO:1905316
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process by which a superior endocardial cushion is generated and organized.","definition_xrefs":["GOC:TermGenie","GO_REF:0000083","GOC:BHF","GOC:rl","PMID:17050629"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endocardial cushion morphogenesis","termid":"GO:0003203"}],"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":"superior endocardial cushion morphogenesis","synonyms":[{"name":"dorsal endocardial cushion morphogenesis","type":"exact"}],"termid":"GO:1905316"}


id: PBO:0053361
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 268-2, pseudogene","termid":"PBO:0053361"}


id: PBO:0086083
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein O-mannosyltransferase; transfers mannose residues from dolichyl phosphate-D-mannose to protein serine/threonine residues; acts in a complex with Pmt5p, can instead interact with Pmt1p in some conditions; antifungal drug target; PMT3 has a paralog, PMT2, that arose from the whole genome duplication","termid":"PBO:0086083"}


id: GO:0060812
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process in which orthodenticle mRNA is transported to and maintained in the oocyte and/or syncytial embryo as part of the process that will specify the anterior/posterior axis.","definition_xrefs":["GOC:dph","GOC:tb","GOC:sdb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intracellular mRNA localization involved in anterior/posterior axis specification","termid":"GO:0060811"}],"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":"orthodenticle mRNA localization","synonyms":[{"name":"orthodenticle mRNA localisation","type":"exact"}],"termid":"GO:0060812"}


id: PBO:0046590
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 32, envelope","termid":"PBO:0046590"}


id: GO:0097116
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The clustering process in which gephyrin molecules are localized to distinct domains in the postsynaptic density as part of postsynaptic density assembly. Gephyrin is a component of the postsynaptic protein network of inhibitory synapses.","definition_xrefs":["GOC:sjp","PMID:15620359","GOC:BHF","PMID:24552784","PMID:25772192"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to synapse","termid":"GO:0035418"},{"relation_name":"part_of","term_name":"postsynaptic density assembly","termid":"GO:0097107"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0044085","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"gephyrin clustering involved in postsynaptic density assembly","synonyms":[{"name":"Geph clustering","type":"broad"}],"termid":"GO:0097116"}


id: PBO:0012553
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HP1/CBX family","termid":"PBO:0012553"}


id: GO:0042778
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the 3'-terminal CCA of a tRNA is removed and restored. This often happens to uncharged tRNA.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tRNA metabolic process","termid":"GO:0006399"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006399"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006399","GO:0008150"],"is_obsolete":false,"name":"tRNA end turnover","termid":"GO:0042778"}


id: GO:0003341
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed, self-propelled movement of a cilium.","definition_xrefs":["GOC:jl","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule-based movement","termid":"GO:0007018"}],"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":"cilium movement","secondary_identifiers":["GO:0036142"],"synonyms":[{"name":"ciliary motility","type":"related"},{"name":"cilium beating","type":"related"},{"name":"flagellar motility","type":"related"},{"name":"flagellar movement","type":"narrow"},{"name":"flagellum movement","type":"narrow"},{"name":"microtubule-based flagellum movement","type":"exact"}],"termid":"GO:0003341"}


id: PBO:0041668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcyclin binding protein pseudogene 1","termid":"PBO:0041668"}


id: PBO:0083458
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene HXT14","termid":"PBO:0083458"}


id: PBO:0064168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipase A2 group IVE","termid":"PBO:0064168"}


id: PBO:0054370
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 1764","termid":"PBO:0054370"}


id: MOD:00462
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-tryptophan residue to L-kynurenine.","definition_xrefs":["OMSSA:66","DeltaMass:357","PubMed:9252331","PubMed:11029593","Unimod:351#W"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-tryptophan residue","termid":"MOD:00918"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"L-kynurenine","synonyms":[{"name":"(2S)-2-amino-4-(2-aminophenyl)-4-oxo-butanoic acid","type":"exact"},{"name":"Trp->Kynurenin","type":"related"},{"name":"kynureninw","type":"exact"},{"name":"tryptophan oxidation to kynurenin","type":"related"}],"termid":"MOD:00462"}


id: PBO:0109228
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLF3 pseudogene 2","termid":"PBO:0109228"}


id: PR:O94350
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC11E10.01 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94350"],"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":"cystathionine beta-lyase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC11E10.01","synonyms":[{"name":"CBL (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-SPCC11E10.01","type":"exact"},{"name":"beta-cystathionase (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"cysteine lyase (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O94350"}


id: GO:0021614
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A developmental process, independent of morphogenetic (shape) change, that is required for the glossopharyngeal nerve to attain its fully functional state. Various sensory and motor branches of the glossopharyngeal nerve supply nerve connections to the pharynx and back of the tongue. The branchial motor component contains motor fibers that innervate muscles that elevate the pharynx and larynx, and the tympanic branch supplies parasympathetic fibers to the otic ganglion.","definition_xrefs":["GOC:jid","ISBN:0838580343","GO_REF:0000021","GOC:dgh","GOC:cls","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cranial nerve maturation","termid":"GO:0021605"},{"relation_name":"part_of","term_name":"glossopharyngeal nerve development","termid":"GO:0021563"}],"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":"glossopharyngeal nerve maturation","synonyms":[{"name":"CN IX maturation","type":"related"}],"termid":"GO:0021614"}


id: PBO:0058312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4685","termid":"PBO:0058312"}


id: GO:0052636
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the transfer of an arabinosyl group from one compound (donor) to another (acceptor).","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentosyltransferase activity","termid":"GO:0016763"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0016757"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0003824","GO:0016757"],"is_obsolete":false,"name":"arabinosyltransferase activity","synonyms":[{"name":"arabinosyl transferase activity","type":"exact"}],"termid":"GO:0052636"}


id: FYECO:0000438
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Experiments were performed in minimal media containing minimal glutamate plus thiamine.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping defined medium","termid":"FYECO:0000013"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ePMGT","secondary_identifiers":["PMID:38133430"],"termid":"FYECO:0000438"}


id: PBO:0003811
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme Ubc7/UbcP3","termid":"PBO:0003811"}


id: GO:0051802
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process in which an organism modulates the frequency, rate or extent of the cytolysis by that organism of cells in a second organism, where the two organisms are in a symbiotic interaction.","definition_xrefs":["GOC:add"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cytolysis in other organism involved in symbiotic interaction (obsolete GO:0051802)","synonyms":[{"name":"regulation of cytolysis of cells in other organism during symbiotic interaction","type":"related"},{"name":"regulation of cytolysis of cells in other organism involved in symbiotic interaction","type":"exact"}],"termid":"GO:0051802"}


id: GO:1902692
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of neuroblast proliferation.","definition_xrefs":["GOC:TermGenie","PMID:21168496","GOC:rl","GOC:PARL","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neural precursor cell proliferation","termid":"GO:2000177"},{"relation_name":"regulates","term_name":"neuroblast proliferation","termid":"GO:0007405"}],"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 neuroblast proliferation","termid":"GO:1902692"}


id: PBO:0070944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18","termid":"PBO:0070944"}


id: PBO:0109356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FLVCR choline and putative heme transporter 2","termid":"PBO:0109356"}


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


id: PBO:0072722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RXYLT1 antisense RNA 1","termid":"PBO:0072722"}


id: PBO:0065473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 26S subunit, non-ATPase 11","termid":"PBO:0065473"}


id: MONDO:0006267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma with cavernous vascular spaces arising from the liver. It is the most frequent benign tumor of the liver and usually affects young females.","definition_xrefs":["NCIT:C96839"],"direct_ancestors":[{"relation_name":"is_a","term_name":"liver hemangioma","termid":"MONDO:0002404"},{"relation_name":"is_a","term_name":"cavernous hemangioma","termid":"MONDO:0003155"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005570","MONDO:0002515"],"is_obsolete":false,"name":"liver cavernous hemangioma","secondary_identifiers":["UMLS:C3282904","MEDGEN:482990"],"synonyms":[{"name":"cavernous hemangioma of liver","type":"exact"},{"name":"liver cavernous hemangioma","type":"exact"}],"termid":"MONDO:0006267","xrefs":{"Monarch":{"xref_id":"0006267"}}}


id: GO:0045297
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The specific behavior of an organism following mating.","definition_xrefs":["GOC:pr","GOC:bf"],"gene_count":0,"genotype_count":0,"name":"obsolete post-mating behavior (obsolete GO:0045297)","synonyms":[{"name":"post-mating behaviour","type":"exact"}],"termid":"GO:0045297"}


id: PBO:0031599
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_cell_cycle_arrest_in_mitotic_anaphase","termid":"PBO:0031599"}


id: PBO:0059814
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CYB pseudogene 40","termid":"PBO:0059814"}


id: GO:0044599
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"An AP-type membrane coat adaptor complex that in humans consists of beta5, zeta, mu5 and sigma5 subunits and is found associated with membranes in the endosomes; it is not clear whether AP-5 forms clathrin coats in vivo.","definition_xrefs":["PMID:22022230"],"direct_ancestors":[{"relation_name":"is_a","term_name":"AP-type membrane coat adaptor complex","termid":"GO:0030119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0032991"},{"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:0032991","GO:0005737","GO:0005575"],"is_obsolete":false,"name":"AP-5 adaptor complex","synonyms":[{"name":"adaptor protein-5 adaptor complex","type":"exact"}],"termid":"GO:0044599"}


id: MONDO:0021046
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign or malignant biphasic neoplasm that arises from the breast parenchyma. It is characterized by the presence of an epithelial and a mesenchymal (stromal) component. The typical examples are fibroadenoma and phyllodes tumor.","definition_xrefs":["NCIT:C40405"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibroepithelial neoplasm","termid":"MONDO:0021045"},{"relation_name":"is_a","term_name":"breast neoplasm","termid":"MONDO:0021100"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"breast fibroepithelial neoplasm","secondary_identifiers":["MEDGEN:267408","UMLS:C1511309","ONCOTREE:BFN"],"synonyms":[{"name":"BFN","type":"related"},{"name":"breast fibroepithelial neoplasm","type":"exact"},{"name":"breast fibroepithelial neoplasms","type":"related"},{"name":"breast fibroepithelial tumor","type":"exact"},{"name":"breast fibroepithelial tumour","type":"exact"}],"termid":"MONDO:0021046","xrefs":{"Monarch":{"xref_id":"0021046"}}}


id: GO:1903206
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of hydrogen peroxide-induced cell death.","definition_xrefs":["GOC:bf","PMID:14749723","PMID:24252804","GOC:TermGenie","GO_REF:0000058","GOC:PARL"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of hydrogen peroxide-induced cell death (obsolete GO:1903206)","synonyms":[{"name":"down regulation of cell death in response to H2O2","type":"exact"},{"name":"down regulation of cell death in response to hydrogen peroxide","type":"exact"},{"name":"down regulation of hydrogen peroxide-mediated cell death","type":"related"},{"name":"down-regulation of cell death in response to H2O2","type":"exact"},{"name":"down-regulation of cell death in response to hydrogen peroxide","type":"exact"},{"name":"down-regulation of hydrogen peroxide-mediated cell death","type":"related"},{"name":"downregulation of cell death in response to H2O2","type":"exact"},{"name":"downregulation of cell death in response to hydrogen peroxide","type":"exact"},{"name":"downregulation of hydrogen peroxide-mediated cell death","type":"related"},{"name":"inhibition of cell death in response to H2O2","type":"narrow"},{"name":"inhibition of cell death in response to hydrogen peroxide","type":"narrow"},{"name":"inhibition of hydrogen peroxide-mediated cell death","type":"related"},{"name":"negative regulation of cell death in response to H2O2","type":"exact"},{"name":"negative regulation of cell death in response to hydrogen peroxide","type":"exact"},{"name":"negative regulation of hydrogen peroxide-mediated cell death","type":"related"},{"name":"protection against H2O2-induced cell death","type":"related"},{"name":"protection against hydrogen peroxide-induced cell death","type":"related"}],"termid":"GO:1903206"}


id: PBO:0042564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase inhibitor 1A","termid":"PBO:0042564"}


id: PBO:0084639
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Mg2+-dependent phosphatidate (PA) phosphatase; dephosphorylates PA to yield diacylglycerol; regulates phospholipid synthesis, nuclear/ER membrane growth, lipid droplet formation, triacylglycerol synthesis, vacuolar homeostasis and cell wall integrity; phosphorylated by Pho85p/Pho80p, Cdc28p/Cyclin B, PKA, PKC, and CKII, regulating activity, localization, and proteosomal degradation; homolog of mammalian lipins 1 and 2; human homologs LPIN1, LPIN2, LPIN3 complement the null","termid":"PBO:0084639"}


id: MONDO:0005080
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Increased blood pressure in the portal venous system. It is most commonly caused by cirrhosis. Other causes include portal vein thrombosis, Budd-Chiari syndrome, and right heart failure. Complications include ascites, esophageal varices, encephalopathy, and splenomegaly.","definition_xrefs":["NCIT:C3119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hepatic vascular disorder","termid":"MONDO:0002405"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"portal hypertension","secondary_identifiers":["SCTID:34742003","UMLS:C0020541","DOID:10762","MEDGEN:9375","EFO:0000666","ICD10CM:K76.6","icd11.foundation:1506184775","ICD9:572.3","MESH:D006975"],"termid":"MONDO:0005080","xrefs":{"Monarch":{"xref_id":"0005080"}}}


id: GO:0016847
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-adenosyl-L-methionine(1+) = 1-aminocyclopropane-1-carboxylate + S-methyl-5'-thioadenosine + H+.","definition_xrefs":["RHEA:21744","EC:4.4.1.14"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-sulfur lyase activity","termid":"GO:0016846"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"1-aminocyclopropane-1-carboxylate synthase activity","secondary_identifiers":["MetaCyc:4.4.1.14-RXN","KEGG_REACTION:R00179","GO:0034100"],"synonyms":[{"name":"1-aminocyclopropane-1-carboxylate synthetase activity","type":"related"},{"name":"1-aminocyclopropane-1-carboxylic acid synthase activity","type":"related"},{"name":"1-aminocyclopropanecarboxylate synthase activity","type":"related"},{"name":"ACC synthase activity","type":"related"},{"name":"L-VG deaminase activity","type":"related"},{"name":"L-vinylglycine deaminase activity","type":"related"},{"name":"S-adenosyl-L-methionine methylthioadenosine-lyase (1-aminocyclopropane-1-carboxylate-forming)","type":"related"},{"name":"S-adenosyl-L-methionine methylthioadenosine-lyase activity","type":"related"},{"name":"aminocyclopropanecarboxylate synthase activity","type":"related"},{"name":"aminocyclopropanecarboxylic acid synthase activity","type":"related"}],"termid":"GO:0016847"}


id: PBO:0060542
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NAV2 antisense RNA 2","termid":"PBO:0060542"}


id: MONDO:0958022
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial partial lipodystrophy","termid":"MONDO:0020088"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0005093"],"is_obsolete":false,"name":"lipodystrophy, familial partial, type 8","secondary_identifiers":["OMIM:620679","UMLS:C5882744","MEDGEN:1846436"],"termid":"MONDO:0958022","xrefs":{"Monarch":{"xref_id":"0958022"}}}


id: GO:1901617
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of organic hydroxy compound.","definition_xrefs":["GOC:pr","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete organic hydroxy compound biosynthetic process (obsolete GO:1901617)","synonyms":[{"name":"organic hydroxy compound anabolism","type":"exact"},{"name":"organic hydroxy compound biosynthesis","type":"exact"},{"name":"organic hydroxy compound formation","type":"exact"},{"name":"organic hydroxy compound synthesis","type":"exact"}],"termid":"GO:1901617"}


id: PR:O74173
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An elongation factor 1-beta that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11595:SF7","PRO:DNx","OMA:SCHPO04800"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"elongation factor 1-beta (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1450.04","secondary_identifiers":["UniProtKB:O74173"],"synonyms":[{"name":"EF-1-beta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-EEF1B2","type":"exact"}],"termid":"PR:O74173"}


id: PBO:0075025
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 115-36","termid":"PBO:0075025"}


id: GO:0033000
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex composed of an Fc-gamma RI alpha chain and an Fc-epsilon RI gamma chain dimer with or without additional signaling components. The complex functions primarily as an activating receptor for IgG.","definition_xrefs":["ISBN:0781735149","PMID:12413532","GOC:add","PMID:11244038"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Fc receptor complex","termid":"GO:0032997"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"Fc-gamma receptor I complex","synonyms":[{"name":"FcgRI complex","type":"exact"},{"name":"IgG receptor complex","type":"broad"},{"name":"immunoglobulin G receptor complex","type":"broad"}],"termid":"GO:0033000"}


id: FYPO:0003744
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 centromeric chromatin is abolished.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished protein localization to centromere during vegetative growth","termid":"FYPO:0000634"},{"relation_name":"is_a","term_name":"abolished protein localization to chromatin during vegetative growth","termid":"FYPO:0001508"},{"relation_name":"is_a","term_name":"abnormal protein localization to centromeric chromatin during vegetative growth","termid":"FYPO:0005306"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"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:0000138","FYPO:0005447","FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abolished protein localization to centromeric chromatin during vegetative growth","synonyms":[{"name":"abolished protein localization to centromeric chromatin during mitotic cell cycle","type":"related"},{"name":"abolished protein localization to chromatin at centromere during vegetative growth","type":"exact"},{"name":"protein localization to centromeric chromatin during vegetative growth abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0003744"}


id: PBO:0071052
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L21 pseudogene 54","termid":"PBO:0071052"}


id: PR:Q9US12
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC607.06c gene.","definition_xrefs":["UniProtKB:Q9US12","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":"zinc metalloproteinase C607.06c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC607.06c","synonyms":[{"name":"Spom972h-SPAC607.06c","type":"exact"}],"termid":"PR:Q9US12"}


id: GO:1902818
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving ethyl acetate.","definition_xrefs":["PMID:16013377","GO_REF:0000068","GOC:mengo_curators","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetate ester metabolic process","termid":"GO:1900619"}],"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":"ethyl acetate metabolic process","synonyms":[{"name":"ethyl acetate metabolism","type":"exact"},{"name":"ethyl ethanoate metabolic process","type":"exact"}],"termid":"GO:1902818"}


id: MONDO:0000467
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intermittent failure of atrial electrical impulse conduction to the ventricles.","definition_xrefs":["NCIT:C111119"],"direct_ancestors":[{"relation_name":"is_a","term_name":"atrioventricular block","termid":"MONDO:0000465"},{"relation_name":"is_a","term_name":"cardiac rhythm disease","termid":"MONDO:0007263"}],"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":"second-degree atrioventricular block","secondary_identifiers":["SCTID:195042002","UMLS:C0264906","MEDGEN:75546","DOID:0050822","ICD9:426.13"],"synonyms":[{"name":"AV block second degree","type":"exact"},{"name":"atrioventricular block second degree","type":"exact"},{"name":"atrioventricular block, second degree","type":"exact"},{"name":"second degree AV block","type":"exact"},{"name":"second degree atrioventricular block","type":"exact"},{"name":"second-degree heart block","type":"exact"}],"termid":"MONDO:0000467","xrefs":{"Monarch":{"xref_id":"0000467"}}}


id: GO:0010238
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 proline stimulus.","definition_xrefs":["GOC:sm"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to organic cyclic compound","termid":"GO:0014070"},{"relation_name":"is_a","term_name":"response to amino acid","termid":"GO:0043200"},{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"},{"relation_name":"is_a","term_name":"response to oxygen-containing compound","termid":"GO:1901700"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to proline","termid":"GO:0010238"}


id: MONDO:0000216
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete congenital bilateral aplasia of vas deferens (obsolete MONDO:0000216)","termid":"MONDO:0000216","xrefs":{"Monarch":{"xref_id":"0000216"}}}


id: PBO:0078628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tripartite motif containing 77B, pseudogene","termid":"PBO:0078628"}


id: PBO:0002802
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nucleoporin Nup155","termid":"PBO:0002802"}


id: MONDO:1012908
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spontaneous systemic inflammation signs and increased delayed hypersensitivity response that occurs in pigs due to a mutation in the NLRP3 gene created by genetic engineering or gene editing.","definition_xrefs":["PMID:34580110"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system disorder, non-human animal","termid":"MONDO:0700106"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cryopyrin-associated periodic syndrome, NLRP3-related, pig","secondary_identifiers":["OMIA:002464-9823"],"termid":"MONDO:1012908","xrefs":{"Monarch":{"xref_id":"1012908"}}}


id: PBO:0060734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH:ubiquinone oxidoreductase complex assembly factor 3","termid":"PBO:0060734"}


id: FYPO:0002781
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 transcription occurs to a greater extent than normal during a cellular response to nitric oxide. All genes, or a specific subset of genes, may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased transcription during vegetative growth","termid":"FYPO:0000780"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000294"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0006551","FYPO:0001320","FYPO:0005447","FYPO:0000294","FYPO:0001985"],"is_obsolete":false,"name":"increased transcription during cellular response to nitric oxide","synonyms":[{"name":"increased transcription during cellular response to NO during vegetative growth","type":"exact"},{"name":"increased transcription during cellular response to nitric oxide during mitotic cell cycle","type":"related"},{"name":"increased transcription during cellular response to nitric oxide during vegetative growth","type":"exact"},{"name":"increased transcription during cellular response to nitric oxide stress","type":"related"}],"termid":"FYPO:0002781"}


id: PBO:0053504
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 487","termid":"PBO:0053504"}


id: GO:1990325
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A collagen homotrimer of alpha1(XXVII) chains. These trimers form thin, non-striated fibrils. Type XXVII collagen triple helices play a role during the calcification of cartilage and the transition of cartilage to bone.","definition_xrefs":["PMID:17876790","GOC:bhm","PMID:21421911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fibrillar collagen trimer","termid":"GO:0005583"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005575","GO:0032991"],"is_obsolete":false,"name":"collagen type XXVII trimer","termid":"GO:1990325"}


id: PBO:0017753
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaphase-promoting complex, platform subcomplex scaffold subunit Apc4/Cut20","termid":"PBO:0017753"}


id: GO:0006868
data:
  {"annotated_genes":["SJAG_03400"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[63056],"is_not":false,"summary":null,"term":"GO:0006868"}]},"cv_name":"biological_process","definition":"The directed movement of glutamine, 2-amino-4-carbamoylbutanoic acid, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neutral amino acid transport","termid":"GO:0015804"},{"relation_name":"is_a","term_name":"carboxylic acid transport","termid":"GO:0046942"},{"relation_name":"is_a","term_name":"nitrogen compound transport","termid":"GO:0071705"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03400":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:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"glutamine transport","references_by_uniquename":{"GO_REF:0000108":null},"secondary_identifiers":["GO:0015815"],"synonyms":[{"name":"L-glutamine transport","type":"narrow"}],"termid":"GO:0006868","terms_by_termid":{"GO:0006868":null}}


id: MONDO:0018974
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pemphigus is a group of chronic autoimmune skin diseases characterized by blisters formation on the outer layer of the skin and the mucous membranes. Three clinical forms have been characterized, of which paraneoplastic pemphigus is extremely rare.","definition_xrefs":["Orphanet:63455"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune bullous skin disease","termid":"MONDO:0019337"},{"relation_name":"is_a","term_name":"paraneoplastic cutaneous syndrome","termid":"MONDO:0700266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"paraneoplastic pemphigus","secondary_identifiers":["icd11.foundation:104197957","MedDRA:10057056","ICD10CM:L10.81","UMLS:C1112570","DOID:0080852","EFO:0008602","GARD:18858","NANDO:1200231","MEDGEN:798302"],"termid":"MONDO:0018974","xrefs":{"Monarch":{"xref_id":"0018974"}}}


id: PBO:0011959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase allele types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial_nucleotide_deletion","termid":"PBO:0011959"}


id: PBO:0029181
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_cellular_trehalose_level_during_heat_shock","termid":"PBO:0029181"}


id: GO:1900388
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 vesicle-mediated transport.","definition_xrefs":["PMID:18622392","GOC:mah","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of vesicle-mediated transport by regulation of transcription from RNA polymerase II promoter (obsolete GO:1900388)","synonyms":[{"name":"regulation of vesicle-mediated transport by regulation of transcription from RNA polymerase II promoter","type":"exact"}],"termid":"GO:1900388"}


id: GO:2000127
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of octopamine or tyramine signaling pathway.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of G protein-coupled receptor signaling pathway","termid":"GO:0045745"},{"relation_name":"is_a","term_name":"regulation of octopamine or tyramine signaling pathway","termid":"GO:2000125"},{"relation_name":"positively_regulates","term_name":"octopamine or tyramine signaling pathway","termid":"GO:0007211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"positively_regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of octopamine or tyramine signaling pathway","synonyms":[{"name":"positive regulation of octopamine or tyramine signalling pathway","type":"exact"},{"name":"positive regulation of octopamine/tyramine signaling pathway","type":"exact"}],"termid":"GO:2000127"}


id: PBO:0061177
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"nuclear-encoded mitochondrial tRNA-Gln (TTG) 7-1","termid":"PBO:0061177"}


id: GO:0061439
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the kidney vasculature is generated and organized. Morphogenesis pertains to the creation of form.","definition_xrefs":["GOC:mtg_kidney_jan10","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"renal system vasculature morphogenesis","termid":"GO:0061438"},{"relation_name":"part_of","term_name":"kidney vasculature development","termid":"GO:0061440"}],"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":"kidney vasculature morphogenesis","termid":"GO:0061439"}


id: SO:0001747
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A DNA sequence that in the normal state of the chromosome corresponds to an unfolded, un-complexed stretch of double-stranded DNA.","definition_xrefs":["SO:cb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological_region","termid":"SO:0001411"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"open_chromatin_region","synonyms":[{"name":"open chromatin region","type":"exact"}],"termid":"SO:0001747"}


id: GO:0004206
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-10 activity (obsolete GO:0004206)","synonyms":[{"name":"caspase-10 activity","type":"exact"}],"termid":"GO:0004206"}


id: PBO:0074442
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small integral membrane protein 43","termid":"PBO:0074442"}


id: GO:0110075
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of ferroptosis.","definition_xrefs":["PMID:29290465","PMID:24439385","GOC:sp","PMID:25402683"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of programmed cell death","termid":"GO:0043067"},{"relation_name":"regulates","term_name":"ferroptosis","termid":"GO:0097707"}],"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 ferroptosis","termid":"GO:0110075"}


id: MONDO:0025028
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A viral disease caused by at least two distinct species (serotypes) in the vesiculovirus genus: vesicular stomatitis indiana virus and vesicular stomatitis new jersey virus. It is characterized by vesicular eruptions on the oral mucosa in cattle, horses, pigs, and other animals. In humans, vesicular stomatitis causes an acute influenza-like illness.","definition_xrefs":["MESH:D054243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Rhabdoviridae infectious disease, non-human animal","termid":"MONDO:0700072"},{"relation_name":"is_a","term_name":"inflammatory disease, non-human animal","termid":"MONDO:1011327"},{"relation_name":"is_a","term_name":"mouth mucosa disorder, non-human animal","termid":"MONDO:1011334"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vesicular stomatitis","secondary_identifiers":["SCTID:36921006"],"synonyms":[{"name":"Stomatitides, vesicular","type":"related"},{"name":"stomatitis, vesicular","type":"related"},{"name":"vesicular Stomatitides","type":"related"}],"termid":"MONDO:0025028","xrefs":{"Monarch":{"xref_id":"0025028"}}}


id: GO:0002668
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of T cell anergy.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of T cell tolerance induction","termid":"GO:0002665"},{"relation_name":"is_a","term_name":"regulation of T cell anergy","termid":"GO:0002667"},{"relation_name":"is_a","term_name":"negative regulation of lymphocyte anergy","termid":"GO:0002912"},{"relation_name":"negatively_regulates","term_name":"T cell anergy","termid":"GO:0002870"}],"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 T cell anergy","synonyms":[{"name":"down regulation of T cell anergy","type":"exact"},{"name":"down-regulation of T cell anergy","type":"exact"},{"name":"downregulation of T cell anergy","type":"exact"},{"name":"inhibition of T cell anergy","type":"narrow"},{"name":"negative regulation of T lymphocyte anergy","type":"exact"},{"name":"negative regulation of T-cell anergy","type":"exact"},{"name":"negative regulation of T-lymphocyte anergy","type":"exact"}],"termid":"GO:0002668"}


id: MONDO:0010929
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any craniosynostosis in which the cause of the disease is a mutation in the ERF gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic craniosynostosis","termid":"MONDO:0015338"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"craniosynostosis 4","secondary_identifiers":["MEDGEN:322167","OMIM:600775","UMLS:C1833340"],"synonyms":[{"name":"CRS4","type":"related"},{"name":"ERF craniosynostosis","type":"exact"},{"name":"ERF-related craniosynostosis","type":"exact"},{"name":"craniosynostosis 4","type":"exact"},{"name":"craniosynostosis caused by mutation in ERF","type":"exact"},{"name":"craniosynostosis type 4","type":"exact"}],"termid":"MONDO:0010929","xrefs":{"Monarch":{"xref_id":"0010929"}}}


id: PBO:0030348
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-incomplete,_unequal_mitotic_sister_chromatid_segregation","termid":"PBO:0030348"}


id: PBO:0049110
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 171","termid":"PBO:0049110"}


id: MONDO:0011100
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":"microcephaly, retinitis pigmentosa, and sutural cataract","secondary_identifiers":["UMLS:C1832214","OMIM:601537","MEDGEN:316936","MESH:C563296"],"synonyms":[{"name":"microcephaly, retinitis pigmentosa, and sutural cataract","type":"exact"}],"termid":"MONDO:0011100","xrefs":{"Monarch":{"xref_id":"0011100"}}}


id: FYPO:0003999
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of glutathione synthase activity is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased catalytic activity","termid":"FYPO:0000662"},{"relation_name":"is_a","term_name":"abnormal glutathione synthase activity","termid":"FYPO:0002856"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000661","FYPO:0000652","FYPO:0000707","FYPO:0000002","FYPO:0000654"],"is_obsolete":false,"name":"increased glutathione synthase activity","synonyms":[{"name":"increased GSH synthase activity","type":"exact"},{"name":"increased glutathione synthetase activity","type":"exact"},{"name":"increased phosphoribosylformylglycinamidine cyclo-ligase activity","type":"exact"}],"termid":"FYPO:0003999"}


id: PBO:0030685
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_vegetative_cell_morphology","termid":"PBO:0030685"}


id: MONDO:0001882
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The presence of bacteria in the urine which is normally bacteria-free. These bacteria are from the urinary tract and are not contaminants of the surrounding tissues. Bacteriuria can be symptomatic or asymptomatic. Significant bacteriuria is an indicator of urinary tract infection.","definition_xrefs":["MESH:D001437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urinary system disorder","termid":"MONDO:0002118"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bacteriuria","secondary_identifiers":["DOID:1412","icd11.foundation:626563645","MEDGEN:491","UMLS:C0004659","HP:0012461","CSP:3045-9976","MedDRA:10004056"],"synonyms":[{"name":"bacteriuria","type":"exact"},{"name":"bacteriuria (disease)","type":"exact"}],"termid":"MONDO:0001882","xrefs":{"Monarch":{"xref_id":"0001882"}}}


id: PBO:0070219
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U7 small nuclear 152 pseudogene","termid":"PBO:0070219"}


id: GO:0051850
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The production of structures and/or molecules in an organism that are required for the acquisition and/or utilization of nutrients obtained from its symbiont organism. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:cc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"biological process involved in interaction with symbiont","termid":"GO:0051702"}],"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":"acquisition of nutrients from symbiont","termid":"GO:0051850"}


id: MONDO:0000125
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete fundus dystrophy, pseudoinflammatory (obsolete MONDO:0000125)","termid":"MONDO:0000125","xrefs":{"Monarch":{"xref_id":"0000125"}}}


id: MONDO:0011212
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":"sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth","secondary_identifiers":["MESH:C566560","OMIM:602340","MEDGEN:356334","UMLS:C1865645"],"synonyms":[{"name":"sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth","type":"exact"}],"termid":"MONDO:0011212","xrefs":{"Monarch":{"xref_id":"0011212"}}}


id: GO:0021515
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which relatively unspecialized cells acquire specialized structural and/or functional features that characterize the cells of the spinal cord. Differentiation includes the processes involved in commitment of a cell to a specific fate.","definition_xrefs":["GOC:dph","GOC:dgh","GO_REF:0000021","GOC:cls","GOC:jid","PMID:11262869"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation","termid":"GO:0030154"},{"relation_name":"part_of","term_name":"spinal cord development","termid":"GO:0021510"}],"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 differentiation in spinal cord","termid":"GO:0021515"}


id: GO:1904821
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The disaggregation of a chloroplast into its constituent components.","definition_xrefs":["GO_REF:0000079","PMID:26494759","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chloroplast organization","termid":"GO:0009658"},{"relation_name":"is_a","term_name":"organelle disassembly","termid":"GO:1903008"}],"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":"chloroplast disassembly","synonyms":[{"name":"chloroplast degradation","type":"related"}],"termid":"GO:1904821"}


id: GO:1903502
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex which is capable of translation repressor activity.","definition_xrefs":["GO_REF:0000088","PMID:14723848","GOC:TermGenie","GOC:bhm"],"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:0005575","GO:0032991"],"is_obsolete":false,"name":"translation repressor complex","termid":"GO:1903502"}


id: PBO:0045426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"divergent-paired related homeobox pseudogene 6","termid":"PBO:0045426"}


id: GO:0048439
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the flower are generated and organized.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process involved in reproduction","termid":"GO:0003006"},{"relation_name":"is_a","term_name":"shoot system morphogenesis","termid":"GO:0010016"},{"relation_name":"is_a","term_name":"post-embryonic plant morphogenesis","termid":"GO:0090698"},{"relation_name":"part_of","term_name":"flower development","termid":"GO:0009908"}],"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":"flower morphogenesis","secondary_identifiers":["GO:0048411"],"termid":"GO:0048439"}


id: MONDO:0040870
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of polydipsia characterized by excessive fluid intake in the absence of physiological stimuli to drink.","definition_xrefs":["Wikipedia:Primary_polydipsia"],"direct_ancestors":[{"relation_name":"is_a","term_name":"impulse control disorder","termid":"MONDO:0001162"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary polydipsia","termid":"MONDO:0040870","xrefs":{"Monarch":{"xref_id":"0040870"}}}


id: PATO:0001856
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"An oriented quality inhering in a bearer by virtue of the bearer's being turned inward upon itself.","definition_xrefs":["die.net:die.net"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oriented","termid":"PATO:0000614"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"introverted","termid":"PATO:0001856"}


id: GO:0009029
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2,3-bis(3-hydroxytetradecanoyl)-D-glucosaminyl-(1->6)-beta-D-2,3-bis(3-hydroxytetradecanoyl)-beta-D-glucosaminyl 1-phosphate + ATP = ADP + 2 H+ + lipid IV(a).","definition_xrefs":["EC:2.7.1.130","RHEA:20700"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kinase activity","termid":"GO:0016301"},{"relation_name":"is_a","term_name":"phosphotransferase activity, alcohol group as acceptor","termid":"GO:0016773"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0016740","GO:0003674","GO:0016301","GO:0003824"],"is_obsolete":false,"name":"tetraacyldisaccharide 4'-kinase activity","secondary_identifiers":["MetaCyc:TETRAACYLDISACC4KIN-RXN","KEGG_REACTION:R04657"],"synonyms":[{"name":"ATP:2,3,2',3'-tetrakis(3-hydroxytetradecanoyl)-D-glucosaminyl-beta-D-1,6-glucosaminyl-beta-phosphate 4'-O-phosphotransferase activity","type":"related"},{"name":"lipid-A 4'-kinase activity","type":"related"}],"termid":"GO:0009029"}


id: GO:0102257
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 1-palmitoyl-2-linoleoyl-phosphatidylcholine + H2O = 1-linoleoyl-sn-glycero-3-phosphocholine + hexadecanoate + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete 1-16:0-2-18:2-phosphatidylcholine sn-1 acylhydrolase activity (obsolete GO:0102257)","termid":"GO:0102257"}


id: PBO:0004002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP-dependent RNA helicase Spb4 (predicted)","termid":"PBO:0004002"}


id: PBO:0004403
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pombe LRO 1 Homolog","termid":"PBO:0004403"}


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:0003043
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that is triggered by aortic body-vasomotor excitation and results in a decrease in the diameter of an artery during the chemoreceptor response to decreased blood pressure.","definition_xrefs":["GOC:mtg_cardio"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vasoconstriction of artery involved in chemoreceptor response to lowering of systemic arterial blood pressure","termid":"GO:0002012"},{"relation_name":"part_of","term_name":"regulation of systemic arterial blood pressure by aortic body chemoreceptor signaling","termid":"GO:0003028"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"vasoconstriction of artery involved in aortic body chemoreceptor response to lowering of systemic arterial blood pressure","synonyms":[{"name":"vasoconstriction of artery during aortic body chemoreceptor response to lowering of systemic arterial blood pressure","type":"related"}],"termid":"GO:0003043"}


id: PBO:0012246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dos2 silencing complex subunit Mms19","termid":"PBO:0012246"}


id: PBO:0108986
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm associated microtubule inner protein 10","termid":"PBO:0108986"}


id: GO:0019716
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The monomethylation of the N-terminal alanine of proteins to form the derivative peptidyl-N-methyl-L-alanine.","definition_xrefs":["RESID:AA0061"],"gene_count":0,"genotype_count":0,"name":"obsolete N-terminal peptidyl-alanine monomethylation (obsolete GO:0019716)","termid":"GO:0019716"}


id: GO:0004769
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 3-oxo-delta(5)-steroid = a 3-oxo-delta(4)-steroid.","definition_xrefs":["RHEA:14709"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular oxidoreductase activity, transposing C=C bonds","termid":"GO:0016863"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"}],"interesting_parent_ids":["GO:0003674","GO:0016853","GO:0003824"],"is_obsolete":false,"name":"steroid Delta-isomerase activity","secondary_identifiers":["Reactome:R-HSA-195690","Reactome:R-HSA-6807052","EC:5.3.3.1","MetaCyc:STEROID-DELTA-ISOMERASE-RXN","Reactome:R-HSA-193052","Reactome:R-HSA-193073","Reactome:R-HSA-193961"],"synonyms":[{"name":"3-oxosteroid delta5-delta4-isomerase activity","type":"related"},{"name":"3-oxosteroid isomerase activity","type":"related"},{"name":"delta(5)-3-keto steroid isomerase activity","type":"related"},{"name":"delta(5)-3-ketosteroid isomerase activity","type":"related"},{"name":"delta(5)-3-oxosteroid isomerase activity","type":"related"},{"name":"delta(5)-steroid isomerase activity","type":"related"},{"name":"delta5(or delta4)-3-keto steroid isomerase activity","type":"related"},{"name":"delta5-3-keto steroid isomerase activity","type":"related"},{"name":"delta5-3-ketosteroid isomerase activity","type":"related"},{"name":"delta5-3-oxosteroid isomerase activity","type":"related"},{"name":"delta5-ketosteroid isomerase activity","type":"related"},{"name":"delta5-steroid isomerase activity","type":"related"},{"name":"hydroxysteroid isomerase activity","type":"related"},{"name":"steroid D-isomerase activity","type":"exact"},{"name":"steroid isomerase activity","type":"related"}],"termid":"GO:0004769"}


id: GO:1990829
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to C-rich, single-stranded DNA.","definition_xrefs":["PMID:8127654"],"direct_ancestors":[{"relation_name":"is_a","term_name":"single-stranded DNA binding","termid":"GO:0003697"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003677"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0003677"],"is_obsolete":false,"name":"C-rich single-stranded DNA binding","synonyms":[{"name":"C-rich ssDNA binding","type":"exact"}],"termid":"GO:1990829"}


id: PBO:0027228
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_1,2-dioctanoyl-sn-glycerol","termid":"PBO:0027228"}


id: PBO:0051781
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IQ motif containing D","termid":"PBO:0051781"}


id: FYPO:0000096
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 cadmium. Cells stop growing (and may die) at a concentration of cadmium ions 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:0000003"},{"rel_name":"is_a","termid":"FYPO:0002683"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000139"}],"interesting_parent_ids":["FYPO:0000003","FYPO:0002683","FYPO:0000139","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"sensitive to cadmium","synonyms":[{"name":"hypersensitive to cadmium","type":"exact"},{"name":"sensitive to cadmium during mitotic cell cycle","type":"related"},{"name":"sensitive to cadmium during vegetative growth","type":"exact"},{"name":"sensitive to cadmium ions","type":"exact"}],"termid":"FYPO:0000096"}


id: PBO:0036493
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"26 copies of a 35 amino acid repeat","termid":"PBO:0036493"}


id: PBO:0001637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PP2A","termid":"PBO:0001637"}


id: GO:0016708
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of an oxidation-reduction (redox) reaction in which hydrogen or electrons are transferred from NADH or NADPH and one other donor, and two atoms of oxygen are incorporated into one donor.","definition_xrefs":["EC:1.14.12.-"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"},{"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:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of two atoms of oxygen into one donor","synonyms":[{"name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NADH or NADPH as one donor, and incorporation of two atoms of oxygen into one donor","type":"related"}],"termid":"GO:0016708"}


id: PBO:0030919
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_subcellular_component_during_vegetative_growth","termid":"PBO:0030919"}


id: MONDO:0013852
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hypertrophic cardiomyopathy associated that has material basis in region 7p12.1-q21 variation.","definition_xrefs":["DOID:0110311","PMID:16651466"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial hypertrophic cardiomyopathy","termid":"MONDO:0024573"}],"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":"hypertrophic cardiomyopathy 21","secondary_identifiers":["OMIM:614676","MEDGEN:766356","UMLS:C3553442"],"synonyms":[{"name":"CMH21","type":"exact"},{"name":"cardiomyopathy familial hypertrophic 21","type":"exact"},{"name":"cardiomyopathy, familial hypertrophic, 21","type":"related"},{"name":"cardiomyopathy, hypertrophic, 21","type":"exact"},{"name":"hypertrophic cardiomyopathy type 21","type":"exact"}],"termid":"MONDO:0013852","xrefs":{"Monarch":{"xref_id":"0013852"}}}


id: GO:0051013
data:
  {"annotated_genes":["SJAG_01530","SJAG_04566"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[96028,112220],"is_not":false,"summary":null,"term":"GO:0051013"}]},"cv_name":"biological_process","definition":"The process in which a microtubule is broken down into smaller segments. Severing enzymes remove dimers from the middle of the filament to create new ends, unlike depolymerizing kinesins that use ATP to uncap microtubules at their ends.","definition_xrefs":["PMID:27037673","GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"microtubule cytoskeleton organization","termid":"GO:0000226"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01530":null,"SJAG_04566":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0000226"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0007010","GO:0000226","GO:0008150"],"is_obsolete":false,"name":"microtubule severing","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"microtubule severing activity","type":"related"}],"termid":"GO:0051013","terms_by_termid":{"GO:0051013":null}}


id: GO:0032605
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The appearance of hepatocyte growth factor due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.","definition_xrefs":["GOC:mah","PMID:1838014"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine production","termid":"GO:0001816"},{"relation_name":"is_a","term_name":"protein metabolic process","termid":"GO:0019538"}],"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":"hepatocyte growth factor production","secondary_identifiers":["GO:0048175"],"synonyms":[{"name":"HGF production","type":"exact"},{"name":"hepatocyte growth factor biosynthetic process","type":"narrow"},{"name":"scatter factor production","type":"exact"}],"termid":"GO:0032605"}


id: SO:0001695
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A terminal region of DNA sequence where the end of the region is not blunt ended.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"restriction_enzyme_region","termid":"SO:0001954"},{"relation_name":"part_of","term_name":"sticky_end_restriction_enzyme_cleavage_site","termid":"SO:0001692"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"restriction_enzyme_single_strand_overhang","synonyms":[{"name":"single strand overhang","type":"exact"},{"name":"sticky end","type":"related"}],"termid":"SO:0001695"}


id: GO:0035218
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Progression of the leg imaginal disc over time, from its initial formation through to its metamorphosis to form adult structures including the leg, coxa and ventral thoracic pleura.","definition_xrefs":["GOC:bf","ISBN:0879694238"],"direct_ancestors":[{"relation_name":"is_a","term_name":"imaginal disc development","termid":"GO:0007444"}],"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":"leg disc development","termid":"GO:0035218"}


id: PBO:0046992
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 88 member C","termid":"PBO:0046992"}


id: GO:0098646
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A hexagonal shaped collagen network formed by collagen type X trimer, mostly found in the cartilage hyaline matrix, which located in the interstitial area.","definition_xrefs":["PMID:34948124","PMID:21421911"],"direct_ancestors":[{"relation_name":"is_a","term_name":"collagen network","termid":"GO:0098645"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"interstitial hexagonal collagen network","synonyms":[{"name":"collagen hexagonal network","type":"exact"},{"name":"collagen sheet","type":"exact"}],"termid":"GO:0098646"}


id: GO:0048933
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of an afferent axon in the posterior lateral line nerve over time from its formation to the mature structure. This process includes axonogenesis and pathfinding of the afferent axons in the posterior lateral line nerve.","definition_xrefs":["PMID:15018940"],"direct_ancestors":[{"relation_name":"is_a","term_name":"afferent axon development in lateral line nerve","termid":"GO:0048893"},{"relation_name":"part_of","term_name":"posterior lateral line nerve development","termid":"GO:0048918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"afferent axon development in posterior lateral line nerve","termid":"GO:0048933"}


id: PBO:0046247
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ELOVL fatty acid elongase 3","termid":"PBO:0046247"}


id: GO:0006014
data:
  {"annotated_genes":["SJAG_00070","SJAG_03174"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88453],"is_not":false,"summary":null,"term":"GO:0006014"},{"annotations":[103837],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0019303"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving D-ribose (ribo-pentose). As beta-D-ribofuranose, D-ribose forms the glycose group of all ribonucleosides, ribonucleotides and ribonucleic acids, and also of ribose phosphates, various glycosides, some coenzymes and some forms of vitamin B12.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pentose metabolic process","termid":"GO:0019321"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00070":null,"SJAG_03174":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"D-ribose metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"D-ribose metabolism","type":"exact"}],"termid":"GO:0006014","terms_by_termid":{"GO:0006014":null,"GO:0019303":null}}


id: MONDO:1012074
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"multiple exostoses, non-human animal","termid":"MONDO:1011944"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multiple exostoses, horse","secondary_identifiers":["OMIA:000354-9796"],"termid":"MONDO:1012074","xrefs":{"Monarch":{"xref_id":"1012074"}}}


id: PBO:0066807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 106","termid":"PBO:0066807"}


id: GO:0048937
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process aimed at the progression of a lateral line glial cell over time, from initial commitment of the cell to a specific fate, to the fully functional differentiated cell.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glial cell development","termid":"GO:0021782"},{"relation_name":"part_of","term_name":"lateral line nerve glial cell differentiation","termid":"GO:0048895"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lateral line nerve glial cell development","termid":"GO:0048937"}


id: GO:0070663
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of leukocyte proliferation.","definition_xrefs":["GOC:add","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell population proliferation","termid":"GO:0042127"},{"relation_name":"regulates","term_name":"leukocyte proliferation","termid":"GO:0070661"}],"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 leukocyte proliferation","termid":"GO:0070663"}


id: PBO:0046772
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"exophilin 5","termid":"PBO:0046772"}


id: GO:0004607
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: phosphatidylcholine + a sterol = a sterol ester + 1-acylglycerophosphocholine.","definition_xrefs":["EC:2.3.1.43"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-acyltransferase activity","termid":"GO:0008374"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016746"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016746","GO:0003824","GO:0016740","GO:0003674"],"is_obsolete":false,"name":"phosphatidylcholine-sterol O-acyltransferase activity","secondary_identifiers":["MetaCyc:2.3.1.43-RXN","Reactome:R-HSA-264695","RHEA:21204"],"synonyms":[{"name":"LCAT (lecithin-cholesterol acyltransferase)","type":"related"},{"name":"LCAT activity","type":"related"},{"name":"lecithin--cholesterol acyltransferase activity","type":"related"},{"name":"lecithin:cholesterol acyltransferase activity","type":"related"},{"name":"phosphatidylcholine:sterol O-acyltransferase activity","type":"related"},{"name":"phospholipid--cholesterol acyltransferase activity","type":"related"}],"termid":"GO:0004607"}


id: GO:0120200
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The outer segment of a vertebrate rod photoreceptor that contains sealed membrane discs that are not connected to the ciliary membrane and containing rhodopsin photoreceptor proteins.","definition_xrefs":["GOC:pde","PMID:19501669","GOC:krc","PMID:26574505","PMID:6771304"],"direct_ancestors":[{"relation_name":"is_a","term_name":"photoreceptor outer segment","termid":"GO:0001750"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"rod photoreceptor outer segment","termid":"GO:0120200"}


id: PBO:0049857
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1","termid":"PBO:0049857"}


id: PBO:0080092
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin specific peptidase 54","termid":"PBO:0080092"}


id: PBO:0087748
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the THO complex; THO is a nuclear complex comprised of Hpr1p, Mft1p, Rlr1p, and Thp2p, that is involved in transcription elongation and mitotic recombination; involved in telomere maintenance","termid":"PBO:0087748"}


id: PBO:0054947
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 2361","termid":"PBO:0054947"}


id: MONDO:0005919
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Failure of the placenta to deliver an adequate supply of nutrients and oxygen to the fetus.","definition_xrefs":["MESH:D010927"],"direct_ancestors":[{"relation_name":"is_a","term_name":"placenta disorder","termid":"MONDO:0005917"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"placental insufficiency","secondary_identifiers":["SCTID:237292005","DOID:3891","EFO:0007443","MEDGEN:45942","Orphanet:439167","UMLS:C0032051","ICD9:762.2","GARD:21823"],"synonyms":[{"name":"insufficiency, placental","type":"related"},{"name":"uteroplacental vascular insufficiency","type":"exact"}],"termid":"MONDO:0005919","xrefs":{"Monarch":{"xref_id":"0005919"}}}


id: MONDO:0800110
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Persistent tachypnoe of infancy that presents with additional minor abnormalities upon scanning, including ground-glass opacities in other locations, focal consolidations, parenchymal cysts or bronchial wall thickening (N=80; 37%).","definition_xrefs":["PMID:32761949","PMID:26474448"],"direct_ancestors":[{"relation_name":"is_a","term_name":"persistent tachypnoe of infancy","termid":"MONDO:0800109"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"persistent tachypnoe of infancy, aberrant","synonyms":[{"name":"PTI, aberrant","type":"exact"}],"termid":"MONDO:0800110","xrefs":{"Monarch":{"xref_id":"0800110"}}}


id: PBO:0034453
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_glutamate_dehydrogenase_(NADP+)_activity","termid":"PBO:0034453"}


id: PBO:0046397
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"erythrocyte membrane protein band 4.1 like 3","termid":"PBO:0046397"}


id: MONDO:0013871
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Seckel syndrome in which the cause of the disease is a mutation in the CEP63 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Seckel syndrome","termid":"MONDO:0019342"}],"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":"Seckel syndrome 6","secondary_identifiers":["MEDGEN:766496","DOID:0070006","OMIM:614728","UMLS:C3553582"],"synonyms":[{"name":"CEP63 Seckel syndrome","type":"exact"},{"name":"SCKL6","type":"exact"},{"name":"Seckel syndrome 6","type":"exact"},{"name":"Seckel syndrome caused by mutation in CEP63","type":"exact"},{"name":"Seckel syndrome type 6","type":"exact"}],"termid":"MONDO:0013871","xrefs":{"Monarch":{"xref_id":"0013871"}}}


id: PBO:0082908
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cysteine desulfurase involved in iron-sulfur cluster biogenesis; required for thio-modification of mitochondrial and cytoplasmic tRNAs; involved in DNA damage response by providing Fe–S cluster cofactors for DNA repair enzymes; essential protein located predominantly in mitochondria","termid":"PBO:0082908"}


id: PBO:0076103
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syntaxin 8","termid":"PBO:0076103"}


id: GO:0035364
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of thymine, 5-methyluracil, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GO:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleobase transport","termid":"GO:0015855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"thymine transport","synonyms":[{"name":"5-methyluracil transport","type":"exact"},{"name":"thymine transmembrane transport","type":"exact"}],"termid":"GO:0035364"}


id: PBO:0041304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"C2 calcium dependent domain containing 6","termid":"PBO:0041304"}


id: MONDO:0002085
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"movement disorder","termid":"MONDO:0005395"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign shuddering attacks","secondary_identifiers":["UMLS:C0375200","MEDGEN:580931","SCTID:446995005","DOID:1713","ICD10CM:G25.83","ICD9:333.93"],"termid":"MONDO:0002085","xrefs":{"Monarch":{"xref_id":"0002085"}}}


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":["DOID:1130","MEDGEN:137969","SCTID:95830009","icd11.foundation:765046957","NCIT:C27117","ICD9:253.8","UMLS:C0342405"],"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:0054168
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 1539","termid":"PBO:0054168"}


id: GO:0001714
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell fate determination process that results in a cell becoming capable of differentiating autonomously into an endoderm cell in an environment that is neutral with respect to the developmental pathway; upon specification, the cell fate can be reversed.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell fate specification","termid":"GO:0001708"},{"relation_name":"part_of","term_name":"endodermal cell fate commitment","termid":"GO:0001711"}],"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":"endodermal cell fate specification","synonyms":[{"name":"endoderm cell fate specification","type":"exact"}],"termid":"GO:0001714"}


id: GO:0019653
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The anaerobic chemical reactions and pathways resulting in the breakdown of purine nucleobases, yielding energy in the form of ATP.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleobase catabolic process","termid":"GO:0006145"},{"relation_name":"is_a","term_name":"nitrogenous compound fermentation","termid":"GO:0019666"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006091"}],"interesting_parent_ids":["GO:0006091","GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"anaerobic purine nucleobase catabolic process","synonyms":[{"name":"anaerobic purine base catabolic process","type":"exact"},{"name":"anaerobic purine base catabolism","type":"exact"},{"name":"anaerobic purine catabolic process","type":"related"},{"name":"purine base fermentation","type":"exact"},{"name":"purine fermentation","type":"related"}],"termid":"GO:0019653"}


id: PBO:0080668
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WAP four-disulfide core domain 13","termid":"PBO:0080668"}


id: MONDO:0022892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"craniosynostosis","termid":"MONDO:0015469"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"craniosynostosis alopecia brain defect","secondary_identifiers":["GARD:1586"],"termid":"MONDO:0022892","xrefs":{"Monarch":{"xref_id":"0022892"}}}


id: GO:0008113
data:
  {"annotated_genes":["SJAG_00419"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[95070],"is_not":false,"summary":null,"term":"GO:0008113"}]},"cv_name":"molecular_function","definition":"Catalysis of the reactions: peptide-L-methionine + thioredoxin disulfide + H2O = peptide-L-methionine (S)-S-oxide + thioredoxin, and L-methionine + thioredoxin disulfide + H2O = L-methionine (S)-S-oxide + thioredoxin. Can act on oxidized methionine in peptide linkage with specificity for the S enantiomer. Thioredoxin disulfide is the oxidized form of thioredoxin.","definition_xrefs":["EC:1.8.4.11","PMID:11169920","GOC:mah","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor","termid":"GO:0016671"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00419":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"peptide-methionine (S)-S-oxide reductase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0033742","GO:0072561","Reactome:R-HSA-1222363","Reactome:R-HSA-5676940","MetaCyc:RXN-8668","RHEA:14217"],"synonyms":[{"name":"MsrA","type":"related"},{"name":"methionine S-oxide reductase (S-form oxidizing) activity","type":"related"},{"name":"methionine S-oxide reductase activity","type":"broad"},{"name":"methionine sulfoxide (protein) reductase activity","type":"exact"},{"name":"methionine sulfoxide reductase A activity","type":"related"},{"name":"methionine sulfoxide reductase activity","type":"broad"},{"name":"methionine sulphoxide reductase A activity","type":"related"},{"name":"peptide Met(O) reductase activity","type":"related"},{"name":"peptide methionine sulfoxide reductase activity","type":"related"},{"name":"peptide-L-methionine:thioredoxin-disulfide S-oxidoreductase [L-methionine (S)-S-oxide-forming] activity","type":"related"},{"name":"peptide-methionine-(S)-S-oxide reductase activity","type":"exact"},{"name":"protein-methionine-S-oxide reductase activity","type":"exact"}],"termid":"GO:0008113","terms_by_termid":{"GO:0008113":null}}


id: PATO:0005009
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A 3-D shape inhering in a bearer by virtue of the bearer's having an entity in the form of a molar tooth.","definition_xrefs":["PATOC:WD"],"direct_ancestors":[{"relation_name":"is_a","term_name":"3-D shape","termid":"PATO:0002266"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"molariform","termid":"PATO:0005009"}


id: PBO:0114423
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ciliary microtubule inner protein 5","termid":"PBO:0114423"}


id: PBO:0082134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Actin filament binding protein that enhances actin ring formation; IQGAP family member required for assembly and contraction of the AMR, prior to cytokinesis; localizes to the contractile ring during anaphase in an Mlc1p-dependent manner, recruiting Myo1p and Hof1p to the site, and promoting cytokinetic core complex assembly; specifies bud-site selection, localizing axial markers Bud4p and Cdc12p; regulated by Cdc28p; relocalizes from the bud neck to the cytoplasm upon replication stress","termid":"PBO:0082134"}


id: PBO:0061721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NUT family member 2F","termid":"PBO:0061721"}


id: GO:0060567
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of DNA-dependent transcription termination, the process in which transcription is completed; the formation of phosphodiester bonds ceases, the RNA-DNA hybrid dissociates, and RNA polymerase releases the DNA.","definition_xrefs":["GOC:tb","GOC:dph","GOC:txnOH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of termination of DNA-templated transcription","termid":"GO:0031554"},{"relation_name":"is_a","term_name":"negative regulation of protein-containing complex disassembly","termid":"GO:0043242"},{"relation_name":"is_a","term_name":"negative regulation of DNA-templated transcription","termid":"GO:0045892"},{"relation_name":"negatively_regulates","term_name":"DNA-templated transcription termination","termid":"GO:0006353"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"negatively_regulates","termid":"GO:0006351"}],"interesting_parent_ids":["GO:0006355","GO:0008150","GO:0010467","GO:0006351"],"is_obsolete":false,"name":"negative regulation of termination of DNA-templated transcription","synonyms":[{"name":"negative regulation of DNA-dependent transcription, termination","type":"exact"},{"name":"negative regulation of DNA-templated transcription, termination","type":"exact"},{"name":"negative regulation of termination of DNA-dependent transcription","type":"exact"},{"name":"negative regulation of transcription termination, DNA-dependent","type":"exact"}],"termid":"GO:0060567"}


id: MONDO:0024418
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"muscular fibrosis multifocal obstructed vessels","secondary_identifiers":["Orphanet:2033","GARD:3857"],"termid":"MONDO:0024418","xrefs":{"Monarch":{"xref_id":"0024418"}}}


id: PBO:0058541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 6086","termid":"PBO:0058541"}


id: GO:0034228
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of ethanolamine from one side of a membrane to the other. Ethanolamine (2-aminoethanol, monoethanolamine) is an amino alcohol that occurs widely in living organisms as a constituent of certain types of phospholipids, such as phosphatidylethanolamine.","definition_xrefs":["GOC:rn","PMID:3514579"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amine transmembrane transporter activity","termid":"GO:0005275"},{"relation_name":"is_a","term_name":"organic cation transmembrane transporter activity","termid":"GO:0015101"},{"relation_name":"is_a","term_name":"alcohol transmembrane transporter activity","termid":"GO:0015665"}],"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:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"ethanolamine transmembrane transporter activity","secondary_identifiers":["MetaCyc:TRANS-RXN0-476"],"synonyms":[{"name":"2-aminoethanol transmembrane transporter activity","type":"exact"},{"name":"ethanolamine permease activity","type":"exact"},{"name":"monoethanolamine transmembrane transporter activity","type":"exact"}],"termid":"GO:0034228"}


id: MONDO:0957810
data:
  {"annotated_genes":["SJAG_03995"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85763],"is_not":false,"summary":null,"term":"MONDO:0957810"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03995":null},"genotype_count":0,"is_obsolete":false,"name":"developmental delay, dysmorphic facies, and brain anomalies","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:620535","MEDGEN:1847857","DOID:0060933","UMLS:C5882698"],"termid":"MONDO:0957810","terms_by_termid":{"MONDO:0957810":null},"xrefs":{"Monarch":{"xref_id":"0957810"}}}


id: GO:0043207
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of an external biotic stimulus, an external stimulus caused by, or produced by living things.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to external stimulus","termid":"GO:0009605"},{"relation_name":"is_a","term_name":"response to biotic stimulus","termid":"GO:0009607"}],"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 external biotic stimulus","termid":"GO:0043207"}


id: PBO:0055395
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 2825","termid":"PBO:0055395"}


id: MONDO:0030307
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 55","secondary_identifiers":["UMLS:C5543580","DOID:0112337","MEDGEN:1781781","OMIM:619380"],"synonyms":[{"name":"SPGF55","type":"exact"},{"name":"spermatogenic failure 55","type":"exact"}],"termid":"MONDO:0030307","xrefs":{"Monarch":{"xref_id":"0030307"}}}


id: PBO:0041556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 19 open reading frame 44","termid":"PBO:0041556"}


id: MONDO:0956989
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An EWSERI-negative small round cell tumor that is characterized by a recurrent translocation involving the CIC gene on chromosome 19 and either DUX4 gene on chromosome 4 or DUX4L gene on chromosome 10. The translocation results in either CIC-DUX4, t(4;19)(q35;q13) or CIC-DUX4L, t(10;19)(q26;q13) fusions.","definition_xrefs":["DOID:0081250"],"direct_ancestors":[{"relation_name":"is_a","term_name":"EWSR1-negative small round cell tumor","termid":"MONDO:0858921"}],"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":"CIC-rearranged sarcoma","secondary_identifiers":["UMLS:C3899764","MEDGEN:859358"],"termid":"MONDO:0956989","xrefs":{"Monarch":{"xref_id":"0956989"}}}


id: PR:O94699
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC83.16c gene.","definition_xrefs":["PRO:DNx","UniProtKB:O94699"],"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":"mitochondrial outer membrane protein C83.16c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC83.16c","synonyms":[{"name":"Spom972h-SPBC83.16c","type":"exact"}],"termid":"PR:O94699"}


id: GO:0044542
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont initiates, promotes, or enhances the normal activation of plasminogen, the pathway resulting in the processing of inactive plasminogen to active plasmin in the host organism. This can facilitate the dissemination of the symbiont into host tissues. It can also be used to destroy complement, opsonins as well as antibacterial proteins like histones.","definition_xrefs":["PMID:27533300","PMID:18070889","PMID:34305859"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host cellular process","termid":"GO:0044068"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"symbiont-mediated activation of host plasminogen","synonyms":[{"name":"plasminogen activation in another organism","type":"broad"},{"name":"plasminogen activation in other organism","type":"broad"}],"termid":"GO:0044542"}


id: GO:0008666
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (S)-2,3,4,5-tetrahydrodipicolinate + H2O + succinyl-CoA = L-2-succinylamino-6-oxopimelate + CoA.","definition_xrefs":["EC:2.3.1.117","RHEA:17325"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-succinyltransferase activity","termid":"GO:0016749"}],"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:0016746"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016740","GO:0016746","GO:0003674"],"is_obsolete":false,"name":"2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase activity","secondary_identifiers":["KEGG_REACTION:R04365","MetaCyc:TETHYDPICSUCC-RXN"],"synonyms":[{"name":"THDP N-succinyltransferase activity","type":"exact"},{"name":"succinyl-CoA:(S)-2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase activity","type":"related"},{"name":"succinyl-CoA:2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase activity","type":"related"},{"name":"succinyl-CoA:tetrahydrodipicolinate N-succinyltransferase activity","type":"related"},{"name":"tetrahydrodipicolinate N-succinyltransferase activity","type":"related"},{"name":"tetrahydrodipicolinate succinylase activity","type":"related"},{"name":"tetrahydrodipicolinate succinyltransferase activity","type":"related"},{"name":"tetrahydropicolinate succinylase activity","type":"related"}],"termid":"GO:0008666"}


id: PBO:0016946
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial NADH dehydrogenase (ubiquinone) Nde2 (predicted)","termid":"PBO:0016946"}


id: PBO:0046663
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"estrogen receptor 1","termid":"PBO:0046663"}


id: PBO:0079355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TUBA1B antisense RNA 1","termid":"PBO:0079355"}


id: PBO:0081558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 480","termid":"PBO:0081558"}


id: MONDO:0018700
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete pseudohypoparathyroidism without Albright hereditary osteodystrophy (obsolete MONDO:0018700)","secondary_identifiers":["Orphanet:457062"],"termid":"MONDO:0018700","xrefs":{"Monarch":{"xref_id":"0018700"}}}


id: GO:0060964
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that modulates the rate, frequency, or extent of the downregulation of gene expression through the action of microRNAs (miRNAs).","definition_xrefs":["GOC:aruk","PMID:23985560","PMID:28379604","GOC:tb","GOC:bc","GOC:dph","GOC:rl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of post-transcriptional gene silencing by regulatory ncRNA","termid":"GO:1900368"},{"relation_name":"regulates","term_name":"miRNA-mediated post-transcriptional gene silencing","termid":"GO:0035195"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"regulation of miRNA-mediated gene silencing","secondary_identifiers":["Reactome:R-HSA-5578749"],"synonyms":[{"name":"regulation of gene silencing by miRNA","type":"exact"},{"name":"regulation of gene silencing by microRNA","type":"exact"}],"termid":"GO:0060964"}


id: GO:0044514
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that begins with venom being forced into an organism by the bite or sting of another organism, and ends with the resultant positive regulation of G protein-coupled receptor activity in of the bitten organism.","definition_xrefs":["GOC:jl","PMID:8405712","GOC:fj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"envenomation resulting in modulation of G protein-coupled receptor activity in another organism","termid":"GO:0044513"}],"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":"envenomation resulting in positive regulation of G protein-coupled receptor activity in another organism","synonyms":[{"name":"envenomation resulting in positive regulation of G protein-coupled receptor activity in other organism","type":"exact"},{"name":"envenomation resulting in positive regulation of G-protein coupled receptor activity in other organism","type":"exact"}],"termid":"GO:0044514"}


id: MONDO:0010915
data:
  {"annotated_genes":["SJAG_02431","SJAG_03703"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86276,86277],"is_not":false,"summary":null,"term":"MONDO:0010915"}]},"cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH14 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant nonsyndromic hearing loss","termid":"MONDO:0019587"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02431":null,"SJAG_03703":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0000426"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 4A","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:322209","OMIM:600652","DOID:0110573","MESH:C563460","UMLS:C1833503","GARD:18100"],"synonyms":[{"name":"DFNA4A","type":"narrow"},{"name":"MYH14 autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"autosomal dominant deafness 4A","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 4A","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in MYH14","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 4A","type":"narrow"},{"name":"deafness, autosomal dominant 4","type":"narrow"},{"name":"deafness, autosomal dominant 4A","type":"narrow"},{"name":"deafness, autosomal dominant 4a","type":"narrow"},{"name":"deafness, autosomal dominant type 4A","type":"narrow"}],"termid":"MONDO:0010915","terms_by_termid":{"MONDO:0010915":null},"xrefs":{"Monarch":{"xref_id":"0010915"}}}


id: GO:1905897
data:
  {"annotated_genes":["SJAG_01528","SJAG_02244"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[99364,96041],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904293"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of response to endoplasmic reticulum stress.","definition_xrefs":["GOC:bc","GOC:aruk","PMID:21803450","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"regulates","term_name":"response to endoplasmic reticulum stress","termid":"GO:0034976"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01528":null,"SJAG_02244":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of response to endoplasmic reticulum stress","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of ER stress response","type":"exact"},{"name":"regulation of cellular response to endoplasmic reticulum stress","type":"exact"},{"name":"regulation of response to ER stress","type":"exact"}],"termid":"GO:1905897","terms_by_termid":{"GO:1904293":null}}


id: GO:0001932
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of addition of phosphate groups into an amino acid in a protein.","definition_xrefs":["GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of protein modification process","termid":"GO:0031399"},{"relation_name":"is_a","term_name":"regulation of phosphorylation","termid":"GO:0042325"},{"relation_name":"regulates","term_name":"protein phosphorylation","termid":"GO:0006468"}],"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 protein phosphorylation","synonyms":[{"name":"regulation of protein amino acid phosphorylation","type":"exact"}],"termid":"GO:0001932"}


id: GO:0042635
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the cyclical phases of growth (anagen), regression (catagen), quiescence (telogen), and shedding (exogen) in the life of a hair.","definition_xrefs":["PMID:12230507","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of hair cycle","termid":"GO:0042634"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"hair cycle","termid":"GO:0042633"}],"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 hair cycle","synonyms":[{"name":"activation of hair cycle","type":"narrow"},{"name":"stimulation of hair cycle","type":"narrow"},{"name":"up regulation of hair cycle","type":"exact"},{"name":"up-regulation of hair cycle","type":"exact"},{"name":"upregulation of hair cycle","type":"exact"}],"termid":"GO:0042635"}


id: MONDO:0015397
data:
  {"annotated_genes":["SJAG_00539","SJAG_00322"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85256,85255],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0958175"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic developmental defect of the eye (obsolete MONDO:0015218)","termid":"MONDO:0015218"},{"relation_name":"excluded_subClassOf","term_name":"obsolete branchial arch or oral-acral syndrome (obsolete MONDO:0015334)","termid":"MONDO:0015334"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic palpebral coloboma (obsolete MONDO:0020157)","termid":"MONDO:0020157"},{"relation_name":"excluded_subClassOf","term_name":"obsolete bulbar conjunctival dermoid or conjunctival dermolipoma (obsolete MONDO:0020205)","termid":"MONDO:0020205"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndromic corneal dystrophy (obsolete MONDO:0020215)","termid":"MONDO:0020215"},{"relation_name":"excluded_subClassOf","term_name":"obsolete lens shape anomaly (obsolete MONDO:0020237)","termid":"MONDO:0020237"},{"relation_name":"excluded_subClassOf","term_name":"obsolete genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability (obsolete MONDO:0043008)","termid":"MONDO:0043008"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"oculoauriculovertebral spectrum with radial defects","termid":"MONDO:0007712"},{"relation_name":"is_a","term_name":"neurocristopathy","termid":"MONDO:0021635"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00322":null,"SJAG_00539":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"craniofacial microsomia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:367462009","GARD:12074","ICD9:759.89","MEDGEN:75554","NCIT:C84740","UMLS:C0265240","OMIMPS:164210","Orphanet:141132","Orphanet:141136","MESH:D006053","Orphanet:374","SCTID:109393007","DOID:2907"],"synonyms":[{"name":"Expanded spectrum hemifacial microsomia","type":"exact"},{"name":"Expanded spectrum of hemifacial microsomia","type":"exact"},{"name":"Fav sequence","type":"related"},{"name":"Goldenhar disease","type":"exact"},{"name":"Goldenhar syndrome","type":"exact"},{"name":"HFM","type":"exact"},{"name":"Laterofacial microsomia","type":"exact"},{"name":"OAV (oculoauriculovertebral) dysplasia","type":"exact"},{"name":"OAV dysplasia","type":"exact"},{"name":"OAV spectrum","type":"exact"},{"name":"OAVD","type":"related"},{"name":"OAVS","type":"exact"},{"name":"facio-auriculo-vertebral spectrum","type":"exact"},{"name":"facioauriculovertebral dysplasia","type":"exact"},{"name":"facioauriculovertebral sequence","type":"related"},{"name":"first and second branchial arch syndrome","type":"exact"},{"name":"first arch syndrome","type":"exact"},{"name":"first branchial arch syndrome","type":"exact"},{"name":"hemifacial microsomia","type":"exact"},{"name":"oculo-auriculo-vertebral dysplasia","type":"related"},{"name":"oculo-auriculo-vertebral spectrum","type":"exact"},{"name":"oculoauriculovertebral dysplasia","type":"exact"},{"name":"oculoauriculovertebral spectrum","type":"exact"},{"name":"oculoauriculovertebral syndrome","type":"exact"},{"name":"otomandibular syndrome","type":"exact"},{"name":"unilateral or bilateral and asymmetric otomandibular dysplasia","type":"exact"}],"termid":"MONDO:0015397","terms_by_termid":{"MONDO:0958175":null},"xrefs":{"Monarch":{"xref_id":"0015397"}}}


id: MOD:01307
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"modification from Unimod Chemical derivative -","definition_xrefs":["Unimod:332#S"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thiophosphate labeled with biotin-HPDP","termid":"MOD:00639"},{"relation_name":"is_a","term_name":"modified L-serine residue","termid":"MOD:00916"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thiophosphate labeled with biotin-HPDP -site S","synonyms":[{"name":"Thiophos-S-S-biotin","type":"related"},{"name":"thiophosphate labeled with biotin-HPDP","type":"related"}],"termid":"MOD:01307"}


id: PBO:0000236
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ANC9 family protein","termid":"PBO:0000236"}


id: GO:0103030
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + methylglyoxal + NADH = hydroxyacetone + NAD.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete ethylglyoxal reductase (NADH-dependent, hydroxyacetone-forming) activity (obsolete GO:0103030)","termid":"GO:0103030"}


id: PBO:0045282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dynamin 1 pseudogene 33","termid":"PBO:0045282"}


id: GO:0035909
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of an aorta are generated and organized. An aorta is an artery that carries blood from the heart to other parts of the body.","definition_xrefs":["MA:0000062","Wikipedia:Aorta","GOC:bf","GOC:dgh","UBERON:0000947"],"direct_ancestors":[{"relation_name":"is_a","term_name":"artery morphogenesis","termid":"GO:0048844"},{"relation_name":"part_of","term_name":"aorta development","termid":"GO:0035904"}],"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":"aorta morphogenesis","termid":"GO:0035909"}


id: GO:0034236
data:
  {"annotated_genes":["SJAG_01245"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[70592],"is_not":false,"summary":null,"term":"GO:0034236"}]},"cv_name":"molecular_function","definition":"Binding to one or both of the catalytic subunits of protein kinase A.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase binding","termid":"GO:0019901"},{"relation_name":"is_a","term_name":"protein kinase A binding","termid":"GO:0051018"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01245":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"protein kinase A catalytic subunit binding","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"PKA catalytic subunit binding","type":"exact"}],"termid":"GO:0034236","terms_by_termid":{"GO:0034236":null}}


id: PBO:0077108
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translocase of inner mitochondrial membrane 13","termid":"PBO:0077108"}


id: MONDO:0007283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early-onset non-syndromic cataract in which the cause of the disease is a mutation in the CRYBA2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset non-syndromic cataract","termid":"MONDO:0011060"}],"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 42","secondary_identifiers":["DOID:0110237","MEDGEN:859891","OMIM:115900","UMLS:C4011454"],"synonyms":[{"name":"A cataract that has_material_basis_in heterozygous mutation in the CRYBA2 gene on chromosome 2q35.","type":"exact"},{"name":"CRYBA2 early-onset non-syndromic cataract","type":"exact"},{"name":"CTRCT42","type":"exact"},{"name":"cataract 42","type":"exact"},{"name":"cataract type 42","type":"exact"},{"name":"early-onset non-syndromic cataract caused by mutation in CRYBA2","type":"exact"}],"termid":"MONDO:0007283","xrefs":{"Monarch":{"xref_id":"0007283"}}}


id: PBO:0091249
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha-One, Three-Galactosyltransferase","termid":"PBO:0091249"}


id: MONDO:0019686
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete type 2 collagen-related bone disorder (obsolete MONDO:0019686)","termid":"MONDO:0019686","xrefs":{"Monarch":{"xref_id":"0019686"}}}


id: PBO:0072868
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SAT1 divergent transcript","termid":"PBO:0072868"}


id: PBO:0075979
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STAT4 antisense RNA 1","termid":"PBO:0075979"}


id: MONDO:0016648
data:
  {"annotated_genes":["SJAG_02463","SJAG_01941"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85282,85281],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009189"}]},"cv_name":"mondo","definition":"Multiple epiphyseal dysplasias (MED/EDMs) are characterized by epiphyseal anomalies causing joint pain early in life, recurrent osteochondritis and early arthrosis. The EDMs are a heterogeneous group of diseases with variable expression classed as MED/EDMs 1-6.","definition_xrefs":["Orphanet:251"],"direct_ancestors":[{"relation_name":"is_a","term_name":"osteochondrodysplasia","termid":"MONDO:0005516"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01941":null,"SJAG_02463":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"multiple epiphyseal dysplasia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:756.56","DOID:12721","icd11.foundation:2009123831","NORD:1468","UMLS:C0026760","ICD10CM:Q77.3","OMIMPS:132400","MedDRA:10028197","GARD:10756","MEDGEN:6461","SCTID:59708000","HP:0002654"],"synonyms":[{"name":"Dominant Multiple Epiphyseal Dysplasia","type":"exact"},{"name":"EDM","type":"exact"},{"name":"MED","type":"exact"},{"name":"Polyepiphyseal dysplasia","type":"exact"},{"name":"epiphyseal dysplasia, multiple","type":"related"},{"name":"multiple epiphyseal dysplasia","type":"exact"},{"name":"multiple epiphyseal dysplasia (disease)","type":"exact"},{"name":"polyepiphyseal dysplasia","type":"exact"}],"termid":"MONDO:0016648","terms_by_termid":{"MONDO:0009189":null},"xrefs":{"Monarch":{"xref_id":"0016648"}}}


id: GO:0015480
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Secretins are Gram-negative bacterial outer membrane proteins that form multimeric pores through which macromolecules, usually proteins, can pass. Form homomultimeric ring structures, 10-20 subunits per complex, with large central pores (inner diameters of 5-10 nm).","definition_xrefs":["TC:1.B.22.-.-"],"gene_count":0,"genotype_count":0,"name":"obsolete secretin (sensu Bacteria) (obsolete GO:0015480)","synonyms":[{"name":"secretin (sensu Bacteria)","type":"exact"}],"termid":"GO:0015480"}


id: GO:0030619
data:
  {"annotated_genes":["SJAG_04911","SJAG_04497","SJAG_05009","SJAG_03983"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[91077,97520,110095,112724],"is_not":false,"summary":null,"term":"GO:0030619"}]},"cv_name":"molecular_function","definition":"Binding to a U1 small nuclear RNA (U1 snRNA).","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA binding","termid":"GO:0017069"}],"gene_count":4,"genes_by_uniquename":{"SJAG_03983":null,"SJAG_04497":null,"SJAG_04911":null,"SJAG_05009":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003723","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"U1 snRNA binding","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0030619","terms_by_termid":{"GO:0030619":null}}


id: GO:2000367
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of acrosomal vesicle exocytosis.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of calcium ion-dependent exocytosis","termid":"GO:0017158"},{"relation_name":"regulates","term_name":"acrosomal vesicle exocytosis","termid":"GO:0060478"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"}],"interesting_parent_ids":["GO:0016192","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"regulation of acrosomal vesicle exocytosis","synonyms":[{"name":"regulation of acrosomal granule exocytosis","type":"related"},{"name":"regulation of acrosome exocytosis","type":"exact"}],"termid":"GO:2000367"}


id: MONDO:0000205
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete radioulnar synostosis with amegakaryocytic thrombocytopenia (obsolete MONDO:0000205)","termid":"MONDO:0000205","xrefs":{"Monarch":{"xref_id":"0000205"}}}


id: MONDO:0030947
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":"neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities","secondary_identifiers":["MEDGEN:1781967","GARD:18023","Orphanet:610573","OMIM:619173","UMLS:C5543020"],"synonyms":[{"name":"CONRIBA","type":"exact"},{"name":"neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities","type":"exact"}],"termid":"MONDO:0030947","xrefs":{"Monarch":{"xref_id":"0030947"}}}


id: GO:0033023
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of regulating the proliferation and elimination of mast cells such that the total number of mast cells within a whole or part of an organism is stable over time in the absence of an outside stimulus.","definition_xrefs":["GOC:add","PMID:11292031"],"direct_ancestors":[{"relation_name":"is_a","term_name":"leukocyte homeostasis","termid":"GO:0001776"},{"relation_name":"is_a","term_name":"myeloid cell homeostasis","termid":"GO:0002262"}],"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":"mast cell homeostasis","termid":"GO:0033023"}


id: FYPO:0002383
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cellular process phenotype observed in the vegetative growth phase of the life cycle in which acetylation of lysine at positions 9 and 14 of histone H3 in regions of the genome that are actively transcribed occurs to a greater extent than normal.","definition_xrefs":["PomBase:mah","PMID:23851719"],"gene_count":0,"genotype_count":0,"name":"obsolete increased histone H3-K9 and H3-K14 acetylation at centromere outer repeat during vegetative growth (obsolete FYPO:0002383)","synonyms":[{"name":"increased histone H3 acetylation (K9 and K14) at centromere outer repeat during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 and H3-K14 acetylation at centromere otr during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 and H3-K14 acetylation at centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"increased histone H3-K9 and H3-K14 acetylation at centromeric outer repeat region during vegetative growth","type":"exact"},{"name":"increased histone H3-K9 and H3-K14 acetylation at pericentric region during vegetative growth","type":"related"},{"name":"increased histone H3-K9 and H3-K14 acetylation at pericentromeric region during vegetative growth","type":"related"},{"name":"increased histone H3K9 and H3K14 acetylation at centromere outer repeat during vegetative growth","type":"exact"}],"termid":"FYPO:0002383"}


id: PBO:0049382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"general transcription factor IIIC subunit 4","termid":"PBO:0049382"}


id: MONDO:0100405
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any acute myeloid leukemia that has the chromosomal anomaly Non-KMT2A MLLT10 rearrangement positive. (An indication that a cytogenetic rearrangement involving MLLT10 but not involving KMT2A was detected in a sample.)","definition_xrefs":["NCIT:C168771"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive","synonyms":[{"name":"AML, Non-KMT2A MLLT10 Rearrangement","type":"exact"},{"name":"AML, Non-KMT2A MLLT10 rearrangement positive","type":"exact"},{"name":"AML, Non-MLL MLLT10 Rearrangement","type":"exact"},{"name":"AML, Non-MLL MLLT10 Rearrangement Positive","type":"exact"}],"termid":"MONDO:0100405","xrefs":{"Monarch":{"xref_id":"0100405"}}}


id: FYPO:0003354
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which the glycan moiety of a glycoprotein contains a lower amount of galactose residues than normal. In wild-type cells, glycoprotein glycans contain mannose and galactose residues in a 1:1.2 ratio, and the galactose residues are connected by alpha-1,2 linkages.","definition_xrefs":["PMID:8782411","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal glycoprotein glycan structure","termid":"FYPO:0003290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0002494"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0002274"},{"rel_name":"is_a","termid":"FYPO:0003290"}],"interesting_parent_ids":["FYPO:0003290","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0002274","FYPO:0002494"],"is_obsolete":false,"name":"decreased galactose level in glycoprotein glycan","synonyms":[{"name":"decreased galactose level in glycoprotein oligosaccharide","type":"related"},{"name":"decreased level of alpha 1,2-linked galactose residues in glycoprotein glycan","type":"exact"},{"name":"decreased protein glycan galactosylation","type":"related"},{"name":"reduced galactose level in glycoprotein glycan","type":"exact"}],"termid":"FYPO:0003354"}


id: MONDO:1012951
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Alzheimer disease that occurs in crab-eating macaque due to a mutation in the PSEN1 gene created by genetic engineering or gene editing.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"Alzheimer disease, non-human animal","termid":"MONDO:1011443"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Alzheimer disease, PSEN1-related, crab-eating macaque","secondary_identifiers":["OMIA:002493-9541"],"termid":"MONDO:1012951","xrefs":{"Monarch":{"xref_id":"1012951"}}}


id: PBO:0052721
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 18 pseudogene 13","termid":"PBO:0052721"}


id: PBO:0078925
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon ACG) 2-1","termid":"PBO:0078925"}


id: FYPO:0007867
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to one or both poles of the meiotic spindle is normal (i.e. indistinguishable from wild type) during the first meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:34346498"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to meiotic spindle","termid":"FYPO:0007866"}],"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:0000138"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to meiotic spindle pole during meiosis I","synonyms":[{"name":"normal protein localisation to meiotic spindle pole during meiosis I","type":"exact"},{"name":"normal protein localisation to spindle pole during meiosis I","type":"exact"},{"name":"normal protein localization to meiosis I spindle pole","type":"exact"},{"name":"normal protein localization to spindle pole during first meiotic nuclear division","type":"exact"}],"termid":"FYPO:0007867"}


id: GO:0051333
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The cell cycle process in which the reformation of the nuclear membranes during meiosis occurs.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nuclear membrane reassembly","termid":"GO:0031468"},{"relation_name":"is_a","term_name":"meiotic cell cycle process","termid":"GO:1903046"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0061024"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0007049","GO:0061024","GO:0044085"],"is_obsolete":false,"name":"meiotic nuclear membrane reassembly","synonyms":[{"name":"meiotic nuclear envelope reassembly","type":"related"}],"termid":"GO:0051333"}


id: GO:0060627
data:
  {"annotated_genes":["SJAG_03581","SJAG_03268","SJAG_03970","SJAG_04052","SJAG_00661","SJAG_01373","SJAG_00514","SJAG_04465","SJAG_01166","SJAG_02366","SJAG_04666","SJAG_00845","SJAG_03631","SJAG_02419","SJAG_04343","SJAG_00649","SJAG_00402","SJAG_04509","SJAG_03987","SJAG_03763","SJAG_02684"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[87418,91526],"is_not":false,"summary":null,"term":"GO:0060627"},{"annotations":[94085],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045806"},{"annotations":[87604],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042997"},{"annotations":[103185],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045807"},{"annotations":[99668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045921"},{"annotations":[118291,110471,111119],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000369"},{"annotations":[87413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2001135"},{"annotations":[77816,92214,102418,77104,90475,112678,112805,89383,91933],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030100"},{"annotations":[111098],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0060628"},{"annotations":[97904,87416,93348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0017157"},{"annotations":[113064],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:2000156"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate, frequency, or extent of vesicle-mediated transport, the directed movement of substances, either within a vesicle or in the vesicle membrane, into, out of or within a cell.","definition_xrefs":["GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"is_a","term_name":"regulation of transport","termid":"GO:0051049"},{"relation_name":"regulates","term_name":"vesicle-mediated transport","termid":"GO:0016192"}],"gene_count":21,"genes_by_uniquename":{"SJAG_00402":null,"SJAG_00514":null,"SJAG_00649":null,"SJAG_00661":null,"SJAG_00845":null,"SJAG_01166":null,"SJAG_01373":null,"SJAG_02366":null,"SJAG_02419":null,"SJAG_02684":null,"SJAG_03268":null,"SJAG_03581":null,"SJAG_03631":null,"SJAG_03763":null,"SJAG_03970":null,"SJAG_03987":null,"SJAG_04052":null,"SJAG_04343":null,"SJAG_04465":null,"SJAG_04509":null,"SJAG_04666":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0016192","GO:0006810"],"is_obsolete":false,"name":"regulation of vesicle-mediated transport","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0060627","terms_by_termid":{"GO:0017157":null,"GO:0030100":null,"GO:0042997":null,"GO:0045806":null,"GO:0045807":null,"GO:0045921":null,"GO:0060627":null,"GO:0060628":null,"GO:2000156":null,"GO:2000369":null,"GO:2001135":null}}


id: MONDO:0004660
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma in situ involving a lung.","definition_xrefs":["MONDO:patterns/carcinoma_in_situ"],"direct_ancestors":[{"relation_name":"is_a","term_name":"in situ carcinoma","termid":"MONDO:0004647"},{"relation_name":"is_a","term_name":"lung carcinoma","termid":"MONDO:0005138"}],"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":"lung carcinoma in situ","secondary_identifiers":["DOID:8800","MEDGEN:146894","NCIT:C27467","ICD9:231.2","UMLS:C0685053","SCTID:92649001"],"synonyms":[{"name":"bronchial carcinoma in situ","type":"exact"},{"name":"carcinoma in situ of lung","type":"exact"},{"name":"lung in situ carcinoma","type":"exact"},{"name":"stage 0 lung cancer","type":"exact"},{"name":"stage 0 lung cancer aJCC v6","type":"exact"},{"name":"stage 0 lung cancer aJCC v6 and v7","type":"exact"},{"name":"stage 0 lung cancer aJCC v7","type":"exact"},{"name":"stage 0 lung carcinoma","type":"exact"}],"termid":"MONDO:0004660","xrefs":{"Monarch":{"xref_id":"0004660"}}}


id: PBO:0074789
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 10","termid":"PBO:0074789"}


id: GO:1904552
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of chemotaxis to arachidonic acid.","definition_xrefs":["GOC:TermGenie","GO_REF:0000058","PMID:16382163"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chemotaxis","termid":"GO:0050920"},{"relation_name":"regulates","term_name":"chemotaxis to arachidonate","termid":"GO:0034670"}],"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 chemotaxis to arachidonate","synonyms":[{"name":"regulation of chemotaxis to arachidonic acid","type":"exact"}],"termid":"GO:1904552"}


id: PBO:0030346
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-incomplete,_unequal_mitotic_sister_chromatid_segregation,_with_unseparated_DNA","termid":"PBO:0030346"}


id: PBO:0050320
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 22","termid":"PBO:0050320"}


id: PBO:0053407
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 342","termid":"PBO:0053407"}


id: MOD:00261
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively crosslinks an L-tyrosine residue and 5'-phosphouridine through a phosphodiester bond to form O4'-(phospho-5'-uridine)-L-tyrosine.","definition_xrefs":["RESID:AA0256","PubMed:11467524","DeltaMass:0","PubMed:2885322","Unimod:417#Y"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modified L-tyrosine residue","termid":"MOD:00919"},{"relation_name":"is_a","term_name":"uridylated residue","termid":"MOD:01166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"O4'-(phospho-5'-uridine)-L-tyrosine","synonyms":[{"name":"(S)-2-amino-3-[4-(5'-uridine phosphonoxy)phenyl]propanoic acid","type":"exact"},{"name":"5'-uridylic-O-tyrosine","type":"exact"},{"name":"MOD_RES O-UMP-tyrosine","type":"exact"},{"name":"O-Uridinylylation (of Tyrosine)","type":"exact"},{"name":"O4'-(phospho-5'-uridine)-L-tyrosine","type":"exact"},{"name":"O4'-L-tyrosine 5'-uridine phosphodiester","type":"exact"},{"name":"OUMPTyr","type":"exact"},{"name":"PhosphoUridine","type":"related"},{"name":"hydrogen 5'-uridylate tyrosine ester","type":"exact"},{"name":"uridine phosphodiester","type":"related"}],"termid":"MOD:00261"}


id: GO:0140426
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by a ligand binding of a pattern recognition receptor (PRR) to activate a plant innate immune response. PAMP-triggered immunity PRRs bind pathogen-associated molecular pattern (PAMPs), structures conserved among microbial species.","definition_xrefs":["PMID:25744358"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pattern recognition receptor signaling pathway","termid":"GO:0002221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"pathogen-associated molecular pattern receptor signaling pathway","synonyms":[{"name":"MAMP-triggered immunity signalling","type":"exact"},{"name":"PAMP receptor signaling pathway","type":"exact"},{"name":"PAMP-triggered immunity signalling pathway","type":"exact"},{"name":"PTI signalling","type":"exact"},{"name":"pathogen-associated molecular pattern signalling","type":"exact"}],"termid":"GO:0140426"}


id: GO:0046362
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of ribitol, a pentitol derived formally by reduction of the -CHO group of either D- or L-ribose.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ribitol metabolic process","termid":"GO:0019349"},{"relation_name":"is_a","term_name":"pentitol biosynthetic process","termid":"GO:0019526"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"ribitol biosynthetic process","synonyms":[{"name":"ribitol anabolism","type":"exact"},{"name":"ribitol biosynthesis","type":"exact"},{"name":"ribitol formation","type":"exact"},{"name":"ribitol synthesis","type":"exact"}],"termid":"GO:0046362"}


id: GO:2001315
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a UDP-4-deoxy-4-formamido-beta-L-arabinopyranose.","definition_xrefs":["GOC:yaf","UniPathway:UPA00032"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-sugar biosynthetic process","termid":"GO:0009226"},{"relation_name":"is_a","term_name":"amino sugar biosynthetic process","termid":"GO:0046349"},{"relation_name":"is_a","term_name":"UDP-4-deoxy-4-formamido-beta-L-arabinopyranose metabolic process","termid":"GO:2001313"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0055086","GO:0044281"],"is_obsolete":false,"name":"UDP-4-deoxy-4-formamido-beta-L-arabinopyranose biosynthetic process","synonyms":[{"name":"UDP-4-deoxy-4-formamido-beta-L-arabinopyranose anabolism","type":"exact"},{"name":"UDP-4-deoxy-4-formamido-beta-L-arabinopyranose biosynthesis","type":"exact"},{"name":"UDP-4-deoxy-4-formamido-beta-L-arabinopyranose formation","type":"exact"},{"name":"UDP-4-deoxy-4-formamido-beta-L-arabinopyranose synthesis","type":"exact"}],"termid":"GO:2001315"}


id: PBO:0012267
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SIP/FAR complex striatin subunit, Far8/Csc3","termid":"PBO:0012267"}


id: PBO:0057763
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MIR2052 host gene","termid":"PBO:0057763"}


id: PBO:0082913
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cytochrome b; mitochondrially-encoded subunit of ubiquinol-cytochrome c reductase complex which includes Cobp, Rip1p, Cyt1p, Cor1p, Qcr2p, Qcr6p, Qcr7p, Qcr8p, Qcr9p, and Qcr10p; number of introns varies between strains from 0 to 6, with most having 5","termid":"PBO:0082913"}


id: PR:C6Y4B0
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC27E2.14 gene.","definition_xrefs":["UniProtKB:C6Y4B0","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"uncharacterized protein C27E2.14 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC27E2.14","synonyms":[{"name":"Spom972h-SPAC27E2.14","type":"exact"}],"termid":"PR:C6Y4B0"}


id: PBO:0069856
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1143, pseudogene","termid":"PBO:0069856"}


id: GO:0044622
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of cell migration in a second organism.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of cell migration in another organism (obsolete GO:0044622)","synonyms":[{"name":"envenomation resulting in negative regulation of cell migration in another organism","type":"narrow"},{"name":"envenomation resulting in negative regulation of cell migration in other organism","type":"narrow"},{"name":"negative regulation of cell migration in other organism","type":"exact"}],"termid":"GO:0044622"}


id: GO:0090204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a protein is transported to, or maintained in, a nuclear pore.","definition_xrefs":["GOC:rb","GOC:dph","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein localization to nuclear envelope","termid":"GO:0090435"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0008150"],"is_obsolete":false,"name":"protein localization to nuclear pore","synonyms":[{"name":"protein localisation to nuclear pore","type":"exact"}],"termid":"GO:0090204"}


id: PBO:0083859
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FAD pyrophosphatase; hydrolyzes FAD as the preferred substrate but also acts on NADH and ADP-ribose at lower rates; activity is dependent upon K+ and divalent metal cations; green fluorescent protein (GFP)-fusion protein localizes to both the cytoplasm and nucleus; FPY1 is not an essential gene; protein abundance increases in response to DNA replication stress","termid":"PBO:0083859"}


id: PBO:0091832
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complements S. cerevisiae HAP5","termid":"PBO:0091832"}


id: MONDO:0008411
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Ulnar-mammary syndrome (UMS) is a rare developmental disorder characterized by ulnar defects, mammary and apocrine gland hypoplasia and genital anomalies. Delayed puberty dental anomalies, short stature and obesity have also been described.","definition_xrefs":["Orphanet:3138"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"is_a","term_name":"non-syndromic limb reduction defect","termid":"MONDO:0019713"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ulnar-mammary syndrome","secondary_identifiers":["UMLS:C1866994","ICD9:759.89","icd11.foundation:1508836700","NORD:1695","OMIM:181450","GARD:118","DOID:0060614","MESH:C536937","MEDGEN:357886","SCTID:700211007"],"synonyms":[{"name":"Pallister ulnar-mammary syndrome","type":"exact"},{"name":"Schinzel Syndrome","type":"exact"},{"name":"Schinzel syndrome","type":"exact"},{"name":"UMS","type":"exact"},{"name":"ulnar-mammary syndrome","type":"exact"},{"name":"ulnar-mammary syndrome of Pallister","type":"related"},{"name":"ums","type":"exact"}],"termid":"MONDO:0008411","xrefs":{"Monarch":{"xref_id":"0008411"}}}


id: PBO:0069855
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 1141, pseudogene","termid":"PBO:0069855"}


id: MONDO:0005614
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from the pancreas showing both ductal and squamous differentiation. The squamous component should represent at least 30% of the malignant cellular infiltrate. The prognosis is usually worse than that of ductal adenocarcinoma.","definition_xrefs":["NCIT:C5721"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"pancreatic ductal adenocarcinoma","termid":"MONDO:0005184"},{"relation_name":"is_a","term_name":"adenosquamous carcinoma","termid":"MONDO:0006074"},{"relation_name":"is_a","term_name":"squamous cell carcinoma of pancreas","termid":"MONDO:0018521"}],"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":"pancreatic adenosquamous carcinoma","secondary_identifiers":["EFO:0006732","ONCOTREE:PAASC","DOID:5637","MEDGEN:277489","UMLS:C1335299"],"synonyms":[{"name":"PAASC","type":"related"},{"name":"adenosquamous carcinoma of pancreas","type":"exact"},{"name":"adenosquamous carcinoma of the pancreas","type":"exact"},{"name":"adenosquamous pancreas carcinoma","type":"exact"},{"name":"pancreas adenosquamous carcinoma","type":"exact"},{"name":"pancreatic adenoacanthoma","type":"exact"},{"name":"pancreatic adenosquamous cancer","type":"exact"},{"name":"pancreatic adenosquamous carcinoma","type":"exact"},{"name":"pancreatic mixed squamous and adenocarcinoma","type":"exact"},{"name":"pancreatic mucoepidermoid carcinoma","type":"exact"}],"termid":"MONDO:0005614","xrefs":{"Monarch":{"xref_id":"0005614"}}}


id: MONDO:0004786
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cholangitis that is persistent and long-standing.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cholangitis","termid":"MONDO:0004789"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002515"},{"rel_name":"is_a","termid":"MONDO:0004335"}],"interesting_parent_ids":["MONDO:0002515","MONDO:0004335"],"is_obsolete":false,"name":"chronic cholangitis","secondary_identifiers":["DOID:9439","SCTID:71912000","NCIT:C35335","MEDGEN:82765","UMLS:C0267918"],"synonyms":[{"name":"cholangitis, chronic","type":"exact"}],"termid":"MONDO:0004786","xrefs":{"Monarch":{"xref_id":"0004786"}}}


id: PR:O14235
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pof5 gene.","definition_xrefs":["UniProtKB:O14235","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 pof5 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC6F6.02c","synonyms":[{"name":"Spom972h-pof5","type":"exact"}],"termid":"PR:O14235"}


id: GO:0089721
data:
  {"annotated_genes":["SJAG_00276","SJAG_01960"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[92845,111706],"is_not":false,"summary":null,"term":"GO:0089721"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a phosphoenolpyruvate from one side of a membrane to the other.","definition_xrefs":["GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monocarboxylic acid transmembrane transporter activity","termid":"GO:0008028"},{"relation_name":"is_a","term_name":"organophosphate ester transmembrane transporter activity","termid":"GO:0015605"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00276":null,"SJAG_01960":null},"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:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"phosphoenolpyruvate transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0089721","terms_by_termid":{"GO:0089721":null}}


id: MONDO:0012285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"left ventricular noncompaction","termid":"MONDO:0018901"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"left ventricular noncompaction 2","secondary_identifiers":["GARD:15460","OMIM:609470","MEDGEN:322827","UMLS:C1836118"],"synonyms":[{"name":"LVNC2","type":"exact"},{"name":"left ventricular noncompaction 2","type":"exact"}],"termid":"MONDO:0012285","xrefs":{"Monarch":{"xref_id":"0012285"}}}


id: PR:Q9P6M1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- gst3 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9P6M1"],"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":"glutathione S-transferase 3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC688.04c","synonyms":[{"name":"GST-III (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-gst3","type":"exact"}],"termid":"PR:Q9P6M1"}


id: MONDO:0958178
data:
  {"annotated_genes":["SJAG_04754"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[85551],"is_not":false,"summary":null,"term":"MONDO:0958178"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"cataracts, hearing impairment, nephrotic syndrome, and enterocolitis","termid":"MONDO:0957400"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04754":null},"genotype_count":0,"is_obsolete":false,"name":"cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5829571","OMIM:301108","MEDGEN:1840207"],"termid":"MONDO:0958178","terms_by_termid":{"MONDO:0958178":null},"xrefs":{"Monarch":{"xref_id":"0958178"}}}


id: GO:0014727
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates, maintains or increases the frequency, rate or extent of extraocular skeletal muscle development. Extraocular skeletal muscle development is the process whose specific outcome is the progression of the extraocular skeletal muscle over time, from its formation to the mature structure. The extraocular muscle is derived from cranial mesoderm and controls eye movements. The muscle begins its development with the differentiation of the muscle cells and ends with the mature muscle.","definition_xrefs":["GOC:mtg_muscle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of extraocular skeletal muscle development","termid":"GO:0014725"},{"relation_name":"is_a","term_name":"positive regulation of skeletal muscle tissue development","termid":"GO:0048643"},{"relation_name":"positively_regulates","term_name":"extraocular skeletal muscle development","termid":"GO:0002074"}],"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 extraocular skeletal muscle development","termid":"GO:0014727"}


id: PBO:0057238
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 425","termid":"PBO:0057238"}


id: PBO:0083495
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the verified gene YJL168C/SET2","termid":"PBO:0083495"}


id: MONDO:0800107
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ventricular septal defect","termid":"MONDO:0002070"}],"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":"anterior deviation infundibular septum","secondary_identifiers":["UMLS:C3164404","MEDGEN:756812","SCTID:448619007"],"termid":"MONDO:0800107","xrefs":{"Monarch":{"xref_id":"0800107"}}}


id: PBO:0068301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 6 pseudogene 1","termid":"PBO:0068301"}


id: PATO:0001576
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A pressure which is relatively high.","definition_xrefs":["PATO:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"pressure","termid":"PATO:0001025"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased pressure","synonyms":[{"name":"high pressure","type":"exact"}],"termid":"PATO:0001576"}


id: PBO:0063497
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PDZ and LIM domain 5","termid":"PBO:0063497"}


id: GO:0047100
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: phosphate + NADP+ + glyceraldehyde-3-phosphate = NADPH + 3-phospho-D-glyceroyl-phosphate.","definition_xrefs":["EC:1.2.1.13","MetaCyc:1.2.1.13-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glyceraldehyde-3-phosphate dehydrogenase [NAD(P)+] (phosphorylating) activity","termid":"GO:0043891"}],"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:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"glyceraldehyde-3-phosphate dehydrogenase (NADP+) (phosphorylating) activity","secondary_identifiers":["RHEA:10296"],"synonyms":[{"name":"D-glyceraldehyde-3-phosphate:NADP+ oxidoreductase (phosphorylating)","type":"related"},{"name":"NADP-dependent glyceraldehyde phosphate dehydrogenase activity","type":"related"},{"name":"NADP-dependent glyceraldehyde-3-phosphate dehydrogenase activity","type":"related"},{"name":"NADP-triose phosphate dehydrogenase activity","type":"related"},{"name":"dehydrogenase, glyceraldehyde phosphate (nicotinamide adenine dinucleotide phosphate) (phosphorylating)","type":"related"},{"name":"glyceraldehyde phosphate dehydrogenase (nicotinamide adenine dinucleotide phosphate) (phosphorylating)","type":"related"},{"name":"triosephosphate dehydrogenase (NADP(+)) activity","type":"related"},{"name":"triosephosphate dehydrogenase (NADP)","type":"related"},{"name":"triosephosphate dehydrogenase (NADP+) activity","type":"related"}],"termid":"GO:0047100"}


id: MONDO:0007683
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Grant syndrome is a rare osteogenesis imperfecta-like disorder, described in two patients to date, characterized clinically by persistent wormian bones, blue sclera, mandibular hypoplasia, shallow glenoid fossa, and campomelia. There have been no further descriptions in the literature since 1986.","definition_xrefs":["Orphanet:2097"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with decreased bone density (obsolete MONDO:0019704)","termid":"MONDO:0019704"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Grant syndrome","secondary_identifiers":["OMIM:138930","UMLS:C1841835","MESH:C537293","icd11.foundation:1320218486","GARD:2559","MEDGEN:333925","SCTID:723827003"],"synonyms":[{"name":"Grant syndrome","type":"exact"},{"name":"persistent wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia","type":"related"}],"termid":"MONDO:0007683","xrefs":{"Monarch":{"xref_id":"0007683"}}}


id: SO:0000481
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"An inverted repeat (SO:0000294) occurring at the termini of a DNA transposon.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inverted_repeat","termid":"SO:0000294"},{"relation_name":"part_of","term_name":"terminal_inverted_repeat_element","termid":"SO:0000208"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"terminal_inverted_repeat","synonyms":[{"name":"TIR","type":"exact"},{"name":"terminal inverted repeat","type":"exact"}],"termid":"SO:0000481"}


id: MONDO:0032748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spermatogenic failure","termid":"MONDO:0004983"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005047"}],"interesting_parent_ids":["MONDO:0005047"],"is_obsolete":false,"name":"spermatogenic failure 38","secondary_identifiers":["GARD:18409","OMIM:618433","MEDGEN:1680356","UMLS:C5193095","DOID:0111919"],"synonyms":[{"name":"SPERMATOGENIC FAILURE 38","type":"related"},{"name":"SPGF38","type":"related"}],"termid":"MONDO:0032748","xrefs":{"Monarch":{"xref_id":"0032748"}}}


id: GO:0001759
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The interaction of two or more cells or tissues that causes them to change their fates and specify the development of an organ.","definition_xrefs":["ISBN:0878932437"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of animal organ formation","termid":"GO:0003156"},{"relation_name":"is_a","term_name":"developmental induction","termid":"GO:0031128"},{"relation_name":"is_a","term_name":"positive regulation of animal organ morphogenesis","termid":"GO:0110110"},{"relation_name":"positively_regulates","term_name":"specification of animal organ identity","termid":"GO:0010092"}],"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":"organ induction","synonyms":[{"name":"induction of an organ","type":"exact"}],"termid":"GO:0001759"}


id: GO:0140255
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cellular response to phosphate starvation.","definition_xrefs":["PMID:29414789"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of response to nutrient levels","termid":"GO:0032107"},{"relation_name":"is_a","term_name":"regulation of cellular response to stress","termid":"GO:0080135"},{"relation_name":"regulates","term_name":"cellular response to phosphate starvation","termid":"GO:0016036"}],"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 cellular response to phosphate starvation","termid":"GO:0140255"}


id: FYPO:0002387
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 heterochromatin at subtelomeres is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to heterochromatin during vegetative growth","termid":"FYPO:0002385"},{"relation_name":"is_a","term_name":"decreased protein localization to telomere","termid":"FYPO:0003803"},{"relation_name":"is_a","term_name":"decreased protein localization to subtelomeric heterochromatin","termid":"FYPO:0005918"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0000138","FYPO:0005447","FYPO:0001320"],"is_obsolete":false,"name":"decreased protein localization to subtelomeric heterochromatin during vegetative growth","synonyms":[{"name":"decreased protein localisation to heterochromatin at subtelomere during vegetative growth","type":"exact"},{"name":"decreased protein localization to heterochromatin at subtelomere during vegetative growth","type":"exact"},{"name":"decreased protein localization to subtelomeric heterochromatin during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to telomeric heterochromatin during vegetative growth","type":"related"},{"name":"reduced protein localization to subtelomeric heterochromatin during vegetative growth","type":"exact"}],"termid":"FYPO:0002387"}


id: PBO:0062896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"3-oxoacid CoA-transferase 2","termid":"PBO:0062896"}


id: GO:0044651
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of a symbiont to a host epithelial cell via adhesion molecules, general stickiness etc., either directly or indirectly.","definition_xrefs":["GOC:jl","PMID:10066176"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adhesion of symbiont to host cell","termid":"GO:0044650"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"adhesion of symbiont to host epithelial cell","termid":"GO:0044651"}


id: PBO:0078838
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Pro (anticodon TGG) 3-2","termid":"PBO:0078838"}


id: SO:0001417
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A flanking region located three prime of a specific region.","definition_xrefs":["SO:chado"],"direct_ancestors":[{"relation_name":"is_a","term_name":"flanking_region","termid":"SO:0000239"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"three_prime_flanking_region","synonyms":[{"name":"3' flanking region","type":"related"},{"name":"three prime flanking region","type":"exact"}],"termid":"SO:0001417"}


id: PBO:0050272
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HMGN3 antisense RNA 1","termid":"PBO:0050272"}


id: PBO:0000366
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally represses fip1","termid":"PBO:0000366"}


id: PBO:0040355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit g pseudogene 4","termid":"PBO:0040355"}


id: PBO:0085367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Phosphorylated protein of the mitochondrial outer membrane; localizes only to mitochondria of the bud; interacts with Myo2p to mediate mitochondrial distribution to buds; mRNA is targeted to the bud via the transport system involving She2p","termid":"PBO:0085367"}


id: GO:0140724
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the rate, frequency or extent of the chemical reactions and pathways resulting in the formation of patulin.","definition_xrefs":["PMID:25625822"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of polyketide biosynthetic process","termid":"GO:1900734"},{"relation_name":"is_a","term_name":"positive regulation of alcohol biosynthetic process","termid":"GO:1902932"},{"relation_name":"positively_regulates","term_name":"patulin biosynthetic process","termid":"GO:0140723"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0019748"],"is_obsolete":false,"name":"positive regulation of patulin biosynthetic process","synonyms":[{"name":"positive regulation of patulin anabolism","type":"exact"},{"name":"positive regulation of patulin formation","type":"exact"},{"name":"positive regulation of patulin synthesis","type":"exact"}],"termid":"GO:0140724"}


id: PBO:0052475
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"kelch domain containing 1","termid":"PBO:0052475"}


id: MOD:00791
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-glutamine residue to L-glutamic acid with one (18)O.","definition_xrefs":["PubMed:8382902","Unimod:366#Q"],"direct_ancestors":[{"relation_name":"is_a","term_name":"deamidated L-glutamine","termid":"MOD:00685"},{"relation_name":"is_a","term_name":"1x(18)O labeled deamidated residue","termid":"MOD:00852"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1x(18)O labeled deamidated L-glutamine","synonyms":[{"name":"Deamidated:18O(1)","type":"related"},{"name":"Deamidation in presence of O18","type":"related"}],"termid":"MOD:00791"}


id: PBO:0089689
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vacuolar dipeptidyl peptidase","termid":"PBO:0089689"}


id: PBO:0032714
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_error-free_translesion_synthesis","termid":"PBO:0032714"}


id: FYPO:0008284
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of myo-inositol in a cell is normal when the cell is in the vegetative growth phase of the life cycle.","direct_ancestors":[{"relation_name":"is_a","term_name":"normal level of substance in cell during vegetative growth","termid":"FYPO:0001316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000002","FYPO:0000257","FYPO:0001320"],"is_obsolete":false,"name":"normal cellular myo-inositol level","termid":"FYPO:0008284"}


id: FYPO:0007238
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of two crossovers within a given interval during meiosis I is higher than normal.","definition_xrefs":["PomBase:mah","PMID:30217891"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiotic recombination","termid":"FYPO:0000008"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000293"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000293"],"is_obsolete":false,"name":"increased meiotic double crossover formation","synonyms":[{"name":"decreased crossover interference","type":"exact"}],"termid":"FYPO:0007238"}


id: GO:0060749
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The progression of the mammary gland alveolus over time, from its formation to its mature state. The mammary gland alveolus is a sac-like structure that is found in the mature gland.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure development","termid":"GO:0048856"},{"relation_name":"part_of","term_name":"mammary gland lobule development","termid":"GO:0061377"}],"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":"mammary gland alveolus development","termid":"GO:0060749"}


id: GO:0035708
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The switching of activated B cells from IgM biosynthesis to IgE biosynthesis, accomplished through a recombination process involving an intrachromosomal deletion between switch regions that reside 5' of the IgM and IgE constant region gene segments in the immunoglobulin heavy chain locus, that is dependent on the activity of interleukin 4 (IL-4).","definition_xrefs":["GOC:BHF","PMID:12496423"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isotype switching to IgE isotypes","termid":"GO:0048289"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006259"},{"rel_name":"is_a","termid":"GO:0006310"}],"interesting_parent_ids":["GO:0010467","GO:0006259","GO:0008150","GO:0006310"],"is_obsolete":false,"name":"interleukin-4-dependent isotype switching to IgE isotypes","synonyms":[{"name":"IL-4-dependent isotype switching to IgE isotypes","type":"exact"}],"termid":"GO:0035708"}


id: MONDO:0013021
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoinflammatory disease caused by mutations in the IL1RN gene, which encodes the IL1 receptor antagonist. It presents in infancy, and is characterized by systemic inflammation, pustular rash, bone pain, sterile osteitis, and periostitis.","definition_xrefs":["NCIT:C119056"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic recurrent multifocal osteomyelitis","termid":"MONDO:0009813"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"sterile multifocal osteomyelitis with periostitis and pustulosis","secondary_identifiers":["UMLS:C2748507","OMIM:612852","MEDGEN:411230","NANDO:2200439","MESH:C557815","GARD:10516","Orphanet:210115"],"synonyms":[{"name":"DIRA","type":"exact"},{"name":"Interleukin 1 receptor antagonist deficiency","type":"related"},{"name":"Interleukin-1 receptor antagonist deficiency","type":"exact"},{"name":"OMPP","type":"exact"},{"name":"autoinflammatory disease due to interleukin-1 receptor antagonist deficiency","type":"exact"},{"name":"deficiency of interleukin-1 receptor antagonist","type":"related"},{"name":"deficiency of the Interleukin-1 receptor antagonist","type":"exact"},{"name":"osteomyelitis, STERILE multifocal, with periostitis and pustulosis","type":"related"}],"termid":"MONDO:0013021","xrefs":{"Monarch":{"xref_id":"0013021"}}}


id: PBO:0072969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"secretoglobin family 1C member 1","termid":"PBO:0072969"}


id: PBO:0089800
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pig-U, Gab1","termid":"PBO:0089800"}


id: GO:0032877
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of DNA endoreduplication.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA endoreduplication","termid":"GO:0032875"},{"relation_name":"is_a","term_name":"positive regulation of cell cycle process","termid":"GO:0090068"},{"relation_name":"is_a","term_name":"positive regulation of DNA-templated DNA replication","termid":"GO:2000105"},{"relation_name":"positively_regulates","term_name":"DNA endoreduplication","termid":"GO:0042023"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006259"},{"rel_name":"regulates","termid":"GO:0006260"},{"rel_name":"positively_regulates","termid":"GO:0007049"},{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"positively_regulates","termid":"GO:0006260"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006259","GO:0008150","GO:0007049","GO:0006260"],"is_obsolete":false,"name":"positive regulation of DNA endoreduplication","synonyms":[{"name":"activation of DNA endoreduplication","type":"narrow"},{"name":"positive regulation of DNA endoreplication","type":"exact"},{"name":"positive regulation of DNA re-duplication","type":"exact"},{"name":"stimulation of DNA endoreduplication","type":"narrow"},{"name":"up regulation of DNA endoreduplication","type":"exact"},{"name":"up-regulation of DNA endoreduplication","type":"exact"},{"name":"upregulation of DNA endoreduplication","type":"exact"}],"termid":"GO:0032877"}


id: PBO:0084601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Merged open reading frame; does not encode a discrete protein; YLR312C-B was originally annotated as an independent ORF, but as a result of a sequence change, it was merged with an adjacent ORF into a single reading frame, SPH1/YLR313C","termid":"PBO:0084601"}


id: PBO:0116307
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospho-2-dehydro-3-deoxyheptonate aldolase Aro4","termid":"PBO:0116307"}


id: PBO:0081703
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 624","termid":"PBO:0081703"}


id: PBO:0002125
data:
  {"annotation_feature_type":"gene","cv_name":"genome_org","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alternative transcripts","termid":"PBO:0002125"}


id: PBO:0043332
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"colorectal liver metastasis associated transcript 3","termid":"PBO:0043332"}


id: PBO:0070656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L7 pseudogene 27","termid":"PBO:0070656"}


id: PBO:0045995
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EP300 interacting inhibitor of differentiation 2B","termid":"PBO:0045995"}


id: GO:0030272
data:
  {"annotated_genes":["SJAG_01616"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[104073],"is_not":false,"summary":null,"term":"GO:0030272"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-formyltetrahydrofolate + ATP = 5,10-methenyltetrahydrofolate + ADP + H+ + phosphate.","definition_xrefs":["RHEA:10488","EC:6.3.3.2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cyclo-ligase activity","termid":"GO:0016882"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01616":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016874"],"is_obsolete":false,"name":"5-formyltetrahydrofolate cyclo-ligase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0019006","KEGG_REACTION:R02301","MetaCyc:5-FORMYL-THF-CYCLO-LIGASE-RXN","Reactome:R-HSA-6801342"],"synonyms":[{"name":"5,10-methenyltetrahydrofolate synthetase activity","type":"related"},{"name":"5-Formyltetrahydrofolate cyclodehydrase activity","type":"related"},{"name":"5-formyltetrahydrofolate cyclo-ligase (ADP-forming)","type":"related"},{"name":"5-formyltetrahydrofolate cyclodehydrase","type":"broad"},{"name":"formyltetrahydrofolic cyclodehydrase activity","type":"related"},{"name":"methenyl-THF synthetase activity","type":"related"}],"termid":"GO:0030272","terms_by_termid":{"GO:0030272":null}}


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


id: MONDO:0007874
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Langer-Giedon syndrome, also known as trichorhinophalangeal syndrome type 2, is a very rare, genetic, multiple congenital anomaly disorder characterized by bone abnormalities, distinctive facial features, multiple exostoses, and intellectual disability.","definition_xrefs":["Orphanet:502"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"partial deletion of the long arm of chromosome 8","termid":"MONDO:0016907"},{"relation_name":"is_a","term_name":"trichorhinophalangeal syndrome","termid":"MONDO:0017951"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0005093"],"is_obsolete":false,"name":"trichorhinophalangeal syndrome type II","secondary_identifiers":["MESH:D015826","GARD:7801","icd11.foundation:315453775","UMLS:C0023003","DOID:4998","OMIM:150230","SCTID:41069008","ICD9:759.89","NCIT:C75118","MEDGEN:6009","NORD:1788","MedDRA:10050638"],"synonyms":[{"name":"Giedion-Langer syndrome","type":"related"},{"name":"Langer Giedion syndrome","type":"related"},{"name":"Langer-Giedion syndrome","type":"exact"},{"name":"TRPS 2","type":"related"},{"name":"TRPS2","type":"related"},{"name":"chromosome 8Q24.1 deletion syndrome","type":"related"},{"name":"deletion 8q24.1","type":"exact"},{"name":"monosomy 8q24.1","type":"exact"},{"name":"trichorhinophalangeal dysplasia type II","type":"exact"},{"name":"trichorhinophalangeal syndrome type 2","type":"exact"},{"name":"trichorhinophalangeal syndrome, type 2","type":"related"},{"name":"trichorhinophalangeal syndrome, type II","type":"related"}],"termid":"MONDO:0007874","xrefs":{"Monarch":{"xref_id":"0007874"}}}


id: PBO:0029930
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_5-phosphoribose_1-diphosphate_binding","termid":"PBO:0029930"}


id: MONDO:0100458
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any syndrome in which the cause of the disease is a mutation in the MECOM gene. MECOM-associated syndrome has a variable phenotypic pattern, ranging from isolated radioulnar synostosis with no or mild hematological involvement to severe bone marrow failure without obvious skeletal abnormalities. The clinical picture can also include clinodactyly, cardiac and renal malformations, B-cell deficiency, amegakaryocytic thrombocytopenia, and presenile hearing loss.","definition_xrefs":["PMID:29540340"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MECOM-associated syndrome","termid":"MONDO:0100458","xrefs":{"Monarch":{"xref_id":"0100458"}}}


id: PBO:0089472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WIP family cytoskeletal protein Bbc1","termid":"PBO:0089472"}


id: PBO:0028330
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_rDNA_separation","termid":"PBO:0028330"}


id: MONDO:0013042
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"atypical hemolytic uremic syndrome with complement gene abnormality","termid":"MONDO:0035290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"atypical hemolytic-uremic syndrome with B factor anomaly","secondary_identifiers":["Orphanet:93578","UMLS:C2752038","GARD:18554","OMIM:612924","MEDGEN:416691"],"synonyms":[{"name":"AHUS4","type":"related"},{"name":"D-HUS with B factor anomaly","type":"exact"},{"name":"aHUS with B factor anomaly","type":"exact"},{"name":"aHUS, susceptibility to, 4","type":"related"},{"name":"aHUS4","type":"related"},{"name":"atypical HUS with B factor anomaly","type":"exact"},{"name":"hemolytic uremic syndrome, atypical, susceptibility to, 4","type":"related"},{"name":"hemolytic uremic syndrome, atypical, susceptibility to, type 4","type":"exact"},{"name":"hemolytic-uremic syndrome without diarrhea with B factor anomaly","type":"exact"},{"name":"hemolytic-uremic syndrome without diarrhoea with B factor anomaly","type":"exact"},{"name":"susceptibility to atypical hemolytic uremic syndrome 4","type":"related"}],"termid":"MONDO:0013042","xrefs":{"Monarch":{"xref_id":"0013042"}}}


id: FYPO:0003832
data:
  {"alleles_by_uniquename":{"SJAG_00601:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00601","name":"rip1delta","uniquename":"SJAG_00601:allele-1"},"SJAG_01355:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01355","name":"cox6delta","uniquename":"SJAG_01355:allele-1"},"SJAG_04883:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04883","name":"ptp4delta","uniquename":"SJAG_04883:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[118676],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001007"},{"annotations":[118928,118925],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0000590"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which cell cycle progression is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process","termid":"FYPO:0000627"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00601":null,"SJAG_01355":null,"SJAG_04883":null},"genotype_count":3,"genotypes_by_uniquename":{"cox6delta":{"display_name":"cox6delta","display_uniquename":"cox6delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01355:allele-1","expression":"Null"}]}]},"ptp4delta":{"display_name":"ptp4delta","display_uniquename":"ptp4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04883:allele-1","expression":"Null"}]}]},"rip1delta":{"display_name":"rip1delta","display_uniquename":"rip1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00601:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal cell cycle","references_by_uniquename":{"PMID:36695178":null,"PMID:37164017":null},"single_locus_annotated_genes":["SJAG_01355","SJAG_04883","SJAG_00601"],"single_locus_genotype_uniquenames":["rip1delta","ptp4delta","cox6delta"],"synonyms":[{"name":"cell cycle progression: normal","type":"related"},{"name":"normal cell cycle progression","type":"exact"},{"name":"normal cell-division cycle","type":"exact"}],"termid":"FYPO:0003832","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0000590":null,"FYPO:0001007":null}}


id: PBO:0038733
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin like 6B","termid":"PBO:0038733"}


id: MONDO:0014458
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Fanconi syndrome in which the cause of the disease is a mutation in the HNF4A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maturity-onset diabetes of the young","termid":"MONDO:0018911"},{"relation_name":"is_a","term_name":"inherited Fanconi renotubular syndrome","termid":"MONDO:0100238"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005015"},{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005240"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0019254"},{"rel_name":"is_a","termid":"MONDO:0037792"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005240","MONDO:0005066","MONDO:0019254","MONDO:0005015","MONDO:0037792"],"is_obsolete":false,"name":"Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young","secondary_identifiers":["MEDGEN:863399","GARD:16048","OMIM:616026","UMLS:C4014962","DOID:0080760"],"synonyms":[{"name":"FRTS4","type":"related"},{"name":"FRTS4 with MODY","type":"related"},{"name":"Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young","type":"exact"},{"name":"Fanconi syndrome caused by mutation in HNF4A","type":"exact"},{"name":"HNF4A Fanconi syndrome","type":"exact"},{"name":"fanconi renotubular syndrome 4, with maturity-onset diabetes of the young","type":"exact"}],"termid":"MONDO:0014458","xrefs":{"Monarch":{"xref_id":"0014458"}}}


id: MONDO:0001194
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rickettsialpox (obsolete MONDO:0001194)","termid":"MONDO:0001194","xrefs":{"Monarch":{"xref_id":"0001194"}}}


id: MONDO:0018077
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tularemia is an infection caused by the bacterium Francisella tularensis. It is more common in rodents and rabbits but has been found in other animals including domestic cats, sheep, birds, and hamsters. Humans can become infected in several different ways: by handling infected animals, through tick or deer fly bites, by drinking contaminated water, or by inhaling contaminated dust or aerosols. Person-to-person transmission has not been reported. The type of tularemia and the particular signs and symptoms vary depending on how the bacteria enter the body. However, fever is seen in most cases. Though tularemia can be life-threatening, most infections can be treated with antibiotics.","direct_ancestors":[{"relation_name":"is_a","term_name":"primary bacterial infectious disease","termid":"MONDO:0000314"},{"relation_name":"is_a","term_name":"vector-borne disease","termid":"MONDO:0100120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tularemia","secondary_identifiers":["SCTID:19265001","DOID:2123","GARD:396","ICD10CM:A21","MedDRA:10045146","ICD9:021.9","NORD:1803","NCIT:C85208","Orphanet:3392","EFO:1001444","MEDGEN:22520","MESH:D014406","UMLS:C0041351","ICD9:021.8"],"synonyms":[{"name":"Deerfly fever","type":"related"},{"name":"Francisella tularensis caused disease or disorder","type":"exact"},{"name":"Francisella tularensis disease or disorder","type":"exact"},{"name":"Francisella tularensis infection","type":"related"},{"name":"Francisella tularensis infectious disease","type":"exact"},{"name":"Ohara disease","type":"related"},{"name":"Pahvant Valley plague","type":"related"},{"name":"Yatobyo (Japan)","type":"related"},{"name":"lemming fever","type":"related"},{"name":"rabbit fever","type":"related"}],"termid":"MONDO:0018077","xrefs":{"Monarch":{"xref_id":"0018077"}}}


id: GO:0015676
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of vanadium (V) ions into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transition metal ion transport","termid":"GO:0000041"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0051179","GO:0006810","GO:0008150"],"is_obsolete":false,"name":"vanadium ion transport","termid":"GO:0015676"}


id: FYPO:0004130
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of succinate dehydrogenase (ubiquinone) activity is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased oxidoreductase activity","termid":"FYPO:0000690"},{"relation_name":"is_a","term_name":"abnormal succinate dehydrogenase (ubiquinone) activity","termid":"FYPO:0003322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000707","FYPO:0000654","FYPO:0000661","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"decreased succinate dehydrogenase (ubiquinone) activity","synonyms":[{"name":"reduced succinate dehydrogenase (ubiquinone) activity","type":"exact"}],"termid":"FYPO:0004130"}


id: MONDO:1011925
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder, non-human animal","termid":"MONDO:0700104"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"},{"relation_name":"is_a","term_name":"syndromic disease, non-human animal","termid":"MONDO:1011360"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"primary ciliary dyskinesia, non-human animal","secondary_identifiers":["OMIA:000573"],"termid":"MONDO:1011925","xrefs":{"Monarch":{"xref_id":"1011925"}}}


id: MONDO:0015067
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the colon.","definition_xrefs":["NCIT:C135212"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system neuroendocrine tumor, grade 1/2","termid":"MONDO:0000386"},{"relation_name":"is_a","term_name":"colon neuroendocrine neoplasm","termid":"MONDO:0002882"},{"relation_name":"is_a","term_name":"epithelial tumor of colon","termid":"MONDO:0024479"}],"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":"neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor","secondary_identifiers":["MEDGEN:1617490","UMLS:C4525742"],"synonyms":[{"name":"NET of the colon","type":"exact"},{"name":"carcinoid tumor of colon","type":"broad"},{"name":"carcinoid tumour of colon","type":"broad"},{"name":"colon neuroendocrine tumor","type":"broad"},{"name":"colon neuroendocrine tumour","type":"broad"},{"name":"colonic NET","type":"exact"},{"name":"neuroendocrine neoplasm of the colon","type":"broad"}],"termid":"MONDO:0015067","xrefs":{"Monarch":{"xref_id":"0015067"}}}


id: PBO:0034552
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_cellular_inositol_phosphorylceramide_level","termid":"PBO:0034552"}


id: MONDO:1010813
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Polydactyly that occurs in horse.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polydactyly, non-human animal","termid":"MONDO:1010158"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polydactyly, horse","secondary_identifiers":["OMIA:000810-9796"],"termid":"MONDO:1010813","xrefs":{"Monarch":{"xref_id":"1010813"}}}


id: GO:0010264
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of phytic acid, myo-inositol hexakisphosphate, a regulator of intracellular signaling, a highly abundant animal anti-nutrient and a phosphate and mineral storage compound in plant seeds.","definition_xrefs":["PMID:16107538"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inositol phosphate biosynthetic process","termid":"GO:0032958"},{"relation_name":"is_a","term_name":"myo-inositol hexakisphosphate metabolic process","termid":"GO:0033517"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"myo-inositol hexakisphosphate biosynthetic process","synonyms":[{"name":"myo-inositol hexakisphosphate anabolism","type":"exact"},{"name":"myo-inositol hexakisphosphate biosynthesis","type":"exact"},{"name":"myo-inositol hexakisphosphate formation","type":"exact"},{"name":"myo-inositol hexakisphosphate synthesis","type":"exact"},{"name":"phytate biosynthesis","type":"exact"},{"name":"phytate biosynthetic process","type":"exact"}],"termid":"GO:0010264"}


id: PBO:0113418
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding protein that associates with polysomes; may be involved in regulating mRNA translation; involved in the copper-dependent mineralization of copper sulfide complexes on cell surface in cells cultured in copper salts; role in preventing L-A mycovirus pathogenesis; SLF1 has a paralog, SRO9, that arose from the whole genome duplication; protein abundance increases in response to DNA replication stress","termid":"PBO:0113418"}


id: PBO:0044446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome P450 family 4 subfamily F member 24, pseudogene","termid":"PBO:0044446"}


id: MONDO:0007960
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete megacystis-microcolon-intestinal hypoperistalsis syndrome (obsolete MONDO:0007960)","secondary_identifiers":["NANDO:2200947","NANDO:1200459"],"termid":"MONDO:0007960","xrefs":{"Monarch":{"xref_id":"0007960"}}}


id: FYPO:0002074
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which none of the cells in the population are viable at a high temperature.","definition_xrefs":["PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable cell population at high temperature (obsolete FYPO:0002074)","termid":"FYPO:0002074"}


id: GO:0044657
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The aggregation, arrangement and bonding together of a set of components by an organism to form a pore complex in a membrane of another organism, occurring as part of a symbiotic interaction.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete pore formation in membrane of other organism during symbiotic interaction (obsolete GO:0044657)","termid":"GO:0044657"}


id: GO:0006199
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete ADP reduction (obsolete GO:0006199)","synonyms":[{"name":"ADP reduction","type":"exact"}],"termid":"GO:0006199"}


id: GO:0065003
data:
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id: PBO:0047904
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id: PBO:0017917
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id: PBO:0003231
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id: PBO:0113015
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id: PR:Q9UTB3
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id: MONDO:0800294
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id: PBO:0053570
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id: MONDO:0006372
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id: GO:0034748
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id: PBO:0000751
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id: PBO:0075181
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id: GO:0160196
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id: GO:0034089
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the sister chromatids of a replicated chromosome become joined along the entire length of the chromosome during S phase during a meiotic cell cycle.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"establishment of sister chromatid cohesion","termid":"GO:0034085"},{"relation_name":"part_of","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:0008150","GO:0007049"],"is_obsolete":false,"name":"establishment of meiotic sister chromatid cohesion","termid":"GO:0034089"}


id: GO:0050142
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 6 reduced flavodoxin + 6 H+ + N2 + n ATP = 6 oxidized flavodoxin + 2 NH3 + n ADP + n phosphate.","definition_xrefs":["EC:1.19.6.1","MetaCyc:NITROGENASE-FLAVODOXIN-RXN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on reduced flavodoxin as donor, dinitrogen as acceptor","termid":"GO:0016738"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"nitrogenase (flavodoxin) activity","secondary_identifiers":["RHEA:15645"],"synonyms":[{"name":"reduced flavodoxin:dinitrogen oxidoreductase (ATP-hydrolysing)","type":"related"}],"termid":"GO:0050142"}


id: GO:0106144
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalyzes the reaction fraxetin+ NAD(P)H + 02= sideretin + NAD(P)(+) + H20.","definition_xrefs":["PMID:29581584","RHEA:57844","GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"fraxetin 5-hydroxylase activity","secondary_identifiers":["EC:1.14.14.164"],"termid":"GO:0106144"}


id: PBO:0011985
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"although this is demonstrated to be DNA polymerase epsilon interactor and names Dpb3, it appears to be the ortholog of S. cerevisie BUR6 and human DRAP1 (supported by PSIblast/ Treefam). The real Dpb3 appears to be the newly identified SPCC16C4.22 see Treefam:TF103009","termid":"PBO:0011985"}


id: GO:0019368
data:
  {"annotated_genes":["SJAG_01356","SJAG_02885"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91449,89017],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034625"}]},"cv_name":"biological_process","definition":"Elongation of a fatty acid chain into which one or more C-C double bonds have been introduced.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fatty acid elongation","termid":"GO:0030497"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01356":null,"SJAG_02885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"fatty acid elongation, unsaturated fatty acid","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["MetaCyc:PWY0-862"],"termid":"GO:0019368","terms_by_termid":{"GO:0034625":null}}


id: PBO:0053516
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 506","termid":"PBO:0053516"}


id: PBO:0044367
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cytochrome c, testis, pseudogene","termid":"PBO:0044367"}


id: PBO:0003850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mediator complex subunit Pmc1","termid":"PBO:0003850"}


id: SO:0001544
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A transcript processing variant whereby the process of editing is disrupted with respect to the reference.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transcript_processing_variant","termid":"SO:0001543"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"editing_variant","synonyms":[{"name":"editing variant","type":"exact"}],"termid":"SO:0001544"}


id: PBO:0090558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EKC/KEOPS complex N(6)-L-threonylcarbamoyladenine synthase subunit","termid":"PBO:0090558"}


id: MONDO:0700037
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare testicular sex cord-stromal neoplasm characterized by mixed features of both fibroma and thecoma.","definition_xrefs":["PMID:23715159","PMID:33102067"],"direct_ancestors":[{"relation_name":"is_a","term_name":"testicular sex cord-stromal neoplasm","termid":"MONDO:0003125"},{"relation_name":"is_a","term_name":"fibrothecoma","termid":"MONDO:0700036"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testicular fibrothecoma","termid":"MONDO:0700037","xrefs":{"Monarch":{"xref_id":"0700037"}}}


id: PBO:0066602
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ras homolog family member T1 pseudogene 1","termid":"PBO:0066602"}


id: PBO:0087270
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ser/Thr protein kinase; regulates the organization and function of the actin cytoskeleton; inhibits clathrin-mediated endocytosis; phosphorylates the Pan1p and Sla1p subunits of the Pan1p-Sla1p-End3p complex, resulting in inhibition of complex formation; inhibits Scd5p through phosphorylation; phosphorylates Pan1p-interacting proteins, Ent1/2 and Yap1801/2; negatively regulated through autophosphorylation; functional overlap with ARK1","termid":"PBO:0087270"}


id: PBO:0089466
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane sensing transcription coactivator, ankyrin repeat containing Mga2","termid":"PBO:0089466"}


id: GO:0061815
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the hydrolysis of ubiquitin units from Met1-linked (or linear) polyubiquitin chains.","definition_xrefs":["PMID:26503766","GOC:dph","PMID:27702987"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cysteine-type deubiquitinase activity","termid":"GO:0004843"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008233"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0003824","GO:0008233","GO:0003674","GO:0016787"],"is_obsolete":false,"name":"Met1-linked polyubiquitin deubiquitinase activity","secondary_identifiers":["Reactome:R-HSA-9818975"],"synonyms":[{"name":"Met1 linkage specific DUB","type":"exact"},{"name":"cysteine-type deubiquitinase activity, acting on linear ubiquitin","type":"exact"},{"name":"deubiquitinase, acting on linear ubiquitin","type":"broad"},{"name":"linear ubiquitin specific deubiquitinase activity","type":"exact"},{"name":"ubiquitinyl hydrolase activity, acting on linear ubiquitin","type":"exact"}],"termid":"GO:0061815"}


id: PBO:0065409
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"proteasome 20S subunit alpha 7","termid":"PBO:0065409"}


id: GO:0022413
data:
  {"annotated_genes":["SJAG_00974","SJAG_01943","SJAG_03915","SJAG_04238","SJAG_02079","SJAG_00073","SJAG_04236","SJAG_00486","SJAG_01068","SJAG_03057","SJAG_04140","SJAG_02712","SJAG_00971","SJAG_03997","SJAG_00399","SJAG_02248","SJAG_05309","SJAG_02724","SJAG_02878","SJAG_01076","SJAG_00247","SJAG_04853","SJAG_03221","SJAG_04275","SJAG_02460","SJAG_03557","SJAG_02828","SJAG_02401","SJAG_03688","SJAG_03013","SJAG_04982","SJAG_03097","SJAG_01495","SJAG_04615","SJAG_02320","SJAG_02226","SJAG_04184","SJAG_01410","SJAG_01465","SJAG_03483","SJAG_04080","SJAG_02169","SJAG_00663","SJAG_01531","SJAG_00405","SJAG_00826","SJAG_00757","SJAG_01483","SJAG_03250","SJAG_04922","SJAG_01601","SJAG_03536","SJAG_04887","SJAG_04010","SJAG_04271","SJAG_03090","SJAG_04483","SJAG_04901","SJAG_01662","SJAG_03746","SJAG_03587","SJAG_02556","SJAG_00993","SJAG_04859","SJAG_02241","SJAG_02924","SJAG_04470","SJAG_01321","SJAG_02529","SJAG_00114","SJAG_05239","SJAG_04781","SJAG_00821","SJAG_01677","SJAG_02351","SJAG_00870","SJAG_02319","SJAG_01419","SJAG_04868","SJAG_01769","SJAG_02736"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[112151,104592,96439,103611,110962,96371,107183,109570,100218,113370,117968,94872,96023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0030437"},{"annotations":[93969],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034413"},{"annotations":[91278,89760,88219,87726],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0030476"},{"annotations":[108759],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034412"},{"annotations":[117221,103654,108532,113525,117229],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070591"},{"annotations":[108760,104443,91010,109571,97088],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031321"},{"annotations":[98330,90800,104758,99329,109572,94873,113371,118449,118268,97050,97089,99398,116370,99328,101200,117969,106850],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032120"},{"annotations":[96372,102405,91802,99330,113372,106298,97051,107184,103612,99331],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0031322"},{"annotations":[92018,97222],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0000755"},{"annotations":[116292,87445,118277,98623],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007535"},{"annotations":[116244,106099,109756,100071,96928,118196,114463,98624,95677,110272,88805,87446,105535,107974,88677],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0007534"},{"annotations":[92182,118197,98626,109757,95678,98561,110273,96153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007533"},{"annotations":[102709,107975,102440,93585],"is_not":false,"rel_names":["part_of","is_a"],"summary":null,"term":"GO:0071515"},{"annotations":[110651],"is_not":false,"rel_names":["regulates","negatively_regulates"],"summary":null,"term":"GO:0075297"},{"annotations":[91863,95870,94793,100690,109652],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0032220"},{"annotations":[101779],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0075296"},{"annotations":[90242],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1903024"},{"annotations":[91697],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0034307"},{"annotations":[92857],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071171"},{"annotations":[115415,99332,99333,94010,105479,99610],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070583"}]},"cv_name":"biological_process","definition":"A process, occurring at the cellular level, that is involved in the reproductive function of a single-celled organism.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"reproductive process","termid":"GO:0022414"}],"gene_count":81,"genes_by_uniquename":{"SJAG_00073":null,"SJAG_00114":null,"SJAG_00247":null,"SJAG_00399":null,"SJAG_00405":null,"SJAG_00486":null,"SJAG_00663":null,"SJAG_00757":null,"SJAG_00821":null,"SJAG_00826":null,"SJAG_00870":null,"SJAG_00971":null,"SJAG_00974":null,"SJAG_00993":null,"SJAG_01068":null,"SJAG_01076":null,"SJAG_01321":null,"SJAG_01410":null,"SJAG_01419":null,"SJAG_01465":null,"SJAG_01483":null,"SJAG_01495":null,"SJAG_01531":null,"SJAG_01601":null,"SJAG_01662":null,"SJAG_01677":null,"SJAG_01769":null,"SJAG_01943":null,"SJAG_02079":null,"SJAG_02169":null,"SJAG_02226":null,"SJAG_02241":null,"SJAG_02248":null,"SJAG_02319":null,"SJAG_02320":null,"SJAG_02351":null,"SJAG_02401":null,"SJAG_02460":null,"SJAG_02529":null,"SJAG_02556":null,"SJAG_02712":null,"SJAG_02724":null,"SJAG_02736":null,"SJAG_02828":null,"SJAG_02878":null,"SJAG_02924":null,"SJAG_03013":null,"SJAG_03057":null,"SJAG_03090":null,"SJAG_03097":null,"SJAG_03221":null,"SJAG_03250":null,"SJAG_03483":null,"SJAG_03536":null,"SJAG_03557":null,"SJAG_03587":null,"SJAG_03688":null,"SJAG_03746":null,"SJAG_03915":null,"SJAG_03997":null,"SJAG_04010":null,"SJAG_04080":null,"SJAG_04140":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04238":null,"SJAG_04271":null,"SJAG_04275":null,"SJAG_04470":null,"SJAG_04483":null,"SJAG_04615":null,"SJAG_04781":null,"SJAG_04853":null,"SJAG_04859":null,"SJAG_04868":null,"SJAG_04887":null,"SJAG_04901":null,"SJAG_04922":null,"SJAG_04982":null,"SJAG_05239":null,"SJAG_05309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"reproductive process in single-celled organism","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0022413","terms_by_termid":{"GO:0000755":null,"GO:0007533":null,"GO:0007534":null,"GO:0007535":null,"GO:0030437":null,"GO:0030476":null,"GO:0031321":null,"GO:0031322":null,"GO:0032120":null,"GO:0032220":null,"GO:0034307":null,"GO:0034412":null,"GO:0034413":null,"GO:0070583":null,"GO:0070591":null,"GO:0071171":null,"GO:0071515":null,"GO:0075296":null,"GO:0075297":null,"GO:1903024":null}}


id: GO:0016250
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-sulfo-D-glucosamine + H2O = D-glucosamine + sulfate.","definition_xrefs":["EC:3.10.1.1"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on acid sulfur-nitrogen bonds","termid":"GO:0016826"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"N-sulfoglucosamine sulfohydrolase activity","secondary_identifiers":["Reactome:R-HSA-9036050","RHEA:17881","Reactome:R-HSA-2090043","Reactome:R-HSA-2263444","Reactome:R-HSA-1678708","MetaCyc:N-SULFOGLUCOSAMINE-SULFOHYDROLASE-RXN"],"synonyms":[{"name":"2-desoxy-D-glucoside-2-sulphamate sulphohydrolase (sulphamate sulphohydrolase)","type":"related"},{"name":"N-sulfo-D-glucosamine sulfohydrolase activity","type":"related"},{"name":"N-sulphoglucosamine sulphohydrolase activity","type":"exact"},{"name":"heparin sulfamidase activity","type":"related"},{"name":"sulfoglucosamine sulfamidase activity","type":"related"},{"name":"sulphamidase activity","type":"related"}],"termid":"GO:0016250"}


id: FYPO:0002842
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the centromere outer repeat regions of a chromosome is decreased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization to centromere during vegetative growth","termid":"FYPO:0000449"},{"relation_name":"is_a","term_name":"decreased protein localization to chromosome during vegetative growth","termid":"FYPO:0002839"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to centromere outer repeat","synonyms":[{"name":"decreased protein localisation to centromere outer repeat","type":"exact"},{"name":"decreased protein localisation to centromeric outer repeat region","type":"exact"},{"name":"decreased protein localization to centromere outer repeat during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to centromere outer repeat during vegetative growth","type":"exact"},{"name":"decreased protein localization to chromosome, centric outer repeat region","type":"exact"},{"name":"decreased protein localization to chromosome, centromeric outer repeat region","type":"exact"},{"name":"decreased protein localization to pericentric region","type":"related"},{"name":"decreased protein localization to pericentromeric region","type":"related"},{"name":"reduced protein localization to centromere outer repeat","type":"exact"}],"termid":"FYPO:0002842"}


id: PBO:0062773
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 55 subfamily B member 1 pseudogene","termid":"PBO:0062773"}


id: GO:0070102
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by interleukin-6 binding to a receptor on the surface of a target cell, and ending with the regulation of a downstream cellular process, e.g. transcription.","definition_xrefs":["GOC:signaling","GOC:BHF","GOC:mah","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine-mediated signaling pathway","termid":"GO:0019221"},{"relation_name":"part_of","term_name":"cellular response to interleukin-6","termid":"GO:0071354"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"interleukin-6-mediated signaling pathway","secondary_identifiers":["Reactome:R-HSA-1059683"],"synonyms":[{"name":"IL-6-mediated signaling pathway","type":"related"},{"name":"interleukin-6-mediated signalling pathway","type":"exact"}],"termid":"GO:0070102"}


id: PBO:0050382
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heterogeneous nuclear ribonucleoprotein A3 pseudogene 6","termid":"PBO:0050382"}


id: FYPO:0007144
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of deoxyribonuclease (pyrimidine dimer) activity is increased during a cellular response to ultraviolet light.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased phosphatase activity","termid":"FYPO:0004415"},{"relation_name":"is_a","term_name":"increased 5'-deoxyribonuclease (pyrimidine dimer) activity","termid":"FYPO:0007143"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001985","FYPO:0000002","FYPO:0000661","FYPO:0000654","FYPO:0000707","FYPO:0000652"],"is_obsolete":false,"name":"increased deoxyribonuclease (pyrimidine dimer) activity during cellular response to UV","synonyms":[{"name":"increased 5'-deoxyribonuclease (pyrimidine dimer) activity during cellular response to UV","type":"narrow"},{"name":"increased deoxyribonuclease (pyrimidine dimer) activity during cellular response to ultraviolet light","type":"exact"}],"termid":"FYPO:0007144"}


id: MONDO:0006763
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A painful inflammatory process leads to a mechanical block in active and passive range of motion (ROM) of the shoulder. Adhesive capsulitis of the shoulder is characterized by functional loss of passive and active shoulder motion. This inflammatory process results in fibroblastic proliferation and extensive scar tissue formation. Fibroblastic proliferation, a late phase of the inflammatory process involved in tissue repair, leads to thickening, fibrosis, and adhesion of the capsule to itself and the humerus.","definition_xrefs":["PMID:34772852"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"muscle tissue disorder","termid":"MONDO:0003939"},{"relation_name":"is_a","term_name":"arthropathy","termid":"MONDO:0006816"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"frozen shoulder","secondary_identifiers":["MEDGEN:90227","SCTID:399114005","DOID:14188","MESH:D002062","EFO:1000941","MedDRA:10017391","ICD9:726.0","UMLS:C0311223","ICD10CM:M75.0"],"synonyms":[{"name":"adhesions-capsulitis,shoulder","type":"exact"},{"name":"adhesive capsulitis","type":"exact"},{"name":"adhesive capsulitis of shoulder","type":"exact"}],"termid":"MONDO:0006763","xrefs":{"Monarch":{"xref_id":"0006763"}}}


id: PBO:0059555
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrially encoded tRNA-Trp (UGA/G)","termid":"PBO:0059555"}


id: PBO:0052625
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"keratin 4","termid":"PBO:0052625"}


id: PBO:0047490
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferrochelatase","termid":"PBO:0047490"}


id: PBO:0087963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Transporter; member of the ARN family of transporters that specifically recognize siderophore-iron chelates; responsible for uptake of iron bound to the siderophore triacetylfusarinine C","termid":"PBO:0087963"}


id: GO:0010444
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a meristemoid acquires the specialized features of a guard mother cell.","definition_xrefs":["GOC:expert_db","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plant epidermal cell differentiation","termid":"GO:0090627"},{"relation_name":"part_of","term_name":"stomatal lineage progression","termid":"GO:0010440"}],"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":"guard mother cell differentiation","termid":"GO:0010444"}


id: PBO:0048260
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"galactokinase 2","termid":"PBO:0048260"}


id: MONDO:0007528
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ehlers-Danlos syndrome, autosomal dominant, type unspecified","secondary_identifiers":["MESH:C562424","OMIM:130090","MEDGEN:65083","UMLS:C0220679"],"synonyms":[{"name":"EDS, unspecified type","type":"related"},{"name":"Ehlers-Danlos syndrome, Friedman-Harrod type","type":"related"},{"name":"Ehlers-Danlos syndrome, autosomal dominant, type unspecified","type":"exact"}],"termid":"MONDO:0007528","xrefs":{"Monarch":{"xref_id":"0007528"}}}


id: GO:0051282
data:
  {"annotated_genes":["SJAG_03850"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[108127],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061454"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the binding or confining calcium ions such that they are separated from other components of a biological system.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of localization","termid":"GO:0032879"},{"relation_name":"is_a","term_name":"regulation of cellular process","termid":"GO:0050794"},{"relation_name":"regulates","term_name":"sequestering of calcium ion","termid":"GO:0051208"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03850":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of sequestering of calcium ion","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of calcium ion (Ca2+) retention","type":"exact"},{"name":"regulation of calcium ion (Ca2+) sequestering","type":"exact"},{"name":"regulation of calcium ion (Ca2+) sequestration","type":"exact"},{"name":"regulation of calcium ion (Ca2+) storage","type":"exact"},{"name":"regulation of retention of calcium ion (Ca2+)","type":"exact"},{"name":"regulation of sequestering of calcium ion (Ca2+)","type":"exact"},{"name":"regulation of sequestration of calcium ion (Ca2+)","type":"exact"},{"name":"regulation of storage of calcium ion (Ca2+)","type":"exact"}],"termid":"GO:0051282","terms_by_termid":{"GO:0061454":null}}


id: PBO:0013767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"inorganic pyrophosphatase ipp1 (predicted)","termid":"PBO:0013767"}


id: GO:0009927
data:
  {"annotated_genes":["SJAG_00331","SJAG_06592"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[77296,111274],"is_not":false,"summary":null,"term":"GO:0009927"}]},"cv_name":"molecular_function","definition":"Serves as a phospho-His intermediate enabling the transfer of phospho group between a hybrid kinase and a response regulator.","definition_xrefs":["PMID:11842140","PMID:31386843"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein kinase activity","termid":"GO:0004672"},{"relation_name":"is_a","term_name":"molecular transducer activity","termid":"GO:0060089"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00331":null,"SJAG_06592":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0004672"},{"rel_name":"is_a","termid":"GO:0140096"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0140096","GO:0016301","GO:0016740","GO:0003824","GO:0004672","GO:0003674"],"is_obsolete":false,"name":"histidine phosphotransfer kinase activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0009927","terms_by_termid":{"GO:0009927":null}}


id: PBO:0063156
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"paired box 2","termid":"PBO:0063156"}


id: PBO:0108707
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RabGAP Gyp3","termid":"PBO:0108707"}


id: PBO:0049637
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 40","termid":"PBO:0049637"}


id: PBO:0065208
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRPF39 divergent transcript","termid":"PBO:0065208"}


id: PBO:0054885
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 2299","termid":"PBO:0054885"}


id: PBO:0028034
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_post-anaphase_microtubule_array_organization","termid":"PBO:0028034"}


id: PBO:0060040
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4 pseudogene 28","termid":"PBO:0060040"}


id: MONDO:0017838
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Sclerosteosis is a very rare serious sclerosing hyperostosis syndrome characterized clinically by variable syndactyly and progressive skeletal overgrowth (particularly of the skull), resulting in distinctive facial features (mandibular overgrowth, frontal bossing, midfacial hypoplasia), cranial nerve entrapment causing facial palsy and deafness, and potentially lethal elevation of intracranial pressure.","definition_xrefs":["Orphanet:3152"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete primary bone dysplasia with increased bone density (obsolete MONDO:0019703)","termid":"MONDO:0019703"},{"relation_name":"is_a","term_name":"hyperostosis","termid":"MONDO:0002185"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sclerosteosis","secondary_identifiers":["NANDO:2201369","GARD:4771","OMIMPS:269500","DOID:0060251","SCTID:17568006","ICD9:756.59","NCIT:C131133","UMLS:C0265301","MESH:C537525","icd11.foundation:371637416","MEDGEN:120530"],"synonyms":[{"name":"cortical hyperostosis with syndactyly","type":"exact"},{"name":"cortical hyperostosis-syndactyly syndrome","type":"exact"}],"termid":"MONDO:0017838","xrefs":{"Monarch":{"xref_id":"0017838"}}}


id: PBO:0054980
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 2394","termid":"PBO:0054980"}


id: GO:0097352
data:
  {"annotated_genes":["SJAG_02433","SJAG_03345","SJAG_02414","SJAG_02699","SJAG_06309"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[88772,89594,113088],"is_not":false,"summary":null,"term":"GO:0097352"},{"annotations":[94132],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0016240"},{"annotations":[97122],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:1901098"}]},"cv_name":"biological_process","definition":"Removal of PI3P and Atg8/LC3 after the closure of the phagophore and before the fusion with the endosome/lysosome (e.g. mammals and insects) or vacuole (yeast), and that very likely destabilizes other Atg proteins and thus enables their efficient dissociation and recycling.","definition_xrefs":["PMID:28077293","GOC:autophagy","GOC:lf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex disassembly","termid":"GO:0032984"},{"relation_name":"part_of","term_name":"macroautophagy","termid":"GO:0016236"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02414":null,"SJAG_02433":null,"SJAG_02699":null,"SJAG_03345":null,"SJAG_06309":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006914"}],"interesting_parent_ids":["GO:0006914","GO:0008150"],"is_obsolete":false,"name":"autophagosome maturation","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["GO:0000046"],"synonyms":[{"name":"autophagic vacuole fusion","type":"exact"},{"name":"autophagic vacuole maturation","type":"exact"},{"name":"autophagosome fusion","type":"related"}],"termid":"GO:0097352","terms_by_termid":{"GO:0016240":null,"GO:0097352":null,"GO:1901098":null}}


id: PBO:0001522
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mRNA cleavage and polyadenylation specificity factor complex subunit (predicted)","termid":"PBO:0001522"}


id: GO:1903606
data:
  {"annotated_genes":["SJAG_03199","SJAG_04008"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[93945,106944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903607"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving cytochrome c.","definition_xrefs":["GO_REF:0000068","GOC:TermGenie","PMID:19721088","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytochrome metabolic process","termid":"GO:1903604"}],"gene_count":2,"genes_by_uniquename":{"SJAG_03199":null,"SJAG_04008":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cytochrome c metabolic process","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"cytochrome c metabolism","type":"exact"}],"termid":"GO:1903606","terms_by_termid":{"GO:1903607":null}}


id: PBO:0059611
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ATP6 pseudogene 23","termid":"PBO:0059611"}


id: GO:0009500
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. (Was not defined before being made obsolete).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete dicluster bacterial-type ferredoxin (obsolete GO:0009500)","synonyms":[{"name":"dicluster bacterial-type ferredoxin","type":"exact"}],"termid":"GO:0009500"}


id: PomGeneEx:0000025
data:
  {"annotation_feature_type":"gene","cv_name":"PomGeneExRD","definition":"A qualifier that describes the fraction of ribosomes that are translating each codon of an mRNA, and reflects the average time spent by the ribosome on each codon.","definition_xrefs":["PMID:33313903","PMID:29432178","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"gene expression qualifier","termid":"PomGeneEx:0000001"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal density","synonyms":[{"name":"ribosome density","type":"exact"},{"name":"ribosome occupancy","type":"exact"}],"termid":"PomGeneEx:0000025"}


id: PBO:0050122
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"high mobility group box 1 pseudogene 32","termid":"PBO:0050122"}


id: GO:0034882
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: cis-aconitamide + H2O = cis-aconitate + HN3.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete cis-aconitamide amidase activity (obsolete GO:0034882)","termid":"GO:0034882"}


id: MONDO:0009925
data:
  {"annotated_genes":["SJAG_05213","SJAG_03785","SJAG_01344"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[84699,84700,84701],"is_not":false,"summary":null,"term":"MONDO:0009925"}]},"cv_name":"mondo","definition":"An autosomal recessive form of PXE.","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"excluded_subClassOf","term_name":"familial restrictive cardiomyopathy","termid":"MONDO:0016340"},{"relation_name":"excluded_subClassOf","term_name":"developmental defect during embryogenesis","termid":"MONDO:0019755"},{"relation_name":"excluded_subClassOf","term_name":"pseudoxanthoma elasticum (inherited or acquired)","termid":"MONDO:0024308"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"hereditary disorder of connective tissue","termid":"MONDO:0023603"},{"relation_name":"is_a","term_name":"inherited pseudoxanthoma elasticum","termid":"MONDO:0100091"}],"gene_count":3,"genes_by_uniquename":{"SJAG_01344":null,"SJAG_03785":null,"SJAG_05213":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive inherited pseudoxanthoma elasticum","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:698415","MESH:D011561","SCTID:402782006","NORD:1629","Orphanet:758","DOID:2738","MedDRA:10037150","NCIT:C85036","icd11.foundation:1516160852","OMIM:264800","SCTID:239140003","SCTID:72744008","UMLS:C1275116","ICD9:757.39"],"synonyms":[{"name":"AR inherited pseudoxanthoma elasticum","type":"exact"},{"name":"Gronblad Strandberg syndrome","type":"related"},{"name":"Gronblad-Strandberg syndrome","type":"exact"},{"name":"Gronblad-Strandberg-Touraine syndrome","type":"exact"},{"name":"PXE","type":"exact"},{"name":"PXE, modifier of severity of","type":"related"},{"name":"Pseudoxanthoma Elasticum","type":"exact"},{"name":"pseudoxanthoma elasticum","type":"related"},{"name":"pseudoxanthoma elasticum, modifier of severity of","type":"related"}],"termid":"MONDO:0009925","terms_by_termid":{"MONDO:0009925":null},"xrefs":{"Monarch":{"xref_id":"0009925"}}}


id: PBO:0065125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase D3","termid":"PBO:0065125"}


id: PBO:0056796
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"multifunctional ROCO family signaling regulator 1","termid":"PBO:0056796"}


id: GO:0004216
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of peptide bonds. Has a broad proteolytic activity. With small-molecule substrates and inhibitors, the major determinant of specificity is P2, which is preferably Leu, Met > Phe, and not Arg.","definition_xrefs":["EC:3.4.22.38"],"gene_count":0,"genotype_count":0,"name":"obsolete cathepsin K activity (obsolete GO:0004216)","synonyms":[{"name":"cathepsin K activity","type":"exact"},{"name":"cathepsin O activity","type":"related"},{"name":"cathepsin O2 activity","type":"related"},{"name":"cathepsin X activity","type":"related"}],"termid":"GO:0004216"}


id: PBO:0077306
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM44 antisense RNA 1","termid":"PBO:0077306"}


id: GO:1903729
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of plasma membrane organization.","definition_xrefs":["PMID:24514900","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cellular component organization","termid":"GO:0051128"},{"relation_name":"regulates","term_name":"plasma membrane organization","termid":"GO:0007009"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0061024"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0061024","GO:0008150"],"is_obsolete":false,"name":"regulation of plasma membrane organization","synonyms":[{"name":"regulation of plasma membrane organisation","type":"exact"},{"name":"regulation of plasma membrane organization and biogenesis","type":"related"}],"termid":"GO:1903729"}


id: PBO:0071983
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S6 pseudogene 12","termid":"PBO:0071983"}


id: GO:0042311
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An increase in the internal diameter of blood vessels, especially arterioles or capillaries, due to relaxation of smooth muscle cells that line the vessels, and usually resulting in a decrease in blood pressure.","definition_xrefs":["GOC:pr","ISBN:0192800981"],"direct_ancestors":[{"relation_name":"is_a","term_name":"blood vessel diameter maintenance","termid":"GO:0097746"}],"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":"vasodilation","secondary_identifiers":["GO:0045909","Wikipedia:Vasodilation"],"synonyms":[{"name":"positive regulation of blood vessel size","type":"exact"},{"name":"vasodilatation","type":"exact"}],"termid":"GO:0042311"}


id: FYPO:0005844
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the trimethylation of lysine at position 9 of histone H3 in silent mating-type cassettes does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone H3-K9 trimethylation during vegetative growth","termid":"FYPO:0000787"},{"relation_name":"is_a","term_name":"abolished histone H3-K9 methylation during vegetative growth","termid":"FYPO:0002566"},{"relation_name":"is_a","term_name":"abnormal histone methylation at silent mating-type cassette during vegetative growth","termid":"FYPO:0007373"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0002494","FYPO:0002274","FYPO:0001985","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abolished histone H3-K9 trimethylation at silent mating-type cassette during vegetative growth","synonyms":[{"name":"abolished histone H3 K9 trimethylation at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"abolished histone H3-K9 trimethylation at mating-type region heterochromatin during vegetative growth","type":"exact"},{"name":"abolished histone H3-K9 trimethylation at silent mating-type cassette during mitotic cell cycle","type":"related"},{"name":"abolished histone H3K9 trimethylation at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"abolished histone H3K9me3 at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"abolished histone lysine H3 K9 trimethylation at silent mating-type cassette during vegetative growth","type":"exact"},{"name":"abolished silent mating-type cassette histone H3-K9 trimethylation during vegetative growth","type":"exact"},{"name":"histone H3-K9 trimethylation abolished at silent mating-type cassette during vegetative growth","type":"exact"}],"termid":"FYPO:0005844"}


id: MONDO:0017050
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intraocular medulloepithelioma is a rare eye tumor characterized by a white, gray or yellow-colored cystic mass that arises from the primitive neuroectodermal, nonpigmented epithelium of the ciliary body, or occasionally from the optic nerve, optic disk, retina or iris. Typically it has a benign clinical course with good prognosis and generally presents with childhood onset of poor vision and pain, glaucoma, and/or cataract. Leukocoria, exotropia, exophthalmos, strabismus, epiphora, change in eye color, hyphema, and raised intraocular pressure are also remarkable manifestations.","definition_xrefs":["Orphanet:268139"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonal neoplasm","termid":"MONDO:0005564"},{"relation_name":"is_a","term_name":"eye neoplasm","termid":"MONDO:0021220"}],"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":"intraocular medulloepithelioma","secondary_identifiers":["NCIT:C66806","UMLS:C1883694","MEDGEN:408140","GARD:20945"],"synonyms":[{"name":"intraocular medulloepithelioma","type":"exact"},{"name":"orbital medulloepithelioma","type":"exact"}],"termid":"MONDO:0017050","xrefs":{"Monarch":{"xref_id":"0017050"}}}


id: FYPO:0007504
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which H3-K9 specific histone demethylase activity is absent.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abolished catalytic activity","termid":"FYPO:0000664"},{"relation_name":"is_a","term_name":"abnormal histone demethylase activity","termid":"FYPO:0007503"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000654"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000641"}],"interesting_parent_ids":["FYPO:0000661","FYPO:0000652","FYPO:0000002","FYPO:0000707","FYPO:0001985","FYPO:0000654","FYPO:0000641","FYPO:0005447"],"is_obsolete":false,"name":"abolished histone demethylase activity (H3-K9 specific)","synonyms":[{"name":"histone demethylase activity (H3-K9 specific) abolished","type":"exact"}],"termid":"FYPO:0007504"}


id: PBO:0011430
data:
  {"annotation_feature_type":"gene","cv_name":"species_dist","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conserved in vertebrate","termid":"PBO:0011430"}


id: GO:0102434
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a 10-formyltetrahydrofolate-4a-carbinolamine = H2O + a 10-formyldihydrofolate.","definition_xrefs":["PMID:20959559","GOC:pz","PMID:18245455"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydro-lyase activity","termid":"GO:0016836"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016829"}],"interesting_parent_ids":["GO:0003674","GO:0016829","GO:0003824"],"is_obsolete":false,"name":"pterin-4alpha-carbinolamine dehydratase activity","secondary_identifiers":["MetaCyc:RXN-13908"],"termid":"GO:0102434"}


id: PR:Q9HDY2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAPB1A10.08 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9HDY2"],"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 protein PB1A10.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAPB1A10.08","synonyms":[{"name":"Spom972h-SPAPB1A10.08","type":"exact"}],"termid":"PR:Q9HDY2"}


id: PBO:0038889
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adducin 2","termid":"PBO:0038889"}


id: PATO:0002190
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A molecular quality that inheres in a molecular entity by virtue of the presence of a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals that exhibit a stabilization stronger than would be expected by the stabilization of conjugation alone.","definition_xrefs":["PATOC:JH"],"direct_ancestors":[{"relation_name":"is_a","term_name":"molecular quality","termid":"PATO:0002182"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aromaticity","termid":"PATO:0002190"}


id: MOD:01428
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that forms an adduct with a (13)C labeled compound used as a reagent.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isotope tagged reagent derivatized residue","termid":"MOD:01426"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"(13)C isotope tagged reagent","termid":"MOD:01428"}


id: PBO:0078714
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Leu (anticodon CAG) 2-2","termid":"PBO:0078714"}


id: PBO:0087702
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the RES complex; RES complex is required for nuclear retention of unspliced pre-mRNAs; acts in the same pathway as Pml39p and Mlp1p","termid":"PBO:0087702"}


id: FYPO:0001137
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 the mature 25S rRNA measured in a cell is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased mature rRNA level","termid":"FYPO:0006470"}],"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":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000002","FYPO:0006551","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased mature 25S rRNA level","synonyms":[{"name":"decreased 25S rRNA level","type":"broad"},{"name":"decreased mature 25S rRNA accumulation","type":"related"},{"name":"decreased mature 25S rRNA level during mitotic cell cycle","type":"related"},{"name":"decreased mature 25S rRNA level during vegetative growth","type":"exact"},{"name":"decreased mature 25S rRNA transcript level","type":"exact"},{"name":"reduced mature 25S rRNA level","type":"exact"}],"termid":"FYPO:0001137"}


id: MONDO:0011265
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"tooth agenesis","termid":"MONDO:0005486"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tooth agenesis, selective, 2","secondary_identifiers":["MEDGEN:400679","MESH:C566513","UMLS:C1865092","OMIM:602639"],"synonyms":[{"name":"STHAG2","type":"exact"},{"name":"hypodontia/oligodontia 2","type":"related"},{"name":"tooth agenesis, selective, 2","type":"exact"}],"termid":"MONDO:0011265","xrefs":{"Monarch":{"xref_id":"0011265"}}}


id: PBO:0041314
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 2 open reading frame 69","termid":"PBO:0041314"}


id: FYPO:0003416
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which cells contain more cytoplasmic membrane-bounded vesicles than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"cytoplasmic vesicles present in increased numbers","synonyms":[{"name":"additional cytoplasmic vesicles present during vegetative growth","type":"exact"},{"name":"cytoplasmic vesicles present in greater numbers","type":"exact"},{"name":"cytoplasmic vesicles present in increased numbers during mitotic cell cycle","type":"related"},{"name":"cytoplasmic vesicles present in increased numbers during vegetative growth","type":"exact"},{"name":"extra cytoplasmic vesicles during vegetative growth","type":"exact"}],"termid":"FYPO:0003416"}


id: MONDO:1012285
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"ventricular arrhythmias and sudden death, non-human animal","termid":"MONDO:1011645"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ventricular arrhythmias and sudden death, dog","secondary_identifiers":["OMIA:001040-9615"],"termid":"MONDO:1012285","xrefs":{"Monarch":{"xref_id":"1012285"}}}


id: GO:0042950
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the transfer of salicin (saligenin-beta-D-glucopyranoside), a glucoside of o-hydroxybenzylalcohol, from one side of a membrane to the other.","definition_xrefs":["GOC:mtg_transport","GOC:jl","ISBN:0815340729"],"direct_ancestors":[{"relation_name":"is_a","term_name":"beta-glucoside transmembrane transporter activity","termid":"GO:0015573"},{"relation_name":"is_a","term_name":"alcohol transmembrane transporter activity","termid":"GO:0015665"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"salicin transmembrane transporter activity","termid":"GO:0042950"}


id: MONDO:0017083
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete lipoma associated with neurospinal dysraphism (obsolete MONDO:0017083)","secondary_identifiers":["Orphanet:268832"],"termid":"MONDO:0017083","xrefs":{"Monarch":{"xref_id":"0017083"}}}


id: GO:0102323
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-isopropylphenol + O2 + NADH + H+ = 3-isopropylcatechol + H2O + NAD.","definition_xrefs":["GOC:pz","RHEA:63520"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen","termid":"GO:0016709"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"2-isopropylphenol monooxygenase activity","secondary_identifiers":["MetaCyc:RXN-13152"],"termid":"GO:0102323"}


id: FYPO:0003620
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 any unspliced or incompletely spliced mRNA precursor measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal RNA level during vegetative growth","termid":"FYPO:0001317"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000257","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"normal pre-mRNA level","synonyms":[{"name":"normal pre-mRNA accumulation","type":"related"},{"name":"normal pre-mRNA level during mitotic cell cycle","type":"related"},{"name":"normal pre-mRNA level during vegetative growth","type":"exact"},{"name":"normal pre-mRNA transcript level","type":"exact"}],"termid":"FYPO:0003620"}


id: GO:1901807
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving capsanthin.","definition_xrefs":["UniPathway:UPA00806","GOC:TermGenie","GOC:yaf","PMID:10995282"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xanthophyll metabolic process","termid":"GO:0016122"}],"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":"capsanthin metabolic process","synonyms":[{"name":"capsanthin metabolism","type":"exact"}],"termid":"GO:1901807"}


id: MONDO:0018634
data:
  {"annotated_genes":["SJAG_04300"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86744],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0971004"}]},"cv_name":"mondo","definition":"Hereditary amyloidosis refers to a group of inherited conditions that make up one of the subtypes of amyloidosis. Hereditary amyloidosisis characterized by the deposit of an abnormal protein called amyloid in multiple organs of the body where it should not be, which causes disruption of organ tissue structure and function. In hereditary amyloidosis, amyloid deposits most often occur in tissues of the heart, kidneys, and nervous system. While symptoms of hereditary amyloidosis may appear in childhood, most individuals do not experience symptoms until adulthood. There are many types of hereditary amyloidosis associated with different gene mutations and abnormal proteins. The most common type of hereditary amyloidosis is transthyretin amyloidosis (ATTR),a condition in which the amyloid deposits are most often made up of the transthyretin protein which is made in the liver. Other examplesof hereditary amyloidosis include, but are not limited to, apolipoprotein AI amyloidosis (A ApoAI), gelsolin amyloidosis (A Gel), lysozyme amyloidosis (A Lys), cystatin C amyloidosis (A Cys), fibrinogen Aα-chain amyloidosis (A Fib), and apolipoprotein AII amyloidosis (A ApoAII). Most types of hereditary amyloidosis are inherited in an autosomal dominant manner. Treatment is focused on addressing symptoms of organ damage and slowing down the production of amyloid when possible through methods such as liver transplants.","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn errors of metabolism","termid":"MONDO:0019052"},{"relation_name":"is_a","term_name":"amyloidosis","termid":"MONDO:0019065"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04300":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0021179"}],"interesting_parent_ids":["MONDO:0021179","MONDO:0005066"],"is_obsolete":false,"name":"hereditary amyloidosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:367601000119103","MESH:D028226","UMLS:C0740340","NCIT:C84555","MEDGEN:148146","Orphanet:444116","icd11.foundation:1152878652","GARD:6611"],"synonyms":[{"name":"amyloidosis hereditary","type":"related"},{"name":"amyloidosis, Familial","type":"exact"},{"name":"familial amyloidosis","type":"related"},{"name":"hereditary amyloidosis (disease)","type":"exact"}],"termid":"MONDO:0018634","terms_by_termid":{"MONDO:0971004":null},"xrefs":{"Monarch":{"xref_id":"0018634"}}}


