# terms

id: GO:0061701
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A spherical, bilayered proteolipid vesicle released from gram-negative bacterial outer membranes.","definition_xrefs":["GOC:pr","PMID:20596524","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"extracellular vesicle","termid":"GO:1903561"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005576"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005576","GO:0005575"],"is_obsolete":false,"name":"bacterial outer membrane vesicle","termid":"GO:0061701"}


id: PBO:0044072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CSTB pseudogene 1","termid":"PBO:0044072"}


id: PBO:0060739
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 4 pseudogene 4","termid":"PBO:0060739"}


id: PBO:0061573
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurotrophin 6 alpha (pseudogene)","termid":"PBO:0061573"}


id: PBO:0047125
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"family with sequence similarity 168 member B","termid":"PBO:0047125"}


id: PBO:0077574
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA element modulatory factor 1 pseudogene 1","termid":"PBO:0077574"}


id: PBO:0028160
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_ATPase_activity","termid":"PBO:0028160"}


id: PBO:0091506
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromeric lncRNA","termid":"PBO:0091506"}


id: GO:0001408
data:
  {"annotated_genes":["SJAG_00760"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[64693],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903790"}]},"cv_name":"biological_process","definition":"The directed movement of guanine nucleotides, GTP, GDP, and/or GMP, into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mcc"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide transport","termid":"GO:0015865"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00760":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"guanine nucleotide transport","references_by_uniquename":{"GO_REF:0000108":null},"termid":"GO:0001408","terms_by_termid":{"GO:1903790":null}}


id: PBO:0045564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dual specificity phosphatase 12 pseudogene 1","termid":"PBO:0045564"}


id: FYPO:0004090
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the microtubule cytoskeleton is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal protein localization","termid":"FYPO:0001370"}],"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:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000138","FYPO:0001985","FYPO:0000002"],"is_obsolete":false,"name":"abnormal protein localization to microtubule cytoskeleton","synonyms":[{"name":"abnormal protein localisation to microtubule cytoskeleton","type":"exact"}],"termid":"FYPO:0004090"}


id: PBO:0085595
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in bud-site selection; diploid mutants display a unipolar budding pattern instead of the wild-type bipolar pattern, and bud at the proximal pole; BUD8 has a paralog, BUD9, that arose from the whole genome duplication","termid":"PBO:0085595"}


id: FYPO:0007788
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of macroautophagy is increased.","definition_xrefs":["PomBase:mah","PMID:17121544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased macroautophagy","termid":"FYPO:0000384"}],"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:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased macroautophagy during vegetative growth","synonyms":[{"name":"increased macroautophagy during mitotic cell cycle","type":"related"}],"termid":"FYPO:0007788"}


id: GO:0034050
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Cell death resulting from activation of endogenous cellular processes after interaction with a symbiont (defined as the smaller of two, or more, organisms engaged in symbiosis, a close interaction encompassing mutualism through parasitism). This can be triggered by direct interaction with the organism, for example, contact with penetrating hyphae of a fungus; or an indirect interaction such as symbiont-secreted molecules.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"programmed cell death","termid":"GO:0012501"},{"relation_name":"is_a","term_name":"defense response to symbiont","termid":"GO:0140546"}],"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-induced defense-related programmed cell death","synonyms":[{"name":"host programmed cell death induced by symbiont","type":"exact"},{"name":"programmed cell death induced by symbiont","type":"exact"}],"termid":"GO:0034050"}


id: PBO:0073681
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sirtuin 3","termid":"PBO:0073681"}


id: PBO:0070457
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L4","termid":"PBO:0070457"}


id: PBO:0074197
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 39 member 7","termid":"PBO:0074197"}


id: PATO:0001551
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A sensitivity of a process which is higher than normal or average.","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":"sensitivity of a process","termid":"PATO:0001457"},{"relation_name":"is_a","term_name":"increased process quality","termid":"PATO:0002304"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased sensitivity of a process","synonyms":[{"name":"high sensitivity of occurrent","type":"exact"},{"name":"increased sensitivity of occurrent","type":"exact"}],"termid":"PATO:0001551"}


id: PBO:0042731
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"centromere protein I pseudogene 1","termid":"PBO:0042731"}


id: GO:0008973
data:
  {"annotated_genes":["SJAG_00134"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[75178],"is_not":false,"summary":null,"term":"GO:0008973"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: D-ribose 1-phosphate = D-ribose 5-phosphate. Also converts 2-deoxy-alpha-D-ribose 1-phosphate into 2-deoxy-D-ribose 5-phosphate.","definition_xrefs":["EC:5.4.2.7"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intramolecular phosphotransferase activity","termid":"GO:0016868"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00134":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016853"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016853","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"phosphopentomutase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["MetaCyc:PPENTOMUT-RXN","Reactome:R-HSA-6787329","Reactome:R-HSA-8982667"],"synonyms":[{"name":"D-ribose 1,5-phosphomutase activity","type":"related"},{"name":"alpha-D-glucose-1,6-bisphosphate:deoxy-D-ribose-1-phosphate phosphotransferase activity","type":"related"},{"name":"alpha-D-ribose 1,5-phosphomutase activity","type":"related"},{"name":"deoxyribomutase activity","type":"related"},{"name":"deoxyribose phosphomutase activity","type":"related"},{"name":"phosphodeoxyribomutase activity","type":"related"},{"name":"phosphoribomutase activity","type":"related"}],"termid":"GO:0008973","terms_by_termid":{"GO:0008973":null}}


id: PBO:0026724
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_level_of_histone_H2A_in_cell","termid":"PBO:0026724"}


id: PBO:0031667
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_modification_during_vegetative_growth","termid":"PBO:0031667"}


id: GO:0007204
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the concentration of calcium ions in the cytosol.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of biological quality","termid":"GO:0065008"}],"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 cytosolic calcium ion concentration","synonyms":[{"name":"cytoplasmic calcium ion concentration elevation","type":"broad"},{"name":"cytosolic calcium ion concentration elevation","type":"exact"},{"name":"elevation of calcium ion concentration in cytoplasm","type":"broad"},{"name":"elevation of calcium ion concentration in cytosol","type":"exact"},{"name":"elevation of cytoplasmic calcium ion concentration","type":"broad"},{"name":"elevation of cytosolic calcium ion concentration","type":"exact"}],"termid":"GO:0007204"}


id: GO:1903141
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 endothelial barrier.","definition_xrefs":["GOC:als","GOC:TermGenie","GO_REF:0000058","PMID:24851274"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of endothelial cell development","termid":"GO:1901551"},{"relation_name":"is_a","term_name":"regulation of establishment of endothelial barrier","termid":"GO:1903140"},{"relation_name":"negatively_regulates","term_name":"establishment of endothelial barrier","termid":"GO:0061028"}],"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 endothelial barrier","synonyms":[{"name":"down regulation of establishment of endothelial barrier","type":"exact"},{"name":"down-regulation of establishment of endothelial barrier","type":"exact"},{"name":"downregulation of establishment of endothelial barrier","type":"exact"},{"name":"inhibition of establishment of endothelial barrier","type":"narrow"}],"termid":"GO:1903141"}


id: PBO:0044463
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 62, pseudogene","termid":"PBO:0044463"}


id: MONDO:0011881
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any striate palmoplantar keratoderma in which the cause of the disease is a mutation in the KRT1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"striate palmoplantar keratoderma","termid":"MONDO:0018865"}],"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":"keratosis palmoplantaris striata 3","secondary_identifiers":["MESH:C536163","OMIM:607654","DOID:0081110","MEDGEN:418996","UMLS:C2931123","GARD:9173"],"synonyms":[{"name":"KRT1 striate palmoplantar keratoderma","type":"exact"},{"name":"PPKS3","type":"related"},{"name":"keratoderma palmoplantar striate form 3","type":"related"},{"name":"keratoderma, palmoplantar, striate form 3","type":"related"},{"name":"keratosis palmoplantaris striata III","type":"related"},{"name":"keratosis palmoplantaris striata type 3","type":"exact"},{"name":"striate palmoplantar keratoderma 3","type":"related"},{"name":"striate palmoplantar keratoderma caused by mutation in KRT1","type":"exact"}],"termid":"MONDO:0011881","xrefs":{"Monarch":{"xref_id":"0011881"}}}


id: FYPO:0004594
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is branched, septated and elongated.","definition_xrefs":["PomBase:jh","PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"branched, elongated cell","termid":"FYPO:0001512"},{"relation_name":"is_a","term_name":"elongated septated vegetative cell","termid":"FYPO:0004750"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000005","FYPO:0001320","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"branched, elongated, septated cell","synonyms":[{"name":"branched, elongated, septated cell during mitotic cell cycle","type":"related"},{"name":"branched, elongated, septated cell during vegetative growth","type":"exact"},{"name":"branched, elongated, septated vegetative cell","type":"exact"},{"name":"branched, long, septated cell","type":"exact"}],"termid":"FYPO:0004594"}


id: PBO:0005450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine/threonine protein kinase Bub1","termid":"PBO:0005450"}


id: GO:2001143
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed movement of a N-methylnicotinateacetate into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic cation transport","termid":"GO:0015695"},{"relation_name":"is_a","term_name":"quaternary ammonium group transport","termid":"GO:0015697"}],"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:0006810","GO:0051179","GO:0008150"],"is_obsolete":false,"name":"N-methylnicotinate transport","termid":"GO:2001143"}


id: MONDO:0021154
data:
  {"annotated_genes":["SJAG_04008","SJAG_03846","SJAG_03199"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88745],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007145"},{"annotations":[87742,87741],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0024552"}]},"cv_name":"mondo","definition":"A disease that involves the dermis.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete rare genetic dermis disorder (obsolete MONDO:0019291)","termid":"MONDO:0019291"},{"relation_name":"is_a","term_name":"skin disorder","termid":"MONDO:0005093"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03199":null,"SJAG_03846":null,"SJAG_04008":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"dermis disorder","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5681483","MEDGEN:1843083","Orphanet:79381"],"synonyms":[{"name":"dermis disease","type":"exact"},{"name":"dermis disease or disorder","type":"exact"},{"name":"disease of dermis","type":"exact"},{"name":"disease or disorder of dermis","type":"exact"},{"name":"disorder of dermis","type":"exact"},{"name":"other dermis disorder","type":"exact"}],"termid":"MONDO:0021154","terms_by_termid":{"MONDO:0007145":null,"MONDO:0024552":null},"xrefs":{"Monarch":{"xref_id":"0021154"}}}


id: PR:O13794
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A cleavage and polyadenylation specificity factor subunit 3 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11203:SF11","OMA:SCHPO01509","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":"endoribonuclease ysh1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC17G6.16c","secondary_identifiers":["UniProtKB:O13794"],"synonyms":[{"name":"Spom972h-CPSF3","type":"exact"},{"name":"mRNA 3'-end-processing protein ysh1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O13794"}


id: PBO:0044661
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"defective in cullin neddylation 1 domain containing 3","termid":"PBO:0044661"}


id: PBO:0004214
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoglucomutase (predicted)","termid":"PBO:0004214"}


id: PBO:0068536
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 139, pseudogene","termid":"PBO:0068536"}


id: PBO:0051444
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 3-30 (pseudogene)","termid":"PBO:0051444"}


id: PBO:0048539
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GEN1 Holliday junction 5' flap endonuclease","termid":"PBO:0048539"}


id: MONDO:0005349
data:
  {"annotated_genes":["SJAG_04755","SJAG_05313"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88986,88987],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0968980"}]},"cv_name":"mondo","definition":"Formation of spongy bone in the labyrinth capsule which can progress toward the stapes (stapedial fixation) or anteriorly toward the cochlea leading to conductive, sensorineural, or mixed hearing loss. Several genes are associated with familial otosclerosis with varied clinical signs.","definition_xrefs":["MESH:D010040"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inner ear disorder","termid":"MONDO:0002467"},{"relation_name":"is_a","term_name":"hereditary otorhinolaryngologic disease","termid":"MONDO:0018751"},{"relation_name":"is_a","term_name":"inherited auditory system disease","termid":"MONDO:0037940"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04755":null,"SJAG_05313":null},"genotype_count":0,"is_obsolete":false,"name":"otosclerosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD10CM:H80","EFO:0004213","NCIT:C185242","Orphanet:2794","SCTID:11543004","icd11.foundation:1242649410","ICD9:387.8","ICD9:387","UMLS:C0029899","DOID:12185","ICD9:387.9","MEDGEN:10508","HP:0000362","OMIMPS:166800"],"synonyms":[{"name":"otosclerosis","type":"exact"},{"name":"otosclerosis (disease)","type":"exact"}],"termid":"MONDO:0005349","terms_by_termid":{"MONDO:0968980":null},"xrefs":{"Monarch":{"xref_id":"0005349"}}}


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


id: MONDO:0009798
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic intellectual disability syndrome characterized by macrocephaly, hypotonia, dysmorphic facial features (wide forehead, ptosis, downslanting palpebral fissures, enlarged and calcified external ears, large jaw), sparse body hair, tall stature, and intellectual disability. Hearing loss, insulin-resistant diabetes, and progressive distal muscle wasting (leading to joint contractures) have also been reported in adulthood. Rare manifestations include behavioral abnormalities (aggression and restlessness), hypothyroidism, cerebral calcification, ataxia, and peripheral neuropathy.","definition_xrefs":["Orphanet:3042"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Primrose syndrome","secondary_identifiers":["MESH:C536420","GARD:4488","OMIM:259050","SCTID:726709001","MEDGEN:162911","UMLS:C0796121"],"synonyms":[{"name":"PRIMS","type":"related"},{"name":"Primrose syndrome","type":"exact"},{"name":"intellectual disability-cataracts-calcified pinnae-myopathy syndrome","type":"exact"},{"name":"ossified EAR cartilages with mental deficiency, muscle wasting, and BONY changes","type":"related"}],"termid":"MONDO:0009798","xrefs":{"Monarch":{"xref_id":"0009798"}}}


id: PATO:0002511
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A shape quality inhering in a bearer by virtue of the bearer's similarity to the appearance of a cane.","definition_xrefs":["PATOC:EJS"],"direct_ancestors":[{"relation_name":"is_a","term_name":"shape","termid":"PATO:0000052"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cane-like","synonyms":[{"name":"cane-shaped","type":"related"}],"termid":"PATO:0002511"}


id: PBO:0087170
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA polymerase II largest subunit B220; part of central core; phosphorylation of C-terminal heptapeptide repeat domain regulates association with transcription and splicing factors; similar to bacterial beta-prime","termid":"PBO:0087170"}


id: MONDO:0100139
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A COVID-19 infection where individuals test positive for SARS-CoV-2 but have no symptoms across the entire course of the disease.","gene_count":0,"genotype_count":0,"name":"obsolete asymptomatic COVID-19 infection (obsolete MONDO:0100139)","termid":"MONDO:0100139","xrefs":{"Monarch":{"xref_id":"0100139"}}}


id: SO:0001884
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A feature translocation where the region contains a regulatory region.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"feature_translocation","termid":"SO:0001881"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulatory_region_translocation","synonyms":[{"name":"regulatory region translocation","type":"exact"}],"termid":"SO:0001884"}


id: MONDO:0016977
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thymic neuroendocrine carcinoma","termid":"MONDO:0020516"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570","MONDO:0004992"],"is_obsolete":false,"name":"moderately-differentiated thymic neuroendocrine carcinoma","secondary_identifiers":["UMLS:C5680730","GARD:20896","icd11.foundation:1165208895","MEDGEN:1843377","Orphanet:263335"],"termid":"MONDO:0016977","xrefs":{"Monarch":{"xref_id":"0016977"}}}


id: PBO:0073235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SUMO peptidase family member, NEDD8 specific","termid":"PBO:0073235"}


id: MONDO:0044246
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Voluntary nystagmus is a rapid to-and-fro synchronous movement of the eyes that is initiated and maintained by conscious effort. Voluntary nystagmus has a frequency of 10-25 Hz, with an amplitude of up to 6 degrees, and can be maintained for up to 35 seconds. It usually has its first appearance between ages 8 to 15 years. It can be produced in both light and darkness, without fixation, at all eye positions, and even with closed eyes. It is accompanied by oscillopsia with visual blurring (summary by {1:Aschoff et al., 1976}).","definition_xrefs":["OMIM:164170"],"gene_count":0,"genotype_count":0,"name":"obsolete nystagmus, voluntary (obsolete MONDO:0044246)","synonyms":[{"name":"NYSTAGMUS, voluntary","type":"related"}],"termid":"MONDO:0044246","xrefs":{"Monarch":{"xref_id":"0044246"}}}


id: _global:regulates_o_results_in_maturation_of
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"This is the combination of the regulates relation with the results_in_maturation_of relation.","definition_xrefs":["GOC:mtg_berkeley_2013"],"direct_ancestors":[{"relation_name":"is_a","term_name":"go_annotation_extension_relation","termid":"_global:go_annotation_extension_relation"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulates_maturation_of","secondary_identifiers":["GOREL:0001012"],"termid":"_global:regulates_o_results_in_maturation_of"}


id: PBO:0005414
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxin Pex32 (predicted)","termid":"PBO:0005414"}


id: GO:0043252
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The directed, sodium-independent, movement of organic anions into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transport","termid":"GO:0015711"}],"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:0006810"}],"interesting_parent_ids":["GO:0051179","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"sodium-independent organic anion transport","secondary_identifiers":["Reactome:R-HSA-879518"],"termid":"GO:0043252"}


id: GO:0010812
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the frequency, rate or extent of cell-substrate adhesion. Cell-substrate adhesion is the attachment of a cell to the underlying substrate via adhesion molecules.","definition_xrefs":["GOC:dph","GOC:tb","GOC:pf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell adhesion","termid":"GO:0007162"},{"relation_name":"is_a","term_name":"regulation of cell-substrate adhesion","termid":"GO:0010810"},{"relation_name":"negatively_regulates","term_name":"cell-substrate adhesion","termid":"GO:0031589"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007155"},{"rel_name":"negatively_regulates","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"negative regulation of cell-substrate adhesion","termid":"GO:0010812"}


id: PBO:0069464
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 729, pseudogene","termid":"PBO:0069464"}


id: PBO:0091410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein P1 Rpp101","termid":"PBO:0091410"}


id: MONDO:0004861
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"eye disorder","termid":"MONDO:0005328"}],"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":"ophthalmia nodosa","secondary_identifiers":["ICD10CM:H16.24","icd11.foundation:691596189","MEDGEN:509654","DOID:9722","ICD9:360.14","UMLS:C0154775","SCTID:12371008"],"termid":"MONDO:0004861","xrefs":{"Monarch":{"xref_id":"0004861"}}}


id: PBO:0018241
data:
  {"annotation_feature_type":"gene","cv_name":"misc","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"provides a telomeric cap that prevents Ku from recognising telomeres as double strand breaks (Ku-dependent end-to-end fusions)","termid":"PBO:0018241"}


id: PBO:0076737
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"t-complex 10 like 3, pseudogene","termid":"PBO:0076737"}


id: PBO:0089286
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferrochelatase Hem15","termid":"PBO:0089286"}


id: MONDO:0013229
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Hot water reflex epilepsy is a rare neurologic disease characterized by the onset of generalized or focal seizures following immersion of the head in hot water, or with hot water being poured over the head. Primary generalized tonic-clonic seizures have been reported in rare cases.","definition_xrefs":["Orphanet:166412"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited reflex epilepsy","termid":"MONDO:0023224"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"hot water reflex epilepsy","secondary_identifiers":["UMLS:C4706506","ICD9:345.10","DOID:0081104","SCTID:230454005","GARD:17028","OMIMPS:613339","MEDGEN:1631373"],"synonyms":[{"name":"bathing epilepsy","type":"related"},{"name":"epilepsy, hot water","type":"exact"},{"name":"hot water epilepsy","type":"exact"},{"name":"water immersion epilepsy","type":"related"}],"termid":"MONDO:0013229","xrefs":{"Monarch":{"xref_id":"0013229"}}}


id: PBO:0074885
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 63","termid":"PBO:0074885"}


id: MONDO:0026782
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete chondrodysplasia punctata 2, X-linked dominant (obsolete MONDO:0026782)","termid":"MONDO:0026782","xrefs":{"Monarch":{"xref_id":"0026782"}}}


id: PBO:0011968
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autophagy C terminal domain family protein Atg10 (predicted)","termid":"PBO:0011968"}


id: PBO:0029401
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_duration_of_protein_localization_to_cell_division_site","termid":"PBO:0029401"}


id: GO:0048532
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that gives rise to the configuration of the constituent parts of an anatomical structure. This process pertains to the physical shaping of a rudimentary structure. Anatomical structures can be macroscopic such as a carpel, or microscopic such as an acrosome.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process","termid":"GO:0032502"},{"relation_name":"part_of","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"}],"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":"anatomical structure arrangement","synonyms":[{"name":"anatomical structure organization","type":"broad"},{"name":"anatomical structure structural organization","type":"exact"},{"name":"organization of an anatomical structure","type":"exact"},{"name":"structural organization","type":"exact"}],"termid":"GO:0048532"}


id: PBO:0041964
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coiled-coil domain containing 7","termid":"PBO:0041964"}


id: MONDO:0005601
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An invasive adenocarcinoma that arises from the ovary and is characterized by the presence of malignant epithelial cells that contain intracytoplasmic mucin. There is cellular atypia, increased layering of cells, complexity of glands, and papillary formations.","definition_xrefs":["NCIT:C5243"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ovarian adenocarcinoma","termid":"MONDO:0002752"},{"relation_name":"is_a","term_name":"mucinous adenocarcinoma","termid":"MONDO:0004957"},{"relation_name":"is_a","term_name":"mucinous ovarian cancer","termid":"MONDO:0024282"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"ovarian mucinous adenocarcinoma","secondary_identifiers":["UMLS:C1335167","EFO:0006462","Orphanet:398961","GARD:21651","DOID:3606","icd11.foundation:869438441","MEDGEN:235418"],"synonyms":[{"name":"mucinous adenocarcinoma of ovary","type":"exact"},{"name":"mucinous adenocarcinoma of the ovary","type":"exact"},{"name":"mucinous carcinoma of ovary","type":"exact"},{"name":"mucinous carcinoma of the ovary","type":"exact"},{"name":"ovarian mucinous adenocarcinoma","type":"exact"},{"name":"ovarian mucinous carcinoma","type":"exact"},{"name":"ovary mucinous adenocarcinoma","type":"exact"}],"termid":"MONDO:0005601","xrefs":{"Monarch":{"xref_id":"0005601"}}}


id: PBO:0055255
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 2682","termid":"PBO:0055255"}


id: MONDO:0037937
data:
  {"annotated_genes":["SJAG_00694","SJAG_00885","SJAG_02658","SJAG_00964","SJAG_03164"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86898],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014647"},{"annotations":[87143],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011283"},{"annotations":[88864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013350"},{"annotations":[88109],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012792"},{"annotations":[87023,87022],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009797"}]},"cv_name":"mondo","definition":"A disease that has its basis in the disruption of pyrimidine nucleobase metabolic process.","definition_xrefs":["MONDO:patterns/basis_in_disruption_of_process"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease","termid":"MONDO:0005066"}],"gene_count":5,"genes_by_uniquename":{"SJAG_00694":null,"SJAG_00885":null,"SJAG_00964":null,"SJAG_02658":null,"SJAG_03164":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0005066"],"is_obsolete":false,"name":"pyrimidine metabolism disease","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:85444005"],"synonyms":[{"name":"disorder of pyrimidine metabolism","type":"exact"},{"name":"disorder of pyrimidine nucleobase metabolic process","type":"exact"},{"name":"pyrimidine nucleobase metabolic process disease","type":"exact"}],"termid":"MONDO:0037937","terms_by_termid":{"MONDO:0009797":null,"MONDO:0011283":null,"MONDO:0012792":null,"MONDO:0013350":null,"MONDO:0014647":null},"xrefs":{"Monarch":{"xref_id":"0037937"}}}


id: PBO:0086007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein of unknown function; structure defines a new subfamily of the split beta-alpha-beta sandwiches; green fluorescent protein (GFP)-fusion protein localizes to the cytoplasm and nucleus; YML108W is not an essential gene; relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0086007"}


id: GO:0150012
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of the process in which the anatomical structures of a neuron projection are generated and organized into branches.","definition_xrefs":["PMID:17114044","GOC:bc","GOC:aruk"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell projection organization","termid":"GO:0031346"},{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"regulation of neuron projection arborization","termid":"GO:0150011"},{"relation_name":"positively_regulates","term_name":"neuron projection arborization","termid":"GO:0140058"}],"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 neuron projection arborization","synonyms":[{"name":"positive regulation of neurite arborization","type":"exact"},{"name":"positive regulation of neurite branching","type":"exact"},{"name":"positive regulation of neuron projection branching","type":"exact"}],"termid":"GO:0150012"}


id: PBO:0064312
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phospholipid phosphatase 1","termid":"PBO:0064312"}


id: MONDO:0012973
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An inflammatory bowel disease that has material basis in variation in the chromosome region 12q15.","definition_xrefs":["DOID:0110901","PMID:19122664"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inflammatory bowel disease","termid":"MONDO:0005265"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"inflammatory bowel disease 26","secondary_identifiers":["OMIM:612639","MESH:C567217","MEDGEN:382561","UMLS:C2675249"],"synonyms":[{"name":"IBD26","type":"exact"},{"name":"inflammatory bowel disease 26","type":"exact"},{"name":"inflammatory bowel disease type 26","type":"exact"}],"termid":"MONDO:0012973","xrefs":{"Monarch":{"xref_id":"0012973"}}}


id: GO:0038091
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals initiated by vascular endothelial growth factor (VEGF) binding to a platelet-derived growth factor receptor (PDGFR) on the surface of a cell, which activates or increases the frequency, rate or extent of cell proliferation.","definition_xrefs":["GOC:signaling","PMID:17470632"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of cell population proliferation","termid":"GO:0008284"},{"relation_name":"is_a","term_name":"VEGF-activated platelet-derived growth factor receptor signaling pathway","termid":"GO:0038086"}],"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":"positive regulation of cell proliferation by VEGF-activated platelet derived growth factor receptor signaling pathway","synonyms":[{"name":"VEGF-A-induced cell proliferation","type":"narrow"},{"name":"positive regulation of cell proliferation by VEGF-activated platelet derived growth factor receptor signalling pathway","type":"exact"},{"name":"positive regulation of cell proliferation by VEGF/PDGFR signaling pathway","type":"exact"}],"termid":"GO:0038091"}


id: SO:0001336
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"Wyosine is a modified guanosine base feature.","direct_ancestors":[{"relation_name":"is_a","term_name":"modified_guanosine","termid":"SO:0001276"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"wyosine","secondary_identifiers":["RNAMOD:041"],"synonyms":[{"name":"IMG","type":"exact"}],"termid":"SO:0001336"}


id: PBO:0054005
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 1333","termid":"PBO:0054005"}


id: GO:0042723
data:
  {"annotated_genes":["SJAG_04067","SJAG_01970","SJAG_00827","SJAG_04866","SJAG_02406","SJAG_02047","SJAG_03538","SJAG_01742","SJAG_00381","SJAG_02421","SJAG_04282","SJAG_02420","SJAG_03362"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90852,115541],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090180"},{"annotations":[71804,75730,62213,78755,75672,80196],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009228"},{"annotations":[66840,68868,115447,117880,115453,79953],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009229"},{"annotations":[67375,59299],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006772"},{"annotations":[112295,101341,112296],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036172"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving thiamine (vitamin B1), and compounds derived from it.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"water-soluble vitamin metabolic process","termid":"GO:0006767"},{"relation_name":"is_a","term_name":"sulfur compound metabolic process","termid":"GO:0006790"},{"relation_name":"is_a","term_name":"pyrimidine-containing compound metabolic process","termid":"GO:0072527"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00381":null,"SJAG_00827":null,"SJAG_01742":null,"SJAG_01970":null,"SJAG_02047":null,"SJAG_02406":null,"SJAG_02420":null,"SJAG_02421":null,"SJAG_03362":null,"SJAG_03538":null,"SJAG_04067":null,"SJAG_04282":null,"SJAG_04866":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0006766","GO:0006790","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"thiamine-containing compound metabolic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"secondary_identifiers":["Reactome:R-HSA-196819"],"synonyms":[{"name":"thiamin and derivative metabolic process","type":"exact"},{"name":"thiamin and derivative metabolism","type":"exact"},{"name":"thiamin-containing compound metabolic process","type":"exact"},{"name":"thiamine and derivative metabolic process","type":"exact"},{"name":"thiamine and derivative metabolism","type":"exact"},{"name":"thiamine-containing compound metabolism","type":"exact"},{"name":"vitamin B1 and derivative metabolic process","type":"exact"},{"name":"vitamin B1 and derivative metabolism","type":"exact"}],"termid":"GO:0042723","terms_by_termid":{"GO:0006772":null,"GO:0009228":null,"GO:0009229":null,"GO:0036172":null,"GO:0090180":null}}


id: PBO:0069671
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 948, pseudogene","termid":"PBO:0069671"}


id: PBO:0036104
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_transport_on_microtubule_tip_to_cell_tip_cortex_during_vegetative_growth","termid":"PBO:0036104"}


id: GO:0036109
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving alpha-linolenic acid, an unsaturated omega-6 fatty acid that has the molecular formula C18H32O2.","definition_xrefs":["PMID:15538555"],"direct_ancestors":[{"relation_name":"is_a","term_name":"long-chain fatty acid metabolic process","termid":"GO:0001676"},{"relation_name":"is_a","term_name":"unsaturated fatty acid metabolic process","termid":"GO:0033559"},{"relation_name":"is_a","term_name":"olefinic compound metabolic process","termid":"GO:0120254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"alpha-linolenic acid metabolic process","secondary_identifiers":["Reactome:R-HSA-2046106","Wikipedia:Linoleic_acid"],"synonyms":[{"name":"ALA metabolism","type":"exact"},{"name":"alpha-linolenic acid metabolism","type":"exact"}],"termid":"GO:0036109"}


id: MONDO:0000454
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete multiple synostoses syndrome (obsolete MONDO:0000454)","termid":"MONDO:0000454","xrefs":{"Monarch":{"xref_id":"0000454"}}}


id: GO:0052557
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process by which an organism activates, maintains or increases the frequency, rate or extent of the immune response of the symbiont organism; the immune response is any immune system process that functions in the calibrated response of an organism to a potential internal or invasive threat. The symbiont is defined as the smaller of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:mtg_pamgo"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation by organism of symbiont immune response (obsolete GO:0052557)","synonyms":[{"name":"positive regulation by organism of symbiont immune response","type":"exact"}],"termid":"GO:0052557"}


id: MONDO:0017535
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"central polydactyly of fingers","termid":"MONDO:0017456"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"central polydactyly of fingers, unilateral","secondary_identifiers":["Orphanet:295171","icd11.foundation:738371690"],"synonyms":[{"name":"mesoaxial polydactyly of fingers, unilateral","type":"exact"},{"name":"mirror hand, unilateral","type":"exact"}],"termid":"MONDO:0017535","xrefs":{"Monarch":{"xref_id":"0017535"}}}


id: MONDO:0007955
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A congenital pouch in the distal ileum. It may cause painless rectal bleeding and bowel obstruction.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"digestive system disorder","termid":"MONDO:0004335"}],"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":"Meckel diverticulum","secondary_identifiers":["MESH:D008467","MedDRA:10027055","ICD9:751.0","MEDGEN:9917","NCIT:C12264","SCTID:37373007","OMIM:155140","UMLS:C0025037","EFO:1001036","icd11.foundation:216192536","ICD10CM:Q43.0","DOID:9487"],"synonyms":[{"name":"Meckel diverticulum","type":"exact"},{"name":"Meckel's diverticulum","type":"exact"},{"name":"persistent vitelline duct","type":"exact"}],"termid":"MONDO:0007955","xrefs":{"Monarch":{"xref_id":"0007955"}}}


id: _global:during_which_ends
data:
  {"annotation_feature_type":"gene","cv_name":"external","direct_ancestors":[{"relation_name":"is_a","term_name":"temporally_related_to","termid":"_global:temporally_related_to"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"during_which_ends","secondary_identifiers":["RO:0002084"],"termid":"_global:during_which_ends"}


id: MONDO:0015386
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Epignathus is a very rare and life threatening intraoral teratoma, usually arising from the maxilla, mandible, palate or base of skull and invading the cranium, nasopharynx or oral cavity. Epignathus is more commonly seen in females, and presents with various manifestations (depending on the tumor size) including obstructive polyhydramnios in the prenatal period and dyspnea, cyanosis, cough, difficulty in sucking and swallowing, and rarely vomiting (due to swallowing difficulties) postnatally. When large, they can lead to airway obstruction, asphyxia and death in the neonatal period.","definition_xrefs":["Orphanet:141077"],"direct_ancestors":[{"relation_name":"is_a","term_name":"head and neck neoplasm","termid":"MONDO:0005586"},{"relation_name":"is_a","term_name":"extragonadal teratoma","termid":"MONDO:0019500"},{"relation_name":"is_a","term_name":"otorhinolaryngologic disease","termid":"MONDO:0024623"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"epignathus","secondary_identifiers":["SCTID:31248004","UMLS:C0266725","GARD:19943","HP:0030767","icd11.foundation:7319064","MEDGEN:540117"],"synonyms":[{"name":"Epignathus","type":"exact"},{"name":"epignathus (disease)","type":"exact"},{"name":"oropharyngeal teratoma","type":"exact"}],"termid":"MONDO:0015386","xrefs":{"Monarch":{"xref_id":"0015386"}}}


id: MONDO:0010797
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pearson syndrome is characterized by refractory sideroblastic anemia, vacuolization of bone marrow precursors and exocrine pancreatic dysfunction.","definition_xrefs":["Orphanet:699"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"constitutional neutropenia","termid":"MONDO:0015134"},{"relation_name":"excluded_subClassOf","term_name":"obsolete metabolic disorder with intestinal involvement (obsolete MONDO:0015188)","termid":"MONDO:0015188"},{"relation_name":"excluded_subClassOf","term_name":"obsolete syndrome with hypoparathyroidism (obsolete MONDO:0015895)","termid":"MONDO:0015895"},{"relation_name":"excluded_subClassOf","term_name":"obsolete mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA (obsolete MONDO:0016792)","termid":"MONDO:0016792"},{"relation_name":"excluded_subClassOf","term_name":"inherited sideroblastic anemia","termid":"MONDO:0020099"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pearson syndrome","secondary_identifiers":["MedDRA:10062941","icd11.foundation:452521132","MEDGEN:87459","SCTID:237985009","UMLS:C0342784","NCIT:C115326","DOID:0060067","GARD:7343","ICD9:277.87","OMIM:557000"],"synonyms":[{"name":"Pearson marrow-pancreas syndrome","type":"exact"},{"name":"Pearson's marrow/pancreas syndrome","type":"related"},{"name":"Pearson's syndrome","type":"related"},{"name":"sideroblastic Anaemia with marrow cell vacuolization and exocrine pancreatic dysfunction","type":"related"},{"name":"sideroblastic Anemia with marrow cell vacuolization and exocrine pancreatic dysfunction","type":"related"},{"name":"sideroblastic anaemia with marrow cell vacuolization and exocrine pancreatic dysfunction (formerly)","type":"related"},{"name":"sideroblastic anemia with marrow cell vacuolization and exocrine pancreatic dysfunction (formerly)","type":"related"}],"termid":"MONDO:0010797","xrefs":{"Monarch":{"xref_id":"0010797"}}}


id: GO:0045160
data:
  {"annotated_genes":["SJAG_04781","SJAG_04001","SJAG_04901"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[97184,98678,105072],"is_not":false,"summary":null,"term":"GO:0045160"}]},"cv_name":"cellular_component","definition":"A myosin complex containing a class I myosin heavy chain and associated light chains; myosin I heavy chains are single-headed, possess tails of various lengths, and do not self-associate into bipolar filaments; myosin I complexes are involved in diverse processes related to membrane traffic and cell movement.","definition_xrefs":["PMID:9438839","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"unconventional myosin complex","termid":"GO:0016461"}],"gene_count":3,"genes_by_uniquename":{"SJAG_04001":null,"SJAG_04781":null,"SJAG_04901":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015629"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0015629","GO:0005575"],"is_obsolete":false,"name":"myosin I complex","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0045160","terms_by_termid":{"GO:0045160":null}}


id: PBO:0055581
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 3017","termid":"PBO:0055581"}


id: MONDO:1010286
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Pneumothorax that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"respiratory system disorder, non-human animal","termid":"MONDO:0700104"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pneumothorax, non-human animal","secondary_identifiers":["OMIA:000804"],"termid":"MONDO:1010286","xrefs":{"Monarch":{"xref_id":"1010286"}}}


id: MONDO:0020493
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Haddad syndrome is a rare congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease.","definition_xrefs":["Orphanet:99803"],"direct_ancestors":[{"relation_name":"is_a","term_name":"intestinal motility disease","termid":"MONDO:0021189"}],"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":"Haddad syndrome","secondary_identifiers":["SCTID:719972004","icd11.foundation:1685926536","ICD10CM:G47.3","GARD:16909","MEDGEN:347052","UMLS:C1859049"],"synonyms":[{"name":"Haddad syndrome","type":"exact"},{"name":"congenital central alveolar hypoventilation-Hirschsprung disease syndrome","type":"exact"},{"name":"ondine-Hirschsprung disease","type":"exact"},{"name":"ondine-Hirschsprung syndrome","type":"exact"}],"termid":"MONDO:0020493","xrefs":{"Monarch":{"xref_id":"0020493"}}}


id: PBO:0051209
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 4-55 (pseudogene)","termid":"PBO:0051209"}


id: MONDO:0012471
data:
  {"annotated_genes":["SJAG_01884"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86957],"is_not":false,"summary":null,"term":"MONDO:0012471"}]},"cv_name":"mondo","definition":"Any Aicardi-Goutieres syndrome in which the cause of the disease is a mutation in the RNASEH2C gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Aicardi-Goutieres syndrome","termid":"MONDO:0018866"},{"relation_name":"is_a","term_name":"RNASEH2C-related type 1 interferonopathy","termid":"MONDO:0700258"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01884":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005046","MONDO:0005559"],"is_obsolete":false,"name":"Aicardi-Goutieres syndrome 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:610329","UMLS:C1835916","NANDO:2200895","GARD:15479","MEDGEN:324389","MESH:C563683"],"synonyms":[{"name":"AGS3","type":"related"},{"name":"Aicardi-Goutieres syndrome 3","type":"exact"},{"name":"Aicardi-Goutieres syndrome caused by mutation in RNASEH2C","type":"exact"},{"name":"Aicardi-Goutieres syndrome type 3","type":"exact"},{"name":"RNASEH2C -related Aicardi-Goutieres syndrome","type":"related"},{"name":"RNASEH2C Aicardi-Goutieres syndrome","type":"exact"}],"termid":"MONDO:0012471","terms_by_termid":{"MONDO:0012471":null},"xrefs":{"Monarch":{"xref_id":"0012471"}}}


id: MONDO:0016873
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndrome caused by partial chromosomal deletion","termid":"MONDO:0000761"},{"relation_name":"is_a","term_name":"chromosome 8 disorder","termid":"MONDO:0700015"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial deletion of chromosome 8","secondary_identifiers":["UMLS:C5679652","GARD:20796","MEDGEN:1825961","Orphanet:261801"],"synonyms":[{"name":"partial deletion of chromosome type 8","type":"exact"},{"name":"partial monosomy of chromosome 8","type":"exact"}],"termid":"MONDO:0016873","xrefs":{"Monarch":{"xref_id":"0016873"}}}


id: PBO:0049478
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H1.2 linker histone, cluster member","termid":"PBO:0049478"}


id: PBO:0065047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PRELI domain containing 3B pseudogene 1","termid":"PBO:0065047"}


id: PBO:0065140
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase Y-linked (pseudogene)","termid":"PBO:0065140"}


id: PBO:0070783
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L12 pseudogene 13","termid":"PBO:0070783"}


id: GO:0009026
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: D-altronate + NAD+ = D-tagaturonate + H+ + NADH.","definition_xrefs":["RHEA:17813","EC:1.1.1.58"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor","termid":"GO:0016616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003824","GO:0003674","GO:0016491"],"is_obsolete":false,"name":"tagaturonate reductase activity","secondary_identifiers":["MetaCyc:ALTRO-OXIDOREDUCT-RXN","KEGG_REACTION:R02555"],"synonyms":[{"name":"D-altronate:NAD+ 3-oxidoreductase activity","type":"related"},{"name":"D-tagaturonate reductase activity","type":"related"},{"name":"TagUAR","type":"related"},{"name":"altronate dehydrogenase activity","type":"related"},{"name":"altronate oxidoreductase activity","type":"related"},{"name":"altronic oxidoreductase activity","type":"related"},{"name":"tagaturonate dehydrogenase activity","type":"related"}],"termid":"GO:0009026"}


id: MONDO:0008699
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Achalasia-microcephaly is an extremely rare genetic syndrome, reported in a few families to date, characterized by the association of microcephaly, intellectual deficit and achalasia (with symptoms of coughing, dysphagia, vomiting, failure to thrive and aspiration appearing in infancy/early-childhood). Antenatal exposure to Mefloquine was reported in one simplex case. An autosomal recessive inheritance has been proposed.","definition_xrefs":["Orphanet:929"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"}],"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":"achalasia microcephaly syndrome","secondary_identifiers":["MEDGEN:349753","OMIM:200450","UMLS:C1860212","DOID:0050796","SCTID:718573009","GARD:456","MESH:C536010"],"synonyms":[{"name":"achalasia microcephaly","type":"exact"},{"name":"achalasia-microcephaly syndrome","type":"exact"}],"termid":"MONDO:0008699","xrefs":{"Monarch":{"xref_id":"0008699"}}}


id: GO:0071594
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The adhesion of one thymocyte (an immature T cell) to one or more other thymocytes via adhesion molecules.","definition_xrefs":["GOC:sl","PMID:1382990"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell aggregation","termid":"GO:0070489"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0007155"}],"interesting_parent_ids":["GO:0008150","GO:0007155"],"is_obsolete":false,"name":"thymocyte aggregation","synonyms":[{"name":"T cell precursor aggregation","type":"exact"},{"name":"immature T cell aggregation","type":"broad"},{"name":"immature T-cell aggregation","type":"broad"},{"name":"immature T-lymphocyte aggregation","type":"exact"},{"name":"thymic lymphocyte aggregation","type":"exact"}],"termid":"GO:0071594"}


id: MONDO:0004239
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A variant of cervical squamous cell carcinoma characterized by the presence of keratin pearls. Intercellular bridges and cytoplasmic keratinization are usually present.","definition_xrefs":["NCIT:C40187"],"direct_ancestors":[{"relation_name":"is_a","term_name":"keratinizing squamous cell carcinoma","termid":"MONDO:0005056"},{"relation_name":"is_a","term_name":"cervical squamous cell carcinoma","termid":"MONDO:0006143"}],"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":"cervical keratinizing squamous cell carcinoma","secondary_identifiers":["MEDGEN:309255","UMLS:C1517658","DOID:7483"],"synonyms":[{"name":"cervical keratinizing squamous cell carcinoma","type":"exact"}],"termid":"MONDO:0004239","xrefs":{"Monarch":{"xref_id":"0004239"}}}


id: PBO:0003246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNAPII degradation factor Def1 (predicted)","termid":"PBO:0003246"}


id: PBO:0040896
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bone morphogenetic protein receptor type 2","termid":"PBO:0040896"}


id: GO:0033877
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: (R)-2-benzylsuccinate + succinyl-CoA = (R)-2-benzylsuccinyl-CoA + succinate.","definition_xrefs":["EC:2.8.3.15","RHEA:16469"],"direct_ancestors":[{"relation_name":"is_a","term_name":"CoA-transferase activity","termid":"GO:0008410"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016782"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"}],"interesting_parent_ids":["GO:0003674","GO:0016740","GO:0016782","GO:0003824"],"is_obsolete":false,"name":"succinyl-CoA:(R)-benzylsuccinate CoA-transferase activity","secondary_identifiers":["UM-BBD_reactionID:r0329","MetaCyc:RXN-864","GO:0018728","KEGG_REACTION:R05588"],"synonyms":[{"name":"benzylsuccinate CoA-transferase activity","type":"related"},{"name":"succinyl-CoA:(R)-2-benzylsuccinate CoA-transferase activity","type":"related"},{"name":"succinyl-CoA:benzylsuccinate CoA-transferase activity","type":"exact"}],"termid":"GO:0033877"}


id: MONDO:0005190
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. Macroglobulinemia is the presence of increased levels of macroglobulins in the circulating blood. It is a Plasma cell dyscrasia, resembling leukemia, with cells of lymphocytic, plasmacytic, or intermediate morphology, which secrete a monoclonal immunoglobulin M component. There is diffuse infiltration by the malignant cells of the bone marrow and also, in many cases, of the spleen, liver, or lymph nodes. The circulating macroglobulin can produce symptoms of hyperviscosity syndrome: weakness, fatigue, bleeding disorders, and visual disturbances. Peak incidence of macroglobulinemia is in the sixth and seventh decades of life.","definition_xrefs":["EFO:0002616"],"gene_count":0,"genotype_count":0,"name":"obsolete macroglobulinemia (obsolete MONDO:0005190)","secondary_identifiers":["DOID:9080","ICD10CM:C88.0","NCIT:C80307","Wikipedia:Macroglobulinemia","MESH:D008258","SCTID:190817009","ICD9:273.3","NCIT:C3212"],"synonyms":[{"name":"primary macroglobulinemia","type":"exact"}],"termid":"MONDO:0005190","xrefs":{"Monarch":{"xref_id":"0005190"}}}


id: GO:0002571
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The addition of variable numbers of random nucleotides by terminal deoxytransferase in the N regions of T cell receptor genes. N regions are found at the V-D, D-D, V-J, and D-J recombinational junctions, depending on the T cell receptor gene.","definition_xrefs":["GOC:add","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"somatic diversification of T cell receptor genes","termid":"GO:0002568"},{"relation_name":"is_a","term_name":"somatic diversification of immune receptors by N region addition","termid":"GO:0002569"},{"relation_name":"part_of","term_name":"somatic recombination of T cell receptor gene segments","termid":"GO:0002681"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0006259"},{"rel_name":"part_of","termid":"GO:0006310"}],"interesting_parent_ids":["GO:0008150","GO:0006259","GO:0006310"],"is_obsolete":false,"name":"somatic diversification of T cell receptor genes by N region addition","synonyms":[{"name":"somatic diversification of TCR genes by N region addition","type":"exact"}],"termid":"GO:0002571"}


id: PBO:0044334
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CYCS pseudogene 17","termid":"PBO:0044334"}


id: MONDO:1012425
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"congenital merosin-deficient muscular dystrophy, non-human animal","termid":"MONDO:1011802"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital merosin-deficient muscular dystrophy, domestic cat","secondary_identifiers":["OMIA:001619-9685"],"termid":"MONDO:1012425","xrefs":{"Monarch":{"xref_id":"1012425"}}}


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


id: MONDO:0013823
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the CEACAM16 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":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0019497"],"is_obsolete":false,"name":"autosomal dominant nonsyndromic hearing loss 4B","secondary_identifiers":["MEDGEN:482927","GARD:18136","OMIM:614614","DOID:0110574","UMLS:C3281297"],"synonyms":[{"name":"CEACAM16 autosomal dominant nonsyndromic deafness","type":"narrow"},{"name":"DFNA4B","type":"narrow"},{"name":"autosomal dominant deafness 4B","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness 4B","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness caused by mutation in CEACAM16","type":"narrow"},{"name":"autosomal dominant nonsyndromic deafness type 4B","type":"narrow"},{"name":"deafness, autosomal dominant 4B","type":"narrow"},{"name":"deafness, autosomal dominant 4b","type":"narrow"},{"name":"deafness, autosomal dominant type 4B","type":"narrow"}],"termid":"MONDO:0013823","xrefs":{"Monarch":{"xref_id":"0013823"}}}


id: PBO:0001463
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ornithine carbamoyltransferase Arg3","termid":"PBO:0001463"}


id: PBO:0027884
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_histone_H4-K20_methylation","termid":"PBO:0027884"}


id: GO:0005515
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binding","type":"exact"}],"termid":"GO:0005515","terms_by_termid":{"GO:0000149":null,"GO:0000993":null,"GO:0000994":null,"GO:0001042":null,"GO:0001096":null,"GO:0001097":null,"GO:0001156":null,"GO:0001179":null,"GO:0001664":null,"GO:0001965":null,"GO:0003779":null,"GO:0003785":null,"GO:0003786":null,"GO:0005102":null,"GO:0005515":null,"GO:0005516":null,"GO:0005519":null,"GO:0008017":null,"GO:0008179":null,"GO:0017025":null,"GO:0019902":null,"GO:0019903":null,"GO:0019905":null,"GO:0030276":null,"GO:0030332":null,"GO:0030544":null,"GO:0031072":null,"GO:0031267":null,"GO:0031369":null,"GO:0031593":null,"GO:0031624":null,"GO:0031625":null,"GO:0032036":null,"GO:0032050":null,"GO:0032051":null,"GO:0032182":null,"GO:0034236":null,"GO:0035226":null,"GO:0036435":null,"GO:0042393":null,"GO:0043130":null,"GO:0043175":null,"GO:0043424":null,"GO:0043548":null,"GO:0044389":null,"GO:0045503":null,"GO:0045504":null,"GO:0048487":null,"GO:0051010":null,"GO:0051011":null,"GO:0051015":null,"GO:0051020":null,"GO:0051082":null,"GO:0051087":null,"GO:0051117":null,"GO:0051787":null,"GO:0051879":null,"GO:0070063":null,"GO:0071074":null,"GO:0071889":null,"GO:0097602":null,"GO:0099122":null,"GO:1990269":null}}


id: GO:0050464
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: nitrite + NADP+ + H2O = nitrate + NADPH + H+.","definition_xrefs":["RHEA:19061"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nitrate reductase [NAD(P)H] activity","termid":"GO:0050463"}],"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:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"nitrate reductase (NADPH) activity","secondary_identifiers":["EC:1.7.1.3","MetaCyc:NITRATE-REDUCTASE-NADPH-RXN"],"synonyms":[{"name":"NADPH-nitrate reductase activity","type":"related"},{"name":"NADPH:nitrate oxidoreductase activity","type":"related"},{"name":"NADPH:nitrate reductase activity","type":"related"},{"name":"assimilatory NADPH-nitrate reductase activity","type":"related"},{"name":"assimilatory nitrate reductase activity","type":"broad"},{"name":"assimilatory reduced nicotinamide adenine dinucleotide phosphate-nitrate reductase activity","type":"related"},{"name":"nitrate reductase (NADPH(2)) activity","type":"related"},{"name":"nitrate reductase (NADPH2)","type":"related"},{"name":"nitrite:NADP+ oxidoreductase activity","type":"related"},{"name":"triphosphopyridine nucleotide-nitrate reductase activity","type":"related"}],"termid":"GO:0050464"}


id: GO:0019487
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving acetylene, a colorless, volatile, explosive gas, that occur in the absence of oxygen.","definition_xrefs":["ISBN:0721662544"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acetylene metabolic process","termid":"GO:0018864"},{"relation_name":"is_a","term_name":"xenobiotic catabolic process","termid":"GO:0042178"},{"relation_name":"is_a","term_name":"alkyne catabolic process","termid":"GO:0043454"}],"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":"anaerobic acetylene catabolic process","secondary_identifiers":["MetaCyc:P161-PWY"],"synonyms":[{"name":"anaerobic acetylene breakdown","type":"exact"},{"name":"anaerobic acetylene catabolism","type":"exact"},{"name":"anaerobic acetylene degradation","type":"exact"},{"name":"anaerobic ethyne catabolic process","type":"exact"},{"name":"anaerobic ethyne catabolism","type":"exact"}],"termid":"GO:0019487"}


id: PBO:0034274
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_start_sequence","termid":"PBO:0034274"}


id: FYPO:0000314
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce an elongated germ tube, and does not go on to give rise to a viable cell population.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable elongated vegetative cell","termid":"FYPO:0001490"},{"relation_name":"is_a","term_name":"inviable after spore germination with abnormal germ tube morphology","termid":"FYPO:0002281"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000004","FYPO:0001320","FYPO:0000002","FYPO:0000005"],"is_obsolete":false,"name":"inviable after spore germination with elongated germ tube","synonyms":[{"name":"inviable after spore germination, elongated cell","type":"exact"},{"name":"inviable following spore germination with elongated germ tube","type":"exact"},{"name":"inviable germinated spore with elongated germ tube","type":"exact"},{"name":"lethal after spore germination with elongated germ tube","type":"exact"}],"termid":"FYPO:0000314"}


id: PBO:0042547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cyclin dependent kinase 11B","termid":"PBO:0042547"}


id: MONDO:0010436
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic X-linked intellectual disability Lubs type","termid":"MONDO:0010283"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"chromosome Xq28 duplication syndrome","secondary_identifiers":["OMIM:300815","GARD:15266","UMLS:C2749007","MEDGEN:411727","MESH:C567580"],"synonyms":[{"name":"chromosome Xq28 duplication syndrome","type":"exact"}],"termid":"MONDO:0010436","xrefs":{"Monarch":{"xref_id":"0010436"}}}


id: PR:O74837
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- pmp31 gene.","definition_xrefs":["UniProtKB:O74837","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":"plasma membrane proteolipid 31 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1183.09c","synonyms":[{"name":"Spom972h-pmp31","type":"exact"},{"name":"meiotically up-regulated gene 75 protein (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O74837"}


id: MONDO:1010081
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autoimmune thrombocytopenic purpura that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autoimmune thrombocytopenia, non-human animal","termid":"MONDO:1010069"},{"relation_name":"is_a","term_name":"hereditary disease, non-human animal","termid":"MONDO:1011321"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"autoimmune thrombocytopenic purpura, non-human animal","secondary_identifiers":["OMIA:001104"],"termid":"MONDO:1010081","xrefs":{"Monarch":{"xref_id":"1010081"}}}


id: PATO:0000303
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A speed which is relatively high.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"increased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"speed","termid":"PATO:0000008"},{"relation_name":"is_a","term_name":"increased object quality","termid":"PATO:0002305"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"increased speed","synonyms":[{"name":"fast speed","type":"related"},{"name":"high speed","type":"exact"}],"termid":"PATO:0000303"}


id: PBO:0034294
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-visited_by","termid":"PBO:0034294"}


id: PBO:0073663
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SINHCAF pseudogene 3","termid":"PBO:0073663"}


id: MONDO:0014531
data:
  {"annotated_genes":["SJAG_04387","SJAG_02509"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87180,87181],"is_not":false,"summary":null,"term":"MONDO:0014531"}]},"cv_name":"mondo","definition":"Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the TUBA4A gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial amyotrophic lateral sclerosis","termid":"MONDO:0005144"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02509":null,"SJAG_04387":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"amyotrophic lateral sclerosis type 22","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:616208","DOID:0060355","GARD:16068","UMLS:C4015512","MEDGEN:863949"],"synonyms":[{"name":"ALS 22","type":"exact"},{"name":"ALS22","type":"related"},{"name":"TUBA4A amyotrophic lateral sclerosis","type":"exact"},{"name":"amyotrophic lateral sclerosis 22","type":"exact"},{"name":"amyotrophic lateral sclerosis 22 with or without frontotemporal dementia","type":"exact"},{"name":"amyotrophic lateral sclerosis caused by mutation in TUBA4A","type":"exact"},{"name":"amyotrophic lateral sclerosis type 22","type":"exact"}],"termid":"MONDO:0014531","terms_by_termid":{"MONDO:0014531":null},"xrefs":{"Monarch":{"xref_id":"0014531"}}}


id: GO:0043771
data:
  {"annotated_genes":["SJAG_00533","SJAG_03708"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[94786,116779],"is_not":false,"summary":null,"term":"GO:0043771"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + cytidine = ADP + CMP.","definition_xrefs":["PMID:211379","RHEA:24674"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleoside kinase activity","termid":"GO:0019206"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00533":null,"SJAG_03708":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016301","GO:0016740"],"is_obsolete":false,"name":"cytidine kinase activity","references_by_uniquename":{"GO_REF:0000107":null},"secondary_identifiers":["EC:2.7.1.213"],"synonyms":[{"name":"uridine-cytidine kinase activity","type":"narrow"}],"termid":"GO:0043771","terms_by_termid":{"GO:0043771":null}}


id: PBO:0085630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in fluoride export; nearly identical to FEX1, and deletion of both proteins results in a large increase in fluoride sensitivity compared with the single mutant; contains two FEX domains connected by a linker; part of a widespread family of conserved fluoride export proteins","termid":"PBO:0085630"}


id: PR:O94337
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A deoxyhypusine synthase that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR11703:SF0","OMA:SCHPO02423","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":"deoxyhypusine synthase (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1271.04c","secondary_identifiers":["UniProtKB:O94337"],"synonyms":[{"name":"DHS (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-DHPS","type":"exact"}],"termid":"PR:O94337"}


id: PBO:0058996
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MLX interacting protein like","termid":"PBO:0058996"}


id: PBO:0038947
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acireductone dioxygenase 1 pseudogene 2","termid":"PBO:0038947"}


id: GO:0141118
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: Fe(II)-heme b-[protein] + nitric oxide + O2 = Fe(III)-heme b-[protein] + nitrate.","definition_xrefs":["PMID:20511233"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on a heme group of donors","termid":"GO:0016675"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"nitric oxide dioxygenase activity, heme protein as donor","secondary_identifiers":["Reactome:R-HSA-5340226","RHEA:78091"],"termid":"GO:0141118"}


id: PBO:0062724
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 52 subfamily A member 1","termid":"PBO:0062724"}


id: PBO:0001358
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rho family GTPase Rho5","termid":"PBO:0001358"}


id: PBO:0067774
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 5S ribosomal pseudogene 74","termid":"PBO:0067774"}


id: GO:0034071
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: ATP + aminoglycoside = ADP + phosphoaminoglycoside.","definition_xrefs":["GOC:cb","GOC:mah"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016301"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016740","GO:0016301","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"aminoglycoside phosphotransferase activity","secondary_identifiers":["EC:2.7.1.190"],"synonyms":[{"name":"aminoglycoside kinase activity","type":"exact"}],"termid":"GO:0034071"}


id: GO:0060926
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a pacemaker cell over time, from its formation to the mature state. Pacemaker cells are specialized cardiomyocytes that are responsible for regulating the timing of heart contractions.","definition_xrefs":["GOC:mtg_cardiac_conduct_nov11","GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cardiac muscle cell development","termid":"GO:0055013"},{"relation_name":"part_of","term_name":"cardiac pacemaker cell differentiation","termid":"GO:0060920"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cardiac pacemaker cell development","synonyms":[{"name":"pacemaker cell development","type":"broad"}],"termid":"GO:0060926"}


id: GO:0098787
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Cleavage of an immature mRNA transcript to produce one or more more mature mRNA transcripts, prior to translation into polypeptide.","definition_xrefs":["GOC:dos"],"gene_count":0,"genotype_count":0,"name":"obsolete mRNA cleavage involved in mRNA processing (obsolete GO:0098787)","termid":"GO:0098787"}


id: GO:0033070
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways leading to the formation of ansamycins, any of a group of complex macrolactam compounds characterized by a cyclic structure in which an aliphatic ansa chain forms a bridge between two non-adjacent positions of a cyclic p-system; many exhibit antibacterial, antifungal or antitumor activity.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polyketide biosynthetic process","termid":"GO:0030639"},{"relation_name":"is_a","term_name":"ansamycin metabolic process","termid":"GO:0033069"},{"relation_name":"is_a","term_name":"lactam biosynthetic process","termid":"GO:0072339"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"ansamycin biosynthetic process","synonyms":[{"name":"ansamycin anabolism","type":"exact"},{"name":"ansamycin biosynthesis","type":"exact"},{"name":"ansamycin formation","type":"exact"},{"name":"ansamycin synthesis","type":"exact"}],"termid":"GO:0033070"}


id: MONDO:0000706
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A colitis caused by the introduction of harsh chemicals to the colon by an enema or other procedure. Chemical colitis can resemble ulcerative colitis, infectious colitis and pseudomembranous colitis endoscopically.","direct_ancestors":[{"relation_name":"is_a","term_name":"colitis","termid":"MONDO:0005292"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0004335"],"is_obsolete":false,"name":"chemical colitis","secondary_identifiers":["SCTID:72965009","ICD9:558","ICD9:558.9","DOID:0060186"],"termid":"MONDO:0000706","xrefs":{"Monarch":{"xref_id":"0000706"}}}


id: PBO:0000829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GTPase Ryh1","termid":"PBO:0000829"}


id: PBO:0079676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 W pseudogene 1","termid":"PBO:0079676"}


id: GO:0070687
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"The part of the cortical actin cytoskeleton that forms part of a macropinocytic cup.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"cortical actin cytoskeleton","termid":"GO:0030864"},{"relation_name":"part_of","term_name":"macropinocytic cup","termid":"GO:0070685"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0015629"},{"rel_name":"part_of","termid":"GO:0005737"},{"rel_name":"part_of","termid":"GO:0005938"}],"interesting_parent_ids":["GO:0005737","GO:0015629","GO:0005938","GO:0005575"],"is_obsolete":false,"name":"macropinocytic cup cytoskeleton","synonyms":[{"name":"crown cytoskeleton","type":"exact"}],"termid":"GO:0070687"}


id: GO:0071987
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a WD40 repeat domain of a protein. The WD40 repeat is a short structural motif of approximately 40 amino acids, often terminating in a tryptophan-aspartic acid (W-D) dipeptide. Several of these repeats are combined to form a type of protein domain called the WD domain.","definition_xrefs":["InterPro:IPR017986","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0005488","GO:0005515"],"is_obsolete":false,"name":"WD40-repeat domain binding","synonyms":[{"name":"WD domain binding","type":"exact"},{"name":"beta-transducin repeat domain binding","type":"exact"}],"termid":"GO:0071987"}


id: GO:0016170
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an interleukin-15 receptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cytokine receptor binding","termid":"GO:0005126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"interleukin-15 receptor binding","synonyms":[{"name":"IL-15","type":"narrow"},{"name":"interleukin-15 receptor ligand","type":"narrow"}],"termid":"GO:0016170"}


id: MONDO:0002571
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A non-Hodgkin or Hodgkin lymphoma that arises in the brain or spinal cord as a primary lesion. There is no evidence of lymphoma outside the central nervous system at the time of diagnosis.","definition_xrefs":["NCIT:C9301"],"direct_ancestors":[{"relation_name":"is_a","term_name":"immune system cancer","termid":"MONDO:0000621"},{"relation_name":"is_a","term_name":"central nervous system cancer","termid":"MONDO:0002714"},{"relation_name":"is_a","term_name":"central nervous system hematopoietic neoplasm","termid":"MONDO:0003641"},{"relation_name":"is_a","term_name":"neoplasm of mature B-cells","termid":"MONDO:0004949"},{"relation_name":"is_a","term_name":"primary organ-specific lymphoma","termid":"MONDO:0017207"},{"relation_name":"is_a","term_name":"Epstein-Barr virus-associated malignant lymphoproliferative disorder","termid":"MONDO:0017343"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"primary central nervous system lymphoma","secondary_identifiers":["Orphanet:46135","MONDO:0018732","DOID:3234","MedDRA:10036685","ONCOTREE:PCNSL","ICD9:200.5","NORD:2002","GARD:9318","EFO:1000157","SCTID:307649006","UMLS:C0280803","icd11.foundation:1133193893","MEDGEN:79187"],"synonyms":[{"name":"CNS lymphoma","type":"exact"},{"name":"PCNSL","type":"exact"},{"name":"central nervous system lymphoma","type":"exact"},{"name":"lymphoma of central nervous system","type":"exact"},{"name":"malignant lymphomas of CNS","type":"exact"},{"name":"malignant lymphomas of the CNS","type":"exact"},{"name":"microglioma","type":"exact"},{"name":"primary CNS lymphoma","type":"exact"},{"name":"primary brain lymphoma","type":"exact"},{"name":"primary central nervous system lymphoma","type":"exact"},{"name":"primary lymphoma, CNS","type":"related"}],"termid":"MONDO:0002571","xrefs":{"Monarch":{"xref_id":"0002571"}}}


id: GO:0021707
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which neuroblasts acquire specialized structural and/or functional features that characterize the mature cerebellar granule cell. Differentiation includes the processes involved in commitment of a neuroblast to a granule cell fate. A granule cell is a glutamatergic interneuron found in the cerebellar cortex.","definition_xrefs":["GO_REF:0000021","GOC:dgh","GOC:dph","PMID:15157725","GOC:jid","GOC:cls"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell differentiation in hindbrain","termid":"GO:0021533"},{"relation_name":"is_a","term_name":"central nervous system neuron differentiation","termid":"GO:0021953"},{"relation_name":"is_a","term_name":"glutamatergic neuron differentiation","termid":"GO:1905962"},{"relation_name":"part_of","term_name":"cerebellar granular layer formation","termid":"GO:0021684"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cerebellar granule cell differentiation","termid":"GO:0021707"}


id: PR:Q4LB35
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- fol1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q4LB35"],"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":"folic acid synthesis protein fol1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1734.03","synonyms":[{"name":"Spom972h-fol1","type":"exact"}],"termid":"PR:Q4LB35"}


id: MONDO:1012891
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hearing loss that occurs in sheep due to a mutation in the OTOF 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":"hearing loss disorder, non-human animal","termid":"MONDO:1012969"},{"relation_name":"is_a","term_name":"inherited auditory system disease, non-human animal","termid":"MONDO:1012970"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deafness, OTOF-related, sheep","secondary_identifiers":["OMIA:002413-9940"],"termid":"MONDO:1012891","xrefs":{"Monarch":{"xref_id":"1012891"}}}


id: GO:1904772
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 tetrachloromethane stimulus.","definition_xrefs":["GO_REF:0000071","GOC:TermGenie","PMID:7852267"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chemical","termid":"GO:0042221"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to tetrachloromethane","synonyms":[{"name":"response to CCL4","type":"exact"},{"name":"response to carbon tetrachloride","type":"exact"}],"termid":"GO:1904772"}


id: GO:0047659
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 1,2-dihydrosantonin + NAD(P)+ = alpha-santonin + NAD(P)H + H+.","definition_xrefs":["MetaCyc:ALPHA-SANTONIN-12-REDUCTASE-RXN","EC:1.3.1.47"],"direct_ancestors":[{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor","termid":"GO:0016628"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003824","GO:0016491","GO:0003674"],"is_obsolete":false,"name":"alpha-santonin 1,2-reductase activity","synonyms":[{"name":"1,2-dihydrosantonin:NAD(P)+ 1,2-oxidoreductase activity","type":"related"},{"name":"a-santonin 1,2-reductase activity","type":"exact"}],"termid":"GO:0047659"}


id: MONDO:0030978
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"EN1-related dorsoventral syndrome","termid":"MONDO:1040032"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ENDOVE syndrome, limb-only type","secondary_identifiers":["GARD:18560","MEDGEN:1787128","UMLS:C5543128","OMIM:619217"],"synonyms":[{"name":"ENDOVESL","type":"exact"},{"name":"Mesomelia of Lower Extremities With Hand and Foot Anomalies","type":"exact"}],"termid":"MONDO:0030978","xrefs":{"Monarch":{"xref_id":"0030978"}}}


id: MONDO:0043172
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":"pfeiffer rockelein syndrome","secondary_identifiers":["MESH:C537890","UMLS:C2931656","MEDGEN:419465"],"synonyms":[{"name":"asymmetrical coronal synostosis, cutaneous syndactyly of fingers and toes, and jejunal atresia","type":"related"}],"termid":"MONDO:0043172","xrefs":{"Monarch":{"xref_id":"0043172"}}}


id: PBO:0050956
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interferon gamma receptor 2","termid":"PBO:0050956"}


id: PBO:0047510
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"FERM domain containing kindlin 2","termid":"PBO:0047510"}


id: PBO:0091969
data:
  {"annotation_feature_type":"gene","cv_name":"warning","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"was previously annotated as SPNCRNA.503","termid":"PBO:0091969"}


id: PBO:0068869
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 109, pseudogene","termid":"PBO:0068869"}


id: SO:0000245
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"name":"OBSOLETE SO:0000245 mRNA_by_polyadenylation_status (obsolete SO:0000245)","termid":"SO:0000245"}


id: PBO:0052459
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KLF transcription factor 8","termid":"PBO:0052459"}


id: PBO:0111808
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SR family","termid":"PBO:0111808"}


id: PBO:0027072
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_mitotic_DNA_replication_lagging_strand_elongation_at_telomere","termid":"PBO:0027072"}


id: MONDO:1012840
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any polyneuropathy that occurs in dogs due to a mutation in the SBF2 gene.","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":"polyneuropathy, dog","termid":"MONDO:1012354"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"polyneuropathy, SBF2-related, dog","secondary_identifiers":["OMIA:002284-9615"],"synonyms":[{"name":"demyelinating polyneuropathy, dog","type":"related"}],"termid":"MONDO:1012840","xrefs":{"Monarch":{"xref_id":"1012840"}}}


id: GO:0102684
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: L-phenylalanine + 2 NADPH + 2 O2 + 2 H+ = (E)-phenylacetaldehyde oxime + 2 NADP + 3 H2O + carbon dioxide.","definition_xrefs":["GOC:pz","EC:1.14.14.40"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"L-phenylalanine N-monooxygenase activity","secondary_identifiers":["RHEA:33263","MetaCyc:RXN-4602"],"termid":"GO:0102684"}


id: GO:0044490
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of the activity of a voltage-gated sodium channel in another organism.","definition_xrefs":["PMID:21781281","GOC:fj","GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of voltage-gated sodium channel activity in another organism (obsolete GO:0044490)","synonyms":[{"name":"positive regulation of voltage-gated sodium channel activity in other organism","type":"exact"}],"termid":"GO:0044490"}


id: PBO:0038309
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein_degradation","termid":"PBO:0038309"}


id: GO:0090567
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of a reproductive shoot system over time, from its formation to the mature structure.","definition_xrefs":["GOC:pj"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic development","termid":"GO:0009791"},{"relation_name":"is_a","term_name":"shoot system development","termid":"GO:0048367"},{"relation_name":"is_a","term_name":"reproductive structure development","termid":"GO:0048608"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"reproductive shoot system development","termid":"GO:0090567"}


id: PBO:0074626
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, H/ACA box 22C","termid":"PBO:0074626"}


id: GO:0090630
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that initiates the activity of an inactive GTPase through the replacement of GDP by GTP.","definition_xrefs":["GOC:dph","GOC:mah","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of GTPase activity","termid":"GO:0043547"}],"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":"activation of GTPase activity","secondary_identifiers":["GO:0032856","GO:0032857","GO:0032862","GO:0032860","GO:0032858","GO:0032864","GO:0032859","GO:0032863","GO:0032861"],"synonyms":[{"name":"ARF GTPase activation","type":"narrow"},{"name":"Cdc42 GTPase activation","type":"narrow"},{"name":"Rab GTPase activation","type":"narrow"},{"name":"Rac GTPase activation","type":"narrow"},{"name":"Ral GTPase activation","type":"narrow"},{"name":"Ran GTPase activation","type":"narrow"},{"name":"Rap GTPase activation","type":"narrow"},{"name":"Ras GTPase activation","type":"narrow"},{"name":"Rho GTPase activation","type":"narrow"},{"name":"activation of ARF GTPase activity","type":"narrow"},{"name":"activation of Cdc42 GTPase activity","type":"narrow"},{"name":"activation of Rab GTPase activity","type":"narrow"},{"name":"activation of Rac GTPase activity","type":"narrow"},{"name":"activation of Ral GTPase activity","type":"narrow"},{"name":"activation of Ran GTPase activity","type":"narrow"},{"name":"activation of Rap GTPase activity","type":"narrow"},{"name":"activation of Ras GTPase activity","type":"narrow"},{"name":"activation of Rho GTPase activity","type":"narrow"}],"termid":"GO:0090630"}


id: PBO:0080428
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"VPS51 pseudogene 12","termid":"PBO:0080428"}


id: PBO:0051422
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 2-33 (non-functional)","termid":"PBO:0051422"}


id: PBO:0109841
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPATA31 subfamily G member 1","termid":"PBO:0109841"}


id: PBO:0066413
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RRAD and GEM like GTPase 1","termid":"PBO:0066413"}


id: GO:2000786
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of autophagic vacuole assembly.","definition_xrefs":["GOC:autophagy","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of macroautophagy","termid":"GO:0016239"},{"relation_name":"is_a","term_name":"positive regulation of vacuole organization","termid":"GO:0044090"},{"relation_name":"is_a","term_name":"positive regulation of organelle assembly","termid":"GO:1902117"},{"relation_name":"is_a","term_name":"regulation of autophagosome assembly","termid":"GO:2000785"},{"relation_name":"positively_regulates","term_name":"autophagosome assembly","termid":"GO:0000045"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006914"},{"rel_name":"regulates","termid":"GO:0044085"},{"rel_name":"positively_regulates","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0006914"}],"interesting_parent_ids":["GO:0008150","GO:0006914","GO:0044085"],"is_obsolete":false,"name":"positive regulation of autophagosome assembly","synonyms":[{"name":"positive regulation of PAS formation","type":"related"},{"name":"positive regulation of autophagic vacuole assembly","type":"exact"},{"name":"positive regulation of autophagic vacuole formation","type":"related"},{"name":"positive regulation of autophagosome biosynthesis","type":"exact"},{"name":"positive regulation of autophagosome formation","type":"exact"}],"termid":"GO:2000786"}


id: MONDO:0971031
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An acquired metabolic disease that is characterized by the endogenous production of ethanol produced through endogenous fermentation by fungi or bacteria in the gastrointestinal system, oral cavity, or urinary system and typically presents with the signs of alcohol intoxication.","definition_xrefs":["DOID:0081455"],"direct_ancestors":[{"relation_name":"is_a","term_name":"acquired metabolic disease","termid":"MONDO:0006504"}],"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":"auto-brewery syndrome","secondary_identifiers":["MEDGEN:1853294","UMLS:C4552195"],"termid":"MONDO:0971031","xrefs":{"Monarch":{"xref_id":"0971031"}}}


id: PBO:0034032
data:
  {"annotation_feature_type":"gene","cv_name":"pubprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canto_message_for_curators","termid":"PBO:0034032"}


id: PBO:0053789
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 1040","termid":"PBO:0053789"}


id: PBO:0116410
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S. pombe specific DUF999 family protein 6","termid":"PBO:0116410"}


id: GO:0051643
data:
  {"annotated_genes":["SJAG_04413","SJAG_01564","SJAG_04417","SJAG_00053","SJAG_01437","SJAG_01168","SJAG_01116","SJAG_02626","SJAG_03170","SJAG_04221"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[120028,62294,92220,99268,73602,60982,113516,62919],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0061817"},{"annotations":[92221,59785],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051685"},{"annotations":[108859,117062],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1990854"}]},"cv_name":"biological_process","definition":"Any process in which endoplasmic reticulum is transported to, and/or maintained in, a specific location within the cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organelle localization","termid":"GO:0051640"},{"relation_name":"part_of","term_name":"endoplasmic reticulum organization","termid":"GO:0007029"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_01116":null,"SJAG_01168":null,"SJAG_01437":null,"SJAG_01564":null,"SJAG_02626":null,"SJAG_03170":null,"SJAG_04221":null,"SJAG_04413":null,"SJAG_04417":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0051179"],"is_obsolete":false,"name":"endoplasmic reticulum localization","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"ER localization","type":"exact"},{"name":"endoplasmic reticulum localisation","type":"exact"},{"name":"establishment and maintenance of ER localization","type":"exact"}],"termid":"GO:0051643","terms_by_termid":{"GO:0051685":null,"GO:0061817":null,"GO:1990854":null}}


id: GO:0050969
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of events involved in magnetoception in which a chemical stimulus is received and converted into a molecular signal. It is believed that organisms such as birds and salamanders interpret product ratios in chemical reactions which involve transitions between different spin states.","definition_xrefs":["GOC:ai","GOC:dos"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detection of chemical stimulus involved in sensory perception","termid":"GO:0050907"},{"relation_name":"part_of","term_name":"magnetoreception by sensory perception of chemical stimulus","termid":"GO:0050977"}],"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":"detection of chemical stimulus involved in magnetoreception","synonyms":[{"name":"magnetoception, sensory transduction of chemical stimulus","type":"exact"},{"name":"magnetoreception, detection of chemical stimulus","type":"exact"},{"name":"magnetoreception, sensory detection of chemical stimulus","type":"exact"},{"name":"magnetoreception, sensory transduction of chemical stimulus","type":"exact"},{"name":"sensory detection of chemical stimulus during magnetoreception","type":"exact"},{"name":"sensory transduction of chemical stimulus during magnetoreception","type":"exact"}],"termid":"GO:0050969"}


id: PBO:0038310
data:
  {"annotation_feature_type":"gene","cv_name":"pubprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canto_first_sent_to_curator_date","termid":"PBO:0038310"}


id: GO:0180050
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"The binding activity of a molecule that brings together a protein or protein complex and a mitochondrial outer membrane lipid or membrane-associated protein, in order to maintain the localization of the protein, or protein complex at a specific mitochondrial outer membrane location.","definition_xrefs":["GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-membrane adaptor activity","termid":"GO:0043495"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0030674"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0060090"}],"interesting_parent_ids":["GO:0060090","GO:0030674","GO:0003674"],"is_obsolete":false,"name":"protein-mitochondrial outer membrane tethering activity","termid":"GO:0180050"}


id: PBO:0003190
data:
  {"annotation_feature_type":"gene","cv_name":"EC numbers","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"2.6.1.42","termid":"PBO:0003190"}


id: PBO:0058352
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4725","termid":"PBO:0058352"}


id: PBO:0040806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"betaine--homocysteine S-methyltransferase 2","termid":"PBO:0040806"}


id: PBO:0116501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin-repeat related protein","termid":"PBO:0116501"}


id: MONDO:0018002
data:
  {"annotated_genes":["SJAG_06022"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86907],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014656"}]},"cv_name":"mondo","definition":"Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy is a rare mitochondrial disease characterized by adult onset of progressive external ophthalmoplegia, exercise intolerance, muscle weakness, manifestations of spinocerebellar ataxia (e.g. impaired gait, dysarthria) and mild motor peripheral neuropathy. Respiratory insufficiency has been reported in some cases.","definition_xrefs":["Orphanet:329336"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inborn mitochondrial myopathy","termid":"MONDO:0009637"},{"relation_name":"is_a","term_name":"mitochondrial oxidative phosphorylation disorder","termid":"MONDO:0016387"}],"gene_count":1,"genes_by_uniquename":{"SJAG_06022":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004069"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004069","MONDO:0005336"],"is_obsolete":false,"name":"adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1393682","GARD:17503","SCTID:725464001","UMLS:C4511138"],"synonyms":[{"name":"adult-onset CPEO with mitochondrial myopathy","type":"exact"}],"termid":"MONDO:0018002","terms_by_termid":{"MONDO:0014656":null},"xrefs":{"Monarch":{"xref_id":"0018002"}}}


id: GO:0070985
data:
  {"annotated_genes":["SJAG_04614","SJAG_03618","SJAG_00150"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[61470,67369,77961],"is_not":false,"summary":null,"term":"GO:0070985"}]},"cv_name":"cellular_component","definition":"A transcription factor complex that forms part of the holo TFIIH complex. In Saccharomyces/human, TFIIK contains Ccl1p/Cyclin H, Tfb3p/MAT1 and Kin28p/CDK7.","definition_xrefs":["PMID:19818408","GOC:mah","PMID:22572993"],"direct_ancestors":[{"relation_name":"is_a","term_name":"RNA polymerase II transcription regulator complex","termid":"GO:0090575"},{"relation_name":"part_of","term_name":"transcription factor TFIIH holo complex","termid":"GO:0005675"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00150":null,"SJAG_03618":null,"SJAG_04614":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005654"},{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"part_of","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005654","GO:0005634","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"transcription factor TFIIK complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000117":null},"synonyms":[{"name":"Mcs6/Mcs2/Pmh1 complex","type":"narrow"},{"name":"TFIIK complex","type":"exact"},{"name":"cyclin H-CDK7 complex","type":"related"}],"termid":"GO:0070985","terms_by_termid":{"GO:0070985":null}}


id: PBO:0083795
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential protein of unknown function; exhibits variable expression during colony morphogenesis; overexpression permits survival without protein phosphatase 2A, inhibits growth, and induces a filamentous phenotype; PAM1 has a paralog, SVL3, that arose from the whole genome duplication","termid":"PBO:0083795"}


id: GO:1901581
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of telomeric RNA transcription from RNA pol II promoter.","definition_xrefs":["GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of telomeric RNA transcription from RNA pol II promoter (obsolete GO:1901581)","synonyms":[{"name":"down regulation of telomeric RNA transcription from Pol II promoter","type":"exact"},{"name":"down regulation of telomeric RNA transcription from RNA pol II promoter","type":"exact"},{"name":"down-regulation of telomeric RNA transcription from Pol II promoter","type":"exact"},{"name":"down-regulation of telomeric RNA transcription from RNA pol II promoter","type":"exact"},{"name":"downregulation of telomeric RNA transcription from Pol II promoter","type":"exact"},{"name":"downregulation of telomeric RNA transcription from RNA pol II promoter","type":"exact"},{"name":"inhibition of telomeric RNA transcription from Pol II promoter","type":"exact"},{"name":"inhibition of telomeric RNA transcription from RNA pol II promoter","type":"narrow"},{"name":"negative regulation of telomeric RNA transcription from Pol II promoter","type":"exact"}],"termid":"GO:1901581"}


id: PBO:0085106
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear response regulator and transcription factor; physically interacts with the Tup1-Cyc8 complex and recruits Tup1p to its targets; part of a branched two-component signaling system; required for optimal induction of heat-shock genes in response to oxidative stress; involved in osmoregulation; relocalizes to the cytosol in response to hypoxia; SKN7 has a paralog, HMS2, that arose from the whole genome duplication","termid":"PBO:0085106"}


id: MONDO:0012522
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any transient neonatal diabetes mellitus in which the cause of the disease is a mutation in the KCNJ11 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transient neonatal diabetes mellitus","termid":"MONDO:0020525"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0005015"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0005015","MONDO:0005066"],"is_obsolete":false,"name":"diabetes mellitus, transient neonatal, 3","secondary_identifiers":["SCTID:609581006","MESH:C566432","OMIM:610582","UMLS:C1864623","MEDGEN:351177","GARD:15490"],"synonyms":[{"name":"KCNJ11 transient neonatal diabetes mellitus (disease)","type":"exact"},{"name":"Tndm3","type":"related"},{"name":"diabetes mellitus, transient neonatal 3","type":"exact"},{"name":"diabetes mellitus, transient neonatal, 3","type":"exact"},{"name":"diabetes mellitus, transient neonatal, type 3","type":"exact"},{"name":"diabetes mellitus, type II, autosomal dominant","type":"related"},{"name":"transient neonatal diabetes mellitus (disease) caused by mutation in KCNJ11","type":"exact"}],"termid":"MONDO:0012522","xrefs":{"Monarch":{"xref_id":"0012522"}}}


id: PBO:0039570
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ankyrin repeat domain 65","termid":"PBO:0039570"}


id: PBO:0059635
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 1","termid":"PBO:0059635"}


id: PBO:0045054
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deleted in lymphocytic leukemia 2","termid":"PBO:0045054"}


id: PBO:0083183
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; completely overlaps the tRNA ORF tI(AAU)N2","termid":"PBO:0083183"}


id: PBO:0074077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SLC25A51 pseudogene 1","termid":"PBO:0074077"}


id: MONDO:0022963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A WHO grade I large cystic tumor that occurs almost exclusively in infants, with a prominent desmoplastic stroma having a neuroepithelial population consisting mainly of neoplastic astrocytes. It involves the superficial cerebral cortex and leptomeninges, and often attaches to the dura. Although clinically it presents as large tumor, it generally has a good prognosis following surgical resection. (Adapted from WHO)","definition_xrefs":["NCIT:C9476"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mixed neuronal-glial tumor","termid":"MONDO:0016729"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"desmoplastic infantile astrocytoma","secondary_identifiers":["ICDO:9412/1","GARD:9617","UMLS:C0457179","MEDGEN:141595","ONCOTREE:DIA"],"synonyms":[{"name":"DIA","type":"exact"},{"name":"Desmoplastic astrocytoma of infancy","type":"exact"},{"name":"Desmoplastic infantile astrocytoma","type":"exact"}],"termid":"MONDO:0022963","xrefs":{"Monarch":{"xref_id":"0022963"}}}


id: FYPO:0003638
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which occurrence of ADP binding by a gene product (usually a protein) in a mutant is increased. The affected gene product may be encoded by the mutated gene, or by a different gene.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal ADP binding","termid":"FYPO:0003637"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000652","FYPO:0000707"],"is_obsolete":false,"name":"increased ADP binding","termid":"FYPO:0003638"}


id: PBO:0060067
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 14","termid":"PBO:0060067"}


id: GO:1904504
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of lipophagy.","definition_xrefs":["GOC:dph","GOC:autophagy","PMID:25383539","GOC:TermGenie","GO_REF:0000058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of macroautophagy","termid":"GO:0016239"},{"relation_name":"is_a","term_name":"regulation of lipophagy","termid":"GO:1904502"},{"relation_name":"positively_regulates","term_name":"lipophagy","termid":"GO:0061724"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006914"},{"rel_name":"positively_regulates","termid":"GO:0006914"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006914"],"is_obsolete":false,"name":"positive regulation of lipophagy","synonyms":[{"name":"activation of lipophagy","type":"narrow"},{"name":"up regulation of lipophagy","type":"exact"},{"name":"up-regulation of lipophagy","type":"exact"},{"name":"upregulation of lipophagy","type":"exact"}],"termid":"GO:1904504"}


id: PBO:0005355
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA snR10","termid":"PBO:0005355"}


id: PBO:0063962
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphatidylinositol-4-phosphate 5-kinase like 1","termid":"PBO:0063962"}


id: PBO:0002017
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"UBA domain protein Dph1","termid":"PBO:0002017"}


id: FYPO:0006617
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype in which a vegetative cell is viable, elongated, and has a greater diameter than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viable elongated vegetative cell","termid":"FYPO:0001492"},{"relation_name":"is_a","term_name":"viable vegetative cell with increased cell diameter","termid":"FYPO:0006616"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0000004","FYPO:0000005"],"is_obsolete":false,"name":"viable elongated vegetative cell with increased cell diameter","synonyms":[{"name":"viable elongated cell with increased cell diameter during vegetative growth","type":"exact"},{"name":"viable elongated vegetative cell with increased cell diameter during mitotic cell cycle","type":"related"},{"name":"viable elongated vegetative cell with increased cell thickness","type":"exact"},{"name":"viable elongated vegetative cell with increased cell width","type":"exact"}],"termid":"FYPO:0006617"}


id: PBO:0071141
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L22 pseudogene 4","termid":"PBO:0071141"}


id: GO:0060339
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that decreases the rate, frequency or extent of a type I interferon-mediated signaling pathway.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine-mediated signaling pathway","termid":"GO:0001960"},{"relation_name":"is_a","term_name":"negative regulation of innate immune response","termid":"GO:0045824"},{"relation_name":"is_a","term_name":"regulation of type I interferon-mediated signaling pathway","termid":"GO:0060338"},{"relation_name":"negatively_regulates","term_name":"type I interferon-mediated signaling pathway","termid":"GO:0060337"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"negative regulation of type I interferon-mediated signaling pathway","synonyms":[{"name":"negative regulation of type I interferon-mediated signalling pathway","type":"exact"}],"termid":"GO:0060339"}


id: PBO:0011107
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Rapadilino syndrome","termid":"PBO:0011107"}


id: PBO:0028584
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-elongated_cell_during_stationary_phase","termid":"PBO:0028584"}


id: MONDO:0035426
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete rare disorder potentially indicated for transplant or complication after transplantation (obsolete MONDO:0035426)","secondary_identifiers":["Orphanet:565779"],"termid":"MONDO:0035426","xrefs":{"Monarch":{"xref_id":"0035426"}}}


id: GO:1904111
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of plus-end directed microfilament motor activity.","definition_xrefs":["GOC:kmv","GO_REF:0000059","GOC:TermGenie","PMID:25717181"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of plus-end directed microfilament motor activity (obsolete GO:1904111)","synonyms":[{"name":"down regulation of barbed-end directed actin-filament motor activity","type":"exact"},{"name":"down regulation of plus-end directed actin filament motor activity","type":"related"},{"name":"down regulation of plus-end directed actin-filament motor activity","type":"exact"},{"name":"down regulation of plus-end directed microfilament motor activity","type":"exact"},{"name":"down-regulation of barbed-end directed actin-filament motor activity","type":"exact"},{"name":"down-regulation of plus-end directed actin filament motor activity","type":"related"},{"name":"down-regulation of plus-end directed actin-filament motor activity","type":"exact"},{"name":"down-regulation of plus-end directed microfilament motor activity","type":"exact"},{"name":"downregulation of barbed-end directed actin-filament motor activity","type":"exact"},{"name":"downregulation of plus-end directed actin filament motor activity","type":"related"},{"name":"downregulation of plus-end directed actin-filament motor activity","type":"exact"},{"name":"downregulation of plus-end directed microfilament motor activity","type":"exact"},{"name":"inhibition of barbed-end directed actin-filament motor activity","type":"narrow"},{"name":"inhibition of plus-end directed actin filament motor activity","type":"related"},{"name":"inhibition of plus-end directed actin-filament motor activity","type":"narrow"},{"name":"inhibition of plus-end directed microfilament motor activity","type":"narrow"},{"name":"negative regulation of barbed-end directed actin-filament motor activity","type":"exact"},{"name":"negative regulation of plus-end directed actin filament motor activity","type":"related"},{"name":"negative regulation of plus-end directed actin-filament motor activity","type":"exact"}],"termid":"GO:1904111"}


id: FYPO:0002336
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A transcription regulation phenotype observed in the vegetative growth phase of the life cycle in which chromatin silencing at the silent mating-type cassettes is normal (i.e. indistinguishable from wild type). Chromatin silencing is the observed effect of processes that repress transcription in a region of the genome that is normally assembled into heterochromatin.","definition_xrefs":["PomBase:vw","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal chromatin silencing","termid":"FYPO:0002335"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000257","FYPO:0001320","FYPO:0001312","FYPO:0000002"],"is_obsolete":false,"name":"normal chromatin silencing at silent mating-type cassette","synonyms":[{"name":"normal chromatin silencing at mating-type region heterochromatin","type":"exact"},{"name":"normal chromatin silencing at silent mating-type cassette during mitotic cell cycle","type":"related"},{"name":"normal chromatin silencing at silent mating-type cassette during vegetative growth","type":"exact"}],"termid":"FYPO:0002336"}


id: GO:0042400
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of ectoine (1,4,5,6-tetrahydro-2-methyl-4-pyrimidinecarboxylic acid), a tetrahydropyrimidine commonly synthesized by halophilic bacteria.","definition_xrefs":["GOC:jl","PMID:11823218"],"direct_ancestors":[{"relation_name":"is_a","term_name":"ectoine metabolic process","termid":"GO:0042399"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"ectoine catabolic process","synonyms":[{"name":"ectoine breakdown","type":"exact"},{"name":"ectoine catabolism","type":"exact"},{"name":"ectoine degradation","type":"exact"}],"termid":"GO:0042400"}


id: FYPO:0006212
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, when spore germination takes place under conditions of copper ion starvation. 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, before germ tube formation","termid":"FYPO:0006211"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000004","FYPO:0001320"],"is_obsolete":false,"name":"inviable after spore germination, before germ tube formation, during copper ion starvation","synonyms":[{"name":"inviable after spore germination, before germ tube formation, during cellular response to copper ion starvation","type":"exact"},{"name":"inviable after spore germination, before germ tube formation, during copper starvation","type":"exact"},{"name":"inviable following spore germination, before germ tube formation, during copper ion starvation","type":"exact"},{"name":"inviable germinated spore, without germ tube formation, during copper ion starvation","type":"exact"},{"name":"lethal after spore germination, before germ tube formation, during copper ion starvation","type":"exact"}],"termid":"FYPO:0006212"}


id: MONDO:0030472
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"genetic developmental and epileptic encephalopathy","termid":"MONDO:0100062"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"},{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0005027","MONDO:0700092"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy 98","secondary_identifiers":["MEDGEN:1794227","OMIM:619605","DOID:0070384","UMLS:C5562017"],"synonyms":[{"name":"DEE98","type":"exact"}],"termid":"MONDO:0030472","xrefs":{"Monarch":{"xref_id":"0030472"}}}


id: GO:0033342
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents, or reduces the frequency, rate or extent of collagen binding.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of collagen binding (obsolete GO:0033342)","synonyms":[{"name":"down regulation of collagen binding","type":"exact"},{"name":"down-regulation of collagen binding","type":"exact"},{"name":"downregulation of collagen binding","type":"exact"},{"name":"inhibition of collagen binding","type":"narrow"}],"termid":"GO:0033342"}


id: GO:2000979
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of forebrain neuron differentiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of neuron differentiation","termid":"GO:0045666"},{"relation_name":"is_a","term_name":"regulation of forebrain neuron differentiation","termid":"GO:2000977"},{"relation_name":"positively_regulates","term_name":"forebrain neuron differentiation","termid":"GO:0021879"}],"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 forebrain neuron differentiation","termid":"GO:2000979"}


id: MONDO:0100348
data:
  {"annotated_genes":["SJAG_02517"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87563],"is_not":false,"summary":null,"term":"MONDO:0100348"}]},"cv_name":"mondo","definition":"An autosomal recessive disorder characterized by global developmental delay apparent in infancy. Affected individuals have delayed walking with variable gait abnormalities, impaired intellectual development with poor or absent speech and language, and progressive microcephaly. More variable features include hypotonia, early-onset seizures, and a peripheral demyelinating or axonal peripheral sensorimotor neuropathy. The disease follows a neurodegenerative course in many patients; clinical features suggest involvement of both the central and peripheral nervous systems.","definition_xrefs":["OMIM:619091"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02517":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1731507","GARD:18534","UMLS:C5436783"],"synonyms":[{"name":"NEDMILG, AR","type":"exact"},{"name":"neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive","type":"exact"}],"termid":"MONDO:0100348","terms_by_termid":{"MONDO:0100348":null},"xrefs":{"Monarch":{"xref_id":"0100348"}}}


id: MONDO:0013773
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any porencephaly in which the cause of the disease is a mutation in the COL4A2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"familial porencephaly","termid":"MONDO:0020496"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"porencephaly 2","secondary_identifiers":["DOID:0112314","UMLS:C3280970","GARD:15808","MEDGEN:482600","OMIM:614483"],"synonyms":[{"name":"COL4A2 porencephaly","type":"exact"},{"name":"POREN2","type":"related"},{"name":"brain small vessel disease 2","type":"exact"},{"name":"porencephaly 2","type":"exact"},{"name":"porencephaly caused by mutation in COL4A2","type":"exact"},{"name":"porencephaly type 2","type":"exact"}],"termid":"MONDO:0013773","xrefs":{"Monarch":{"xref_id":"0013773"}}}


id: PBO:0066577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RHEB pseudogene 1","termid":"PBO:0066577"}


id: MONDO:0003344
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete hemangioblastoma (obsolete MONDO:0003344)","termid":"MONDO:0003344","xrefs":{"Monarch":{"xref_id":"0003344"}}}


id: PBO:0063124
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"poly(ADP-ribose) polymerase family member 9","termid":"PBO:0063124"}


id: GO:0106402
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of a Lewis x epitope, a trisaccharide (beta-D-galactosyl-(1,4)-[alpha-L-fucosyl-(1,3)]-N-acetyl-beta-D-glucosamine) expressed on several glycolipids, glycoproteins, and proteoglycans of the nervous system. The related Lewis x epitope is formed by alpha(1,3) fucosylation of the N-acetylglucosaminyl residue of a type 2 histo-blood group antigen precursor disaccharide.","definition_xrefs":["PMID:16973732","PMID:23000574"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbohydrate derivative biosynthetic process","termid":"GO:1901137"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"Lewis x epitope biosynthetic process","synonyms":[{"name":"sLeX biosynthetic process","type":"related"},{"name":"sialyl-Lewis X biosynthetic process","type":"related"}],"termid":"GO:0106402"}


id: PBO:0109969
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CIA machinery iron sulphur cluster to apoprotein adaptor Mms19","termid":"PBO:0109969"}


id: PR:O59743
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPBC530.07c gene.","definition_xrefs":["UniProtKB:O59743","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 C530.07c (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC530.07c","synonyms":[{"name":"Spom972h-SPBC530.07c","type":"exact"}],"termid":"PR:O59743"}


id: PBO:0072822
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sterile alpha motif domain containing 15","termid":"PBO:0072822"}


id: FYPO:0001179
data:
  {"alleles_by_uniquename":{"SJAG_01050:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01050","name":"nur1delta","uniquename":"SJAG_01050:allele-1"},"SJAG_01143:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01143","name":"mid1delta","uniquename":"SJAG_01143:allele-1"},"SJAG_02392:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02392","name":"pom1delta","uniquename":"SJAG_02392:allele-1"},"SJAG_03892:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03892","name":"vps4delta","uniquename":"SJAG_03892:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"multi_locus_phenotype":[{"annotations":[121311],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0001132"},{"annotations":[121355],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007177"}],"single_locus_phenotype":[{"annotations":[121345,121344,121352,121356],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"FYPO:0007177"}]},"cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which a protein does not localize to, and is therefore absent from, a place where it is normally found in the vegetative growth phase of the life cycle.","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":"abolished protein localization","termid":"FYPO:0001375"}],"gene_count":4,"genes_by_uniquename":{"SJAG_01050":null,"SJAG_01143":null,"SJAG_01665":null,"SJAG_01745":null,"SJAG_02392":null,"SJAG_03596":null,"SJAG_03703":null,"SJAG_03892":null,"SJAG_04498":null},"genotype_count":3,"genotypes_by_uniquename":{"mid1delta":{"display_name":"mid1delta","display_uniquename":"mid1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]}]},"mid1delta__pom1delta":{"display_name":"mid1delta pom1delta","display_uniquename":"mid1delta__pom1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01143:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_02392:allele-1","expression":"Null"}]}]},"nur1delta__vps4delta":{"display_name":"nur1delta vps4delta","display_uniquename":"nur1delta__vps4delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01050:allele-1","expression":"Null"}]},{"expressed_alleles":[{"allele_uniquename":"SJAG_03892:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000002","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"multi_locus_annotated_genes":["SJAG_03892","SJAG_01050","SJAG_01143","SJAG_02392"],"name":"abolished protein localization during vegetative growth","references_by_uniquename":{"PMID:25866389":null,"PMID:32109380":null},"single_locus_annotated_genes":["SJAG_01143"],"single_locus_genotype_uniquenames":["mid1delta"],"synonyms":[{"name":"abolished protein localisation during vegetative growth","type":"exact"},{"name":"abolished protein localization during mitotic cell cycle","type":"related"},{"name":"protein absent from specific location in cell during vegetative growth","type":"related"},{"name":"protein localization abolished during vegetative growth","type":"exact"}],"termid":"FYPO:0001179","terms_by_termid":{"FYECO:0000005":null,"FYECO:0000137":null,"FYPO:0001132":null,"FYPO:0007177":null,"FYPO_EXT:0000001":null}}


id: MONDO:0800354
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"febrile seizures, familial","termid":"MONDO:0000032"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"febrile seizures, familial, 3b","secondary_identifiers":["UMLS:C3151229","MEDGEN:462579"],"synonyms":[{"name":"FEB3B","type":"exact"}],"termid":"MONDO:0800354","xrefs":{"Monarch":{"xref_id":"0800354"}}}


id: GO:0102413
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 6-O-methyl-N-deacetylisoipecoside + H2O = 6-O-methyl-N-deacetylisoipecoside aglycon + D-glucose.","definition_xrefs":["RHEA:78891"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, hydrolyzing O-glycosyl compounds","termid":"GO:0004553"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0016798"}],"interesting_parent_ids":["GO:0016798","GO:0003824","GO:0016787","GO:0003674"],"is_obsolete":false,"name":"6-O-methyl-deacetylisoipecoside beta-glucosidase activity","secondary_identifiers":["MetaCyc:RXN-13791"],"termid":"GO:0102413"}


id: PBO:0000549
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"serine carboxypeptidase Sxa2","termid":"PBO:0000549"}


id: PBO:0046391
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EP400 pseudogene 1","termid":"PBO:0046391"}


id: MONDO:0003948
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hemangioma arising from the cerebral hemisphere.","definition_xrefs":["NCIT:C5433"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain hemangioma","termid":"MONDO:0003428"},{"relation_name":"is_a","term_name":"benign neoplasm of cerebrum","termid":"MONDO:0021497"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cerebral hemangioma","secondary_identifiers":["MEDGEN:164084","UMLS:C0877388","DOID:6621"],"synonyms":[{"name":"angioma of cerebral hemispheres","type":"exact"},{"name":"angioma of cerebrum","type":"exact"},{"name":"angioma of the cerebral hemispheres","type":"exact"},{"name":"angioma of the cerebrum","type":"exact"},{"name":"cerebral angioma","type":"exact"},{"name":"cerebral hemangioma","type":"exact"},{"name":"cerebral hemispheric angioma","type":"exact"},{"name":"cerebral hemispheric hemangioma","type":"exact"},{"name":"hemangioma of cerebral hemispheres","type":"exact"},{"name":"hemangioma of cerebrum","type":"exact"},{"name":"hemangioma of telencephalon","type":"exact"},{"name":"hemangioma of the cerebral hemispheres","type":"exact"},{"name":"hemangioma of the cerebrum","type":"exact"},{"name":"telencephalon hemangioma","type":"exact"}],"termid":"MONDO:0003948","xrefs":{"Monarch":{"xref_id":"0003948"}}}


id: FYPO:0001290
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 a phosphoinositide measured in a cell differs from normal. A phosphoinositide is any phosphatidylinositol that is phosphorylated at one or more of the hydroxy groups of inositol.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered phospholipid level","termid":"FYPO:0001287"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000002","FYPO:0001320"],"is_obsolete":false,"name":"altered cellular phosphoinositide level","synonyms":[{"name":"abnormal cellular phosphoinositide level","type":"exact"},{"name":"altered PI accumulation","type":"related"},{"name":"altered cellular PI level","type":"related"},{"name":"altered cellular phosphoinositide level during mitotic cell cycle","type":"related"},{"name":"altered cellular phosphoinositide level during vegetative growth","type":"exact"}],"termid":"FYPO:0001290"}


id: PR:O94691
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- jmj3 gene.","definition_xrefs":["UniProtKB:O94691","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":"lid2 complex component jmj3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC83.07","synonyms":[{"name":"Lid2C component jmj3 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-jmj3","type":"exact"}],"termid":"PR:O94691"}


id: FYPO:0002266
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 one or more polysaccharides measured in the cell wall is lower than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased polysaccharide level during vegetative growth","termid":"FYPO:0001080"},{"relation_name":"is_a","term_name":"decreased level of substance in cell wall during vegetative growth","termid":"FYPO:0002628"},{"relation_name":"output_of","term_name":"abnormal cell wall biogenesis","termid":"FYPO:0000174"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased cell wall polysaccharide level","synonyms":[{"name":"decreased cell wall polysaccharide accumulation","type":"related"},{"name":"decreased cell wall polysaccharide level during mitotic cell cycle","type":"related"},{"name":"decreased cell wall polysaccharide level during vegetative growth","type":"exact"},{"name":"reduced cell wall polysaccharide level","type":"exact"}],"termid":"FYPO:0002266"}


id: GO:0034581
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 4-methyloct-2-enoyl-CoA + H2O = 3-hydroxy-4-methyloctanoyl-CoA.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 4-methyloct-2-enoyl-CoA hydratase activity (obsolete GO:0034581)","termid":"GO:0034581"}


id: PBO:0087248
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Serine-threonine kinase and endoribonuclease; transmembrane protein that mediates the unfolded protein response (UPR) by regulating Hac1p synthesis through HAC1 mRNA splicing; role in homeostatic adaptation to ER stress; Kar2p binds inactive Ire1p and releases from it upon ER stress","termid":"PBO:0087248"}


id: GO:1901300
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of hydrogen peroxide-mediated programmed cell death.","definition_xrefs":["GOC:TermGenie","GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of programmed cell death","termid":"GO:0043068"},{"relation_name":"is_a","term_name":"regulation of hydrogen peroxide-mediated programmed cell death","termid":"GO:1901298"},{"relation_name":"positively_regulates","term_name":"hydrogen peroxide-mediated programmed cell death","termid":"GO:0010421"}],"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 hydrogen peroxide-mediated programmed cell death","synonyms":[{"name":"activation of hydrogen peroxide-mediated programmed cell death","type":"narrow"},{"name":"up regulation of hydrogen peroxide-mediated programmed cell death","type":"exact"},{"name":"up-regulation of hydrogen peroxide-mediated programmed cell death","type":"exact"},{"name":"upregulation of hydrogen peroxide-mediated programmed cell death","type":"exact"}],"termid":"GO:1901300"}


id: FYPO:0007992
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the mitotic spindle pole body is decreased during metaphase.","definition_xrefs":["PomBase:mlr","PMID:35286199"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to mitotic spindle pole body during mitosis","termid":"FYPO:0002822"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0001320","FYPO:0005447","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased protein localization to mitotic spindle pole body during metaphase","synonyms":[{"name":"decreased protein localisation to mitotic spindle pole body during metaphase","type":"exact"},{"name":"decreased protein localization to mitotic SPB during metaphase","type":"exact"}],"termid":"FYPO:0007992"}


id: MONDO:1011878
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sensory ataxic neuropathy, non-human animal","secondary_identifiers":["OMIA:001467"],"termid":"MONDO:1011878","xrefs":{"Monarch":{"xref_id":"1011878"}}}


id: PR:000037082
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A tropomyosin cdc8 (Schizosaccharomyces pombe) that has not been post-translationally modified to include an acetylated N-terminal methionine.","definition_xrefs":["PRO:DAN"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tropomyosin cdc8 (Schizosaccharomyces pombe)","termid":"PR:000027986"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cdc8/UnMod(M1)","pombase_gene_id":"SPAC27F1.02c","synonyms":[{"name":"PomBase_original_PRO_term_name: tropomyosin cdc8, non-acetylated form (Schizosaccharomyces pombe)","type":"exact"},{"name":"Spom-cdc8/AcRes-","type":"exact"},{"name":"cdc8/UnMod(M1)","type":"exact"}],"termid":"PR:000037082"}


id: PBO:0002036
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"40S ribosomal protein S4 (predicted)","termid":"PBO:0002036"}


id: MONDO:0000909
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes.","definition_xrefs":["PMID:15044642","DOID:0110146"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Bartter syndrome type 4","termid":"MONDO:0019524"}],"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":"Bartter disease type 4B","secondary_identifiers":["GARD:15612","MEDGEN:934772","UMLS:C4310805","OMIM:613090"],"synonyms":[{"name":"BARTS4B","type":"exact"},{"name":"Bartter disease type 4B","type":"exact"},{"name":"Bartter syndrome, infantile, with sensorineural deafness","type":"related"},{"name":"Bartter syndrome, type 4B","type":"exact"},{"name":"Bartter syndrome, type 4B, neonatal, with sensorineural deafness","type":"related"},{"name":"Bartter syndrome, type 4b, digenic","type":"exact"},{"name":"neonatal Bartter syndrome type 4B with sensorineural deafness","type":"exact"}],"termid":"MONDO:0000909","xrefs":{"Monarch":{"xref_id":"0000909"}}}


id: PBO:0051527
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 1 receptor antagonist","termid":"PBO:0051527"}


id: PBO:0012582
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cell Wall Lysis","termid":"PBO:0012582"}


id: MONDO:0005611
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"The most common morphologic subtype of urinary bladder carcinoma (over 90% of cases). It arises from the transitional epithelium. It most often affects males in their sixth and seventh decades of life. Hematuria is the most common symptom at presentation. Pathologic stage is the strongest predictor of survival.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urinary bladder carcinoma","termid":"MONDO:0004986"},{"relation_name":"is_a","term_name":"urothelial carcinoma","termid":"MONDO:0040679"}],"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":"bladder transitional cell carcinoma","secondary_identifiers":["EFO:0006544","NCIT:C39851","ONCOTREE:BLCA","MEDGEN:76013","DOID:4006","SCTID:255109008","UMLS:C0279680"],"synonyms":[{"name":"BLCA","type":"related"},{"name":"bladder transitional cell carcinoma","type":"exact"},{"name":"bladder urothelial cancer","type":"exact"},{"name":"bladder urothelial carcinoma","type":"exact"},{"name":"transitional cell carcinoma of bladder","type":"exact"},{"name":"transitional cell carcinoma of the urinary bladder","type":"exact"},{"name":"urinary bladder transitional cell carcinoma","type":"exact"},{"name":"urinary bladder urothelial carcinoma","type":"exact"},{"name":"urothelial bladder carcinoma","type":"exact"},{"name":"urothelial carcinoma of the urinary bladder","type":"exact"}],"termid":"MONDO:0005611","xrefs":{"Monarch":{"xref_id":"0005611"}}}


id: PBO:0038654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acid phosphatase 4","termid":"PBO:0038654"}


id: GO:1904894
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of receptor signaling pathway via STAT.","definition_xrefs":["GOC:TermGenie","PMID:24587195","GO_REF:0000058","GOC:rjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of signal transduction","termid":"GO:0009967"},{"relation_name":"is_a","term_name":"regulation of receptor signaling pathway via STAT","termid":"GO:1904892"},{"relation_name":"positively_regulates","term_name":"cell surface receptor signaling pathway via STAT","termid":"GO:0097696"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0023052","GO:0008150"],"is_obsolete":false,"name":"positive regulation of receptor signaling pathway via STAT","secondary_identifiers":["Reactome:R-HSA-9027283"],"synonyms":[{"name":"activation of STAT cascade","type":"narrow"},{"name":"activation of STAT signalling pathway","type":"narrow"},{"name":"activation of kinase activated-STAT cascade","type":"narrow"},{"name":"activation of kinase-STAT cascade","type":"narrow"},{"name":"positive regulation of STAT signalling pathway","type":"exact"},{"name":"positive regulation of kinase activated-STAT cascade","type":"exact"},{"name":"positive regulation of kinase-STAT cascade","type":"exact"},{"name":"up regulation of STAT cascade","type":"exact"},{"name":"up regulation of STAT signalling pathway","type":"exact"},{"name":"up regulation of kinase activated-STAT cascade","type":"exact"},{"name":"up regulation of kinase-STAT cascade","type":"exact"},{"name":"up-regulation of STAT cascade","type":"exact"},{"name":"up-regulation of STAT signalling pathway","type":"exact"},{"name":"up-regulation of kinase activated-STAT cascade","type":"exact"},{"name":"up-regulation of kinase-STAT cascade","type":"exact"},{"name":"upregulation of STAT cascade","type":"exact"},{"name":"upregulation of STAT signalling pathway","type":"exact"},{"name":"upregulation of kinase activated-STAT cascade","type":"exact"},{"name":"upregulation of kinase-STAT cascade","type":"exact"}],"termid":"GO:1904894"}


id: FYPO:0002821
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to the mitotic spindle pole body is decreased during interphase.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to mitotic spindle pole body","termid":"FYPO:0000940"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0000138","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to mitotic spindle pole body during interphase","synonyms":[{"name":"decreased protein localisation to mitotic spindle pole body during interphase","type":"exact"},{"name":"decreased protein localization to mitotic SPB during interphase","type":"exact"},{"name":"decreased protein localization to mitotic spindle pole body during mitotic interphase","type":"exact"},{"name":"decreased protein localization to spindle pole body during interphase during vegetative growth","type":"exact"},{"name":"reduced protein localization to mitotic spindle pole body during interphase","type":"exact"}],"termid":"FYPO:0002821"}


id: MONDO:0003135
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Inflammation of a specific segment of glomeruli, which is associated with subacute bacterial endocarditis, and frequently produces microscopic hematuria without azotemia.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glomerulonephritis","termid":"MONDO:0002462"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0005240"],"is_obsolete":false,"name":"focal embolic glomerulonephritis","secondary_identifiers":["UMLS:C0238143","NCIT:C35707","DOID:4779","MEDGEN:65950"],"termid":"MONDO:0003135","xrefs":{"Monarch":{"xref_id":"0003135"}}}


id: GO:0061692
data:
  {"annotated_genes":["SJAG_01199","SJAG_04823","SJAG_04953","SJAG_00141","SJAG_01216","SJAG_02515"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[97013,101819,106876,110676,119232,120168],"is_not":false,"summary":null,"term":"GO:0061692"}]},"cv_name":"biological_process","definition":"Any process that reduces or removes the toxicity of hydrogen peroxide in a cell. These include transport of hydrogen peroxide away from sensitive areas and to compartments or complexes whose purpose is sequestration.","definition_xrefs":["GOC:dph","GOC:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"detoxification of hydrogen peroxide","termid":"GO:0061691"},{"relation_name":"is_a","term_name":"cellular oxidant detoxification","termid":"GO:0098869"},{"relation_name":"part_of","term_name":"cellular response to hydrogen peroxide","termid":"GO:0070301"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00141":null,"SJAG_01199":null,"SJAG_01216":null,"SJAG_02515":null,"SJAG_04823":null,"SJAG_04953":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0098754"}],"interesting_parent_ids":["GO:0008150","GO:0098754"],"is_obsolete":false,"name":"cellular detoxification of hydrogen peroxide","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0061692","terms_by_termid":{"GO:0061692":null}}


id: FYPO:0003104
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 small RNA (such as siRNA) derived from mRNA transcripts measured in a cell is greater than normal.","definition_xrefs":["PomBase:mah","PMID:24095277"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased RNA level during vegetative growth","termid":"FYPO:0000825"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0005447","FYPO:0001985","FYPO:0006551"],"is_obsolete":false,"name":"increased mRNA-derived small RNA level","synonyms":[{"name":"increased accumulation of mRNA-derived small RNAs","type":"related"},{"name":"increased mRNA-derived small RNA accumulation","type":"related"},{"name":"increased mRNA-derived small RNA level during mitotic cell cycle","type":"related"},{"name":"increased mRNA-derived small RNA level during vegetative growth","type":"exact"},{"name":"increased mRNA-derived small transcript level","type":"exact"},{"name":"increased protein-coding gene-derived small RNA level","type":"related"}],"termid":"FYPO:0003104"}


id: PBO:0000109
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"aldo/keto reductase, unknown biological role","termid":"PBO:0000109"}


id: PBO:0079304
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"testis-specific transcript, Y-linked 2","termid":"PBO:0079304"}


id: GO:0032280
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A synapse that lacks an electron dense postsynaptic specialization. In vertebtrates, these occur primarily on dendrite shafts and neuronal cell bodies and involve persynapses containing clusters of predominantly flattened or elongated vesicles and are typically inhibitory.","definition_xrefs":["GOC:ef","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuron to neuron synapse","termid":"GO:0098984"}],"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":"symmetric synapse","synonyms":[{"name":"Gray's type II synapse","type":"exact"}],"termid":"GO:0032280"}


id: PATO:0000488
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  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A response quality inhering in a bearer by virtue of the bearer's lack of reaction to a stimulus or an agent.","definition_xrefs":["PATOC:GVG"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to","termid":"PATO:0000077"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"unresponsive to","synonyms":[{"name":"unresponsive","type":"exact"}],"termid":"PATO:0000488"}


id: PBO:0111834
data:
  {"annotation_feature_type":"gene","cv_name":"pombase_family_or_domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"jmjN domain","termid":"PBO:0111834"}


id: PBO:0088348
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH-dependent reductase for Dph3, Cbr1","termid":"PBO:0088348"}


id: MONDO:0001962
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"endocrine pancreas disorder","termid":"MONDO:0001933"}],"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":"abnormality of glucagon secretion","secondary_identifiers":["MEDGEN:509540","ICD9:251.4","UMLS:C0154191","DOID:14427","SCTID:11178005"],"synonyms":[{"name":"glucagon secretion abnormality","type":"exact"}],"termid":"MONDO:0001962","xrefs":{"Monarch":{"xref_id":"0001962"}}}


id: PR:O74750
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A UDP-xylose and UDP-N-acetylglucosamine transporter that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR10778:SF4","PRO:DNx","OMA:SCHPO02706"],"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":"UDP-N-acetylglucosamine transporter yea4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1734.09","secondary_identifiers":["UniProtKB:O74750"],"synonyms":[{"name":"Spom972h-SLC35B4","type":"exact"}],"termid":"PR:O74750"}


id: MONDO:0005225
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  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acute myeloblastic leukemia with maturation (obsolete MONDO:0005225)","termid":"MONDO:0005225","xrefs":{"Monarch":{"xref_id":"0005225"}}}


id: MONDO:0957003
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  {"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":"hereditary neuro-ophthalmological disease","secondary_identifiers":["Orphanet:183616","GARD:20309","MEDGEN:1842469","UMLS:C5680540"],"synonyms":[{"name":"genetic neuro-ophthalmological disease","type":"exact"}],"termid":"MONDO:0957003","xrefs":{"Monarch":{"xref_id":"0957003"}}}


id: PR:Q8NKC2
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  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- eno102 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q8NKC2"],"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":"enolase 1-2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBPB21E7.01c","synonyms":[{"name":"2-phospho-D-glycerate hydro-lyase 1-2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"2-phosphoglycerate dehydratase 1-2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-eno102","type":"exact"}],"termid":"PR:Q8NKC2"}


id: PBO:0073508
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH2 domain containing 3A","termid":"PBO:0073508"}


id: GO:0032952
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  {"annotated_genes":["SJAG_04771","SJAG_01787","SJAG_04668","SJAG_04666","SJAG_04462","SJAG_01255","SJAG_03705","SJAG_00610","SJAG_04659"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[89326,94233],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0140748"},{"annotations":[107172,107743,119769,69409,94217,119902,92582],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0090334"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the chemical reactions and pathways involving (1->3)-beta-D-glucans.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of beta-glucan metabolic process","termid":"GO:0032950"},{"relation_name":"regulates","term_name":"(1->3)-beta-D-glucan metabolic process","termid":"GO:0006074"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00610":null,"SJAG_01255":null,"SJAG_01787":null,"SJAG_03705":null,"SJAG_04462":null,"SJAG_04659":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04771":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0005975"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0005975","GO:0008150"],"is_obsolete":false,"name":"regulation of (1->3)-beta-D-glucan metabolic process","references_by_uniquename":{"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"regulation of (1->3)-beta-D-glucan metabolism","type":"exact"},{"name":"regulation of 1,3-beta-D-glucan metabolic process","type":"exact"},{"name":"regulation of 1,3-beta-glucan metabolic process","type":"broad"},{"name":"regulation of 1,3-beta-glucan metabolism","type":"exact"}],"termid":"GO:0032952","terms_by_termid":{"GO:0090334":null,"GO:0140748":null}}


id: PATO:0000113
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000113 radiation sensitivity (obsolete PATO:0000113)","termid":"PATO:0000113"}


id: PBO:0064630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"peroxisome proliferator activated receptor delta","termid":"PBO:0064630"}


id: GO:0043639
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of benzoate, the anion of benzoic acid (benzenecarboxylic acid), a fungistatic compound widely used as a food preservative; it is conjugated to glycine in the liver and excreted as hippuric acid.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benzoate metabolic process","termid":"GO:0018874"},{"relation_name":"is_a","term_name":"monocarboxylic acid catabolic process","termid":"GO:0072329"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150"],"is_obsolete":false,"name":"benzoate catabolic process","synonyms":[{"name":"benzoate breakdown","type":"exact"},{"name":"benzoate catabolism","type":"exact"},{"name":"benzoate degradation","type":"exact"}],"termid":"GO:0043639"}


id: PBO:0002564
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sm snRNP core protein Smd1","termid":"PBO:0002564"}


id: MONDO:1011416
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Calcinosis circumscripta that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"metabolic disease, non-human animal","termid":"MONDO:1011331"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcinosis circumscripta, non-human animal","secondary_identifiers":["OMIA:000158"],"termid":"MONDO:1011416","xrefs":{"Monarch":{"xref_id":"1011416"}}}


id: MONDO:0035743
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"coagulation protein disease","termid":"MONDO:0002242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570"],"is_obsolete":false,"name":"factor V amsterdam bleeding disorder","secondary_identifiers":["GARD:22414","Orphanet:599579","UMLS:C5681605","MEDGEN:1842961"],"termid":"MONDO:0035743","xrefs":{"Monarch":{"xref_id":"0035743"}}}


id: GO:0048361
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving mucilage that occur in the root epithelium; mucilage is normally synthesized during root growth.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"mucilage metabolic process","termid":"GO:0010191"}],"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":"root epithelial mucilage metabolic process","synonyms":[{"name":"root epithelial mucilage metabolism","type":"exact"}],"termid":"GO:0048361"}


id: FYPO:0000577
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  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype observed in the vegetative growth phase of the life cycle in which the occurrence of gene silencing is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_output","term_name":"decreased RNA level during vegetative growth","termid":"FYPO:0001117"},{"relation_name":"is_a","term_name":"abnormal gene silencing","termid":"FYPO:0000574"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0006551"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0006551","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased gene silencing","synonyms":[{"name":"increased gene silencing during mitotic cell cycle","type":"related"},{"name":"increased gene silencing during vegetative growth","type":"exact"},{"name":"silencing: increased","type":"related"}],"termid":"FYPO:0000577"}


id: PBO:0038907
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"adhesion G protein-coupled receptor E2","termid":"PBO:0038907"}


id: GO:0048878
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biological process involved in the maintenance of an internal steady state of a chemical.","definition_xrefs":["GOC:isa_complete"],"direct_ancestors":[{"relation_name":"is_a","term_name":"homeostatic 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homeostasis","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000108":null,"GO_REF:0000117":null},"termid":"GO:0048878","terms_by_termid":{"GO:0001678":null,"GO:0006808":null,"GO:0006874":null,"GO:0006878":null,"GO:0006879":null,"GO:0006882":null,"GO:0007035":null,"GO:0009992":null,"GO:0010106":null,"GO:0010619":null,"GO:0010960":null,"GO:0010961":null,"GO:0019676":null,"GO:0019740":null,"GO:0030007":null,"GO:0030026":null,"GO:0030641":null,"GO:0030643":null,"GO:0032468":null,"GO:0033212":null,"GO:0033214":null,"GO:0033215":null,"GO:0050801":null,"GO:0051453":null,"GO:0055064":null,"GO:0055075":null,"GO:0055082":null,"GO:0055088":null,"GO:0055091":null,"GO:0055092":null,"GO:0090156":null,"GO:0098711":null}}


id: MONDO:0060664
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Mendelian neurodevelopmental disorder","termid":"MONDO:0100500"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"}],"interesting_parent_ids":["MONDO:0700092"],"is_obsolete":false,"name":"neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities","secondary_identifiers":["UMLS:C4693567","OMIM:617913","MEDGEN:1634867","DOID:0081263"],"synonyms":[{"name":"NEDMCR","type":"related"},{"name":"neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities","type":"exact"}],"termid":"MONDO:0060664","xrefs":{"Monarch":{"xref_id":"0060664"}}}


id: GO:0036358
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The formation of a D-alanyl ester of lipoteichoic acid by transfer of D-Ala onto a membrane-associated lipoteichoic acid (LTA).","definition_xrefs":["GOC:crds","PMID:22750871","PMID:8682792"],"direct_ancestors":[{"relation_name":"is_a","term_name":"teichoic acid D-alanylation","termid":"GO:0070400"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0044281","GO:0071554"],"is_obsolete":false,"name":"lipoteichoic acid D-alanylation","synonyms":[{"name":"D-alanyl LTA formation","type":"exact"},{"name":"D-alanyl lipoteichoic acid formation","type":"exact"},{"name":"LTA D-alanylation","type":"exact"}],"termid":"GO:0036358"}


id: GO:0051581
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of a neurotransmitter into a neuron or glial cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of neurotransmitter uptake","termid":"GO:0051580"},{"relation_name":"is_a","term_name":"negative regulation of neurotransmitter transport","termid":"GO:0051589"},{"relation_name":"negatively_regulates","term_name":"neurotransmitter uptake","termid":"GO:0001504"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0006810","GO:0008150"],"is_obsolete":false,"name":"negative regulation of neurotransmitter uptake","synonyms":[{"name":"down regulation of neurotransmitter uptake","type":"exact"},{"name":"down-regulation of neurotransmitter uptake","type":"exact"},{"name":"downregulation of neurotransmitter uptake","type":"exact"},{"name":"negative regulation of neurotransmitter import","type":"exact"}],"termid":"GO:0051581"}


id: PBO:0058876
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 10392","termid":"PBO:0058876"}


id: MONDO:0010448
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Moyamoya angiopathy - short stature - facial dysmorphism - hypergonadotropic hypogonadism is a very rare, hereditary, neurological, dysmorphic syndrome characterized by moyamoya disease, short stature of postnatal onset, and stereotyped facial dysmorphism.","definition_xrefs":["Orphanet:280679"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome","termid":"MONDO:0015160"},{"relation_name":"is_a","term_name":"Moyamoya disease","termid":"MONDO:0016820"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome","secondary_identifiers":["icd11.foundation:673174743","OMIM:300845","UMLS:C3151857","GARD:17301","MEDGEN:463207"],"synonyms":[{"name":"MYMY4","type":"related"},{"name":"Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism, and facial dysmorphism","type":"related"},{"name":"Moyamoya disease-short stature-facial dysmorphism-hypergonadotropic hypogonadism","type":"exact"},{"name":"chromosome Xq28 deletion syndrome, 3.4-Kb","type":"related"},{"name":"moyamoya disease 4, X-linked recessive","type":"exact"},{"name":"syndromic Moyamoya disease","type":"related"}],"termid":"MONDO:0010448","xrefs":{"Monarch":{"xref_id":"0010448"}}}


id: MONDO:0014379
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of ADNP on chromosome 20q13.13.","definition_xrefs":["DOID:0070058"],"direct_ancestors":[{"relation_name":"is_a","term_name":"congenital nervous system disorder","termid":"MONDO:0002320"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"autosomal dominant syndromic intellectual disability","termid":"MONDO:0100601"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426","MONDO:0002320"],"is_obsolete":false,"name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","secondary_identifiers":["GARD:12931","NORD:1965","MEDGEN:862975","SCTID:766824003","UMLS:C4014538","Orphanet:404448","OMIM:615873"],"synonyms":[{"name":"ADNP Syndrome","type":"exact"},{"name":"ADNP syndrome","type":"exact"},{"name":"ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder","type":"exact"},{"name":"HVDAS","type":"exact"},{"name":"Helsmoortel-Van der Aa syndrome","type":"exact"},{"name":"MRD28","type":"exact"},{"name":"autosomal dominant intellectual disability 28","type":"exact"},{"name":"autosomal dominant mental retardation 28","type":"exact"},{"name":"intellectual disability, autosomal dominant 28","type":"related"},{"name":"mental retardation, autosomal dominant 28","type":"related"}],"termid":"MONDO:0014379","xrefs":{"Monarch":{"xref_id":"0014379"}}}


id: MONDO:0850283
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An asthma that is characterized by severe and sudden onset of increasing wheezing, airways closing, smooth muscle contraction, mucus plugging and lower airway edema that may be reversible upon treatment.","definition_xrefs":["DOID:0080810"],"direct_ancestors":[{"relation_name":"is_a","term_name":"asthma","termid":"MONDO:0004979"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"acute asthma","secondary_identifiers":["UMLS:C0349790","MEDGEN:578946"],"termid":"MONDO:0850283","xrefs":{"Monarch":{"xref_id":"0850283"}}}


id: GO:0022013
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of pallium cells in the forebrain, resulting in the expansion of the cell population.","definition_xrefs":["GOC:dph","GOC:jid","GOC:dgh","GOC:cls","GO_REF:0000021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell proliferation in forebrain","termid":"GO:0021846"},{"relation_name":"part_of","term_name":"pallium development","termid":"GO:0021543"}],"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":"pallium cell proliferation in forebrain","termid":"GO:0022013"}


id: MONDO:0003020
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete orofaciodigital syndrome (obsolete MONDO:0003020)","termid":"MONDO:0003020","xrefs":{"Monarch":{"xref_id":"0003020"}}}


id: PBO:0050722
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"heat shock protein family D (Hsp60) member 1 pseudogene 8","termid":"PBO:0050722"}


id: GO:0015423
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 + maltose(out) = ADP + phosphate + maltose(in).","definition_xrefs":["RHEA:22132"],"direct_ancestors":[{"relation_name":"is_a","term_name":"maltose transmembrane transporter activity","termid":"GO:0005363"},{"relation_name":"is_a","term_name":"ABC-type oligosaccharide transporter activity","termid":"GO:0015422"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0022857","GO:0003674","GO:0005215"],"is_obsolete":false,"name":"ABC-type maltose transporter activity","secondary_identifiers":["MetaCyc:ABC-16-RXN","EC:7.5.2.1"],"synonyms":[{"name":"ABC-type maltose transporter","type":"exact"},{"name":"ATP-dependent maltose transmembrane transporter activity","type":"related"},{"name":"ATPase-coupled maltose transmembrane transporter activity","type":"related"},{"name":"maltooligosaccharide-importing ATPase activity","type":"related"},{"name":"maltose ABC transporter","type":"exact"},{"name":"maltose-transporting ATPase activity","type":"related"}],"termid":"GO:0015423"}


id: PBO:0078676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Lys (TTT) 9-1","termid":"PBO:0078676"}


id: MONDO:0012186
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Fanconi anemia caused by mutations in the FANCI gene, encoding Fanconi anemia group I protein.","definition_xrefs":["NCIT:C129026"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Fanconi anemia","termid":"MONDO:0019391"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0021190"},{"rel_name":"is_a","termid":"MONDO:0002280"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0021190","MONDO:0005046","MONDO:0005570","MONDO:0005066","MONDO:0002280"],"is_obsolete":false,"name":"Fanconi anemia complementation group I","secondary_identifiers":["MEDGEN:323016","OMIM:609053","DOID:0111091","GARD:15448","UMLS:C1836861","MESH:C563802"],"synonyms":[{"name":"FANCI","type":"exact"},{"name":"Fanconi Anemia, complementation Group 1","type":"related"},{"name":"Fanconi Anemia, complementation group type 1","type":"exact"},{"name":"Fanconi anaemia complementation group type I","type":"exact"},{"name":"Fanconi anemia complementation group I","type":"exact"},{"name":"Fanconi anemia complementation group type I","type":"exact"},{"name":"Fanconi anemia, complementation group I","type":"related"}],"termid":"MONDO:0012186","xrefs":{"Monarch":{"xref_id":"0012186"}}}


id: GO:0070070
data:
  {"annotated_genes":["SJAG_00301","SJAG_04454","SJAG_01939","SJAG_00771","SJAG_05306","SJAG_06514"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[68771,64873,103801,112009,65298,118409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070072"}]},"cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a proton-transporting V-type ATPase complex, proton-transporting two-sector ATPase complex that couples ATP hydrolysis to the transport of protons across a concentration gradient.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton-transporting two-sector ATPase complex assembly","termid":"GO:0070071"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00301":null,"SJAG_00771":null,"SJAG_01939":null,"SJAG_04454":null,"SJAG_05306":null,"SJAG_06514":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0065003"],"is_obsolete":false,"name":"proton-transporting V-type ATPase complex assembly","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000107":null},"synonyms":[{"name":"V-ATPase assembly","type":"related"},{"name":"V-ATPase complex assembly","type":"related"}],"termid":"GO:0070070","terms_by_termid":{"GO:0070072":null}}


id: PATO:0001753
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A peramorphic growth quality which is due to an increased rate.","definition_xrefs":["PATOC:mh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"peramorphic growth","termid":"PATO:0001752"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"accelerated growth","termid":"PATO:0001753"}


id: PBO:0028922
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_transcription_during_glucose_starvation","termid":"PBO:0028922"}


id: PBO:0059024
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"matrix metallopeptidase 13","termid":"PBO:0059024"}


id: GO:0051400
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a Bcl-2 homology (BH) protein domain. Bcl-2-related proteins share homology in one to four conserved regions designated the Bcl-2 homology (BH) domains BH1, BH2, BH3 and BH4. These domains contribute at multiple levels to the function of these proteins in cell death and survival. Anti-apoptotic members of the Bcl-2 family have four BH domains (BH1-BH4). Pro-apoptotic members have fewer BH domains.","definition_xrefs":["PMID:11048732","PMID:9020082","PMID:9704409","PMID:12133724"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein domain specific binding","termid":"GO:0019904"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0005515","GO:0005488","GO:0003674"],"is_obsolete":false,"name":"BH domain binding","synonyms":[{"name":"Bcl-2 homology domain binding","type":"exact"}],"termid":"GO:0051400"}


id: GO:0009017
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: N-succinyl-L-glutamate + H2O = L-glutamate + succinate.","definition_xrefs":["EC:3.5.1.96","RHEA:15169"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides","termid":"GO:0016811"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016810","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"succinylglutamate desuccinylase activity","secondary_identifiers":["MetaCyc:SUCCGLUDESUCC-RXN","KEGG_REACTION:R00411"],"synonyms":[{"name":"AstE","type":"related"},{"name":"N-succinyl-L-glutamate amidohydrolase activity","type":"related"},{"name":"N2-succinylglutamate desuccinylase activity","type":"exact"},{"name":"SGDS","type":"related"}],"termid":"GO:0009017"}


id: GO:0047510
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: S-citramalate = H2O + mesaconate.","definition_xrefs":["RHEA:13529"],"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:0016829"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016829","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"(S)-2-methylmalate dehydratase activity","secondary_identifiers":["KEGG_REACTION:R03693","MetaCyc:S-2-METHYLMALATE-DEHYDRATASE-RXN","EC:4.2.1.34"],"synonyms":[{"name":"(+)-citramalate hydro-lyase activity","type":"related"},{"name":"(+)-citramalic hydro-lyase activity","type":"related"},{"name":"(S)-2-methylmalate hydro-lyase (2-methylfumarate-forming)","type":"related"},{"name":"(S)-2-methylmalate hydro-lyase activity","type":"related"},{"name":"L-citramalate hydrolase activity","type":"related"},{"name":"citramalate dehydratase activity","type":"related"},{"name":"mesaconase activity","type":"related"},{"name":"mesaconate hydratase activity","type":"related"},{"name":"mesaconate mesaconase activity","type":"related"}],"termid":"GO:0047510"}


id: GO:0070880
data:
  {"annotated_genes":["SJAG_00218","SJAG_00876","SJAG_01835","SJAG_01290","SJAG_05285","SJAG_02222","SJAG_03587","SJAG_01288","SJAG_04771","SJAG_04666","SJAG_04483","SJAG_01453","SJAG_03123"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[79965,104462],"is_not":false,"summary":null,"term":"GO:0070880"},{"annotations":[96277],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034413"},{"annotations":[74739],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034412"},{"annotations":[76257,74742,72800,117679,107933,77603,115020,93413],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0071970"},{"annotations":[89326,94233],"is_not":false,"rel_names":["positively_regulates","regulates"],"summary":null,"term":"GO:0140748"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of beta-glucans, compounds composed of glucose residues linked by beta-D-glucosidic bonds, found in the walls of fungal cells.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell wall beta-glucan biosynthetic process","termid":"GO:0034410"},{"relation_name":"is_a","term_name":"fungal-type cell wall polysaccharide biosynthetic process","termid":"GO:0051278"},{"relation_name":"is_a","term_name":"fungal-type cell wall beta-glucan metabolic process","termid":"GO:0070879"}],"gene_count":13,"genes_by_uniquename":{"SJAG_00218":null,"SJAG_00876":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01453":null,"SJAG_01835":null,"SJAG_02222":null,"SJAG_03123":null,"SJAG_03587":null,"SJAG_04483":null,"SJAG_04666":null,"SJAG_04771":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0005975"},{"rel_name":"part_of","termid":"GO:0071554"}],"interesting_parent_ids":["GO:0008150","GO:0044085","GO:0071554","GO:0005975"],"is_obsolete":false,"name":"fungal-type cell wall beta-glucan biosynthetic process","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"fungal-type cell wall beta-glucan anabolism","type":"exact"},{"name":"fungal-type cell wall beta-glucan biosynthesis","type":"exact"},{"name":"fungal-type cell wall beta-glucan formation","type":"exact"},{"name":"fungal-type cell wall beta-glucan synthesis","type":"exact"}],"termid":"GO:0070880","terms_by_termid":{"GO:0034412":null,"GO:0034413":null,"GO:0070880":null,"GO:0071970":null,"GO:0140748":null}}


id: MONDO:0957303
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"palmoplantar keratoderma, epidermolytic","termid":"MONDO:0968949"}],"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":"palmoplantar keratoderma, epidermolytic, 2","secondary_identifiers":["DOID:0070551","MEDGEN:445412","UMLS:C2936837","OMIM:620411"],"termid":"MONDO:0957303","xrefs":{"Monarch":{"xref_id":"0957303"}}}


id: PBO:0070723
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L9 pseudogene 28","termid":"PBO:0070723"}


id: MONDO:1011886
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"nervous system disorder, non-human animal","termid":"MONDO:1011336"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuroaxonal dystrophy with cerebellar abiotrophy, non-human animal","secondary_identifiers":["OMIA:001606"],"termid":"MONDO:1011886","xrefs":{"Monarch":{"xref_id":"1011886"}}}


id: FYPO:0005230
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A gene expression phenotype observed in the vegetative growth phase of the life cycle in which regulation of translation in response to ultraviolet light is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PMID:26493332","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular process during vegetative growth","termid":"FYPO:0001319"},{"relation_name":"is_a","term_name":"cellular response phenotype during vegetative growth","termid":"FYPO:0001342"},{"relation_name":"is_a","term_name":"translation regulation phenotype during vegetative growth","termid":"FYPO:0005044"}],"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:0000002"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001312","FYPO:0000257","FYPO:0000002","FYPO:0000298","FYPO:0001320"],"is_obsolete":false,"name":"normal regulation of translation in response to UV","synonyms":[{"name":"normal regulation of translation in response to UV during mitotic cell cycle","type":"related"},{"name":"normal regulation of translation in response to UV during vegetative growth","type":"exact"},{"name":"normal regulation of translation in response to ultraviolet light","type":"exact"}],"termid":"FYPO:0005230"}


id: MONDO:0004595
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acute pulmonary heart disease (obsolete MONDO:0004595)","termid":"MONDO:0004595","xrefs":{"Monarch":{"xref_id":"0004595"}}}


id: MONDO:0029135
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"muscular dystrophy-dystroglycanopathy, type C","termid":"MONDO:0000173"},{"relation_name":"is_a","term_name":"autosomal recessive limb-girdle muscular dystrophy","termid":"MONDO:0015152"},{"relation_name":"is_a","term_name":"congenital muscular dystrophy caused by variation in POMGNT2","termid":"MONDO:0700075"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0024322"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320","MONDO:0005066","MONDO:0024322","MONDO:0006025"],"is_obsolete":false,"name":"muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8","secondary_identifiers":["GARD:16294","OMIM:618135","UMLS:C4748320","MEDGEN:1648468","DOID:0112382"],"synonyms":[{"name":"LGMD-POMGNT2 related myopathy","type":"exact"},{"name":"MDDGC8","type":"related"},{"name":"Muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT2-related","type":"related"},{"name":"muscular dystrophy, limb-girdle, autosomal recessive 24","type":"related"},{"name":"muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 8","type":"exact"},{"name":"muscular dystrophy-dystroglycanopathy (limb-girdle), TYPE C, 8","type":"related"}],"termid":"MONDO:0029135","xrefs":{"Monarch":{"xref_id":"0029135"}}}


id: GO:1904046
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of vascular endothelial growth factor production.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:19404486"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cytokine production","termid":"GO:0001818"},{"relation_name":"is_a","term_name":"regulation of vascular endothelial growth factor production","termid":"GO:0010574"},{"relation_name":"negatively_regulates","term_name":"vascular endothelial growth factor production","termid":"GO:0010573"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"negative regulation of vascular endothelial growth factor production","synonyms":[{"name":"down regulation of VEGF production","type":"exact"},{"name":"down regulation of vascular endothelial growth factor production","type":"exact"},{"name":"down-regulation of VEGF production","type":"exact"},{"name":"down-regulation of vascular endothelial growth factor production","type":"exact"},{"name":"downregulation of VEGF production","type":"exact"},{"name":"downregulation of vascular endothelial growth factor production","type":"exact"},{"name":"inhibition of VEGF production","type":"narrow"},{"name":"inhibition of vascular endothelial growth factor production","type":"narrow"},{"name":"negative regulation of VEGF production","type":"exact"}],"termid":"GO:1904046"}


id: MONDO:0022993
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Diabetes insipidus caused by excessive intake of water due to psychological factors or damage to the thirst-regulating mechanism.","definition_xrefs":["NCIT:C129735"],"direct_ancestors":[{"relation_name":"is_a","term_name":"diabetes insipidus","termid":"MONDO:0004782"},{"relation_name":"is_a","term_name":"primary polydipsia","termid":"MONDO:0040870"}],"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":"dipsogenic diabetes insipidus","secondary_identifiers":["DOID:0081058","UMLS:C0268813","SCTID:82800008","MESH:C548013","MEDGEN:82829"],"synonyms":[{"name":"Dipsogenic diabetes insipidus","type":"exact"},{"name":"dipsogenic diabetes insipidus","type":"exact"},{"name":"primary polydipsia","type":"broad"}],"termid":"MONDO:0022993","xrefs":{"Monarch":{"xref_id":"0022993"}}}


id: MONDO:0018248
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Intellectual disability-seizures-macrocephaly-obesity syndrome is a rare syndromic obesity due to complex chromosomal rearrangement characterized by development delay and intellectual disability, childhood-onset obesity, seizures, poor coordination and broad-based gait, macrocephaly and mild dysmorphic features (such as narrow palpebral fissures, malar hypoplasia and thin upper lips), eczema, ocular abnormalities and a social personality.","definition_xrefs":["Orphanet:369950"],"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":"intellectual disability-seizures-macrocephaly-obesity syndrome","secondary_identifiers":["GARD:21583","MEDGEN:1650833","UMLS:C4749455"],"synonyms":[{"name":"Der(8)t(8;12)","type":"exact"}],"termid":"MONDO:0018248","xrefs":{"Monarch":{"xref_id":"0018248"}}}


id: MONDO:0022675
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":"cataract skeletal anomalies","termid":"MONDO:0022675","xrefs":{"Monarch":{"xref_id":"0022675"}}}


id: GO:0018298
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The covalent or noncovalent attachment of a chromophore to a protein.","definition_xrefs":["GOC:ma"],"gene_count":0,"genotype_count":0,"name":"obsolete protein-chromophore linkage (obsolete GO:0018298)","termid":"GO:0018298"}


id: PBO:0060002
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND4L pseudogene 22","termid":"PBO:0060002"}


id: MONDO:0002005
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete acrodysostosis (obsolete MONDO:0002005)","termid":"MONDO:0002005","xrefs":{"Monarch":{"xref_id":"0002005"}}}


id: MONDO:0018413
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete female infertility due to an anomaly of ovarian function of genetic origin (obsolete MONDO:0018413)","secondary_identifiers":["Orphanet:400022"],"termid":"MONDO:0018413","xrefs":{"Monarch":{"xref_id":"0018413"}}}


id: MONDO:0011157
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A syndrome, which may be classified among the neurocutaneous syndromes, associates abnormalities of the cerebellum (rhombencephalosynapsis), cranial nerves (trigeminal anesthesia), and scalp (alopecia). It has been reported in 11 individuals so far. Other features observed in patients were craniosynostosis, midfacial hypoplasia, bilateral corneal opacities, low-set ears, short stature, moderate intellectual impairment and ataxia. Hyperactivity, depression, self-injurious behavior and bipolar disorder have also been reported.","definition_xrefs":["Orphanet:1532"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"central nervous system malformation","termid":"MONDO:0020022"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0020022"}],"interesting_parent_ids":["MONDO:0020022"],"is_obsolete":false,"name":"Gomez-Lopez-Hernandez syndrome","secondary_identifiers":["MEDGEN:163201","GARD:229","UMLS:C0795959","SCTID:722451006","MESH:C537285","OMIM:601853"],"synonyms":[{"name":"Cerebellotrigeminal dermal dysplasia","type":"related"},{"name":"Cerebellotrigeminal dermal dysplasia cerebello-trigeminal-dermal dysplasia","type":"related"},{"name":"Cerebellotrigeminal-dermal dysplasia","type":"related"},{"name":"Cerebellotrigeminal-dermal dysplasia syndrome","type":"exact"},{"name":"GLHS","type":"related"},{"name":"GOMEZ-LOPEZ-HERNANDEZ syndrome","type":"related"},{"name":"Gomez Lopez Hernandez syndrome","type":"related"},{"name":"Gomez-Lopez-Hernandez syndrome","type":"exact"},{"name":"Gomez-Lopez-Hernández syndrome","type":"related"},{"name":"Gómez-López-Hernández syndrome","type":"related"},{"name":"craniosynostosis-alopecia-brain defect syndrome","type":"exact"}],"termid":"MONDO:0011157","xrefs":{"Monarch":{"xref_id":"0011157"}}}


id: PBO:0089747
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin-protein ligase E4 Ufd2","termid":"PBO:0089747"}


id: MONDO:0010819
data:
  {"annotated_genes":["SJAG_01356","SJAG_02885"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87889,87890],"is_not":false,"summary":null,"term":"MONDO:0010819"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Stargardt disease","termid":"MONDO:0019353"},{"relation_name":"is_a","term_name":"ELOVL4-related maculopathy","termid":"MONDO:0700227"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01356":null,"SJAG_02885":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"Stargardt disease 3","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:600110","UMLS:C1838644","GARD:15314","MEDGEN:333146","MESH:C535805"],"synonyms":[{"name":"STGD3","type":"related"},{"name":"Stargardt disease 3","type":"exact"},{"name":"Stargardt disease type 3","type":"exact"},{"name":"Stargardt-like macular dystrophy, autosomal dominant","type":"related"},{"name":"macular dystrophy with flecks, type 3","type":"related"}],"termid":"MONDO:0010819","terms_by_termid":{"MONDO:0010819":null},"xrefs":{"Monarch":{"xref_id":"0010819"}}}


id: PBO:0085119
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar protein; constituent of 66S pre-ribosomal particles; depletion leads to defects in rRNA processing and a block in the assembly of large ribosomal subunits; possesses a sigma(70)-like RNA-binding motif","termid":"PBO:0085119"}


id: GO:0008029
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with a pentraxin and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity.","definition_xrefs":["GOC:add","GOC:signaling","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"opsonin receptor activity","termid":"GO:0001847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0038023"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0038023","GO:0003674"],"is_obsolete":false,"name":"pentraxin receptor activity","synonyms":[{"name":"pentaxin receptor","type":"exact"}],"termid":"GO:0008029"}


id: GO:0007027
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of the depolymerization of the specialized microtubules of the axoneme.","definition_xrefs":["GOC:mah","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of microtubule depolymerization","termid":"GO:0007026"},{"relation_name":"is_a","term_name":"regulation of cytoplasmic microtubule depolymerization","termid":"GO:0010937"},{"relation_name":"is_a","term_name":"negative regulation of cell projection organization","termid":"GO:0031345"},{"relation_name":"is_a","term_name":"regulation of plasma membrane bounded cell projection organization","termid":"GO:0120035"},{"relation_name":"negatively_regulates","term_name":"axonemal microtubule depolymerization","termid":"GO:0060404"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0000226"},{"rel_name":"negatively_regulates","termid":"GO:0007010"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0007010"},{"rel_name":"regulates","termid":"GO:0000226"}],"interesting_parent_ids":["GO:0008150","GO:0007010","GO:0000226"],"is_obsolete":false,"name":"negative regulation of axonemal microtubule depolymerization","synonyms":[{"name":"axonemal microtubule stabilization","type":"exact"},{"name":"negative regulation of microtubule depolymerization in axoneme","type":"related"}],"termid":"GO:0007027"}


id: PBO:0113243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nuclear peptidyl-prolyl cis-trans isomerase (PPIase); impacts expression of multiple genes via its role in nucleosome assembly; catalyzes isomerization of proline residues in histones H3 and H4, which affects lysine methylation of those histones; role in rDNA maintenance; PPIase domain acts as a transcriptional repressor when tethered to DNA by lexA, and repressor activity is dependent on PPIase activity; contains a nucleoplasmin-like fold and can form pentamers","termid":"PBO:0113243"}


id: PBO:0080525
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WASP family homolog 7, pseudogene","termid":"PBO:0080525"}


id: GO:0034992
data:
  {"annotated_genes":["SJAG_03783","SJAG_03491","SJAG_05207","SJAG_01242","SJAG_01538","SJAG_04489","SJAG_05196","SJAG_04558","SJAG_05303"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[72282],"is_not":false,"summary":null,"term":"GO:0034992"},{"annotations":[114695],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034993"},{"annotations":[89767,116565,105544,99767,102706],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0180028"},{"annotations":[104637,98527],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:1990612"}]},"cv_name":"cellular_component","definition":"A region of the nuclear envelope to which a microtubule organizing center (MTOC) attaches; protein complexes embedded in the nuclear envelope mediate direct or indirect linkages between the microtubule cytoskeleton and the nuclear envelope.","definition_xrefs":["GOC:mah","PMID:18692466"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"nuclear envelope","termid":"GO:0005635"}],"gene_count":9,"genes_by_uniquename":{"SJAG_01242":null,"SJAG_01538":null,"SJAG_03491":null,"SJAG_03783":null,"SJAG_04489":null,"SJAG_04558":null,"SJAG_05196":null,"SJAG_05207":null,"SJAG_05303":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005634"],"is_obsolete":false,"name":"microtubule organizing center attachment site","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"MAS","type":"exact"},{"name":"MTOC attachment site","type":"exact"},{"name":"microtubule organising centre attachment site","type":"exact"}],"termid":"GO:0034992","terms_by_termid":{"GO:0034992":null,"GO:0034993":null,"GO:0180028":null,"GO:1990612":null}}


id: GO:0032656
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of interleukin-13 production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cytokine production","termid":"GO:0001817"},{"relation_name":"regulates","term_name":"interleukin-13 production","termid":"GO:0032616"}],"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:0008150","GO:0010467"],"is_obsolete":false,"name":"regulation of interleukin-13 production","secondary_identifiers":["GO:2000665","GO:0045366"],"synonyms":[{"name":"regulation of IL-13 production","type":"exact"},{"name":"regulation of interleukin-13 biosynthetic process","type":"narrow"},{"name":"regulation of interleukin-13 secretion","type":"narrow"}],"termid":"GO:0032656"}


id: PBO:0038728
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin gamma 1 pseudogene 23","termid":"PBO:0038728"}


id: GO:0090644
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An innate immune response that is positively correlated with host plant development. As a plant develops, its innate resistance to pathogenic infections increases. The mechanisms involved in age-related resistance differ in nature or in aspects of regulation from the hypersensitive response (HR), systemic acquired resistance (SAR), or induced systemic resistance (ISR).","definition_xrefs":["PMID:17635216","PMID:19694953"],"direct_ancestors":[{"relation_name":"is_a","term_name":"developmental process","termid":"GO:0032502"},{"relation_name":"is_a","term_name":"innate immune response","termid":"GO:0045087"}],"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":"age-related resistance","synonyms":[{"name":"ARR","type":"exact"},{"name":"adult seedling resistance","type":"narrow"},{"name":"developmental resistance","type":"broad"},{"name":"flowering-induced resistance","type":"narrow"},{"name":"mature seedling resistance","type":"narrow"},{"name":"ontogenic resistance","type":"broad"},{"name":"senescence-induced resistance","type":"narrow"}],"termid":"GO:0090644"}


id: PBO:0062077
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily A member 8 (gene/pseudogene)","termid":"PBO:0062077"}


id: PBO:0072691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RUNX family transcription factor 2","termid":"PBO:0072691"}


id: PBO:0011129
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"AAA ATPase Like Fidgetin","termid":"PBO:0011129"}


id: MONDO:0010208
data:
  {"annotated_genes":["SJAG_00516"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87386],"is_not":false,"summary":null,"term":"MONDO:0010208"}]},"cv_name":"mondo","definition":"A type of cutis laxa that is characterized by wrinkling of the skin of the dorsum of the hands and feet, an increased number of palmar and plantar creases, wrinkled abdominal skin, multiple skeletal abnormalities (joint laxity and congenital hip dislocation), late closing of the anterior fontanel, microcephaly, pre- and postnatal growth retardation, developmental delay and facial dysmorphism (a broad nasal bridge, downslanting palpebral fissures and hypertelorism).","definition_xrefs":["Orphanet:2834"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive cutis laxa type 2A","termid":"MONDO:0018163"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00516":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"},{"rel_name":"is_a","termid":"MONDO:0005093"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0004736","MONDO:0005066","MONDO:0006025","MONDO:0005497"],"is_obsolete":false,"name":"wrinkly skin syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["ICD9:259.8","SCTID:238875009","DOID:0112171","MEDGEN:98030","GARD:273","OMIM:278250","UMLS:C0406587","icd11.foundation:638767040","MESH:C536750"],"synonyms":[{"name":"WSS","type":"exact"},{"name":"wrinkled skin syndrome","type":"exact"},{"name":"wrinkly skin syndrome","type":"exact"}],"termid":"MONDO:0010208","terms_by_termid":{"MONDO:0010208":null},"xrefs":{"Monarch":{"xref_id":"0010208"}}}


id: MONDO:0011540
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Spinocerebellar ataxia type 14 (SCA14) is a rare mild subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by slowly progressive ataxia, dysarthria and nystagmus.","definition_xrefs":["Orphanet:98763"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant cerebellar ataxia type I","termid":"MONDO:0019792"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0002039","MONDO:0000426"],"is_obsolete":false,"name":"spinocerebellar ataxia type 14","secondary_identifiers":["icd11.foundation:736357100","UMLS:C1854369","OMIM:605361","GARD:9867","MESH:C537196","DOID:0050964","SCTID:719210007","MEDGEN:343106"],"synonyms":[{"name":"SCA14","type":"exact"},{"name":"spinocerebellar ataxia 14","type":"related"},{"name":"spinocerebellar ataxia type 14","type":"exact"}],"termid":"MONDO:0011540","xrefs":{"Monarch":{"xref_id":"0011540"}}}


id: PBO:0002585
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endoplasmic reticulum resident protein required for packaging into COPII vesicles (predicted)","termid":"PBO:0002585"}


id: MONDO:0005541
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A defect in the pars interarticularis of a vertebral bone.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disease of bone structure","termid":"MONDO:0000836"},{"relation_name":"is_a","term_name":"vertebral disorder","termid":"MONDO:0045002"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spondylolysis","secondary_identifiers":["HP:0003304","MEDGEN:21294","MESH:D013169","UMLS:C0038018","icd11.foundation:790009325","DOID:2300","SCTID:240221008","ICD10CM:M43.0","EFO:0005649","NCIT:C35034"],"synonyms":[{"name":"spondylolysis","type":"exact"},{"name":"spondylolysis (disease)","type":"exact"}],"termid":"MONDO:0005541","xrefs":{"Monarch":{"xref_id":"0005541"}}}


id: GO:0071852
data:
  {"annotated_genes":["SJAG_05285","SJAG_04864","SJAG_01227","SJAG_03188","SJAG_03646","SJAG_04238","SJAG_03587","SJAG_03057","SJAG_01963","SJAG_04184","SJAG_01426","SJAG_02192","SJAG_02845","SJAG_00610","SJAG_02278","SJAG_03483","SJAG_04483","SJAG_04851","SJAG_04073","SJAG_02684","SJAG_04595","SJAG_02733","SJAG_03295","SJAG_04236","SJAG_00218","SJAG_01181","SJAG_03705","SJAG_01028","SJAG_04878","SJAG_04666","SJAG_02590","SJAG_05001","SJAG_01453","SJAG_00661","SJAG_00667","SJAG_01321","SJAG_02718","SJAG_00974","SJAG_01835","SJAG_03123","SJAG_04771","SJAG_01288","SJAG_04620","SJAG_04668","SJAG_00876","SJAG_03013","SJAG_01888","SJAG_04327","SJAG_03631","SJAG_03444","SJAG_01290","SJAG_00163","SJAG_02916","SJAG_02468","SJAG_00310","SJAG_05272","SJAG_04868","SJAG_02649","SJAG_00424","SJAG_04551","SJAG_01017","SJAG_04462","SJAG_03753","SJAG_01171","SJAG_02446","SJAG_01774","SJAG_04850","SJAG_02727","SJAG_02222"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91547,94076,119321,64648],"is_not":false,"summary":null,"term":"GO:0071852"},{"annotations":[96277],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034413"},{"annotations":[92060,93587,90026,90515],"is_not":false,"rel_names":["is_a","part_of"],"summary":null,"term":"GO:0030476"},{"annotations":[74739],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0034412"},{"annotations":[110913,105990,119642,119650,115939],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0070591"},{"annotations":[72372,75267,75095,80516,73157],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070600"},{"annotations":[117679,77603,115020,107933,74742,76257,93413,72800],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071970"},{"annotations":[104462,79965],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070880"},{"annotations":[103761,109905,96918,103762],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0070879"},{"annotations":[119767,104273,76758,95146,97068,73105,71937,72278,81132,72438,102439],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009272"},{"annotations":[109906,90092,101969,103764,103763,95832,90909,113169],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904541"},{"annotations":[81992,77602,72835,76256,79640,91149,76919,104274,72799,78546,77019,73068,111896,78178,79656,81307],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0031505"},{"annotations":[108526,74262],"is_not":false,"rel_names":["part_of"],"summary":null,"term":"GO:0071966"},{"annotations":[89326,94233],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0140748"},{"annotations":[94239,104669,96755,91254],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0070610"},{"annotations":[67929,102001,103967],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0032995"},{"annotations":[112832,89409,73285],"is_not":false,"rel_names":["regulates"],"summary":null,"term":"GO:0060237"}]},"cv_name":"biological_process","definition":"A process that results in the biosynthesis of constituent macromolecules, assembly, arrangement of constituent parts, or disassembly of a fungal-type cell wall.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell wall organization or biogenesis","termid":"GO:0071554"}],"gene_count":69,"genes_by_uniquename":{"SJAG_00163":null,"SJAG_00218":null,"SJAG_00310":null,"SJAG_00424":null,"SJAG_00610":null,"SJAG_00661":null,"SJAG_00667":null,"SJAG_00876":null,"SJAG_00974":null,"SJAG_01017":null,"SJAG_01028":null,"SJAG_01171":null,"SJAG_01181":null,"SJAG_01227":null,"SJAG_01288":null,"SJAG_01290":null,"SJAG_01321":null,"SJAG_01426":null,"SJAG_01453":null,"SJAG_01774":null,"SJAG_01835":null,"SJAG_01888":null,"SJAG_01963":null,"SJAG_02192":null,"SJAG_02222":null,"SJAG_02278":null,"SJAG_02446":null,"SJAG_02468":null,"SJAG_02590":null,"SJAG_02649":null,"SJAG_02684":null,"SJAG_02718":null,"SJAG_02727":null,"SJAG_02733":null,"SJAG_02845":null,"SJAG_02916":null,"SJAG_03013":null,"SJAG_03057":null,"SJAG_03123":null,"SJAG_03188":null,"SJAG_03295":null,"SJAG_03444":null,"SJAG_03483":null,"SJAG_03587":null,"SJAG_03631":null,"SJAG_03646":null,"SJAG_03705":null,"SJAG_03753":null,"SJAG_04073":null,"SJAG_04184":null,"SJAG_04236":null,"SJAG_04238":null,"SJAG_04327":null,"SJAG_04462":null,"SJAG_04483":null,"SJAG_04551":null,"SJAG_04595":null,"SJAG_04620":null,"SJAG_04666":null,"SJAG_04668":null,"SJAG_04771":null,"SJAG_04850":null,"SJAG_04851":null,"SJAG_04864":null,"SJAG_04868":null,"SJAG_04878":null,"SJAG_05001":null,"SJAG_05272":null,"SJAG_05285":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0071554"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0071554","GO:0008150"],"is_obsolete":false,"name":"fungal-type cell wall organization or biogenesis","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"fungal-type cell wall organisation or biogenesis","type":"exact"},{"name":"fungal-type cell wall organization and biogenesis","type":"related"}],"termid":"GO:0071852","terms_by_termid":{"GO:0009272":null,"GO:0030476":null,"GO:0031505":null,"GO:0032995":null,"GO:0034412":null,"GO:0034413":null,"GO:0060237":null,"GO:0070591":null,"GO:0070600":null,"GO:0070610":null,"GO:0070879":null,"GO:0070880":null,"GO:0071852":null,"GO:0071966":null,"GO:0071970":null,"GO:0140748":null,"GO:1904541":null}}


id: MONDO:0000506
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete Caroli disease (obsolete MONDO:0000506)","termid":"MONDO:0000506","xrefs":{"Monarch":{"xref_id":"0000506"}}}


id: GO:1900800
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways involving cspyrone B1.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"secondary metabolic process","termid":"GO:0019748"},{"relation_name":"is_a","term_name":"carboxylic acid metabolic process","termid":"GO:0019752"},{"relation_name":"is_a","term_name":"ketone metabolic process","termid":"GO:0042180"},{"relation_name":"is_a","term_name":"lactone metabolic process","termid":"GO:1901334"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0019748","GO:0044281","GO:0008150"],"is_obsolete":false,"name":"cspyrone B1 metabolic process","synonyms":[{"name":"cspyrone B1 metabolism","type":"exact"}],"termid":"GO:1900800"}


id: MONDO:0024675
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Wilms tumor of the kidney which occurs in adults.","definition_xrefs":["NCIT:C6180"],"direct_ancestors":[{"relation_name":"is_a","term_name":"kidney Wilms tumor","termid":"MONDO:0019004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"},{"rel_name":"is_a","termid":"MONDO:0005240"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0005240"],"is_obsolete":false,"name":"adult kidney Wilms tumor","secondary_identifiers":["UMLS:C1332219","MEDGEN:231045"],"synonyms":[{"name":"adenosarcoma of adult kidney","type":"exact"},{"name":"adenosarcoma of the adult kidney","type":"exact"},{"name":"adult kidney Wilms tumor","type":"exact"},{"name":"adult kidney adenosarcoma","type":"exact"},{"name":"adult nephroblastoma","type":"exact"},{"name":"adult renal Wilms tumor","type":"exact"},{"name":"adult renal Wilms tumour","type":"exact"},{"name":"adult renal Wilms' tumor","type":"exact"},{"name":"adult renal Wilms' tumour","type":"exact"},{"name":"adult renal adenosarcoma","type":"exact"},{"name":"kidney Wilms tumor of adults","type":"exact"},{"name":"kidney Wilms tumour of adults","type":"exact"}],"termid":"MONDO:0024675","xrefs":{"Monarch":{"xref_id":"0024675"}}}


id: PBO:0076212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small ubiquitin like modifier 3","termid":"PBO:0076212"}


id: PBO:0076503
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"taste 2 receptor member 3","termid":"PBO:0076503"}


id: GO:1900052
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of retinoic acid biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:yaf"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of ketone metabolic process","termid":"GO:0010565"},{"relation_name":"is_a","term_name":"regulation of isoprenoid metabolic process","termid":"GO:0019747"},{"relation_name":"is_a","term_name":"regulation of vitamin metabolic process","termid":"GO:0030656"},{"relation_name":"is_a","term_name":"regulation of hormone metabolic process","termid":"GO:0032350"},{"relation_name":"is_a","term_name":"regulation of lipid biosynthetic process","termid":"GO:0046890"},{"relation_name":"regulates","term_name":"retinoic acid biosynthetic process","termid":"GO:0002138"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006766"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0006766","GO:0006629"],"is_obsolete":false,"name":"regulation of retinoic acid biosynthetic process","synonyms":[{"name":"regulation of retinoic acid anabolic process","type":"exact"}],"termid":"GO:1900052"}


id: PBO:0049628
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H3 histone pseudogene 31","termid":"PBO:0049628"}


id: MONDO:0015267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Feingold syndrome (FS), also known as oculo-digito-esophageal-duodenal (ODED) syndrome, is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies and is comprised of two subtypes: FS type 1 (FS1) and FS type 2 (FS2). FS1 is by far the most common form while FS2 has only been reported in 3 patients and has the same clinical characteristics as FS1, apart from the absence of gastrointestinal atresia and short palpebral fissures.","definition_xrefs":["Orphanet:1305"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete non-syndromic respiratory or mediastinal malformation (obsolete MONDO:0015221)","termid":"MONDO:0015221"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Feingold syndrome","secondary_identifiers":["DOID:0060464","NCIT:C74987","UMLS:C0796068","GARD:8407","MEDGEN:163209","OMIMPS:164280"],"synonyms":[{"name":"Brunner-Winter syndrome","type":"exact"},{"name":"FGLDS","type":"exact"},{"name":"FS","type":"exact"},{"name":"MMT","type":"exact"},{"name":"MODED syndrome","type":"exact"},{"name":"ODED syndrome","type":"exact"},{"name":"digital anomalies with short palpebral fissures and atresia of esophagus or duodenum","type":"exact"},{"name":"digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum","type":"related"},{"name":"digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum","type":"exact"},{"name":"microcephaly-digital anomalies-normal intelligence syndrome","type":"exact"},{"name":"microcephaly-intellectual disability-tracheoesophageal fistula syndrome","type":"exact"},{"name":"microcephaly-oculo-digito-esophageal-duodenal syndrome","type":"exact"},{"name":"microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome","type":"exact"},{"name":"oculo-digito-esophageal-duodenal syndrome","type":"exact"}],"termid":"MONDO:0015267","xrefs":{"Monarch":{"xref_id":"0015267"}}}


id: MONDO:0000145
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete premature aging syndrome (obsolete MONDO:0000145)","termid":"MONDO:0000145","xrefs":{"Monarch":{"xref_id":"0000145"}}}


id: FYPO:0005314
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 promoters that contain MCB sites is decreased.","definition_xrefs":["PMID:26912660","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to chromatin during vegetative growth","termid":"FYPO:0002909"},{"relation_name":"is_a","term_name":"decreased protein localization to chromatin at promoter","termid":"FYPO:0007505"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000138","FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"decreased protein localization to chromatin at MCB promoters during vegetative growth","synonyms":[{"name":"decreased protein localisation to chromatin at MCB promoters during vegetative growth","type":"exact"},{"name":"decreased protein localization to chromatin at MCB promoters during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to chromatin at MCB target genes during vegetative growth","type":"related"},{"name":"decreased protein localization to chromatin at MCB-containing promoters during vegetative growth","type":"exact"},{"name":"reduced protein localization to chromatin at MCB promoters during vegetative growth","type":"exact"}],"termid":"FYPO:0005314"}


id: PBO:0062135
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily F member 2 pseudogene","termid":"PBO:0062135"}


id: RO:HOM0000000
data:
  {"annotation_feature_type":"gene","cv_name":"relationship","definition":"Relation between biological objects that resemble or are related to each other sufficiently to warrant a comparison.","definition_xrefs":["BGEE:curator"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"in_similarity_relationship_with","synonyms":[{"name":"correspondence","type":"related"},{"name":"resemblance","type":"related"},{"name":"sameness","type":"exact"},{"name":"similar to","type":"exact"}],"termid":"RO:HOM0000000"}


id: GO:1990923
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that is composed of at least EXD1, TDRD12 and some PIWI protein. The complex is required for MILI slicing-triggered biogenesis and loading of MIWI2 piRNAs.","definition_xrefs":["PMID:26669262"],"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":"PET complex","termid":"GO:1990923"}


id: MONDO:0017807
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A condition characterized by the presence of a growing mature teratoma in a patient during or after chemotherapy for a non-seminomatous germ cell tumor, with normal serum markers for human chorionic gonadotropin and alpha fetoprotein. Complete surgical resection is the preferred treatment.","definition_xrefs":["NCIT:C118370"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"extragonadal non-dysgerminomatous germ cell tumor","termid":"MONDO:0020539"},{"relation_name":"is_a","term_name":"neoplastic syndrome","termid":"MONDO:0021058"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"growing teratoma syndrome","secondary_identifiers":["Orphanet:314613","UMLS:C3891714","MEDGEN:856083","GARD:21380"],"synonyms":[{"name":"GTS","type":"exact"}],"termid":"MONDO:0017807","xrefs":{"Monarch":{"xref_id":"0017807"}}}


id: PBO:0089129
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Hsp70 nucleotide exchange factor Fes1","termid":"PBO:0089129"}


id: MONDO:0034022
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"Bethlem myopathy","termid":"MONDO:0008029"},{"relation_name":"is_a","term_name":"Ehlers-Danlos syndrome","termid":"MONDO:0020066"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"},{"rel_name":"is_a","termid":"MONDO:0005336"}],"interesting_parent_ids":["MONDO:0002320","MONDO:0005336"],"is_obsolete":false,"name":"Bethlem myopathy 2","secondary_identifiers":["OMIM:616471","MEDGEN:907426","GARD:16121","UMLS:C4225313","Orphanet:536516"],"synonyms":[{"name":"BTHLM2","type":"exact"},{"name":"Bethlem myopathy 2","type":"exact"},{"name":"Bethlem myopathy caused by mutation in COL12A1","type":"exact"},{"name":"Bethlem myopathy type 2","type":"exact"},{"name":"COL12A1 Bethlem myopathy","type":"exact"},{"name":"EDS, myopathic type","type":"exact"},{"name":"Ehlers-Danlos syndrome, myopathic type","type":"exact"},{"name":"myopathic EDS","type":"exact"},{"name":"myopathic Ehlers-Danlos syndrome","type":"exact"}],"termid":"MONDO:0034022","xrefs":{"Monarch":{"xref_id":"0034022"}}}


id: MONDO:0007892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Lenz-Majewski hyperostotic dwarfism is an extremely rare syndrome associating dwarfism, characteristic facial appearance, cutis laxa and progressive bone sclerosis.","definition_xrefs":["Orphanet:2658"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"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":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lenz-Majewski hyperostotic dwarfism","secondary_identifiers":["icd11.foundation:1509425242","MEDGEN:98483","UMLS:C0432269","MESH:C537115","DOID:0111507","GARD:3223","OMIM:151050"],"synonyms":[{"name":"LMHD","type":"related"},{"name":"Lenz Majewski hyperostotic dwarfism","type":"related"},{"name":"Lenz-Majewski hyperostotic dwarfism","type":"exact"},{"name":"Lenz-Majewski hyperostotic dysplasia","type":"related"},{"name":"Lenz-Majewski syndrome","type":"related"},{"name":"hyperostotic dwarfism Lenz-Majewski type","type":"related"},{"name":"multiple congenital anomalies, intellectual disability and progressive skeletal sclerosis","type":"related"},{"name":"multiple congenital anomalies, mental retardation and progressive skeletal sclerosis","type":"related"}],"termid":"MONDO:0007892","xrefs":{"Monarch":{"xref_id":"0007892"}}}


id: PBO:0083072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dihydroxyacid dehydratase; putative 2Fe-2S protein; catalyzes third step in the common pathway leading to biosynthesis of branched-chain amino acids","termid":"PBO:0083072"}


id: GO:0003409
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to creating the structural organization of the optic cup. This process pertains to the physical shaping of the rudimentary structure.","definition_xrefs":["GOC:tb","GOC:ascb_2009","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure arrangement","termid":"GO:0048532"},{"relation_name":"part_of","term_name":"optic cup morphogenesis involved in camera-type eye development","termid":"GO:0002072"}],"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":"optic cup structural organization","synonyms":[{"name":"optic cup structural organisation","type":"exact"}],"termid":"GO:0003409"}


id: PBO:0062446
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 7 subfamily E member 111F pseudogene","termid":"PBO:0062446"}


id: GO:0046725
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process where the infecting virus reduces the levels of viral proteins in a cell.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation by virus of viral protein levels in host cell","termid":"GO:0046719"},{"relation_name":"is_a","term_name":"negative regulation of viral process","termid":"GO:0048525"}],"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 by virus of viral protein levels in host cell","synonyms":[{"name":"down regulation of viral protein levels in host cell","type":"exact"},{"name":"down-regulation of viral protein levels in host cell","type":"exact"},{"name":"downregulation of viral protein levels in host cell","type":"exact"},{"name":"inhibition of viral protein levels in host cell","type":"narrow"},{"name":"negative regulation of viral protein levels","type":"exact"}],"termid":"GO:0046725"}


id: PBO:0075086
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 136","termid":"PBO:0075086"}


id: PATO:0001801
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A composition quality inhering in an bearer by virtue of the reduction in amount of water the bearer contains.","definition_xrefs":["Wikipedia:http://en.wikipedia.org/wiki/Dehydrated"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"water composition","termid":"PATO:0001800"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased water composition","synonyms":[{"name":"dehydrated","type":"exact"},{"name":"dry","type":"related"}],"termid":"PATO:0001801"}


id: PBO:0017635
data:
  {"annotation_feature_type":"gene","cv_name":"disease_associated","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Lesch-Nyhan Syndrome","termid":"PBO:0017635"}


id: FYPO:0006509
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which telomere length is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal telomere morphology","termid":"FYPO:0006508"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000641","FYPO:0000002","FYPO:0005447","FYPO:0000293"],"is_obsolete":false,"name":"abnormal telomere length","termid":"FYPO:0006509"}


id: PBO:0060058
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND5 pseudogene 5","termid":"PBO:0060058"}


id: PBO:0049021
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GPN-loop GTPase 3","termid":"PBO:0049021"}


id: MONDO:0004170
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"scleral disorder","termid":"MONDO:0001269"}],"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":"nodular episcleritis","secondary_identifiers":["MEDGEN:509927","icd11.foundation:134477595","UMLS:C0155352","DOID:728","ICD10CM:H15.12","SCTID:70558001","ICD9:379.02"],"termid":"MONDO:0004170","xrefs":{"Monarch":{"xref_id":"0004170"}}}


id: PBO:0091011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NADH-dependent flavin oxidoreductase, implicated in cellular detoxification from family members","termid":"PBO:0091011"}


id: GO:0001777
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The non-specific expansion of T cell populations within a whole or part of an organism to reach to a total number of T cells which will then remain stable over time in the absence of an external stimulus.","definition_xrefs":["GOC:mgi_curators","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"T cell proliferation","termid":"GO:0042098"},{"relation_name":"part_of","term_name":"T cell homeostasis","termid":"GO:0043029"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"T cell homeostatic proliferation","synonyms":[{"name":"T lymphocyte homeostatic proliferation","type":"exact"},{"name":"T-cell homeostatic proliferation","type":"exact"},{"name":"T-lymphocyte homeostatic proliferation","type":"exact"},{"name":"resting T cell proliferation","type":"exact"},{"name":"resting T-cell proliferation","type":"exact"}],"termid":"GO:0001777"}


id: MONDO:0032753
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"spastic ataxia","termid":"MONDO:0017845"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"spastic ataxia 9, autosomal recessive","secondary_identifiers":["UMLS:C5193100","MEDGEN:1680026","OMIM:618438"],"synonyms":[{"name":"SPASTIC ATAXIA 9, AUTOSOMAL RECESSIVE","type":"related"},{"name":"SPAX9","type":"related"}],"termid":"MONDO:0032753","xrefs":{"Monarch":{"xref_id":"0032753"}}}


id: PBO:0066742
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 39","termid":"PBO:0066742"}


id: PBO:0031344
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_tacrolimus","termid":"PBO:0031344"}


id: GO:0052154
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process in which a symbiont alters or subverts the B-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:mtg_pamgo_17jul06"],"direct_ancestors":[{"relation_name":"is_a","term_name":"symbiont-mediated perturbation of host immune response","termid":"GO:0052553"}],"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 B-cell mediated immune response","secondary_identifiers":["GO:0052293"],"synonyms":[{"name":"modulation by organism of B-cell mediated immune response of other organism involved in symbiotic interaction","type":"broad"},{"name":"modulation by symbiont of host B-cell mediated immune response","type":"exact"},{"name":"perturbation of host B-cell mediated immune response","type":"exact"},{"name":"regulation by organism of host B-cell mediated immune response","type":"exact"},{"name":"symbiont-mediated perturbation of host humoral immune response","type":"exact"}],"termid":"GO:0052154"}


id: MONDO:0011405
data:
  {"annotated_genes":["SJAG_01798"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88579],"is_not":false,"summary":null,"term":"MONDO:0011405"}]},"cv_name":"mondo","definition":"A skin disease characterized by poikiloderma, hyperkeratotic nails, generalized hyperkeratosis on palms and soles, neutropenia, short stature, and recurrent pulmonary infections. It has material basis in mutation in the C16ORF57 gene on chromosome 16q13.","definition_xrefs":["DOID:0060551","PMID:20734427"],"direct_ancestors":[{"relation_name":"is_a","term_name":"constitutional neutropenia","termid":"MONDO:0015134"},{"relation_name":"is_a","term_name":"hereditary poikiloderma","termid":"MONDO:0016382"},{"relation_name":"is_a","term_name":"hereditary skin disorder","termid":"MONDO:0100118"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01798":null},"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:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"poikiloderma with neutropenia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:388129","GARD:4085","OMIM:604173","Orphanet:221046","UMLS:C1858723","NCIT:C177535","NANDO:2200749","NORD:2022"],"synonyms":[{"name":"Clericuzio type poikiloderma with neutropenia","type":"related"},{"name":"PN","type":"related"},{"name":"Prurigo Nodularis","type":"exact"},{"name":"poikiloderma with neutropenia","type":"exact"},{"name":"poikiloderma with neutropenia Clericuzio type","type":"related"},{"name":"poikiloderma with neutropenia, Clericuzio type","type":"exact"},{"name":"poikiloderma with neutropenia, Clericuzio-type","type":"related"}],"termid":"MONDO:0011405","terms_by_termid":{"MONDO:0011405":null},"xrefs":{"Monarch":{"xref_id":"0011405"}}}


id: PBO:0072093
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S12 pseudogene 24","termid":"PBO:0072093"}


id: FYPO:0004513
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"An increased chemical resistance phenotype observed in the vegetative growth phase of the life cycle in which cells grow in the presence of a higher concentration of latrunculin A than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased resistance to chemical during vegetative growth","termid":"FYPO:0000126"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002682"},{"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:0005447","FYPO:0001985","FYPO:0000003","FYPO:0002682","FYPO:0000139"],"is_obsolete":false,"name":"resistance to latrunculin A","synonyms":[{"name":"resistance to LatA","type":"exact"},{"name":"resistance to latrunculin A during mitotic cell cycle","type":"related"},{"name":"resistance to latrunculin A during vegetative growth","type":"exact"},{"name":"resistant to latrunculin A","type":"exact"}],"termid":"FYPO:0004513"}


id: GO:0033181
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A proton-transporting two-sector ATPase complex found in the plasma membrane.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton-transporting V-type ATPase complex","termid":"GO:0033176"},{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005886"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0005886","GO:0032991","GO:0005575"],"is_obsolete":false,"name":"plasma membrane proton-transporting V-type ATPase complex","synonyms":[{"name":"plasma membrane hydrogen ion-transporting ATPase","type":"exact"}],"termid":"GO:0033181"}


id: GO:0007044
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of a set of components to form a junction between a cell and its substrate.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell junction assembly","termid":"GO:0034329"},{"relation_name":"is_a","term_name":"cell-substrate junction organization","termid":"GO:0150115"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0044085"}],"interesting_parent_ids":["GO:0008150","GO:0044085"],"is_obsolete":false,"name":"cell-substrate junction assembly","secondary_identifiers":["GO:0007045"],"synonyms":[{"name":"cell-substrate adherens junction assembly","type":"related"}],"termid":"GO:0007044"}


id: SO:0001646
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A genetic marker, discovered using Diversity Arrays Technology (DArT) technology.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"genetic_marker","termid":"SO:0001645"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DArT_marker","synonyms":[{"name":"DArT marker","type":"exact"}],"termid":"SO:0001646"}


id: GO:0046933
data:
  {"annotated_genes":["SJAG_03925","SJAG_MIT37","SJAG_02564","SJAG_07003","SJAG_03114","SJAG_00133","SJAG_00915","SJAG_MIT09","SJAG_05204","SJAG_02598","SJAG_00985","SJAG_MIT15","SJAG_00836","SJAG_04122","SJAG_00542","SJAG_00438","SJAG_02105"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[58106,71627,71919,74478,77559,79560,79880,81066,95094,95683,96663,103638,109647,109739,120945,120951,120958],"is_not":false,"summary":null,"term":"GO:0046933"}]},"cv_name":"molecular_function","definition":"Enables the synthesis of ATP from ADP and phosphate by the transfer of protons from one side of a membrane to the other by a rotational mechanism driven by a gradient according to the reaction: ADP + H2O + phosphate + H+(in) -> ATP + H+(out).","definition_xrefs":["RHEA:57722"],"direct_ancestors":[{"relation_name":"is_a","term_name":"proton channel activity","termid":"GO:0015252"},{"relation_name":"is_a","term_name":"ligase activity","termid":"GO:0016874"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00133":null,"SJAG_00438":null,"SJAG_00542":null,"SJAG_00836":null,"SJAG_00915":null,"SJAG_00985":null,"SJAG_02105":null,"SJAG_02564":null,"SJAG_02598":null,"SJAG_03114":null,"SJAG_03925":null,"SJAG_04122":null,"SJAG_05204":null,"SJAG_07003":null,"SJAG_MIT09":null,"SJAG_MIT15":null,"SJAG_MIT37":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016874"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016874","GO:0003824","GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"proton-transporting ATP synthase activity, rotational mechanism","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["Reactome:R-HSA-164832","TC:3.A.2.1.1"],"synonyms":[{"name":"H+-transporting ATP synthase activity","type":"related"},{"name":"hydrogen ion transporting ATP synthase activity, rotational mechanism","type":"exact"}],"termid":"GO:0046933","terms_by_termid":{"GO:0046933":null}}


id: MONDO:0971127
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"parasitic eye infection","termid":"MONDO:0020947"}],"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":"diffuse unilateral subacute neuroretinitis","secondary_identifiers":["MEDGEN:573129","Orphanet:674947","UMLS:C0339404"],"termid":"MONDO:0971127","xrefs":{"Monarch":{"xref_id":"0971127"}}}


id: GO:0002384
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"An immune response taking place in the liver.","definition_xrefs":["GO_REF:0000022","GOC:jal","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organ or tissue specific immune response","termid":"GO:0002251"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"hepatic immune response","termid":"GO:0002384"}


id: GO:0070466
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A protein complex that consists of an alpha2-beta1 integrin complex bound to a type VI collagen triple helix containing an alpha3(VI) chain.","definition_xrefs":["PMID:8387021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"plasma membrane protein complex","termid":"GO:0098797"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO: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":"alpha2-beta1 integrin-alpha3(VI) complex","synonyms":[{"name":"ITGA2-ITGB1-COL6A3 complex","type":"narrow"}],"termid":"GO:0070466"}


id: GO:0102804
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: oripavine + 2-oxoglutarate + O2 = morphinone + formaldehyde + succinate + carbon dioxide.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete oripavine 6-O-demethylase activity (obsolete GO:0102804)","termid":"GO:0102804"}


id: PBO:0051003
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin (CD79A) binding protein 1 family member C","termid":"PBO:0051003"}


id: PBO:0085481
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Probable multiple transmembrane protein; involved in diploid invasive and pseudohyphal growth upon nitrogen starvation; is glycosylated and phosphorylated; interacts with Rim21p and Rim9p in the plasma membrane to form a pH-sensing complex in the Rim101 pathway and is required to maintain Rim21p levels; required for accumulation of processed Rim101p","termid":"PBO:0085481"}


id: PBO:0087126
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA binding protein; has similarity to mammalian heterogeneous nuclear RNP K protein, involved in the regulation of telomere position effect and telomere length; relative distribution to the nucleus increases upon DNA replication stress","termid":"PBO:0087126"}


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


id: PBO:0083387
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 essential, verified gene PLP2/YOR281C","termid":"PBO:0083387"}


id: GO:0033134
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a ubiquitin activating enzyme, any of the E1 proteins.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small protein activating enzyme binding","termid":"GO:0044388"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0005515","GO:0003674"],"is_obsolete":false,"name":"ubiquitin activating enzyme binding","termid":"GO:0033134"}


id: PBO:0085750
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein kinase; implicated in Slt2p mitogen-activated (MAP) kinase signaling pathway; interacts with numerous components in the mating pheromone and CWI MAPK pathways; associates with Rlm1p; KDX1 has a paralog, SLT2, that arose from the whole genome duplication","termid":"PBO:0085750"}


id: PR:O75006
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sec15 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O75006"],"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":"exocyst complex component sec15 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1183.01","synonyms":[{"name":"Spom972h-sec15","type":"exact"}],"termid":"PR:O75006"}


id: PBO:0049665
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H19 imprinted maternally expressed transcript","termid":"PBO:0049665"}


id: GO:0051013
data:
  {"annotated_genes":["SJAG_01530","SJAG_04566"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[75790,78202],"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":["GOC:ai","PMID:27037673"],"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:0008150"},{"rel_name":"is_a","termid":"GO:0000226"}],"interesting_parent_ids":["GO:0000226","GO:0007010","GO:0008150"],"is_obsolete":false,"name":"microtubule severing","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"microtubule severing activity","type":"related"}],"termid":"GO:0051013","terms_by_termid":{"GO:0051013":null}}


id: GO:0005856
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id: PBO:0002526
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id: PBO:0077493
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id: GO:0020013
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id: PBO:0075204
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id: PBO:0001119
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id: MONDO:0011641
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id: GO:1900011
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id: FYPO:0005575
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id: PBO:0069970
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id: MONDO:0008769
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id: FYPO:0004301
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id: MONDO:0004264
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id: FYECO:0000193
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id: SO:0000237
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id: FYPO:0002591
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id: MONDO:0004917
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A hordeolum that results from infection of a meibomian gland.","direct_ancestors":[{"relation_name":"is_a","term_name":"hordeolum","termid":"MONDO:0005800"},{"relation_name":"is_a","term_name":"sebaceous gland disorder","termid":"MONDO:0006607"},{"relation_name":"is_a","term_name":"skin appendage disorder","termid":"MONDO:0024481"}],"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:0005328","MONDO:0005093"],"is_obsolete":false,"name":"internal hordeolum","secondary_identifiers":["UMLS:C0085690","SCTID:414521009","ICD9:373.12","DOID:9908","MEDGEN:43227"],"synonyms":[{"name":"hordeolum internum","type":"related"},{"name":"hordeolum of tarsal gland","type":"exact"},{"name":"infected chalazion","type":"related"},{"name":"infected cyst of meibomian gland","type":"related"},{"name":"infected meibomian cyst","type":"related"},{"name":"infection of meibomian gland","type":"related"},{"name":"internal hordeolum","type":"exact"},{"name":"meibomian adenitis","type":"related"},{"name":"tarsal gland hordeolum","type":"exact"}],"termid":"MONDO:0004917","xrefs":{"Monarch":{"xref_id":"0004917"}}}


id: MONDO:0011747
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"excluded_subClassOf","term_name":"dyslexia","termid":"MONDO:0005489"},{"relation_name":"is_a","term_name":"inherited disease susceptibility","termid":"MONDO:0020573"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dyslexia, susceptibility to, 5","secondary_identifiers":["UMLS:C1847184","OMIM:606896","MEDGEN:337746"],"synonyms":[{"name":"DYX5","type":"exact"},{"name":"dyslexia, susceptibility to, 5","type":"exact"}],"termid":"MONDO:0011747","xrefs":{"Monarch":{"xref_id":"0011747"}}}


id: GO:0042754
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate or extent of a circadian rhythm behavior.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of circadian rhythm","termid":"GO:0042752"},{"relation_name":"is_a","term_name":"negative regulation of biological process","termid":"GO:0048519"},{"relation_name":"negatively_regulates","term_name":"circadian rhythm","termid":"GO:0007623"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"negative regulation of circadian rhythm","synonyms":[{"name":"down regulation of circadian rhythm","type":"exact"},{"name":"down-regulation of circadian rhythm","type":"exact"},{"name":"downregulation of circadian rhythm","type":"exact"},{"name":"inhibition of circadian rhythm","type":"narrow"}],"termid":"GO:0042754"}


id: GO:0030566
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Specifies the site of a posttranscriptional modification in an snRNA molecule by base pairing with a short sequence around the target residue.","definition_xrefs":["GOC:mah","PMID:12457565"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snRNA binding","termid":"GO:0017069"},{"relation_name":"is_a","term_name":"RNA modification guide activity","termid":"GO:0030555"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003723"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0003723","GO:0005488"],"is_obsolete":false,"name":"snRNA modification guide activity","termid":"GO:0030566"}


id: MONDO:0007617
data:
  {"annotated_genes":["SJAG_02254"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87763],"is_not":false,"summary":null,"term":"MONDO:0007617"}]},"cv_name":"mondo","definition":"Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the ARID1B gene.","definition_xrefs":["MONDO:patterns/OMIM_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"autosomal dominant non-syndromic intellectual disability","termid":"MONDO:0015802"},{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"Coffin-Siris syndrome","termid":"MONDO:0015452"},{"relation_name":"is_a","term_name":"BAFopathy","termid":"MONDO:0700120"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02254":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0000426"],"is_obsolete":false,"name":"Coffin-Siris syndrome 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["GARD:15072","DOID:0070042","MESH:C538391","MEDGEN:482831","OMIM:135900","UMLS:C3281201","OMIM:609943","OMIM:614562"],"synonyms":[{"name":"ARID1B-related BAFopathy","type":"exact"},{"name":"COFFIN-SIRIS syndrome","type":"related"},{"name":"COFFIN-SIRIS syndrome 1","type":"exact"},{"name":"CSS","type":"related"},{"name":"CSS1","type":"exact"},{"name":"Coffin-Siris syndrome 1","type":"exact"},{"name":"MRD12","type":"exact"},{"name":"autosomal dominant mental retardation 12","type":"exact"},{"name":"fifth digit syndrome","type":"broad"},{"name":"hypertrichosis, hyperkeratosis, intellectual disability, and distinctive facial features","type":"exact"},{"name":"hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features","type":"exact"},{"name":"intellectual disability, autosomal dominant 12","type":"exact"},{"name":"mental retardation, autosomal dominant 12","type":"related"},{"name":"mental retardation, autosomal dominant type 12","type":"exact"}],"termid":"MONDO:0007617","terms_by_termid":{"MONDO:0007617":null},"xrefs":{"Monarch":{"xref_id":"0007617"}}}


id: PBO:0016909
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces pombe specific protein Mug115","termid":"PBO:0016909"}


id: PBO:0002821
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Set3 complex subunit Snt1","termid":"PBO:0002821"}


id: MONDO:0014849
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete autosomal recessive nonsyndromic deafness 105 (obsolete MONDO:0014849)","secondary_identifiers":["OMIM:616958"],"termid":"MONDO:0014849","xrefs":{"Monarch":{"xref_id":"0014849"}}}


id: GO:0003007
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process in which the heart is generated and organized. The heart is a hollow, muscular organ, which, by contracting rhythmically, keeps up the circulation of the blood.","definition_xrefs":["GOC:isa_complete","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ morphogenesis","termid":"GO:0009887"},{"relation_name":"part_of","term_name":"heart development","termid":"GO:0007507"}],"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":"heart morphogenesis","synonyms":[{"name":"cardiac morphogenesis","type":"related"}],"termid":"GO:0003007"}


id: MONDO:0019885
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Distal trisomy 11q is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the long arm of chromosome 11, with high phenotypic variability principally characterized by craniofacial dysmorphism (brachycephaly/plagiocephaly, low-set, posteriorly rotated ears, short philtrum, micrognathia) and intellectual disability. Short stature and seizures, as well as cardiac (e.g. atrial septal defect), skeletal (incl. brachy/syndactyly) and genital (e.g. micropenis, cryptorchidism) abnormalities may also be associated. Neurodevelopmental anomalies (pain insensitivity, sensorineural hearing loss, expressive language deficiency) and neuropsychiatric disorders (autistic features, auditory hallucination, self-talking) have also been reported.","definition_xrefs":["Orphanet:96103"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome 11q trisomy","termid":"MONDO:0022173"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"distal trisomy 11q","secondary_identifiers":["NORD:937","MEDGEN:419166","SCTID:764447009","UMLS:C2931797","MESH:C538294","GARD:19318"],"synonyms":[{"name":"Chromosome 11, Partial Trisomy 11q","type":"exact"},{"name":"distal duplication 11q","type":"exact"},{"name":"distal trisomy type 11q","type":"exact"},{"name":"telomeric duplication 11q","type":"exact"},{"name":"trisomy 11qter","type":"exact"}],"termid":"MONDO:0019885","xrefs":{"Monarch":{"xref_id":"0019885"}}}


id: FYPO:0000223
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell morphology phenotype observed in the vegetative growth phase of the life cycle in which a cell is longer, and has a greater length:diameter ratio, than normal, and has more than one septum.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"multiseptate vegetative cell","termid":"FYPO:0000118"},{"relation_name":"is_a","term_name":"multiseptate vegetative cell","termid":"FYPO:0000118"},{"relation_name":"is_a","term_name":"elongated septated vegetative cell","termid":"FYPO:0004750"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0000631"},{"rel_name":"output_of","termid":"FYPO:0000032"},{"rel_name":"is_a","termid":"FYPO:0000005"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000032","FYPO:0000631","FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0000005"],"is_obsolete":false,"name":"elongated multiseptate vegetative cell","synonyms":[{"name":"elongated multiseptate cell during mitotic cell cycle","type":"related"},{"name":"elongated multiseptate cells during vegetative growth","type":"exact"},{"name":"long multiseptate cells","type":"exact"}],"termid":"FYPO:0000223"}


id: GO:0006478
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The sulfation of peptidyl-tyrosine residues to form peptidyl-O4'-sulfo-L-tyrosine.","definition_xrefs":["RESID:AA0172"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein sulfation","termid":"GO:0006477"},{"relation_name":"is_a","term_name":"peptidyl-tyrosine modification","termid":"GO:0018212"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006790","GO:0008150"],"is_obsolete":false,"name":"peptidyl-tyrosine sulfation","synonyms":[{"name":"peptidyl-tyrosine sulphation","type":"exact"}],"termid":"GO:0006478"}


id: GO:0034216
data:
  {"annotated_genes":["SJAG_04673"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[102496],"is_not":false,"summary":null,"term":"GO:0034216"}]},"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: thiamine(out) + H+(out) = thiamine(in) + H+(in). In high-affinity transport the transporter is able to bind the solute even if it is only present at very low concentrations.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thiamine:proton symporter activity","termid":"GO:0034215"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04673":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0022857","GO:0005215"],"is_obsolete":false,"name":"high-affinity thiamine:proton symporter activity","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"high affinity thiamin:hydrogen symporter activity","type":"exact"},{"name":"high-affinity thiamin:hydrogen symporter activity","type":"exact"},{"name":"high-affinity thiamin:proton symporter activity","type":"exact"},{"name":"high-affinity thiamine:hydrogen symporter activity","type":"exact"}],"termid":"GO:0034216","terms_by_termid":{"GO:0034216":null}}


id: PR:O59748
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- lsc1 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O59748"],"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":"CTD kinase subunit beta (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC530.13","synonyms":[{"name":"CTD kinase subunit 2 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"CTDK-I subunit beta (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-lsc1","type":"exact"},{"name":"latrunculin sensitive cyclin knockout protein 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O59748"}


id: PBO:0027033
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_duration_of_protein_localization_to_mitotic_spindle_midzone","termid":"PBO:0027033"}


id: GO:0009327
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"OBSOLETE. A protein complex that possesses NAD(P)+ transhydrogenase (AB-specific) activity. Homodimeric, trimeric, and heterotetrameric complexes have been identified.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete NAD(P)+ transhydrogenase complex (AB-specific) (obsolete GO:0009327)","termid":"GO:0009327"}


id: GO:0019042
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process by which, after initial infection, a virus lies dormant within a cell and viral production ceases. The process ends when the virus switches from latency and starts to replicate.","definition_xrefs":["VZ:3970","GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral process","termid":"GO:0016032"}],"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":"viral latency","secondary_identifiers":["GO:0030069","GO:0075710"],"synonyms":[{"name":"latent virus infection","type":"exact"},{"name":"phage lysogeny","type":"exact"},{"name":"viral dormancy","type":"exact"}],"termid":"GO:0019042"}


id: GO:0015015
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification, often by sulfation, of sugars incorporated into heparan sulfate after polymerization.","definition_xrefs":["ISBN:0815316194"],"gene_count":0,"genotype_count":0,"name":"obsolete heparan sulfate proteoglycan biosynthetic process, enzymatic modification (obsolete GO:0015015)","synonyms":[{"name":"heparan sulfate proteoglycan anabolism, enzymatic modification","type":"exact"},{"name":"heparan sulfate proteoglycan formation, enzymatic modification","type":"exact"},{"name":"heparan sulfate proteoglycan synthesis, enzymatic modification","type":"exact"},{"name":"heparan sulphate proteoglycan biosynthesis, enzymatic modification","type":"exact"},{"name":"heparan sulphate proteoglycan biosynthetic process, enzymatic modification","type":"exact"},{"name":"heparin proteoglycan biosynthetic process, enzymatic modification","type":"related"}],"termid":"GO:0015015"}


id: PBO:0051817
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"interleukin 1 receptor associated kinase 2","termid":"PBO:0051817"}


id: SO:0001892
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A feature amplification of a region containing a transcription factor binding site.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulatory_region_amplification","termid":"SO:0001891"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TFBS_amplification","secondary_identifiers":["http:www.ensembl.org/info/genome/variation/predicted_data.html#consequences"],"synonyms":[{"name":"TFBS amplification ","type":"exact"},{"name":"VEP:TFBS_amplification","type":"exact"},{"name":"transcription factor binding site amplification","type":"exact"}],"termid":"SO:0001892"}


id: MONDO:0011088
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the CHRNA1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"postsynaptic congenital myasthenic syndrome","termid":"MONDO:0020344"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0002320"],"is_obsolete":false,"name":"congenital myasthenic syndrome 1A","secondary_identifiers":["DOID:0110663","MEDGEN:419336","UMLS:C2931107","GARD:15330","OMIM:601462"],"synonyms":[{"name":"CHRNA1 congenital myasthenic syndrome","type":"exact"},{"name":"CMS IIa","type":"exact"},{"name":"CMS1A","type":"exact"},{"name":"Cms IIa","type":"related"},{"name":"Cms IIa, formerly","type":"related"},{"name":"congenital myasthenic syndrome 1A, slow-channel","type":"exact"},{"name":"congenital myasthenic syndrome caused by mutation in CHRNA1","type":"exact"},{"name":"congenital myasthenic syndrome type 1A","type":"exact"},{"name":"congenital myasthenic syndrome type IIa","type":"exact"},{"name":"myasthenic syndrome, congenital, 1A, slow-channel","type":"related"},{"name":"myasthenic syndrome, congenital, type IIa","type":"related"},{"name":"myasthenic syndrome, congenital, type IIa, formerly","type":"related"}],"termid":"MONDO:0011088","xrefs":{"Monarch":{"xref_id":"0011088"}}}


id: PBO:0069011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 255, pseudogene","termid":"PBO:0069011"}


id: PBO:0049178
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"GREB1 like retinoic acid receptor coactivator","termid":"PBO:0049178"}


id: PBO:0080473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vesicle transport through interaction with t-SNAREs 1B pseudogene 4","termid":"PBO:0080473"}


id: PATO:0000898
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000898 intercross fertility value (obsolete PATO:0000898)","termid":"PATO:0000898"}


id: PBO:0076181
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sulfotransferase family 6B member 1","termid":"PBO:0076181"}


id: GO:0021721
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process that contributes to the act of creating the structural organization of the superior olivary nucleus structure. In mice, the superior olivary nucleus is a small cylindrical mass on the dorsal surface of the lateral part of the trapezoid body of the pons, and it is situated immediately above the inferior olivary nucleus. It receives projections from the cochlear nucleus and thus is involved in the perception of sound.","definition_xrefs":["GOC:jid","GOC:dph","GOC:cls","GO_REF:0000021","ISBN:0838580343","GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure arrangement","termid":"GO:0048532"},{"relation_name":"part_of","term_name":"pons structural organization","termid":"GO:0021585"},{"relation_name":"part_of","term_name":"superior olivary nucleus morphogenesis","termid":"GO:0021719"}],"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 olivary nucleus structural organization","synonyms":[{"name":"superior olivary nucleus structural organisation","type":"exact"}],"termid":"GO:0021721"}


id: GO:0004401
data:
  {"annotated_genes":["SJAG_00248"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78348],"is_not":false,"summary":null,"term":"GO:0004401"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: L-histidinol phosphate + H2O = L-histidinol + phosphate.","definition_xrefs":["RHEA:14465","EC:3.1.3.15"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphatase activity","termid":"GO:0016791"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00248":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016788"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016787"}],"interesting_parent_ids":["GO:0016788","GO:0003674","GO:0016787","GO:0003824"],"is_obsolete":false,"name":"histidinol-phosphatase activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["KEGG_REACTION:R03013","MetaCyc:HISTIDPHOS-RXN"],"synonyms":[{"name":"HPpase activity","type":"related"},{"name":"L-histidinol phosphate phosphatase activity","type":"related"},{"name":"L-histidinol-phosphate phosphohydrolase activity","type":"related"},{"name":"histidinol phosphate phosphatase activity","type":"related"},{"name":"histidinolphosphatase activity","type":"related"},{"name":"histidinolphosphate phosphatase activity","type":"related"}],"termid":"GO:0004401","terms_by_termid":{"GO:0004401":null}}


id: PR:Q9P7X5
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- ppk32 gene.","definition_xrefs":["UniProtKB:Q9P7X5","PRO:DNx"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Schizosaccharomyces pombe 972h- protein","termid":"PR:000029043"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"protein kinase domain-containing protein ppk32 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBP23A10.10","synonyms":[{"name":"Spom972h-ppk32","type":"exact"}],"termid":"PR:Q9P7X5"}


id: FYPO:0007102
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype in which a cell contains more than one meiotic spindle per nucleus during the second meiotic nuclear division.","definition_xrefs":["PomBase:mah","PMID:22292001"],"direct_ancestors":[{"relation_name":"is_a","term_name":"multiple meiotic spindles","termid":"FYPO:0006390"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000120"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000054"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0002399","FYPO:0005447","FYPO:0000120","FYPO:0000054"],"is_obsolete":false,"name":"multiple spindles during meiosis II","synonyms":[{"name":"additional spindles present during meiosis II","type":"exact"},{"name":"extra spindles during meiosis II","type":"exact"},{"name":"increased number of spindles during meiosis II","type":"exact"},{"name":"multiple meiotic spindles during meiosis II","type":"exact"},{"name":"spindles present in greater numbers during meiosis II","type":"exact"}],"termid":"FYPO:0007102"}


id: PBO:0068347
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ring finger protein 123","termid":"PBO:0068347"}


id: PBO:0055676
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"LIPE antisense RNA 1","termid":"PBO:0055676"}


id: FYPO:0008074
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the localization of a protein to the medial cortical nodes is increased during mitotic interphase.","definition_xrefs":["PMID:10930468"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein localization to medial cortical node","termid":"FYPO:0007156"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000138","FYPO:0001320","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"increased protein localization to medial cortical node during interphase","termid":"FYPO:0008074"}


id: FYPO:0001022
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell population growth phenotype in which vegetative cells grow normally (i.e. indistinguishably from wild type) during a cellular response to high osmolarity.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal growth during cellular response to osmotic stress","termid":"FYPO:0001021"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0002058"}],"interesting_parent_ids":["FYPO:0002057","FYPO:0000139","FYPO:0000257","FYPO:0000003","FYPO:0002058","FYPO:0002060"],"is_obsolete":false,"name":"normal growth during cellular response to high osmolarity","synonyms":[{"name":"normal cell population growth during cellular response to high osmolarity","type":"exact"},{"name":"normal cell population growth during cellular response to hyperosmotic conditions","type":"exact"},{"name":"normal cellular response to high osmolarity","type":"related"},{"name":"normal vegetative cell population growth during cellular response to high osmolarity","type":"exact"}],"termid":"FYPO:0001022"}


id: PBO:0026745
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_phosphorylation_during_glucose_starvation","termid":"PBO:0026745"}


id: GO:0005925
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A cell-substrate junction that anchors the cell to the extracellular matrix and that forms a point of termination of actin filaments. In insects focal adhesion has also been referred to as hemi-adherens junction (HAJ).","definition_xrefs":["ISBN:0124325653","PMID:23033047","PMID:12191915","PMID:1643657","PMID:16805308","PMID:19197329","PMID:8314002","GOC:bc","PMID:10419689","GOC:aruk","ISBN:0815316208","PMID:15246682","PMID:26923917","PMID:28796323"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell-substrate junction","termid":"GO:0030055"}],"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":"focal adhesion","secondary_identifiers":["Wikipedia:Focal_adhesion","GO:0005926","GO:0008357"],"synonyms":[{"name":"HAJ","type":"exact"},{"name":"adhesion plaque","type":"related"},{"name":"connecting hemi-adherens junction","type":"exact"},{"name":"focal contact","type":"exact"},{"name":"hemi-adherens junction","type":"exact"}],"termid":"GO:0005925"}


id: GO:0048520
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of behavior, the internally coordinated responses (actions or inactions) of whole living organisms (individuals or groups) to internal or external stimuli.","definition_xrefs":["GOC:pr","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of behavior","termid":"GO:0050795"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"positively_regulates","term_name":"behavior","termid":"GO:0007610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"positive regulation of behavior","synonyms":[{"name":"activation of behavior","type":"narrow"},{"name":"stimulation of behavior","type":"narrow"},{"name":"up regulation of behavior","type":"exact"},{"name":"up-regulation of behavior","type":"exact"},{"name":"upregulation of behavior","type":"exact"}],"termid":"GO:0048520"}


id: PBO:0070971
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L18 pseudogene 9","termid":"PBO:0070971"}


id: PATO:0000807
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000807 proprioreception value (obsolete PATO:0000807)","termid":"PATO:0000807"}


id: PBO:0062105
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 4 subfamily C member 3","termid":"PBO:0062105"}


id: PBO:0053801
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 1056","termid":"PBO:0053801"}


id: PATO:0002211
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A curvature quality inhering in a bearer by virtue of the bearer's being curved backward or inward.","definition_xrefs":["merriam-webster:http://www.merriam-webster.com/dictionary/recurved"],"direct_ancestors":[{"relation_name":"is_a","term_name":"curved","termid":"PATO:0000406"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"recurved","termid":"PATO:0002211"}


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


id: PBO:0113300
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in axial bud site selection; prevents repolarization of cells at previous division sites; recruited with Nba1p to the cell cortex and to cytokinesis remnants (bud scars) by Aim44p and Nap1p where Nba1p prevents Rsr1p-mediated activation of Cdc24p, and therefore Cdc42p activation; acts with Nba1p to establish transient bud scar localization of Rga1p, a Cdc42p GAP; localizes to the nucleus and to cell division site during G2/M, and is then stably recruited to cytokinesis remnants","termid":"PBO:0113300"}


id: PBO:0027488
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_protein_level_during_G0","termid":"PBO:0027488"}


id: PBO:0044901
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"derlin 3","termid":"PBO:0044901"}


id: PBO:0002937
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translation initiation factor eIF3i","termid":"PBO:0002937"}


id: GO:0072764
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a reversine stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular response to purine-containing compound","termid":"GO:0071415"},{"relation_name":"is_a","term_name":"response to reversine","termid":"GO:1901596"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cellular response to reversine","termid":"GO:0072764"}


id: PBO:0088734
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Armadillo-type fold protein, zf-MYND type zinc finger protein, Mub1-Rad6-Ubr2 ubiquitin ligase complex Mub1","termid":"PBO:0088734"}


id: PBO:0050609
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HSD17B2 antisense RNA 1","termid":"PBO:0050609"}


id: PBO:0038710
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"actin gamma 1 pseudogene 4","termid":"PBO:0038710"}


id: PBO:0057659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 1251","termid":"PBO:0057659"}


id: PBO:0036488
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphoribosylanthranilate transferase Trp4","termid":"PBO:0036488"}


id: MONDO:0100591
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"TOR1AIP1-related multisystem disorder is a rare, early-onset disorder affecting multiple organ systems that is caused by variation in the TOR1AIP1 gene. Clinical features reported in affected individuals are variable but may include hypotonia, dystonia, cerebellar atrophy, contractures, cardiomyopathy, microcephaly, cataract, deafness, skeletal anomalies, progeroid appearance and other facial dysmorphism, and nephrolithiasis.","definition_xrefs":["PMID:32055997","PMID:25425325","PMID:30723199"],"direct_ancestors":[{"relation_name":"is_a","term_name":"TOR1AIP1-related nuclear envelopathy","termid":"MONDO:0100604"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TOR1AIP1-related multisystem disorder","termid":"MONDO:0100591","xrefs":{"Monarch":{"xref_id":"0100591"}}}


id: MONDO:0017503
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acheiria","termid":"MONDO:0017445"}],"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":"acheiria, bilateral","secondary_identifiers":["MEDGEN:672347","Orphanet:295103","UMLS:C0685394","icd11.foundation:1430605018","SCTID:371189003"],"synonyms":[{"name":"congenital absence of hand, bilateral","type":"exact"}],"termid":"MONDO:0017503","xrefs":{"Monarch":{"xref_id":"0017503"}}}


id: PATO:0002222
data:
  {"annotation_feature_type":"gene","cv_name":"quality","definition":"A quality inhering in a bearer by virtue of the bearer's being phosphorylated to a lesser than normal extent, or less than fully.","definition_xrefs":["Wikipedia:http://en.wiktionary.org/wiki/hypophosphorylated"],"direct_ancestors":[{"relation_name":"decreased_in_magnitude_relative_to","term_name":"normal","termid":"PATO:0000461"},{"relation_name":"is_a","term_name":"phosphorylated","termid":"PATO:0002220"},{"relation_name":"is_a","term_name":"decreased object quality","termid":"PATO:0002303"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"decreased phosphorylation","synonyms":[{"name":"hypophosporylated ","type":"exact"}],"termid":"PATO:0002222"}


id: PBO:0016975
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Schizosaccharomyces specific protein Mug95","termid":"PBO:0016975"}


id: PBO:0047784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"forkhead box D4","termid":"PBO:0047784"}


id: MONDO:0009393
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic disorder of urea cycle metabolism characterized by either a neonatal-onset with manifestations of lethargy, poor feeding, vomiting and tachypnea or, more commonly, presentations in infancy, childhood or adulthood with chronic neurocognitive deficits, acute encephalopathy and/or coagulation defects or other chronic liver dysfunction.","definition_xrefs":["Orphanet:415"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"urea cycle disorder or inherited hyperammonemia","termid":"MONDO:0800153"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0004736"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0004736"],"is_obsolete":false,"name":"ornithine translocase deficiency","secondary_identifiers":["MEDGEN:82815","MESH:C538380","NCIT:C129029","OMIM:238970","SCTID:30287008","GARD:2830","NANDO:2200485","UMLS:C0268540","DOID:0050720"],"synonyms":[{"name":"HHH","type":"related"},{"name":"HHH syndrome","type":"exact"},{"name":"HHHS","type":"related"},{"name":"Hhh syndrome","type":"related"},{"name":"ORNT1 deficiency","type":"exact"},{"name":"hyperornithinemia-hyperammonemia-homocitrullinemia syndrome","type":"exact"},{"name":"hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome","type":"exact"},{"name":"hyperornithinemia-hyperammonemia-homocitrullinuria syndrome","type":"related"},{"name":"ornithine carrier deficiency","type":"exact"},{"name":"ornithine translocase deficiency","type":"exact"},{"name":"ornithine translocase deficiency syndrome","type":"related"},{"name":"triple H syndrome","type":"exact"}],"termid":"MONDO:0009393","xrefs":{"Monarch":{"xref_id":"0009393"}}}


id: FYPO:0001667
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of cyclic AMP measured in a cell during glucose starvation is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cAMP level","termid":"FYPO:0001666"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000257"],"is_obsolete":false,"name":"normal cAMP level during glucose starvation","synonyms":[{"name":"normal cAMP accumulation during glucose starvation","type":"related"},{"name":"normal cAMP level during glucose depletion","type":"exact"},{"name":"normal cAMP level during glucose deprivation","type":"exact"},{"name":"normal cAMP level during glucose limitation","type":"related"},{"name":"normal cellular cAMP level during glucose starvation","type":"exact"},{"name":"normal cyclic AMP level during glucose starvation","type":"exact"}],"termid":"FYPO:0001667"}


id: GO:0006473
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The addition of an acetyl group to a protein amino acid. An acetyl group is CH3CO-, derived from acetic [ethanoic] acid.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein acylation","termid":"GO:0043543"}],"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":"protein acetylation","synonyms":[{"name":"protein amino acid acetylation","type":"exact"}],"termid":"GO:0006473"}


id: PBO:0075014
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 115-25","termid":"PBO:0075014"}


id: GO:0018270
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of a C-terminal peptidyl-alanine ethanolamide-linked glycosylphosphatidylinositol (GPI) anchor following hydrolysis of an alanyl-peptide bond in the carboxy-terminal region of a membrane-associated protein.","definition_xrefs":["RESID:AA0163"],"gene_count":0,"genotype_count":0,"name":"obsolete GPI anchor biosynthetic process via N-alanyl-glycosylphosphatidylinositolethanolamine (obsolete GO:0018270)","termid":"GO:0018270"}


id: FYPO:0000280
data:
  {"alleles_by_uniquename":{"SJAG_00514:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00514","name":"scd1delta","uniquename":"SJAG_00514:allele-1"},"SJAG_00993:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_00993","name":"byr1delta","uniquename":"SJAG_00993:allele-1"},"SJAG_01718:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01718","name":"byr2delta","uniquename":"SJAG_01718:allele-1"},"SJAG_01794:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_01794","name":"scd2delta","uniquename":"SJAG_01794:allele-1"},"SJAG_02379:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02379","name":"gap1delta","uniquename":"SJAG_02379:allele-1"},"SJAG_02486:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02486","name":"ste6delta","uniquename":"SJAG_02486:allele-1"},"SJAG_02592:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02592","name":"sty1delta","uniquename":"SJAG_02592:allele-1"},"SJAG_02923:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_02923","name":"spk1delta","uniquename":"SJAG_02923:allele-1"},"SJAG_03453:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_03453","name":"ras1delta","uniquename":"SJAG_03453:allele-1"},"SJAG_04009:allele-1":{"allele_type":"deletion","description":"deletion","gene_uniquename":"SJAG_04009","name":"ste11delta","uniquename":"SJAG_04009:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121150,121190,121196,121197,121201,121204,121206,121207,121220,121222],"is_not":false,"summary":null,"term":"FYPO:0000280"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which conjugation does not occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating","termid":"FYPO:0000031"},{"relation_name":"is_a","term_name":"abolished biological process","termid":"FYPO:0005448"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00514":null,"SJAG_00993":null,"SJAG_01718":null,"SJAG_01794":null,"SJAG_02379":null,"SJAG_02486":null,"SJAG_02592":null,"SJAG_02923":null,"SJAG_03453":null,"SJAG_04009":null},"genotype_count":10,"genotypes_by_uniquename":{"byr1delta":{"display_name":"byr1delta","display_uniquename":"byr1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00993:allele-1","expression":"Null"}]}]},"byr2delta":{"display_name":"byr2delta","display_uniquename":"byr2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01718:allele-1","expression":"Null"}]}]},"gap1delta":{"display_name":"gap1delta","display_uniquename":"gap1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02379:allele-1","expression":"Null"}]}]},"ras1delta":{"display_name":"ras1delta","display_uniquename":"ras1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_03453:allele-1","expression":"Null"}]}]},"scd1delta":{"display_name":"scd1delta","display_uniquename":"scd1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_00514:allele-1","expression":"Null"}]}]},"scd2delta":{"display_name":"scd2delta","display_uniquename":"scd2delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_01794:allele-1","expression":"Null"}]}]},"spk1delta":{"display_name":"spk1delta","display_uniquename":"spk1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02923:allele-1","expression":"Null"}]}]},"ste11delta":{"display_name":"ste11delta","display_uniquename":"ste11delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04009:allele-1","expression":"Null"}]}]},"ste6delta":{"display_name":"ste6delta","display_uniquename":"ste6delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02486:allele-1","expression":"Null"}]}]},"sty1delta":{"display_name":"sty1delta","display_uniquename":"sty1delta","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_02592:allele-1","expression":"Null"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000301"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0000301","FYPO:0005447"],"is_obsolete":false,"name":"sterile","references_by_uniquename":{"PMID:29566183":null,"PMID:31150379":null},"secondary_identifiers":["FYPO:0000638"],"single_locus_annotated_genes":["SJAG_02379","SJAG_02592","SJAG_04009","SJAG_03453","SJAG_02923","SJAG_01718","SJAG_01794","SJAG_00514","SJAG_00993","SJAG_02486"],"single_locus_genotype_uniquenames":["byr2delta","scd1delta","ste6delta","spk1delta","gap1delta","byr1delta","ste11delta","sty1delta","ras1delta","scd2delta"],"synonyms":[{"name":"conjugation abolished","type":"exact"},{"name":"zygote formation abolished","type":"related"}],"termid":"FYPO:0000280","terms_by_termid":{"FYECO:0000272":null,"FYPO:0000280":null,"FYPO_EXT:0000001":null}}


id: GO:0050091
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 3-(2-hydroxyphenyl)propanoate + H+ + NADH + O2 = 3-(2,3-dihydroxyphenyl)propanoate + H2O + NAD+.","definition_xrefs":["EC:1.14.13.4","RHEA:17669"],"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:0003824"},{"rel_name":"is_a","termid":"GO:0016491"}],"interesting_parent_ids":["GO:0003674","GO:0003824","GO:0016491"],"is_obsolete":false,"name":"melilotate 3-monooxygenase activity","secondary_identifiers":["KEGG_REACTION:R03369","MetaCyc:MELILOTATE-3-MONOOXYGENASE-RXN"],"synonyms":[{"name":"2-hydroxyphenylpropionate hydroxylase activity","type":"related"},{"name":"2-hydroxyphenylpropionic hydroxylase activity","type":"related"},{"name":"3-(2-hydroxyphenyl)propanoate,NADH:oxygen oxidoreductase (3-hydroxylating)","type":"related"},{"name":"melilotate hydroxylase activity","type":"exact"},{"name":"melilotic hydroxylase activity","type":"related"}],"termid":"GO:0050091"}


id: PBO:0087840
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Threonine aldolase; catalyzes the cleavage of L-allo-threonine and L-threonine to glycine; involved in glycine biosynthesis","termid":"PBO:0087840"}


id: GO:0035124
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process, occurring in the embryo, by which the anatomical structures of the caudal fin are generated and organized. The caudal fin is an unpaired medial fin mounted at the caudal end of the fish and is the main fin used for propulsion.","definition_xrefs":["GOC:dgh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"embryonic medial fin morphogenesis","termid":"GO:0035122"},{"relation_name":"is_a","term_name":"caudal fin morphogenesis","termid":"GO:0035143"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"embryonic caudal fin morphogenesis","termid":"GO:0035124"}


id: PR:O14345
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A palmitoyltransferase ZDHHC21 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","OMA:SCHPO02966"],"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":"palmitoyltransferase pfa3 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC2F12.15c","secondary_identifiers":["UniProtKB:O14345"],"synonyms":[{"name":"Spom972h-ZDHHC21","type":"exact"},{"name":"protein fatty acyltransferase 3 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O14345"}


id: GO:0017168
data:
  {"annotated_genes":["SJAG_01995"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[78825],"is_not":false,"summary":null,"term":"GO:0017168"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: 5-oxo-L-proline + ATP + 2 H2O = L-glutamate + ADP + 2 H+ + phosphate.","definition_xrefs":["RHEA:10348","EC:3.5.2.9"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides","termid":"GO:0016812"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01995":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016787"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016810"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016810","GO:0016787","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"5-oxoprolinase (ATP-hydrolyzing) activity","references_by_uniquename":{"GO_REF:0000033":null},"secondary_identifiers":["Wikipedia:5-oxoprolinase_(ATP-hydrolysing)","MetaCyc:5-OXOPROLINASE-ATP-HYDROLYSING-RXN","KEGG_REACTION:R00251","Reactome:R-HSA-1247935","Reactome:R-HSA-5603208"],"synonyms":[{"name":"5-OPase activity","type":"related"},{"name":"5-oxo-L-prolinase activity","type":"related"},{"name":"5-oxo-L-proline amidohydrolase (ATP-hydrolysing)","type":"related"},{"name":"5-oxoprolinase (ATP-hydrolysing)","type":"related"},{"name":"5-oxoprolinase activity","type":"related"},{"name":"L-pyroglutamate hydrolase activity","type":"related"},{"name":"oxoprolinase activity","type":"related"},{"name":"pyroglutamase (ATP-hydrolysing)","type":"related"},{"name":"pyroglutamase (ATP-hydrolyzing) activity","type":"related"},{"name":"pyroglutamase activity","type":"related"},{"name":"pyroglutamate hydrolase activity","type":"related"},{"name":"pyroglutamic hydrolase activity","type":"related"}],"termid":"GO:0017168","terms_by_termid":{"GO:0017168":null}}


id: PBO:0048076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ferritin heavy chain 1 pseudogene 27","termid":"PBO:0048076"}


id: PBO:0003551
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"But2 family protein But2","termid":"PBO:0003551"}


id: FYPO:0005349
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 mitotic spindle pole body (SPB) moves rapidly back and forth to a greater extent and over a larger area than normal, causing increased chromosome movement. Normally, SPB oscillation occurs during mitotic interphase (as well as prophase) but is restricted to a small space.","definition_xrefs":["PMID:19001497","PMID:12390246","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal spindle pole body-led chromosome movement during mitotic interphase","termid":"FYPO:0005348"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000138"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0005447","FYPO:0000138"],"is_obsolete":false,"name":"increased spindle pole body-led chromosome movement during mitotic interphase","synonyms":[{"name":"increased SPB-led chromosome movement during mitotic interphase","type":"exact"},{"name":"increased mitotic SPB oscillation during mitotic interphase","type":"exact"},{"name":"increased mitotic spindle pole body movement during mitotic interphase","type":"exact"},{"name":"increased mitotic spindle pole body oscillation during mitotic interphase","type":"exact"},{"name":"increased spindle pole body-led chromosome movement during interphase of mitotic cell cycle","type":"exact"},{"name":"increased spindle pole body-led chromosome movement during mitotic interphase during vegetative growth","type":"exact"}],"termid":"FYPO:0005349"}


id: MOD:00801
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-cysteine residue, an L-histidine residue, homocitric acid and an eight-iron nine-sulfur cluster to L-cysteinyl-L-histidino-homocitryl octairon nonasulfide.","definition_xrefs":["RESID:AA0394","PubMed:8392330"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iron-sulfur cluster containing modification","termid":"MOD:00739"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-cysteine residue","termid":"MOD:02067"},{"relation_name":"is_a","term_name":"metal or metal cluster coordinated L-histidine residue","termid":"MOD:02070"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:00905"}],"interesting_parent_ids":["MOD:00905"],"is_obsolete":false,"name":"L-cysteinyl-L-histidino-homocitryl octairon nonasulfide","synonyms":[{"name":"CysHis-[8Fe9S]","type":"exact"},{"name":"L-cysteinyl-L-histidino-homocitryl octairon nonasulfide carbide","type":"exact"},{"name":"nitrogenase iron-iron cofactor","type":"exact"}],"termid":"MOD:00801"}


