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id: FYPO:0006956
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id: GO:0032925
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id: PBO:0054316
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id: GO:0018529
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id: PBO:0028065
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id: PBO:0047021
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id: GO:0016746
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id: MONDO:0001305
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Narrowing of the laryngeal airway.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"laryngeal disorder","termid":"MONDO:0004382"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"laryngostenosis","secondary_identifiers":["ICD9:478.74","ICD10CM:J38.6","MESH:D007829","DOID:11527","SCTID:75547007","MEDGEN:7274","UMLS:C0023075","HP:0001602"],"synonyms":[{"name":"stenosis of larynx","type":"exact"}],"termid":"MONDO:0001305","xrefs":{"Monarch":{"xref_id":"0001305"}}}


id: PBO:0045544
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dihydrouridine synthase 4 like","termid":"PBO:0045544"}


id: MONDO:0005403
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete neonatal systemic lupus erthematosus (obsolete MONDO:0005403)","termid":"MONDO:0005403","xrefs":{"Monarch":{"xref_id":"0005403"}}}


id: PBO:0018104
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"name description Alpha Amylase Homolog","termid":"PBO:0018104"}


id: GO:0097314
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The aggregation, arrangement and bonding together of the apoptosome, a multisubunit protein complex involved in the signaling phase of the apoptotic process.","definition_xrefs":["GOC:mtg_apoptosis"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein-containing complex assembly","termid":"GO:0065003"},{"relation_name":"part_of","term_name":"apoptotic signaling pathway","termid":"GO:0097190"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0065003"},{"rel_name":"part_of","termid":"GO:0044085"},{"rel_name":"part_of","termid":"GO:0023052"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0023052","GO:0065003","GO:0008150","GO:0044085"],"is_obsolete":false,"name":"apoptosome assembly","synonyms":[{"name":"apoptosome formation","type":"exact"}],"termid":"GO:0097314"}


id: PATO:0000294
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000294 process value (obsolete PATO:0000294)","termid":"PATO:0000294"}


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


id: MONDO:0011988
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A primary immunodeficiency characterized by neutrophilia with severe neutrophil dysfunction, leukocytosis, a predisposition to bacterial infections and poor wound healing, including an absence of pus in infected areas.","definition_xrefs":["Orphanet:183707"],"direct_ancestors":[{"relation_name":"is_a","term_name":"functional neutrophil defect","termid":"MONDO:0015978"},{"relation_name":"is_a","term_name":"T-B- severe combined immunodeficiency","termid":"MONDO:0017855"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0005046"],"is_obsolete":false,"name":"neutrophil immunodeficiency syndrome","secondary_identifiers":["icd11.foundation:1459690929","DOID:0112064","GARD:17087","MESH:C564275","OMIM:608203","MEDGEN:374920","SCTID:723443003","UMLS:C1842398"],"synonyms":[{"name":"immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis","type":"exact"},{"name":"neutrophil immunodeficiency syndrome","type":"exact"}],"termid":"MONDO:0011988","xrefs":{"Monarch":{"xref_id":"0011988"}}}


id: PBO:0109010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"G protein-coupled receptor 143 Y-linked pseudogene","termid":"PBO:0109010"}


id: PR:O43089
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cbp6 gene.","definition_xrefs":["PRO:DNx","UniProtKB:O43089"],"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":"cytochrome B pre-mRNA-processing protein 6 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC947.14c","synonyms":[{"name":"Spom972h-cbp6","type":"exact"}],"termid":"PR:O43089"}


id: PR:Q9USR2
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A U4/U6.U5 tri-snRNP-associated protein 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PANTHER:PTHR24006:SF31","PRO:DNx","OMA:SCHPO02581"],"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":"mRNA-splicing protein ubp10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC577.07","secondary_identifiers":["UniProtKB:Q9USR2"],"synonyms":[{"name":"Spom972h-USP39","type":"exact"},{"name":"inactive ubiquitin-specific-processing protease 10 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9USR2"}


id: PBO:0088398
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sorting nexin Snx3","termid":"PBO:0088398"}


id: PBO:0052322
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KIAA1328","termid":"PBO:0052322"}


id: PBO:0055615
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 3054","termid":"PBO:0055615"}


id: GO:0048087
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the frequency, rate or extent of the developmental process that results in the deposition of coloring matter in an organism.","definition_xrefs":["GOC:tb","GOC:dph","GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of developmental pigmentation","termid":"GO:0048070"},{"relation_name":"is_a","term_name":"positive regulation of biological process","termid":"GO:0048518"},{"relation_name":"positively_regulates","term_name":"developmental pigmentation","termid":"GO:0048066"}],"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 developmental pigmentation","synonyms":[{"name":"activation of developmental pigmentation","type":"narrow"},{"name":"stimulation of developmental pigmentation","type":"narrow"},{"name":"up regulation of developmental pigmentation","type":"exact"},{"name":"up-regulation of developmental pigmentation","type":"exact"},{"name":"upregulation of developmental pigmentation","type":"exact"}],"termid":"GO:0048087"}


id: FYPO:0000471
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 mating type switching is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating type switching","termid":"FYPO:0000468"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000293"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0000293","FYPO:0001985","FYPO:0005447"],"is_obsolete":false,"name":"increased mating type switching","synonyms":[{"name":"increased mating type switching during mitotic cell cycle","type":"related"},{"name":"increased mating type switching during vegetative growth","type":"exact"},{"name":"mating type switching: increased","type":"related"}],"termid":"FYPO:0000471"}


id: PATO:0000524
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000524 plant growth hormone sensitivity value (obsolete PATO:0000524)","termid":"PATO:0000524"}


id: MONDO:0016328
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy (obsolete MONDO:0016328)","secondary_identifiers":["Orphanet:217591"],"termid":"MONDO:0016328","xrefs":{"Monarch":{"xref_id":"0016328"}}}


id: MONDO:0002719
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neoplasm (disease) that involves the conus medullaris.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spinal cord cancer","termid":"MONDO:0003544"},{"relation_name":"is_a","term_name":"spinal cord neoplasm","termid":"MONDO:0021234"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"conus medullaris neoplasm","secondary_identifiers":["UMLS:C1333153","DOID:3641","MEDGEN:232392","NCIT:C5443"],"synonyms":[{"name":"conus medullaris neoplasm","type":"exact"},{"name":"conus medullaris neoplasm (disease)","type":"exact"},{"name":"conus medullaris tumor","type":"exact"},{"name":"conus medullaris tumour","type":"exact"},{"name":"neoplasm of conus medullaris","type":"exact"},{"name":"neoplasm of the conus medullaris","type":"exact"},{"name":"tumor of conus medullaris","type":"exact"},{"name":"tumor of the conus medullaris","type":"exact"},{"name":"tumour of conus medullaris","type":"exact"},{"name":"tumour of the conus medullaris","type":"exact"}],"termid":"MONDO:0002719","xrefs":{"Monarch":{"xref_id":"0002719"}}}


id: PBO:0040349
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ATP synthase membrane subunit f pseudogene 6","termid":"PBO:0040349"}


id: MONDO:0858998
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"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":"mesomelic dysplasia-digital anomalies-intellectual disability syndrome","secondary_identifiers":["UMLS:C5816803","MEDGEN:1843408","Orphanet:632603"],"termid":"MONDO:0858998","xrefs":{"Monarch":{"xref_id":"0858998"}}}


id: MONDO:0032777
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"generalized epilepsy with febrile seizures plus","termid":"MONDO:0018214"}],"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":"generalized epilepsy with febrile seizures plus, type 10","secondary_identifiers":["GARD:18671","MEDGEN:1676426","OMIM:618482","DOID:0111296","UMLS:C5193120"],"synonyms":[{"name":"GEFSP10","type":"related"},{"name":"GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 10","type":"related"},{"name":"Gefs+, Type 10","type":"related"}],"termid":"MONDO:0032777","xrefs":{"Monarch":{"xref_id":"0032777"}}}


id: MONDO:0006748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"OBSOLETE. A variant of epilepsy characterized by continuous focal jerking of a body part over a period of hours, days, or even years without spreading to other body regions. Contractions may be aggravated by movement and are reduced, but not abolished during sleep. electroencephalography demonstrates epileptiform (spike and wave) discharges over the hemisphere opposite to the affected limb in most instances. The repetitive movements may originate from the cerebral cortex or from subcortical structures (e.g., brain stem; basal ganglia). This condition is associated with Russian Spring and Summer encephalitis; Rasmussen syndrome; multiple sclerosis; diabetes mellitus; brain neoplasms; and cerebrovascular disorders.","definition_xrefs":["MESH:D017036","PMID:7681771","PMID:8800935"],"gene_count":0,"genotype_count":0,"name":"obsolete epilepsia partialis continua (obsolete MONDO:0006748)","secondary_identifiers":["icd11.foundation:669338526","ICD9:345.70","MedDRA:10015034","EFO:1000924","ICD9:345.7","SCTID:241006","DOID:11349"],"termid":"MONDO:0006748","xrefs":{"Monarch":{"xref_id":"0006748"}}}


id: FYPO:0006713
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 malonyl-CoA measured in a cell is higher than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased level of substance in cell during vegetative growth","termid":"FYPO:0001330"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"increased cellular malonyl-CoA level","synonyms":[{"name":"increased cellular malonyl-CoA level during mitotic cell cycle","type":"related"},{"name":"increased cellular malonyl-CoA level during vegetative growth","type":"exact"},{"name":"increased malonyl-CoA accumulation","type":"related"}],"termid":"FYPO:0006713"}


id: GO:0032784
data:
  {"annotated_genes":["SJAG_01707","SJAG_02057","SJAG_00150","SJAG_03967","SJAG_01151","SJAG_01213","SJAG_01149","SJAG_03118","SJAG_03061"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[119937],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034244"},{"annotations":[72152,81695],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032786"},{"annotations":[81431,118999,65907,73393,72983,80073],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032968"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of transcription elongation, the extension of an RNA molecule after transcription initiation and promoter clearance by the addition of ribonucleotides catalyzed by a DNA-dependent RNA polymerase.","definition_xrefs":["GOC:txnOH","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of DNA-templated transcription","termid":"GO:0006355"},{"relation_name":"regulates","term_name":"DNA-templated transcription elongation","termid":"GO:0006354"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00150":null,"SJAG_01149":null,"SJAG_01151":null,"SJAG_01213":null,"SJAG_01707":null,"SJAG_02057":null,"SJAG_03061":null,"SJAG_03118":null,"SJAG_03967":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006351"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006355"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467","GO:0006351","GO:0006355"],"is_obsolete":false,"name":"regulation of DNA-templated transcription elongation","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null,"GO_REF:0000117":null},"synonyms":[{"name":"regulation of DNA-dependent transcription, elongation","type":"exact"},{"name":"regulation of DNA-templated transcription, elongation","type":"exact"},{"name":"regulation of RNA elongation","type":"broad"},{"name":"regulation of transcription elongation, DNA-dependent","type":"exact"},{"name":"regulation of transcriptional elongation","type":"broad"},{"name":"transcription elongation regulator activity","type":"related"}],"termid":"GO:0032784","terms_by_termid":{"GO:0032786":null,"GO:0032968":null,"GO:0034244":null}}


id: GO:0070915
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Combining with the phospholipid derivative lysophosphatidic acid, and transmitting the signal across the membrane by activating an associated G-protein.","definition_xrefs":["PMID:15755723","GOC:bf","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bioactive lipid receptor activity","termid":"GO:0045125"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0038023"}],"interesting_parent_ids":["GO:0003674","GO:0038023"],"is_obsolete":false,"name":"lysophosphatidic acid receptor activity","synonyms":[{"name":"LPA receptor activity","type":"exact"}],"termid":"GO:0070915"}


id: PBO:0085263
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Permease of basic amino acids in the vacuolar membrane","termid":"PBO:0085263"}


id: PBO:0066852
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RN7SK pseudogene 152","termid":"PBO:0066852"}


id: GO:0097596
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A partial left-handed spiral array of microtubules that lies generally dorsal to the main ventral disc microtubule array in Giardia species (trophozoite stage).","definition_xrefs":["GOC:giardia","ISBN:9780124260207"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cellular anatomical structure","termid":"GO:0110165"},{"relation_name":"part_of","term_name":"ventral disc","termid":"GO:0097597"}],"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":"ventral disc supernumerary microtubule array","synonyms":[{"name":"supernumerary microtubule array","type":"broad"},{"name":"ventral disk supernumerary microtubule array","type":"related"}],"termid":"GO:0097596"}


id: GO:1903777
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to melibiose.","definition_xrefs":["PMID:11471732","GOC:mr","GOC:TermGenie","GO_REF:0000067"],"direct_ancestors":[{"relation_name":"is_a","term_name":"disaccharide binding","termid":"GO:0048030"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"melibiose binding","termid":"GO:1903777"}


id: MONDO:0001144
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"paralytic strabismus","termid":"MONDO:0001143"},{"relation_name":"is_a","term_name":"oculomotor nerve paralysis","termid":"MONDO:0001309"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"partial third-nerve palsy","secondary_identifiers":["ICD9:378.51","DOID:10864","MEDGEN:75745","SCTID:194118007","UMLS:C0271370"],"synonyms":[{"name":"partial third nerve palsy","type":"exact"},{"name":"third nerve palsy with pupil sparing","type":"exact"},{"name":"third or oculomotor nerve palsy, partial","type":"exact"}],"termid":"MONDO:0001144","xrefs":{"Monarch":{"xref_id":"0001144"}}}


id: PBO:0108954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TMEM69 pseudogene 2","termid":"PBO:0108954"}


id: MONDO:0018434
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"acute myeloid leukemia","termid":"MONDO:0018874"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0005570","MONDO:0004992","MONDO:0005046"],"is_obsolete":false,"name":"acute myeloid leukemia with t(9;11)(p22;q23)","secondary_identifiers":["MEDGEN:753997","Orphanet:402017","UMLS:C2919692","GARD:21711"],"synonyms":[{"name":"AML with t(9;11)(p22;q23)","type":"exact"}],"termid":"MONDO:0018434","xrefs":{"Monarch":{"xref_id":"0018434"}}}


id: PBO:0059674
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-CO1 pseudogene 40","termid":"PBO:0059674"}


id: GO:0031323
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that modulates the frequency, rate or extent of the chemical reactions and pathways by which individual cells transform chemical substances.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete regulation of cellular metabolic process (obsolete GO:0031323)","synonyms":[{"name":"regulation of cellular metabolism","type":"exact"}],"termid":"GO:0031323"}


id: MONDO:0016730
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, slow growing neuroepithelial neoplasm composed of neoplastic, mature ganglion cells.","definition_xrefs":["NCIT:C6934"],"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":"gangliocytoma","secondary_identifiers":["MESH:D005729","NANDO:2200097","ONCOTREE:GNC","GARD:10638","UMLS:C5779630","MEDGEN:1830324","SCTID:116371000119107","ICDO:9492/0","DOID:2426","Orphanet:251937"],"synonyms":[{"name":"GNC","type":"related"}],"termid":"MONDO:0016730","xrefs":{"Monarch":{"xref_id":"0016730"}}}


id: GO:0048038
data:
  {"annotated_genes":["SJAG_04223","SJAG_03198","SJAG_02398"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[72695],"is_not":false,"summary":null,"term":"GO:0048038"},{"annotations":[117215,78700],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0048039"}]},"cv_name":"molecular_function","definition":"Binding to a quinone, any member of a class of diketones derivable from aromatic compounds by conversion of two CH groups into CO groups with any necessary rearrangement of double bonds.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"small molecule binding","termid":"GO:0036094"}],"gene_count":3,"genes_by_uniquename":{"SJAG_02398":null,"SJAG_03198":null,"SJAG_04223":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005488"}],"interesting_parent_ids":["GO:0003674","GO:0005488"],"is_obsolete":false,"name":"quinone binding","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"termid":"GO:0048038","terms_by_termid":{"GO:0048038":null,"GO:0048039":null}}


id: MOD:01433
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue into 1-amino-2-propanone.","definition_xrefs":["ChEBI:17906","RESID:AA0486","PubMed:19196969","PubMed:12715872"],"direct_ancestors":[{"relation_name":"is_a","term_name":"dehydrogenated residue","termid":"MOD:00683"},{"relation_name":"is_a","term_name":"modified L-threonine residue","termid":"MOD:00917"},{"relation_name":"is_a","term_name":"decarboxylated residue","termid":"MOD:00960"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"1-amino-2-propanone","synonyms":[{"name":"1-amino-2-propanone","type":"exact"},{"name":"1-aminopropan-2-one","type":"exact"},{"name":"1-aminopropanone","type":"exact"},{"name":"MOD_RES 1-amino-2-propanone","type":"exact"},{"name":"aminoacetone","type":"exact"}],"termid":"MOD:01433"}


id: PBO:0046037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eukaryotic translation initiation factor 2 subunit 2 beta pseudogene 5","termid":"PBO:0046037"}


id: PBO:0038801
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ADAM metallopeptidase domain 7","termid":"PBO:0038801"}


id: PBO:0108548
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"clathrin adaptor End4","termid":"PBO:0108548"}


id: PBO:0018220
data:
  {"annotation_feature_type":"gene","cv_name":"feature_relationshipprop_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"expression","termid":"PBO:0018220"}


id: PBO:0075940
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SH3 and cysteine rich domain 3","termid":"PBO:0075940"}


id: PATO:0000659
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000659 temparature_quantity (obsolete PATO:0000659)","termid":"PATO:0000659"}


id: PBO:0050806
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HTT antisense RNA","termid":"PBO:0050806"}


id: MONDO:0007258
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"canine teeth, absence of upper permanent","secondary_identifiers":["UMLS:C1861899","OMIM:114600","MEDGEN:396244"],"synonyms":[{"name":"canine teeth, absence of upper permanent","type":"exact"}],"termid":"MONDO:0007258","xrefs":{"Monarch":{"xref_id":"0007258"}}}


id: PBO:0050729
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 15","termid":"PBO:0050729"}


id: FYECO:0000192
data:
  {"annotation_feature_type":"gene","cv_name":"fission_yeast_phenotype_condition","definition":"Biotin was completely excluded from the experimental medium/buffer.","definition_xrefs":["PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"grouping absent","termid":"FYECO:0000120"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"biotin absent","termid":"FYECO:0000192"}


id: MONDO:0006009
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Encephalitis resulting from viral infection.","definition_xrefs":["NCIT:C35302"],"direct_ancestors":[{"relation_name":"is_a","term_name":"infectious encephalitis","termid":"MONDO:0020067"},{"relation_name":"is_a","term_name":"viral infection of central nervous system","termid":"MONDO:0024318"},{"relation_name":"is_a","term_name":"primary viral infectious disease","termid":"MONDO:0100329"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"viral encephalitis","secondary_identifiers":["UMLS:C0243010","MEDGEN:116719","EFO:0007538","MedDRA:10058805","Orphanet:98252","SCTID:34476008","GARD:19433","DOID:646"],"synonyms":[{"name":"Viruses caused encephalitis","type":"exact"},{"name":"Viruses encephalitis","type":"exact"},{"name":"viral encephalitis","type":"exact"}],"termid":"MONDO:0006009","xrefs":{"Monarch":{"xref_id":"0006009"}}}


id: PBO:0054464
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 1863","termid":"PBO:0054464"}


id: PBO:0109088
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sperm microtubule inner protein 2","termid":"PBO:0109088"}


id: MONDO:0021510
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A benign neoplasm that involves the prostate gland.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"benign male reproductive system neoplasm","termid":"MONDO:0000625"},{"relation_name":"is_a","term_name":"prostate neoplasm","termid":"MONDO:0021259"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"benign neoplasm of prostate","secondary_identifiers":["MEDGEN:57577","NCIT:C3613","SCTID:92308005","UMLS:C0154009","ICD10CM:D29.1","icd11.foundation:1144614287","ICD9:222.2"],"synonyms":[{"name":"benign neoplasm of the prostate","type":"exact"},{"name":"benign prostate neoplasm","type":"exact"},{"name":"benign prostate tumor","type":"exact"},{"name":"benign prostate tumour","type":"exact"},{"name":"benign prostatic neoplasm","type":"exact"},{"name":"benign tumor of prostate","type":"exact"},{"name":"benign tumor of the prostate","type":"exact"},{"name":"benign tumour of prostate","type":"exact"},{"name":"benign tumour of the prostate","type":"exact"},{"name":"prostate gland benign neoplasm","type":"exact"}],"termid":"MONDO:0021510","xrefs":{"Monarch":{"xref_id":"0021510"}}}


id: MONDO:0021329
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A carcinoma that arises from the soft palate. The majority are squamous cell carcinomas.","definition_xrefs":["NCIT:C8395"],"direct_ancestors":[{"relation_name":"is_a","term_name":"soft palate cancer","termid":"MONDO:0004611"},{"relation_name":"is_a","term_name":"oral cavity carcinoma","termid":"MONDO:0044925"},{"relation_name":"is_a","term_name":"oropharyngeal carcinoma","termid":"MONDO:0044926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992","MONDO:0004335"],"is_obsolete":false,"name":"carcinoma of soft palate","secondary_identifiers":["MEDGEN:87505","SCTID:254435009","UMLS:C0345555"],"synonyms":[{"name":"carcinoma of soft palate","type":"exact"},{"name":"carcinoma of the soft palate","type":"exact"},{"name":"soft palate cancer","type":"broad"},{"name":"soft palate carcinoma","type":"exact"}],"termid":"MONDO:0021329","xrefs":{"Monarch":{"xref_id":"0021329"}}}


id: MONDO:1011213
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Coloboma that occurs in chicken.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bird disease","termid":"MONDO:0024905"},{"relation_name":"is_a","term_name":"coloboma, non-human animal","termid":"MONDO:1010319"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"coloboma, chicken","secondary_identifiers":["OMIA:000219-9031"],"termid":"MONDO:1011213","xrefs":{"Monarch":{"xref_id":"1011213"}}}


id: GO:0034309
data:
  {"annotated_genes":["SJAG_03362","SJAG_03538","SJAG_02406","SJAG_04866","SJAG_01970","SJAG_04067","SJAG_00827","SJAG_00381","SJAG_02421","SJAG_04282","SJAG_02420"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[90984,115680],"is_not":false,"rel_names":["regulates","positively_regulates"],"summary":null,"term":"GO:0090180"},{"annotations":[75821,62377,75879,78897,80331,71956],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009228"},{"annotations":[112435,112436,101478],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0036172"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of primary alcohols. A primary alcohol is any alcohol in which a hydroxy group, -OH, is attached to a saturated carbon atom which has either three hydrogen atoms attached to it or only one other carbon atom and two hydrogen atoms attached to it.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary alcohol metabolic process","termid":"GO:0034308"},{"relation_name":"is_a","term_name":"alcohol biosynthetic process","termid":"GO:0046165"}],"gene_count":11,"genes_by_uniquename":{"SJAG_00381":null,"SJAG_00827":null,"SJAG_01970":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:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281"],"is_obsolete":false,"name":"primary alcohol biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"monohydric alcohol biosynthetic process","type":"exact"},{"name":"primary alcohol anabolism","type":"exact"},{"name":"primary alcohol biosynthesis","type":"exact"},{"name":"primary alcohol formation","type":"exact"},{"name":"primary alcohol synthesis","type":"exact"}],"termid":"GO:0034309","terms_by_termid":{"GO:0009228":null,"GO:0036172":null,"GO:0090180":null}}


id: MONDO:0002527
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A dome-shaped, rapidly growing skin lesion composed of well differentiated squamous cells. It represents a proliferation of the infundibular epithelium of the hair follicle and its morphologic distinction from a well differentiated carcinoma may be difficult or impossible. Keratoacanthomas affect males more frequently than females and the majority tend to regress spontaneously. It has been suggested that keratoacanthoma represents a distinct subtype of squamous cell carcinoma of the skin.","definition_xrefs":["NCIT:C3146"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"skin squamous cell carcinoma","termid":"MONDO:0002529"},{"relation_name":"is_a","term_name":"epithelial skin neoplasm","termid":"MONDO:0021634"}],"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":"keratoacanthoma","secondary_identifiers":["DOID:3149","SCTID:254662007","icd11.foundation:516478127","UMLS:C0022572","MESH:D007636","ICDO:8071/1","MEDGEN:5954"],"termid":"MONDO:0002527","xrefs":{"Monarch":{"xref_id":"0002527"}}}


id: GO:0032198
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process involved in the transposition of miniature inverted-repeat transposable elements (MITEs).","definition_xrefs":["GOC:jp","ISBN:1555812090"],"gene_count":0,"genotype_count":0,"name":"obsolete MITE transposition (obsolete GO:0032198)","termid":"GO:0032198"}


id: PBO:0058394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 4766","termid":"PBO:0058394"}


id: MONDO:0016594
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Superficial siderosis is a rare neurologic disease characterized by progressive sensorineural hearing loss, cerebellar ataxia, pyramidal signs, and neuroimaging findings revealing hemosiderin deposits in the spinal and cranial leptomeninges and subpial layer. The disease progresses slowly and patients may present with mild cognitive impairment, nystagmus, dysmetria, spasticity, dysdiadochokinesia, dysarthria, hyperreflexia, and Babinski signs. Additional features reported include dementia, urinary incontinence, anosmia, ageusia, and anisocoria.","definition_xrefs":["Orphanet:247245"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"acquired ataxia","termid":"MONDO:0016593"},{"relation_name":"is_a","term_name":"neurodegenerative disease","termid":"MONDO:0005559"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"superficial siderosis","secondary_identifiers":["UMLS:C2938918","MEDGEN:1371500","GARD:9484","NANDO:1200543"],"synonyms":[{"name":"hemosiderosis of the central nervous system","type":"exact"},{"name":"superficial hemosiderosis of the CNS","type":"exact"},{"name":"superficial hemosiderosis of the central nervous system","type":"exact"},{"name":"superficial siderosis of the CNS","type":"exact"},{"name":"superficial siderosis of the central nervous system","type":"exact"}],"termid":"MONDO:0016594","xrefs":{"Monarch":{"xref_id":"0016594"}}}


id: GO:2000846
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of corticosteroid hormone secretion.","definition_xrefs":["GOC:sl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of steroid hormone secretion","termid":"GO:2000831"},{"relation_name":"regulates","term_name":"corticosteroid hormone secretion","termid":"GO:0035930"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0023052"],"is_obsolete":false,"name":"regulation of corticosteroid hormone secretion","synonyms":[{"name":"regulation of corticosteroid secretion","type":"related"}],"termid":"GO:2000846"}


id: MONDO:0000099
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete trichoepithelioma, multiple familial (obsolete MONDO:0000099)","termid":"MONDO:0000099","xrefs":{"Monarch":{"xref_id":"0000099"}}}


id: PBO:0054094
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 1447","termid":"PBO:0054094"}


id: PBO:0081255
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 25","termid":"PBO:0081255"}


id: GO:0006940
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of smooth muscle contraction.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of muscle contraction","termid":"GO:0006937"},{"relation_name":"regulates","term_name":"smooth muscle contraction","termid":"GO:0006939"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of smooth muscle contraction","termid":"GO:0006940"}


id: GO:0110110
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of animal organ morphogenesis.","definition_xrefs":["GOC:kmv"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of developmental process","termid":"GO:0051094"},{"relation_name":"is_a","term_name":"positive regulation of multicellular organismal process","termid":"GO:0051240"},{"relation_name":"is_a","term_name":"regulation of animal organ morphogenesis","termid":"GO:2000027"},{"relation_name":"positively_regulates","term_name":"animal organ morphogenesis","termid":"GO:0009887"}],"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 animal organ morphogenesis","termid":"GO:0110110"}


id: MONDO:0018790
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete COL4A1 or COL4A2-related cerebral small vessel disease with hemorrhagic tendency (obsolete MONDO:0018790)","secondary_identifiers":["Orphanet:477765"],"synonyms":[{"name":"COL4A1 or COL4A2-related cerebral angiopathy with hemorrhagic tendency","type":"exact"}],"termid":"MONDO:0018790","xrefs":{"Monarch":{"xref_id":"0018790"}}}


id: PBO:0002098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIIB","termid":"PBO:0002098"}


id: PBO:0030021
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_asymmetric_protein_localization_to_old_or_new_mitotic_spindle_pole_body_during_anaphase,_with_protein_symmetrically_localized_to_both_spindle_pole_bodies","termid":"PBO:0030021"}


id: GO:0034634
data:
  {"annotated_genes":["SJAG_01660","SJAG_03577"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[97477,115129],"is_not":false,"summary":null,"term":"GO:0034634"}]},"cv_name":"molecular_function","definition":"Enables the transfer of glutathione, the tripeptide glutamylcysteinylglycine, from one side of a membrane to the other.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"organic anion transmembrane transporter activity","termid":"GO:0008514"},{"relation_name":"is_a","term_name":"tripeptide transmembrane transporter activity","termid":"GO:0042937"},{"relation_name":"is_a","term_name":"modified amino acid transmembrane transporter activity","termid":"GO:0072349"},{"relation_name":"is_a","term_name":"sulfur compound transmembrane transporter activity","termid":"GO:1901682"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01660":null,"SJAG_03577":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"}],"interesting_parent_ids":["GO:0005215","GO:0022857","GO:0003674"],"is_obsolete":false,"name":"glutathione transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0034634","terms_by_termid":{"GO:0034634":null}}


id: MONDO:0019963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neuroendocrine neoplasm that involves the bronchus.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bronchial neoplasm","termid":"MONDO:0002807"},{"relation_name":"is_a","term_name":"neuroendocrine neoplasm","termid":"MONDO:0019496"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"bronchial endocrine tumor","secondary_identifiers":["GARD:19360","Orphanet:97287"],"synonyms":[{"name":"bronchial NET","type":"exact"},{"name":"bronchial neuroendocrine tumor","type":"related"},{"name":"bronchial neuroendocrine tumour","type":"related"},{"name":"bronchus NET","type":"exact"},{"name":"bronchus neuroendocrine neoplasm","type":"exact"},{"name":"bronchus neuroendocrine tumor","type":"exact"},{"name":"bronchus neuroendocrine tumor, well differentiated, low or intermediate grade","type":"exact"},{"name":"bronchus neuroendocrine tumour","type":"exact"},{"name":"neuroendocrine neoplasm of bronchus","type":"exact"}],"termid":"MONDO:0019963","xrefs":{"Monarch":{"xref_id":"0019963"}}}


id: MONDO:0016612
data:
  {"annotated_genes":["SJAG_02457","SJAG_01400"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87533],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010547"},{"annotations":[87664],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010524"}]},"cv_name":"mondo","definition":"X-linked form of cerebellar ataxia.","definition_xrefs":["MONDO:patterns/x_linked"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked disease","termid":"MONDO:0000425"},{"relation_name":"is_a","term_name":"hereditary cerebellar ataxia","termid":"MONDO:0100310"}],"gene_count":2,"genes_by_uniquename":{"SJAG_01400":null,"SJAG_02457":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"X-linked cerebellar ataxia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["DOID:0111828","DOID:0050953","GARD:20665","Orphanet:247765"],"synonyms":[{"name":"X-linked hereditary ataxia","type":"exact"},{"name":"cerebellar ataxia, X-linked","type":"exact"},{"name":"hereditary ataxia, X-linked","type":"exact"}],"termid":"MONDO:0016612","terms_by_termid":{"MONDO:0010524":null,"MONDO:0010547":null},"xrefs":{"Monarch":{"xref_id":"0016612"}}}


id: FYPO:0007997
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A physical cellular phenotype observed in the vegetative growth phase of the life cycle in which actin cortical patches are localized to only the new end of a cell following cell division.","definition_xrefs":["PomBase:mlr","PMID:15184402"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monopolar actin cortical patch localization during vegetative growth","termid":"FYPO:0001019"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0000138"},{"rel_name":"output_of","termid":"FYPO:0004803"},{"rel_name":"output_of","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0004803","FYPO:0000138","FYPO:0005447","FYPO:0001320","FYPO:0000002"],"is_obsolete":false,"name":"monopolar actin cortical patch localization to new end","termid":"FYPO:0007997"}


id: PBO:0040132
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ASB16 antisense RNA 1","termid":"PBO:0040132"}


id: PBO:0002052
data:
  {"annotation_feature_type":"gene","cv_name":"complementation","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"functionally complemented by human HSET","termid":"PBO:0002052"}


id: PBO:0013029
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splicing factor Cwf16","termid":"PBO:0013029"}


id: GO:0015491
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Enables the transfer of a solute or solutes from one side of a membrane to the other according to the reaction: cation A(out) + cation B(in) = cation A(in) + cation B(out).","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete cation:cation antiporter activity (obsolete GO:0015491)","termid":"GO:0015491"}


id: PBO:0054084
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 1435","termid":"PBO:0054084"}


id: PBO:0042134
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cholecystokinin","termid":"PBO:0042134"}


id: MONDO:0012448
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the ZFYVE27 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"hereditary spastic paraplegia 33","secondary_identifiers":["MESH:C565214","MEDGEN:339943","OMIM:610244","DOID:0110784","UMLS:C1853251"],"synonyms":[{"name":"SPG33","type":"exact"},{"name":"ZFYVE27 hereditary spastic paraplegia","type":"exact"},{"name":"autosomal dominant spastic paraplegia 33","type":"exact"},{"name":"hereditary spastic paraplegia caused by mutation in ZFYVE27","type":"exact"},{"name":"hereditary spastic paraplegia type 33","type":"exact"},{"name":"spastic paraplegia 33, autosomal dominant","type":"related"}],"termid":"MONDO:0012448","xrefs":{"Monarch":{"xref_id":"0012448"}}}


id: PR:P87050
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- cdr2 gene.","definition_xrefs":["UniProtKB:P87050","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":"mitosis inducer protein kinase cdr2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC57A10.02","synonyms":[{"name":"Spom972h-cdr2","type":"exact"}],"termid":"PR:P87050"}


id: PBO:0034631
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-increased_rRNA_level","termid":"PBO:0034631"}


id: PATO:0000834
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000834 relative visual threshold value (obsolete PATO:0000834)","termid":"PATO:0000834"}


id: MONDO:0007341
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cleidorhizomelic syndrome is a rhizo-mesomelic dysplasia characterized by rhizomelic short stature/dwarfism in combination with lateral clavicular defects. Additional manifestations include brachydactyly with bilateral clinodactyly and hypoplastic middle phalanx of the fifth digit. X-ray demonstrated an apparent Y-shaped or bifid distal clavicle. Cleidorhizomelic syndrome has been reported in one family (mother and son) and is suspected to be transmitted in an autosomal dominant manner. There have been no further descriptions in the literature since 1988.","definition_xrefs":["Orphanet:1453"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cleidorhizomelic syndrome","secondary_identifiers":["MEDGEN:350042","OMIM:119650","GARD:5532","MESH:C536428","SCTID:719471002","UMLS:C1861515"],"synonyms":[{"name":"Wallis Zieff Goldblatt syndrome","type":"related"},{"name":"Wallis-Zieff-Goldblatt syndrome","type":"exact"},{"name":"brachydactyly, enlarged diaphysis, rhizomelic micromelia, short stature and abnormal clavicle","type":"related"},{"name":"cleido rhizomelic syndrome","type":"related"},{"name":"cleidorhizomelic syndrome","type":"exact"},{"name":"rhizomelic shortness with clavicular defect","type":"exact"}],"termid":"MONDO:0007341","xrefs":{"Monarch":{"xref_id":"0007341"}}}


id: PBO:0029094
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-resistance_to_quinidine","termid":"PBO:0029094"}


id: GO:0090325
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of the self-propelled movement of a cell or organism from one location to another in a behavioral context; the aspect of locomotory behavior having to do with movement.","definition_xrefs":["GOC:dph","GOC:kmv","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of locomotion","termid":"GO:0040012"},{"relation_name":"is_a","term_name":"regulation of behavior","termid":"GO:0050795"},{"relation_name":"regulates","term_name":"locomotion involved in locomotory behavior","termid":"GO:0031987"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of locomotion involved in locomotory behavior","termid":"GO:0090325"}


id: GO:0102696
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + cis-zeatin = H+ + 9-(alpha-D-glucosyl)-cis-zeatin + UDP.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete cis-zeatin UDP glycosyltransferase activity (obsolete GO:0102696)","termid":"GO:0102696"}


id: PBO:0029110
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_mitotic_cell_cycle_process","termid":"PBO:0029110"}


id: PR:O74977
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- vms1 gene.","definition_xrefs":["UniProtKB:O74977","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":"VMS1 homolog C1827.04 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1827.04","synonyms":[{"name":"Spom972h-vms1","type":"exact"}],"termid":"PR:O74977"}


id: PBO:0083848
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Exosome non-catalytic core component; involved in 3'-5' RNA processing and degradation in both the nucleus and the cytoplasm; has similarity to E. coli RNase PH and to human hRrp42p (EXOSC7)","termid":"PBO:0083848"}


id: GO:0043301
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the rate of leukocyte degranulation.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of immune effector process","termid":"GO:0002698"},{"relation_name":"is_a","term_name":"regulation of leukocyte degranulation","termid":"GO:0043300"},{"relation_name":"is_a","term_name":"negative regulation of regulated secretory pathway","termid":"GO:1903306"},{"relation_name":"negatively_regulates","term_name":"leukocyte degranulation","termid":"GO:0043299"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"},{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"negatively_regulates","termid":"GO:0016192"},{"rel_name":"negatively_regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0016192","GO:0008150","GO:0006810"],"is_obsolete":false,"name":"negative regulation of leukocyte degranulation","synonyms":[{"name":"down regulation of leukocyte degranulation","type":"exact"},{"name":"down-regulation of leukocyte degranulation","type":"exact"},{"name":"downregulation of leukocyte degranulation","type":"exact"},{"name":"inhibition of leukocyte degranulation","type":"narrow"},{"name":"negative regulation of immune cell degranulation","type":"exact"},{"name":"negative regulation of leucocyte degranulation","type":"exact"}],"termid":"GO:0043301"}


id: MONDO:0004361
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An ependymoma of the spinal cord occurring in adults.","definition_xrefs":["NCIT:C27399"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spinal cord ependymoma","termid":"MONDO:0003473"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"adult spinal cord ependymoma","secondary_identifiers":["DOID:7788","UMLS:C1332215","MEDGEN:231359"],"synonyms":[{"name":"adult spinal cord ependymoma","type":"exact"},{"name":"spinal cord ependymoma","type":"broad"},{"name":"spinal cord ependymoma of adults","type":"exact"}],"termid":"MONDO:0004361","xrefs":{"Monarch":{"xref_id":"0004361"}}}


id: FYPO:0000573
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which mating projection assembly is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal cellular component organization","termid":"FYPO:0006003"}],"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:0000257","FYPO:0000002"],"is_obsolete":false,"name":"normal shmoo formation","synonyms":[{"name":"normal conjugation tube formation","type":"exact"},{"name":"normal mating projection assembly","type":"exact"},{"name":"normal mating projection formation","type":"exact"},{"name":"normal shmoo assembly","type":"exact"},{"name":"shmoo formation: normal","type":"related"}],"termid":"FYPO:0000573"}


id: PBO:0083757
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Essential evolutionarily-conserved nucleolar protein; component of the box C/D snoRNP complexes that direct 2'-O-methylation of pre-rRNA during its maturation; overexpression causes spindle orientation defects","termid":"PBO:0083757"}


id: GO:0060820
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Compensating for the two-fold variation in X-chromosome: autosome ratios between sexes by a global inactivation of all, or most of, the genes on one of the X-chromosomes in the XX sex by the mechanism of heterochromatin formation.","definition_xrefs":["GOC:sdb_2009","GOC:dph","GOC:tb"],"gene_count":0,"genotype_count":0,"name":"obsolete inactivation of X chromosome by heterochromatin formation (obsolete GO:0060820)","synonyms":[{"name":"inactivation of X chromosome by heterochromatin assembly","type":"exact"}],"termid":"GO:0060820"}


id: PBO:0048966
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glycosylphosphatidylinositol anchor attachment 1 pseudogene 1","termid":"PBO:0048966"}


id: MONDO:0044320
data:
  {"annotated_genes":["SJAG_04334","SJAG_04495"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88636,88637],"is_not":false,"summary":null,"term":"MONDO:0044320"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"retinitis pigmentosa","termid":"MONDO:0019200"}],"gene_count":2,"genes_by_uniquename":{"SJAG_04334":null,"SJAG_04495":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005328"},{"rel_name":"is_a","termid":"MONDO:0005066"}],"interesting_parent_ids":["MONDO:0004736","MONDO:0005328","MONDO:0005066"],"is_obsolete":false,"name":"retinitis pigmentosa 79","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:617460","DOID:0061108","GARD:16231","UMLS:C4479526","MEDGEN:1386200"],"synonyms":[{"name":"RP79","type":"related"},{"name":"retinitis pigmentosa 79","type":"exact"}],"termid":"MONDO:0044320","terms_by_termid":{"MONDO:0044320":null},"xrefs":{"Monarch":{"xref_id":"0044320"}}}


id: PR:P56288
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A translation initiation factor eIF-2B subunit gamma that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02228","PANTHER:PTHR22572:SF8","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":"translation initiation factor eIF-2B subunit gamma (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC4D7.09","secondary_identifiers":["UniProtKB:P56288"],"synonyms":[{"name":"Spom972h-EIF2B3","type":"exact"},{"name":"eIF-2B GDP-GTP exchange factor subunit gamma (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:P56288"}


id: PBO:0072047
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S10 pseudogene 17","termid":"PBO:0072047"}


id: GO:0034876
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: isoniazid + H2O = isonicotinate + hydrazine.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete isonicotinic acid hydrazide hydrolase activity (obsolete GO:0034876)","termid":"GO:0034876"}


id: PBO:0061069
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"NFKB activating protein pseudogene 1","termid":"PBO:0061069"}


id: PBO:0082688
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of the GARP (Golgi-associated retrograde protein) complex; GARP is required for the recycling of proteins from endosomes to the late Golgi, and for mitosis after DNA damage induced checkpoint arrest; required for vacuolar protein sorting; members of the GARP complex are Vps51p-Vps52p-Vps53p-Vps54p; human ortholog is implicated in progressive cerebello-cerebral atrophy type 2 (PCCA2)","termid":"PBO:0082688"}


id: PBO:0109282
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MTX2 pseudogene 1","termid":"PBO:0109282"}


id: FYPO:0002564
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 mature transfer RNA (tRNA) measured in a cell is higher than normal. Total tRNA or a specific tRNA may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered mature tRNA level during vegetative growth","termid":"FYPO:0002579"},{"relation_name":"is_a","term_name":"increased ncRNA level during vegetative growth","termid":"FYPO:0008146"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0001320","FYPO:0000002","FYPO:0001985","FYPO:0006551"],"is_obsolete":false,"name":"increased mature tRNA level during vegetative growth","synonyms":[{"name":"increased mature tRNA accumulation during vegetative growth","type":"related"},{"name":"increased mature tRNA level during mitotic cell cycle","type":"related"},{"name":"increased mature tRNA transcript level during vegetative growth","type":"exact"},{"name":"increased mature transfer RNA level during vegetative growth","type":"exact"},{"name":"increased tRNA level during vegetative growth","type":"broad"}],"termid":"FYPO:0002564"}


id: PBO:0035799
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-complete_but_unequal_mitotic_sister_chromatid_segregation_with_unseparated_chromosomes","termid":"PBO:0035799"}


id: PBO:0057296
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 513a-1","termid":"PBO:0057296"}


id: MONDO:0034092
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"hereditary peripheral neuropathy","termid":"MONDO:0020127"},{"relation_name":"is_a","term_name":"FDXR-related optic atrophy mitochondrial dysfunction syndrome","termid":"MONDO:1060116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005244"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0005244","MONDO:0006025"],"is_obsolete":false,"name":"optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome","secondary_identifiers":["MEDGEN:1807322","GARD:22231","Orphanet:543470","UMLS:C5681321"],"termid":"MONDO:0034092","xrefs":{"Monarch":{"xref_id":"0034092"}}}


id: MOD:01494
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively replaces the N6'-hydrogen atom of a lysine residue with the Applied Biosystems iTRAQ4plex-115 reporter+balance group.","definition_xrefs":["OMSSA:171","Unimod:533#K"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iTRAQ4plex-115 reporter+balance reagent acylated residue","termid":"MOD:01492"},{"relation_name":"is_a","term_name":"iTRAQ4plex reporter+balance reagent N-acylated residue","termid":"MOD:01709"},{"relation_name":"is_a","term_name":"N6-acylated L-lysine","termid":"MOD:01875"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01875"}],"interesting_parent_ids":["MOD:01875"],"is_obsolete":false,"name":"iTRAQ4plex-115 reporter+balance reagent N6-acylated lysine","synonyms":[{"name":"(4-methylpiperazin-1-yl)acetyl","type":"exact"},{"name":"Accurate mass for 115","type":"related"},{"name":"Applied Biosystems iTRAQ(TM) multiplexed quantitation chemistry","type":"related"},{"name":"iTRAQ115","type":"related"},{"name":"iTRAQ115K","type":"exact"},{"name":"iTRAQ4plex115","type":"related"}],"termid":"MOD:01494"}


id: GO:0010201
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 the detection of a continuous far red light stimulus by the high-irradiance response system. Far red light is electromagnetic radiation of wavelength 700-800nm. The activity of the high-irradiance response system is characterized by stronger effects of continuous than pulsed light at equal total fluence.","definition_xrefs":["GOC:sm","GOC:mtg_far_red"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to far red light","termid":"GO:0010218"}],"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 continuous far red light stimulus by the high-irradiance response system","termid":"GO:0010201"}


id: FYPO:0004352
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 nucleus is decreased during a cellular response to methylglyoxal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased protein localization to nucleus during vegetative growth","termid":"FYPO:0001514"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000138"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0001320","FYPO:0005447","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"decreased protein localization to nucleus during cellular response to methylglyoxal","synonyms":[{"name":"decreased protein localisation to nucleus during cellular response to methylglyoxal","type":"exact"},{"name":"decreased protein localization to nucleus during cellular response to methylglyoxal during mitotic cell cycle","type":"related"},{"name":"decreased protein localization to nucleus during cellular response to methylglyoxal during vegetative growth","type":"exact"},{"name":"reduced protein localization to nucleus during cellular response to methylglyoxal","type":"exact"}],"termid":"FYPO:0004352"}


id: PBO:0075212
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"syntrophin beta 2","termid":"PBO:0075212"}


id: PBO:0071712
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L39 pseudogene 10","termid":"PBO:0071712"}


id: GO:0071246
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 chlorate stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to chlorate","termid":"GO:0010157"},{"relation_name":"is_a","term_name":"cellular response to oxygen-containing compound","termid":"GO:1901701"}],"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 chlorate","termid":"GO:0071246"}


id: PBO:0005829
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcription factor TFIID complex subunit Taf13 (predicted)","termid":"PBO:0005829"}


id: PBO:0078224
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 11-2","termid":"PBO:0078224"}


id: PBO:0120959
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"IGF2BP2 pseudogene 1","termid":"PBO:0120959"}


id: FYPO:0004208
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which the observed rate of H3-K4 specific histone methyltransferase activity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal histone methyltransferase activity","termid":"FYPO:0004783"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0000707"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0000661"},{"rel_name":"is_a","termid":"FYPO:0000654"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0000652","FYPO:0001985","FYPO:0000641","FYPO:0000707","FYPO:0000661","FYPO:0000654","FYPO:0005447"],"is_obsolete":false,"name":"abnormal histone methyltransferase activity (H3-K4 specific)","synonyms":[{"name":"abnormal H3-K4 specific histone methyltransferase activity","type":"exact"}],"termid":"FYPO:0004208"}


id: PBO:0075653
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"splA/ryanodine receptor domain and SOCS box containing 2","termid":"PBO:0075653"}


id: GO:1900836
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate or extent of emericellin biosynthetic process.","definition_xrefs":["GOC:di","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of xanthone-containing compound biosynthetic process","termid":"GO:1900185"},{"relation_name":"is_a","term_name":"positive regulation of secondary metabolite biosynthetic process","termid":"GO:1900378"},{"relation_name":"is_a","term_name":"regulation of emericellin biosynthetic process","termid":"GO:1900834"},{"relation_name":"positively_regulates","term_name":"emericellin biosynthetic process","termid":"GO:1900766"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0019748"},{"rel_name":"regulates","termid":"GO:0019748"},{"rel_name":"positively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0044281","GO:0019748","GO:0008150"],"is_obsolete":false,"name":"positive regulation of emericellin biosynthetic process","termid":"GO:1900836"}


id: GO:0009759
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of indole glucosinolates, sulfur-containing compounds that have a common structure linked to an R group derived from tryptophan.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"glucosinolate biosynthetic process","termid":"GO:0019761"},{"relation_name":"is_a","term_name":"indole glucosinolate metabolic process","termid":"GO:0042343"},{"relation_name":"is_a","term_name":"indole-containing compound biosynthetic process","termid":"GO:0042435"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006790"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006790","GO:0044281"],"is_obsolete":false,"name":"indole glucosinolate biosynthetic process","synonyms":[{"name":"indole glucosinolate anabolism","type":"exact"},{"name":"indole glucosinolate biosynthesis","type":"exact"},{"name":"indole glucosinolate formation","type":"exact"},{"name":"indole glucosinolate synthesis","type":"exact"}],"termid":"GO:0009759"}


id: PBO:0065076
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"prickle planar cell polarity protein 3","termid":"PBO:0065076"}


id: FYPO:0003984
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of an amino acid measured in a cell differs from normal when the cell is in the vegetative growth phase of the life cycle.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"altered level of substance in cell during vegetative growth","termid":"FYPO:0001323"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"altered cellular amino acid level during vegetative growth","synonyms":[{"name":"abnormal cellular amino acid level during vegetative growth","type":"exact"},{"name":"altered cellular amino acid level during mitotic cell cycle","type":"related"},{"name":"altered level of amino acid in cell","type":"exact"}],"termid":"FYPO:0003984"}


id: PBO:0068591
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U2 small nuclear 42, pseudogene","termid":"PBO:0068591"}


id: MONDO:0007833
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"iris pigment layer, cleavage of","secondary_identifiers":["OMIM:147610","UMLS:C1840140","MEDGEN:326664"],"synonyms":[{"name":"iris pigment layer, cleavage of","type":"exact"}],"termid":"MONDO:0007833","xrefs":{"Monarch":{"xref_id":"0007833"}}}


id: PBO:0088493
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"membrane trafficking protein, ER to Golgi Psg1","termid":"PBO:0088493"}


id: GO:0007512
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the adult heart over time, from its formation to the mature structure.","definition_xrefs":["GOC:bf"],"direct_ancestors":[{"relation_name":"is_a","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":"adult heart development","synonyms":[{"name":"adult cardiac development","type":"related"}],"termid":"GO:0007512"}


id: MONDO:0700280
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disorder caused by the infection in Lyme disease and manifesting after the original infection.","definition_xrefs":["PMID:36958992","PMID:27407225","MONDO:patterns/post_infectious_disease","PMID:37209716"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-bacterial disorder","termid":"MONDO:0021673"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"post-treatment Lyme disease syndrome","secondary_identifiers":["UMLS:C3890422","NCIT:C119039","MEDGEN:855646"],"synonyms":[{"name":"PLDS","type":"exact"},{"name":"disorder due to consequences of Lyme disease","type":"exact"},{"name":"post-Lyme disease","type":"exact"},{"name":"post-Lyme disease syndrome","type":"exact"},{"name":"post-treatment Lyme disease syndrome","type":"exact"}],"termid":"MONDO:0700280","xrefs":{"Monarch":{"xref_id":"0700280"}}}


id: MONDO:0008520
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Brachydactyly-elbow wrist dysplasia syndrome is a rare, genetic bone development disorder characterized by dysplasia of all the bony components of the elbow joint, abnormally shaped carpal bones, wrist joint radial deviation and brachydactyly. Patients typically present with slight flexion at the elbow joints (with impossibility to perform active extension) and usually associate a limited range of motion of the elbow, wrist and finger articulations. Camptodactyly and syndactyly have also been reported.","definition_xrefs":["Orphanet:1275"],"direct_ancestors":[{"relation_name":"is_a","term_name":"bone development disease","termid":"MONDO:0005497"},{"relation_name":"is_a","term_name":"skeletal dysplasia","termid":"MONDO:0018230"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"brachydactyly-elbow wrist dysplasia syndrome","secondary_identifiers":["GARD:966","MESH:C566090","MEDGEN:396103","SCTID:764437006","UMLS:C1861313","OMIM:186550"],"synonyms":[{"name":"LBNBG","type":"related"},{"name":"LIEBENBERG syndrome","type":"related"},{"name":"Liebenberg syndrome","type":"exact"},{"name":"brachydactyly elbow wrist dysplasia","type":"related"},{"name":"brachydactyly with Joint dysplasia","type":"related"},{"name":"brachydactyly with joint dysplasia","type":"related"},{"name":"brachydactyly-joint dysplasia syndrome","type":"exact"},{"name":"carpal synostosis with dysplastic elbow joints and brachydactyly","type":"related"},{"name":"synostosis, carpal, with dysplastic elbow joints and brachydactyly","type":"related"}],"termid":"MONDO:0008520","xrefs":{"Monarch":{"xref_id":"0008520"}}}


id: PBO:0042659
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"CEA cell adhesion molecule 8","termid":"PBO:0042659"}


id: PBO:0052292
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"KH domain containing 1 like","termid":"PBO:0052292"}


id: GO:0061209
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The multiplication or reproduction of cells, resulting in the expansion of the population in the mesonephros.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cell proliferation involved in kidney development","termid":"GO:0072111"},{"relation_name":"part_of","term_name":"mesonephros development","termid":"GO:0001823"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"cell proliferation involved in mesonephros development","termid":"GO:0061209"}


id: GO:0060197
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The separation of the single opening of the digestive, urinary, and reproductive tracts, the cloaca, into multiple isolated openings during development.","definition_xrefs":["GOC:st","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"tube morphogenesis","termid":"GO:0035239"},{"relation_name":"part_of","term_name":"cloaca development","termid":"GO:0035844"}],"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":"cloacal septation","synonyms":[{"name":"cloaca septation","type":"exact"}],"termid":"GO:0060197"}


id: PBO:0092011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial DNA binding endonuclease (intron encoded)","termid":"PBO:0092011"}


id: GO:0099192
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A synapse formed by a cerebellar Golgi cell synapsing on to a cerebellar granule cell.","definition_xrefs":["PMID:26134650"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synapse","termid":"GO:0045202"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575"],"is_obsolete":false,"name":"cerebellar Golgi cell to granule cell synapse","termid":"GO:0099192"}


id: MONDO:0005555
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Cycloplegia is paralysis of the ciliary muscle of the eye, resulting in a loss of accommodation.","definition_xrefs":["EFO:0005758"],"direct_ancestors":[{"relation_name":"is_a","term_name":"eye accommodation disease","termid":"MONDO:0000926"}],"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":"cycloplegia","secondary_identifiers":["Wikipedia:Cycloplegia","DOID:10033","ICD9:367.51","SCTID:68158006","MEDGEN:536368","UMLS:C0235238","ICD10CM:H52.52"],"synonyms":[{"name":"accommodative paresis","type":"related"},{"name":"ciliary muscle paresis","type":"exact"},{"name":"cycloplegia","type":"exact"},{"name":"cycloplegic paralysis of accommodation","type":"exact"},{"name":"loss of accommodation","type":"related"},{"name":"paralysis of accommodation","type":"related"},{"name":"paresis of accommodation","type":"exact"},{"name":"visual accommodation paralysis","type":"related"}],"termid":"MONDO:0005555","xrefs":{"Monarch":{"xref_id":"0005555"}}}


id: GO:0072710
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 hydroxyurea stimulus.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to nitrogen compound","termid":"GO:1901698"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"response to hydroxyurea","synonyms":[{"name":"response to HU","type":"exact"}],"termid":"GO:0072710"}


id: PBO:0030777
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_growth_on_sodium_dodecyl_sulfate","termid":"PBO:0030777"}


id: GO:0006207
data:
  {"annotated_genes":["SJAG_00694","SJAG_00197","SJAG_00779","SJAG_00444","SJAG_00392","SJAG_05024","SJAG_03164","SJAG_00964"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[58034,71628,71867,73495,73794,75212,75949,89731],"is_not":false,"summary":null,"term":"GO:0006207"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the formation of pyrimidine nucleobases, 1,3-diazine, organic nitrogenous bases, beginning with the synthesis of a pyrimidine ring from simpler precursors.","definition_xrefs":["ISBN:0716720094","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleobase biosynthetic process","termid":"GO:0019856"}],"gene_count":8,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00392":null,"SJAG_00444":null,"SJAG_00694":null,"SJAG_00779":null,"SJAG_00964":null,"SJAG_03164":null,"SJAG_05024":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"'de novo' pyrimidine nucleobase biosynthetic process","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"'de novo' pyrimidine base anabolism","type":"exact"},{"name":"'de novo' pyrimidine base biosynthesis","type":"exact"},{"name":"'de novo' pyrimidine base biosynthetic process","type":"exact"},{"name":"'de novo' pyrimidine base formation","type":"exact"},{"name":"'de novo' pyrimidine base synthesis","type":"exact"}],"termid":"GO:0006207","terms_by_termid":{"GO:0006207":null}}


id: PBO:0065982
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"retinoic acid early transcript 1F pseudogene","termid":"PBO:0065982"}


id: PBO:0055287
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 2714","termid":"PBO:0055287"}


id: FYPO:0006014
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which one cell forms multiple mating projections that engage multiple partner cells.","definition_xrefs":["PMID:28410370","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal mating","termid":"FYPO:0000031"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000301"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0001985","FYPO:0005447","FYPO:0000301"],"is_obsolete":false,"name":"promiscuous mating","synonyms":[{"name":"conjugation with multiple partner cells","type":"exact"},{"name":"formation of multiple mating projections","type":"related"},{"name":"formation of multiple shmoos","type":"related"},{"name":"mating with multiple partner cells","type":"exact"},{"name":"promiscuous conjugation","type":"exact"}],"termid":"FYPO:0006014"}


id: GO:0034090
data:
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id: PBO:0029999
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id: GO:0010749
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id: MONDO:0012521
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id: MONDO:0007149
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id: MONDO:0043303
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id: PATO:0000278
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id: GO:1900736
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id: PR:Q10140
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id: PBO:0027687
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id: PBO:0074438
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id: PR:000027626
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id: MONDO:0858988
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id: PBO:0076473
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id: MONDO:0100500
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id: GO:0102899
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: H+ + dehydroabietadienol + NADPH + O2 = dehydroabietadiene-diol + NADP + H2O.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete dehydroabietadienol hydroxylase activity (obsolete GO:0102899)","termid":"GO:0102899"}


id: GO:0002279
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  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The change in morphology and behavior of a mast cell resulting from exposure to a cytokine, chemokine, soluble factor, or to (at least in mammals) an antigen which the mast cell has specifically bound via IgE bound to Fc-epsilonRI receptors, leading to the initiation or perpetuation of an immune response.","definition_xrefs":["ISBN:0781735149","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"myeloid cell activation involved in immune response","termid":"GO:0002275"},{"relation_name":"is_a","term_name":"mast cell activation","termid":"GO:0045576"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"mast cell activation involved in immune response","synonyms":[{"name":"mast cell activation during immune response","type":"related"}],"termid":"GO:0002279"}


id: GO:1904838
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of male germ-line stem cell asymmetric division.","definition_xrefs":["GO_REF:0000058","PMID:19339709","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of asymmetric cell division","termid":"GO:0009786"},{"relation_name":"is_a","term_name":"regulation of multicellular organismal process","termid":"GO:0051239"},{"relation_name":"is_a","term_name":"regulation of stem cell division","termid":"GO:2000035"},{"relation_name":"regulates","term_name":"male germ-line stem cell asymmetric division","termid":"GO:0048133"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of male germ-line stem cell asymmetric division","synonyms":[{"name":"regulation of male germ-line stem cell renewal","type":"exact"}],"termid":"GO:1904838"}


id: GO:1900132
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that activates or increases the frequency, rate or extent of lipid binding.","definition_xrefs":["GOC:pm","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete positive regulation of lipid binding (obsolete GO:1900132)","synonyms":[{"name":"activation of lipid binding","type":"narrow"},{"name":"up regulation of lipid binding","type":"exact"},{"name":"up-regulation of lipid binding","type":"exact"},{"name":"upregulation of lipid binding","type":"exact"}],"termid":"GO:1900132"}


id: SO:0000596
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A primary transcript encoding a small nucleolar RNA of the box H/ACA family.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"snoRNA_primary_transcript","termid":"SO:0000232"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H_ACA_box_snoRNA_primary_transcript","synonyms":[{"name":"H ACA box snoRNA primary transcript","type":"exact"}],"termid":"SO:0000596"}


id: MONDO:0014290
data:
  {"annotated_genes":["SJAG_05277"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87551],"is_not":false,"summary":null,"term":"MONDO:0014290"}]},"cv_name":"mondo","definition":"COASY protein-associated neurodegeneration (CoPAN) is a very rare, slowly progressive form of neurodegeneration with brain iron accumulation (NBIA) characterized by classic NBIA features. The clinical manifestations include early-onset spastic-dystonic paraparesis, oromandibular dystonia, dysarthria, parkinsonism, axonal neuropathy, progressive cognitive impairment, complex motor tics, and obsessive-compulsive disorder.","definition_xrefs":["Orphanet:397725"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neurodegeneration with brain iron accumulation","termid":"MONDO:0018307"}],"gene_count":1,"genes_by_uniquename":{"SJAG_05277":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005066","MONDO:0002039","MONDO:0005559"],"is_obsolete":false,"name":"neurodegeneration with brain iron accumulation 6","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:615643","DOID:0110740","GARD:12571","UMLS:C4517377","MEDGEN:1387791","SCTID:732264002"],"synonyms":[{"name":"COASY neurodegeneration with brain iron accumulation","type":"exact"},{"name":"COASY protein-associated neurodegeneration","type":"related"},{"name":"CoPAN","type":"exact"},{"name":"NBIA6","type":"exact"},{"name":"neurodegeneration with brain iron accumulation 6","type":"exact"},{"name":"neurodegeneration with brain iron accumulation caused by mutation in COASY","type":"exact"},{"name":"neurodegeneration with brain iron accumulation due to COASY mutation","type":"exact"},{"name":"neurodegeneration with brain iron accumulation type 6","type":"exact"}],"termid":"MONDO:0014290","terms_by_termid":{"MONDO:0014290":null},"xrefs":{"Monarch":{"xref_id":"0014290"}}}


id: PBO:0044867
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"DENN domain containing 2B","termid":"PBO:0044867"}


id: GO:0047546
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2-hydroxypyridine + AH(2) + O2 = 2,5-dihydroxypyridine + A + H2O.","definition_xrefs":["RHEA:16973","EC:1.14.99.26"],"direct_ancestors":[{"relation_name":"is_a","term_name":"monooxygenase activity","termid":"GO:0004497"},{"relation_name":"is_a","term_name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen","termid":"GO:0016705"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0003674","GO:0016491","GO:0003824"],"is_obsolete":false,"name":"2-hydroxypyridine 5-monooxygenase activity","secondary_identifiers":["MetaCyc:2-HYDROXYPYRIDINE-5-MONOOXYGENASE-RXN","KEGG_REACTION:R03206"],"synonyms":[{"name":"2-hydroxypyridine oxygenase activity","type":"related"},{"name":"2-hydroxypyridine,hydrogen-donor:oxygen oxidoreductase (5-hydroxylating)","type":"related"}],"termid":"GO:0047546"}


id: PBO:0109630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"napsin B aspartic peptidase (pseudogene)","termid":"PBO:0109630"}


id: GO:0061163
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The endoplasmic reticulum organization process that results in the structure of the endoplasmic reticulum being oriented in the cell. Endoplasmic reticulum polarization serves as a mechanism to compartmentalize cellular activities and to establish cell polarity.","definition_xrefs":["GOC:vw","GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"endoplasmic reticulum organization","termid":"GO:0007029"}],"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":"endoplasmic reticulum polarization","secondary_identifiers":["GO:0061166","GO:0061167","GO:0061164","GO:0061165"],"synonyms":[{"name":"ER localization involved in ER polarization at cell division site","type":"narrow"},{"name":"ER polarization","type":"exact"},{"name":"endoplasmic reticulum localisation involved in endoplasmic reticulum polarization at cell division site","type":"narrow"},{"name":"endoplasmic reticulum localization involved in endoplasmic reticulum polarization at cell division site","type":"narrow"},{"name":"establishment of endoplasmic reticulum localisation involved in endoplasmic reticulum polarization at cell division site","type":"narrow"},{"name":"establishment of endoplasmic reticulum localization involved in endoplasmic reticulum polarization at cell division site","type":"narrow"},{"name":"maintenance of endoplasmic reticulum location involved in endoplasmic reticulum polarization at cell division site","type":"narrow"},{"name":"transitional endoplasmic reticulum polarization at cell division site","type":"narrow"}],"termid":"GO:0061163"}


id: MONDO:0010171
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A form of Usher syndrome type I that is caused by homozygous or compound heterozygous mutation in the gene encoding harmonin on chromosome 11p15. It is inherited in an autosomal recessive manner.","definition_xrefs":["OMIM:276904"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Usher syndrome type 1","termid":"MONDO:0010168"}],"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":"Usher syndrome type 1C","secondary_identifiers":["MEDGEN:338506","ICD10CM:H35.5","GARD:5437","UMLS:C1848604","DOID:0110830"],"synonyms":[{"name":"USH1C","type":"exact"},{"name":"USHER syndrome, type IC","type":"related"},{"name":"Usher syndrome type 1C","type":"exact"},{"name":"Usher syndrome type I Acadian variety","type":"exact"},{"name":"Usher syndrome type IC","type":"exact"},{"name":"Usher syndrome, Acadian variety","type":"related"},{"name":"Usher syndrome, type 1C","type":"related"},{"name":"Usher syndrome, type I, Acadian variety","type":"related"}],"termid":"MONDO:0010171","xrefs":{"Monarch":{"xref_id":"0010171"}}}


id: MONDO:0012609
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An Alzheimer's disease that is characterized by an associated with variation in the region 8p12-q22.","definition_xrefs":["PMID:16825432","DOID:0110045"],"direct_ancestors":[{"relation_name":"is_a","term_name":"early-onset autosomal dominant Alzheimer disease","termid":"MONDO:0015140"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0002039"},{"rel_name":"is_a","termid":"MONDO:0005559"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0002039","MONDO:0000426","MONDO:0005559"],"is_obsolete":false,"name":"Alzheimer disease 12","secondary_identifiers":["MEDGEN:410013","MESH:C567022","UMLS:C1970209","OMIM:611073","GARD:16516"],"synonyms":[{"name":"AD12","type":"exact"},{"name":"Ad12","type":"related"},{"name":"Alzheimer disease 12","type":"exact"},{"name":"Alzheimer disease familial 12","type":"exact"},{"name":"Alzheimer disease type 12","type":"exact"},{"name":"Alzheimer disease, familial, 12","type":"related"},{"name":"Alzheimer's disease 12","type":"exact"},{"name":"Alzheimer's disease type 12","type":"exact"}],"termid":"MONDO:0012609","xrefs":{"Monarch":{"xref_id":"0012609"}}}


id: PBO:0072246
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein S20 pseudogene 21","termid":"PBO:0072246"}


id: PBO:0050501
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"HOXC cluster antisense RNA 1","termid":"PBO:0050501"}


id: GO:0009176
data:
  {"annotated_genes":["SJAG_04627","SJAG_03771","SJAG_04487"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[71801,81348],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006231"},{"annotations":[71800,81371],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0006226"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving pyrimidine deoxynucleoside monophosphate, a compound consisting of a pyrimidine base linked to a deoxyribose sugar esterified with phosphate on the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleoside monophosphate metabolic process","termid":"GO:0009129"}],"gene_count":3,"genes_by_uniquename":{"SJAG_03771":null,"SJAG_04487":null,"SJAG_04627":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"pyrimidine deoxyribonucleoside monophosphate metabolic process","references_by_uniquename":{"GO_REF:0000033":null},"synonyms":[{"name":"pyrimidine deoxyribonucleoside monophosphate metabolism","type":"exact"}],"termid":"GO:0009176","terms_by_termid":{"GO:0006226":null,"GO:0006231":null}}


id: GO:0032261
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  {"annotated_genes":["SJAG_01298","SJAG_04123","SJAG_01500","SJAG_01070","SJAG_01859","SJAG_06634","SJAG_04634","SJAG_03298"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[57535,75829],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044209"},{"annotations":[77528,103153],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032263"},{"annotations":[66114,77529],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032264"},{"annotations":[72700,81952],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034355"},{"annotations":[77530,110250],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0032265"}]},"cv_name":"biological_process","definition":"Any process which produces a purine nucleotide from derivatives of it, without de novo synthesis.","definition_xrefs":["GOC:jp"],"direct_ancestors":[{"relation_name":"is_a","term_name":"purine nucleotide biosynthetic process","termid":"GO:0006164"},{"relation_name":"is_a","term_name":"purine-containing compound salvage","termid":"GO:0043101"},{"relation_name":"is_a","term_name":"nucleotide salvage","termid":"GO:0043173"}],"gene_count":8,"genes_by_uniquename":{"SJAG_01070":null,"SJAG_01298":null,"SJAG_01500":null,"SJAG_01859":null,"SJAG_03298":null,"SJAG_04123":null,"SJAG_04634":null,"SJAG_06634":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0044281","GO:0008150","GO:0055086"],"is_obsolete":false,"name":"purine nucleotide salvage","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000041":null,"GO_REF:0000107":null},"termid":"GO:0032261","terms_by_termid":{"GO:0032263":null,"GO:0032264":null,"GO:0032265":null,"GO:0034355":null,"GO:0044209":null}}


id: PBO:0080356
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"vomeronasal 2 receptor 11 pseudogene","termid":"PBO:0080356"}


id: GO:0007088
data:
  {"annotated_genes":["SJAG_01805","SJAG_04884","SJAG_04968","SJAG_03126","SJAG_04699","SJAG_01297","SJAG_02380","SJAG_03353","SJAG_02058","SJAG_02169","SJAG_03681","SJAG_01082","SJAG_00666","SJAG_02498","SJAG_03048","SJAG_02336","SJAG_01679","SJAG_00883","SJAG_04126","SJAG_01330","SJAG_01837","SJAG_04573","SJAG_04259","SJAG_04999","SJAG_02451"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[112918],"is_not":false,"summary":null,"term":"GO:0007088"},{"annotations":[105846,110230,116267,117899,101540,92668,109202,113954,115780],"is_not":false,"rel_names":["is_a","negatively_regulates","regulates"],"summary":null,"term":"GO:1902426"},{"annotations":[117557,101382,111891,116497,103755,108285],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0007094"},{"annotations":[96146],"is_not":false,"rel_names":["regulates","negatively_regulates","is_a"],"summary":null,"term":"GO:0140499"},{"annotations":[118675],"is_not":false,"rel_names":["positively_regulates","regulates","is_a"],"summary":null,"term":"GO:0090267"},{"annotations":[104063,99646,102101,95754,113368,116763,104335],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045842"}]},"cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of mitosis.","definition_xrefs":["GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of mitotic cell cycle","termid":"GO:0007346"},{"relation_name":"is_a","term_name":"regulation of cell cycle process","termid":"GO:0010564"},{"relation_name":"is_a","term_name":"regulation of nuclear division","termid":"GO:0051783"},{"relation_name":"regulates","term_name":"mitotic nuclear division","termid":"GO:0140014"}],"gene_count":25,"genes_by_uniquename":{"SJAG_00666":null,"SJAG_00883":null,"SJAG_01082":null,"SJAG_01297":null,"SJAG_01330":null,"SJAG_01679":null,"SJAG_01805":null,"SJAG_01837":null,"SJAG_02058":null,"SJAG_02169":null,"SJAG_02336":null,"SJAG_02380":null,"SJAG_02451":null,"SJAG_02498":null,"SJAG_03048":null,"SJAG_03126":null,"SJAG_03353":null,"SJAG_03681":null,"SJAG_04126":null,"SJAG_04259":null,"SJAG_04573":null,"SJAG_04699":null,"SJAG_04884":null,"SJAG_04968":null,"SJAG_04999":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of mitotic nuclear division","references_by_uniquename":{"GO_REF:0000107":null},"synonyms":[{"name":"regulation of mitosis","type":"exact"}],"termid":"GO:0007088","terms_by_termid":{"GO:0007088":null,"GO:0007094":null,"GO:0045842":null,"GO:0090267":null,"GO:0140499":null,"GO:1902426":null}}


id: MONDO:1010122
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any form of vitiligo characterized by a tan zone of varying width between normal and depigmented skin. This intermediate tan zone has more inflammatory cells, Langerhans cells, and melanophages than vitiliginous or normal skin. The number of melanocytes is greater than in vitiliginous skin but fewer than in normal skin.","definition_xrefs":["PMID:21839315"],"direct_ancestors":[{"relation_name":"is_a","term_name":"vitiligo","termid":"MONDO:0008661"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005093"],"is_obsolete":false,"name":"trichrome vitiligo","secondary_identifiers":["UMLS:C1274649","MEDGEN:697977","SCTID:403270009"],"termid":"MONDO:1010122","xrefs":{"Monarch":{"xref_id":"1010122"}}}


id: FYPO:0000558
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the occurrence of re-entry into the mitotic cell cycle after pheromone arrest is increased.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal re-entry into mitotic cell cycle after pheromone arrest","termid":"FYPO:0000555"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000298"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000298","FYPO:0005447","FYPO:0000631","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"increased re-entry into mitotic cell cycle after pheromone arrest","synonyms":[{"name":"increased recovery from pheromone-induced cell cycle arrest","type":"exact"},{"name":"recovery from pheromone-induced cell cycle arrest: increased","type":"related"}],"termid":"FYPO:0000558"}


id: PBO:0042987
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"checkpoint kinase 2","termid":"PBO:0042987"}


id: MONDO:0019652
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"familial idiopathic steroid-resistant nephrotic syndrome","termid":"MONDO:0019006"}],"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":"familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation","secondary_identifiers":["Orphanet:93214"],"termid":"MONDO:0019652","xrefs":{"Monarch":{"xref_id":"0019652"}}}


id: MONDO:0003619
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Acute or chronic inflammation of the fallopian tube. It is most often caused by Neisseria gonorrhoeae and Chlamydia trachomatis infections. The infections usually originate in the vagina and ascend to the fallopian tube. Symptoms include abdominal, pelvic, and lower back pain, pain during ovulation and sexual intercourse, fever, nausea, and vomiting. Complications include infertility and ectopic pregnancy.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pelvic inflammatory disease","termid":"MONDO:0000922"},{"relation_name":"is_a","term_name":"fallopian tube disorder","termid":"MONDO:0002156"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"salpingitis","secondary_identifiers":["UMLS:C0036130","SCTID:88157006","MEDGEN:20646","DOID:5733","MESH:D012488","NCIT:C26880"],"synonyms":[{"name":"fallopian tube inflammation","type":"exact"},{"name":"inflammation of fallopian tube","type":"exact"}],"termid":"MONDO:0003619","xrefs":{"Monarch":{"xref_id":"0003619"}}}


id: PBO:0086883
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative transcription factor containing a WOPR domain; binds DNA in vitro; similar to C. albicans Wor1p transcription factor that regulates white-opaque switching; overexpression causes a cell cycle delay or arrest","termid":"PBO:0086883"}


id: PBO:0000280
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Fen1 family nuclease, XP-G family (predicted)","termid":"PBO:0000280"}


id: GO:2000722
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of cardiac vascular smooth muscle cell differentiation.","definition_xrefs":["GOC:BHF"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of vascular associated smooth muscle cell differentiation","termid":"GO:1905063"},{"relation_name":"is_a","term_name":"regulation of cardiocyte differentiation","termid":"GO:1905207"},{"relation_name":"regulates","term_name":"cardiac vascular smooth muscle cell differentiation","termid":"GO:0060947"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of cardiac vascular smooth muscle cell differentiation","synonyms":[{"name":"regulation of heart vascular smooth muscle cell differentiation","type":"exact"}],"termid":"GO:2000722"}


id: GO:0038100
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a nodal protein, a member of the transforming growth factor-beta superfamily.","definition_xrefs":["GOC:bf","PMID:20629020"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein binding","termid":"GO:0005515"}],"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":"nodal binding","termid":"GO:0038100"}


id: PR:O94702
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An endoplasmic reticulum metallopeptidase 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO04550","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":"endoplasmic reticulum metallopeptidase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC1259.02c","secondary_identifiers":["UniProtKB:O94702"],"synonyms":[{"name":"FXNA-like protease (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-ERMP1","type":"exact"}],"termid":"PR:O94702"}


id: GO:1904736
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of fatty acid beta-oxidation using acyl-CoA dehydrogenase.","definition_xrefs":["PMID:25416781","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of fatty acid beta-oxidation","termid":"GO:0031999"},{"relation_name":"is_a","term_name":"regulation of fatty acid beta-oxidation using acyl-CoA dehydrogenase","termid":"GO:1904735"},{"relation_name":"negatively_regulates","term_name":"fatty acid beta-oxidation using acyl-CoA dehydrogenase","termid":"GO:0033539"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0006629"},{"rel_name":"negatively_regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006629"}],"interesting_parent_ids":["GO:0008150","GO:0006629","GO:0044281"],"is_obsolete":false,"name":"negative regulation of fatty acid beta-oxidation using acyl-CoA dehydrogenase","synonyms":[{"name":"down regulation of fatty acid beta-oxidation using acyl-CoA dehydrogenase","type":"exact"},{"name":"down-regulation of fatty acid beta-oxidation using acyl-CoA dehydrogenase","type":"exact"},{"name":"downregulation of fatty acid beta-oxidation using acyl-CoA dehydrogenase","type":"exact"},{"name":"inhibition of fatty acid beta-oxidation using acyl-CoA dehydrogenase","type":"narrow"}],"termid":"GO:1904736"}


id: PBO:0075630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small proline rich protein 1B","termid":"PBO:0075630"}


id: PBO:0071884
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RPS3A pseudogene 22","termid":"PBO:0071884"}


id: GO:2000593
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of metanephric DCT cell differentiation.","definition_xrefs":["GOC:obol"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell differentiation","termid":"GO:0045596"},{"relation_name":"is_a","term_name":"regulation of metanephric DCT cell differentiation","termid":"GO:2000592"},{"relation_name":"negatively_regulates","term_name":"metanephric DCT cell differentiation","termid":"GO:0072240"}],"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 metanephric DCT cell differentiation","synonyms":[{"name":"negative regulation of metanephric distal convoluted tubule cell differentiation","type":"exact"}],"termid":"GO:2000593"}


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:0046494
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"endoplasmic reticulum-golgi intermediate compartment 1","termid":"PBO:0046494"}


id: GO:0160238
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: reduced [NADPH-hemoprotein reductase] + O2 + a long-chain fatty aldehyde = oxidized [NADPH-hemoprotein reductase] + CO2 + H2O + H+ + a long-chain alkane.","definition_xrefs":["PMID:22927409","RHEA:83563"],"direct_ancestors":[{"relation_name":"is_a","term_name":"carbon-carbon lyase activity","termid":"GO:0016830"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016829"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016829","GO:0003674","GO:0003824"],"is_obsolete":false,"name":"long-chain fatty aldehyde oxidative decarbonylase activity","synonyms":[{"name":"aldehyde oxidative decarbonylase activity","type":"broad"}],"termid":"GO:0160238"}


id: GO:0102763
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: a ribonucleoside 5'-triphosphate + phytyl phosphate = a ribonucleoside 5'-diphosphate + phytyl diphosphate.","definition_xrefs":["RHEA:38099"],"direct_ancestors":[{"relation_name":"is_a","term_name":"phosphotransferase activity, phosphate group as acceptor","termid":"GO:0016776"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0016740","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"phytyl-P kinase activity","secondary_identifiers":["MetaCyc:RXN-7763"],"termid":"GO:0102763"}


id: PBO:0086755
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Putative protein of unknown function; proposed to be an inactive evolutionary remnant that along with neighboring gene YOL162W may have constituted a second sulfonate transporter and SOA1 paralog that is intact in S. uvarum, S. eubayanus and S. arboricola and named SOA2; member of the Dal5p subfamily of the major facilitator family","termid":"PBO:0086755"}


id: PBO:0074582
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 2A","termid":"PBO:0074582"}


id: PBO:0116720
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"popeye domain cAMP effector 2","termid":"PBO:0116720"}


id: GO:0032245
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the directed movement of a purine nucleoside into, out of or within a cell, or between cells, by means of some agent such as a transporter or pore.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of nucleoside transport","termid":"GO:0032242"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810"],"is_obsolete":false,"name":"regulation of purine nucleoside transport","termid":"GO:0032245"}


id: PBO:0017485
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-bearer_of","termid":"PBO:0017485"}


id: GO:1902314
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to hydroquinone.","definition_xrefs":["GOC:bhm","GOC:TermGenie","PMID:15667223"],"direct_ancestors":[{"relation_name":"is_a","term_name":"binding","termid":"GO:0005488"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0003674"],"is_obsolete":false,"name":"hydroquinone binding","synonyms":[{"name":"quinol binding","type":"exact"}],"termid":"GO:1902314"}


id: MONDO:0005144
data:
  {"annotated_genes":["SJAG_02289","SJAG_04178","SJAG_03923","SJAG_00053","SJAG_03170","SJAG_00668","SJAG_04387","SJAG_02242","SJAG_02695","SJAG_07000","SJAG_01317","SJAG_04489","SJAG_02509","SJAG_03345","SJAG_03598"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88508],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0859529"},{"annotations":[87160,89223],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007103"},{"annotations":[88703],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012945"},{"annotations":[88821],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010459"},{"annotations":[87566],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013715"},{"annotations":[87314,87313],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014531"},{"annotations":[88433,88434],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011223"},{"annotations":[88563,88564],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012077"},{"annotations":[88668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013501"},{"annotations":[87241],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010936"},{"annotations":[89213],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008458"}]},"cv_name":"mondo","definition":"An instance of amyotrophic lateral sclerosis that is caused by an inherited modification of the individual's genome.","definition_xrefs":["MONDO:patterns/hereditary"],"direct_ancestors":[{"relation_name":"is_a","term_name":"amyotrophic lateral sclerosis","termid":"MONDO:0004976"},{"relation_name":"is_a","term_name":"hereditary motor neuron disease","termid":"MONDO:0024257"}],"gene_count":15,"genes_by_uniquename":{"SJAG_00053":null,"SJAG_00668":null,"SJAG_01317":null,"SJAG_02242":null,"SJAG_02289":null,"SJAG_02509":null,"SJAG_02695":null,"SJAG_03170":null,"SJAG_03345":null,"SJAG_03598":null,"SJAG_03923":null,"SJAG_04178":null,"SJAG_04387":null,"SJAG_04489":null,"SJAG_07000":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"familial amyotrophic lateral sclerosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C4551993","OMIMPS:105400","EFO:0001356","MEDGEN:1642547"],"synonyms":[{"name":"hereditary amyotrophic lateral sclerosis","type":"exact"}],"termid":"MONDO:0005144","terms_by_termid":{"MONDO:0007103":null,"MONDO:0008458":null,"MONDO:0010459":null,"MONDO:0010936":null,"MONDO:0011223":null,"MONDO:0012077":null,"MONDO:0012945":null,"MONDO:0013501":null,"MONDO:0013715":null,"MONDO:0014531":null,"MONDO:0859529":null},"xrefs":{"Monarch":{"xref_id":"0005144"}}}


id: PBO:0041357
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement component 4 binding protein alpha","termid":"PBO:0041357"}


id: GO:1900647
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of chanoclavine-I aldehyde biosynthetic process.","definition_xrefs":["GOC:TermGenie","GOC:di"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of chanoclavine-I aldehyde biosynthetic process","termid":"GO:1900646"},{"relation_name":"is_a","term_name":"negative regulation of ergot alkaloid biosynthetic process","termid":"GO:1900823"},{"relation_name":"negatively_regulates","term_name":"chanoclavine-I aldehyde biosynthetic process","termid":"GO:1900569"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"negatively_regulates","termid":"GO:0019748"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0019748"}],"interesting_parent_ids":["GO:0019748","GO:0008150"],"is_obsolete":false,"name":"negative regulation of chanoclavine-I aldehyde biosynthetic process","synonyms":[{"name":"down regulation of chanoclavine-I aldehyde anabolism","type":"exact"},{"name":"down regulation of chanoclavine-I aldehyde biosynthesis","type":"exact"},{"name":"down regulation of chanoclavine-I aldehyde biosynthetic process","type":"exact"},{"name":"down regulation of chanoclavine-I aldehyde formation","type":"exact"},{"name":"down regulation of chanoclavine-I aldehyde synthesis","type":"exact"},{"name":"down-regulation of chanoclavine-I aldehyde anabolism","type":"exact"},{"name":"down-regulation of chanoclavine-I aldehyde biosynthesis","type":"exact"},{"name":"down-regulation of chanoclavine-I aldehyde biosynthetic process","type":"exact"},{"name":"down-regulation of chanoclavine-I aldehyde formation","type":"exact"},{"name":"down-regulation of chanoclavine-I aldehyde synthesis","type":"exact"},{"name":"downregulation of chanoclavine-I aldehyde anabolism","type":"exact"},{"name":"downregulation of chanoclavine-I aldehyde biosynthesis","type":"exact"},{"name":"downregulation of chanoclavine-I aldehyde biosynthetic process","type":"exact"},{"name":"downregulation of chanoclavine-I aldehyde formation","type":"exact"},{"name":"downregulation of chanoclavine-I aldehyde synthesis","type":"exact"},{"name":"inhibition of chanoclavine-I aldehyde anabolism","type":"exact"},{"name":"inhibition of chanoclavine-I aldehyde biosynthesis","type":"exact"},{"name":"inhibition of chanoclavine-I aldehyde biosynthetic process","type":"narrow"},{"name":"inhibition of chanoclavine-I aldehyde formation","type":"exact"},{"name":"inhibition of chanoclavine-I aldehyde synthesis","type":"exact"},{"name":"negative regulation of chanoclavine-I aldehyde anabolism","type":"exact"},{"name":"negative regulation of chanoclavine-I aldehyde biosynthesis","type":"exact"},{"name":"negative regulation of chanoclavine-I aldehyde formation","type":"exact"},{"name":"negative regulation of chanoclavine-I aldehyde synthesis","type":"exact"}],"termid":"GO:1900647"}


id: PATO:0000435
data:
  {"annotation_feature_type":"gene","cv_name":"quality","gene_count":0,"genotype_count":0,"name":"OBSOLETE PATO:0000435 pattern value (obsolete PATO:0000435)","termid":"PATO:0000435"}


id: PBO:0073954
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 22 member 3","termid":"PBO:0073954"}


id: GO:0010331
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a gibberellin, a plant hormone that regulates aspects of plant growth.","definition_xrefs":["GOC:tair_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"isoprenoid binding","termid":"GO:0019840"},{"relation_name":"is_a","term_name":"carboxylic acid binding","termid":"GO:0031406"},{"relation_name":"is_a","term_name":"hormone binding","termid":"GO:0042562"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0008289"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005488","GO:0008289","GO:0003674"],"is_obsolete":false,"name":"gibberellin binding","synonyms":[{"name":"gibberellic acid receptor","type":"related"},{"name":"gibberellin receptor","type":"related"}],"termid":"GO:0010331"}


id: GO:0120323
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which one or more ubiquitin groups are added to a lipid.","definition_xrefs":["GOC:sp","PMID:34012115"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipid modification by small protein conjugation","termid":"GO:0120322"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006629","GO:0008150"],"is_obsolete":false,"name":"lipid ubiquitination","termid":"GO:0120323"}


id: PBO:0090472
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein subunit L44","termid":"PBO:0090472"}


id: PBO:0081450
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zinc finger protein 317 pseudogene 1","termid":"PBO:0081450"}


id: GO:0051508
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-glucose + stigmasterol = UDP + O-glucosyl-stigmasterol.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete stigmasterol UDP-glucosyltransferase activity (obsolete GO:0051508)","termid":"GO:0051508"}


id: FYPO:0003303
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 post-anaphase array of microtubules is present in an abnormal location.","definition_xrefs":["PMID:9348288","PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal post-anaphase array","termid":"FYPO:0004316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0000054"},{"rel_name":"is_a","termid":"FYPO:0002399"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000002","FYPO:0000054","FYPO:0002399","FYPO:0001320","FYPO:0001985"],"is_obsolete":false,"name":"mislocalized post-anaphase array","synonyms":[{"name":"mislocalised post-anaphase array","type":"exact"},{"name":"mislocalized PAA","type":"exact"},{"name":"mislocalized post-anaphase array during mitotic cell cycle","type":"related"},{"name":"mislocalized post-anaphase array during vegetative growth","type":"exact"},{"name":"mislocalized post-anaphase microtubule array","type":"exact"}],"termid":"FYPO:0003303"}


id: PBO:0005736
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Cut3 interacting protein Cti1, predicted exosome subunit","termid":"PBO:0005736"}


id: GO:1905220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the frequency, rate or extent of platelet formation.","definition_xrefs":["GO_REF:0000058","GOC:TermGenie","PMID:10606160"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of myeloid cell differentiation","termid":"GO:0045638"},{"relation_name":"is_a","term_name":"regulation of platelet formation","termid":"GO:1905219"},{"relation_name":"negatively_regulates","term_name":"platelet formation","termid":"GO:0030220"}],"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 platelet formation","synonyms":[{"name":"down regulation of platelet extrusion","type":"exact"},{"name":"down regulation of platelet formation","type":"exact"},{"name":"down-regulation of platelet extrusion","type":"exact"},{"name":"down-regulation of platelet formation","type":"exact"},{"name":"downregulation of platelet extrusion","type":"exact"},{"name":"downregulation of platelet formation","type":"exact"},{"name":"inhibition of platelet extrusion","type":"narrow"},{"name":"inhibition of platelet formation","type":"narrow"},{"name":"negative regulation of platelet extrusion","type":"exact"}],"termid":"GO:1905220"}


id: MONDO:0019151
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Oligocone trichromacy is a rare non-progressive form of cone photoreceptor dysfunction characterized by reduced visual acuity, normal retinal appearance, absent or reduced cone responses on electroretinography but normal color vision.","definition_xrefs":["Orphanet:75378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"oligocone trichromacy","secondary_identifiers":["MEDGEN:928545","GARD:18925","icd11.foundation:645985320","SCTID:722066001","UMLS:C4302876"],"synonyms":[{"name":"Oligocone syndrome","type":"exact"}],"termid":"MONDO:0019151","xrefs":{"Monarch":{"xref_id":"0019151"}}}


id: PBO:0077911
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TPT1 pseudogene 2","termid":"PBO:0077911"}


id: GO:0043313
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate, or extent of neutrophil degranulation.","definition_xrefs":["ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of myeloid leukocyte mediated immunity","termid":"GO:0002886"},{"relation_name":"is_a","term_name":"regulation of leukocyte degranulation","termid":"GO:0043300"},{"relation_name":"is_a","term_name":"regulation of immune response","termid":"GO:0050776"},{"relation_name":"regulates","term_name":"neutrophil degranulation","termid":"GO:0043312"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0016192"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0006810"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0016192"],"is_obsolete":false,"name":"regulation of neutrophil degranulation","synonyms":[{"name":"regulation of neutrophil granule exocytosis","type":"exact"}],"termid":"GO:0043313"}


id: GO:0052849
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Catalysis of the reaction: 2 NADP+ + tetrahydrocurcumin = curcumin + 2 H+ + 2 NADPH.","definition_xrefs":["RHEA:34815"],"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:0003674"},{"rel_name":"is_a","termid":"GO:0016491"},{"rel_name":"is_a","termid":"GO:0003824"}],"interesting_parent_ids":["GO:0016491","GO:0003824","GO:0003674"],"is_obsolete":false,"name":"curcumin reductase (NADP+) activity","secondary_identifiers":["MetaCyc:RXN0-6676"],"synonyms":[{"name":"NADPH-dependent curcumin reductase activity","type":"exact"}],"termid":"GO:0052849"}


id: MONDO:0044720
data:
  {"annotated_genes":["SJAG_00863"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88375],"is_not":false,"summary":null,"term":"MONDO:0044720"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary otorhinolaryngologic disease","termid":"MONDO:0018751"},{"relation_name":"is_a","term_name":"autosomal recessive syndromic cerebellar ataxia","termid":"MONDO:0020047"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00863":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559","MONDO:0006025"],"is_obsolete":false,"name":"cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:504476","OMIM:614575","MEDGEN:482853","GARD:17937","UMLS:C3281223"],"synonyms":[{"name":"CABV syndrome","type":"exact"},{"name":"CANVAS","type":"exact"},{"name":"cerebellar ataxia with bilateral vestibulopathy syndrome","type":"exact"},{"name":"cerebellar ataxia, neuropathy, and vestibular areflexia syndrome","type":"exact"}],"termid":"MONDO:0044720","terms_by_termid":{"MONDO:0044720":null},"xrefs":{"Monarch":{"xref_id":"0044720"}}}


id: PBO:0087711
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of the RNA polymerase II mediator complex; associates with core polymerase subunits to form the RNA polymerase II holoenzyme; essential for transcriptional regulation; relocalizes to the cytosol in response to hypoxia","termid":"PBO:0087711"}


id: MONDO:0018260
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"melanocytic nevus","termid":"MONDO:0005073"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"scalp syndrome","secondary_identifiers":["Orphanet:370052","GARD:21592","UMLS:C4751599","MEDGEN:1665599"],"synonyms":[{"name":"sebaceous nevus-CNS malformations-aplasia cutis congenital-limbal dermoid-pigmented nevus syndrome","type":"exact"},{"name":"sebaceous nevus-central nervous system malformations-aplasia cutis congenital-limbal dermoid-pigmented nevus syndrome","type":"exact"}],"termid":"MONDO:0018260","xrefs":{"Monarch":{"xref_id":"0018260"}}}


id: FYPO:0003738
data:
  {"alleles_by_uniquename":{"SJAG_04464:allele-1":{"allele_type":"amino_acid_mutation","description":"R152C","gene_uniquename":"SJAG_04464","name":"pim1-R152C","synonyms":[{"name":"Inferred CDK-phospho-mimic mutation","reference":"PMID:28954740","type":"exact"}],"uniquename":"SJAG_04464:allele-1"}},"annotation_feature_type":"genotype","cv_annotations":{"single_locus_phenotype":[{"annotations":[121467],"is_not":false,"summary":null,"term":"FYPO:0003738"}]},"cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which progression through the mitotic cell cycle is arrested when cells have condensed chromosomes, but show no other signs of having entered mitosis or M phase, under conditions where arrest does not normally occur.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormally arrested mitotic cell cycle progression","termid":"FYPO:0000502"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04464":null},"genotype_count":1,"genotypes_by_uniquename":{"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type":{"display_name":"pim1-R152C(aa)","display_uniquename":"pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type","loci":[{"expressed_alleles":[{"allele_uniquename":"SJAG_04464:allele-1","expression":"Not assayed or wild type"}]}]}},"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000631","FYPO:0001985","FYPO:0000002","FYPO:0005447"],"is_obsolete":false,"name":"abnormal mitotic cell cycle arrest with condensed chromosomes","references_by_uniquename":{"PMID:28954740":null},"single_locus_annotated_genes":["SJAG_04464"],"single_locus_genotype_uniquenames":["pim1-R152C-R152C-amino_acid_mutation-expression-not_assayed_or_wild_type"],"synonyms":[{"name":"abnormal cell cycle arrest with condensed chromosomes during mitotic cell cycle","type":"related"},{"name":"abnormal mitotic cell cycle arrest with condensed chromosomes during vegetative growth","type":"exact"}],"termid":"FYPO:0003738","terms_by_termid":{"FYECO:0000004":null,"FYPO:0003738":null}}


id: PBO:0112988
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Acetyltransferase required for sister chromatid cohesion; elicits cohesin dimerization during S phase; acetylates Mps3p to regulate nuclear organization; modifies Smc3p at replication forks and Mcd1p in response to dsDNA breaks; phosphorylated by Cdc28p, Cdc7p, Mck1p to generate pair of phosphates spaced precisely for recognition by ubiquitin ligase SCF-Cdc4; relative distribution to nucleus increases upon DNA replication stress; mutations in human homolog ESCO2 cause Roberts syndrome","termid":"PBO:0112988"}


id: PBO:0067007
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 14, pseudogene","termid":"PBO:0067007"}


id: MONDO:0009717
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare, genetic neuromuscular disease characterized by permanent myotonia, mask-like facies (with blepharospasm, narrow palpebral fissures, small mouth with pursed lips and puckered chin) , and chondrodysplasia (variably manifesting with short stature, pectus carinatum, kyphoscoliosis, bowing of long bones, epiphyseal, metaphyseal, and hip dysplasia).","definition_xrefs":["Orphanet:800"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"progressive muscular dystrophy","termid":"MONDO:0016106"},{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"qualitative or quantitative defects of perlecan","termid":"MONDO:0016151"},{"relation_name":"is_a","term_name":"spondyloepiphyseal dysplasia","termid":"MONDO:0016761"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0005497"],"is_obsolete":false,"name":"Schwartz-Jampel syndrome","secondary_identifiers":["NANDO:2200876","UMLS:C0036391","icd11.foundation:1725668060","NANDO:1200224","NANDO:2100235","ICD10CM:G71.13","GARD:250","MEDGEN:19892","NCIT:C35008","NORD:1697","SCTID:29145002","ICD9:759.89"],"synonyms":[{"name":"Aberfeld syndrome","type":"exact"},{"name":"Catel-Hempel syndrome","type":"exact"},{"name":"Catel-Hempel type dysostosis enchondralis metaepiphysaria","type":"exact"},{"name":"Osteochondromuscular dystrophy","type":"exact"},{"name":"SJS","type":"exact"},{"name":"Schwartz Jampel Aberfeld syndrome","type":"related"},{"name":"Schwartz Jampel Syndrome","type":"exact"},{"name":"Schwartz Jampel syndrome","type":"related"},{"name":"Schwartz-Jampel syndrome","type":"exact"},{"name":"Schwartz-Jampel-Aberfeld syndrome","type":"exact"},{"name":"burton skeletal dysplasia","type":"exact"},{"name":"burton syndrome","type":"exact"},{"name":"dysostosis enchondralis metaepiphysaria, Catel-Hempel type","type":"exact"},{"name":"myotonic chondrodystrophy","type":"exact"},{"name":"myotonic myopathy dwarfism chondrodystrophy and ocular and facial abnormalities","type":"related"},{"name":"myotonic myopathy, dwarfism, chondrodystrophy, and ocular and Facial abnormalities","type":"related"},{"name":"myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies","type":"exact"},{"name":"osteochondromuscular dystrophy","type":"exact"}],"termid":"MONDO:0009717","xrefs":{"Monarch":{"xref_id":"0009717"}}}


id: MONDO:0009910
data:
  {"annotated_genes":["SJAG_04934"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88083],"is_not":false,"summary":null,"term":"MONDO:0009910"}]},"cv_name":"mondo","definition":"Wiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism.","definition_xrefs":["Orphanet:3455"],"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":"multiple congenital anomalies/dysmorphic syndrome-intellectual disability","termid":"MONDO:0015159"},{"relation_name":"is_a","term_name":"developmental anomaly of metabolic origin","termid":"MONDO:0015327"},{"relation_name":"is_a","term_name":"hereditary lipodystrophy","termid":"MONDO:0020087"},{"relation_name":"is_a","term_name":"progeria","termid":"MONDO:0020732"},{"relation_name":"is_a","term_name":"POLR3A-related disorder","termid":"MONDO:0700276"},{"relation_name":"is_a","term_name":"osteogenesis imperfecta and a reduction of bone mineral density.","termid":"MONDO:0800064"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04934":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:0019303"}],"interesting_parent_ids":["MONDO:0019303","MONDO:0005497","MONDO:0005093","MONDO:0005066"],"is_obsolete":false,"name":"Wiedemann-Rautenstrauch syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["NORD:1852","OMIM:264090","NCIT:C121565","SCTID:238874008","UMLS:C0406586","MEDGEN:140806","MESH:C536423","ICD9:259.8","GARD:330","DOID:0081333"],"synonyms":[{"name":"Wiedemann Rautenstrauch Syndrome","type":"exact"},{"name":"Wiedemann Rautenstrauch syndrome","type":"related"},{"name":"Wiedemann-Rautenstrauch syndrome","type":"exact"},{"name":"neonatal progeroid syndrome","type":"exact"},{"name":"progeroid syndrome neonatal","type":"related"},{"name":"progeroid syndrome, neonatal","type":"related"}],"termid":"MONDO:0009910","terms_by_termid":{"MONDO:0009910":null},"xrefs":{"Monarch":{"xref_id":"0009910"}}}


id: CHEBI:84327
data:
  {"annotation_feature_type":"gene","cv_name":"chebi_ontology","direct_ancestors":[{"relation_name":"is_a","term_name":"chemical entity","termid":"CHEBI:24431"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"torin 1","termid":"CHEBI:84327"}


id: PBO:0076435
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TATA-box binding protein associated factor 11 like 11","termid":"PBO:0076435"}


id: MONDO:0033853
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome","secondary_identifiers":["MEDGEN:1814478","GARD:22144","Orphanet:521432","UMLS:C5681444"],"termid":"MONDO:0033853","xrefs":{"Monarch":{"xref_id":"0033853"}}}


id: MONDO:0001184
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Chronic form of rapidly progressive glomerulonephritis.","definition_xrefs":["MONDO:patterns/chronic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic kidney disease","termid":"MONDO:0005300"},{"relation_name":"is_a","term_name":"rapidly progressive glomerulonephritis","termid":"MONDO:0017236"}],"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":"chronic rapidly progressive glomerulonephritis","secondary_identifiers":["MEDGEN:574584","SCTID:197614002","ICD9:582.4","DOID:11036","UMLS:C0341694"],"synonyms":[{"name":"chronic glomerulonephritis with lesion of rapidly progressive glomerulonephritis","type":"exact"},{"name":"rapidly progressive glomerulonephritis, chronic","type":"exact"}],"termid":"MONDO:0001184","xrefs":{"Monarch":{"xref_id":"0001184"}}}


id: MONDO:0044748
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A disease of cattle caused by parasitization of the red blood cells by bacteria of the genus ANAPLASMA.","definition_xrefs":["MESH:D000712"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cattle disease","termid":"MONDO:0024913"},{"relation_name":"is_a","term_name":"Anaplasmataceae infectious disease, non-human animal","termid":"MONDO:0700113"},{"relation_name":"is_a","term_name":"tick-borne infectious disease, non-human animal","termid":"MONDO:0700201"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"anaplasmosis in cattle","synonyms":[{"name":"Anaplasmoses","type":"related"}],"termid":"MONDO:0044748","xrefs":{"Monarch":{"xref_id":"0044748"}}}


id: GO:1905806
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of synapse pruning.","definition_xrefs":["GO_REF:0000058","PMID:27779093","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of synapse organization","termid":"GO:0050807"},{"relation_name":"regulates","term_name":"synapse pruning","termid":"GO:0098883"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of synapse pruning","synonyms":[{"name":"regulation of synapse clearance","type":"exact"},{"name":"regulation of synapse disassembly","type":"exact"},{"name":"regulation of synapse elimination","type":"exact"},{"name":"regulation of synapse removal","type":"exact"}],"termid":"GO:1905806"}


id: MONDO:1011723
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","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":"mitochondrial fission encephalopathy, non-human animal","secondary_identifiers":["OMIA:002551"],"termid":"MONDO:1011723","xrefs":{"Monarch":{"xref_id":"1011723"}}}


id: MONDO:0700202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Bunyaviridae infectious disease that occurs in non-human animals.","definition_xrefs":["MONDO:patterns/nonhuman_disease"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral infectious disease, non-human animal","termid":"MONDO:0700053"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Bunyaviridae infectious disease, non-human animal","termid":"MONDO:0700202","xrefs":{"Monarch":{"xref_id":"0700202"}}}


id: PBO:0068235
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 18S ribosomal N1","termid":"PBO:0068235"}


id: PR:Q9UTS8
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of any of the following genes in Schizosaccharomyces pombe 972h-: fex1/fex2.","definition_xrefs":["UniProtKB:Q9UTS8","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":"UPF0695 membrane protein C977.11/PB8B6.06c (Schizosaccharomyces pombe 972h-)","synonyms":[{"name":"Spom972h-fex2","type":"exact"}],"termid":"PR:Q9UTS8"}


id: MONDO:0956993
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A posterior fossa ependymoma that arises in the posterior fossa with characteristic DNA methylation patterns including retention of nuclear H3 p.K28me3 (K27me3) expression, absence of CpG island hypermethylation, absence of global DNA hypomethylation, and absence of EZHIP overexpression.","definition_xrefs":["DOID:0081255"],"direct_ancestors":[{"relation_name":"is_a","term_name":"posterior fossa ependymoma","termid":"MONDO:0850339"}],"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":"posterior fossa group B ependymoma","secondary_identifiers":["NCIT:C186451"],"termid":"MONDO:0956993","xrefs":{"Monarch":{"xref_id":"0956993"}}}


id: MONDO:0009486
data:
  {"annotated_genes":["SJAG_02672"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86982],"is_not":false,"summary":null,"term":"MONDO:0009486"}]},"cv_name":"mondo","definition":"An autosomal recessive form of Kenny-Caffey syndrome due to mutation(s) in the TBCE gene, encoding tubulin-specific chaperone E. This condition is characterized by hypoparathyroidism with hypocalcemia, marked growth retardation, craniofacial anomalies, absent diploic space in the skull, cortical thickening of long bones with medullary stenosis, and small hands and feet.","definition_xrefs":["NCIT:C130992"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal recessive disease","termid":"MONDO:0006025"},{"relation_name":"is_a","term_name":"Kenny-Caffey syndrome","termid":"MONDO:0016516"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02672":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive Kenny-Caffey syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["Orphanet:93324","UMLS:C1855648","GARD:8367","MESH:C537021","OMIM:244460","MEDGEN:340923","DOID:0080722"],"synonyms":[{"name":"KCS1","type":"related"},{"name":"Kcs","type":"related"},{"name":"Kenny-Caffey syndrome type 1","type":"exact"},{"name":"Kenny-Caffey syndrome, autosomal recessive","type":"exact"},{"name":"Kenny-Caffey syndrome, type 1","type":"related"}],"termid":"MONDO:0009486","terms_by_termid":{"MONDO:0009486":null},"xrefs":{"Monarch":{"xref_id":"0009486"}}}


id: PBO:0034542
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_glutamate_synthase_(NADH)_activity","termid":"PBO:0034542"}


id: GO:0005171
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to an hepatocyte growth factor receptor.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"growth factor receptor binding","termid":"GO:0070851"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005515"}],"interesting_parent_ids":["GO:0003674","GO:0005515","GO:0005488"],"is_obsolete":false,"name":"hepatocyte growth factor receptor binding","synonyms":[{"name":"HGF receptor binding","type":"exact"},{"name":"hepatocyte growth factor","type":"narrow"},{"name":"hepatocyte growth factor receptor ligand","type":"narrow"}],"termid":"GO:0005171"}


id: MOD:01837
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively cross-links two L-cysteine residues with a thioether bond to form L-lanthionine.","definition_xrefs":["PubMed:6007887","ChEBI:21347","PubMed:20805503","RESID:AA0110#CYS2"],"direct_ancestors":[{"relation_name":"is_a","term_name":"L-lanthionine","termid":"MOD:01839"}],"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-lanthionine (Cys-Cys)","synonyms":[{"name":"(2R,2'R)-3,3'-sulfanediylbis(2-aminopropanoic acid)","type":"exact"},{"name":"(R)-S-(2-amino-2-carboxyethyl)-L-cysteine","type":"exact"},{"name":"(R,R)-2,6-diamino-4-thiaheptanedioic acid","type":"exact"},{"name":"(R,R)-3,3'-thiobis-(2-aminopropanoic acid)","type":"exact"},{"name":"(R,R)-bis(2-amino-2-carboxyethyl)sulfide","type":"exact"},{"name":"2-amino-3-(2-amino-2-carboxyethyl)sulfanylpropanoic acid","type":"exact"},{"name":"3,3'-thiobis-L-alanine","type":"exact"},{"name":"L-lanthionine","type":"exact"}],"termid":"MOD:01837"}


id: PBO:0004601
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"U3 snoRNP-associated protein Utp16 (predicted)","termid":"PBO:0004601"}


id: PBO:0085654
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Protein involved in mitochondrial function; interacts with Hsp82p and copurifies with Ipl1p; expression is copper responsive and downregulated in strains deleted for MAC1, a copper-responsive transcription factor; human homolog MYG1 complements yeast null mutant","termid":"PBO:0085654"}


id: MONDO:0017892
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal recessive myogenic arthrogryposis multiplex congenita is a rare inherited neuromuscular disease characterized by prenatal presentation (usually in the second trimester) of reduced fetal movements and abnormal positioning resulting in joint abnormalities that may involve both lower and upper extremities and is usually symmetric, severe hypotonia at birth with bilateral club foot, motor development delay, mild facial weakness without opthalmoplegia, absent deep tendon reflexes, normal motor and sensory nerve conduction velocities, no cerebellar or pyramidal involvement, and progressive disease course with loss of ambulation after the first decade of life.","definition_xrefs":["Orphanet:319332"],"direct_ancestors":[{"relation_name":"is_a","term_name":"arthrogryposis multiplex congenita","termid":"MONDO:0015168"},{"relation_name":"is_a","term_name":"congenital muscular dystrophy","termid":"MONDO:0019950"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005336"},{"rel_name":"is_a","termid":"MONDO:0002320"}],"interesting_parent_ids":["MONDO:0005336","MONDO:0002320"],"is_obsolete":false,"name":"autosomal recessive myogenic arthrogryposis multiplex congenita","secondary_identifiers":["GARD:17447","MEDGEN:1647450","SCTID:764812008","UMLS:C4707155"],"synonyms":[{"name":"SYNE1-related AMC","type":"exact"},{"name":"SYNE1-related arthrogryposis multiplex congenita","type":"exact"},{"name":"autosomal recessive myogenic AMC","type":"exact"}],"termid":"MONDO:0017892","xrefs":{"Monarch":{"xref_id":"0017892"}}}


id: MONDO:0013503
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any familial chronic mucocutaneous candidiasis in which the cause of the disease is a mutation in the IL17F gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chronic mucocutaneous candidiasis","termid":"MONDO:0015279"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093","MONDO:0005046"],"is_obsolete":false,"name":"candidiasis, familial, 6","secondary_identifiers":["MEDGEN:462755","UMLS:C3151405","OMIM:613956","GARD:15093"],"synonyms":[{"name":"CANDF6","type":"related"},{"name":"IL17F familial chronic mucocutaneous candidiasis","type":"exact"},{"name":"candidiasis, familial chronic mucocutaneous, autosomal dominant","type":"related"},{"name":"candidiasis, familial, 6","type":"exact"},{"name":"candidiasis, familial, 6, autosomal dominant","type":"exact"},{"name":"candidiasis, familial, type 6","type":"exact"},{"name":"familial chronic mucocutaneous candidiasis caused by mutation in IL17F","type":"exact"}],"termid":"MONDO:0013503","xrefs":{"Monarch":{"xref_id":"0013503"}}}


id: GO:0072197
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which the anatomical structures of the ureter are generated and organized. The ureter is a muscular tube that transports urine from the kidney to the urinary bladder.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"animal organ morphogenesis","termid":"GO:0009887"},{"relation_name":"is_a","term_name":"tube morphogenesis","termid":"GO:0035239"},{"relation_name":"part_of","term_name":"ureter development","termid":"GO:0072189"}],"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":"ureter morphogenesis","termid":"GO:0072197"}


id: PBO:0053494
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 472","termid":"PBO:0053494"}


id: PBO:0047385
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"F-box protein 22","termid":"PBO:0047385"}


id: PBO:0005650
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cAMP-specific phosphodiesterase Cgs2","termid":"PBO:0005650"}


id: MONDO:0019518
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Waardenburg-Shah syndrome (WSS) is a neurocristopathy characterized by the association of Waardenburg syndrome (sensorineural hearing loss and pigmentary abnormalities) and Hirschsprung disease.","definition_xrefs":["Orphanet:897"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"eye disorder","termid":"MONDO:0005328"},{"relation_name":"excluded_subClassOf","term_name":"hypopigmentation of the skin","termid":"MONDO:0019290"},{"relation_name":"is_a","term_name":"Waardenburg syndrome","termid":"MONDO:0018094"},{"relation_name":"is_a","term_name":"intestinal motility disease","termid":"MONDO:0021189"},{"relation_name":"is_a","term_name":"neurocristopathy","termid":"MONDO:0021635"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0000426"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0000426"],"is_obsolete":false,"name":"Waardenburg-Shah syndrome","secondary_identifiers":["icd11.foundation:1420151003","NCIT:C124842","GARD:5524"],"synonyms":[{"name":"Hirschsprung disease with pigmentary anomaly","type":"related"},{"name":"Shah-Waardenburg syndrome","type":"exact"},{"name":"WS4","type":"exact"},{"name":"Waardenburg syndrome type 4","type":"exact"},{"name":"Waardenburg syndrome type IV","type":"exact"},{"name":"Waardenburg-Hirschsprung disease","type":"related"},{"name":"Waardenburg-Hirschsprung syndrome","type":"exact"},{"name":"Waardenburg-Shah syndrome","type":"exact"}],"termid":"MONDO:0019518","xrefs":{"Monarch":{"xref_id":"0019518"}}}


id: PBO:0039759
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"APPBP2 divergent transcript","termid":"PBO:0039759"}


id: GO:0075004
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The attachment of a spore of the symbiont to its host via adhesion molecules, general stickiness etc. The host is defined as the larger of the organisms involved in a symbiotic interaction.","definition_xrefs":["GOC:pamgo_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"adhesion of symbiont to host cell","termid":"GO:0044650"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"adhesion of symbiont spore to host","synonyms":[{"name":"adhesion of symbiont spore to host during symbiotic interaction","type":"exact"}],"termid":"GO:0075004"}


id: PR:O59730
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A methionine aminopeptidase 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO03371","PRO:DNx","PANTHER:PTHR10804:SF13"],"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":"methionine aminopeptidase 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC3E7.10","secondary_identifiers":["UniProtKB:O59730"],"synonyms":[{"name":"MAP 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"MetAP 1 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-METAP1","type":"exact"},{"name":"peptidase M 1 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:O59730"}


id: GO:0002161
data:
  {"annotated_genes":["SJAG_04738","SJAG_00443","SJAG_02015","SJAG_04285","SJAG_02428","SJAG_03545","SJAG_01797","SJAG_01248","SJAG_01259"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[57338,57642,59405,64640,65422,68433,77763],"is_not":false,"summary":null,"term":"GO:0002161"},{"annotations":[107890],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0043907"},{"annotations":[75473],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051500"},{"annotations":[102410],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0106026"}]},"cv_name":"molecular_function","definition":"The hydrolysis of an incorrectly aminoacylated tRNA.","definition_xrefs":["PMID:16087889","PMID:14663147","GOC:hjd"],"direct_ancestors":[{"relation_name":"is_a","term_name":"catalytic activity, acting on a tRNA","termid":"GO:0140101"}],"gene_count":9,"genes_by_uniquename":{"SJAG_00443":null,"SJAG_01248":null,"SJAG_01259":null,"SJAG_01797":null,"SJAG_02015":null,"SJAG_02428":null,"SJAG_03545":null,"SJAG_04285":null,"SJAG_04738":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0003674","GO:0140098","GO:0003824","GO:0140101"],"is_obsolete":false,"name":"aminoacyl-tRNA deacylase activity","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"amino acid proofreading activity","type":"related"},{"name":"aminoacyl-tRNA hydrolysis activity","type":"related"}],"termid":"GO:0002161","terms_by_termid":{"GO:0002161":null,"GO:0043907":null,"GO:0051500":null,"GO:0106026":null}}


id: PBO:0045037
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"dispatched RND transporter family member 2","termid":"PBO:0045037"}


id: MONDO:0006208
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A serous adenocarcinoma that arises from the fallopian tube. It is usually a high grade invasive adenocarcinoma.","definition_xrefs":["NCIT:C40099"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fallopian tube adenocarcinoma","termid":"MONDO:0002746"},{"relation_name":"is_a","term_name":"serous adenocarcinoma","termid":"MONDO:0005278"}],"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":"fallopian tube serous adenocarcinoma","secondary_identifiers":["MEDGEN:274490","DOID:5598","EFO:1000253","UMLS:C1517124"],"synonyms":[{"name":"fallopian tube serous adenocarcinoma","type":"exact"}],"termid":"MONDO:0006208","xrefs":{"Monarch":{"xref_id":"0006208"}}}


id: PBO:0044243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cutC copper transporter","termid":"PBO:0044243"}


id: GO:0048057
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the R3 and R4 pair of photoreceptors in the eye over time, from their formation to the mature structures. R3 and R4 are paired photoreceptors that contribute to the outer rhabdomeres. An example of this process is found in Drosophila melanogaster.","definition_xrefs":["GOC:jid"],"direct_ancestors":[{"relation_name":"is_a","term_name":"compound eye photoreceptor development","termid":"GO:0042051"},{"relation_name":"part_of","term_name":"R3/R4 cell differentiation","termid":"GO:0048056"}],"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":"R3/R4 development","termid":"GO:0048057"}


id: MONDO:0012258
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A basal subtype of epidermolysis bullosa simplex (EBS) characterized by belt-like areas of erythema with multiple vesicles and small blisters at the advancing edge of erythema.","definition_xrefs":["Orphanet:158681"],"direct_ancestors":[{"relation_name":"is_a","term_name":"epidermolysis bullosa simplex","termid":"MONDO:0017610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005093"}],"interesting_parent_ids":["MONDO:0005093"],"is_obsolete":false,"name":"epidermolysis bullosa simplex 2E, with migratory circinate erythema","secondary_identifiers":["MEDGEN:324475","GARD:16990","OMIM:609352","SCTID:716700003","UMLS:C1836284","MESH:C563730"],"synonyms":[{"name":"EBS-migr","type":"exact"},{"name":"epidermolysis bullosa simplex 2E, with migratory circinate erythema","type":"exact"},{"name":"epidermolysis bullosa simplex with migratory circinate erythema","type":"exact"}],"termid":"MONDO:0012258","xrefs":{"Monarch":{"xref_id":"0012258"}}}


id: PBO:0078196
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"T cell receptor beta variable 5-6","termid":"PBO:0078196"}


id: MONDO:0015073
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the gallbladder.","definition_xrefs":["NCIT:C96918"],"direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system neuroendocrine tumor, grade 1/2","termid":"MONDO:0000386"},{"relation_name":"is_a","term_name":"extrahepatic bile duct neoplasm","termid":"MONDO:0021385"},{"relation_name":"is_a","term_name":"gallbladder neuroendocrine neoplasm","termid":"MONDO:0024502"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004335"},{"rel_name":"is_a","termid":"MONDO:0002515"}],"interesting_parent_ids":["MONDO:0004335","MONDO:0002515"],"is_obsolete":false,"name":"gallbladder neuroendocrine tumor, grade 1/2","secondary_identifiers":["Orphanet:100086","MEDGEN:474749","GARD:19761","UMLS:C3273116"],"synonyms":[{"name":"gallbladder NET","type":"exact"},{"name":"gallbladder neuroendocrine tumor","type":"exact"},{"name":"gallbladder neuroendocrine tumour","type":"exact"},{"name":"gallbladder well differentiated endocrine tumor","type":"exact"},{"name":"gallbladder well differentiated endocrine tumor/carcinoma","type":"exact"},{"name":"gallbladder well differentiated endocrine tumour","type":"exact"}],"termid":"MONDO:0015073","xrefs":{"Monarch":{"xref_id":"0015073"}}}


id: MONDO:0007943
data:
  {"annotated_genes":["SJAG_00504"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87094],"is_not":false,"summary":null,"term":"MONDO:0007943"}]},"cv_name":"mondo","definition":"Nager syndrome, also called Nager acrofacial dysostosis (NAFD) is a congenital malformation syndrome characterized by mandibulofacial dystosis (malar hypoplasia, micrognathia, external ear malformations) and variable preaxial limb defects.","definition_xrefs":["Orphanet:245"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"multiple congenital anomalies/dysmorphic syndrome without intellectual disability","termid":"MONDO:0015161"},{"relation_name":"is_a","term_name":"SF3B4-related acrofacial dysostosis","termid":"MONDO:0800483"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00504":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"Nager acrofacial dysostosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:35520007","GARD:498","MESH:C538184","MEDGEN:120519","UMLS:C0265245","NORD:1487","OMIM:154400","DOID:5768"],"synonyms":[{"name":"AFD","type":"related"},{"name":"AFD, Nager type","type":"related"},{"name":"AFD1","type":"related"},{"name":"NAFD","type":"exact"},{"name":"Nager Syndrome","type":"exact"},{"name":"Nager acrofacial dysostosis","type":"exact"},{"name":"Nager acrofacial dysostosis syndrome","type":"exact"},{"name":"Nager syndrome","type":"exact"},{"name":"acrofacial dysostosis 1, Nager type","type":"exact"},{"name":"mandibulofacial dysostosis with preaxial limb anomalies","type":"exact"},{"name":"mandibulofacial dysostosis, Treacher Collins type, with limb anomalies","type":"related"},{"name":"preaxial acrodysostosis","type":"exact"},{"name":"preaxial acrofacial dysostosis","type":"related"},{"name":"preaxial manibulofacial dysostosis","type":"related"},{"name":"split hand deformity-mandibulofacial dysostosis","type":"related"}],"termid":"MONDO:0007943","terms_by_termid":{"MONDO:0007943":null},"xrefs":{"Monarch":{"xref_id":"0007943"}}}


id: GO:0072220
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the metanephric descending thin limb over time, from its formation to the mature structure. The metanephric descending thin limb is a part of the metanephric loop of Henle situated just after the proximal straight tubule (S3). It extends to the tip of the metanephric loop of Henle.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"descending thin limb development","termid":"GO:0072022"},{"relation_name":"part_of","term_name":"metanephric loop of Henle development","termid":"GO:0072236"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"metanephric descending thin limb development","termid":"GO:0072220"}


id: GO:0015205
data:
  {"annotated_genes":["SJAG_02147","SJAG_04717","SJAG_04714","SJAG_03777"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[79954],"is_not":false,"summary":null,"term":"GO:0015205"},{"annotations":[114542],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015207"},{"annotations":[114543],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015208"},{"annotations":[97489],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0015505"},{"annotations":[81819],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0042907"}]},"cv_name":"molecular_function","definition":"Enables the transfer of a nucleobase, any nitrogenous base that is a constituent of a nucleoside, nucleotide, or nucleic acidfrom one side of a membrane to the other.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"transmembrane transporter activity","termid":"GO:0022857"}],"gene_count":4,"genes_by_uniquename":{"SJAG_02147":null,"SJAG_03777":null,"SJAG_04714":null,"SJAG_04717":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0005215"}],"interesting_parent_ids":["GO:0003674","GO:0005215","GO:0022857"],"is_obsolete":false,"name":"nucleobase transmembrane transporter activity","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"secondary_identifiers":["GO:0015392"],"termid":"GO:0015205","terms_by_termid":{"GO:0015205":null,"GO:0015207":null,"GO:0015208":null,"GO:0015505":null,"GO:0042907":null}}


id: GO:0036376
data:
  {"annotated_genes":["SJAG_01541"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[68470],"is_not":false,"summary":null,"term":"GO:0036376"}]},"cv_name":"biological_process","definition":"The directed movement of sodium ions from inside of a cell, across the plasma membrane and into the extracellular region.","definition_xrefs":["GOC:vw","PMID:14674689"],"direct_ancestors":[{"relation_name":"is_a","term_name":"sodium ion transmembrane transport","termid":"GO:0035725"},{"relation_name":"is_a","term_name":"export across plasma membrane","termid":"GO:0140115"}],"gene_count":1,"genes_by_uniquename":{"SJAG_01541":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0051179"},{"rel_name":"is_a","termid":"GO:0055085"},{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0006810","GO:0055085","GO:0008150","GO:0051179"],"is_obsolete":false,"name":"sodium ion export across plasma membrane","references_by_uniquename":{"GO_REF:0000002":null},"secondary_identifiers":["GO:0071436","GO:0098667"],"synonyms":[{"name":"sodium export","type":"related"},{"name":"sodium ion export","type":"related"},{"name":"sodium ion export from cell","type":"exact"}],"termid":"GO:0036376","terms_by_termid":{"GO:0036376":null}}


id: PBO:0089615
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"post-Golgi vesicle-mediated transport protein Avl9","termid":"PBO:0089615"}


id: MONDO:0859146
data:
  {"annotated_genes":["SJAG_02461"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88441],"is_not":false,"summary":null,"term":"MONDO:0859146"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_02461":null},"genotype_count":0,"is_obsolete":false,"name":"growth restriction, hypoplastic kidneys, alopecia, and distinctive facies","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:1784590","OMIM:619321","UMLS:C5543375"],"termid":"MONDO:0859146","terms_by_termid":{"MONDO:0859146":null},"xrefs":{"Monarch":{"xref_id":"0859146"}}}


id: PBO:0034526
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-decreased_mitotic_recombination_at_hotspot","termid":"PBO:0034526"}


id: MONDO:1012274
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"thrombopathia, non-human animal","termid":"MONDO:1011695"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombopathia, pig","secondary_identifiers":["OMIA:001003-9823"],"termid":"MONDO:1012274","xrefs":{"Monarch":{"xref_id":"1012274"}}}


id: PBO:0074834
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"small nucleolar RNA, C/D box 29","termid":"PBO:0074834"}


id: PR:O94726
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An ER degradation-enhancing alpha-mannosidase-like protein 1 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["PRO:DNx","PANTHER:PTHR11742:SF11"],"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":"ER degradation-enhancing alpha-mannosidase-like protein 1 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC23A1.04c","secondary_identifiers":["UniProtKB:O94726"],"synonyms":[{"name":"SPAC23A1.04c","type":"related"},{"name":"Spom972h-EDEM1","type":"exact"}],"termid":"PR:O94726"}


id: PBO:0034038
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-has_plasma_membrane_part","termid":"PBO:0034038"}


id: GO:0120141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of the activity of any ecdysone receptor signaling pathway.","definition_xrefs":["GOC:ha","PMID:23072462"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of intracellular steroid hormone receptor signaling pathway","termid":"GO:0033143"},{"relation_name":"is_a","term_name":"regulation of cellular response to alcohol","termid":"GO:1905957"},{"relation_name":"regulates","term_name":"ecdysone receptor signaling pathway","termid":"GO:0035076"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"regulation of ecdysone receptor signaling pathway","synonyms":[{"name":"regulation of ecdysone receptor-mediated signaling pathway","type":"exact"}],"termid":"GO:0120141"}


id: PBO:0038391
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-assayed_transcript","termid":"PBO:0038391"}


id: GO:0002701
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of the production of molecular mediator of immune response.","definition_xrefs":["GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of immune effector process","termid":"GO:0002698"},{"relation_name":"is_a","term_name":"regulation of production of molecular mediator of immune response","termid":"GO:0002700"},{"relation_name":"is_a","term_name":"negative regulation of gene expression","termid":"GO:0010629"},{"relation_name":"negatively_regulates","term_name":"production of molecular mediator of immune response","termid":"GO:0002440"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"negative regulation of production of molecular mediator of immune response","synonyms":[{"name":"down regulation of production of molecular mediator of immune response","type":"exact"},{"name":"down-regulation of production of molecular mediator of immune response","type":"exact"},{"name":"downregulation of production of molecular mediator of immune response","type":"exact"},{"name":"inhibition of production of molecular mediator of immune response","type":"narrow"}],"termid":"GO:0002701"}


id: MONDO:0030714
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"osteogenesis imperfecta","termid":"MONDO:0019019"}],"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":"osteogenesis imperfecta, IIA 22","secondary_identifiers":["MEDGEN:1801631","UMLS:C5676943","OMIM:619795"],"synonyms":[{"name":"OI22","type":"exact"},{"name":"osteogenesis imperfecta, IIA 22","type":"exact"}],"termid":"MONDO:0030714","xrefs":{"Monarch":{"xref_id":"0030714"}}}


id: PBO:0075547
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPECC1 pseudogene 1","termid":"PBO:0075547"}


id: PBO:0051168
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 3-52 (pseudogene)","termid":"PBO:0051168"}


id: PBO:0049533
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"H2A.Z histone pseudogene 4","termid":"PBO:0049533"}


id: MONDO:0001840
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","gene_count":0,"genotype_count":0,"name":"obsolete schistosomiasis (obsolete MONDO:0001840)","termid":"MONDO:0001840","xrefs":{"Monarch":{"xref_id":"0001840"}}}


id: FYPO:0000191
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A regulation phenotype observed in the vegetative growth phase of the life cycle in which regulation of the establishment or maintenance of cell polarity is abnormal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation phenotype during vegetative growth","termid":"FYPO:0001334"},{"relation_name":"is_a","term_name":"abnormal cellular process during vegetative growth","termid":"FYPO:0001362"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0005447","FYPO:0001985","FYPO:0001320"],"is_obsolete":false,"name":"abnormal regulation of establishment or maintenance of cell polarity","synonyms":[{"name":"abnormal regulation of establishment or maintenance of cell polarity during mitotic cell cycle","type":"related"},{"name":"abnormal regulation of establishment or maintenance of cell polarity during vegetative growth","type":"exact"}],"termid":"FYPO:0000191"}


id: MONDO:0012871
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any Jervell and Lange-Nielsen syndrome in which the cause of the disease is a mutation in the KCNE1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Jervell and Lange-Nielsen syndrome","termid":"MONDO:0002441"},{"relation_name":"is_a","term_name":"long QT syndrome 5","termid":"MONDO:0013372"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267"],"is_obsolete":false,"name":"Jervell and Lange-Nielsen syndrome 2","secondary_identifiers":["OMIM:612347","MEDGEN:394108","GARD:10364","UMLS:C2676723","MESH:C567343"],"synonyms":[{"name":"JLNS2","type":"related"},{"name":"Jervell and Lange-Nielsen syndrome 2","type":"exact"},{"name":"Jervell and Lange-Nielsen syndrome caused by mutation in KCNE1","type":"exact"},{"name":"Jervell and Lange-Nielsen syndrome type 2","type":"exact"},{"name":"KCNE1 Jervell and Lange-Nielsen syndrome","type":"exact"}],"termid":"MONDO:0012871","xrefs":{"Monarch":{"xref_id":"0012871"}}}


id: MONDO:0012542
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"psoriasis, susceptibility to","termid":"MONDO:0100171"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"psoriasis 8, susceptibility to","secondary_identifiers":["UMLS:C1853143","DOID:0111288","MEDGEN:377839","OMIM:610707"],"synonyms":[{"name":"PSORS8","type":"exact"},{"name":"psoriasis 8, susceptibility to","type":"exact"},{"name":"psoriasis susceptibility 8","type":"exact"}],"termid":"MONDO:0012542","xrefs":{"Monarch":{"xref_id":"0012542"}}}


id: GO:0010540
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The unidirectional movement of auxin from the apex to base of an organ, including the shoot, leaf, primary root, or lateral root.","definition_xrefs":["PMID:10677441"],"direct_ancestors":[{"relation_name":"is_a","term_name":"auxin polar transport","termid":"GO:0009926"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0006810"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0051179"}],"interesting_parent_ids":["GO:0008150","GO:0006810","GO:0051179"],"is_obsolete":false,"name":"basipetal auxin transport","termid":"GO:0010540"}


id: PBO:0003069
data:
  {"annotation_feature_type":"gene","cv_name":"DNA_binding_specificity","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"binds rDIS 5'-AGGTAAGGGTAATGCAC-3'","termid":"PBO:0003069"}


id: GO:0035079
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The decondensing (loosening) and swelling of the chromosomal sites of target genes on polytene chromosomes following response to a stimulus, to facilitate sudden bursts of transcriptional activity in response to transient environmental signals.","definition_xrefs":["GOC:bf","PMID:12543962"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chromosome organization","termid":"GO:0051276"}],"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":"polytene chromosome puffing","termid":"GO:0035079"}


id: PBO:0056778
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"methyltransferase like 27","termid":"PBO:0056778"}


id: MONDO:0023138
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":"Feingold trainer syndrome","secondary_identifiers":["MEDGEN:419341","MESH:C536179","UMLS:C2931126"],"synonyms":[{"name":"unusual facies, cleft palate, short stature, and intellectual disability","type":"related"},{"name":"unusual facies, cleft palate, short stature, and mental retardation","type":"related"}],"termid":"MONDO:0023138","xrefs":{"Monarch":{"xref_id":"0023138"}}}


id: PR:P78797
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPCC70.10 gene.","definition_xrefs":["PRO:DNx","UniProtKB:P78797"],"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 proline-rich protein C70.10 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPCC70.10","synonyms":[{"name":"Spom972h-SPCC70.10","type":"exact"}],"termid":"PR:P78797"}


id: PR:Q9C113
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- SPAC1F8.08 gene.","definition_xrefs":["PRO:DNx","UniProtKB:Q9C113"],"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 C1F8.08 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC1F8.08","synonyms":[{"name":"Spom972h-SPAC1F8.08","type":"exact"}],"termid":"PR:Q9C113"}


id: MONDO:0014551
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"short stature with nonspecific skeletal abnormalities","termid":"MONDO:0975810"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"short stature with nonspecific skeletal abnormalities 1","secondary_identifiers":["OMIM:616255"],"synonyms":[{"name":"SNSK","type":"exact"},{"name":"short stature with nonspecific skeletal abnormalities 1","type":"exact"}],"termid":"MONDO:0014551","xrefs":{"Monarch":{"xref_id":"0014551"}}}


id: MONDO:0008889
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare inflammatory non-necrotizing vascular disease affecting the small- and medium-sized arteries and veins of the upper and lower extremities characterized by endarteritis and vaso-occlusion due to occlusive thrombus development. The development and progression of the disease is consistently associated with exposure to tobacco.","definition_xrefs":["Orphanet:36258"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"obsolete secondary glomerular disease (obsolete MONDO:0019724)","termid":"MONDO:0019724"},{"relation_name":"is_a","term_name":"peripheral vascular disease","termid":"MONDO:0005294"},{"relation_name":"is_a","term_name":"inflammatory disease","termid":"MONDO:0021166"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thromboangiitis obliterans","secondary_identifiers":["NCIT:C35070","UMLS:C0040021","DOID:12918","ICD10CM:I73.1","GARD:5969","NANDO:1200266","icd11.foundation:1000683110","MedDRA:10043540","OMIM:211480","MESH:D013919","NORD:880","MEDGEN:21531","SCTID:52403007","EFO:1001211","ICD9:443.1"],"synonyms":[{"name":"BUERGER disease","type":"related"},{"name":"Buerger's Disease","type":"exact"},{"name":"Buerger's disease","type":"exact"},{"name":"TAO","type":"related"},{"name":"inflammatory occlusive peripheral vascular disease","type":"related"},{"name":"occlusive peripheral vascular disease","type":"related"},{"name":"presenile gangrene","type":"exact"},{"name":"thromboangiitis obliterans","type":"exact"},{"name":"thromboangiitis obliterans [Buerger's disease]","type":"exact"}],"termid":"MONDO:0008889","xrefs":{"Monarch":{"xref_id":"0008889"}}}


id: MONDO:0008742
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Autosomal dominant form of severe congenital neutropenia.","definition_xrefs":["MONDO:patterns/autosomal_dominant"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autosomal dominant disease","termid":"MONDO:0000426"},{"relation_name":"is_a","term_name":"severe congenital neutropenia","termid":"MONDO:0018542"}],"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:0000426"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0000426","MONDO:0005570"],"is_obsolete":false,"name":"autosomal dominant severe congenital neutropenia","secondary_identifiers":["DOID:0112130","NCIT:C166155","MEDGEN:1665322","GARD:9558","Orphanet:486","UMLS:C4749612"],"synonyms":[{"name":"severe congenital neutropenia autosomal dominant","type":"related"},{"name":"severe congenital neutropenia, autosomal dominant","type":"exact"}],"termid":"MONDO:0008742","xrefs":{"Monarch":{"xref_id":"0008742"}}}


id: PBO:0052412
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"killer cell immunoglobulin like receptor, three Ig domains and long cytoplasmic tail 1","termid":"PBO:0052412"}


id: PBO:0028630
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abolished_U6_2'-O-snRNA_methylation_at_residue_A41","termid":"PBO:0028630"}


id: PBO:0063215
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"propionyl-CoA carboxylase subunit beta","termid":"PBO:0063215"}


id: MONDO:1010886
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any neuronal ceroid lipofuscinosis that occurs in pigs due to a mutation in the TPP1 gene created using gene editing.","definition_xrefs":["OMIA:001472-9823"],"direct_ancestors":[{"relation_name":"is_a","term_name":"neuronal ceroid lipofuscinosis, pig","termid":"MONDO:1011577"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neuronal ceroid lipofuscinosis, TPP1-related, pig","synonyms":[{"name":"neuronal ceroid lipofuscinosis, 2, pig","type":"related"}],"termid":"MONDO:1010886","xrefs":{"Monarch":{"xref_id":"1010886"}}}


id: PBO:0079223
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tetratricopeptide repeat domain 3","termid":"PBO:0079223"}


id: FYPO:0002250
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 inviable, is curved along the long axis, and in which vacuoles are more visible (usually by microscopy) than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"has_part","term_name":"vacuolated","termid":"FYPO:0001581"},{"relation_name":"is_a","term_name":"abnormal subcellular component during vegetative growth","termid":"FYPO:0001322"},{"relation_name":"is_a","term_name":"inviable curved vegetative cell","termid":"FYPO:0002113"}],"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:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0001985"},{"rel_name":"has_part","termid":"FYPO:0001320"},{"rel_name":"has_part","termid":"FYPO:0000004"},{"rel_name":"has_part","termid":"FYPO:0000005"},{"rel_name":"is_a","termid":"FYPO:0000005"}],"interesting_parent_ids":["FYPO:0000002","FYPO:0001320","FYPO:0001985","FYPO:0000005","FYPO:0000004"],"is_obsolete":false,"name":"inviable curved vacuolated vegetative cell","synonyms":[{"name":"inviable curved vacuolated cell during vegetative growth","type":"exact"},{"name":"inviable curved vacuolated vegetative cell during mitotic cell cycle","type":"related"},{"name":"lethal; curved vacuolated vegetative cell","type":"exact"}],"termid":"FYPO:0002250"}


id: PBO:0017541
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial iron ion transmembrane transporter (predicted)","termid":"PBO:0017541"}


id: PBO:0078943
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Arg (anticodon TCG) 1-1","termid":"PBO:0078943"}


id: GO:1900565
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the breakdown of chanoclavine-I.","definition_xrefs":["GOC:di","GOC:TermGenie"],"gene_count":0,"genotype_count":0,"name":"obsolete chanoclavine-I catabolic process (obsolete GO:1900565)","synonyms":[{"name":"chanoclavine-I breakdown","type":"exact"},{"name":"chanoclavine-I catabolism","type":"exact"},{"name":"chanoclavine-I degradation","type":"exact"}],"termid":"GO:1900565"}


id: PBO:0088079
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Ubiquitin (Ub) chain assembly factor (E4); forms branched Ub chains on substrates destined for degradation, catalyzing K48-linked multi-monoubiquitination of K29-linked Ub chains assembled by the Ub-ligase Ufd4p; involved in the Ub-fusion degradation pathway, OLE membrane fluidity pathway, stress response survival and the ERAD pathway for misfolded proteins, where it promotes ubiquitination and transfer of ERAD substrates to Rad23p; U-box family member; homologous to human Ufd2a and Ufd2b","termid":"PBO:0088079"}


id: MONDO:0005099
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A serious neurological disorder characterized by intracranial hemorrhage into the subarachnoid space.","definition_xrefs":["PMID:7807157","NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"brain disorder","termid":"MONDO:0005560"},{"relation_name":"is_a","term_name":"neurovascular disorder","termid":"MONDO:0043218"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"subarachnoid hemorrhage","secondary_identifiers":["UMLS:C0038525","SCTID:21454007","EFO:0000713","HP:0002138","MEDGEN:11625","ICD9:430","MESH:D013345"],"synonyms":[{"name":"subarachnoid haemorrhage (disease)","type":"exact"},{"name":"subarachnoid hemorrhage","type":"exact"},{"name":"subarachnoid hemorrhage (disease)","type":"exact"}],"termid":"MONDO:0005099","xrefs":{"Monarch":{"xref_id":"0005099"}}}


id: FYPO:0001582
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which vegetative cell population growth is normal (i.e. indistinguishable from wild type) in a medium containing glutathione.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal vegetative cell population growth","termid":"FYPO:0001357"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0002058"},{"rel_name":"is_a","termid":"FYPO:0002060"},{"rel_name":"is_a","termid":"FYPO:0000003"},{"rel_name":"is_a","termid":"FYPO:0000257"},{"rel_name":"is_a","termid":"FYPO:0000139"},{"rel_name":"is_a","termid":"FYPO:0002057"}],"interesting_parent_ids":["FYPO:0002060","FYPO:0000003","FYPO:0000257","FYPO:0000139","FYPO:0002057","FYPO:0002058"],"is_obsolete":false,"name":"normal growth on glutathione","synonyms":[{"name":"normal cell population growth in presence of glutathione","type":"exact"},{"name":"normal cell population growth on GSH","type":"exact"},{"name":"normal cell population growth on L-gamma-glutamyl-L-cysteinylglycine","type":"exact"},{"name":"normal cell population growth on glutathione","type":"exact"},{"name":"normal cell population growth on reduced glutathione","type":"exact"},{"name":"normal cellular response to glutathione","type":"related"},{"name":"normal vegetative cell population growth on glutathione","type":"exact"}],"termid":"FYPO:0001582"}


id: PBO:0048179
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"alpha glucosidase","termid":"PBO:0048179"}


id: PBO:0081180
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"zymogen granule protein 16B","termid":"PBO:0081180"}


id: GO:0032730
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of interleukin-1 alpha production.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of interleukin-1 alpha production","termid":"GO:0032650"},{"relation_name":"is_a","term_name":"positive regulation of interleukin-1 production","termid":"GO:0032732"},{"relation_name":"positively_regulates","term_name":"interleukin-1 alpha production","termid":"GO:0032610"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"},{"rel_name":"regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0008150","GO:0010467"],"is_obsolete":false,"name":"positive regulation of interleukin-1 alpha production","secondary_identifiers":["GO:0050726","GO:0050717"],"synonyms":[{"name":"activation of interleukin-1 alpha production","type":"narrow"},{"name":"positive regulation of IL-1 alpha production","type":"exact"},{"name":"positive regulation of interleukin-1 alpha biosynthetic process","type":"narrow"},{"name":"positive regulation of interleukin-1 alpha secretion","type":"narrow"},{"name":"stimulation of interleukin-1 alpha production","type":"narrow"},{"name":"up regulation of interleukin-1 alpha production","type":"exact"},{"name":"up-regulation of interleukin-1 alpha production","type":"exact"},{"name":"upregulation of interleukin-1 alpha production","type":"exact"}],"termid":"GO:0032730"}


id: PBO:0074991
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 115-2","termid":"PBO:0074991"}


id: MOD:01769
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively converts an L-threonine residue to O-palmitoleyl-L-threonine.","definition_xrefs":["RESID:AA0079#var","OMSSA:188","PubMed:6642431","Unimod:431#T","PubMed:8413602"],"direct_ancestors":[{"relation_name":"is_a","term_name":"O-palmitoleylated residue","termid":"MOD:01768"},{"relation_name":"is_a","term_name":"O3-acylated L-threonine","termid":"MOD:02004"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MOD:01155"}],"interesting_parent_ids":["MOD:01155"],"is_obsolete":false,"name":"O-palmitoleyl-L-threonine","synonyms":[{"name":"(2S,3R)-2-amino-3-((Z)-9-hexadecenoyloxy)butanoic acid","type":"exact"},{"name":"L-threonine cis-9-hexadecenoate ester","type":"exact"},{"name":"O-palmitoleylated L-threonine","type":"exact"},{"name":"O3-palmitoleyl-threonine","type":"exact"},{"name":"Palmitoleyl","type":"related"},{"name":"mod188","type":"exact"},{"name":"palmitoleyl","type":"related"}],"termid":"MOD:01769"}


id: MONDO:1011666
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"digestive system disorder, non-human animal","termid":"MONDO:1011311"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"non-specific digestive disorder, non-human animal","secondary_identifiers":["OMIA:001768"],"termid":"MONDO:1011666","xrefs":{"Monarch":{"xref_id":"1011666"}}}


id: PBO:0076827
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"telomerase associated protein 1","termid":"PBO:0076827"}


id: FYPO:0002132
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A molecular function phenotype in which an interaction between a protein and RNA is abnormal. One of the relevant gene products may be encoded by the mutated gene, or both the RNA and protein may be encoded by genes other than the mutated one.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal molecular function","termid":"FYPO:0000707"},{"relation_name":"is_a","term_name":"protein-RNA interaction phenotype","termid":"FYPO:0002131"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000652"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0002131"},{"rel_name":"is_a","termid":"FYPO:0000707"}],"interesting_parent_ids":["FYPO:0002131","FYPO:0000707","FYPO:0000652","FYPO:0001985"],"is_obsolete":false,"name":"abnormal protein-RNA interaction","synonyms":[{"name":"abnormal RNA binding","type":"exact"},{"name":"abnormal RNA-protein interaction","type":"exact"}],"termid":"FYPO:0002132"}


id: SO:0001605
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A sequence variant within a CDS resulting in the gain of an amino acid to the resulting polypeptide.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"polypeptide_sequence_variant","termid":"SO:0001603"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amino_acid_insertion","synonyms":[{"name":"amino acid insertion","type":"exact"}],"termid":"SO:0001605"}


id: PBO:0051189
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin heavy variable 3/OR16-7 (pseudogene)","termid":"PBO:0051189"}


id: GO:0016575
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The modification of histones by removal of acetyl groups.","definition_xrefs":["GOC:ai"],"gene_count":0,"genotype_count":0,"name":"obsolete histone deacetylation (obsolete GO:0016575)","termid":"GO:0016575"}


id: PBO:0080807
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"X-ray repair cross complementing 3","termid":"PBO:0080807"}


id: GO:0046155
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The chemical reactions and pathways resulting in the breakdown of rhodopsin, a brilliant purplish-red, light-sensitive visual pigment found in the rod cells of the retinas.","definition_xrefs":["ISBN:0198506732"],"direct_ancestors":[{"relation_name":"is_a","term_name":"xanthophyll catabolic process","termid":"GO:0016124"},{"relation_name":"is_a","term_name":"protein catabolic process","termid":"GO:0030163"},{"relation_name":"is_a","term_name":"eye pigment catabolic process","termid":"GO:0046151"},{"relation_name":"is_a","term_name":"alcohol catabolic process","termid":"GO:0046164"},{"relation_name":"is_a","term_name":"tertiary alcohol metabolic process","termid":"GO:1902644"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0030163"},{"rel_name":"is_a","termid":"GO:0006629"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0030163","GO:0006629","GO:0008150","GO:0044281"],"is_obsolete":false,"name":"rhodopsin catabolic process","synonyms":[{"name":"rhodopsin breakdown","type":"exact"},{"name":"rhodopsin catabolism","type":"exact"},{"name":"rhodopsin degradation","type":"exact"}],"termid":"GO:0046155"}


id: PBO:0082624
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Component of both the SWI/SNF and RSC chromatin remodeling complexes; actin-related protein involved in transcriptional regulation","termid":"PBO:0082624"}


id: MONDO:0019628
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Rieger's anomaly is a congenital ocular defect caused by anterior segment dysgenesis and is characterized by severe anterior chamber deformity with prominent strands and marked atrophy of the iris stroma, with hole or pseudo-hole formation and corectopia. The term covers the association of these iris and pupil anomalies with the features of AxenfeldBs anomaly.","definition_xrefs":["Orphanet:91483"],"direct_ancestors":[{"relation_name":"is_a","term_name":"iridogoniodysgenesis","termid":"MONDO:0011119"}],"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":"Rieger anomaly","secondary_identifiers":["UMLS:C0265341","MedDRA:10059198","GARD:16482","MEDGEN:78558"],"termid":"MONDO:0019628","xrefs":{"Monarch":{"xref_id":"0019628"}}}


id: PBO:0044438
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 3","termid":"PBO:0044438"}


id: GO:0062022
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The ATP-dependent protein localization to chromatin by which a cohesin ring complex is topologically linked to ssDNA (lagging strand) which is already linked to a dsDNA (leading strand) molecule as part of the mitotic cell cycle.","definition_xrefs":["GOC:vw","PMID:29358048"],"gene_count":0,"genotype_count":0,"name":"obsolete mitotic cohesin ssDNA (lagging strand) loading (obsolete GO:0062022)","synonyms":[{"name":"second-DNA capture","type":"exact"}],"termid":"GO:0062022"}


id: PBO:0068311
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNF13 pseudogene 1","termid":"PBO:0068311"}


id: MONDO:0013097
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"glioma susceptibility","termid":"MONDO:0100242"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glioma susceptibility 8","secondary_identifiers":["MEDGEN:416601","UMLS:C2751637","OMIM:613033"],"synonyms":[{"name":"GLM8","type":"exact"},{"name":"glioma susceptibility 8","type":"exact"}],"termid":"MONDO:0013097","xrefs":{"Monarch":{"xref_id":"0013097"}}}


id: PR:Q9UUJ1
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"An actin-related protein 2 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO01984","PRO:DNx","PANTHER:PTHR11937:SF37"],"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":"actin-related protein 2 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPAC11H11.06","secondary_identifiers":["UniProtKB:Q9UUJ1"],"synonyms":[{"name":"Spom972h-ACTR2","type":"exact"},{"name":"actin-like protein 2 (Schizosaccharomyces pombe 972h-)","type":"exact"}],"termid":"PR:Q9UUJ1"}


id: GO:0009414
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 water deprivation stimulus, prolonged deprivation of water.","definition_xrefs":["GOC:lr"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to stress","termid":"GO:0006950"},{"relation_name":"is_a","term_name":"response to water","termid":"GO:0009415"}],"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 water deprivation","synonyms":[{"name":"drought tolerance","type":"related"},{"name":"response to dehydration","type":"exact"},{"name":"response to drought","type":"exact"},{"name":"response to thirst","type":"exact"}],"termid":"GO:0009414"}


id: SOFP:source
data:
  {"annotation_feature_type":"gene","cv_name":"feature_property","definition":"Source from which feature originates - may be a computer program or analysis, or a group. Corresponds to GFF column 2","direct_ancestors":[{"relation_name":"is_a","term_name":"feature_property","termid":"SOFP:feature_property"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"source","termid":"SOFP:source"}


id: PBO:0056963
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"microRNA 23a","termid":"PBO:0056963"}


id: MONDO:0002598
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A malignant germ cell tumor arising in the central nervous system. It is characterized by the presence of primitive, large malignant germ cells and lymphocytes.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"malignant germ cell tumor","termid":"MONDO:0006290"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"germinoma","secondary_identifiers":["DOID:3304","UMLS:C0206660","MESH:D018237","ICDO:9064/3","NCIT:C3753","ONCOTREE:GMN","MEDGEN:64626","HP:0100620"],"synonyms":[{"name":"germinoma","type":"exact"},{"name":"germinoma (disease)","type":"exact"}],"termid":"MONDO:0002598","xrefs":{"Monarch":{"xref_id":"0002598"}}}


id: PBO:0048477
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glucosaminyl (N-acetyl) transferase 1 pseudogene 4","termid":"PBO:0048477"}


id: GO:0018767
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: 2-hydroxy-6-oxo-7-methylocta-2,4-dienoate + H2O = cis-2-hydroxypenta-2,4-dienoate + isobutyrate.","definition_xrefs":["GOC:curators"],"gene_count":0,"genotype_count":0,"name":"obsolete 2-hydroxy-6-oxo-7-methylocta-2,4-dienoate hydrolase activity (obsolete GO:0018767)","termid":"GO:0018767"}


id: MONDO:0700235
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any retinopathy caused by variants in the RD3 gene.","direct_ancestors":[{"relation_name":"is_a","term_name":"inherited retinal dystrophy","termid":"MONDO:0019118"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005328"}],"interesting_parent_ids":["MONDO:0005328"],"is_obsolete":false,"name":"RD3-related retinopathy","synonyms":[{"name":"RD3-related retinopathy","type":"exact"}],"termid":"MONDO:0700235","xrefs":{"Monarch":{"xref_id":"0700235"}}}


id: FYPO:0004682
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 polyadenylated 5S rRNA measured in a cell is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal rRNA or precursor level","termid":"FYPO:0006000"}],"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 polyadenylated 5S rRNA level","synonyms":[{"name":"normal polyadenylated 5S rRNA accumulation","type":"related"},{"name":"normal polyadenylated 5S rRNA level during mitotic cell cycle","type":"related"},{"name":"normal polyadenylated 5S rRNA level during vegetative growth","type":"exact"},{"name":"normal polyadenylated 5S rRNA transcript level","type":"exact"}],"termid":"FYPO:0004682"}


id: GO:0022829
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Enables the energy-independent facilitated diffusion of propanediol through a large pore, un-gated channel. Examples include gap junctions, which transport substances from one cell to another; and porins which transport substances in and out of bacteria, mitochondria and chloroplasts.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport"],"direct_ancestors":[{"relation_name":"is_a","term_name":"channel activity","termid":"GO:0015267"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005215"},{"rel_name":"is_a","termid":"GO:0022857"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0022857","GO:0005215","GO:0003674"],"is_obsolete":false,"name":"wide pore channel activity","synonyms":[{"name":"gap junction activity","type":"narrow"},{"name":"non-gated, wide pore channel activity","type":"exact"}],"termid":"GO:0022829"}


id: SO:0002365
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A gene that codes for mitochondrial SSU rRNA.","direct_ancestors":[{"relation_name":"is_a","term_name":"mt_rRNA_gene","termid":"SO:0002363"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mt_SSU_rRNA_gene","synonyms":[{"name":"mitochondrial small subunit rRNA gene","type":"exact"}],"termid":"SO:0002365"}


id: PBO:0039950
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ARIH2 opposite strand lncRNA","termid":"PBO:0039950"}


id: MONDO:0004363
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare spinal tumor which is highly malignant and tends to be locally invasive of surrounding neural tissue. The tumor also tends to spread throughout the neuroaxis and is often rapidly progressive. Histologically the tumors are highly cellular with nuclear and cellular pleomorphism, endothelial proliferation, mitotic figures, and, often, necrosis. This tumor has a relatively poor prognosis. Clinical features may include pain followed by rapidly progressive neurologic deficits such as extremity weakness, sensory changes, spasticity, and incontinence. (From Innocenzi et al., Clin Neurol Neurosurg 1997 Feb;99(1):1-5)","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"spinal cord glioma","termid":"MONDO:0002542"},{"relation_name":"is_a","term_name":"spinal cord glioma","termid":"MONDO:0002542"},{"relation_name":"is_a","term_name":"adult glioblastoma","termid":"MONDO:0020690"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0004992"}],"interesting_parent_ids":["MONDO:0004992"],"is_obsolete":false,"name":"adult spinal cord glioblastoma","secondary_identifiers":["MEDGEN:107849","NCIT:C27183","UMLS:C0559185","SCTID:276829003","DOID:7806"],"synonyms":[{"name":"adult spinal cord glioblastoma","type":"exact"},{"name":"adult spinal cord glioblastoma multiforme","type":"exact"},{"name":"glioblastoma multiforme of spinal cord","type":"exact"}],"termid":"MONDO:0004363","xrefs":{"Monarch":{"xref_id":"0004363"}}}


id: FYPO:0008367
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 duration of heterochromatin maintenance is shorter than normal in the context of chromatin silencing at silent mating type cassettes.","definition_xrefs":["PomBase:vw"],"direct_ancestors":[{"relation_name":"is_a","term_name":"decreased duration of heterochromatin maintenance","termid":"FYPO:0008366"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0000641"},{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0005447"},{"rel_name":"is_a","termid":"FYPO:0001320"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0001985","FYPO:0000641","FYPO:0005447","FYPO:0000002"],"is_obsolete":false,"name":"decreased duration of heterochromatin maintenance involved in chromatin silencing at silent mating type cassette","termid":"FYPO:0008367"}


id: PBO:0048767
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"glia maturation factor beta","termid":"PBO:0048767"}


id: PBO:0059948
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MT-ND2 pseudogene 34","termid":"PBO:0059948"}


id: MONDO:0014949
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the FGF12 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"undetermined early-onset epileptic encephalopathy","termid":"MONDO:0018614"},{"relation_name":"is_a","term_name":"neonatal-onset developmental and epileptic encephalopathy","termid":"MONDO:0100455"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0700092"},{"rel_name":"is_a","termid":"MONDO:0004736"},{"rel_name":"is_a","termid":"MONDO:0005066"},{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0700092","MONDO:0004736","MONDO:0005027","MONDO:0005066"],"is_obsolete":false,"name":"developmental and epileptic encephalopathy, 47","secondary_identifiers":["DOID:0080425","OMIM:617166","GARD:16206","MEDGEN:934652","UMLS:C4310685"],"synonyms":[{"name":"DEE47","type":"exact"},{"name":"EIEE47","type":"exact"},{"name":"FGF12 early infantile epileptic encephalopathy","type":"exact"},{"name":"developmental and epileptic encephalopathy 47","type":"exact"},{"name":"early infantile epileptic encephalopathy caused by mutation in FGF12","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 47","type":"exact"},{"name":"epileptic encephalopathy, early infantile, 47; EIEE47","type":"exact"},{"name":"epileptic encephalopathy, early infantile, type 47","type":"exact"}],"termid":"MONDO:0014949","xrefs":{"Monarch":{"xref_id":"0014949"}}}


id: PBO:0003072
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fructose-1,6-bisphosphatase Fbp1","termid":"PBO:0003072"}


id: PBO:0053470
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 434","termid":"PBO:0053470"}


id: PBO:0114213
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial matrix protease Sdd3","termid":"PBO:0114213"}


id: PBO:0062477
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 H member 1 pseudogene","termid":"PBO:0062477"}


id: GO:0006378
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The enzymatic addition of a sequence of 40-200 adenylyl residues at the 3' end of a eukaryotic mRNA primary transcript.","definition_xrefs":["ISBN:0198506732"],"gene_count":0,"genotype_count":0,"name":"obsolete mRNA polyadenylation (obsolete GO:0006378)","termid":"GO:0006378"}


id: PBO:0110500
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"STMN3 pseudogene 1","termid":"PBO:0110500"}


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


id: GO:0040021
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The determination of sex and sexual phenotype in the germ line of a hermaphrodite.","definition_xrefs":["GOC:ems"],"direct_ancestors":[{"relation_name":"is_a","term_name":"germ-line sex determination","termid":"GO:0018992"}],"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":"hermaphrodite germ-line sex determination","secondary_identifiers":["GO:0042005"],"termid":"GO:0040021"}


id: PBO:0047616
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"fin bud initiation factor homolog","termid":"PBO:0047616"}


id: PBO:0120010
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TENM2 antisense RNA 1","termid":"PBO:0120010"}


id: PBO:0077011
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"THBS1 antisense RNA 1","termid":"PBO:0077011"}


id: PBO:0068482
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U1 small nuclear 63, pseudogene","termid":"PBO:0068482"}


id: PBO:0078394
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tRNA-Phe (anticodon GAA) 4-1","termid":"PBO:0078394"}


id: MONDO:0003202
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"leukocyte disorder","termid":"MONDO:0004805"},{"relation_name":"is_a","term_name":"pituitary adenocarcinoma","termid":"MONDO:0017582"}],"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":"pituitary gland basophilic carcinoma","secondary_identifiers":["NCIT:C27392","MEDGEN:352901","UMLS:C1704778","DOID:4915"],"synonyms":[{"name":"basophil adenocarcinoma","type":"exact"},{"name":"basophil carcinoma","type":"exact"},{"name":"basophil carcinoma (morphologic abnormality)","type":"exact"},{"name":"basophilic carcinoma","type":"related"},{"name":"pituitary gland basophil carcinoma","type":"exact"}],"termid":"MONDO:0003202","xrefs":{"Monarch":{"xref_id":"0003202"}}}


id: PBO:0071359
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ribosomal protein L29 pseudogene 18","termid":"PBO:0071359"}


id: MONDO:0015150
data:
  {"annotated_genes":["SJAG_04292","SJAG_04537","SJAG_04506","SJAG_00199","SJAG_00660","SJAG_01537","SJAG_03320","SJAG_04145","SJAG_00308","SJAG_00773","SJAG_04123","SJAG_01854","SJAG_04757","SJAG_04110","SJAG_02306","SJAG_03457","SJAG_03866"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[86917,86916],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014702"},{"annotations":[88933,88932],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014975"},{"annotations":[89205],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030669"},{"annotations":[87352],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014567"},{"annotations":[87567],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009748"},{"annotations":[87092],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0010043"},{"annotations":[88230],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012787"},{"annotations":[87202,87200,87201],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014018"},{"annotations":[87199],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014020"},{"annotations":[87559],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014305"},{"annotations":[87029],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014644"},{"annotations":[88410,88409],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011006"},{"annotations":[87013],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014679"},{"annotations":[88669],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0012651"},{"annotations":[87959],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030482"},{"annotations":[88005],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0030512"}]},"cv_name":"mondo","definition":"A hereditary spastic paraplegia that is part of a larger syndrome.","definition_xrefs":["MONDO:patterns/syndromic"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic disease","termid":"MONDO:0002254"},{"relation_name":"is_a","term_name":"hereditary spastic paraplegia","termid":"MONDO:0019064"}],"gene_count":17,"genes_by_uniquename":{"SJAG_00199":null,"SJAG_00308":null,"SJAG_00660":null,"SJAG_00773":null,"SJAG_01537":null,"SJAG_01854":null,"SJAG_02306":null,"SJAG_03320":null,"SJAG_03457":null,"SJAG_03866":null,"SJAG_04110":null,"SJAG_04123":null,"SJAG_04145":null,"SJAG_04292":null,"SJAG_04506":null,"SJAG_04537":null,"SJAG_04757":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"complex hereditary spastic paraplegia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:230261006","MEDGEN:581446","NANDO:1200054","GARD:19823","UMLS:C0393556","Orphanet:102013"],"synonyms":[{"name":"Complex HSP","type":"exact"},{"name":"Complex SPG","type":"exact"},{"name":"Complex familial spastic paraplegia","type":"exact"},{"name":"complicated HSP","type":"exact"},{"name":"complicated SPG","type":"exact"},{"name":"complicated familial spastic paraplegia","type":"exact"},{"name":"complicated hereditary spastic paraplegia","type":"exact"},{"name":"syndrome associated with hereditary spastic paraplegia","type":"exact"},{"name":"syndromic hereditary spastic paraplegia","type":"exact"}],"termid":"MONDO:0015150","terms_by_termid":{"MONDO:0009748":null,"MONDO:0010043":null,"MONDO:0011006":null,"MONDO:0012651":null,"MONDO:0012787":null,"MONDO:0014018":null,"MONDO:0014020":null,"MONDO:0014305":null,"MONDO:0014567":null,"MONDO:0014644":null,"MONDO:0014679":null,"MONDO:0014702":null,"MONDO:0014975":null,"MONDO:0030482":null,"MONDO:0030512":null,"MONDO:0030669":null},"xrefs":{"Monarch":{"xref_id":"0015150"}}}


id: PBO:0002230
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"translationally controlled tumor protein homolog (predicted)","termid":"PBO:0002230"}


id: PBO:0068850
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, U6 small nuclear 88, pseudogene","termid":"PBO:0068850"}


id: MONDO:0005333
data:
  {"annotated_genes":["SJAG_04300"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88420],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007785"}]},"cv_name":"mondo","definition":"Abnormally elevated thyroxine level in the blood.","definition_xrefs":["EFO:0004127"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thyroid gland disorder","termid":"MONDO:0003240"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04300":null},"genotype_count":0,"is_obsolete":false,"name":"hyperthyroxinemia","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C0020551","MESH:D006981","MEDGEN:6973","HGNC:399","DOID:2855"],"termid":"MONDO:0005333","terms_by_termid":{"MONDO:0007785":null},"xrefs":{"Monarch":{"xref_id":"0005333"}}}


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


id: PBO:0055086
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 2504","termid":"PBO:0055086"}


id: PBO:0074675
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 59B","termid":"PBO:0074675"}


id: MONDO:0013963
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the CABP2 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"},{"rel_name":"is_a","termid":"MONDO:0019497"}],"interesting_parent_ids":["MONDO:0019497","MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 93","secondary_identifiers":["GARD:22645","MEDGEN:854875","DOID:0110537","UMLS:C3888355","OMIM:614899"],"synonyms":[{"name":"CABP2 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"DFNB93","type":"narrow"},{"name":"autosomal recessive deafness 93","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 93","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in CABP2","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 93","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 93","type":"exact"},{"name":"deafness, autosomal recessive 93","type":"narrow"},{"name":"deafness, autosomal recessive type 93","type":"narrow"}],"termid":"MONDO:0013963","xrefs":{"Monarch":{"xref_id":"0013963"}}}


id: GO:0072399
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"A process that occurs in response to signals generated as a result of cytokinesis checkpoint signaling.","definition_xrefs":["GOC:mtg_cell_cycle"],"direct_ancestors":[{"relation_name":"is_a","term_name":"response to cell cycle checkpoint signaling","termid":"GO:0072396"}],"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 cytokinesis checkpoint signaling","secondary_identifiers":["GO:0072420"],"synonyms":[{"name":"cytokinesis checkpoint effector process","type":"exact"},{"name":"response to signal involved in cytokinesis checkpoint","type":"exact"}],"termid":"GO:0072399"}


id: PBO:0114434
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"S-adenosylmethionine sensor upstream of mTORC1","termid":"PBO:0114434"}


id: SO:0000425
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"The long terminal repeat found at the five-prime end of the sequence to be inserted into the host genome.","direct_ancestors":[{"relation_name":"is_a","term_name":"long_terminal_repeat","termid":"SO:0000286"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"five_prime_LTR","synonyms":[{"name":"5' LTR","type":"exact"},{"name":"5' long terminal repeat","type":"exact"},{"name":"five prime LTR","type":"exact"}],"termid":"SO:0000425"}


id: GO:0000720
data:
  {"annotated_genes":["SJAG_00500","SJAG_03613"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[118692,118693],"is_not":false,"summary":null,"term":"GO:0000720"}]},"cv_name":"biological_process","definition":"The repair of UV-induced T-T, C-T, and C-C dimers by the recognition and removal of the damaged DNA strand from the DNA helix as an oligonucleotide. The small gap left in the DNA helix is filled in by the sequential action of DNA polymerase and DNA ligase.","definition_xrefs":["GOC:elh"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nucleotide-excision repair","termid":"GO:0006289"},{"relation_name":"is_a","term_name":"pyrimidine dimer repair","termid":"GO:0006290"}],"gene_count":2,"genes_by_uniquename":{"SJAG_00500":null,"SJAG_03613":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0006281"},{"rel_name":"is_a","termid":"GO:0006259"}],"interesting_parent_ids":["GO:0006281","GO:0006259","GO:0008150"],"is_obsolete":false,"name":"pyrimidine dimer repair by nucleotide-excision repair","references_by_uniquename":{"GO_REF:0000107":null},"termid":"GO:0000720","terms_by_termid":{"GO:0000720":null}}


id: PBO:0079981
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"USP9Y pseudogene 19","termid":"PBO:0079981"}


id: MONDO:0019430
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"X-linked intellectual disability-ataxia-apraxia syndrome is characterized by ataxia, apraxia, intellectual deficit and/or seizures. It has been described in nine males in two unrelated Danish families. It is transmitted as an X-linked recessive syndrome with partial clinical expression in obligate female carriers.","definition_xrefs":["Orphanet:85338"],"direct_ancestors":[{"relation_name":"is_a","term_name":"X-linked cerebellar ataxia","termid":"MONDO:0016612"},{"relation_name":"is_a","term_name":"X-linked syndromic intellectual disability","termid":"MONDO:0020119"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005559"}],"interesting_parent_ids":["MONDO:0005559"],"is_obsolete":false,"name":"X-linked intellectual disability-ataxia-apraxia syndrome","secondary_identifiers":["UMLS:C4305139","GARD:19063","MEDGEN:930808"],"termid":"MONDO:0019430","xrefs":{"Monarch":{"xref_id":"0019430"}}}


id: GO:0097526
data:
  {"annotated_genes":["SJAG_04405","SJAG_02455","SJAG_02279","SJAG_03410","SJAG_01819","SJAG_03070","SJAG_01634","SJAG_03469","SJAG_02295","SJAG_03460","SJAG_04497","SJAG_04433","SJAG_05240","SJAG_00147","SJAG_01870","SJAG_04529","SJAG_04538","SJAG_00531","SJAG_04222","SJAG_01327","SJAG_00643","SJAG_03369","SJAG_00989","SJAG_02843","SJAG_01308","SJAG_00414","SJAG_03954","SJAG_02469","SJAG_01301","SJAG_02304"],"annotation_feature_type":"gene","cv_annotations":{"cellular_component":[{"annotations":[76186,64359,80263,95062,72363,118399,110510,113130,79223,99959,102589,77581,107796,112616,63128,72666,81860,73520,79456,79252,81219,97133,112051,80380,80772,79540,116857,78294,107841,74573],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0046540"}]},"cv_name":"cellular_component","definition":"A spliceosomal snRNP complex that is formed by the association of the U4/U6 (or U4atac/U6atac) snRNP with the U5 snRNP.","definition_xrefs":["GOC:krc","GOC:pr","ISBN:0879695897","PMID:9452384"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal snRNP complex","termid":"GO:0097525"}],"gene_count":30,"genes_by_uniquename":{"SJAG_00147":null,"SJAG_00414":null,"SJAG_00531":null,"SJAG_00643":null,"SJAG_00989":null,"SJAG_01301":null,"SJAG_01308":null,"SJAG_01327":null,"SJAG_01634":null,"SJAG_01819":null,"SJAG_01870":null,"SJAG_02279":null,"SJAG_02295":null,"SJAG_02304":null,"SJAG_02455":null,"SJAG_02469":null,"SJAG_02843":null,"SJAG_03070":null,"SJAG_03369":null,"SJAG_03410":null,"SJAG_03460":null,"SJAG_03469":null,"SJAG_03954":null,"SJAG_04222":null,"SJAG_04405":null,"SJAG_04433":null,"SJAG_04497":null,"SJAG_04529":null,"SJAG_04538":null,"SJAG_05240":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0005575"},{"rel_name":"is_a","termid":"GO:0032991"}],"interesting_parent_ids":["GO:0032991","GO:0005634","GO:0005575"],"is_obsolete":false,"name":"spliceosomal tri-snRNP complex","references_by_uniquename":{"GO_REF:0000002":null,"GO_REF:0000033":null,"GO_REF:0000104":null,"GO_REF:0000107":null},"termid":"GO:0097526","terms_by_termid":{"GO:0046540":null}}


id: GO:0071023
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A spliceosomal complex that forms during the addition of a specific spliced leader (SL) sequence to the 5'-end of a messenger RNA primary transcript, a process which occurs in a number of eukaryotic organisms, including trypanosomatid protozoans, euglenoids, nematodes, trematodes, and chordates.","definition_xrefs":["GOC:krc","ISBN:0879697393"],"direct_ancestors":[{"relation_name":"is_a","term_name":"spliceosomal complex","termid":"GO:0005681"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"part_of","termid":"GO:0005634"},{"rel_name":"is_a","termid":"GO:0032991"},{"rel_name":"is_a","termid":"GO:0005575"}],"interesting_parent_ids":["GO:0005575","GO:0005634","GO:0032991"],"is_obsolete":false,"name":"trans spliceosomal complex","termid":"GO:0071023"}


id: MONDO:0024325
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A glomangiomyoma that involves the zone of skin.","definition_xrefs":["MONDO:patterns/location"],"direct_ancestors":[{"relation_name":"is_a","term_name":"skin glomus tumor","termid":"MONDO:0002295"},{"relation_name":"is_a","term_name":"glomangiomyoma","termid":"MONDO:0024323"}],"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":"cutaneous glomangiomyoma","secondary_identifiers":["MEDGEN:698513","UMLS:C1275227","ICD9:227.6","SCTID:403971002"],"synonyms":[{"name":"glomangiomyoma of skin","type":"exact"},{"name":"zone of skin glomangiomyoma","type":"exact"}],"termid":"MONDO:0024325","xrefs":{"Monarch":{"xref_id":"0024325"}}}


id: MONDO:0009850
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"},{"relation_name":"is_a","term_name":"chronic periodontitis","termid":"MONDO:0005593"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"periodontitis, chronic, adult","secondary_identifiers":["MEDGEN:120593","SCTID:74797001","OMIM:260950","UMLS:C0266929"],"synonyms":[{"name":"periodontitis, adult","type":"broad"},{"name":"periodontitis, chronic","type":"broad"}],"termid":"MONDO:0009850","xrefs":{"Monarch":{"xref_id":"0009850"}}}


id: GO:0045067
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process of sparing extrathymically maturing T cells which react with self-MHC protein complexes with low affinity levels from apoptotic death.","definition_xrefs":["PMID:7880383","ISBN:0781735149"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive T cell selection","termid":"GO:0043368"},{"relation_name":"is_a","term_name":"extrathymic T cell selection","termid":"GO:0045062"}],"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 extrathymic T cell selection","synonyms":[{"name":"positive extrathymic T lymphocyte selection","type":"exact"},{"name":"positive extrathymic T-cell selection","type":"exact"},{"name":"positive extrathymic T-lymphocyte selection","type":"exact"}],"termid":"GO:0045067"}


id: FYPO:0002416
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"OBSOLETE. A cell population phenotype in which a cell undergoes one or a few rounds of cell division before cells die, resulting in the formation a colony that contains only a few inviable cells in which cell shape is altered and cell volume is larger than normal. Up to 6 rounds of cell division (generating 64 cells) may be observed, but 3 divisions or fewer is more typical.","definition_xrefs":["PomBase:vw","PomBase:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete inviable microcolony, swollen cells, abnormal cell shape (obsolete FYPO:0002416)","synonyms":[{"name":"inviable microcolonies swollen misshapen cells","type":"related"},{"name":"inviable microcolony, enlarged vegetative cells with abnormal cell shape","type":"related"},{"name":"inviable microcolony, large vegetative cells with abnormal cell shape","type":"related"},{"name":"inviable microcolony, vegetative cells with increased cell size and abnormal cell shape","type":"related"},{"name":"inviable microcolony, vegetative cells with increased cell volume and abnormal cell shape","type":"exact"}],"termid":"FYPO:0002416"}


id: GO:0140913
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The dissemination of mature viral particles from a host cell, caused by a virus hydrolyzing the peptidoglycan cell wall of the host organism. Peptidoglycans are any of a class of glycoconjugates found in bacterial cell walls.","definition_xrefs":["PMID:24585055","PMID:29495305","PMID:26085488"],"direct_ancestors":[{"relation_name":"is_a","term_name":"viral release from host cell by cytolysis","termid":"GO:0044659"}],"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 release via disruption of host peptidoglycan cell wall","termid":"GO:0140913"}


id: PBO:0117071
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PALB2 antisense RNA 1","termid":"PBO:0117071"}


id: PBO:0078098
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"trafficking protein particle complex subunit 6A","termid":"PBO:0078098"}


id: MONDO:0013119
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LOXHD1 gene.","definition_xrefs":["MONDO:patterns/disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hearing loss, autosomal recessive","termid":"MONDO:0019588"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0019497"},{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025","MONDO:0019497"],"is_obsolete":false,"name":"autosomal recessive nonsyndromic hearing loss 77","secondary_identifiers":["DOID:0110525","GARD:22631","MEDGEN:412541","MESH:C567543","OMIM:613079","UMLS:C2746083"],"synonyms":[{"name":"DFNB77","type":"narrow"},{"name":"LOXHD1 autosomal recessive nonsyndromic deafness","type":"narrow"},{"name":"autosomal recessive deafness 77","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness 77","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness caused by mutation in LOXHD1","type":"narrow"},{"name":"autosomal recessive nonsyndromic deafness type 77","type":"narrow"},{"name":"autosomal recessive nonsyndromic hearing loss 77","type":"exact"},{"name":"deafness, autosomal recessive 77","type":"narrow"},{"name":"deafness, autosomal recessive type 77","type":"narrow"}],"termid":"MONDO:0013119","xrefs":{"Monarch":{"xref_id":"0013119"}}}


id: PBO:0051455
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"immunoglobulin lambda variable 6-57","termid":"PBO:0051455"}


id: _global:sequence_of
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"sequence_of","termid":"_global:sequence_of"}


id: PBO:0079107
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"TSC22 domain family member 2","termid":"PBO:0079107"}


id: MONDO:0100598
data:
  {"annotated_genes":["SJAG_02774","SJAG_02523"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88632],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0044319"},{"annotations":[87520],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014832"}]},"cv_name":"mondo","definition":"Autosomal recessive form of syndromic intellectual disability.","definition_xrefs":["MONDO:patterns/autosomal_recessive"],"direct_ancestors":[{"relation_name":"is_a","term_name":"syndromic intellectual disability","termid":"MONDO:0000508"},{"relation_name":"is_a","term_name":"intellectual disability, autosomal recessive","termid":"MONDO:0100597"}],"gene_count":2,"genes_by_uniquename":{"SJAG_02523":null,"SJAG_02774":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0006025"}],"interesting_parent_ids":["MONDO:0006025"],"is_obsolete":false,"name":"autosomal recessive syndromic intellectual disability","references_by_uniquename":{"PB_REF:0000006":null},"termid":"MONDO:0100598","terms_by_termid":{"MONDO:0014832":null,"MONDO:0044319":null},"xrefs":{"Monarch":{"xref_id":"0100598"}}}


id: MONDO:0002226
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An urogenital tuberculosis involving a pathogenic inflammatory response in the ovary.","definition_xrefs":["MONDO:patterns/specific_inflammatory_disease_by_site"],"direct_ancestors":[{"relation_name":"is_a","term_name":"urogenital tuberculosis","termid":"MONDO:0006002"},{"relation_name":"is_a","term_name":"oophoritis","termid":"MONDO:0006877"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"tuberculous oophoritis","secondary_identifiers":["icd11.foundation:1634640694","ICD9:016.60","SCTID:84194006","UMLS:C0275932","DOID:2148","MEDGEN:546959","ICD9:016.6"],"termid":"MONDO:0002226","xrefs":{"Monarch":{"xref_id":"0002226"}}}


id: MONDO:0005638
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A rare disorder characterized by the lack of ability to recognize individuals, objects, shapes, sounds, or smells. There is no loss of memory. It is caused by neurological damage in the brain, specifically in the occipital or parietal lobes.","definition_xrefs":["NCIT:C84542"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"communication disorder","termid":"MONDO:0002182"},{"relation_name":"is_a","term_name":"perceptual disorders","termid":"MONDO:0024417"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"agnosia","secondary_identifiers":["EFO:0007136","DOID:4090","SCTID:68345001","UMLS:C0001816","icd11.foundation:1315065296","ICD10CM:R48.1","MEDGEN:174","MESH:D000377","MESH:D001072","ICD10CM:R48.2"],"synonyms":[{"name":"Monomodal visual amnesia","type":"narrow"},{"name":"agnosia","type":"exact"},{"name":"dyspraxia (finding)","type":"related"},{"name":"dyspraxia syndrome","type":"related"},{"name":"primary visual agnosia","type":"narrow"},{"name":"visual amnesia","type":"narrow"}],"termid":"MONDO:0005638","xrefs":{"Monarch":{"xref_id":"0005638"}}}


id: GO:0034125
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents, or reduces the frequency, rate, or extent of MyD88-dependent toll-like receptor signaling pathway.","definition_xrefs":["PMID:16551253","PMID:17328678","GOC:add"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of toll-like receptor signaling pathway","termid":"GO:0034122"},{"relation_name":"is_a","term_name":"regulation of MyD88-dependent toll-like receptor signaling pathway","termid":"GO:0034124"},{"relation_name":"negatively_regulates","term_name":"MyD88-dependent toll-like receptor signaling pathway","termid":"GO:0002755"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"negatively_regulates","termid":"GO:0023052"},{"rel_name":"regulates","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"negative regulation of MyD88-dependent toll-like receptor signaling pathway","synonyms":[{"name":"negative regulation of MyD88-dependent TLR signaling pathway","type":"exact"},{"name":"negative regulation of MyD88-dependent toll-like receptor signalling pathway","type":"exact"}],"termid":"GO:0034125"}


id: MONDO:0007544
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Familial occurrence, with more than one generation being affected, of persistent eosinophilia, an increase in the number of eosinophils in the blood, in the absence of known causal factors.","definition_xrefs":["PMID:14176021"],"direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"eosinophilia, familial","secondary_identifiers":["SCTID:79336007","OMIM:131400","UMLS:C0272192","MEDGEN:78796","MESH:C562722"],"synonyms":[{"name":"Eos","type":"related"},{"name":"eosinophilia, familial","type":"exact"},{"name":"familial eosinophilia","type":"related"}],"termid":"MONDO:0007544","xrefs":{"Monarch":{"xref_id":"0007544"}}}


id: GO:0031801
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"Binding to a type 4 metabotropic glutamate receptor.","definition_xrefs":["GOC:nln","GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"G protein-coupled glutamate receptor binding","termid":"GO:0035256"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0005488"},{"rel_name":"is_a","termid":"GO:0005515"},{"rel_name":"is_a","termid":"GO:0003674"}],"interesting_parent_ids":["GO:0005515","GO:0003674","GO:0005488"],"is_obsolete":false,"name":"type 4 metabotropic glutamate receptor binding","synonyms":[{"name":"type 4 metabotropic glutamate receptor ligand","type":"narrow"}],"termid":"GO:0031801"}


id: MONDO:0008104
data:
  {"annotated_genes":["SJAG_02342","SJAG_01181","SJAG_00993"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[89206,89207,89208],"is_not":false,"summary":null,"term":"MONDO:0008104"}]},"cv_name":"mondo","definition":"Noonan syndrome caused by mutations in the PTPN11 gene.","definition_xrefs":["NCIT:C75459"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Noonan syndrome","termid":"MONDO:0018997"}],"gene_count":3,"genes_by_uniquename":{"SJAG_00993":null,"SJAG_01181":null,"SJAG_02342":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005267"}],"interesting_parent_ids":["MONDO:0005267","MONDO:0005046"],"is_obsolete":false,"name":"Noonan syndrome 1","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["OMIM:163950","GARD:7223","MEDGEN:1638960","UMLS:C4551602","DOID:0060578"],"synonyms":[{"name":"Male Turner syndrome","type":"related"},{"name":"NS1","type":"exact"},{"name":"Noonan syndrome","type":"related"},{"name":"Noonan syndrome 1","type":"exact"},{"name":"Noonan syndrome type 1","type":"exact"},{"name":"Turner phenotype with normal karyotype","type":"related"},{"name":"female pseudo-Turner syndrome","type":"related"},{"name":"pterygium colli syndrome","type":"related"}],"termid":"MONDO:0008104","terms_by_termid":{"MONDO:0008104":null},"xrefs":{"Monarch":{"xref_id":"0008104"}}}


id: PBO:0083426
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Dubious open reading frame; unlikely to encode a functional protein, based on available experimental and comparative sequence data; partially overlaps the uncharacterized ORF YAR029W and the verified gene PRM9","termid":"PBO:0083426"}


id: GO:0072025
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the distal convoluted tubule over time, from its formation to the mature structure. The distal convoluted tubule is the first segment of the nephron lying just downstream from the loop of Henle, immediately after the macula densa. Among other functions, in humans it is responsible for the reabsorption of about 5% of filtered sodium via the thiazide-sensitive Na-Cl symporter.","definition_xrefs":["GOC:mtg_kidney_jan10"],"direct_ancestors":[{"relation_name":"is_a","term_name":"nephron tubule development","termid":"GO:0072080"},{"relation_name":"part_of","term_name":"distal tubule development","termid":"GO:0072017"}],"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":"distal convoluted tubule development","termid":"GO:0072025"}


id: GO:0046561
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the hydrolysis of proteins with broad specificity similar to that of pepsin A, preferring hydrophobic residues at P1 and P1', but also cleaving Gly20-Glu in the B chain of insulin. Clots milk, and activates trypsinogen.","definition_xrefs":["EC:3.4.23.20"],"gene_count":0,"genotype_count":0,"name":"obsolete penicillopepsin activity (obsolete GO:0046561)","synonyms":[{"name":"Penicillium aspartic proteinase activity","type":"related"},{"name":"Penicillium caseicolum aspartic proteinase activity","type":"related"},{"name":"Penicillium citrinum acid proteinase activity","type":"related"},{"name":"Penicillium citrinum aspartic proteinase activity","type":"related"},{"name":"Penicillium cyclopium acid proteinase activity","type":"related"},{"name":"Penicillium duponti aspartic proteinase activity","type":"related"},{"name":"Penicillium expansum acid proteinase activity","type":"related"},{"name":"Penicillium expansum aspartic proteinase activity","type":"related"},{"name":"Penicillium janthinellum acid proteinase activity","type":"related"},{"name":"Penicillium janthinellum aspartic protease activity","type":"related"},{"name":"Penicillium janthinellum aspartic proteinase activity","type":"related"},{"name":"Penicillium roqueforti acid proteinase activity","type":"related"},{"name":"acid protease A","type":"exact"},{"name":"penicillopepsin activity","type":"exact"},{"name":"peptidase A activity","type":"broad"}],"termid":"GO:0046561"}


id: GO:0009173
data:
  {"annotated_genes":["SJAG_04709","SJAG_04713","SJAG_03164","SJAG_00197","SJAG_04354","SJAG_00964","SJAG_00533","SJAG_03708","SJAG_00444","SJAG_00694"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[62871,60023,61874,59649,57503],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044205"},{"annotations":[69760],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0009224"},{"annotations":[90399,69761,89403,93922,94919],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0044206"}]},"cv_name":"biological_process","definition":"The chemical reactions and pathways involving pyrimidine ribonucleoside monophosphate, a compound consisting of a pyrimidine base linked to a ribose sugar esterified with phosphate on the sugar.","definition_xrefs":["ISBN:0198506732","GOC:go_curators"],"direct_ancestors":[{"relation_name":"is_a","term_name":"pyrimidine nucleoside monophosphate metabolic process","termid":"GO:0009129"}],"gene_count":10,"genes_by_uniquename":{"SJAG_00197":null,"SJAG_00444":null,"SJAG_00533":null,"SJAG_00694":null,"SJAG_00964":null,"SJAG_03164":null,"SJAG_03708":null,"SJAG_04354":null,"SJAG_04709":null,"SJAG_04713":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0044281"},{"rel_name":"is_a","termid":"GO:0055086"}],"interesting_parent_ids":["GO:0008150","GO:0044281","GO:0055086"],"is_obsolete":false,"name":"pyrimidine ribonucleoside monophosphate metabolic process","references_by_uniquename":{"GO_REF:0000041":null,"GO_REF:0000107":null,"GO_REF:0000108":null},"synonyms":[{"name":"pyrimidine ribonucleoside monophosphate metabolism","type":"exact"}],"termid":"GO:0009173","terms_by_termid":{"GO:0009224":null,"GO:0044205":null,"GO:0044206":null}}


id: PBO:0041630
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"calcium voltage-gated channel subunit alpha1 C","termid":"PBO:0041630"}


id: PBO:0055061
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 2477","termid":"PBO:0055061"}


id: PBO:0064293
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"perilipin 1","termid":"PBO:0064293"}


id: GO:0003271
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The series of molecular signals generated as a consequence of activation of the transmembrane protein Smoothened contributing to the modulation of the frequency, rate or extent of cardioblast proliferation in the secondary heart field. A cardioblast is a cardiac precursor cell. It is a cell that has been committed to a cardiac fate, but will undergo more cell division rather than terminally differentiating.","definition_xrefs":["GOC:mtg_heart"],"direct_ancestors":[{"relation_name":"is_a","term_name":"smoothened signaling pathway","termid":"GO:0007224"},{"relation_name":"is_a","term_name":"cell surface receptor signaling pathway involved in heart development","termid":"GO:0061311"},{"relation_name":"part_of","term_name":"regulation of secondary heart field cardioblast proliferation","termid":"GO:0003266"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"part_of","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"smoothened signaling pathway involved in regulation of secondary heart field cardioblast proliferation","synonyms":[{"name":"hedgehog signaling pathway involved in regulation of second heart field cardioblast proliferation","type":"exact"},{"name":"hh signaling pathway involved in regulation of second heart field cardioblast proliferation","type":"exact"},{"name":"smoothened receptor signaling pathway involved in regulation of second heart field cardioblast proliferation","type":"exact"},{"name":"smoothened receptor signaling pathway involved in regulation of secondary heart field cardioblast proliferation","type":"exact"},{"name":"smoothened receptor signalling pathway involved in regulation of secondary heart field cardioblast proliferation","type":"exact"}],"termid":"GO:0003271"}


id: PBO:0002942
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"amidophosphoribosyltransferase Ade4","termid":"PBO:0002942"}


id: PBO:0085145
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Nucleolar S-adenosylmethionine-dependent rRNA methyltransferase; methylates adenine (m1A) of large subunit (LSU) rRNA at position 645; involved in pre-rRNA cleavage at site A2; mutation is synthetically lethal with gar1 mutation; deletion disrupts telomere maintenance by influencing expression of neighboring gene STN1; mammalian homolog nucleomethylin has been linked to nutrient availability signaling pathways and obesity","termid":"PBO:0085145"}


id: PBO:0080715
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"WRN RecQ like helicase","termid":"PBO:0080715"}


id: PBO:0039268
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ALDOA pseudogene 1","termid":"PBO:0039268"}


id: MONDO:0019838
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"An autoimmune disease of the pituitary gland which can present with varying degrees of pituitary hormonal impairment and/or with symptoms related to pituitary enlargement. It predominantly affects young women in pregnancy or the peripartum period.","definition_xrefs":["PMID:21592417"],"direct_ancestors":[{"relation_name":"is_a","term_name":"primary hypophysitis","termid":"MONDO:0019835"},{"relation_name":"is_a","term_name":"anterior pituitary gland disorder","termid":"MONDO:0024468"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"adenohypophysitis","secondary_identifiers":["MEDGEN:1677203","UMLS:C5190880","GARD:19284","Orphanet:95512"],"synonyms":[{"name":"adenohypophysis inflammation","type":"exact"},{"name":"anterior pituitary hypophysitis","type":"exact"},{"name":"inflammation of adenohypophysis","type":"exact"},{"name":"lymphocytic adenohypophysitis","type":"exact"}],"termid":"MONDO:0019838","xrefs":{"Monarch":{"xref_id":"0019838"}}}


id: GO:0042136
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. The chemical reactions and pathways resulting in the formation of any of a group of substances that are released on excitation from the axon terminal of a presynaptic neuron of the central or peripheral nervous system and travel across the synaptic cleft to either excite or inhibit the target cell.","definition_xrefs":["GOC:jl"],"gene_count":0,"genotype_count":0,"name":"obsolete neurotransmitter biosynthetic process (obsolete GO:0042136)","synonyms":[{"name":"neurotransmitter anabolism","type":"exact"},{"name":"neurotransmitter biosynthesis","type":"exact"},{"name":"neurotransmitter biosynthesis and storage","type":"broad"},{"name":"neurotransmitter biosynthetic process and storage","type":"broad"},{"name":"neurotransmitter formation","type":"exact"},{"name":"neurotransmitter synthesis","type":"exact"}],"termid":"GO:0042136"}


id: PBO:0075649
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"SPRY domain containing 4","termid":"PBO:0075649"}


id: PBO:0076944
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transferrin receptor 2","termid":"PBO:0076944"}


id: PR:P48011
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A DNA-directed RNA polymerases I, II, and III subunit RPABC4 that is encoded in the genome of Schizosaccharomyces pombe 972h-.","definition_xrefs":["OMA:SCHPO02953","PANTHER:PTHR12056:SF0","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":"DNA-directed RNA polymerases I, II, and III subunit RPABC4 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC19C2.03","secondary_identifiers":["UniProtKB:P48011"],"synonyms":[{"name":"ABC10-alpha (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"RNA polymerases I, II, and III subunit ABC4 (Schizosaccharomyces pombe 972h-)","type":"exact"},{"name":"Spom972h-POLR2K","type":"exact"}],"termid":"PR:P48011"}


id: _global:regulates_o_has_participant
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"This is the combination of the regulates relation with the has_participant relation.","definition_xrefs":["GOC:mtg_berkeley_2013"],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"regulates_o_has_participant","secondary_identifiers":["GOREL:0001016"],"termid":"_global:regulates_o_has_participant"}


id: MOD:00786
data:
  {"annotation_feature_type":"gene","cv_name":"PSI-MOD","definition":"A protein modification that effectively substitutes one or more (2)H deuterium atoms for (1)H protium atoms.","definition_xrefs":["PubMed:18688235"],"direct_ancestors":[{"relation_name":"is_a","term_name":"(2)H deuterium labeled residue","termid":"MOD:00839"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"deuterium substituted residue","synonyms":[{"name":"D(H)Res","type":"exact"}],"termid":"MOD:00786"}


id: PBO:0088473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"pseudopeptidase Ecm14","termid":"PBO:0088473"}


id: GO:1903266
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency, rate or extent of ornithine catabolic process.","definition_xrefs":["PMID:12679340","GOC:bhm","GO_REF:0000058","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of catabolic process","termid":"GO:0009894"},{"relation_name":"is_a","term_name":"regulation of ornithine metabolic process","termid":"GO:0090368"},{"relation_name":"regulates","term_name":"L-ornithine catabolic process","termid":"GO:0006593"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0044281"},{"rel_name":"regulates","termid":"GO:0006520"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0006520","GO:0044281"],"is_obsolete":false,"name":"regulation of ornithine catabolic process","synonyms":[{"name":"regulation of ornithine breakdown","type":"exact"},{"name":"regulation of ornithine catabolism","type":"exact"},{"name":"regulation of ornithine degradation","type":"exact"}],"termid":"GO:1903266"}


id: GO:0071648
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that activates or increases the frequency, rate, or extent of production of macrophage inflammatory protein-1 gamma.","definition_xrefs":["GOC:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"positive regulation of chemokine production","termid":"GO:0032722"},{"relation_name":"is_a","term_name":"regulation of macrophage inflammatory protein-1 gamma production","termid":"GO:0071646"},{"relation_name":"positively_regulates","term_name":"macrophage inflammatory protein-1 gamma production","termid":"GO:0071607"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0010467"},{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"positively_regulates","termid":"GO:0010467"}],"interesting_parent_ids":["GO:0010467","GO:0008150"],"is_obsolete":false,"name":"positive regulation of macrophage inflammatory protein-1 gamma production","synonyms":[{"name":"positive regulation of CCL9 production","type":"exact"},{"name":"positive regulation of MIP-1g production","type":"exact"},{"name":"positive regulation of chemokine (C-C motif) ligand 9 production","type":"exact"}],"termid":"GO:0071648"}


id: GO:0000937
data:
  {"annotation_feature_type":"gene","cv_name":"cellular_component","definition":"A septum, or cross-wall, between two portions of a cell or hypha; contains a central pore around which the septum is swollen to form a barrel-shaped structure; pore is covered on each side of the septum by a septal pore cap (parenthosome).","definition_xrefs":["GOC:clt"],"direct_ancestors":[{"relation_name":"is_a","term_name":"porous cell septum","termid":"GO:0000934"}],"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":"dolipore septum","termid":"GO:0000937"}


id: PBO:0011121
data:
  {"annotation_feature_type":"gene","cv_name":"name_description","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Pombe Chromsome segregation in Meiosis","termid":"PBO:0011121"}


id: PBO:0090784
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"COPII-coated vesicle component Erv46","termid":"PBO:0090784"}


id: PBO:0062691
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"olfactory receptor family 51 subfamily B member 2","termid":"PBO:0062691"}


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


id: MONDO:0002163
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A well-circumscribed tumor of the thymus composed of islands of normal thymic parenchyma and mature adipose tissue. It is not clear if thymolipoma is a neoplastic or non-neoplastic lesion.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"lipoma","termid":"MONDO:0005106"},{"relation_name":"is_a","term_name":"benign neoplasm of thymus","termid":"MONDO:0021512"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"},{"rel_name":"is_a","termid":"MONDO:0005570"}],"interesting_parent_ids":["MONDO:0005046","MONDO:0005570"],"is_obsolete":false,"name":"thymus lipoma","secondary_identifiers":["NCIT:C6452","UMLS:C1336744","DOID:1975","MEDGEN:234427"],"synonyms":[{"name":"Thymolipoma","type":"exact"},{"name":"Thymolipomatous hamartoma","type":"exact"},{"name":"lipoma of thymus","type":"exact"},{"name":"thymus lipoma","type":"exact"}],"termid":"MONDO:0002163","xrefs":{"Monarch":{"xref_id":"0002163"}}}


id: MONDO:0009464
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"inborn error of immunity","termid":"MONDO:0003778"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005046"}],"interesting_parent_ids":["MONDO:0005046"],"is_obsolete":false,"name":"immunodeficiency with defective T-cell response to interleukin 1","secondary_identifiers":["OMIM:243110","MEDGEN:340948","UMLS:C1855735"],"synonyms":[{"name":"Interleukin 1, defective T-cell response to","type":"related"},{"name":"immunodeficiency with defective T-cell response to Interleukin type 1","type":"exact"},{"name":"immunodeficiency with defective T-cell response to interleukin 1","type":"exact"}],"termid":"MONDO:0009464","xrefs":{"Monarch":{"xref_id":"0009464"}}}


id: MONDO:0013796
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"17q12 microduplication syndrome is a rare chromosomal anomaly with variable phenotypic expression and reduced penetrance associated with developmental delay, mild to severe intellectual disability, speech delay, seizures, microcephaly, behavioral abnormalities, autism spectrum disorder, eye or vision defects (such as strabismus, astigmatism, amblyopia, cataract, coloboma, and microphthalmia), non-specific dysmorphic features, hypotonia, cardiac and renal anomalies, schizophrenia.","definition_xrefs":["Orphanet:261272"],"direct_ancestors":[{"relation_name":"is_a","term_name":"partial duplication of the long arm of chromosome 17","termid":"MONDO:0016967"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"chromosome 17q12 duplication syndrome","secondary_identifiers":["DOID:0060433","SCTID:764435003","MEDGEN:482767","GARD:13296","UMLS:C3281137","OMIM:614526"],"synonyms":[{"name":"17q12 duplication","type":"related"},{"name":"17q12 microduplication","type":"related"},{"name":"17q12 microduplication syndrome","type":"exact"},{"name":"chromosome 17q12 duplication syndrome","type":"exact"},{"name":"dup(17)(q12)","type":"exact"},{"name":"recurrent duplication of 17q12","type":"related"},{"name":"trisomy 17q12","type":"exact"}],"termid":"MONDO:0013796","xrefs":{"Monarch":{"xref_id":"0013796"}}}


id: MONDO:0850461
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A fetal alcohol spectrum disorder that is characterized by one or more deficits in neurocognition and in self-regulation plus two or more deficits in adaptive functioning, with at least 1 in communication or social communication and interaction.","definition_xrefs":["DOID:0081052"],"direct_ancestors":[{"relation_name":"is_a","term_name":"fetal alcohol spectrum disorder","termid":"MONDO:0000408"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"neurobehavioral disorder with prenatal alcohol exposure","termid":"MONDO:0850461","xrefs":{"Monarch":{"xref_id":"0850461"}}}


id: PBO:0073752
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"solute carrier family 2 member 7","termid":"PBO:0073752"}


id: GO:0018184
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The modification of a protein amino acid by polyamination.","definition_xrefs":["GOC:ai"],"direct_ancestors":[{"relation_name":"is_a","term_name":"protein modification process","termid":"GO:0036211"}],"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 polyamination","synonyms":[{"name":"protein amino acid polyamination","type":"exact"}],"termid":"GO:0018184"}


id: MONDO:0018214
data:
  {"annotated_genes":["SJAG_03536"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88648],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014517"}]},"cv_name":"mondo","definition":"A familial epilepsy syndrome in which family members display a seizure disorder from the generalized epilepsy with febrile seizures plus spectrum which ranges from simple febrile seizures (FS) to the more severe phenotype of myoclonic-astatic epilepsy (MAE) or Dravet syndrome (DS).","definition_xrefs":["Orphanet:36387"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"idiopathic generalized epilepsy","termid":"MONDO:0005579"},{"relation_name":"is_a","term_name":"hereditary generalized epilepsy","termid":"MONDO:0100576"}],"gene_count":1,"genes_by_uniquename":{"SJAG_03536":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005027"}],"interesting_parent_ids":["MONDO:0005027"],"is_obsolete":false,"name":"generalized epilepsy with febrile seizures plus","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["SCTID:699688008","NCIT:C122811","MEDGEN:503203","MESH:C565808","DOID:0060170","GARD:18641","OMIMPS:604233","UMLS:C3502809"],"synonyms":[{"name":"GEFS+","type":"exact"},{"name":"epilepsy, generalized, with febrile seizures plus","type":"exact"},{"name":"generalised epilepsy with febrile seizures-plus","type":"exact"},{"name":"generalized epilepsy with febrile seizures plus","type":"exact"},{"name":"genetic epilepsy with febrile seizures plus","type":"exact"},{"name":"genetic epilepsy with febrile seizures-plus","type":"exact"}],"termid":"MONDO:0018214","terms_by_termid":{"MONDO:0014517":null},"xrefs":{"Monarch":{"xref_id":"0018214"}}}


id: FYPO:0005893
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype in which the amount of protein found associated with chromatin is higher than normal when the cell is in the vegetative growth phase of the life cycle. Total protein or a specific protein may be affected.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"increased protein level during vegetative growth","termid":"FYPO:0001327"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"output_of","termid":"FYPO:0005447"},{"rel_name":"output_of","termid":"FYPO:0006551"},{"rel_name":"output_of","termid":"FYPO:0001985"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0006551","FYPO:0000002","FYPO:0005447","FYPO:0001985"],"is_obsolete":false,"name":"increased protein level in chromatin","synonyms":[{"name":"increased protein level at chromatin during vegetative growth","type":"exact"},{"name":"increased protein level in chromatin during mitotic cell cycle","type":"related"},{"name":"increased protein level in chromatin during vegetative growth","type":"exact"},{"name":"protein accumulation in chromatin","type":"exact"}],"termid":"FYPO:0005893"}


id: MONDO:0000448
data:
  {"annotated_genes":["SJAG_00260","SJAG_03163","SJAG_03920","SJAG_01895","SJAG_01671","SJAG_02398"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87758],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008192"},{"annotations":[88965],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011121"},{"annotations":[88864],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0011544"},{"annotations":[87548],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0007273"},{"annotations":[87755],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013602"},{"annotations":[89112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0032771"}]},"cv_name":"mondo","definition":"A benign or malignant neoplasm arising from paraganglia located along the sympathetic or parasympathetic nerves. Infrequently, it may arise outside the usual distribution of the sympathetic and parasympathetic paraganglia. Tumors arising from the adrenal gland medulla are called pheochromocytomas. Morphologically, paragangliomas usually display a nesting (Zellballen) growth pattern. There are no reliable morphologic criteria to distinguish between benign and malignant paragangliomas. The only definitive indicator of malignancy is the presence of regional or distant metastases.","definition_xrefs":["NCIT:C3308"],"direct_ancestors":[{"relation_name":"is_a","term_name":"autonomic nervous system neoplasm","termid":"MONDO:0002366"},{"relation_name":"is_a","term_name":"neuroendocrine neoplasm","termid":"MONDO:0019496"},{"relation_name":"is_a","term_name":"neurocristopathy","termid":"MONDO:0021635"},{"relation_name":"is_a","term_name":"hereditary neurological disease","termid":"MONDO:0100545"}],"gene_count":6,"genes_by_uniquename":{"SJAG_00260":null,"SJAG_01671":null,"SJAG_01895":null,"SJAG_02398":null,"SJAG_03163":null,"SJAG_03920":null},"genotype_count":0,"is_obsolete":false,"name":"paraganglioma","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MEDGEN:10571","MESH:D010235","ICD9:239.7","ICDO:8680/1","SCTID:127027008","EFO:1000453","UMLS:C0030421","DOID:0050773","OMIMPS:168000","ONCOTREE:PGNG"],"synonyms":[{"name":"Paraganglionic neoplasm","type":"exact"},{"name":"Paraganglionic tumor","type":"exact"},{"name":"Paraganglionic tumour","type":"exact"},{"name":"chemodectoma","type":"narrow"},{"name":"neoplasm of paraganglion","type":"exact"},{"name":"neoplasm of the paraganglion","type":"exact"},{"name":"paraganglioma","type":"exact"},{"name":"paragangliomas","type":"exact"},{"name":"paraganglion neoplasm","type":"exact"},{"name":"paraganglion tumor","type":"exact"},{"name":"paraganglion tumour","type":"exact"},{"name":"tumor of paraganglion","type":"exact"},{"name":"tumor of the paraganglion","type":"exact"},{"name":"tumour of paraganglion","type":"exact"},{"name":"tumour of the paraganglion","type":"exact"}],"termid":"MONDO:0000448","terms_by_termid":{"MONDO:0007273":null,"MONDO:0008192":null,"MONDO:0011121":null,"MONDO:0011544":null,"MONDO:0013602":null,"MONDO:0032771":null},"xrefs":{"Monarch":{"xref_id":"0000448"}}}


id: MONDO:0005738
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A parasitic infection caused by tapeworm larvae of Echinococcus. It affects livestock and humans. It is characterized by the formation of hydatid cysts mainly in the liver, lungs, spleen, and kidneys. Rupture of the cysts may lead to shock.","definition_xrefs":["NCIT:P378"],"direct_ancestors":[{"relation_name":"is_a","term_name":"Cestode infectious disease","termid":"MONDO:0042488"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"echinococcosis","secondary_identifiers":["icd11.foundation:1456802165","EFO:0007245","ICD9:122.9","MEDGEN:4438","MESH:D004443","ICD10CM:B67","NCIT:C84682","SCTID:74942003","ICD9:122","UMLS:C0013502","DOID:1496","ICD10WHO:B67"],"synonyms":[{"name":"Echinococcus caused disease or disorder","type":"exact"},{"name":"Echinococcus disease or disorder","type":"exact"},{"name":"Echinococcus infectious disease","type":"exact"},{"name":"echinococcal disease","type":"narrow"},{"name":"echinococciasis","type":"related"},{"name":"echinococcosis","type":"exact"},{"name":"echinococcosis of liver","type":"exact"},{"name":"echinococcosis, unspecified, of liver","type":"narrow"},{"name":"echinococcus disease","type":"related"},{"name":"hepatic echinococcosis","type":"narrow"},{"name":"hydatid disease","type":"narrow"},{"name":"hydatidosis","type":"narrow"},{"name":"liver echinococcus","type":"exact"},{"name":"pulmonary echinococcosis","type":"narrow"}],"termid":"MONDO:0005738","xrefs":{"Monarch":{"xref_id":"0005738"}}}


id: SO:0000620
data:
  {"annotation_feature_type":"gene","cv_name":"sequence","definition":"A variably distant linear promoter region recognized by TFIIIC, with consensus sequence AGGTTCCAnnCC.","definition_xrefs":["SO:ke"],"direct_ancestors":[{"relation_name":"is_a","term_name":"core_eukaryotic_promoter_element","termid":"SO:0001660"},{"relation_name":"part_of","term_name":"RNApol_III_promoter_type_2","termid":"SO:0000618"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"B_box","synonyms":[{"name":"B-box","type":"exact"}],"termid":"SO:0000620"}


id: PBO:0087345
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Sphinganine C4-hydroxylase; catalyses the conversion of sphinganine to phytosphingosine in sphingolipid biosyntheis","termid":"PBO:0087345"}


id: PBO:0059091
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"MORC family CW-type zinc finger 3","termid":"PBO:0059091"}


id: PBO:0028897
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_pear-shaped_vegetative_cell","termid":"PBO:0028897"}


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


id: GO:0043030
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that modulates the frequency or rate of macrophage activation.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of leukocyte activation","termid":"GO:0002694"},{"relation_name":"regulates","term_name":"macrophage activation","termid":"GO:0042116"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"regulation of macrophage activation","synonyms":[{"name":"regulation of macrophage polarization","type":"exact"}],"termid":"GO:0043030"}


id: PBO:0048656
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gap junction protein epsilon 1","termid":"PBO:0048656"}


id: MONDO:1011267
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Any cone-rod dystrophy that occurs in black-footed cats due to a mutation in the IQCB1 gene.","definition_xrefs":["MONDO:patterns/nonhuman_disease_series_by_gene"],"direct_ancestors":[{"relation_name":"is_a","term_name":"cone-rod dystrophy, non-human animal","termid":"MONDO:1012582"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"cone-rod dystrophy, IQCB1-related, black-footed cat","secondary_identifiers":["OMIA:001675-61379"],"synonyms":[{"name":"retinal atrophy - cone-rod dystrophy 2, black-footed cat","type":"related"}],"termid":"MONDO:1011267","xrefs":{"Monarch":{"xref_id":"1011267"}}}


id: PBO:0060310
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin light chain kinase","termid":"PBO:0060310"}


id: FYPO:0002430
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A phenotype in which a spore germinates to produce a cell that undergoes two or more rounds of cell division, and then dies.","definition_xrefs":["PomBase:mah","PomBase:al"],"direct_ancestors":[{"relation_name":"is_a","term_name":"inviable after spore germination","termid":"FYPO:0000316"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001320"},{"rel_name":"is_a","termid":"FYPO:0000004"},{"rel_name":"is_a","termid":"FYPO:0000002"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000004","FYPO:0000002"],"is_obsolete":false,"name":"inviable after spore germination, multiple cell divisions","synonyms":[{"name":"inviable following spore germination, multiple cell divisions","type":"exact"},{"name":"inviable germinated spore, multiple cell divisions","type":"exact"},{"name":"lethal after spore germination, multiple cell divisions","type":"exact"}],"termid":"FYPO:0002430"}


id: GO:0048527
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process whose specific outcome is the progression of the lateral root over time, from its formation to the mature structure. A lateral root is one formed from pericycle cells located on the xylem radius of the root, as opposed to the initiation of the main root from the embryo proper.","definition_xrefs":["GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"post-embryonic root development","termid":"GO:0048528"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150"],"is_obsolete":false,"name":"lateral root development","termid":"GO:0048527"}


id: PBO:0117193
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"EPB41L3 antisense RNA 1","termid":"PBO:0117193"}


id: PBO:0064370
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"phosphomannomutase 2 pseudogene 2","termid":"PBO:0064370"}


id: PBO:0087558
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Subunit of SEACAT, a subcomplex of the SEA complex; Sea4p, along with Rtc1p and Mtc5p, redundantly inhibit the TORC1 inhibitory role of the Iml1p/SEACIT (Iml1p-Npr2p-Npr3p) subcomplex, a GAP for GTPase Gtr1p (EGOC subunit) in response to amino acid limitation, thereby resulting in activation of TORC1 signaling; SEA is a coatomer-related complex that associates dynamically with the vacuole; contains an N-terminal beta-propeller fold and a C-terminal RING motif","termid":"PBO:0087558"}


id: GO:0102723
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of the reaction: UDP-alpha-D-glucose + curcumin = curcumin monoglucoside + UDP + H+.","definition_xrefs":["GOC:pz"],"gene_count":0,"genotype_count":0,"name":"obsolete UDP-glucose:curcumin glucosyltransferase activity (obsolete GO:0102723)","termid":"GO:0102723"}


id: PBO:0004243
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase family or domain","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"PPP3/PP2B/calcineurin subfamily","termid":"PBO:0004243"}


id: PBO:0029392
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-abnormal_protein_localization_to_nucleoplasm_during_cellular_response_to_hydroxyurea","termid":"PBO:0029392"}


id: PBO:0067473
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"RNA, 7SL, cytoplasmic 604, pseudogene","termid":"PBO:0067473"}


id: MONDO:0015469
data:
  {"annotated_genes":["SJAG_04995","SJAG_02165","SJAG_02200","SJAG_04270","SJAG_03249"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[87526],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0008726"},{"annotations":[87000],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0020667"},{"annotations":[87349],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0014558"},{"annotations":[87455,87456],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0009039"},{"annotations":[88535],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"MONDO:0013740"}]},"cv_name":"mondo","definition":"Craniosynostosis is defined as the premature fusion of one or more cranial sutures leading to secondary distortion of skull shape resulting in skull deformities with a variable presentation. Craniosynostosis may occur in an isolated setting or as part of a syndrome.","definition_xrefs":["Orphanet:1531"],"direct_ancestors":[{"relation_name":"is_a","term_name":"synostosis","termid":"MONDO:0001411"},{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":5,"genes_by_uniquename":{"SJAG_02165":null,"SJAG_02200":null,"SJAG_03249":null,"SJAG_04270":null,"SJAG_04995":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"MONDO:0005497"}],"interesting_parent_ids":["MONDO:0005497"],"is_obsolete":false,"name":"craniosynostosis","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["MESH:D003398","NCIT:C84655","OMIMPS:123100","ICD10CM:Q75.0","NANDO:2100227","DOID:2340","GARD:6209","MEDGEN:1163","UMLS:C0010278","icd11.foundation:458033798","MedDRA:10049889","MedDRA:10048907"],"synonyms":[{"name":"CSO","type":"related"},{"name":"craniosynostosis syndrome","type":"exact"},{"name":"premature closure of cranial sutures","type":"exact"}],"termid":"MONDO:0015469","terms_by_termid":{"MONDO:0008726":null,"MONDO:0009039":null,"MONDO:0013740":null,"MONDO:0014558":null,"MONDO:0020667":null},"xrefs":{"Monarch":{"xref_id":"0015469"}}}


id: GO:0006886
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id: FYPO:0005293
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id: PBO:0067036
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id: GO:0000412
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id: PBO:0002695
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id: PR:O60187
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id: MOD:00575
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id: MONDO:0024430
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A neurological disorder in which a sensory stimulus, usually tactile but more rarely other sensory modalities, is misperceived in a location distant from the original stimulus.","definition_xrefs":["MESH:D066190"],"direct_ancestors":[{"relation_name":"is_a","term_name":"perceptual disorders","termid":"MONDO:0024417"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"allesthesia","secondary_identifiers":["MEDGEN:827104","UMLS:C3850010"],"synonyms":[{"name":"Allachesthesia","type":"related"},{"name":"Allachesthesias","type":"related"},{"name":"Allesthesias","type":"related"},{"name":"Alloesthesia","type":"related"},{"name":"Alloesthesias","type":"related"},{"name":"Dyschirias","type":"related"},{"name":"allochiria","type":"related"},{"name":"dyschiria","type":"related"},{"name":"false allochiria","type":"related"}],"termid":"MONDO:0024430","xrefs":{"Monarch":{"xref_id":"0024430"}}}


id: _global:process_has_causal_agent
data:
  {"annotation_feature_type":"gene","cv_name":"external","definition":"Inverse of 'causal agent in process'","direct_ancestors":[{"relation_name":"is_a","term_name":"causally_related_to","termid":"_global:causally_related_to"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"process_has_causal_agent","secondary_identifiers":["RO:0002608"],"termid":"_global:process_has_causal_agent"}


id: GO:0015477
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. A porin of the bacterial outer membrane that forms transmembrane pores and transports relatively large molecules from the external milieu to the periplasm in an energized process. Energizing of transport across the outer membrane requires a heterotrimeric complex of proteins, the TonB-ExbB-ExbD complex, or in some cases, the TolA-TolQ-TolR complex. Energizing requires proton motive force across the cytoplasmic membrane.","definition_xrefs":["ISBN:0815340729","GOC:mtg_transport","TC:1.B.13.-.-"],"gene_count":0,"genotype_count":0,"name":"obsolete receptor porin activity (obsolete GO:0015477)","synonyms":[{"name":"receptor porin activity","type":"exact"}],"termid":"GO:0015477"}


id: GO:0060244
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that stops, prevents or reduces the rate or extent of cell proliferation in response to cell density.","definition_xrefs":["GOC:dph"],"direct_ancestors":[{"relation_name":"is_a","term_name":"negative regulation of cell population proliferation","termid":"GO:0008285"},{"relation_name":"part_of","term_name":"contact inhibition","termid":"GO:0060242"}],"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 cell proliferation involved in contact inhibition","termid":"GO:0060244"}


id: GO:0044867
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The process in which a host organism effects a change in the enzyme activity of a virus with which it is infected.","definition_xrefs":["GOC:jl"],"direct_ancestors":[{"relation_name":"is_a","term_name":"modulation by host of viral molecular function","termid":"GO:0044868"}],"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":"modulation by host of viral catalytic activity","termid":"GO:0044867"}


id: PBO:0059389
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"mitochondrial ribosomal protein S24","termid":"PBO:0059389"}


id: MONDO:0001954
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"A thrombophlebitis that is characterized by repeated occurrences of thrombophlebitis in different locations.","definition_xrefs":["DOID:14392"],"direct_ancestors":[{"relation_name":"is_a","term_name":"thrombophlebitis","termid":"MONDO:0002800"}],"gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"thrombophlebitis migrans","secondary_identifiers":["SCTID:31268005","ICD9:453.1","UMLS:C0152250","MEDGEN:508947","icd11.foundation:674623750","ICD10CM:I82.1"],"termid":"MONDO:0001954","xrefs":{"Monarch":{"xref_id":"0001954"}}}


id: MONDO:0032901
data:
  {"annotated_genes":["SJAG_00143"],"annotation_feature_type":"gene","cv_annotations":{"mondo":[{"annotations":[88616],"is_not":false,"summary":null,"term":"MONDO:0032901"}]},"cv_name":"mondo","direct_ancestors":[{"relation_name":"is_a","term_name":"hereditary disease","termid":"MONDO:0003847"}],"gene_count":1,"genes_by_uniquename":{"SJAG_00143":null},"genotype_count":0,"is_obsolete":false,"name":"Catifa syndrome","references_by_uniquename":{"PB_REF:0000006":null},"secondary_identifiers":["UMLS:C5231492","MEDGEN:1684686","OMIM:618761"],"synonyms":[{"name":"CATIFA","type":"related"},{"name":"CATIFA SYNDROME","type":"related"},{"name":"Cleft Lip, Cataract, Tooth Abnormality, Impaired Intellectual Development, Facial Dysmorphism, and Attention-Deficit Hyperactivity Disorder","type":"related"}],"termid":"MONDO:0032901","terms_by_termid":{"MONDO:0032901":null},"xrefs":{"Monarch":{"xref_id":"0032901"}}}


id: GO:0090127
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"Any process that increases the extent of synaptic maturation as a result of the communication from a pre-synaptic cell to a post-synaptic cell across a synapse.","definition_xrefs":["GOC:tb","GOC:dph","GOC:ascb_2009"],"direct_ancestors":[{"relation_name":"is_a","term_name":"chemical synaptic transmission","termid":"GO:0007268"},{"relation_name":"is_a","term_name":"positive regulation of synapse maturation","termid":"GO:0090129"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0008150"},{"rel_name":"is_a","termid":"GO:0023052"}],"interesting_parent_ids":["GO:0008150","GO:0023052"],"is_obsolete":false,"name":"positive regulation of synapse maturation by synaptic transmission","termid":"GO:0090127"}


id: PBO:0029537
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-inviable_mixed_population_including_germinated_spores_and_tapered_cells_(obsolete_FYPO:0002185)","termid":"PBO:0029537"}


id: GO:1905392
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"The developmental process by which a plant organ is generated and organized.","definition_xrefs":["GO_REF:0000083","GOC:tb","GOC:TermGenie"],"direct_ancestors":[{"relation_name":"is_a","term_name":"anatomical structure morphogenesis","termid":"GO:0009653"},{"relation_name":"part_of","term_name":"plant organ development","termid":"GO:0099402"}],"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":"plant organ morphogenesis","termid":"GO:1905392"}


id: PR:Q9USW9
data:
  {"annotation_feature_type":"gene","cv_name":"protein","definition":"A protein that is a translation product of the Schizosaccharomyces pombe 972h- sgf29 gene.","definition_xrefs":["UniProtKB:Q9USW9","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":"SAGA-associated factor 29 (Schizosaccharomyces pombe 972h-)","pombase_gene_id":"SPBC1921.07c","synonyms":[{"name":"Spom972h-sgf29","type":"exact"}],"termid":"PR:Q9USW9"}


id: GO:0160102
data:
  {"annotated_genes":["SJAG_04181"],"annotation_feature_type":"gene","cv_annotations":{"molecular_function":[{"annotations":[64125],"is_not":false,"summary":null,"term":"GO:0160102"}]},"cv_name":"molecular_function","definition":"Catalysis of the reaction: guanosine(10) in tRNA + S-adenosyl-L-methionine = H+ + N(2)-methylguanosine(10) in tRNA + S-adenosyl-L-homocysteine.","definition_xrefs":["EC:2.1.1.214"],"direct_ancestors":[{"relation_name":"is_a","term_name":"N-methyltransferase activity","termid":"GO:0008170"},{"relation_name":"is_a","term_name":"tRNA (guanine) methyltransferase activity","termid":"GO:0016423"}],"gene_count":1,"genes_by_uniquename":{"SJAG_04181":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"GO:0016740"},{"rel_name":"is_a","termid":"GO:0140098"},{"rel_name":"is_a","termid":"GO:0003674"},{"rel_name":"is_a","termid":"GO:0003824"},{"rel_name":"is_a","termid":"GO:0140101"},{"rel_name":"is_a","termid":"GO:0016741"}],"interesting_parent_ids":["GO:0016740","GO:0140098","GO:0003674","GO:0003824","GO:0140101","GO:0016741"],"is_obsolete":false,"name":"tRNA (guanine(10)-N2)-methyltransferase activity","references_by_uniquename":{"GO_REF:0000002":null},"secondary_identifiers":["Reactome:R-HSA-6786501","RHEA:43128"],"synonyms":[{"name":"tRNA (guanine(10)-N(2))-methyltransferase activity","type":"exact"},{"name":"tRNA (guanosine(10)-N(2))-methyltransferase activity","type":"exact"}],"termid":"GO:0160102","terms_by_termid":{"GO:0160102":null}}


id: PBO:0055137
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 2556","termid":"PBO:0055137"}


id: PBO:0079615
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"ubiquitin conjugating enzyme E2 K","termid":"PBO:0079615"}


id: GO:0150141
data:
  {"annotation_feature_type":"gene","cv_name":"biological_process","definition":"OBSOLETE. Any process that stops, prevents or reduces the frequency, rate or extent of CD86 biosynthetic process.","definition_xrefs":["PMID:26936882","GOC:aruk"],"gene_count":0,"genotype_count":0,"name":"obsolete negative regulation of CD86 production (obsolete GO:0150141)","synonyms":[{"name":"negative regulation of CD86 biosynthetic process","type":"exact"}],"termid":"GO:0150141"}


id: FYPO:0005083
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cell phenotype observed in the vegetative growth phase of the life cycle in which the localization of a protein to chromatin at non-coding RNA (ncRNA) genes is normal (i.e. indistinguishable from wild type).","definition_xrefs":["PomBase:mah","PMID:21151114"],"direct_ancestors":[{"relation_name":"is_a","term_name":"normal protein localization to chromatin during vegetative growth","termid":"FYPO:0001509"}],"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:0001320"},{"rel_name":"is_a","termid":"FYPO:0001312"},{"rel_name":"is_a","termid":"FYPO:0000257"}],"interesting_parent_ids":["FYPO:0001320","FYPO:0000257","FYPO:0001312","FYPO:0000138","FYPO:0000002"],"is_obsolete":false,"name":"normal protein localization to chromatin at ncRNA gene","synonyms":[{"name":"normal protein localisation to chromatin at ncRNA gene","type":"exact"},{"name":"normal protein localization to chromatin at ncRNA gene during mitotic cell cycle","type":"related"},{"name":"normal protein localization to chromatin at ncRNA gene during vegetative growth","type":"exact"}],"termid":"FYPO:0005083"}


id: PBO:0000340
data:
  {"annotation_feature_type":"gene","cv_name":"gene_ex","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"transcriptionally regulates ctr4","termid":"PBO:0000340"}


id: PBO:0031638
data:
  {"annotation_feature_type":"gene","cv_name":"cvterm_property_type","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"annotation_extension_relation-normal_shmoo_formation","termid":"PBO:0031638"}


id: PBO:0041396
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"complement C6","termid":"PBO:0041396"}


id: PBO:0060301
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"myosin light chain 11","termid":"PBO:0060301"}


id: GO:0051445
data:
  {"annotated_genes":["SJAG_02712","SJAG_00457","SJAG_04682","SJAG_05153","SJAG_03327","SJAG_00993","SJAG_02169","SJAG_04332","SJAG_00364","SJAG_02481","SJAG_01401","SJAG_01680","SJAG_01345","SJAG_03486","SJAG_02723","SJAG_04126","SJAG_01515","SJAG_02771","SJAG_03720","SJAG_01113","SJAG_04813","SJAG_02404","SJAG_01082","SJAG_03887","SJAG_03501","SJAG_00987","SJAG_03525","SJAG_04287","SJAG_04853","SJAG_04280","SJAG_03438","SJAG_03371","SJAG_02592","SJAG_00266","SJAG_03048","SJAG_01837","SJAG_05288","SJAG_01330","SJAG_04259","SJAG_00145","SJAG_03854","SJAG_01000","SJAG_01956","SJAG_04140","SJAG_06638","SJAG_01311"],"annotation_feature_type":"gene","cv_annotations":{"biological_process":[{"annotations":[91762,94087,95243,96324,106286],"is_not":false,"summary":null,"term":"GO:0051445"},{"annotations":[109944],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010846"},{"annotations":[92290,97109],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051728"},{"annotations":[108283,116494],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905318"},{"annotations":[108585,93377,118056],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033315"},{"annotations":[118057,91006,108586,116257],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051598"},{"annotations":[77267,118668],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0033316"},{"annotations":[113191],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075297"},{"annotations":[120386,107773,108619,104317,106397,107938,111249],"is_not":false,"rel_names":["negatively_regulates","is_a","regulates"],"summary":null,"term":"GO:0110045"},{"annotations":[80472,72579],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110031"},{"annotations":[118379],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051447"},{"annotations":[100643],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1902103"},{"annotations":[109947],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0045128"},{"annotations":[104242],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0075296"},{"annotations":[92673],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1903024"},{"annotations":[120241,118483],"is_not":false,"rel_names":["is_a","regulates","positively_regulates"],"summary":null,"term":"GO:0140648"},{"annotations":[75368],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0110032"},{"annotations":[108591,118231,91007,104329],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1904514"},{"annotations":[115785],"is_not":false,"rel_names":["regulates","is_a","positively_regulates"],"summary":null,"term":"GO:1905326"},{"annotations":[121116,121117,98993,109023],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0051446"},{"annotations":[97112],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:1905191"},{"annotations":[91008],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0010845"},{"annotations":[94135],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0034307"},{"annotations":[106882,96493,111025,103580],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:0110044"},{"annotations":[103297],"is_not":false,"rel_names":["is_a","regulates"],"summary":null,"term":"GO:1905325"},{"annotations":[98886],"is_not":false,"rel_names":["is_a"],"summary":null,"term":"GO:0040020"}]},"cv_name":"biological_process","definition":"Any process that modulates the rate or extent of progression through the meiotic cell cycle.","definition_xrefs":["GOC:dph","GOC:ai","GOC:tb"],"direct_ancestors":[{"relation_name":"is_a","term_name":"regulation of cell cycle","termid":"GO:0051726"},{"relation_name":"is_a","term_name":"regulation of reproductive process","termid":"GO:2000241"},{"relation_name":"regulates","term_name":"meiotic cell cycle","termid":"GO:0051321"}],"gene_count":46,"genes_by_uniquename":{"SJAG_00145":null,"SJAG_00266":null,"SJAG_00364":null,"SJAG_00457":null,"SJAG_00987":null,"SJAG_00993":null,"SJAG_01000":null,"SJAG_01082":null,"SJAG_01113":null,"SJAG_01311":null,"SJAG_01330":null,"SJAG_01345":null,"SJAG_01401":null,"SJAG_01515":null,"SJAG_01680":null,"SJAG_01837":null,"SJAG_01956":null,"SJAG_02169":null,"SJAG_02404":null,"SJAG_02481":null,"SJAG_02592":null,"SJAG_02712":null,"SJAG_02723":null,"SJAG_02771":null,"SJAG_03048":null,"SJAG_03327":null,"SJAG_03371":null,"SJAG_03438":null,"SJAG_03486":null,"SJAG_03501":null,"SJAG_03525":null,"SJAG_03720":null,"SJAG_03854":null,"SJAG_03887":null,"SJAG_04126":null,"SJAG_04140":null,"SJAG_04259":null,"SJAG_04280":null,"SJAG_04287":null,"SJAG_04332":null,"SJAG_04682":null,"SJAG_04813":null,"SJAG_04853":null,"SJAG_05153":null,"SJAG_05288":null,"SJAG_06638":null},"genotype_count":0,"interesting_parent_details":[{"rel_name":"regulates","termid":"GO:0007049"},{"rel_name":"is_a","termid":"GO:0008150"}],"interesting_parent_ids":["GO:0008150","GO:0007049"],"is_obsolete":false,"name":"regulation of meiotic cell cycle","references_by_uniquename":{"GO_REF:0000033":null,"GO_REF:0000107":null},"synonyms":[{"name":"meiotic cell cycle modulation","type":"exact"},{"name":"meiotic cell cycle regulation","type":"exact"},{"name":"meiotic cell cycle regulator","type":"related"},{"name":"modulation of meiotic cell cycle progression","type":"exact"},{"name":"regulation of meiotic cell cycle progression","type":"exact"},{"name":"regulation of progression through meiotic cell cycle","type":"exact"}],"termid":"GO:0051445","terms_by_termid":{"GO:0010845":null,"GO:0010846":null,"GO:0033315":null,"GO:0033316":null,"GO:0034307":null,"GO:0040020":null,"GO:0045128":null,"GO:0051445":null,"GO:0051446":null,"GO:0051447":null,"GO:0051598":null,"GO:0051728":null,"GO:0075296":null,"GO:0075297":null,"GO:0110031":null,"GO:0110032":null,"GO:0110044":null,"GO:0110045":null,"GO:0140648":null,"GO:1902103":null,"GO:1903024":null,"GO:1904514":null,"GO:1905191":null,"GO:1905318":null,"GO:1905325":null,"GO:1905326":null}}


id: PBO:0116577
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase feature property types","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"gocam_title_termid","termid":"PBO:0116577"}


id: FYPO:0003606
data:
  {"annotation_feature_type":"genotype","cv_name":"fission_yeast_phenotype","definition":"A cellular process phenotype in which the duration of prophase of the first meiotic nuclear division is shorter than normal.","definition_xrefs":["PomBase:mah"],"direct_ancestors":[{"relation_name":"is_a","term_name":"abnormal meiosis","termid":"FYPO:0000051"},{"relation_name":"is_a","term_name":"decreased duration of meiotic cell cycle phase","termid":"FYPO:0006851"}],"gene_count":0,"genotype_count":0,"interesting_parent_details":[{"rel_name":"is_a","termid":"FYPO:0001985"},{"rel_name":"is_a","termid":"FYPO:0000631"},{"rel_name":"is_a","termid":"FYPO:0000002"},{"rel_name":"is_a","termid":"FYPO:0005447"}],"interesting_parent_ids":["FYPO:0005447","FYPO:0000631","FYPO:0000002","FYPO:0001985"],"is_obsolete":false,"name":"decreased duration of meiotic prophase I","synonyms":[{"name":"reduced duration of meiotic prophase I","type":"exact"},{"name":"short meiotic prophase I","type":"exact"}],"termid":"FYPO:0003606"}


id: PBO:0090556
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"assembly chaperone for ribosomal protein Rpl4, TPR repeat protein Acl4","termid":"PBO:0090556"}


id: PBO:0113278
data:
  {"annotation_feature_type":"gene","cv_name":"PomBase gene products","gene_count":0,"genotype_count":0,"is_obsolete":false,"name":"Plasma membrane transporter for choline, ethanolamine, and carnitine; involved in the uptake of nitrogen mustard and the uptake of glycine betaine during hypersaline stress; co-regulated with phospholipid biosynthetic genes and negatively regulated by choline and myo-inositol; human FLVCR2 (MFSD7c), a choline transporter involved in Fowler syndrome, can complement the yeast null mutant","termid":"PBO:0113278"}


id: GO:0046996
data:
  {"annotation_feature_type":"gene","cv_name":"molecular_function","definition":"OBSOLETE. Catalysis of an oxidation-reduction (redox) reaction in which hydrogen or electrons are transferred from NADH or NADPH and one other donor, and the latter donor is dehydrogenated.","definition_xrefs":["GOC:mah"],"gene_count":0,"genotype_count":0,"name":"obsolete oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with NAD(P)H as one donor, and the other dehydrogenated (obsolete GO:0046996)","synonyms":[{"name":"oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with NADH or NADPH as one donor, and the other dehydrogenated","type":"related"}],"termid":"GO:0046996"}


id: MONDO:0005768
data:
  {"annotation_feature_type":"gene","cv_name":"mondo","definition":"Tuberculosis that involves any region of the gastrointestinal tract, mostly in the distal ileum and the cecum. In most cases, mycobacterium tuberculosis is the pathogen. Clinical features include abdominal pain; fever; and palpable mass in the ileocecal area.","definition_xrefs":["MESH:D014385"],"direct_ancestors":[{"relation_name":"excluded_subClassOf","term_name":"abdominal tuberculosis","termid":"MONDO:0000369"},{"relation_name":"is_a","term_name":"extrapulmonary tuberculosis","termid":"MONDO:0000368"},{"relation_name":"is_a","term_name":"digestive system infectious disorder","termid":"MONDO:0043424"}],"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":"gastrointestinal tuberculosis","secondary_identifiers":["ICD9:014.81","EFO:0007280","ICD9:014.80","UMLS:C0041312","ICD9:014.86","DOID:404","MEDGEN:52885","SCTID:186225008"],"synonyms":[{"name":"tuberculosis of gastrointestinal tract","type":"exact"},{"name":"tuberculosis of intestines, peritoneum and mesenteric glands","type":"exact"},{"name":"tuberculosis of intestines, peritoneum, and mesenteric glands","type":"exact"}],"termid":"MONDO:0005768","xrefs":{"Monarch":{"xref_id":"0005768"}}}


